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Ethan and Prime

May 14, 2023

you are you crying?

May 14, 2023

May 14, 2023

I have some news for everybody at Brandom account. I am going to have an interview on Tuesday for the Nextep in my educational journey. Hopefully doing how do you say super level 1030 thank you for updates on Tuesday about my interview outcome

look Prime you know for five months #Holidaying #Dog #Spaniel😘👩🏾‍🦽

May 14, 2023

video that I promise, click on the link to watch it

May 14, 2023

https://vm.tiktok.com/ZGJHuQgwr/

your happen saying ,from me to you

May 14, 2023

from choir on Thursday, footage of me joining in the choir dancer on Thursday to you. We’re going to habita on Sunday. love the tune would love to visit Habita. To see the video which I am talking about, probably on Sunday afternoon.

May 14, 2023

colour by number that I did last Sunday with my support person from my activity book

May 14, 2023

https://www.justgiving.com/crowdfunding/maya-richards?utm_term=YQabBEeA4

May 14, 2023

how hot are pulling the tornado pretty tomato three years ago today #Art #SarahBucharest

May 14, 2023

💜♥️♥️♥️🥳😘😆🥳

May 13, 2023

please help me by donating to my just giving page, just a little to help me reach the a £1000 goal. # £1000 #FundraisingGirl, #CerebralPalsy #RespiteSupport #DoYouHaveASupportHowDo

May 13, 2023

https://www.justgiving.com/crowdfunding/maya-richards?utm_term=dN7GwMGDm

my scrapbook page that I completed with my support worker this afternoon hashtags for today at work. #OutWithMySupportWorker #HaveISpentManchester

May 13, 2023

your weekend WORDsearch, which I promise you, you would see over the weekend that I was able to do just with assistance of identifying some letters and writing using a regular pen. whereas the other one just a couple of months ago. so now I am able to write using the pen with assistance to complete the words search successfully and identify was able to identify the letter S successfully and independently for the first time in 23years. I was able to identify when told which letters we are looking for. I would like to celebrate this success with you by sharing this so that people that will be aware that the smallest things are the biggest things when you are disabled and trying to be as independent as humanly possible with your challenges that you face.

May 13, 2023

https://www.justgiving.com/crowdfunding/maya-richards?utm_term=vrRnVARBV

May 13, 2023

Saturday saying, wishing everybody a good weekend 💕🤩👩🏾‍🦽

May 13, 2023

May 13, 2023

💕💖

May 12, 2023

😎🥳🥳

May 12, 2023

you? Friday motivation

May 12, 2023

how do you take a papier-mâché balloon about three years ago today? #ForYou #Painting #CerebralPalsyHasTheLockdownAt

May 12, 2023

https://www.justgiving.com/crowdfunding/maya-richards?utm_term=Pjrn6gp8R Brandom, are you saying ready for those that want to contribute towards emoji because support and my respite care

May 12, 2023

💜❤️💖😇 two year old three-year memory of me squeezy burn orange to get the Duke Of Edinburg to make orange flavoured butters. Hello#OrangeFlavouredBellSouthHas also making #SarahRecruitment

May 12, 2023

Blind Presenter Lucy Edwards Hosts Eurovision Description Show

May 12, 2023

    A blind presenter has launched a new podcast which will include audio descriptions of iconic moments from the Eurovision Song Contest.

    Lucy Edwards, from Birmingham, lost her vision 10 years ago when she was 17.

    Since then, she said she has “missed out” on cultural moments and wanted to describe elements from the competition for other blind and visually impaired fans.

    She hosts Eurovision Described on BBC Sounds with Abi Clarke.

    “Ultimately, when you’re blind or visually impaired, there’s a lot of things online that aren’t accessible to you at all,” said Ms Edwards.

    “We thought it was really important to bring this podcast to everyone who hasn’t seen those moments, has never had those cultural moments described to them.”

    Ms Edwards, who has more than half a million followers online, is a self-described Eurovision super fan but admitted she has not watched any of this year’s competition, hosted in Liverpool, so far.

    “The semi final, my dad always has it on, I’m always like ‘don’t show me’ because I’m so invested in the final, I don’t want the acts to be spoilers,” she said.

    As part of the podcast, she and Ms Clarke have interviewed the likes of Lordi, Bucks Fizz and Scooch and her co-host has described their performances to her.

    “I had vision 10 years back when I saw some of these performances but I’d forgotten,” Ms Edwards said.

    “A lot of my visual memory has faded over the years, so having them described by Abi my co-presenter was amazing, just putting a lot of colour into the performances.”

    She said it was “amazing” to see more televised events, like the Coronation, being audio described to be more inclusive.

    “It brings me to tears when live shows are audio described because I haven’t had that being blind for the last 10 years,” she said.

    “There have been times when I have been shut out from major moments.”

    For the final on Friday, Ms Edwards is planning to enjoy the show with her family, adding her dad normally describes the action for her.

    All episodes of Eurovision Described, hosted by Lucy Edwards and Abi Clarke, are available to stream on BBC Sounds.

    oh you memory of a workshop I went to to celebrate the Watford football game #4Years #OncallWorkshop

    May 11, 2023

    https://www.justgiving.com/crowdfunding/maya-richards?utm_term=b4gwyBDAv to my dear game, support and care and my response to grow

    May 11, 2023

    what are you even saying pretty illustration

    May 11, 2023

    My car being chewed on my bed 😍💕

    May 11, 2023

    💕

    May 11, 2023

    on the way to my phone today selfie

    May 11, 2023

    colouring and writing and counting activity today that I did and enjoyed my Sunday last week doing this.

    May 11, 2023

    DWP Work Coaches: No Qualifications, Appointed Without Ever Being Met, Interview Questions Supplied For Under A Tenner

    May 11, 2023

    With many thanks to Benefits And Work.

    Work coaches, who will decide whether claimants are fit for work-related activities under DWP plans, need not have even a single GCSE it has been revealed. In addition, job interviews are conducted without the DWP ever meeting the candidate and the questions asked, as well as suggested answers, are available online for under a tenner.

    Disability News Service revealed last week that that the DWP had admitted that there are no minimum academic qualifications required to become a work coach in a jobcentre.

    Yet under DWP plans, the work capability assessment (WCA) is to be abolished and it will be unqualified work coaches who will decide whether a universal credit claimant must undertake work-related activities.

    This is a decision which is currently made by registered health professionals and the fact that it is to be handed over to work coaches with no medical knowledge whatsoever is causing alarm amongst claimants and many voluntary sector organisations.

    Benefits and Work can reveal that not only do work coaches not need qualifications, but that the DWP never meet them before offering them a job and that there are websites that claim to offer a full list of questions and suggested answers for passing the online work coach interviews.

    In 2020, the government announced it was going to double the number of work coaches in jobcentres by hiring an extra 13,500 people.

    It wanted the first 4,500 new recruits in place within just three months of the announcement

    Civils Service World explained how the DWP tackled this mass hiring challenge by using an outside company to create an entirely online, prerecorded recruitment process.

    The high-speed, remote interview system that was devised at that stage is still in use today to recruit work coaches, with details of the process available on the DWP workcoach microsite.

    After completing an application form, candidates are asked to undertake an online situational judgement test in which they have 40 minutes to consider 20 hypothetical scenarios. For each scenario there is a list of possible responses which candidates have to rank on a five-point scale from ‘extremely desirable’ to ‘extremely undesirable’.

    Applicants who pass this test are then invited to take part in an online “interview”. A pre-recorded interviewer asks six questions, two each on: communicating and influencing; managing a quality service; and making effective decisions.

    After each question, the candidate gets a minute’s thinking time and then automatic video recording begins and the candidate has three minutes to give their answer.

    The video recording is then evaluated by DWP staff and successful candidates are offered a job at a local jobcentre.

    A small industry has grown up to help people complete the application process successfully.

    One website offers a “DWP Work Coach Mock Interview” with 30 interview questions and answer examples. A subscription to the site costs £6 for a week with anytime cancellation.

    Other sites have forums where people who have been through the interview process share their experiences and lists of questions they were asked, such as:

    “How do you explain something complex taking into account the end-users’ needs.”

    “Tell me about a time you had to manage a complex issue to bring about great service.”

    A forum poster on one site explained that some jobcentres even run groups where you can discuss the application process and talk to other people who are going through it.

    All of this may be fine for people whose aim is to get a job where they can support other people into employment.

    Buts as DNS pointed out, decisions about whether a disabled person must carry out work-related activity are “life-changing – and potentially life-ending – decisions”.

    To have a recruitment and selection process where candidates don’t need any qualifications whatsoever and where you appoint people before you meet them seems ill-conceived and dangerous.

    Under the DWP plans, entirely unqualified work coaches will decide whether someone with a complex mental health condition or a serious physical health issue is able to undertake work-related activities. They will then then decide precisely what those activities should be, without the claimant having any right of appeal. And they will then have the power to recommend that the claimant is sanctioned and suffers a catastrophic loss of income if they are unable to carry out those activities.

    Abolishing the WCA and replacing it with the  decisions of unqualified work coaches selected according to their ability to answer multiple choice questions and perform in front of a web cam is not progress, it’s irresponsible and potentially deadly cost-cutting.

    https://www.justgiving.com/crowdfunding/maya-richards?utm_term=nBxgZvNYD my friend, Rosa drink if you want to join

    May 10, 2023

    WORD-search, I did a couple of months ago. please stay tuned for recent word searches over the weekend. This is one that I did with full assistance from my PA. compare to the one that i did with my PA today which you will see on Saturday morning.

    May 10, 2023

    scrapbook page which I did with my support tonight, which celebrate me and my friend trip to boom Battle bar, a fairground bar that does excellent cocktails and give you an excellent time. #CerebralPalsy, #CompetitiveStreak #Friends #CerebralPalsy,Twins

    May 10, 2023

    Autistic Teenager Was Stuck On General Hospital Ward For Months

    May 10, 2023

      An autistic girl aged 16 spent nearly seven months in a busy general hospital due to a lack of suitable children’s mental health services in England.

      Her local health and care system said it was “very sorry” for how she was treated “when she was most vulnerable”.

      Campaigners describe the shortage of appropriate support for people with autism as a human rights crisis.

      Directors of council care services are calling for an urgent government review of children’s mental health services.

      The teenager, called Molly, spent about 200 days living in a side-room of a children’s ward at the Queen Alexandra Hospital in Portsmouth. It is not a mental health unit.

      Experts say a general hospital was not the right place for her, but she had nowhere else to go because of a lack of help in the community.

      Warning: Molly’s story contains details that some people may find upsetting

      Agency mental health nurses were brought in because she needed constant, three-to-one observations to keep her safe. Her family says security guards were also often stationed outside her room.

      Molly’s autism is at the root of the deep anxiety and eating problems that she struggles with.

      Like many autistic people, she finds dealing with noise difficult. The clamour of the hospital overloaded her senses and her behaviour sometimes became challenging. She was restrained numerous times.

      In the final 10 days she was at the hospital, her family says the children’s ward was closed to other patients because she became so distressed.

      A spokesperson for Hampshire and Isle of Wight Integrated Care System (ICS) said it was sorry Molly “did not receive care in an environment better suited to her needs”, adding: “Molly’s safety has always been our priority.”

      The National Autistic Society says it is hearing from hundreds of autistic people who cannot get the support they need.

      A spokesperson for the Department of Health and Social Care says it recognises “the importance of getting people the right care in the right place”.

      This may be one person’s experience, but it tells us so much about how the health and care system is failing too many young people who are struggling.

      Short presentational grey line

      Molly is a bright, engaging teenager, who loves animals and finds the outdoors calming. She was diagnosed as autistic when she was 10 years old. She is also partially sighted.

      For nearly a year, I’ve been speaking to Molly and her parents. Through the many emails, phone calls, video meetings and visits I’ve followed the frustrating fight they’ve faced to try to get Molly the right support.

      When I first sat talking to Molly in the kitchen of her family home last August, she had already spent 90 days on the children’s ward of the general hospital because there was no support available elsewhere.

      She had initially been taken there because her weight had fallen dangerously low, but described the loud, bright, busy hospital environment as like “living in hell”.

      “It feels like they’re torturing you,” she said. “It’s almost like the hospital room is like a small box, and you’re not allowed to leave it. There are phones going off, alarms, children screaming.”

      The three-person restraint team that moved in when she became distressed or if she was refusing to eat “just made things 100 times worse”, she remembered.

      In the past four years, Molly has also spent time on four child and adolescent mental health units. Two of the units have since closed after highly critical inspection reports. Her family believes none of the places provided Molly with the therapy or autism support she needed.

      Her father Richard said: “There is no long-term strategy. No planning really, other than reacting to crises.”

      The Hampshire and Isle of Wight ICS spokesperson said there had been “a significant and rapid rise” in the number of children and young people with complex mental health conditions requiring care and support since the Covid pandemic.

      It says across England, the proportion of children aged five to 16 years identified as having a probable mental disorder increased from 10.8% in 2017 to 16% in 2020. In south-east England the proportion is even higher at 17.4%.

      When I asked Molly why she wanted to speak to us, she was very clear. She didn’t want others to be treated as she had been treated.

      “The system really needs to change,” she said.

      Once Molly was back at home after being discharged from the last unit, they hoped she would get intensive support in the community to help with her disordered eating and anxiety.

      Her family says this proved patchy, with many changes of staff.

      Last October, Molly reached another crisis. Her weight dropped again and she was taken back to the Queen Alexandra Hospital. Her parents asked us to delay telling her story, hoping she would be home soon. Nearly seven months later she was still there.

      Her family says she was traumatised by the hospital environment, being frequently restrained and largely isolated from other young people.

      “It’s a vicious cycle,” Richard said. “The more distressed she gets, the more her behaviour becomes challenging and then the more intense support they’ve got around her, which is more oppressive and more sensory-overloading.”

      Despite the close supervision, she has also harmed herself seriously on several occasions.

      “I think we know something is wrong before we even pick up, if the phone rings at night,” said her mother, Mandy.

      They are both exhausted and when I asked how they were coping, Mandy said: “You have to cope, there is no other way.”

      In March, Molly’s parents told me that the teams involved in her care seemed to agree she was stuck.

      Richard said past experience had shown that “off-the-shelf solutions”, including stays in mental health units, were “very negative for her and completely don’t meet her autistic needs”.

      An ICS spokesperson said: “Everyone involved has done all they can to ensure she receives safe and compassionate care and sought to move Molly to a setting that better meets her needs as quickly as possible. Teams continue to do their very best to help ensure Molly gets the care she needs.”

      The National Autistic Society says it hears from hundreds of people trapped in a similar cycle.

      It wants the government and NHS to put more money into mental health services that support people at home and to intervene early when there are problems.

      The charity’s head of research, Tim Nicholls, says that unless this is done the pattern will repeat itself and “one of the great human rights crises of our generation” will continue.

      It is hard to calculate how much Molly’s latest stay in the general hospital will have cost, but according to the Nuffield Trust health think-tank, a paediatric NHS hospital bed costs nearly £500 a day. If a child has an eating disorder that rises to about £1,400 a day.

      The NHS hasn’t commented on the financial impact of the nearly 200 days Molly has spent at the hospital, but with the costs of employing agency mental health staff included, it could easily have reached a quarter of a million pounds.

      While the NHS runs most mental health services for children, councils also provide community-based support.

      In a recent survey, 79% of directors who run council children’s services in England said there was “rarely” or “never” appropriate beds available for children with complex needs.

      Steve Crocker from the Association of Directors of Children’s Services in England said they had seen “a real increase in the number of children stuck on hospital wards with mental health issues”.

      Until recently he ran children’s social care in Hampshire, where Molly lives. While he can’t comment on individual cases, he says generally the need for change is urgent and “we also need to push government for a full review around children’s mental health services”.

      The government says its ambition is to halve the number of autistic people and those with a learning disability in mental health hospitals by March 2024. A Department of Health and Social Care spokesperson added that this is backed by extra funding and “our action plan to improve community support and reduce over-reliance on mental health hospitals”.

      In April, Molly’s family says she became so distressed the children’s ward was closed to other patients. Ten days later she was moved to a mental health unit – even though that has not worked for her in the past. It is meant to be a short-term solution but her family say no other options are currently being discussed.

      I last spoke to Molly a couple of days ago. She had had a few trips out with her parents and was desperate to get on with life.

      And if she can get the right support, her hopes of staying out of hospital and going to college should be possible.

      playing of the day for everybody in the community ATM 💚😊🍕🌸

      May 10, 2023

      https://www.justgiving.com/crowdfunding/maya-richards?utm_term=yb6P7n39v

      May 10, 2023

      https://www.justgiving.com/crowdfunding/maya-richards?utm_term=yb6P7n39v fundraising mint, #SarahBecauseIDon’tHaveATextFromReidiForRespiteAndMyTVFootball

      May 10, 2023

      celebrating as program at the virtual day service two years ago today

      May 10, 2023

      Fundraising link for anyone who wants to donate to my respite – to get appropriate respite and appropriate support staff 💖 i have now raised enough money for DofE!

      May 10, 2023

      https://www.justgiving.com/crowdfunding/maya-richards

      stay tuned to see how I made these soaps 🧼

      May 10, 2023

      Meet Melanie And Chayse: The Disabled Woman And Her Sex Worker

      May 10, 2023

        While Melanie was in social isolation in her Australian home due to Covid-19, she made a promise to herself. Once she was allowed out again she was going to hire a sex worker, lose her virginity and put a halt to those anxieties she had developed around love and intimacy as a disabled person. Chayse was the man she booked.

        It was Melanie’s support worker who first suggested it. While they were isolating together, Tracey gave Melanie a massage.

        No one had touched Melanie before in a non-medical way and, at 43 years old, she realised she wanted more.

        Tracey, not her real name, revealed to Melanie she had once been a sex worker and thought that personal services could be an option for her to explore.

        “It just opened my eyes to the fact that maybe I could experience this,” Melanie told BBC Access All.

        She found an escort agency online, where a profile for a man called Chayse caught her eye.

        Excited, she arranged a booking and travelled to his apartment for the first session.

        “When I got out of my powerchair and my support worker left, it was just the two of us. I had no idea what I was in for.”

        Short presentational grey line

        Melanie has used a wheelchair since the age of three having been diagnosed with inflammation of the spinal cord – a condition known as transverse myelitis. It has given her paralysis in her legs and limited movement in her arms. As an adult, she uses support workers to help with daily tasks.

        She has lived and worked in Japan and is now a video editor, but romance never seemed to be on the cards. “I just thought if it happens, it happens.”

        Dating and opening yourself up to others can feel intimidating and the world doesn’t always acknowledge disabled people as sexual beings.

        According to the UK Disability Survey, published by the government in 2021, just 56% of the general population said they would feel comfortable in an intimate relationship with a disabled person.

        Melanie, herself, had never been sure how to approach it, so had left it to chance.

        After emailing an inquiry to Chayse, he arranged several videocalls so they could get to know each other and discuss any potential challenges.

        “I asked a million questions,” Melanie says: “Have you ever used a hoist before? Is your apartment wheelchair accessible? How often does the lift in your place break down?”

        “About once every six months,” Chayse replied.

        For Melanie, Chayse’s answers were good enough to book a session at his apartment. And far from nervous, she brought the appointment forward, too excited to wait as he had been so warm and reassuring.

        Legally, the arrangement between Melanie and Chayse was above board.

        In Western Australia, under the Prostitution Act 2000, while it is illegal to carry out street-based sex work or run a brothel, the act of prostitution is not against the law and escort agencies are legal. This differs across Australia’s states with Victoria, New South Wales and the Northern Territory having decriminalised sex work.

        It is similar in the UK. While the exchange of sexual services for money is legal in the UK, apart from in Northern Ireland, related activities such as soliciting or running a brothel are not.

        When Melanie arrived at Chayse’s property, the enormity of the situation began to sink in.

        “I knew I was out of my depth with sexual knowledge and I felt completely overwhelmed with the expert that was standing in front of me.”

        But as the appointment tentatively got under way, Melanie had a revelation.

        “I am an expert with disability and Chayse had no idea. We ended up laughing at each other’s ignorance and naivety. Two hours later we were the best of buddies.”

        Chayse, who has worked in the industry for six years, says “sexpectations” are the biggest problem when it comes to new clients – people put too much pressure on guaranteeing “the big O”.

        Presentational grey line

        LISTEN: You can hear more from Melanie and Chayse on the BBC Access All podcast with Nikki Fox and Emma Tracey.

        Presentational grey line

        “You’ve got to figure out what is going to work,” just like any intimate relationship, he says.

        Before hiring Chayse, Melanie had no idea how her body might respond in an intimate setting, whether she would be able to get into a conducive position or whether fatigue would obliterate any enjoyment.

        “That was the whole reason I booked Chayse,” she says. “I didn’t want to go home with a guy from a bar and find out these things and be awkward, vulnerable and unsafe.”

        As it happens, she found she could achieve plenty of enjoyment with Chayse and didn’t have to limit herself.

        Another thing she discovered was that her legs can be unpredictable and “fling off the bed” and she often needs a physio session afterwards to refresh her limbs.

        “I’ve worked out that my legs need to be fastened to the bed beforehand and then there’s no worry,” she says.

        This raises questions about power and control.

        As a disabled woman in an unfamiliar house, Melanie is more vulnerable than most.

        “It was the first time I’d been naked in front of a man, outside of a hospital,” she says.

        Chayse, who has previously worked with those who have experienced trauma, says “creating a safe welcoming space where she’s in control,” is his top priority.

        But it’s not just the physical power imbalance where the vulnerability lies. Disability can sometimes infantilise people and make them feel unworthy of certain experiences that other people think of as just normal – some disabled people call this internalised ableism.

        These recent intimate encounters have gone on to give Melanie greater power in every aspect of her life.

        “I knew that by booking Chayse, and paying for a service, that I was in control. I knew that if Chayse treated me differently or did something I didn’t like he would stop.”

        She said if that did happen she knew she wouldn’t have booked with him again.

        But it does come at a financial cost.

        “It’s in the thousands,” Chayse says wryly of his 48-hour price. His hourly rate is about 400 Australian dollars (£211).

        Justifying the cost, he says: “What a lot of people don’t understand is when you’re seeing someone for 48 hours, as rewarding as it can be, you’re not doing anything else you want to do in your life.”

        But he adds that he does get a huge amount of satisfaction from his work.

        “Who doesn’t want to help people explore different things? Why can’t I be there for other people that need that and want and deserve to feel beautiful?”

        “It’s hard not to fall in love with Chayse,” Melanie admits. “But I have to remind myself that it is a professional relationship.”

        Melanie and Chayse have been seeing each other since January, but it’s not just about a quick fix and sex.

        As well as providing his skills as a sex worker, Chayse has also been talking with a dating coach to see how he can support Melanie navigate the “tango of dating” and help her build future romantic partnerships with other people.

        “I’m looking for a Chayse replacement. Somebody who loves me and loves what I like and does everything for free,” she says.

        “I never thought I would go on dating apps and talk to men online and now I’m doing it pretty much daily. My only regret is not doing it sooner.”

        For Melanie, the experience is more than just sexual liberation and she has got so much out of this ongoing experience she believes governments should pay and support disabled people in accessing sexual services.

        “My confidence has grown heaps, I’m happier than I’ve ever been and you can’t put a price on that life-changing experience.”

        And she has been excited to share her new experiences with friends and family.

        “I was a bit embarrassed to say anything at first, but it made such a huge difference in my life. I just couldn’t stop telling people and they’re really happy for me. I can’t wipe the smile off my face.”

        https://www.justgiving.com/crowdfunding/maya-richards?utm_term=g9JBG32gY

        May 9, 2023

        Day, whatever you are doing tomorrow, where do you are going to college university all paid voluntary employment oh yeah #Disability #DisabilityLife #HaveANiceDay #FromOneDisabledPersonToAnotherHouse3PartOfTheDisabilityCommunity

        May 9, 2023

        https://www.justgiving.com/crowdfunding/maya-richards?utm_term=v43vgpPy7 my friend, Grace in Prime for my respite care of the Rees group💖💖💖💖💜💜💕😎😎😍😇😇😍😍😇

        May 9, 2023

        ❤️❤️😎♥️

        May 9, 2023

        Play video of me acting in drama class today as the drama car. #CerebralPalsy #”EmojiMeanOkay

        May 9, 2023

        https://vm.tiktok.com/ZGJHLpuGS/

        Selfie of me today all ready to go to drama after having lunch at Morrisons!

        May 9, 2023

        https://www.justgiving.com/crowdfunding/maya-richards?utm_term=aNqzwgQe8❤️

        May 9, 2023

        phone of the day ♥️

        May 9, 2023

        😆😆💖💖💖 A drawing activity that I did on Sunday with my support person.

        May 9, 2023

        good morning good morning to everybody. I hope you have a nice day at work College who volunteer employment after the long weekend that we just had

        May 9, 2023

        please donate to my fundraiser if you can i’d be really grateful ♥️ this is to help with respite care and DofE support

        May 9, 2023

        https://www.justgiving.com/crowdfunding/maya-richards

        Royal School For The Deaf Derby Signs National Anthem With Choir

        May 9, 2023

          A school for deaf children has used British Sign Language to perform the national anthem for the Coronation.

          Pupils from Royal School for the Deaf Derby’s choir used British Sign Language for the performance, while Derby Cathedral’s choir sang in accompaniment.

          The school said it wanted to do something special for the Coronation.

          The performance was recorded and has been shared on the school’s social media sites.

          Head teacher Paul Burrows said: “Our school is the only Royal school in the area and we wanted to do something really special to mark the Coronation and Deaf Awareness Week.

          “We have established very good links with Derby Cathedral and it was a genuine joy to work with the choir on this performance.

          “The result is incredibly moving and I think you can see on the children’s faces just how proud they were to be able to record this tribute to the new King.

          “We hope everyone enjoys this performance as much as the choir did performing it.

          “Who knows, maybe the King himself will visit our school one day in the future?”

          The performance also marked the start of National Deaf Awareness Week.

          The school had previously marked the death of Queen Elizabeth II by signing the national anthem as a tribute to her.

          Mr Burrows added: “Derby is well known as the city of planes, trains and automobiles, as it should be, of course.

          “But it is also the home of our wonderful school which has helped create the largest deaf community outside of London – a fact which should be celebrated too.

          “It is the only school for deaf children which has a royal status, which was granted by Queen Victoria during her Diamond Jubilee celebrations.”

          happy tuesday everyone :)

          May 9, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=b873gnzVn😎💜💕❤️❤️💜💜💜🙂💕

          May 8, 2023

          pan grading for my website, please click on this link if you would like to donate thanks Meyer to every member of this community, and every reader who reads this broke because your engagement and effort to read my content means more to me than anything

          have a nice evening and remember to check out my just giving ring 💜💜❤️

          May 8, 2023

          is saying from one over human program who enjoys reading this book. I know I certainly do.

          May 8, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=vRdJakV27

          May 8, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=vRdJakV27

          May 8, 2023

          postcode fundraising. #Foundations #AppreciatedByMe #ClickHereToDonate

          Afternoon Oaklands, saying of this Tuesday,, saying overhaul and beyond

          May 8, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=8Qx43PPpm

          May 8, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=W6ywy5dzK my fundraising route to help raise money for my respite care and easy support if you would like to donate to come it is very much appreciated. Prime me and my family💕🙂🙂💕💕💕

          May 8, 2023

          movies with my friend, Joe, I really enjoy spending time with her 💖💖💖💖💖💖

          May 8, 2023

          Here is the saying for those that won’t be celebrating the UK‘s king coming into power this weekend, but are still having a bank holiday.

          May 8, 2023

          A drawing activity that I did with my support yesterday afternoon.

          May 8, 2023

          even more pictures of me at choir last thursday :)

          May 8, 2023

          your Sunday saying 💜

          May 7, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=89ZXEx2aN

          May 7, 2023

          my fundraising group click on this to donate to wards my respite and they are really care

          some are retarded one year ago today this is scratch oh

          May 7, 2023

          Colour by letter I did this afternoon with my support. I loved it. I was able to complete it with only a little bit of assistance.

          May 7, 2023

          more pictures from choir last thursday that i enjoyed very much with my friends 🎤

          May 7, 2023

          me on the stage at choir on thursday singing with my group 🎵

          May 7, 2023

          Picture of my scrapbook page which I completed today with my support. Just a reminder about my just giving page as well. I will stick cooling down those that want to donate towards my respite can do so thanks Maya Maya

          May 6, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=qnnY6D6Ge

          me or my evening walk to go to the chip shop. Look at my new cute hat. I love it as it is a bit windy to eat outside today.

          May 6, 2023

          no no “who everybody in this community. Good afternoon, same difference

          May 6, 2023

          A page of my scrapbook, which I made yesterday evening with my support person

          May 6, 2023

          Models using stencils and air dry clay that I made with my friend 3 years ago who I went to school with!

          May 6, 2023

          Picture of me doing some painting of an activity from my activity book that I was gifted for my birthday in November.

          May 6, 2023

          Hi SameDifference Community – Good Morning!

          May 6, 2023

          I have some wonderful news to announce to my community on here.

          As you may all know, I’ve been fighting to get back into education for the next academic year. I have been accepted onto my Maths course starting in September and have an interview for my Health and Social Care, due to start in October but I will be enrolling in August!

          I will update after my interview but I hope to tell you all that I have a place on Health and Social Care Level 2. Fingers crossed for me!

          #Furthereducation #CerebralPalsy #Fightforaccesstoeducation #Wanttoqualify

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=QGPYG48X7🙃

          May 5, 2023

          Hastye Grace, very high standard cerebral palsy #FromRaising #HelpMeToGetToTheThousandPounds

          fundraising route for those that want to donate this Friday during me today for my Friday, too busy, including another string out. Click on the link to donate all donations are very much appreciated by me and I will put it to good use for my dear Rees support and restaurant. #Respite #CerebralPalsy #Son

          May 5, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=xdzpJQXQ6

          Full length picture of me all dressed up when I went out on Tuesday night! :D

          May 5, 2023

          Stay tuned for this evenings String Art that I am going to finish off with my PA. This time its all about decorating the word ‘Love’ in string :)

          May 5, 2023

          Join me on Monday to see the process of me making your raffle prizes with my PA! #Soapmakingproject #Creative #Creatingsomethinguseful

          May 5, 2023

          Your raffle prizes are going to be as unique as me ❤

          Click Here: Twitter Alt Text Meme That Isn’t Funny For Blind People

          May 5, 2023

           

          You’ve probably seen one of the latest Twitter memes doing the rounds.

          There’s black text – “click here” – on a white background. And an arrow pointing to the ALT image description label. Behind that, there’s a joke or a punchline.

          Brands including McDonald’s (ALT: “Extra pickles life”) and Red Bull Gaming (ALT: “Ice cold Red Bull”) have jumped on the trend.

          Just a bit of light-hearted content to make their followers laugh, right?

          Well, alt text, short for alternative text, is a description of an image used by blind or partially sighted people to help them navigate social media.

          So if you’re visually impaired, this joke’s not for you. And that’s got people upset.

          ‘A meme for sighted people’

          Connor Scott-Gardner is blind and says alt text is so important to him because so much content posted online relies on images.

          “There are entire social media platforms like Instagram, which are image-based,” he says.

          “And we share a lot of information through images, whether that’s text or through memes, whether we’re making a joke or just through culturally significant things.

          “So for me alt text gives me access to all of that content, and it means that I’m able to have an equitable experience on the web.”

          So Connor, 29, says that the “click here” meme left him feeling “excluded on a very fundamental level”.

          “It actually took sighted people calling out the meme for blind people to even know what it was,” he tells BBC Newsbeat.

          “It’s very much a meme that is created for sighted people.”

          Connor and other users hit out at some brands who’d jumped on the meme. McDonald’s Canada actually replied with an apology and deleted their post.

          It took another company, Specsavers, to turn the trend on its head.

          In a tweet that’s been seen millions of times, the company posted its own version of the “click here” meme.

          But it used the alt text to make a serious point instead of cracking a joke.

          It wrote: “Alt text is a hugely important accessibility tool designed to help people navigate the internet more easily, so it shouldn’t be used as a punchline.

          “This is especially true if the Alt text doesn’t describe the image, leaving blind and visually impaired people out of the joke.”

          ‘Inclusive content is good content’

          Becky Brynolf, who’s the head of social media at the Royal National Institute of Blind People (RNIB), agrees.

          “Adding good alt text is such a quick win, I’m really surprised that more people don’t do it,” she says.

          “Inclusive content is just good content. So you really shouldn’t be excluding anyone, especially not for a joke.

          “If you wouldn’t take someone’s guide cane to show off how well you can twirl it about, you absolutely shouldn’t be misusing alt text for the sake of a joke.”

          How to make your feeds more accessible

          Becky says you can be really descriptive with your alt text, because you have 1,000 characters to play with.

          “I’ve been really disappointed by all the tweets coming from the Met Gala, for example, that just say something like ‘Jeremy Strong attends the Met Gala’,” she says.

          “But what is he wearing? What’s his facial expression? What’s the vibe like? Does he look happy to be there?

          “Blind people want to hear about the fashion too. So don’t feel like people aren’t interested just because they can’t see the visuals.

          “And just always think of accessibility as like a love note. Like it tells people we want you here as well.”

          Connor says he’s especially annoyed that so many of the brands jumping on the bandwagon don’t use alt text in their other posts.

          He says some have even posted things since without alt text.

          “So it’s very clear that they have no interest in including blind people or giving us access to information,” he says.

          “They’re only using that accessibility feature when it’s convenient to them and brings something to their sighted followers.”

          Newsbeat contacted Twitter for a comment but it replied in the same way it does to all media, with a poo emoji.

          Yay it’s Friday!

          May 5, 2023

          my evening, saying to everybody in the community 😆😆👩🏾‍🦽😆

          May 4, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=8z2PkGGda fundraising link who am I with sprite

          May 4, 2023

          my first ever night out 4 years ago today with friends :)

          May 4, 2023

          Please stay tuned for my Soap Making which I am planning to raffle off as part of my fundraising efforts for my respite care and DofE support <3 comment down below if you would like a raffle ticket and I will send an electric one through SameDifference!

          May 4, 2023

          Keep Calm and Keep Fundraising! I’d appreciate and put any donations to good use this summer when I do DofE and any respite trips with a PA! So please donate to help me reach my £1000 goal on my JustGiving page which will be linked below <3

          May 4, 2023

          https://www.justgiving.com/crowdfunding/maya-richards

          Happy Thursday! :)

          May 4, 2023

          You could be in for a chance of winning these prizes when you enter my raffle for respite care fundraiser!

          May 4, 2023

          Flavours of soap are:

          Vanilla

          Rose

          Gardenia

          Chamomile

          Cherry Blossom

          White Tea

          To enter, please put the word “Raffle”, with your name (can be your real name or username) in the comments below this post in the comments. You will then receive a raffle number electronically.

          Not quite sure when it will be drawn, details to be announced. Donate to my JustGiving or GoFundMe, linked below for a chance to win. Please use the same name to donate as the name in the comments.

          I will put up a video to reveal who has won after I have announced the draw of the raffle, and the date and time of it. Thanks and have fun with this!

          https://www.justgiving.com/crowdfunding/maya-richards

          DWP Needs To Come Clean About How Many Desperate Callers They Deliberately Disconnect

          May 4, 2023

          With many thanks to Benefits And Work.

           

          Claimants are waiting over half an hour, on average, for PIP and DLA helpline calls to be answered, DWP minister Tom Pursglove admitted in a written parliamentary answer last week. But the minister now needs to come clean about how many callers never get an answer at all, because they are deliberately disconnected using a practice the department refers to as ‘call-blocking’.

          Labour MP Beth Winter asked about waiting times for calls last month.

          The response from the minister for disabled people was that the average waiting times for the PIP, DLA and AA telephone enquiry lines for the month of March 2023 were:

          PIP – 37 minutes

          DLA – 33.5 minutes

          DLA65+ – 6 minutes

          AA – 2 minutes

          Clearly average waiting times of over half an hour for PIP and DLA are absolutely unacceptable, although many people who contact us have waited much longer without getting an answer at all.

          But Pursglove’s response hides much more than it reveals. Because we also need to know about the number and proportion of calls that don’t get answered.

          This would include claimants who hang up after waiting often for an hour or more.

          And, crucially, it would include callers who are being deliberately and repeatedly cut-off by the DWP.

          Back in March of this year a parliamentary question was asked about waiting times for the DWP Future Pension Centre. Call volumes had increased ten-fold as people tried to check their national insurance contribution record before a deadline.

          The answer revealed that in March 443,000 calls out of a total of 517,00 had been blocked by the DWP – almost nine in ten callers. The practice is known by the DWP as ‘call-blocking’ and means that the DWP does not allow the call to enter the call waiting queue because there are too many people in it already. Instead, the line simply gets cut-off.

          This sounds very similar to what has been happening to many callers to the PIP helpline, who report being repeatedly cut-off:

          “Received PiP review form but my partner who it relates to is unwell in bed for last 3 days. Time scale for return quite short. Rang to get extension today. Keep getting cut off. Must have tried 10 times.”

          “Been trying for Weeks to get through to change bank account details and it cuts off as soon as you go through all the automated talk. Three weeks ago got through the talk on the ‘make a new claim’ section only to hold for an hour and a half. I gave up without speaking to someone.”

          “Ridiculous wait times, been trying to phone for 4 days now and each time it either cuts me off during asking for my details, or there is an hour 30 wait time and it cuts off. Only need to ask for an extension to my date as the forms only just arrived giving me 7 working days to reply back. I can’t even get an appointment with CAB in the next 2 weeks, let alone my doctors to request supporting documentation and they give 7 working days?”

          In his written answer, the minister’s explanation for the long waiting times was:

          “We are currently experiencing higher than forecast call volumes to the PIP and DLA telephony enquiry lines. We have recruited additional staff onto our telephony teams and have on-going recruitment to further increase resources.”

          But, without knowing how many staff are being recruited and how many staff are already in post it is impossible to tell whether the extra staff are likely to make any real difference.

          So, it’s good news that MPs have begun raising the issue of DWP call handling with ministers, but there are a lot more questions that need to be asked.

          A picture of me dressed up from last night :)

          May 3, 2023

          lianne, one of my Bestie from the first year of my private education, college, Joe name, two years ago, she died having some Snapchat Mum was sitting together having for tea when re allowed to visit six people outside when restrictions started to be a little less restricted #Friends #2YearsAgoHasTextReminderWhenWeWhereAreYouLikeToMeet6PeopleOutside #Fun #DayOut #2

          May 3, 2023

          Picture of me out last night. I had fun and enjoy seeing some of tomorrow study with

          May 3, 2023

          https://www.justgiving.com/crowdfunding/maya-richards?utm_term=52QBdeXgG phone, if I am do you have a qualification support thank you

          May 3, 2023