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Me at crazy golf with my friends playing crazy golf in my wheelchair. 👩‍🦽 I never thought I’d try and find it got some amazing and proud of myself when I did

January 28, 2023

This was 4 years ago when I first left school.

How far I’ve got with my scrap with my support worker this Friday night please see the pages that I have completed tonight in pictures bro thank you ☺️

January 27, 2023

Disabled Woman And Service Dog Asked To Leave Hanley Pub

January 27, 2023

A disabled woman said she was reduced to tears when asked to leave a pub because of her assistance dog.

Louise Harris, who has multiple sclerosis, was approached by a manager in Hanley Wetherspoons on 13 January.

“I was in utter shock, I could not believe it,” said Ms Harris, adding she had provided proof cockapoo Bella was a service dog.

Wetherspoons said in a statement it had a “no-dog policy”, but assistance dogs were allowed in its pubs.

The chain added it was in contact with Ms Harris to understand her concerns.

Ms Harris was socialising with friends over food and cups of tea at the Reginald Mitchell on Parliament Row, when the staff member came over about 19:00 GMT, she said.

Bella, who helps her owner with daily tasks made difficult by her limited mobility, was lying on a mat under the table in a clearly marked jacket.

“We’d been in there for a good few hours and then the manager come over to me and asked me to leave,” Ms Harris told BBC Radio Stoke.

“[He said] ‘we don’t allow your kind of dog in’ and I said, ‘she’s an assistance dog she has a coat on saying she’s an assistance dog, please do not ignore me’.”

Ms Harris, who was wearing a hidden disability lanyard and had crutches with her, said she felt intimidated and frustrated during the incident.

“I came outside and just cried because I was humiliated, discriminated and in front of my friends and that we’d been in there for five hours,” she said.

She added that an action card listing her disabilities and paperwork on her phone were “ignored” by the manager.

The Equality Act 2010 prevents businesses refusing entry to those who need an assistance dog with them.

Ms Harris said she and Bella had previously been allowed entry to the same Wetherspoons, and another in nearby Newcastle-under-Lyme, and she had “no idea” why she had been challenged on this occasion.

She has contacted the Equality Advisory and Support Service to intervene with the venue on her behalf.

How I didn’t let the pandemic stop me enjoying Friday nights with my friends instead I turned Grandma’s living room into a nightclub disco lights and all. Here is a picture of me partying with my friends on zoom after I turned Grandma’s living room into nightclub.

January 27, 2023

Video of fun and games

January 26, 2023

https://www.facebook.com/messenger_media/?attachment_id=1192107841681042&message_id=mid.%24cAABa-avRNxeMFXFYaWF5CulSbgx-&thread_id=100027676781699

Visually-Impaired Nottingham Law Student Praises Book Scheme

January 26, 2023

    A visually-impaired law student has said he used books from a sight loss charity to help him achieve top exam grades and a place at university.

    Charlie Beeston, 19, from Lincoln, has had optic nerve hypoplasia, nystagmus and ocular albinism from birth.

    During his studies, he made extensive use of the Bookshare service operated by sight loss charity, Royal National Institute of Blind People (RNIB).

    He is now studying law at the University of Nottingham.

    The service provides books, worksheets and resources free of charge to teachers, pupils and students, which can be downloaded in accessible formats including electronic braille, PDF and audio.

    ‘Flick of a switch’

    Mr Beeston, who is in his second year at the university, said: “It basically provides alternative formats of loads of books and when I was at school, it was very important to me.

    “I could sit and learn alongside other students, rather than going elsewhere to have something read to me.”

    Mr Beeston, who has severe sight impairment, achieved As in A-level psychology and history and a B in politics.

    He said it was hard to gauge if he would have got those grades without the service, as his school – The Priory Academy LSST in Lincoln – had been hugely supportive, but he said the books had simplified things.

    “It made everything available to me at the flick of a switch,” he said.

    During the Covid lockdown, he said he had also used Bookshare to help guide his sister, who has autism, through her own GCSE examinations.

    The service recently announced it had reached the millionth title in its collection.

    David Clarke, RNIB’s chief operating officer, added: “I am delighted that RNIB Bookshare has reached this incredible number of one million titles.

    “This means more children and young people are getting support with their learning and are able to do this alongside their sighted classmates.

    “I know from my own experience as a student how vital it is to have materials available in formats other than print.”

    The most expensive cruise in the world what I thought of the general make up of it and the excursions they have on board their ships.

    January 26, 2023

    I thought that having fridge space or refrigerated areas the size of 5 regular bungalows was a bit excessive and I think it was just for all the expensive alcohol such as the champagne the rosé and lemonade what do you think. But I suppose if you are rich you can have your cake and eat it. What would you do if you are rich would you go on the most expensive cruise in the world or buy a fast car. I know if I was rich I would live in a place with a spa that could be reached by hoist. I would go to Revitalise which is a specialist hotel for disabled individuals to have their needs met but it is extortionate and is marketed by the price they charge to the rich disabled and not the one who have to rely on benefits and government assistance and are students and don’t yet have a career because they are studying for the career they wish to have.

    £1 appeal! If all you who follow me could donate £1 tonight to my Crowd Funding page I would very much appreciate it, as the crowd funding page hasn’t even had one donation yet. If you wish to donate more than £1 then you can but you do not have to, just as many of you as you can donate £1💕 thank you for continuing to help me reach my goal of my DofE qualification 🥰💵 (see below for link)

    January 25, 2023

    https://www.justgiving.com/crowdfunding/maya-richards?fbclid=IwAR1U_olyAJnOUQHQlXw21-p_pvECH-nRtcX1i5D6fRF6ueB7sBmP9tzSojk

    I Have Low Vision, So I Built An App To Help Others Like Me

    January 25, 2023

    Rebecca Rosenberg, who has an uncorrectable visual impairment, found that there was no suitable technology to help her.

    She decided to create ReBokeh, an app which has adjustable smartphone camera filters to allow users to change how things look, and navigate the world more easily.

    Ms Rosenberg hopes it will help other people with low vision.

    BBC Click’s Paul Carter reports.

    See more at Click’s website and @BBCClick.

    Which camping or blow up bed do you think would be the most comfortable for someone with cerebral palsey that I can purchase of Amazon.

    January 25, 2023

    I am thinking of purchasing one to make me more comfortable when I am on my DofE expedition. Have you ever seen a human dog bed they look so fluffy and something I would be comfortable in but unsure whether they would be suitable for a tent does anybody know because I love fluffy things and the fluffier the better and the less spasms I would have during the night especially as it is obviously going to be cold when I go camping. Let me know whether anybody has used these in tents please.

    £1 appeal if all you follow you could donate £1 tonight landing page I would very much appreciate it as the crown landing page hasn’t even had one donation yet if you wish to donate more than £1 then you can but you do not have to just as many of you as you can donate £1 thanks a different continue to help me reach my goal of my baby qualification 🥰💵

    January 24, 2023

    looking me inspection of say different where you will find my cloud landing pages or in my recent log and I didn’t smoke with the crowd standing attack very recently thank you

    Visiting my grandma’s dog this weekend, he looks so cute in his jacket that we all bought him this Christmas

    January 24, 2023

    Hollyoaks Boss Confirms New Storyline For Brooke Hathaway This Year

    January 24, 2023

    Hollyoaks is lining up a new storyline for Brooke Hathaway this year.

     

    The character (played by Tylan Grant) was first introduced in 2018, and they made history as the first regular autistic character in the soap.

    While things have been quieter for Brooke lately – apart from a relationship with Ripley, who left last year – executive producer Lucy Allan has teased more onscreen time for the character in 2023.


     
     

    We’ll be looking at Brooke in terms of a young person with autism entering the workplace, and how they go about seeking employment,” Allan told Inside Soap. “That will also see a building friendship between Brooke and Lizzie.”There’s a real joy to Lizzie as a character, she’s a mother hen. But sometimes the assumptions people make about what they know about autism might not be quite right. It’ll be a learning process.”

    Brooke shared that they are non-binary in 2021 in powerful scenes on the soap after spending months questioning their gender identity with the support of Ripley.

    Speaking at the time, Tylan spoke about how the storyline chimed with him, saying: “This storyline in particular means a lot to me – being non-binary myself, seeing the progression of Brooke’s self-growth and self-discovery has been emotional and empowering for me.”I hope anyone out there who is coming to terms (or confused) with their identity can feel heard, encouraged or that I can be the representation that I so needed when I was younger.”

    Has anybody seen that programme on channel 4 about the biggest cruise ship in the world.

    January 24, 2023

    If so what did you think of it. As I watched one episode today and will continue watching the rest of the episodes tonight and tomorrow morning before my care assistant comes to take me to choir but I thought they had more money than sense but it could make for a good retirement home if they just cruise around all the time instead of paying to go into a care home or assisted or sheltered housing provision. What did you think of it compared to other cruise ships that you may have seen on TV or been on, on holiday? I thought it was over the top and I would be more scared of breaking some of the precious crockery or staining one of the sweets sofas or something like that and having to replace what I broke.

    Disabled People Stuck At Home Over PIP Travel Pass Problems

    January 23, 2023

      Disabled people are “stuck in their homes” and feel excluded from society because travel passes have stopped working, a charity has said.

      These allow them to use Transport for Wales (TfW) services for reduced fares.

      But users must prove evidence of receiving a benefit called Personal Independence Payments (PIPs), and many are still waiting for assessments.

      The Department of Work and Pensions, which assesses people, said waiting times have “greatly improved”.

      “I don’t leave the house,” said Lara Warlow, 42, of Bridgend.

      “I’ve kind of got to the stage where I’m not even noticing that I don’t do anything any more, it’s just the way my life is now.”

      Lara struggles to afford travel without the reduced fares. She has been unable to work since 2017 after an accident where she fell 30ft (9 metres) from a window.

      She was left with vocal chord paralysis, hearing loss and Bell’s palsy, which causes weakness in facial muscles.

      The only social thing she has done in the last couple of months is a weekly samba drumming class in Cardiff.

      While she is waiting for her PIP assessment, she has been limiting her travel to save money, but admits it could be months away.

      TfW offers a number of concessions to people with disabilities, including a third off for some services.

      Disability Wales said Lara’s is a common story, with more and more people telling the organisation they cannot go out because discounted passes have stopped working, meaning limited funds will not stretch.

      “It’s making disabled people really anxious because their day-to-day lives tend to cost more than non-disabled people,” said the charity’s Alex Osborne.

      “Then when we are at a time like now, with the cost of everything increasing, they haven’t got a lot of money left over each month.

      “The fact that they now have to try and pay full price for their travel, it means they can’t afford that, and it means that they’re just not going out or they’re having to give up something else.”

      She said it should be made easier for people to prove their status to access discounted services, adding many felt “excluded and stuck in their homes because they can’t renew their travel passes”.

      Ms Osborne called on TfW to consider accepting other documents as proof of eligibility, adding: “Maybe accepting a blue badge as evidence, or even a doctor’s note.”

      The Welsh government, which sets travelcard criteria rules, said it is “fully committed to supporting the rights of disabled people in Wales and are working closely with local authorities to ensure assessments are carried out in a timely manner”.

      TfW said: “We give individuals plenty of notice of up-coming reviews so they can make PIP appointments to get the evidence required for a disabled person’s bus pass.

      “If someone is deemed to be permanently disabled by their local authority, we no longer ask them to prove their eligibility on a regular basis.”

      The UK government’s Department of Work and Pensions, which is responsible for PIP assessments, said it was “committed to ensuring people can access financial support through PIP in a timely manner”.

      A spokesman said it was working constantly to make improvements, adding: “The latest statistics show clearance times have greatly improved, returning to pre-pandemic levels.”

      Doing experiments with balloons also my group last Monday

      January 23, 2023

      Picture of me sitting at my youth group talking to everybody that attended their and discussing what we are going to do through for our mad science experiment about static electricity

      January 22, 2023

      My Backpage of my scrapbook completed tonight.

      January 21, 2023

      Look how cute the baby picture of me is at nursery.

      Gofundme Page link

      January 20, 2023

      If you didn’t see it yesterday in the fundraising section of same difference. Here’s the gofundme link, you can click it where my full page will pop up and you can donate through this. Thanks Myah

      https://gofund.me/cc0199d7

      Fix Relationship With SEND Parents, Bristol City Council Told

      January 20, 2023

      A council must fix its “fractured relationship” with the parents of special educational needs (SEND) children, the government has said.

      Bristol City Council was referred to Whitehall last year after failing to reverse years of mistrust, a situation exacerbated by the SEND spying scandal.

      One campaigner said there are hundreds of unhappy parent carers in Bristol.

      The council said it is now planning to re-establish a “formal body to represent parents and carers”.

      It has been ordered to complete an “accelerated progress plan”, which needs to be submitted to the Department for Education (DfE) by 1 February, explaining how it intends to improve its relationship with parents and carers.

      In a statement to Bristol’s health and wellbeing board on Thursday, SEND parent and campaigner Jen Smith said “the number of unhappy parent carers in Bristol runs into the hundreds”.

      She said the council had “made it abundantly clear throughout 2022 that it does not wish to engage in co-production”.

      She accused the council of “tokenistic box ticking” and added: “The relationship with parent carers is fractured due to the way the council continues to behave.”

      Last year, leaked documents showed that council staff monitored the social media posts of SEND parents who were critical of the service’s poor quality.

      It later emerged the authority had also blocked DfE funding to Bristol Parent Carer Forum, the charity that had been liaising with it on improving SEND provision, and whose members were subject to the surveillance. The council insisted the two issues were unrelated.

      Improvement in four areas

      Ofsted and the CQC revisited the city in October to check progress in five areas of “significant weakness” identified by the original inspection in 2019, according to the Local Democracy Reporting Service

      A report published in November found sufficient improvements had been made in four of the areas – including lack of accountability of leaders at all levels, inconsistent timeliness and effectiveness in assessing SEND pupils, inadequate EHCPs, and high levels of underachievement, absenteeism and exclusions.

      But the fifth – “the fractured relationships with parents and carers” – had not been sorted.

      Inspectors said this “continues to affect the quality of co-production that takes place between area leaders and parents and carers” and added it would be referring the council to the DfE for “further action”.

      City council interim director of education and skills, Richard Hanks, told the board that although inspectors found a “more mixed view” from parents on the quality of support to youngsters than before, “it is not where it needed to be by this point”.

      Ofsted’s report said some parents “continue to lack trust in the system and feel that leaders are not acting in the best interests of children”.

      But the inspectors said the majority of those accessing services more recently had a positive experience – a conclusion disputed by SEND campaigners.

      Mr Hanks said the council acknowledged “that not all young people with SEND get the support they need as quickly as they could”, something they “need to continue to work on”.

      He said while they can make changes to the systems and processes in schools and settings, it would take time for it to “lead to a positive experience for all parents”.

      Does anybody know of any apps that you can find care assistant from that can take people on residential holidays/courses.

      January 19, 2023

      I want to start getting prices for the cost of a caregiver, but I’ve never used apps before to do this but want one that is recommended as I cannot go through reading reviews as my voice reader reads it like Darth Vader and I can’t understand it. Please let me know in the comment section below which one you would recommend or if there is any out there. If you know how much hiring a caregiver would be through the apps as I am normally funded through my local authority but for this trip they said they will not fund this trip and to do it through the company my local authority commissions would cost over £1000 for 24hr care for 5 days and that is for one expedition not two. I am based in the UK if that helps for the apps.

      my fair date for my training has been Putin and I am talking to you next month intern dogs near the end of the next level is different to the first level I did whitwood from now I will be training to silver and sleepy silver I want to see what the differences between levels I want to see whether it’s tired or not 🤣👩🏽‍🦽

      January 19, 2023

      NHS Crisis: Why Are Disabled People Disproportionately Affected?

      January 19, 2023

      The NHS is at crisis point. For many disabled people, trips to A&E or GPs can be quite regular, but the current hospital delays and lack of staff is impacting their overall health and has made them scared.

      Laura Miller, 50, is no stranger to hospitals, but she’s never seen anything like this winter.

      “I witnessed and experienced such severe conditions I feared for my life,” the 50-year-old wheelchair-user told BBC Access All. After her last hospital visit, she sought counselling for PTSD.

      This winter is the worst in NHS history. After two years of Covid-19, when people did their best to avoid hospitals, they are returning with exacerbated conditions. A fifth wave of Covid and the worst flu season in a decade have hit, alongside low staffing levels and strike action.

      The latest government figures revealed that in December, the average wait for an ambulance hit 90 minutes while A&E waits of over four-hours reached their highest level.

      For disabled people – a community which disproportionately relies on the NHS to keep them healthy – these statistics are worrying.

      Laura uses a wheelchair and has multiple health conditions including asthma and Postural Tachycardia Syndrome (PoTS), which is an abnormal heart rate which can cause fainting.

      She regularly needs emergency care, but remains traumatised by an incident in September when she went to A&E with Covid-19.

      LISTEN: You can hear more from disabled patients and doctors and their particular fears about this crisis on BBC Access All.

      Plus Lauren Mahon from You, Me and the Big C chats about cancer and bringing the award-winning podcast to an end.

      “The nursing staff told me I had to leave the bed I was in, as other patients were dying. As soon as I attempted to get out of bed, I collapsed and was shouted at by a doctor.”

      She says she was then “wheeled through to a room by myself” and left there despite needing the bathroom and water but couldn’t achieve these alone.

      Unable to remain in a sitting position, she manoeuvred herself out of the wheelchair.

      “I lay on the floor in a room that staff were walking by. No one came to my assistance.”

      Eventually, a hospital manager found her, but she had already spent significant time without the care she required.

      “The staff had left a disabled adult, sick with Covid, in a room with no access to the toilet, to water, and who was now traumatised after being forcibly removed and shouted at.

      “I realised that day that my disabled friends were about to enter a level of neglect even worse than they have previously experienced.”

      The disabled community is already feeling scarred. In 2021, the Office For National Statistics revealed that disabled people accounted for six in 10 Covid-19 deaths and many are fearful of returning to those numbers.

      GP, Dr Hannah Barham-Brown, based in Selby, understands those fears as a doctor who is disabled herself.

      “The whole NHS, right now, is a bin-fire,” she says.

      “Disabled people disproportionately need the NHS. We have conditions that need NHS care a lot more often, so we’re more likely to need the NHS in an emergency capacity.”

      As well as emergency care, she says regular appointments, that many disabled people require to maintain basic good health, are being postponed while clinicians are pulled away to deal with the crisis in A&E and on wards.

      “So the waiting lists grow and so our health outcomes are getting worse.”

      Earlier this month the government said the NHS would receive £250m to buy 2,500 beds in care homes, so some patients who are ready to be discharged from hospital, but need additional support, can be relocated.

      Labour’s shadow health secretary, Wes Streeting, called it “another sticking plaster” but frustrated Dr Hannah takes his analogy further.

      “It’s a wet plaster hanging off, letting infection in because we don’t have beds sitting empty in social care [settings].”

      She says disabled people are struggling to get adequate care anyway, let alone re-allocating available beds in a social care industry with 160,000 job vacancies.

      “If the staff don’t exist, if the beds don’t exist, then this is not a solution, is it?”

      It’s not just a physical medical emergency. The toll on patients with mental health needs or developmental conditions is acute.

      Anna Morell, who uses crutches to help with her mobility and works for Disability Rights UK, regularly needs to visit her local hospital. She says she was “gobsmacked” by the lack of pastoral care when she made several visits to A&E over Christmas.

      “There were people that were in mental health distress who’d been waiting 14 hours while suicidal with no help. It’s the worst place for mental health.”

      She said others with learning disabilities and autism were left in waiting rooms, “rocking” back and forth.

      Following the shocking statistics related to outcomes for disabled people in the pandemic, she says: “It’s scary for disabled people because the upshot is with this kind of crisis, we’re going to die.”

      Anna says as well as cash and staffing injections into the NHS, she wants Cabinet members, whose remit covers health, to spend time on the front line to understand the reality.

      “They’re looking at spreadsheets. If they’re not doing things on a human basis, they have no idea what needs to be done.”

      The Department for Health and Social Care said it was “prioritising health and care services with up to £14.1bn over the next two years to address the most pressing issues facing the NHS and social care”.

      It recently introduced a new requirement that health and care staff receive learning disability and autism training “appropriate to their role”.

      Despite the crisis, Dr Hannah, who used to be deputy leader of the Women’s Equality Party, says if you need health care, you must seek it out.

      She advises disabled people to make the most of available services including pharmacies and walk-in centres which might be able to help. She also says many GP surgeries are open to email queries if you need advice.

      “I think it’s about being quite savvy about all the different options that are available.”

      All of this really paints a pretty depressing picture.

      I’m sure every hospital is trying very hard to accommodate everyone. But like so many other issues in the NHS, waiting times – that experience of going into that very crowded, noisy environment – is one of the things that needs to be addressed.

      I think everyone should be concerned as a citizen. And for disabled people, there are extra concerns on top of that.

      Ultimately, this is a workforce problem . There aren’t enough staff and the issue is often pay. Sometimes you can earn more working for a local retailer.

      I’ve talked to staff, nurses, doctors and health care assistants. They really want to make it work and they’re trying extremely hard. It’s not their fault. It’s a system that is finding it really tough, coping with all the extra patient numbers.

      But I think the whole country wants the NHS to succeed and do well, but how to do that is a big debate for all of us.

       

      GoFundme/Crowdfunding Page

      January 18, 2023

      Please see the link to the crowdfunder and a picture of what the gofundme looks like on the front page of it. Please donate if you can as every little helps to go on my DofE awards and the support that I will need. My gofundme page is in the fundraising section of same difference, but here is a picture for you to ensure you are donating to the right person if you want to support my cause. Please go over to that section and donate if you would like to as the full page is there. I appreciate every single donation that I receive. I’m very keen to achieve this qualification in this new year of 2023 💵💰. Every little helps and matters to me, please share this post on your social media pages if you can so that we can spread the word and people can be aware of my story and the goal I am trying to achieve. Thank you same difference community for all your interactions and support. Thanks Myah

      Tube Feed Questions And Face Touching Upset Girl

      January 18, 2023

        How would you feel if the first question many strangers asked was “what’s wrong with you?” or “what’s that on your face?”

        That is the reality for 11-year-old Imogen from Caldicot, Monmouthshire, who said she has had enough after people started touching her face.

        Imogen has cerebral palsy and has been fed through a tube since last March because she was unwell and losing weight.

        “The most annoying thing possible with people, and adults do this too, is they stare at you and because it’s on my face they keep eye contact with me the whole time,” she said.

        “Normally I just stare at the floor and then they stop.”

        BBC Wales is following Imogen and her mum Catherine over the next year, as they navigate challenges that are faced by many families with a disabled child – accessing education and other services and seemingly endless medical appointments.

        Imogen has been home-schooled since she was six because her mum has been in dispute with the council about her needs, including over the provision of disabled toilets.

        Monmouthshire Council said all schools in the county had disabled toilets.

        Bespoke toilet facilities had been installed for Imogen, it added, in schools identified by the family, as well providing training and resources to staff.

        She hopes to re-enter mainstream education this year and start secondary school in September.

        Imogen has been undergoing treatment to try to help her walk and since September she has been in casts to stretch her muscles and could walk short distances in them.

        Last week, she tried new splints to give her better support, but the transition has not been straightforward, so for the moment it means that Imogen has to rely on her wheelchair again and crawl up the stairs in her house.

        There will be more doctors appointments, so it is a big year ahead, but one of the main things Imogen wants is to talk about is how people behave around her.

        “People grab your face. Touch you,” she said. “Once a random child picked this up [her tube] and said ‘what is this?’

        “The thing I struggle with is when I am with my friends who are all in wheelchairs, they get it,” she said. “But when I am trying to make friends with new people, the first question is always ‘what’s that thing on your face?’

        “It’s sometimes hard to explain because, especially a lot of children don’t understand the medical terms of it,” she said. “Sometimes I just say to the younger ones, it helps me stay strong like a superhero. It’s annoying.”

        Catherine says they became used to people staring when Imogen was younger and in her wheelchair but that was happening less as she has got older.

        But since having the tube fitted last year, Catherine said it became much more noticeable, recalling a difficult shopping trip before Christmas when they were stared at the whole time.

        “Staring at her makes her feel really uncomfortable and self-conscious,” said Catherine, who is Imogen’s full-time carer. “And I think people probably just don’t realise how uncomfortable it makes her feel.

        “Actually if they were to decide to spark up a conversation, not just touch her and stare. But it’s also how they ask. Sometimes we get ‘what’s wrong with you? Or ‘we hope it’s not permanent’.”

        “I would happily talk about it, if they asked me,” Imogen said. “They could have said, ‘if you don’t mind me asking, not meaning to be rude, why are you a wheelchair user?’

        “It just depends how they ask really. It’s ok to ask questions. We are not going to take offence.”

        Imogen is sport mad and plays tennis for Wales, as well as loving horse riding and basketball, swimming and surfing.

        So if you see her and her mum out on the court or on the beach, they are hoping you might stop and think about what you say and do around her and other people with disabilities.

        photos yesterday of my night haircut on Fri thank you for Monday work ewheels content later on today hope you all had an enjoyable Friday and happy Monday to Thursday 😆day hope you

        January 17, 2023

        help with cerebral palsy how terrible called me from doing the things I want to and participating in team but I enjoy and concert is one of them🎞️🎟️

        https://www.facebook.com/messenger_media/?attachment_id=5761504423933983&message_id=mid.%24cAABa-avRNxeL8abbG2FwGF74xRIq&thread_id=100027676781699

        WCA May Be Scrapped Or Overhauled

        January 17, 2023

        With many thanks to Benefits And Work.

        A number of national media outlets are reporting that the government is considering scrapping or overhauling the work capability assessment (WCA) as well as making it easier for claimants to return to their former benefits if an attempt at working fails.

        The WCA is a points based system used to decide if a claimant is eligible for employment and support allowance or universal credit.

        A white paper on benefits is due out in the next few months and it is claimed it will include changes to the WCA.  Ministers are said to be unhappy that the system currently focuses on what a claimant cannot do rather than what job they could do.

        Many Benefits and Work readers may feel that they have heard all these pledges before and that little ever comes of them.

        But with employers now struggling to fill vacancies and the number of people leaving the workforce because of illness at a record high, there is a strong incentive for the government to make changes.

        Allowing claimants to return to their former benefits if an attempt at working is not successful sounds attractive on the face of it.

        But given the enormous delays in processing claims, the impossibility of getting through to the DWP on the telephone and the department’s savage eagerness to sanction claimants, how many are likely to believe a smooth transition back to benefits would be possible?

        And how many employers will be willing to take on claimants with a long history of ill-health, especially if their condition is one that varies in its severity?

        Abolishing the WCA is clearly long overdue.  But the idea of replacing it with a system that tests what claimants can do instead ignores the fact that this is exactly what the WCA was allegedly designed to do.

        The reality is that replacing the WCA with a new assessment which is independent of a claimant’s own health practitioners is likely to lead to exactly the same problems as the current WCA.

        But, it seems to be increasingly likely that another attempt to overhaul the system to get more sick and disabled claimants into work is about to begin. 

        Would you welcome changes to the system?  And would you trust the DWP to return you swiftly and smoothly to your benefits if you tried work and had to stop again?  Let us know in the comments section below.

        You can read the full report in the Guardian

        Quadriplegic Cerebral Palsy: Mum Sees Son Walk For First Time

        January 17, 2023

          Lynsey Summers says she dreams about seeing her son walk.

          Jacob, 19, has quadriplegic cerebral palsy, which affects his arms and legs and means he uses a wheelchair.

          But thanks to a new machine at his school, Jacob has now stood upright and moved his legs for the first time.

          “I have dreams where he walks and that’s emotional, so to actually see that start to be real, I suppose it’s the closest I can ever hope for a dream coming true,” said Lynsey.

          “It’s a sensation he could never have experienced before.”

          Jacob, from Cardiff, cannot sit unaided so most of his movement has traditionally come from physiotherapy sessions.

          “We’d try to do a little bit in the morning, just to loosen him up,” Lynsey said, describing doing ankle turns and leg movements with him, which could be quite “stilted”.

          “It’s also very tiring for the person doing it, so it can only be done for a short time, especially because Jacob’s an adult now,” she added.

          “So to have a machine he can go in for a longer period and give him the sensation of walking that he’s never experienced before… he goes on there and you see the smile on him.”

          Ysgol y Deri is a special school in Penarth, Vale of Glamorgan, which caters for students aged between three and 19 with a range of learning and physical needs and autism.

          Physiotherapists at the school trialled the Innowalk device to see if it could help pupils.

          Eighteen months on, paediatric physiotherapist Amelia Stubbs, 31, said they had seen real benefits for pupils.

          “In the basic terms, it’s their wellbeing,” said Ms Stubbs.

          “They’re up and doing something active, which they wouldn’t normally be able to do.

          “We notice they’re much happier when they come to physiotherapy and really like engaging with us.”

          Lynsey said Jacob looks forward to his sessions: “He gets an endorphin rush when he’s been on it, so he’s in a much better mood.

          “He’s happy and jokey. He sleeps really well when he’s been on it. It helps with his personal care, bowel movements and achy-ness in his muscles. He really, really enjoys it.”

          Fellow pupil Seren, 14, also enjoys using the device.

          “It’s actually kind of nice. It’s fun if you have something fun to do in it,” she said.

          The school’s assistive technology technician, Aaron Hawxwell, had the idea of introducing virtual reality (VR) headsets to the experience.

          Using the perspective of children who used to be able to walk but cannot any longer, they tested a series of VR videos to determine which one offered the most realistic walking experience to the user.

          “Some of the kids who can’t talk, when you see their faces… you can’t put it into words,” said Mr Hawxwell.

          “Even us, who’ve been here a long time, we still tear-up. You go home and think about it. It just makes your day.”

          The school chose to purchase two machines after seeing positive results.

          “For us, we need to invest as much in pupils’ wellbeing as we do in their education,” said head teacher Chris Britten.

          “When the kids are well and they’re in a good place they can learn, and that benefits all of us – and that means our whole community, not just me, not just the teachers, but the parents as well and their families.”

          The second series of A Special School – based at Ysgol y Deri – begins on Monday at 20:30 on BBC One Wales and BBC iPlayer.

          Me and my support worker arena in the interval in the interval

          January 16, 2023

          Happy Monday and whatever cream on Monday can you have your whatever career or Monday can you have whether it be volunteering working or a group like me

          January 16, 2023

          Blind Artist Wants To Inspire Younger Generation With Braille Creations

          January 16, 2023

          A blind artist hopes to inspire a new generation with his Braille artwork.

          The Power of Touch is Clarke Reynolds’ first London solo exhibition.

          Born partially sighted in his right eye, Clarke became an artist when the deteriorating eyesight in his other eye forced him to give up his career. Today, he has only 5% of his sight left.

          The exhibition will showcase Clarke’s idiosyncratic, colourful Braille art, where he uses the tactile language of raised dots to recount his journey as an artist and convey the lived experience of blind and visually impaired people.

          Remember about my crowdfunding case that you find in the translation of changes website

          January 15, 2023

          would appreciate any donations gibbons that pain as it will help me ensure that I am able to to ensure the picture of my TV

          my hair braids that I decided to have another hot cake for Friday night

          January 15, 2023

          hairstyle before I went out on Friday night 💕💕💕💕💕

          January 15, 2023

          January 15, 2023

          it’s Friday night of me enjoying myself at the concer

          January 14, 2023

          Morning everybody at same different last night I went to the concert and really enjoyed myself I enjoyed the musical instrument costumes and the genuine atmosphere whatever you did on your pride a night hope you had the plan stage used for photos videos of me and of the concerts really how much than I have

          picture of bath bombs in the mould for them to text but they didn’t but they smell goo

          January 13, 2023

          Workers May Be Able To Still Claim Sickness Benefits

          January 13, 2023

          Some people claiming sickness and disability benefits could be allowed to keep receiving payments even if they find work, under plans being considered by the government.

          The proposals are aimed at getting more people back into employment.

          At the moment, benefits can be reduced or withdrawn altogether when a claimant returns to work.

          A source told the BBC there was to be a “radical rewiring” of how the benefits system operates.

          Recent figures suggest some 2.5 million people are missing from the labour market because of medical conditions.

          In his Autumn Statement last year, Chancellor Jeremy Hunt expressed concern that employment had not returned to pre-pandemic levels.

          And last week, Prime Minister Rishi Sunak said the government was looking at a range of measures to tackle the issue, adding: “We need to look at how our welfare system is operating… we would like to make sure that we are supporting and incentivising people who can be, to be in work.”

          Work and Pensions Secretary Mel Stride has been tasked with finding ways to reduce the number of people out of work.

          A Health and Disability White Paper detailing the new plans – which are yet to be finalised – is expected later this year.

          “One of the biggest challenges we’re facing is how to support people to start or return to work, and we are looking at this issue in depth,” said a spokesperson for the Department for Work and Pensions.

          The spokesperson added that the white paper would be published “in the coming months”, following “consultation with disabled people and people with health conditions to help shape our approach”.

          The Times reported that the white paper would recommend scrapping the “work capability assessment” system used to consider eligibility for benefits, with ministers describing it as a “perverse incentive to prove how sick you are”.

          It could be replaced with a process that instead asks claimants to demonstrate what work they might be able to take.

          The paper also said the Treasury was considering offering tax breaks to people for entering jobs.

          Labour has outlined plans to reform the system should it win power, announcing that claimants who take a job but then have to stop working within a year would not have to undergo another capability assessment in order to claim benefits again.

          Torsten Bell, chief executive of the Resolution Foundation think tank, told the BBC’s Today programme that the Covid pandemic had clearly had a major impact on sickness levels.

          However, he said: “People shouldn’t place much faith in changes to the benefit system leading to people who left during the pandemic returning [to work].

          “Once people have left the labour market for a large period of time they’re very unlikely to come back.”

          However, Mr Bell said that did not mean “you shouldn’t reform the benefit system to prevent rises in inactivity in future”.

          He added that the focus should be on keeping people with a disability or who have become ill in their current jobs.

          Before Christmas, reports suggested that the government was considering plans to persuade retired middle-aged workers back into jobs to boost the economy.

          Older people who have given up work could be offered what is being dubbed a “midlife MoT” to entice them back into employment, the Times reported last month.

          The House of Lords Economic Affairs Committee reported recently that a wave of early retirement following the pandemic helped to cause a huge labour shortage in the UK.

          It said some 565,000 more people were economically inactive in December than at the start of the pandemic.

          Good morning sound of silence good morning to you I hope you have a good Fri paymentsense down blow when I will see if I can have a go at making some of them and let you know whether I think it smells good when I have made them happy smiley Friday 😁day and I would like to know what your favourite bath bomb scent is Chinese vanilla what’s yours

          January 13, 2023

          Local Authorities Spending On SEND

          January 13, 2023

          This is a guest post.

          The i on 18th December 2022 reported that local authorities have spent more than £325m in the past 8 years defending cases against parents in the education tribunal (SENDist), the vast majority of which they lose. This news will be shocking to many, but as a solicitor representing families in this arena, this completely aligns with my own experience.

          I have attended tribunal hearings where local authorities are opposing provision sought by families, but are unable to produce any expert evidence whatsoever to support their position; this is doomed to fail. I have also represented families where Education Health Care Plans (EHCPs) have been denied to children with clearly evidenced special educational needs (SEN) which cannot be met without additional provision – these families have gone on to successfully challenge the local authority and their child has been granted a full EHCP with significant support, including full time 1-2-1 learning support assistance.

          Unconscionable as it seems, one can’t help but think this cynical approach on the part of local authorities is deliberately designed to put families off the process, in the hope that they will lose their nerve before the hearing date or, keeping in mind the many demands on families of children with SEN,  that they will run out of time, energy and resources to engage in the fight. The further explanation, that fighting cases delays local authorities having to pay for support until after the hearing date, is equally plausible.

          One of the main problems is the rarity of costs orders against local authorities in the education tribunal. The default position in these cases is that each party bears their own costs. Therefore, if a parent fights a claim to tribunal and wins, they bear their own legal costs of so doing, which can be significant. Unless local authorities are penalised financially for these kinds of tactics, they have no incentive to change their approach. Surely, they would adopt a different approach if they knew there was a real risk that they would be ordered to pay the successful party’s costs by the tribunal. In this broken system, families are instead forced to incur their own legal costs to fight untenable arguments put forward by local authorities, with no meaningful route to recovering these costs even if they are successful in the tribunal. And all while their child is without the support they often so desperately need.  The structures designed to support children with SEN are crumbling, and it is families and children who are suffering.   

          Claudia Hillemand, Partner in the Child Brain Injury team at Bolt Burdon Kemp

          Going to paint my nails awkward now take nail out take nail night out nail varnish

          January 12, 2023

          lipstick powder and paint lipstick nail varnish and blushes as well well as take sometimes too although I don’t think I will wear tomorrow I will make the evening and I am getting ready because her lovely bit of Google YouTube one of my person along with my Love2Shop for makeup and fashion and yes I have cerebral palsy that price I shocked like drop the same as anybody out and I’m enjoy doing this with friends and family like any other quinti three-year-old yes I’ve got silver cordy but why should people see me different why is it the public you is that you have cerebral palsy so you should do nothing and people give people like me in wheelchairs stairs will be out in public like this there thinking what are you doing here this is why I want to spread the word that I like many other things that other 23 year olds like I just do a lot more of it because I think many of the 22 year olds made like maths science but don’t have the time because they have all time jobs commitments careers and field where is I’m lucky that I can spend more time on my passion so actually in a way I can come lucky to be in this position there is a stigma attached to people who are disabled and are the education because they believe he should be in education and employed as well but this table people in education on our education and employment and wider life so education have been the priority so that we can get called jobs careers and opportunities as homemade Street counter this is why I want to spread positivity and awareness but we are the same as everybody else and should be treated like it and not down on as people who are this table we do the same wear make-up you go out with party and we also good work it experience like everybody else to placement everybody else we just might do it differently differently isn’t to be crowned a prom this is the message that society needs to take note book thank you everybody who is ready awareness with me it’s a different

          12 hours and go to my concert really surprises because this Friday is going to be Frid will be happy and having 🥂🐍🐍🍴🍻🍴🍾🍾ay have a happy Friday everyone at 10 d Friday’s uncle be silly going out for a meal and having wine or champagne Friday #hashtag Tesco #we’ll have come #going out to a concert #love music music lab xxifferent

          January 12, 2023

          January 12, 2023

          Remember my gofundme is remember my gofundme is on my previous post or you can get to it through the grazing bit of same difference if you you can record to please no one leave them sell short back that would help to achieve in the D of E girl thank you all there is just giving page in the prem grazing change different as well thank you just a reminder and remember that I appreciate fuel😆xxxx

          Stream on YouTube which I’m going to wear on my night out tomorrow #christmas boi got with tickets from the box office and all ready to go so excited tonight 💕 going to the concert with Molly lovely and lovely to go with itl outfits for night out 🎉👗😍🎟️

          January 12, 2023

          YouTube for another tomorrow with my support worker and will show you what colours we have chosen and tell the bath bomb turn out and may take a picture of the and action in case you want to try that to yourself keep your eyes out for this thank you you was of 10 different👁️👀👀👁️👀👀👁️😁👁️😁👀👀👀👁️👁️

          January 12, 2023

          public bus drivers attitude towards me as a wheelchair user look at that Pokémon keyboard today in my wheelchair the disrespect that they have for me as a wheelchair user

          January 12, 2023

          play do not realise greatest become disabled everybody disrespect you want to call your back please first driving you so could become the table one day you never know what is around the corner for anybody and please make sure your ramp to work in before you leave the pasta to you for the bath safely and do not be rude to quarter and tell them that they need training because you couldn’t be bothered to check that the rent work before leaving the bus depot just be mindful of our community and people with wheelchairs and walkers that might need to use your best friend and be helpful and respectful little time please I hope you pick this message on board today you know anybody who is above or if you are a bus driver driving for your community because I want to do is water bath with no proper like anybody else I don’t think really that is too much well because we are people we are not yeah equipment to get on and off the bath I had today with the public buses with mood towards me my staff member who was supporting me and embarrassing for the rest of the public that was on the bath he didn’t having a member of the community to get to Wilton and the back without the RAM this is embarrassing not helpful and shouldn’t be happening in this day and age of 2023 get it right and treat us with respect turn to every public transport worker who pick this message on board

          Ready to return to choir today day.of after the Christmas holiday already to return to choir today after the Christmas holiday all wrapped up for the weather about to get the bus

          January 12, 2023

          You, Me And The Big C Podcast: Hosts ‘Ready To Hang Up Headphones’

          January 12, 2023

            The presenters of a BBC podcast about living with cancer have said they are ready to “hang up their headphones”.

            Lauren Mahon and Steve Bland said they planned to stand down from presenting the award-winning podcast You, Me and the Big C.

            The show launched in 2018 with Mahon presenting alongside BBC Radio 5 Live newsreader Rachael Bland and Dame Deborah James.

            Bland died six months later while Dame Deborah died last year.

            The podcast takes a candid look at cancer, discussing matters such as telling your family and friends as well as practical matters, such as hair loss and tips for dealing with finances.

            Steve Bland, Rachael’s husband, took her place on the podcast after she died.

            Speaking to BBC North West Tonight, Mahon, who is five years clear of cancer, said: “I have struggled over the last year getting back in that studio without their seats being filled.”

            The Londoner said: “I’m still processing it all.

            “In what other job than the army would you go into work thinking you may lose colleagues, and so it’s very hard because there’s not many people who get it. It’s challenging.”

            She said she has had “so many chats” with Steve about the podcast continuing as it is a “public service” but “we don’t feel like it’s for us to continue it”.

            “How do we get back into that studio without these two remarkable women that began this podcast?

            “People are getting diagnosed everyday – that’s not going to change. The world of cancer changes. So I think it would be more appropriate and probably more poignant and relevant to get people that are going through it now.”

            Steve said there would not be many more episodes from them and it would be a “long goodbye”.

            He told BBC Breakfast: “We’d like the podcast to carry on because it’s a really important thing for so many people.

            “It just takes a toll and it’s heavy and it’s hard to kind of keep talking about this stuff – particularly when we’ve had to deal with obviously Rachel and Deborah over the last few years.

            “There aren’t many people doing podcasts where two people have died from the subject matter. It’s a tough thing to keep talking about.”

            The announcement comes as the pair announced they will record an episode with a live audience later this month. Those wanting to be a part of the audience can enter an online ballot for a ticket.

            X is everybody at same different today 2023 is so what made it better than the previous year was it it your actual towards the expectation or your work or study environment let me know in the comments everybody get same different to the good 2023 so far and will continue to have a good 2023 best wishes and good luck for 2023 from Maya

            January 11, 2023

            The timer in the winter Viking using a protocol as it is too cold for me in winter to do this

            January 11, 2023

            picture of me ready to go biking in the summer can’t wait until it’s permit again and I get to do this biting is one of my favourite summer activity 🙂

            opinions of the person that are really not helpful or constructed when starting your mu just because they are lazy and cry and disrespect you like if you are a baby York 23 years old and they don’t you use the same as you were 23-year old without noticed ability they don’t you you just need someone who needs assistant away 23-year old save you you like this you are a toddler some of them even poaching you on money so do you want a cup of tea in public and I don’t see to see that you can’t walk that you are not deaf or stupid as cerebral palsy doesn’t affect your internet on its own and certainly for me so it will call you doesn’t affect my internet at all it is a learning disability that expect intellect but not all learning disability can do that some of them han but some of them are just something the individual has to live with ok mum I heard you but this was great as we are not children we are adult in the eyes of the law and in the eyes of we are the same we just use reels instead of leg I will leg whether we use those wheels 24-hours a day like my town or whether we use those real or some of the day like some people with cerebral palsy to to me I am no different that is clearly not how I’m viewed by others this is frustrating and drop call every person would sewable call me in England and across the world everybody with cerebral palsy be respected distain is everybody out respect and respect when they are be spoken to because 30 is also very important to me and not just expecting respect from us but not giving out it it’s making talk to her anyway they want I would be interested to hear your opinions if then you’ve you are cerebral palsy peppers or will chair uses either full-time or part-time would love to hear you on

            January 11, 2023

            From making on Friday I am going to make from which colours do you think I make blue pink yellow green lilac or some ABBA covers put in the comments what colour you would make yours if you were making them and I will make them and showcase then on Friday morning

            January 11, 2023

            forward to Friday’s night out be live music 🎵🎶🎵 music on phone I I love cloud music and blind music the load of the bed and the more context ok she’s the better

            January 11, 2023

            ‘My First Time Going To The Gym As An Amputee’

            January 11, 2023

            A woman has described going to the gym for the first time since having her leg amputated as “like walking into a bit of a lion’s den”.

            Sian Green, 32, from Leicester, had her left leg amputated below the knee after a taxi driver mounted a kerb and crashed into her in Manhattan on 20 August 2013.

            Ms Green said: “I feel it’s very common to feel [nervous] about walking into a gym, even if you don’t have a disability.

            “I have finally done it without any assistance and I feel great.”

            Guide Dog Shortage: The Blind People Who Train Their Own Guide Dogs

            January 10, 2023

              In early January a shortage of available guide dogs was reported. For some visually impaired people the wait is too long and they decide to train their own guide dogs.

              Isabel Holdsworth had been making the daily commute across London from Dagenham to Kings Cross for years. Being visually impaired she had worked with five different guide dogs, until it came to a sad and abrupt end.

              “My dog died suddenly and I had to go to work and college the next day – two tubes, a 40 minute walk – with no dog,” she told BBC Access All.

              She used her white cane instead, knowing it could be a long time before she was matched with another dog. But it wasn’t easy.

              “I was on Liverpool Street Station and almost fell in front of the Tube,” she says. “I thought ‘I can’t do this anymore’.”

              She had an idea – could she train her own dog?

              It’s not a common way to go about it, but for years people have been doing this. The big question for guide dog owners is, if a dog is self-trained and not accredited by a big organisation, will they be allowed to take it to places dogs can’t usually go, like restaurants, shops and in taxis? The answer is yes, the law doesn’t make a distinction.

              Isabel started researching the possibility of training her own dog and spoke to others who had done so.

              She felt confident she could also do this and began searching rescue centres until she found Lucy, a one-year-old Labrador. Lucy hadn’t had the best start in life with little socialisation and family life but Isabel felt she had found the right dog.

              Having taken Lucy home, Isabel invested in a training clicker and food to reward Lucy and then booked a weeks leave from work to get started.

              Abigail Hughes understands Isabel’s drive to do this. She co-founded PAWtected CIC, an organisation that works with about 80 people every year to train their own assistance dogs. She says she started offering online and in-person courses when she realised dogs weren’t always available for people who needed support, including autistic adults.

              “You’ve got lesser-known dogs like allergen detection dogs, so that you don’t come into contact with something you’re severely allergic to,” she says. “There are dogs who can help with PTSD and other traumatic circumstances.”

              Back in London, Isabel ventured out with Lucy. She had bought a harness and, armed with her trusty cane which she used at the same time, they started walking the street they lived on.

              One of the first tasks was to teach Lucy to avoid obstacles. Isabel knew there was a lamppost on her road so she braced herself then “smacked into it and jumped back” yelping in pain.

              Isabel made a huge deal about the pain hoping Lucy would take note. Then they tried the approach again.

              “Lucy did a great big wide circuit around it. I didn’t really have any problem with obstacles after that.”

              This isn’t a standard way to train assistance dogs. It’s usually pain-free and involves lots of repetition and positive reinforcement with treats.

              Crossing roads was another essential and involved Lucy trying to learn that she mustn’t always follow the commands her owner gives her because it might be dangerous – something called “intelligent disobedience”. That means if Isabel instructs Lucy to cross the road but there’s a car coming, Lucy must refuse.

              Being a trainer who is blind, Isabel had to ensure she knew the layout of the road and where cars might appear before practising.

              She says it took about four months until she had “absolute trust” in her dog. But it paid off. When Isabel hadn’t heard a quiet electric car approaching, Lucy stopped Isabel from getting hit.

              Isabel’s aim had always been to get back to commuting with a dog and after just seven days of training she felt Lucy had learned enough to set them on their way.

              But returning to the office wasn’t all plain sailing.

              “The first day Lucy went into the office, she pulled down the soft walls between the offices. She ate through the boss’s phone cable and network cable.”

              Happily the company was understanding.

              Isabel says it took about two years to fully train Lucy. It’s a similar length of time that Guide Dogs, the UKs biggest provider of assistance dogs, takes to train its puppies before they are matched with a partner.

              Guide Dogs is currently struggling to meet demand. The Covid pandemic paused breeding, training and socialising for five months. As well as fewer dogs, the number of those making it through the process dropped from 65% to less than 50% – the lowest in decades – and the average waiting time for a guide dog increased to 18 months.

              The organisation said it was “devastated” by this, in its annual report. “In all our 90 years, we have never had two years as tumultuous and challenging as 2020 and 2021.”

              One way it is trying to mitigate this, and to diversify its gene pools, is by working with international partners. In 2022 it received dogs from America, Japan and Finland.

              Tim Stafford, its director of canine affairs, says dogs bring “incredible benefits” to a person’s life” but he believes guide dogs should be independently assessed rather than owner-trained to “provide clarity, reassure the public and service providers”.

              Although receivers of many guide dogs are used to getting dogs from a big charity, many other assistance dog charities are not so big and so the onus is on disabled people to obtain and train their own dogs.

              Abigail says PAWtected CIC has helped hundreds of people and on a practical level it can be quite “simple” to start training a dog for tasks such as taking your socks off.

              “You start off by playing a game of tug with the sock,” she says. “Then you put the sock on your foot, leaving a tail at the end, and encourage them to play tug at the end of your foot so that they can pull it off. It builds up really slowly through fun games.”

              Sadly, Lucy died at the end of 2022 but for Isabel the hundreds of hours of training paid off. “Lucy was the best guide dog I ever had,” she says, but adds that time and expense, such as vet bills and public liability insurance, need to be factored in before anyone attempts it.

              “It’s not an easy thing to do but it’s not impossible for a blind person to train their own dog. It’s the buzziest feeling ever.”

              Proof of our progress

              January 10, 2023

              night I love live music allowed in the Becca and the best bit is all the musical instrument also love that as well especially romantic when it’s day really try to and really glad that I getnight now on Friday and see some live music

              January 9, 2023

              Can I get her to ruin my jewellery enjoyed any 23-year old cerebral palsy but the cerebral palsy won’t stop me from going to karaoke because I love to park and anybody else my hand and see different band play in concert and have some cocktails or wine all wine music is one of my favourite pudding so I could really enjoyed it when it’s dry I love music in general especially music from the 90s I hope you’re excited to see how much I get up to and what I think of the concert in my comfort with you q🎵🎵🎶🎶🎵🎵🎉🎶🎶🎶🎉🤩

              What to wear?

              January 9, 2023

              what colours should I wear on Friday night the doorway so I wear red as I like white collar or white what do you think of Siri comment below what colour I could wear on Friday night outfits to you with the colour and bacon I have chosen to wear I would appreciate any news on where I’m going on Friday night choose one of these and reveal when I rub it on my own as it is from thank you same difference and happy partying to you guys on Friday anybody else it happened to also be out about opinions share them with me and let’s get me well as it’s unity but we are community of changes we will all the time that is for sure we are all equal here open cerebral palsy or any other disability makes us different but we are all the same we are all different and unique because being unique is good because you can bring different experiences to the table enjoy my message for Monday night xxx

              Science experiments that I am going to do next week as well instruments do a music video with my kids from making but I am going to do with my my Virgin data to see what flavours I make want colours they are and what since they are are I will then take a video of how she’s up when I try them out in in a few weeks time when I visit my grandma Mark and grandad some of the weekend all these things and more including my concert outfit this Friday my makeup that I choose to wear out and many other exciting activities that I am going to do this week and next week stay tuned everybody it’s any difference because your interest matters to me me and I appreciate every bit of interest that I was Steve on my blogs :-) xx

              January 9, 2023

              The making up youth group today making my first use of the year 2023

              January 9, 2023

              Unjust DWP Causes Help Requests To Rise, Says Martlesham Charity

              January 9, 2023

                A charity for people with disabilities has blamed “unjust benefit decisions” and rising living costs for an increase in requests for help.

                Disability Advice Service, based at Martlesham Heath, Suffolk, helped 463 in 2022 compared to 29 people in 2019.

                Trustee Rob Gibson said the “Department for Work and Pensions [DWP] is the enemy as far as we are concerned”.

                The government said it was “protecting the most vulnerable” and it “recognises the extra costs disabled people face”.

                As reported by the Local Democracy Reporting Service, Mr Gibson said: “It is not untypical to get a call from someone who says ‘I haven’t eaten for four days but I have been able to feed the dog’.

                “These were people who were just on the verge of not being able to manage – then along came energy bills and the rising cost of living and they were tipped over the edge.”

                The charity supports residents in East Suffolk with disability-related problems.

                Mr Gibson said: “Over the past three years, the Disability Advice Service has had a 100% success rate in the appeals we’ve supported for unjust benefits decisions by the DWP.”

                A government spokesman said its disability assessors were “all qualified health professionals”.

                “Decisions are made using all the information available to us at the time, but if someone disagrees with that decision then they have the right to ask for a review,” he said.

                East Suffolk Council had provided £33.5m, from a government grant, “to help those who come to us in poverty”, said Mr Gibson.

                The charity uses the grant to provide people with essentials like a week’s worth of food, topping up electricity bills and making sure people are getting the benefit payments they are entitled to, he added.

                The grant originated with the DWP, which Mr Gibson described as “ironic”.

                The government spokesman said six million people with a disability or health condition had received an extra £150 payment last year and low-income households had “received at least £1,200 of direct help, including £400 towards energy costs over 2022-23”.

                Coronation Street Star Cherylee Houston Returns To Filming After Long Absence

                January 9, 2023

                Coronation Street star Cherylee Houston, who plays Izzy Armstrong on the ITV soap, has retuned to filming after a long absence.

                Cherylee has been part of Coronation Street for 12 years, but she hasn’t appeared on the cobbles since 2020 due to the pandemic.

                The actress has a connective tissue disorder called Ehlers-Danlos syndromes, meaning she’s been forced to shield at home for an extended period because it makes her vulnerable to the coronavirus.

                Cherylee made an appearance on Corrie via Zoom in 2021 alongside her real-life husband, Toby Hadoke, to highlight the challenges experienced by disabled people during the pandemic – but now she’s officially heading back to the street.

                Coronation Street told Digital Spy that the soap star returned to filming before Christmas and has made a full-time return.

                In November, Cherylee received an MBE for her services to drama and to people with disabilities.

                Speaking about the importance of disabled people being represented on screen, she said: “If you think when you were growing up who your role models were, who influenced you, if you as a disabled child don’t have that, how do you know what you can do?”

                Cherylee continued: “That’s why I firmly believe the more we’re on our screens, the more we’re going to be understood, the more people care and empathise and will ensure that we will have equal rights and equal opportunity, because it’s about equality.

                “It would be nice if the world was a bit more physically accessible.”

                Just about to start on my diamond art again but this is how far I got last time I got it out look how pretty it is I am proud of it it’s just needs finishing before I can move onto my next diamond project post two of my Art Serieshappy

                January 9, 2023

                Tune for wacky wheels contents returning tomorrow my youth group project happy Sunday so you difference have a successful week from Maya xxxx

                January 8, 2023

                Artwork

                January 8, 2023

                under the sea colour by number that I have done with my support worker on Friday morning

                This is the first post in my Art Series, happy crafting same difference.I would love to see your art which you have been working on or any paintings that you have made which you are proud of. I will be starting some more artistic projects such as bath bomb making and candle making, hobby craft will become my best friend I used chalk and normal coloured pens for this project. Stay tuned for more art to come here is a picture of it

                waiting for the bus on a winter’s morning enjoying the warmth of my woolie hat right now

                January 7, 2023

                bring my birthday time out types of cerebral palsy #bus #accessing the community dressing up for winter and wearing my sunflower lanyard hopefully bus drivers are a bit more respectful#respect members of your community if you buy public transpor

                someone definitely wants attention loving the fact that I was at home over Christmas love you Maddie🐾💕🤩

                January 7, 2023

                CES 2023: Sony Unveils Controller For Disabled Gamers

                January 6, 2023

                  Sony has teamed up with accessibility experts to announce a PlayStation 5 controller for disabled gamers.

                  Project Leonardo is a “highly customisable kit” of different buttons, triggers and sticks that lets players create a set-up that suits their needs.

                  Microsoft’s Adaptive Controller, released in 2018, sells for £74.99 at its UK store – though extra buttons and joysticks can cost much more.

                  But there is currently no release date or price point for Project Leonardo.

                  https://emp.bbc.co.uk/emp/SMPj/2.47.2/iframe.htmlMedia caption,

                  BBC News looks at Microsoft’s Adaptive Controller

                  A Sony Interactive Entertainment official told BBC News it would work “out of the box” to help gamers play “more easily, more comfortably and for longer periods”.

                  “We feel the breadth of hardware and software customisation options in Project Leonardo is unique and stands out from any other accessibility controller on the market today,” the official said.

                  “Project Leonardo is a true passion project for our team. We’ve drawn on 28 years of design expertise at PlayStation to create a controller kit that we hope many players with disabilities will find useful.”

                  Several charities helped, including US-based AbleGamers and UK-based SpecialEffect.

                  SpecialEffect founder and chief executive Mick Donegan said he was “really excited to see the impact of the controller on helping to make access to gaming available to many more people”.

                  The charity has previously championed Microsoft’s Adaptive Controller, which officially works with PC or Xbox only but can be used on rival consoles with a third-party adapter.

                  Other manufacturers, such as Hori, have also developed accessible controllers.

                  Last year, 8BitDo made one for gamers with spinal muscular atrophy, after being contacted by a parent.

                  Gran Turismo

                  Cesar Flores, who has consulted on Project Leonardo, said Sony’s controller was “a big part of what it means to create accessibility”.

                  “I’m so thankful to be a part of it,” he said. “It’s life-changing, not just for me but for so many people in the world.”

                  Also at CES 2023, one of the world’s largest technology shows, Sony:

                  • revealed it had sold more than 30 million PlayStation 5 consoles
                  • unveiled the first trailer for the feature film based on racing game Gran Turismo

                  Happy partying to anybody that is going out this weekend,I’m not going out this weekend but will go out next weekend to see another a concert. Stay tuned for a review of my outfit that I am wearing to the concert. Once I have attended it I will give you a review of the concert and any videos I manage to get of them performing and any pictures of me enjoying the night out , most probably pictures of me at the bar lol🤣

                  January 6, 2023

                  Animal documentaries the Twilight animal documentaries the Twilight that take place easy Rudy I like the days because it shows you how they make him viral moment as habitable as possible for the animal and so you have a silicate enrichment in captivity and now they keep the animals healthy location and create their habitat I also like because it’s all about chimps and meerkat and all sorts of monkeys similarit so you similarities and differences to humans when it comes to the TV on marmoset very cute about them and why why people giving and are not allowed to keep them up next read me the high summer speech animal welfare what exotic pets do you have as many different strokes Is love to hearing the commen🤩🤩🦁🦁🦒🦒🦓 be

                  January 5, 2023

                  some of my course work I had to complete to get my level 2 in common health I was determined the words determined 👍🎉

                  January 5, 2023

                  £1,350 Cost Of Living Payments, 2023 Timetable

                  January 5, 2023

                  With many thanks to Benefits And Work.

                  Claimants will get up to £1,350 in cost of living payments in 2023/24, with the timetable for payments now announced by the government.

                  Over 8 million claimants will get £900 in three payments, whilst 6 million disability benefit will get an additional £150 and 8 million pensioners will get £300 in addition to their winter fuel payments.

                  The rough timetable for the payments is as follows:

                  £301 – First Cost of Living Payment – during Spring 2023

                  £150 – Disability Payment – during Summer 2023

                  £300 – Second Cost of Living Payment – during Autumn 2023

                  £300 – Pensioner Payment – during Winter 2023/4

                  £299 – Third Cost of Living Payment – during Spring 2024

                  These payments will all be tax-free, will not count towards the benefit cap, and will not have any impact on existing benefit awards.

                  Households eligible for the £900 cost of living payment will be on one of the following benefits:

                  • Universal Credit,
                  • Income-based Jobseekers Allowance,
                  • Income-related Employment and Support Allowance,
                  •  Income Support,
                  • Working Tax Credit,
                  • Child Tax Credit,
                  • Pension Credit.

                  If individuals are eligible they will be paid automatically, and there will be no need to apply.

                  Claimants who are eligible for any of the Cost of Living Payments and receive tax credits, and no other means-tested benefits, will receive payment from HMRC shortly after DWP payments are issued.

                  Further details of who will be eligible for the disability payment were not given in the latest statement, but is likely to be people in receipt of one of the following benefits on a yet to be announced date:

                  • disability living allowance,
                  • personal independence payment,
                  • attendance allowance,
                  • Scottish disability benefits,
                  • armed forces independence payment,
                  • constant attendance allowance
                  • war pension mobility supplement.

                  You can read the full cost of living payments statement on the .gov.uk website

                  News I would like to share with my Same Difference Community. I have now passed my common health conditions level 2 qualification just waiting for certification from the exam board.Thank you for being interested in my education and my life in general.I am proud of myself because this is the first level two qualification I’ve passed apart from my English GCSE. I was so excited to share with you this news when I heard that I had passed. This gives me give hope that we will all raise awareness and people will have more respect for people who use wheelchairs and people with cerebral palsy and realise that we are not stupid we are just differently-abled but I wouldn’t call it disabled to me it’s just differently-abled because we just have to be helped to be enabled to participate in our life

                  January 5, 2023

                  I hope everybody has enjoyed their first few days back at college work and probably go if you are in the final years of it happy start of a new academic year everybody at 10 different Maya

                  January 4, 2023

                  Ring to the future to work at Disneyland and go to Disneyland college Disneyland Paris because I think it looks magical there I want to do this because it will meet in experience of a different country although I’m not sure whether this green will be achievable but we’ll see in the future or even to work at Butlins would be agreeing to me also I like the idea of working in a resort where holiday makers create the atmosphere 🎊

                  January 4, 2023

                  What Does It Take To Raise A Guide Dog Puppy?

                  January 4, 2023

                  The pandemic caused a decline in guide dog partnerships, after puppy breeding and training were paused.

                  Lisa Allison’s is one of more than 2,000 households trying to help, in the hope of providing a blind person with independence.

                  One of her dogs, Fergall, is now ready for advanced training, so Lisa has to say a difficult goodbye.

                  my favourite present I got and hobby that I will enjoy in the new year and enjoy doing so.

                  January 3, 2023

                  I received a diamond crystal art clock that I can decorate myself and put on my wall in my bedroom I love my crystal art and will enjoy passing the time in this way I am currently doing a unicorn crystal art and I need to finish that as the crystal lots are very big but I’m enjoy anything out craft we do crystal or diamond as it’s sometimes called when I am finished my unicorn one I will show you in my art project series that I plan to start I will also show you how far I got with the unicorn so far when I start these series some point next week what I like about art or crystal art in particular is it looks pretty it is not too messy and it doesn’t discriminate anybody can do it whether we use a wheelchair air-con frame or on main screen and you do everything totally independently and it is big enough for me and my support workers to work on it together haha sometimes in other pieces of art is too big for me to have a team member working on it with me but diamond art is good for. me because it’s large it gives me something to concentrate on and like everybody else who . i like the fact that it looks pretty and it is something to be immensely proud of please show me your creations if you are an art person other I would love to see them in the comments.

                  Blind BBC News Correspondent Sean Dilley Defeats Mugger Who Stole His Phone

                  January 3, 2023

                  A blind BBC reporter says he “instinctively” leapt on a mugger who had stolen his mobile phone – and managed to get it back.

                  Sean Dilley was targeted on Tuesday while on a break during a night shift at London’s New Broadcasting House.

                  A person riding a bike snatched the phone – but Dilley did not give up easily and instead made a split-second decision to try to detain his attacker.

                  He said afterwards he suspected he was targeted because of his blindness.

                  A member of the public is allowed to attempt an arrest if they suspect a serious criminal act is taking place and they intend to deliver the suspect to the custody of police as soon as possible.

                  The news correspondent took his opportunity when he sensed that his attacker was still next to him so jumped in that direction and managed to get them onto the ground.

                  He then restrained their arms and was able to retrieve his phone.

                  Dilley sustained several cuts and injured his elbow in the incident, which happened just before 0600 GMT. He said he was concerned about protecting himself but also wanted to ensure the person was as safe as possible.

                  He used a voice assistant on his phone to call 999. As he waited for the police, another person arrived and offered to help.

                  At that stage, with his assailant continuing to struggle, Dilley told them he would let them go as long as they left immediately.

                  Three police officers arrived soon after and Dilley said he was grateful to them for their quick response, describing their attitude towards him as “friendly” and “helpful”. The trio walked him back into the BBC newsroom.

                  Dilley said he hoped that his instinctive actions might force the thief to reconsider their actions in future.

                  “He picked the wrong blind person on the wrong day,” he said.

                  He described his own actions as “stupid” and advised anybody in a similar situation that no property is worth risking their life for and to simply call the police.

                  However, Mr Dilley said he can’t pretend he is not happy he got his phone back.

                  Police are investigating the incident as an robbery and are appealing for witnesses who saw what happened in Bolsover Street, in central London. The witness who stopped to help told police the person ran off in the direction of Greenwell Street. Anyone with information should call 101 quoting CAD 1115/27Dec.

                  Blind Man And Guide Dog Refused Taxis Over 30 Times

                  January 3, 2023

                  A blind man who uses taxis and private hire vehicles to get to work says he and his guide dog have been refused trips by some drivers over 30 times.

                  Stephen Anderson, 32, who works as an organist at a London church, has been filming the incidents involving him and his dog Barney and sending them to Transport for London (TfL).

                  His actions have so far seen a dozen successful prosecutions.

                  TfL says it acts against minicab drivers who refuse to take guide dogs.

                  Under section 170 of the Equality Act, it is a criminal offence for private hire drivers to refuse access to a guide dog and its owner.

                  ‘Distress and shame’

                  Mr Anderson said: “I’m not sure whether I can take another guide dog on in the future simply because I cannot deal with the distress and the sense of shame that comes from people treating me so appallingly.

                  “Even when I tell them, they will say that it’s not a criminal offence because, ‘it’s my car’.”

                  Mr Anderson hopes private hire and taxi companies take action to prevent their drivers from discriminating against blind and partially sighted people.

                  TfL said it acted “against mini cab drivers who refuse to carry passengers and their guide dogs”.

                  Mr Anderson is the not the first person to stand up for his rights surrounding guide dogs.

                  In November, a blind woman and her dog were thrown out of a London Premier Inn in the night after she was accused of lying about her assistance dog.

                  Angharad Paget-Jones, 29, said she was woken up and asked for “proof” her dog Tudor was a registered guide dog.

                  She claimed that after providing a Guide Dogs ID booklet, security staff accused Tudor of being a “fake” guide dog.

                  At the time, Premier Inn said it was urgently investigating the allegations.

                  all terrain wheelchair all terrain wheelchair of do

                  January 2, 2023

                  Some other found that you help donate throughnmy JustGiving and gofundme pages will go towards purchasing an all terrain wheelchair so that I can fully participate in the dov experience and enjoy it with my peers who are not disabled on it platform on an equal platform form to them so please donate share my story and become part of this Dov and goes journey that I am in Barking on much appreciated

                  Myah

                  happy New year to everybody at same difference

                  January 1, 2023

                  I hope you all achieve what you set out to achieve this year let It be love You best wishes Myah

                  Appreciating the Christmas decorations they are all lit for the last time this year before they are taking down in the new year

                  December 31, 2022

                  New year’s resolutions and goals for myself and New year’s resolutions for 2023

                  December 30, 2022

                  one of the goals is to go to more concert and live music to complete my dov the silver award to go to a summer festival and camp or Grahamp to start my applied science and forensic science course at college and two gaing all skills level 1 by the end of 2023 join me to tick off this goals list and show the world what people with cerebral cause like me can achieve and what we aspire to describe negative attitudes societal expectations that are rather outlandish and rather silly for this modern age and to show them that people like me do not care about their negative opinions we only care about The Prodigy one and only about the people that care about a ticket or girls the people that have preconceived ideas of disability can go away and be sad in their own little world all they can choose to edit Kate and sells about disability and about the people that live with it and about what causative life they can leave with support as part of this I would love is many of you to donate to my JustGiving page as possible this will help me to achieve my goal or passing my D ov and allow me t on employ support and achieve my goals and me able me to do the qualifying expedition.

                  Review of Alice in Wonderland

                  December 29, 2022

                   

                  my review of the first show of the this series I went to see today and a picture of me in the trestle theatre in the interval. I thought it was very funny, and interactive, lots of audience participation. Increasing my enjoyment of their version of Alice in wonderland. As well as some singing, dancing and excellent costumes.

                  independent schools Maidstone how to tag on your shoulder #paddington pro #independent #support big achievement

                  December 28, 2022

                  picture of me all ready for Christmas Day to see what Santa brought me for Christmas

                  December 27, 2022

                  ⛄🥰🤣

                  sharing competition I would like all of you to design and New year’s Eve Picture.

                  December 27, 2022

                  you can also design a private Christmas picture and I will school room decide the best one and then the best one will get an electronic certificate to appreciate their work this is only a bit of time this is only a bit of fun I look forward to see your New year’s Eve interpretations pictures you cannot different art forms and media forms including crayons and many others I will do this to 2.and log your New year’s Eve pictures and I will pick a winner do New year’s Eve once everything goes back to normal I will look to the mall and give you all Pete back in the comments would love to see your interpretation of New year’s 12 the Christmas and also a present if you would like this could be the best present you received the way the present is wrapped it’s basically your interpretation of a Christmas and New year’s celebration

                  My Prom four years ago.

                  December 27, 2022

                  This is me and my cousin.

                  picture of me wearing when all my presents Christmas 🍾🌲🥰

                  December 26, 2022

                  reviewing shows that I am going to see the Series.

                  December 26, 2022

                  show number one theatre pantomime which I will review on Thursday after I have been to see it I hope that there is money fun and tongue and cheek jokes in the show what do you think the theatre shown might be like out of 10 being the best and one by the way I would love to see your guest ratings and then I will give you my opinion won’t be to see it comment down below what you would like to see in a pantomime show if you ever went to run and heather’s day on how it was made this time I am not participating in the show but I would love to hear your views on what you would like to see in a pantomime show or in any show that you go and see at the theatre all concert places around the country this includes musical concerts.

                  me and the choir sheet

                  December 26, 2022

                  Happy Christmas to all my fellow blogger at same different may 2023 be your year

                  December 25, 2022

                  Xxxx.🤣🤣🤣👩🏾‍🦽👍🤣🥂🥂🥂x 🥂🥂🥂🍾🍾🍾🍾

                  pictures of a singing in the show and looking at choir teacher for direction as you stood up on the same

                  December 24, 2022

                  a very festive wake up call you would get some this alarm clock although this with new Christmas all the moment in the town today I had the pleasure of sitting next to and appreciating

                  December 23, 2022

                  The British Sign Language Project Stretching Back 2,000 Years

                  December 23, 2022

                    Sign language has experienced a surge of interest in the past couple of years.

                    Deaf actress Rose Ayling-Ellis wowed on Strictly Come Dancing last year – and the film Coda, about a teenager who is the only hearing member of a deaf family, won best picture at the 2022 Oscars.

                    Now another project under way, with its roots stretching back more than 2,000 years: the Bible is being translated into British Sign Language (BSL).

                    Rev Dr Hannah Lewis, a Deaf priest based in Liverpool, always believed she had a good understanding of the Bible. As someone who is “completely bilingual in English and BSL”, she didn’t think she was missing out.

                    “I can read it, I can understand it, I can preach on it. But when I see the Bible in BSL it just hits me – emotionally, spiritually – in a way that reading never will.

                    “However good the interpreter, you’re receiving the Bible once-removed,” she told Radio 4’s Sunday programme.

                    BSL is Hannah’s first language and, as such, the most meaningful.

                    Currently, while there are some non-traditional versions of the Bible available in BSL, there has been no official translation until now. Previously it had come down to the subjective reading of individual interpreters – their take on the stories and words on any given day. Come the following week, or a different interpreter, the Bible stories might be signed slightly differently and convey slightly different meanings.

                    The BSL Bible Translation Project is trying to put that right. A team of Christian volunteers have been working with historical and biblical experts to translate the Bible from the original Greek and Hebrew texts into a BSL video version.

                    It will be the only definitive BSL version – and, because it will be a video, the signing will not be subject to change.

                    The project has involved about 20 people, from theological experts to BSL linguists, interpreters and presenters, at a cost of about £1,000 a day – all from sponsorship.

                    Their aim is to strike a balance between scholarly interpretations of the texts while ensuring the translation is accessible, accurate and looks natural in BSL.

                    The team has so far translated Mark’s Gospel and has started on parts of Genesis, both of which are available on the project’s website.

                    But it’s not entirely straightforward. There are many versions of the Bible in English – because translators rarely agree on how to express the meaning of the original texts.

                    Janice Silo, a trustee of the project – who is Deaf and was a teacher of Deaf students before her retirement – says it has given the community a chance to think about its meaning in their own language.

                    “Growing up, it felt like I was always told what to think. When I became a teacher I wanted the children I taught to think for themselves.

                    “I feel that Christians should read the Bible for themselves, but Deaf people don’t have a Bible in their own language so this project will ensure they do.”

                    Signing is often considered the “dynamic interpretation” of language, meaning it is used to convey thought-for-thought rather than word-for-word. It focuses on feelings and nouns, rather than conjunctions such as “for”, “and” or “but”.

                    Rev Canon Gill Behenna, one of the trustees of the project, is a Church of England priest and works with the Deaf community in Bristol. She says the project is using signs that are already widely understood, rather than creating new ones.

                    “We are translating into BSL, which is a language,” she says. “We are not ‘transliterating’ which would be word-for-sign. We’re translating whole concepts.”

                    She herself is hearing and bilingual, speaking both English and BSL. She cites English as her first language and took up BSL for a temporary job 40 years ago.

                    In Mark, chapter 4 – Gill explains – the English text reads: “A sower went out to sow.” In BSL this would be signed as “there is a person with a basket of seed” followed by the signer creating a basket shape with their hands and then scattering seeds.

                    “BSL creates a picture. In English, the picture is created by words,” she says.

                    “When I read the Bible I am sometimes inspired by a single verse or story, and I sense God communicating with me through that. I want the same for Deaf people.

                    “Although a huge number of Deaf people are bilingual, it’s different having the words of scripture in your own heart language – the language you use and you identify with.”

                    Currently, Deaf churchgoers may experience sermons with an interpreter, but sometimes the signing can be done on-the-fly and, as such, some Bible stories can be embellished or added to unnecessarily.

                    Gill remembers a signing of the story of Jesus stilling the storm. With Jesus asleep in the boat, the disciples wake him up.

                    “The version I saw included a conversation between two disciples: ‘Wake him up!’ ‘Me? No, you wake him up!’ We wouldn’t do that in a translation because that would be adding to the [Bible’s] text,” she says.

                    Hannah says going to church as a Deaf person can be a mixed experience and – whether it’s good or bad – it is often taken as God’s opinion of you.

                    If you go to church, and “there’s no access at all, the rejection is not coming from the church, that rejection is felt as if it’s coming from God,” she says.

                    Before the first national lockdown, during the coronavirus pandemic, Hannah was involved in integrated services within her diocese which adopted elements of both hearing and Deaf culture.

                    That included the congregation remaining seated throughout the service so everyone could see the interpreter.

                    “Quite small changes like that change the whole atmosphere,” she says.

                    But Hannah thinks BSL and Deaf culture add more to worship than just inclusivity.

                    “People find that their senses are opened to worship, to God, in a way that they aren’t before.”

                    She says some within the Church of England might close their eyes to listen to a sermon or prayer, but “when I lead in sign language I encourage people to keep their eyes open and people find that it benefits their own faith”.

                    While the BSL Bible Translation Project does not currently have a deadline for completion, a similar project to translate it into American Sign Language took 40 years.

                    But Janice says it will be worth the wait.

                    “Deaf people will be able to watch the Bible for themselves, instead of having to ask for explanation or relying on interpreters all the time.

                    “William Tyndale, who translated the Bible into English, said that he wanted anyone – even a ‘lowly plowboy’ – to read the scriptures. I want that for Deaf people too.”

                    My favourite Christmas cards that I have received this year from my wacky wheels youth group and my volunteer job.

                    December 22, 2022

                    Man To Spend ‘Tough’ Third Christmas Shielding

                    December 22, 2022

                    A man who will spend his third Christmas shielding said it “can be tough” for him.

                    Karl Knights from Leiston, Suffolk, has cerebral palsy and is immuno-supressed.

                    The 26-year-old is continuing to stay at home due to his increased risk of complications from a potential Covid-19 infection.

                    “Outside of the house I haven’t seen anyone in the flesh for three years now,” he said.

                    There are around 500,000 people in the UK with suppressed immune systems.

                    That means their bodies struggle to produce antibodies, so the existing vaccines offer them little or no protection, leaving them very vulnerable to coronavirus.

                    Mr Knights said: “Around the holiday season, special occasions, like birthdays, it can be tough.

                    “I’m lucky that I have family members in the house still, so I see them and talk to them.”

                    ‘Living in a question mark’

                    Mr Knights, who is a writer, has only left the house since to first lockdown to receive his vaccines.

                    “The great thing with where we are with technology is we can Zoom, and call, and email and text, but we’re just not meeting in person,” he said.

                    “One of the few blessings is I’m glad this horrible event and all the shielding is happening in this moment where we have this connectivity.

                    “I’m grateful for it, especially at this time of year.”

                    He described shielding for almost three years as “very strange, very odd, you’re in this kind of bubble, you’re on pause, watching the world go by and you’re still in place”.

                    Mr Knights said he did not know when he would stop shielding.

                    “We never know how this pandemic will develop, you’re living inside of a question mark,” he said.

                    He added he would be having “quite a quiet Christmas” with his father and siblings.

                    “It’ll be just a normal day with a lot more food.”

                     

                    Ukraine War: ‘We Long For Home – But Our Son Has Chances Here’

                    December 21, 2022

                    When war broke out, millions of Ukrainians had to make a life-changing decision to flee their country – with many hoping to return as soon as possible. But for some disabled refugees, this displacement has offered new opportunities, and they now face a dilemma over whether to ever go home.

                    The Kyrychenko family fled Kyiv as missiles rained down. In the space of an hour the parents had packed up their car with three children, a dog and two guinea pigs. Without time to plan a destination, instinct took over and their safety was all that mattered.

                    Nine months later, they are just some of the 1.4m refugees living in small apartments, rooms and shelters across Poland.

                    This means that their eldest son Roman, who has cerebral palsy and learning disabilities, has been given the chance to go to school for the first time. He is 20 years old.

                    “Back in Ukraine we were told he was unteachable, that there was no school for him,” his mum Olga says as she makes packed lunches in the family’s small kitchen.

                    For many disabled children and young people in Ukraine, access to education is rare. Before the war, fewer than 3% were enrolled in mainstream school.

                    Roman needs support to walk, and communicates through sounds and facial expressions. While he spent most of his life stuck at home, his younger sister, Sofia, was in full-time education. Now, in Poland, they both leave the house for school.

                    “Over the years that he didn’t go to school, he lost a lot. And we lost a lot as a family,” Olga says.

                    Widespread abuse

                    Back in Ukraine, Olga and her husband Volodymyr have had to fight to keep Roman from a life in an institution or a “psycho-neurological boarding facility”. The authorities have spent two decades telling them that their son belongs in one of these places.

                    “They said, ‘Give him away, you can always have another one,'” Olga says – the determination on her face making clear that this was never an option.

                    More than 50,000 disabled children and young people exist in this system – a network of more than 700 institutions. They are casualties of a Soviet era that encouraged parents to give their disabled child up to the state in the belief children receive better care in an institution.

                    A BBC News investigation in August uncovered widespread abuse in these establishments and the team were asked to give evidence at the United Nations.

                    Following that, UN experts demanded that the government urgently continue its de-institutionalisation process – returning children to families, increasing community support and closing facilities which abuse and neglect some of the most vulnerable in society.

                    Now in Poland, Roman starts his day with new purpose. Supported by his dad, he navigates the several flights of stairs from their small apartment in the suburbs of Krakow before a taxi takes him to a specialist school a few miles away.

                    There, his face lights up as his music therapy teacher plays the piano for him. She says the aggression he struggled to contain when he first came to the school back in March has left him, he’s a “happy kid” who feels at ease and confident in this new environment.

                    He is given one-to-one support and physiotherapy in the school gym and his walking is steadily improving. For the first time, he can mix with his peers and learn new skills.

                    “I do not understand why he did not go to school in Ukraine,” the head teacher, Urszula Majcher-Legawiec, says in one of the school’s brightly-coloured corridors.

                    “We know his potential. Roman is constantly improving, he is learning new communication skills, he can tell us what he needs. A place like this is the best place for him.”

                    “I am very proud of him that he goes to school,” Olga beams. “He goes with pleasure.”

                    Walking for the first time

                    A few hundred miles away in the north of Poland, I meet another 20-year-old refugee whose world is gradually expanding – but this time from the confines of his bed.

                    Ivan had spent his life lying down in an institution in the east of Ukraine. He is one of 60 disabled evacuees who fled their orphanage in Kharkiv just after the war broke out.

                    It was a gruelling 48-hour journey through Ukraine, during which some were tied to bus seats. Two of them did not survive.

                    “They were in a terrible condition,” said Katarzyna Bogumila, a Polish volunteer who has helped care for them since they first arrived.

                    “They were really skinny. Like dry sticks, and I didn’t think it was because of the war. They came to Poland at the end of February and it was just after the invasion. So it couldn’t be that – it had to be like a system in Ukraine or something.”

                    Ivan looks no older than a six-year-old, undernourished after two decades in confinement. His hair a flash of red against his pale skin.

                    Along with the other evacuees, his new home is a former psychiatric hospital in the city of Torun.

                    It has taken months to raise his fragile frame to a sitting position. If they elevated him too quickly there was a chance he could have had a stroke.

                    His view of the world has completely changed – he can now move around in a wheelchair, his face lights up as he is pushed to his physiotherapy. For the first time, he can see the lives of those around him.

                    Other children have also developed. Eleven-year-old Lillia, who has complex disabilities, is walking for the first time. One young man picks up a feather in the sensory room, an experience he has never had. The look of joy at his new-found capability glows on his face.

                    For Katarzyna, this is a short term solution. Her belief chimes with the UN experts who have criticised the Ukrainian government for insisting disabled children remain in a residential setting even when abroad, rather than being supported in the community. The government maintains it is the best way of being able to track the young evacuees and prevent trafficking.

                    “Every kid should have the chance to be with a family,” she said.

                    “I’m hoping they’re going to stay in Poland and we can find them families. I can see the difference being here is making every day. It’s awesome. I feel like they’re my own kids. I don’t want to let them go.”

                    But the situation is complex, illustrated by the dilemma facing the Kyrychenko family. Olga feels the pull of her homeland, but Poland offers so many opportunities for her son. She knows if they return to Ukraine his life will stagnate again.

                    “Our soul longs to go home while the brain says something different. For Roman, it is better here. It is amazing he can go to school here.

                    “It’s hard to return from good to worse conditions, but abandoning Ukraine – our home is there. I just have to hope that maybe we can bring our experience back to Ukraine and a school for Roman could open there.”

                    Showcase photo of me on stage in August.

                    December 20, 2022

                    A choir group photo of us all on stage from just before we performed showing off our Christmas hat sparkly tiaras and Christmas jumpers

                    December 20, 2022