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make up for karaoke night on 🥰♥️♥️zoom to years ago

March 14, 2023

Play karaoke night two years ago on zoom

Baroness Masham, Paralympian And Longest-Serving Female Peer, Dies Aged 87

March 14, 2023

    Baroness Masham, a Paralympian and the longest-serving female member of the House of Lords ever, has died aged 87.

    Lady Masham won medals in swimming and table tennis at the 1960, 1964 and 1968 games and was created a life peer in 1970.

    She spent much of her career campaigning for disability rights.

    The Spinal Injuries Association, which she founded in 1974, said it was “devastated to have lost our greatest champion”.

    She died peacefully in hospital in Northallerton, Yorkshire, on Sunday, it said.

    Lady Masham, born Susan Sinclair, became a wheelchair user after suffering an injury to her spinal cord in a riding accident in 1958.

    Two years later, she won a gold medal in the 25m breaststroke at the Paralympic games in Rome, and in 1964 won another in the women’s doubles table tennis in Tokyo.

    She won a further six silver medals and two bronze across both sports in the three games at which she competed.

    In 1976, she was the subject of an episode of This Is Your Life.

    She sat as a crossbencher and spent a total of 53 years in the House of Lords, more than any other female peer in history.

    She set up the Spinal Injuries Association to address a lack of specialist care or advice available to newly injured people and served as its president until her death.

    The association described Lady Masham as “the reason we have been able to champion, fight, serve and support thousands of spinal cord injured people ever since”.

    “Our condolences go to her family at this sad time,” it said.

    Lady Masham also sat on a number of all party parliamentary groups (APPGs), including those on global tuberculosis, HIV and Aids, and malaria.

    The APPG on global tuberculosis said she had been “one of parliament’s most vociferous champions for disability rights and has worked tirelessly to advocate on behalf of people around the world living with TB and HIV”.

    “Baroness Masham’s remarkable life serves as a testament of her compassion and dedication. She will be greatly missed by all,” it said.

    karaoke night with disco lights in the living room to

    March 14, 2023

    send where is the airport on the link to go with to help to raise money for qualifications, support, and for this summer and I appreciate all your interacting with my pal thank you :-) my

    March 14, 2023

    https://www.justgiving.com/crowdfunding/maya-richards?utm_term=WnZKEJe2e

    fundraising and three donation link. Thanks for all donations that you may give every thanks mate

    March 14, 2023

    fundraising ring Team I just giving page for those that might want to donate as I am still trying to work toward my goal of my diary planning some respite breaks

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    Jersey Dad Welcomes More Consoles For Disabled Gamers

    March 14, 2023

      A father who has been making video game consoles more accessible for disabled children has welcomed gaming companies getting more involved in the process.

      Rory Steel, from Jersey, made consoles for his children Corban, eight, and Ava, 12, who have spastic paraplegia affecting their motor controls skills.

      He said big gaming firms were now making their own specialised consoles.

      It follows the success of Mr Steel’s YouTube channel on which he shows how to make consoles.

      Mr Steel, the head of Digital Jersey Academy, said he had spent the past three years “putting a lot of effort into these controllers”.

      He said “the good news is… now the actual big companies have £30 accessible controllers”.

      He added: “While it seems frustrating that I’ve wasted my time for three years, I really haven’t because I hope they were learning from that – seeing there’s a demand for disabled gaming.

      “We have really seen a lot of the big names, PlayStation and XBox, put accessibility into their gaming.”

      Mr Steel said he was “a big gamer” in his youth and he wanted his children to have the same fun that he had.

      “Everyone loves to play their games,” he added.

      “Everyone remembers the iconic game they had as a child and I just wanted them to have those same experiences.”

      Me next to a statue of an old fashioned pub a bit like one on Emmerdale.

      March 14, 2023

      travel project at the Dave service two years ago, Wednesday service with Tressel 🛫

      March 13, 2023

      doing about our group travel destinations at Learning Hall leisure in lockdown. Here is a picture of Sam. Oh, I did to represent the thought of her role that I like to do before nobody could travel out side of the UK because of

      James Martin: From Belfast Barista To Beverly Hills

      March 13, 2023

        It’s not often that a Belfast barista gets serenaded by the glitterati of Hollywood.

        But then it’s not often that you win an Oscar and celebrate your birthday at the 95th Academy Awards.

        Cue James Martin. Coffee connoisseur, soccer lover and one of those rocking the night away with Sir Elton John at the Los Angeles After Party.

        Martin, 31, is one of the stars of An Irish Goodbye, which won an Oscar for best live action short film, just weeks after it clinched a Bafta.

        Filmed on location in Londonderry, Templepatrick and Saintfield, Martin previously said an Oscar win would “put the icing on my birthday cake”.

        Who is James Martin?

        The broadcaster Ivan Martin was told when his son was born with Down’s syndrome that he may never speak.

        “But here we are. James not only speaks, once he started speaking he hasn’t shut up since,” Ivan Martin told BBC News NI, just hours after the Oscar win.

        And what a journey it’s been for the former pupil of Harberton Special School in Belfast.

        Martin got the acting bug after joining the Belfast-based Babosh theatre company, which was set up about 20 years ago for children with learning disabilities.

        In 2020, he told the Disability Horizons newsletter that he had agreed to give it a go at the theatre group.

        “I’m very glad I went, as I got to meet Breige Hawkins and her staff,” he told the newsletter.

        “Breige was a great teacher who knew her stuff and inspired us all to improve our acting skills. We did all types of shows and I enjoyed every minute of it.”

        https://emp.bbc.co.uk/emp/SMPj/2.47.3/iframe.htmlMedia caption,

        James Martin was in festive mode jamming on his harmonica in an Irish pub in LA

        From treading the boards in Belfast, Martin landed the lead role in the BBC drama Ups and Downs, alongside actress Susan Lynch.

        Written and directed by fellow Irishman Eoin Cleland, who has a sister with Down’s syndrome, the film focuses on the story of a young man with Down’s Syndrome wanting his own independence.

        “He wants to get his voice to be heard,” Martin told BBC News NI at the time.

        “It makes him more open and honest with his family and that’s good too.”

        Martin then went on to get a part in the ITV and Netflix drama Marcella.

        But arguably his most high-profile acting job to date, certainly the one that has garnered the most publicity, is An Irish Goodbye.

        Directed and written by Ross White and Tom Berkeley, it tells the story of two estranged brothers who came together after their mother’s death.

        The black comedy, set on a rural farm, stars James Martin as Lorcan, alongside Seamus O’Hara who plays his older brother Turlough.

        Ahead of the ceremony, Martin showed up in a Los Angeles pub – playing his harmonica for a rendition of Dirty Old Town in a jam session.

        Mencap ambassador

        Martin is also a Mencap ambassador in Northern Ireland and has previously said that having Down’s Syndrome “doesn’t really hold me back”.

        Martin told the BBC’s Today programme on Monday morning: “It doesn’t matter if you have Down’s Syndrome, as long as you’re doing what you do. I do what I can to be funny.

        https://emp.bbc.co.uk/emp/SMPj/2.47.3/iframe.htmlMedia caption,

        ‘Holding this Oscar is just fantastic’

        “I’m the first person with Down’s Syndrome not just getting a Bafta but also getting an Oscar, especially in the time of my birthday – it’s just fantastic.

        “My drama group to me is very important – I’ve been doing drama a log time. But not just drama, Mencap and Starbucks too, fingers crossed.”

        He is a keen runner and has previously taken part in park runs with The Falcons – a group of young adults with learning difficulties, who are part of the Queen’s parkrun community.

        “It’s more about what you have inside you but not outside of you,” he told BBC News NI several years ago.

        He can also be spotted at Irish league grounds on the weekend – often accompanied by his dad.

        The day job

        Martin’s day job for the past 10 years has been at Starbucks in Castle Lane and Victoria Square as well as Scalini restaurant in south Belfast.

        His work colleagues are said to be very proud of his acting success, with good-luck posters adorning the walls of the coffee chain’s city stores.

        But having traded his green apron of Starbucks for a swanky leopard-skin jacket at the Oscars, will he be swapping the kitchen for the stage permanently?

        His dad said despite the fame, he couldn’t see his son leaving his jobs “any time soon”.

        And Ivan Martin couldn’t be more proud.

        “What an achievement, I’m just delighted,” he told BBC News NI.

        “I haven’t been able to get him – he was at the Elton John After Party.

        He said his son tackles everything with great gusto – and that has now paid off.

        “He loves the acting, he’s loved this ride with the Oscars and the Baftas,” said Ivan.

        “All I ever wanted for James was that he’d be happy; I’ll tell you what, he’s happy now.”

        More here.

        Dame Judi Dench Backs Call To Overturn York Blue Badge Ban

        March 13, 2023

          Dame Judi Dench has given her “wholehearted support” to campaigners calling for a ban on blue badge parking in York city centre to be lifted.

          A permanent ban on disabled parking in pedestrianised areas was introduced in November 2021.

          The decision angered many of those affected, who said they had been made to feel like “second-class citizens”.

          Marilyn Crawshaw, from the group Reverse The Ban, said Dame Judi’s support was “a great boost”.

          She said the group was “absolutely delighted” to have received a message from the James Bond star, who was born in the Heworth area of York.

          The Oscar-winning actor, 88, said: “York city centre is a rare jewel that should be free for all to enjoy, including those with a disability and for whom accessible parking is essential.

          “As someone living with sight loss, I know only too well how gaining access to places can be exceptionally difficult.

          “York city centre should be fully accessible through these types of schemes.

          “I should like to offer my wholehearted support to people in the City of York who are asking the local council to reconsider any ban to the blue badge scheme in the city centre.”

          Ms Crawshaw said “When we have somebody like Dame Judi Dench coming out and supporting us it’s a great boost to us.

          “It’s lovely to think that somebody with such a high profile is willing to speak out.”

          Ms Crawshaw said Dame Judi’s words were “particularly heart-warming and encouraging and we hope it will help the situation change.”

          The parking ban came into force after the council installed anti-terror measures to prevent the risk of so-called hostile vehicle attacks.

          Councillors previously said they had approved a series of mitigation measures, including dropped kerbs, the employment of an access officer and a feasibility study into an accessible shuttle service.

          Ms Crawshaw said postgraduate students from the University of York had conducted research into the way counter-terror measures could be reconciled with meeting the rights of disabled people.

          She told BBC Radio York the group planned to issue findings from the research soon.

          Me and an amazing instrument which I believe is called a harp at the Luton Museum also four years ago.

          March 13, 2023

          what I have achieved at College in 2023/2022. A picture of my certificate for common health conditions. Level two that I have just received.

          March 12, 2023

          neon crab night with Silver Birch the company during lockdown, Royal zoom who is a picture of me rest up in Lyon plus Curve night to you memory came up this morning at two years ago today

          March 12, 2023

          how do you spell today’s time difference my date today going to be making pancakes for breakfast this time and then we are going to go a PowerPoint old secondary school, where I am I gay for preparing for adulthood conference today where I am proud to be selected is what is what is the time

          March 11, 2023

          Me posing as an army soldier at Luton Museum 4 years ago next to a statue of one.

          March 11, 2023

          Eating in the stables restaurant at my old college run by the catering students. Here is a selfie of me and my wonderful lunch I ate there.

          March 11, 2023

          museum fashion, and my interesting person is open for person is my hobby. This is why I like to visit the museum, even crazier than them who is the Japanese a.m. four years ago, I had a whole entire him. I didn’t miss you before we heard fashion retail when people used to make and design their own clothing, such as sewing et cetera. As the details on it looked quite

          March 10, 2023

          Jackets at the museum that people used to wear in the olden days before they were sent

          States Of Jersey To Bring Back Support Worker For Deaf People

          March 10, 2023

            Jersey is to see a British Sign Language (BSL) support worker reinstated after the government cut funding for the role in 2018.

            Deputy Malcom Ferey said the post would return, alongside potentially two part-time social workers and more equipment.

            This would allow members of the deaf or hard-of-hearing community to “live more independent lives”, he said.

            The community had been “left behind” since funding was axed nearly five years ago, he added.

            Deputy Ferey, Assistant Minister for Social Security and Assistant Minister for Health and Social Services, said he did not know why the role was cut in the first place.

            Jersey born Ella-Louise Territt has been deaf since she was 18 months old, and has had to travel for hearing appointments since she was young.

            ‘It doesn’t work’

            She said the support worker had attended medical appointments with her, including flying to London.

            “There’s literally no sign language interpreter in Jersey for hospital or doctors, dentists; pretty much anything for medical terms or bank or tax,” she said.

            “All government do is give us an iPad with Facetime with someone from the UK, but it doesn’t work – we need a professional interpreter.”

            Miss Territt said since the removal of the role, she had volunteered to interpret at appointments for other deaf people.

            “I want to help them because I’ve been through what they’ve been through and I don’t want them to struggle,” she said.

            Gabriele Schiessl from charity Earsay said there had not been adequate and consistent support since funding was axed.

            “After various consultations the government has realised that support is needed and is now looking into finding the right person for Jersey’s deaf and hearing-impaired community,” she said.

            The Royal National Institute for Deaf People (RNID) is a UK charity that campaigns for deaf and hard-of-hearing people to have equal access to spaces, services, health care and job opportunities.

            In the UK, all NHS care and or publicly-funded adult social care services are required to follow the Accessible Information Standard law, introduced in 2016.

            RNID policy lead Ayla Ozmen said the island could introduce legal requirements for all health and social care providers to “meet people’s communication needs”.

            “It’s not just about people losing their autonomy and having to get family and friends to talk about confidential, personal issues at a medical appointment, but… if you can’t communicate in a medical appointment, then of course, it’s a safety issue,” she said.

            Deputy Ferey said Jersey’s legislation was better suited the needs of an islander with disabilities than the UK’s as it was built on a social, rather than medical, model.

            Mr Ferey said the government was also looking at assistive technology, including BSL translation via an app.

            “I think in some ways the deaf community have been a little bit left behind and we’re really keen to make sure that that stops now and that other members of the disability community have the support and structures in place that they need,” he said.

            “So yes, there will be more support coming in all different shapes.”

            Mr Ferey did not confirm how much would be set aside for the social workers, but the roles would return “within the next weeks and months”.

            Me dressed up as a judge 4 years ago being silly at the Luton Museum.

            March 10, 2023

            👍👍👍 who years ago, memory of Harpenden Museum, enjoying learning about old women’s fashion, what that used to be used, retail providers, 👗😛♥️👍👗👍👗

            March 9, 2023

            #Independence #YoungPersonWithCerebralPalsy #JustGraduated4YearsAgo

            March 9, 2023

            memory of me for years ago, when I first left school in a pub, having a lemon and Coke

            ♥️♥️😆 dance festival so that I attended today. I hope that your sister very talented and here is some pictures of me already to attend the show this afternoon.

            March 9, 2023

            Wanted: Aluminium Welder For Wheelchair Design

            March 9, 2023

            Posting by request:

            Please connect me to an aluminium welder who can press steel into aluminium and make this wheelchair frame without technical drawings: retotogni.com/the-reagiro-original

            Harry

            07472 768 414

            My submissions for World Poetry Day that I have done for my volunteer job and written by myself. Hope you enjoy! 📖✒️

            March 9, 2023

            People living with dementia and hearing conditions invited to shape future research

            March 9, 2023

            A press release:

            Programme will give patients a greater voice

            28 February 2023

             

            Embargo: 00.01 Friday, March 3rd, 2023

            People living with dementia and hearing conditions, their families, and their clinicians are being encouraged to make their views known through a new national research prioritisation programme that could drive future research.

            The new programme, called a James Lind Alliance Priority Setting Partnership (PSP) for co-existing dementia and hearing conditions, will be launched on World Hearing Day (3rd March 2023) by the National Institute for Health and Care Research (NIHR) Nottingham Biomedical Research Centre (BRC) and the University of Nottingham.

            The PSP will identify the top priorities for research about the prevention, diagnosis, and treatment of dementia and hearing conditions, such as hearing loss, tinnitus and hyperacusis, by consulting people affected by these conditions and their clinicians. The PSP outcomes will impact research funding, commissioning, and policy in the future, to benefit people living with these conditions.

            With hearing loss affecting one in five of the UK population, including many people living with dementia, and with the prevalence of both dementia and hearing loss increasing, researchers are keen to understand the concerns of people living with these conditions along with those who provide care. The programme is being carried out in partnership with the James Lind Alliance, Alzheimer’s Research UK (ARUK) and the RNID, the charity supporting people who are deaf, have hearing loss, and tinnitus.

            Dr Eithne Heffernan, Senior Research Fellow at the Nottingham BRC and the University of Nottingham, is leading the Priority Setting Partnership alongside a steering group of people who live with dementia and hearing conditions, and clinicians.

            She said: “By ensuring that people living with these life-changing conditions have a voice – along with their families and clinicians – we can make future research into dementia and hearing loss more relevant, beneficial, and impactful for people in the UK and abroad.”

            People living with dementia can experience severe difficulties, including communication problems, diminishing independence and social isolation. Having hearing conditions in addition can significantly exacerbate these difficulties.  It also means that accessing suitable diagnostic assessments and treatment options becomes even more challenging. Furthermore, a commission by The Lancet has highlighted hearing loss as being one of the main risk factors for developing dementia.

            Dr Heffernan added:

            “Through the PSP, people affected by these co-existing conditions will have a strong say in which research programmes are carried out about hearing conditions and dementia in the future. This will avoid research studies being conducted, or treatments being developed, that don’t address the real problems patients face in everyday life.”

            The Nottingham BRC team and its partners will make sure that the outputs of the process are brought to the attention of research funders, research commissioners and policy makers so patients can access the best, most appropriate care in future.

            Hearing experts at Nottingham BRC have previously led three James Lind Alliance PSPs into Ear, Nose and Throat Conditions, on the prevention, diagnosis and management of mild to moderate hearing loss, tinnitus and hyperacusis. The BRC and its partners have more than a decade’s experience in helping shape research programmes through patients’ voices.

            Nahid Ahmad, James Lind Alliance adviser, who is chairing the PSP, said:

            “I’m delighted to be supporting this PSP in using the JLA method to identify and prioritise the research needs of people who live with coexisting dementia and hearing conditions, their families and carers, and the clinicians who work with them. It is an interesting approach for the JLA to consider these two conditions together. The partnership will be consulting widely and working hard to involve communities that are often underrepresented in research.  The Top 10 priorities will be an important call to action for researchers and funders, making them aware of the issues that matter most to people who need to use the research in their everyday lives.” 

            Dr Susan Mitchell, Head of Policy for early detection and diagnosis at Alzheimer’s Research UK, said:

            “Alzheimer’s Research UK is looking forward to being part of the Priority Setting Partnership for dementia and hearing conditions. Despite growing evidence suggesting a relationship between hearing loss and the increased risk of dementia, there is still so much we don’t understand – what are the key mechanisms behind the relationship between the two conditions? What are the suitable interventions to reduce the risk of developing dementia?

            “This partnership gives us a great opportunity to determine the gaps in the current evidence in hearing loss and dementia, and identify top priorities for future research across the UK. This will also help us shape our future research funding and policy work so it benefits people living with hearing loss and dementia.”

            Ralph Holme, Director of Research and Insight at RNID, said: 

            “We are pleased to be involved in this Priority Setting Partnership, driving forward research in this important area that could make a huge difference to millions of people.

            “We know that hearing loss and dementia can often occur together and have an impact on each other, and there is still a lack of understanding about the prevention, diagnosis and treatment options for people who are living with both conditions. As well as being involved in this PSP, we are co-funding three other important research projects to investigate the links between hearing loss and dementia more closely and help find the answers that so many people are looking for.”

            • The PSP will launch on World Hearing Day (3rd March 2023). It will entail reviews of published evidence as well as surveys and a workshop with people affected by dementia and hearing conditions and clinicians. You can contact the partnership by emailing the coordinator at sian.calvert@nottingham.ac.uk. Follow the latest PSP updates on Twitter at @DementiaHearPSP, @NottmBRC and @hearingnihr

             

             

            For more information, images, or interview and filming opportunities, contact Andrew Bennett, email: richard.bennett@nuh.nhs.uk at Nottingham University Hospitals NHS Trust. Mobile +44 07812 275573.

             

             

            About the NIHR Nottingham Biomedical Research Centre

            The NIHR Nottingham Biomedical Research Centre is translating research into breakthroughtreatments, new technologies and advanced medicines for common illnesses like asthmaand arthritis. 

            Our research is led by internationally renowned clinicians, scientists and academics workingtogether to improve the health of our patients and our communities. 

            Our expertise in respiratory medicine and MRI is at the forefront of COVID-19 research foreffective treatments and vaccines, as well as contributing to the world’s understanding ofCoronavirus.The NIHR Nottingham Biomedical Research Centre is funded by the National Institute forHealth and Care Research and is a partnership between Nottingham University HospitalsNHS Trust (NUH) and the University of Nottingham, working with NottinghamshireHealthcare NHS Foundation Trust and NHS and academic partners across the EastMidlands.  It is based at NUH.About the NIHR

            The mission of the National Institute for Health and Care Research (NIHR) is to improve thehealth and wealth of the nation through research. We do this by:· Funding high quality, timely research that benefits the NHS, public health and socialcare;· Investing in world-class expertise, facilities and a skilled delivery workforce totranslate discoveries into improved treatments and services;· Partnering with patients, service users, carers and communities, improving therelevance, quality and impact of our research;· Attracting, training and supporting the best researchers to tackle complex health andsocial care challenges;· Collaborating with other public funders, charities and industry to help shape acohesive and globally competitive research system;· Funding applied global health research and training to meet the needs of the poorestpeople in low and middle income countries.

            NIHR is funded by the Department of Health and Social Care. Its work in low and middleincome countries is principally funded through UK Aid from the UK government.

            Website: https://www.nihr.ac.uk/

            About the University of Nottingham

            Ranked 18th in the UK by the QS World University Rankings 2023, the University of Nottingham is a founding member of Russell Group of research-intensive universities. Studying at the University of Nottingham is a life-changing experience, and we pride ourselves on unlocking the potential of our students. We have a pioneering spirit, expressed in the vision of our founder Sir Jesse Boot, which has seen us lead the way in establishing campuses in China and Malaysia – part of a globally connected network of education, research and industrial engagement.  

            The University is among the best universities in the UK for the strength of our research, positioned seventh for research power in the UK according to REF 2021. The birthplace of discoveries such as MRI and ibuprofen, our innovations transform lives and tackle global problems such as sustainable food supplies, ending modern slavery, developing greener transport, and reducing reliance on fossil fuels.

            The University is a major employer and industry partner – locally and globally – and our graduates are the second most targeted by the UK’s top employers, according to The Graduate Market in 2022 report by High Fliers Research. We lead the Universities for Nottingham initiative, in partnership with Nottingham Trent University, a pioneering collaboration between the city’s two world-class institutions to improve levels of prosperity, opportunity, sustainability, health and wellbeing for residents in the city and region we are proud to call home.

            Hearing Sciences at the University of Nottingham School of Medicine is a flourishing UK centre of auditory research. Its mission is to deliver research-led innovations that can lead to improvements in daily living for people who have hearing-related problems.

             

            About the James Lind Alliance

            The James Lind Alliance (JLA) is a non-profit making initiative bringing patients, carers and clinicians together in JLA Priority Setting Partnerships (PSPs).  JLA PSPs identify and prioritise unanswered questions or evidence uncertainties that they agree are the most important, so that health research funders and researchers are aware of the issues that matter most to the people who need to use the research in their everyday lives.  Over 135 PSPs have been completed, in the UK and internationally.  The JLA is hosted by the National Institute for Health and Care Research (NIHR). 

            For more information, please see https://www.jla.nihr.ac.uk/

            About Alzheimer’s Research UK

            • Alzheimer’s Research UK is the UK’s leading charity specialising in finding preventions, treatments and a cure for dementia.
            • For our latest updates follow us on Twitter @AlzResearchUK
            • Our animation “What is dementia?” explains the essentials of dementia and the diseases that cause it https://youtu.be/HobxLbPhrMc
            • Our incredible supporters make our work possible through donations and fundraising, with 1 in 3 of our research projects funded by gifts in Wills. To learn how you can help fund vital dementia research, visit www.alzheimersresearchuk.org or call 0300 111 5555.
            • We are currently supporting pioneering dementia research projects worth nearly £34 million in leading Universities across the UK.
            • How can we challenge perceptions of dementia using only an orange? Find out more at www.alzheimersresearchuk.org/orange and help us share a better understanding about dementia. #ShareTheOrange

             

            About RNID

            • RNID is the national charity supporting people who are deaf, have hearing loss or tinnitus.

            • Currently, one in five adults in the UK have a form of hearing loss. One in eight people have tinnitus. 

            • RNID was founded in 1911. For more than 100 years the charity has pioneered new treatments for hearing loss and tinnitus. It has promoted access to sign language and subtitles, brought in free hearing tests for new-born babies, worked with technology for cochlear implants and developed techniques to help people cope with tinnitus.  

            • If you (or someone close to you) are deaf, have hearing loss or tinnitus and need free confidential and impartial information and support, contact RNID. We are open 8:30am to 5.00pm, Monday to Friday. Find out how to contact RNID at rnid.org.uk/contact

            celebrating international women’s day with Learning for leisure two years ago, international women’s day out my Grindr me

            March 8, 2023

            donate and share if possible thank you my

            March 8, 2023

            crowdfunding link for anybody that might want to donate or read my journey and share it. It is for my respite care and carers to the DMV training fo

            https://www.justgiving.com/crowdfunding/maya-richards?utm_term=3nEkpagaq

            early morning, Salpi, and

            March 8, 2023

            An Irish Goodbye

            March 8, 2023

              It’s safe to say that actor James Martin is looking forward to his upcoming trip to Hollywood.

              The star of An Irish Goodbye, the short film that has already won a Bafta and is now gunning for an Oscar, has an extra reason to celebrate. Sunday’s ceremony falls on his birthday.

              “The leopard-skin jacket is coming out!” he says.

              “I would love to meet Tom Cruise. His movie Top Gun was fantastic. I would love to meet Robert De Niro as we have something in common. My name is actually Robert James so it would be nice to meet someone who has the same name. We’re both actors and we can both be grumpy on set, so maybe it’s a family thing!”

              Martin, who has also starred in BBC One film Ups and Downs and ITV’s Marcella, plays Lorcan in Ross White and Tom Berkeley’s film about two estranged brothers thrown together again after their mother’s untimely death.

              Younger brother Lorcan lives and works on the family farm in Northern Ireland but with their mother (Michelle Fairley) gone, older brother Turlough (Seamus O’Hara) returns from London to announce that Lorcan – who has Down’s syndrome – will have to move in with their aunt. Lorcan is distinctly unimpressed with the idea.

              “Everyone wants to be independent, I’m very independent of my folks,” Martin says.

              “It’s very important [to show what people with learning disabilities can do]. It’s not often you get your own part on a show if you have Down’s syndrome. But never judge a book by its cover.

              “Lorcan’s very independent but the love and the hate and the emotion towards his brother is fantastic. It’s good to have that special bond. If it wasn’t for that special bond… he’d just look at him (Turlough) as a carer.”

              White says the idea about a homecoming first began to germinate after he and Berkeley made a big life decision a few years ago.

              “Tom and I met about 10 years ago when we trained as actors, we were living in London and writing plays as well acting.

              “As our careers went on, we were writing more and more and acting less. In 2019, we made this big decision to leave London, to go back to our respective home towns, Belfast for myself and Gloucester for Tom, and just write full-time and move from writing for theatre into writing for screen.

              “At that time we were thinking a lot about the idea of having left home, and then returning back home and it feeling a little bit like, ‘Are you from that place again?'”

              But they needed a narrative, which came by chance when Berkeley attended a football match.

              “I just happened to see a couple of brothers who were sat a few rows ahead of me watching the game, and the younger brother, much like in our story, had Down’s syndrome,” he tells me.

              “There was an interesting juxtaposition between what was a very typically ferocious, brotherly kind of relationship, quite combative, as they were watching the game. They were hurling abuse at each other! And then… there was this other added layer of responsibility that was there between them as well, which I found quite compelling. There was just something really poignant about the relationship.”

              Berkeley explains that it got them thinking about how people deal with grief in different ways.

              “It was the idea of two people who see the world very differently and processed emotions very differently. The older brother – stoic, a bit repressed, slightly cynical. And then the younger brother, who wears his heart on his sleeve and has this superhuman capacity for empathy.

              “We thought it would be really interesting to see those two opposites go through the process of grief together.”

              While part of the storyline is linked to Lorcan having a learning disability and needing support after the death of his mum, White and Berkeley were keen not to make that the sole focus.

              “We spoke about the idea of the character having Down’s syndrome… once, and then we just didn’t really speak about it that much, because there were so many other factors of that character that were more interesting,” says White.

              “It wasn’t at the forefront for us… and meeting James as an actor, you see the the multi-faceted sides of his personality, and actually the Down’s syndrome is way down the list of interesting things about James. He’s a natural comedian. He’s charismatic.

              “With representation, it’s not enough just to slap somebody in the thing and say we’ve done our job. The role has to be meaningful.”

              Berkeley adds: “Lorcan has the agency of his own story, he’s not orbiting around the other characters. He drives the plot.”

              The black comedy has generally been given a warm reception, with Amano Miura from Dublin’s EPIC: The Irish Emigration Museum, writing: “The dynamic, hilarious, and heart-warming relationship between brothers confronts the audience with existential questions about what really matters to us and where we really call home.”

              Rukayat Moibi from MySohoTimes wrote: “An Irish Goodbye is an ambitious picture that, in a satisfying and heart-warming sense, almost feels as if it could be outside of the short film genre.”

              A rollercoaster of emotion, the film sends you lurching from tears of sadness one minute to tears of laughter the next.

              White explains: “There’s the kind of space between the tragedy and the comedy that feels like the truth in the middle.

              “Coming from Belfast obviously there’s this kind of gallows humour we’ve got with coping with adversity, and that felt like a very specifically Northern Irish thing in that way.

              “It’s also quite a male thing as well,” adds Berkeley.

              Their previous short film Roy starred David Bradley as an elderly widower suffering from loneliness.

              “Both films are about men struggling or badly coping with with grief. And I suppose that’s something maybe we recognise in our own experience and from the chaps in our lives as well.”

              An Irish Goodbye is available on Mubi.

              Don’t press the wrong show at the open Arena on Thursday I am attending it and hopefully will be amazing owed to a review of water thought about it after I have

              March 7, 2023

              Open pool Thursday is to go to a dance festival tomorrow so I will do a review with this so when I come back from a

              “The Thai believe any students that are still studying, simply then, especially if they are very young adults or young people

              March 7, 2023

              positive quotes about being a student, it’s like me

              staging for tomorrow’s blog about my scrapbook and my poetry

              March 7, 2023

              things I have enjoyed watching today Casualty 24/7 on Channel 5 forensic detective things I will enjoy tomorrow 04 upcoming volunteering and very discreet, 30 and 50 miles ticket into it :-)🦋🦋 turn

              March 7, 2023
              September 2026
              M T W T F S S
               123456
              78910111213
              14151617181920
              21222324252627
              282930  

              Wednesday night quote of the day about cerebral palsy and general positive quotes. #Positivity #CerebralPalsyPostcode think reflect me and Mum, and live in my auntie so true in so many ways❤️❤️🤩🥰

              March 7, 2023

              evening time, difference community searching for poetry tomorrow that I am writing for my one of my many volunteer jobs that I get involved in Dayton to see what I write and Walker come up Please share your poetry ideas this poetry day with me so that I can. I have some inspiration and input from you guys. What would you like me to do a poem disability, different ability or abilities and determination please to hear poetry. I write about in the comment section of my blog TuneIn pro poetry day by a person with 23-year-old young woman who is still in education, has text publicly. #CerebralPalsy, #Student #CerebralPalsyLifeAsPerAndPink#GettingInvolvedInAnOpportunityThatIsPresentedToMe

              March 7, 2023

              March 7, 2023

              ring crowdfunding page rely to raise money for my dear Vicky and Samantha restaurant. Is Tracey carers for the expedition.

              https://www.justgiving.com/crowdfunding/maya-richards?utm_term=264W4Zgvv

              what program I am enjoying this morning. Net impression on Netflix series. Maybe one day I’ll be your person designer who knows, but I love this program because I love fashion that is wearing different types of fashion. I suggest you watch it if you love fashion as a hobby or in prayer or even if you were in anyway, I will let you know this series is right right now I am finished watching it

              March 7, 2023

              happy Tuesday everyone

              March 7, 2023

              good morning, are you different and happy hope you enjoy your day. What ever you are doing whether that be volunteering oh full-time or part-time employment. Hope you’re enjoying your Tuesday good morning and have a good day from where I am

              Vitiligo: Controversial Skin Cream May Come To UK

              March 7, 2023

                A controversial new treatment for a condition called vitiligo that can restore pigment to the skin might soon be offered on the NHS, if UK experts approve it.

                Some call ruxolitinib a miracle cream because it can return skin’s natural colour and get rid of whitened patches.

                But it carries some potentially serious side effects.

                Others question whether vitiligo should be celebrated rather than masked or corrected.

                Ruxolitinib (brand name Opzelura) must be prescribed by a doctor because the treatment requires monitoring.

                Opzelura risks and benefits

                It can affect the body’s immune system, which might leave users more prone to infections such as coughs and colds, for example.

                A stronger pill formulation of the same drug is already used to treat some cancers.

                In trials of the cream for vitiligo, some users developed acne and redness affecting the area of skin where it was applied. But it was an effective treatment for nonsegmental vitiligo – the most common type – where patches or blotches of depigmentation appear on both sides of the body.

                About half of those who used it twice a day experienced a significant improvement, and about one in six had almost a complete repigmentation within three months.

                The list price for a tube is $2,000 (£1,660) in the US where it is already approved for use.

                European regulators look set to recommend it, too, for people aged 12 and over.

                What is vitiligo and what causes it?

                Vitiligo is thought to be an autoimmune condition where the person’s own body starts attacking cells in the skin that make protective pigment. This causes visible whitened patches or blotches that are prone to sun damage.

                Vitiligo affects all races but is more noticeable in people with skin of colour. It is not infectious or contagious.

                Experts say living with vitiligo can be psychologically devastating, causing anxiety, depression, low self-esteem and even suicidal thoughts.

                Dr Viktoria Eleftheriadou from the British Association of Dermatologists says some people with vitiligo may feel like they have lost their ethnic identity.

                She said: “The risk of this can be higher among people of colour, as the condition is more noticeable in people with darker skin tones.”

                She says it would be good to offer people the choice of a treatment.

                Winnie Harlow, one of the world’s most recognisable models, has embraced having vitiligo rather than trying to hide her patches, although she has said she found living with it as a child “incredibly isolating”.

                “I vividly recall being in third grade and trying to befriend two girls who would run away from me because their mothers didn’t want them to ‘catch’ what I had, as if I were contagious,” she told Cosmopolitan magazine.

                She describes her skin condition as one of her “greatest gifts”.

                “It has taught me, from the time I was a little girl, to use it as a megaphone: to be louder, prouder, and always fuelled by passion and love. It’s helped me look beyond my own cover – and everyone else’s, too.”

                Emma Rush, founder and chief executive of Vitiligo Support UK, says while it is great to see models raising public awareness, “there is a gap between the average model and the average person on the street”.

                She says many people find having vitiligo on your face can be particularly distressing. “My face is now covered with it. I don’t recognise old pictures of myself from before I had it. It’s like I was a different person.

                “I can wear make-up to cover it but I can’t just walk around unnoticed without it. It helps with that first encounter so people don’t stare.

                “When it starts on the face it is often around the mouth and eyes and those are the parts that people look at. It can be catastrophic experience in a society that is focused on appearances.

                “Having a condition that can turn your skin white is not just impacting your skin colour, either. When your appearance changes, it can come with a whole raft of assumptions about where you come from and who you are.

                “Some people say they feel like they have lost a depth of their identity or had something taken away from them by the disease.”

                She says having it as a new treatment option would be “an absolute godsend”.

                Teacher Joti Gata-Aura was diagnosed with vitiligo in her early 20s. At that time, she says, she would have been willing to try almost anything to remedy it.

                “I battled with it for a very, very long time. I was constantly searching for treatments,” she said.

                “I hadn’t accepted the skin I was in.”

                “I’m Indian. I have brown skin – I’m not a fair-skinned Asian person. So when I had vitiligo I stood out and I covered up my skin for many, many years.

                “I hid my skin so much.”

                Now aged 45, her outlook has changed and she campaigns about body positivity and mentors young people to help them with self-confidence.

                “I’ve done so much work on being happy in the skin you are in and being confident in who you are.”

                She says identity is still a big issue. “My identity was stripped when I lost my pigment.

                “It’s taken so long for me to accept this white skin.

                “It does, for me, add the extra layer of having to… not justify myself, but explain who I am, and that can sometimes be quite difficult, especially now that my skin is whiter than some of my English friends. That’s difficult because I am proud of my background and culture.”

                She said people needed to make their own choices about living with vitiligo.

                “It might not be a disability, it might not be an illness, but people psychologically have been ripped apart because of this condition and I think it is so important that while I’m in a good place right now, I wasn’t in a good place when I was diagnosed.

                “People are going through what I went through 20 years ago. This could be light at the end of the tunnel for many people.”

                Current treatments for vitiligo that result in a return of patients’ natural skin colour are limited and have variable effectiveness, which means that if one treatment worked well for one patient it might not work for another at all, says the British Association of Dermatologists.

                The most commonly used ones – phototherapy, tacrolimus and topical corticosteroids – can all have their downsides. For example, there are side effects associated with the long-term use of strong topical steroids, and phototherapy sessions usually require repeat trips to hospital for several months.

                Ruxolitinib would need to be approved by the drug regulator, the MHRA, to be sold or prescribed in the UK. The advisory body NICE is planning to assess its merits and risks and whether the cost can be justified for the NHS to provide to patients.

                Huntingdon Cyclist Death: Police Warn Over Ill-Informed Views

                March 7, 2023

                  Police have urged against “ill-informed comments” after an angry pedestrian was jailed for killing a cyclist in 2020.

                  Auriol Grey, 49, swore at and gestured in an “aggressive way” towards Celia Ward, 77, who then fell into the path of a car in Huntingdon, Cambridgeshire.

                  She was convicted of manslaughter and jailed for three years on Thursday.

                  Investigating officer Det Sgt Mark Dollard said that following the sentencing he had seen comments which were “not helpful to anyone”.

                  Grey, who has cerebral palsy and is partially sighted, and Mrs Ward passed each other in opposite directions on the pavement of the town’s ring road, during the afternoon of 20 October.

                  The incident was captured on CCTV which included sound, and Grey could be heard shouting at the retired midwife to “get off the [expletive] pavement”.

                  Grey then gestured at Mrs Ward, who fell into the path of a car and was pronounced dead at the scene.

                  https://emp.bbc.co.uk/emp/SMPj/2.47.3/iframe.htmlMedia caption,

                  Auriol Grey was filmed shouting an expletive at the cyclist in Huntingdon

                  In police interview, Grey said she believed she had made light contact with Mrs Ward.

                  Det Sgt Dollard, who interviewed Grey, told BBC Radio Cambridgeshire: “I’ll always remember the morning after it occurred obtaining the CCTV and watching it in its entirety.

                  “In all honesty it’s horrific and not appropriate for wider release to the public, but, if it were, then I think a lot of the arguments in relation to appropriate responses would be null and void.”

                  He added that there were “considerations in relation to Auriol Grey’s vulnerability” in their investigation.

                  “A lot of medical records… professional expert evidence was sought and presented to a jury, it’s important to note, and with all that, in fact, she was found guilty of an unlawful act and that is why she was convicted,” he said.

                  He said “what [Grey] did was wrong but ultimately that will not bring Celia back”, and he did not believe her family “take any pleasure in the fact that a sentence was passed”.

                  “I certainly urge people to think twice about commenting in relation to this case when they’re not in possession of all the facts,” the detective said.

                  “I’ve seen a number of ill-informed comments on various messaging sites as well and it’s not helpful to anyone.”

                  Shared cycleway?

                  The trial was told that police could not “categorically” state whether the pavement was a shared cycleway, but in his sentencing remarks Judge Sean Enright said it was.

                  Labour county councillor and disability campaigner Gerri Bird said: “The county council ought to have the information and it needs checking urgently.”

                  A Cambridgeshire County Council spokesperson said: “We cannot categorically say it is a shared use path as we could not find any legal records to evidence this.

                  “We know it is used by cyclists and we are looking at this location to see if there is any work required to make things clearer.

                  “We’d urge all users to take care and be considerate to each other.”

                  Falkirk Wheelchair Racer Abby Cook Is New Blue Peter Presenter

                  March 7, 2023
                   
                  Falkirk wheelchair racer Abby Cook said she was “speechless” after being chosen as the 42nd Blue Peter presenter.

                  Abby, 20, will join Mwaka Mudenda, Joel Mawhinney and Henry the dog as she makes her debut on the long-running BBC children’s show on Friday.

                  She trains twice a week with Paralympians as part of the Forth Valley Flyers athletics club.

                  Abby said she “had to check it was true” when she was picked for the high-profile role.

                  The former Grangemouth High School pupil said: “It was a very emotional moment knowing I would actually be presenting a show I love and had grown up with.”

                  She will combat her fear of heights as she takes on her first challenge to collect a Blue Peter badge by abseiling down Millers Dale Viaduct in the Yorkshire Dales National Park.

                  Abby said: “Helen (Skelton) and (dog) Barney were my era, but I also became obsessed with watching You Decide when the public got to choose the latest presenter and they picked Lindsey (Russell).”

                  I remember thinking what a great role model she was, she had never presented before but here was this strong woman going on the show and doing an amazing job.

                  “I’m hoping to do the same because I know what a lasting impression the presenters can have on the audience.”

                  Since studying applied biological science at Forth Valley College, Abby has worked with Forth Valley Disability Sport, supporting disabled and non-disabled young people becoming active.

                  She has also worked as a mental health project administrator for Scottish Disability Sport.

                  Blue Peter editor Ellen Evans said: “When Abby came to the studio, we knew she would be great for the show because she has an unstoppable ‘can do’ attitude.”She’s up for any challenge and we know she’ll connect beautifully with our audience because she has a real affinity for working with young people, but she also has the biggest of hearts.”

                   

                  Mental Health Matters

                  March 6, 2023

                  cerebral palsy “Tuesday, but with disabilities, cerebral palsy

                  how do you say “oh you Tuesday evening? I hope you enjoy the quote about the disability cerebral palsy from your fellow terrible Maya

                  March 6, 2023

                  cerebral palsy

                  complex mean even walk in the park on anybody’s cities has no idea about complex mean that we make choices in our have routines the same as an able bodied. Individual complex needs to be extra things like use. And may have to take auxiliary aid with such is Care assistance, assistance, dogs or special cutlery. a support worker or a PA complex needs needs to be understood across the world and rather than the disrespect, the arse with complex mean face every day, because we have lines the same as then we attend college commitment we can have commitment. Where is the perception is that we count people are preconceived ideas of what completely and aren’t very often willing to learn what they are because their culture tells the complex means it’s something bad to be annoying, sometimes aren’t willing to learn that it is not something to be found upon in the slightest that they think you should live their lives in the way, they should leave it and do what they should do and I believe that you’re lucky for the support you were saying if you’re not lucky it is the necessity for those with complex needs for us to be and community, just please educate yourself and complex thank you as many of you are such a difference will understand and I imagine many of you have made and complex disability but this doesn’t smell pass. In fact for me, it makes me more determined to succeed, gain a career and finish my person would be because I know how much Apple iPad to put in to start these qualifications courses et cetera this just passed me on to bigger and better things. Where is nondisabled people aren’t is motivated. I clean my opinion anyway

                  March 6, 2023

                  people need to understand that we have complex means that we live outside or disability, especially those helping out in a professional messages, supposedly like to work with people with disabilities and complex needs really they think we do yes we have complex needs, but it doesn’t mean that we do nothing we are breaking the law is the same as them complex needs to understand that we have a life, the same as them we may choose to live a life different way, but we have a life and we are not Reidi we are home, rely on their assistance to have a independent and successful life that we have lives that we choose how we leave them. #Sarah WeHaveLives

                  March 6, 2023

                  The first stations that go with Ingleside Road on a Monday, especially when managers come back in from the weekend support worker with me to College, then moaned that it is hard work and then doesn’t want to come again to support me ho, free until the Oval you wonder what career you would have what opportunities you may have and what LOL maybe you like but as a person with complex needs independent, depends on other peoples reliability

                  March 6, 2023

                  FaceTime three years ago, see picture below

                  March 6, 2023

                  perfume and some of the activities I did

                  US Disability Rights Activist Judy Heumann Dies Aged 75

                  March 6, 2023

                    Judy Heumann, a renowned advocate for the rights of disabled people, has died at the age of 75.

                    Heumann was an internationally recognised leader of the disability rights movement whose activism led to the implementation of major legislation in the United States.

                    After contracting polio as a child, she became the first wheelchair user to work as a teacher in New York City.

                    She died in Washington DC on Saturday.

                    Heumann was “widely regarded as ‘the mother’ of the disability rights movement”, according to a message posted on her website announcing her death.

                    She was at the forefront of major disability rights demonstrations, helped spearhead the passage of laws and founded national and international advocacy organisations, it added.

                    Heumann also served in both the Clinton and Obama administrations, and had more than 20 years of non-profit experience.

                    Barack Obama said he was “fortunate” to work with Heumann, and paid tribute to her life-long dedication to fight for civil rights.

                    The American Association of People with Disabilities also led tributes, saying her leadership “advanced the rights and inherent dignity of people with disabilities”.

                    Born in 1947 in Philadelphia and raised in Brooklyn, New York, she contracted polio when she was two years old and lost the ability to walk.

                    She was not allowed to attend pre-school, because her wheelchair was considered a “fire-hazard”, and when she eventually got into a school at age nine, she recounted being treated as a “second-class citizen”.

                    Her parents fought for her rights as a child, and she went on to study speech therapy at Long Island University and earned a masters in public health from the University of California, Berkeley.

                    In the 1970s, she won a lawsuit against the New York Board of Education and became the first teacher in the state to use a wheelchair.

                    Her fight for civil rights led to her staging a 24-day sit-in at a San Francisco federal building in 1977, an event which eventually helped pave the way for the Americans with Disabilities Act (ADA) in 1990.

                    “Disability only becomes a tragedy when society fails to provide the things we need to lead our lives – job opportunities or barrier-free buildings, for example,” she told a reporter in 1987.

                    “It is not a tragedy to me that I’m living in a wheelchair.”

                    Heumann went on to serve in the Clinton administration from 1993 to 2001 as an assistant secretary in the Office of Special Education and Rehabilitation Services in the Department of Education, and was appointed special adviser on International Disability Rights by Barack Obama.

                    Alongside her decades’ long activism, she also co-authored her memoir, Being Heumann, and its Young Adult version, Rolling Warrior, and was featured in the Oscar-nominated documentary, Crip Camp: A Disability Revolution.

                    Heumann is survived by her husband, Jorge, and two brothers, Ricky and Joseph.

                    Happy Monday!

                    March 6, 2023

                    happy Monday to everybody at same difference. Hope you had a good weekend and are looking forward to volunteering employment school or college. I hope this week is the sixth 👿😈🤡

                    Surgeon Amputee From Truro Shortlisted For Astronaut Job

                    March 6, 2023

                      A surgeon specialising in amputation, who lost both legs to sepsis, has made it to the shortlist to become an astronaut.

                      Neil Hopper, consultant vascular surgeon at the Royal Cornwall Hospital Trust, defied advice and expectations by successfully returning to work.

                      He made the European Space Agency’s shortlist for a para-astronaut but was then eliminated from the process.

                      He said: “I got far enough to start worrying that I might get through.”

                      Mr Hopper, who works at Royal Cornwall Hospital based in Truro, added: “When I saw the advertisement from the European Space Agency for a para-astronaut, I had to put in an application.

                      “The criteria were quite specific, you had to have a doctorate in engineering or medicine, you had to have a disability below the knee, and you had to speak a second language – hey, Welsh.”

                      Mr Hopper said his wife Rachel thought he was “completely crazy”.

                      He travelled to Hamburg to take part in the selection process which involved medical, personality, psychometric and memory tests.

                      He said: “I made it reasonably far through the programme but I didn’t get selected in the end.”

                      Mr Hopper has told his story, which includes a gruelling recovery and a return to helping patients with a new perspective, for a Welsh BBC documentary.

                      In the documentary, he explains how he had performed hundreds of amputations during his career when he lost both his legs to sepsis in 2019.

                      “On the other side”

                      He added: “I remember imagining the operation – operations which I do all the time, and thinking that power tools were going to be used on me. That was really difficult to process.”

                      In hospital for seven weeks, Mr Hopper said the physical changes were “fairly easy to understand”, while the psychological changes and “fitting back into family life” were harder to grasp.

                      But with prosthetic legs came a glimmer of hope.

                      He added: “I was starting to think I’d never be able to go back to work, I’d never be able to play football with my son, walk the dog on the beach – that’s the kind of mindset I had.

                      “But once I got legs, things started to change overnight, the future didn’t look so bleak.”

                      On reflection, he believes his experience and ability to relate to patients has made him a “better doctor”, facilitating improvements to services throughout Devon and Cornwall.

                      The surgeon had been advised to reconsider his career, but he said: “I was determined to go back to work.

                      “I wanted to prove that they were completely wrong.”

                      please stay tuned to see how I decide to display my tickets for different show in my scrapbook so that it looks nice and so that I have the tickets and also remember that are you still have my iCloud turning Page live for those that may want to for my support for DMV link with O. Click on it to read my story, and donate if you wish to go to the page with your friends, family or thanks to all those that may choose to donate all my publicity for my just giving page thank you in advance to all of you that my decide to contribute to the pages success👍👍

                      March 5, 2023

                      no, it’s from berries, different shards in my scrapbook as a little souvenir, and to continue with my scrapbooking, as I continue to boom different things are with Mum

                      https://www.justgiving.com/crowdfunding/maya-richards?utm_term=Wavng2gvR

                      Dawn, Thursday, staging for upcoming content ❤️❤️🤖🎃🦋

                      March 5, 2023

                      Play German for dance show content on Thursday when I go and see it with Morrie, the Hertfordshire dance show

                      hope your Sunday was a happy one everybody in this community will you?

                      March 5, 2023

                      happy Sunday. I hope you’ve had a relaxing one. Enjoy preparing for the store. Are you working week for volunteering or college? Enjoy whatever you are doing this week and look forward to next weekend poetry post on Wednesday

                      I have given the honour by my old secondary school to return there to do something rather special to talk to young people about my experiences as an adult who has left the school and has been out in the adult world for four years. About the good experiences navigating services and the rather tricky experiences i have faced and learnt to deal with due to my disability. My mission is to enable these young people to be prepared to fight the rather off putting opinions of professionals and empower them not to get discouraged and enable them to follow their dreams. They will leave school prepared for this as i left school with no clue as to what adulthood would be like as a disabled person. Even though it has been better than I thought it would be there have been some challenges that wouldn’t be challenges for someone in the mainstream community.

                      March 5, 2023

                      my favourite photo from last night when I went out 😁🤪

                      March 4, 2023

                      I think the best musical I’ve ever seen as I never saw the film grease that I plan to watch it now I have seen this musical station. Look at last night pose for pictures of me and the famous Molly last night.

                      March 4, 2023

                      Saturday everybody water I’m going about last night I do like the stage decorations are you

                      and the amount of comedy that was with it in it, because it was very well thought out and scripted as it is very well thought out and scripted

                      tell me a memory of them all at the camera over memory this morning, recorded two years ago. I enjoy it very much emoji one of my hubby

                      March 4, 2023

                      Rees was amazing. Enjoy phone call I really enjoyed it and then the tiredness are also in euros from alcoholic beverages. Yes tonight is Brighton from a night out like this

                      March 3, 2023

                      back for Minaj outfit. Very tired bathroom toilet

                      March 3, 2023

                      what time are you leaving? Where is Mum Road?

                      Grease Performance 😁❤️

                      March 3, 2023

                      I hope you love me with my make-up on the bus on the way to see the show ♥️

                      March 3, 2023

                      Night out tonight with Mollie, who is famous on my page, partying while watching this show! here is me before makeup, and later i will insert a picture of me after makeup on a later blog #NightOut #PeopleWithCerebralPalsyDoParty♥️♥️❤️❤️

                      March 3, 2023

                      happy Friday thank you different. The day has arrived where I am going to see Grace lazy morning this morning and then I was the party at the concert dancing et cetera this evening. Hope you all have a good Friday and treat yourself Friday and three yourself and it 3 am to another working week. So well done Rosa exceed volunteering improvement or college assignment is well done Jane for more musical content to see how much I enjoyed great later this afternoon/evening. 33. Are you in Grace later on this afternoon/evening because I am so I will really enjoy it as I am going with Molly

                      National poetry day is a day where poetry is celebrated. I will be taking part in a poetry competition with one of my volunteering jobs. Stay tuned to see what poems i write for this as i will be posting poems i have written in the lead up to national poetry day on my blog as well as my usual content.

                      March 3, 2023

                      s

                      Grimsby Town Apologises For ‘Inappropriate’ Harvey Price Post

                      March 3, 2023

                        Grimsby Town has apologised for posting an “inappropriate” short video of Harvey Price following its FA Cup win at Southampton.

                        According to reports, the League Two club tweeted a clip showing Mr Price, the disabled son of TV star Katie Price.

                        It was said to have been accompanied with the caption: “Signing off for the night! Enjoy your night, Town fans.”

                        In a statement, the club said it wished to “wholeheartedly apologise”.

                        The club’s full statement reads: “It has come to our attention that an inappropriate gif was posted on the club’s official Twitter account late last night following our game against Southampton in the Emirates FA Cup.

                        “The post was removed this morning as soon as we were made aware. We would like to wholeheartedly apologise for any offence it has caused. UTM.”

                        Mr Price, 20, has septo-optic dysplasia, a rare genetic disorder affecting his eyesight, as well as autism and Prader-Willi syndrome, which can cause learning difficulties and behavioural problems.

                        The incident comes two weeks after Ms Price published a letter from the Met Police telling her officers are facing misconduct proceedings over alleged involvement in a WhatsApp group that targeted her son.

                        Grimsby Town beat their Premier League opponents 2-1, courtesy of a brace from Gavan Holohan at St Mary’s.

                        The win secures The Mariners a quarter-final fixture with European hopefuls Brighton – the first time the club has reached the last eight in the FA Cup since 1938/39, a year they went on to reach the semi-finals.

                        March 2, 2023

                        I believe this playing really just froze me I love this slogan because this is what I do as a 23-year-old disabled woman who likes independence

                        do you not care about general public opinion of me, unless it is positive when out when out I Com because actually, I’d rather educate them, listen to the people that have rather strange opinions of me, and other people who are disabled

                        ring unfortunately I can’t access funding Paul from the government for this as my local authority doesn’t meet my needs and provide what I expect from a respite provision in terms of activities et cetera. They also won’t fund me to complete my DNA qualification so this is why I am reaching out with a “founder thanks to anybody that can donate even £1 even £1 will be appreciated immensely behind me and my family and my friends who I am completing the course with Rees. Look back at previous blogs to see what I have got up to in my training for the expeditions and the qualifying outdoor exams 😍♥️❤️😘🎉 link for the fundraising that continues for my DVD and respite care

                        March 2, 2023

                        https://www.justgiving.com/crowdfunding/maya-richards?utm_term=ZJv5PYPWW

                        happy international wheelchair day for celebrating mobility aids and acknowledge in this case helping a lot wheelchairs users . here is my dream wheelchair look like the only difference is mine will be spanking with glitters

                        March 2, 2023

                        What i went shopping for in Primark this evening. Here is the outfit. Primark sales are the best at the moment for clothes, shoes and accessories. I would recommend that if you love clothes and fashion and/or make up as much as i do go and find some bargains there. My trousers in the photo are only retailing at the moment for £7 and the top was £3 also.

                        March 2, 2023

                        international will per day. Can you guys are celebrated on the 1st of March who all of those that were around the country as this is a nationwide celebratory day apparently celebrate today, but apparently it is the day that some people around the country who you outside, and apparently celebrated in very happy wheelchair, die internationally❤️⭐️❤️

                        March 2, 2023

                        make your wheelchair stylish today for international wheelchair die on the 1st of March every year. Make your wheelchair sparkle. Just like you this international will tear tear

                        Arranged Marriage: Judge Protects Woman With Learning Disabilities

                        March 2, 2023

                          A judge has taken action to protect a woman with learning disabilities in an arranged marriage that happened in Pakistan.

                          Luton Borough Council, which had responsibility for the woman, asked Mrs Justice Theis to consider issues relating to her care.

                          The judge heard the case at a hearing in the Court of Protection in London.

                          She re-imposed a forced marriage protection order made at an earlier hearing.

                          The judge also indicated that she wanted the marriage ended or nullified as soon as possible.

                          She heard the woman had taken part in a marriage ceremony about four years ago.

                          Mrs Justice Theis said the woman, who is in her 20s, could not be identified.

                          She said she would reconsider the case later in the year.

                          The Court of Protection hears cases where issues relating to people who might lack the mental capacity to take decisions are considered.

                          Earlier this week, a new law increasing the legal age of marriage to 18 came into force in England and Wales.

                          Previously people could get married at 16 or 17 if they had parental consent and there was no law against ceremonies for younger children which were not registered with local councils.

                          The new legislation also covers non-legally binding ceremonies.

                          The government said the changes would help protect vulnerable children from being forced into marriage.

                          March 1, 2023

                          I have been joyed this evening. Autistic minds on BBC Two here is a picture of me sitting watching TV this evening. 📺

                          My fundraising efforts are continuing so please donate to my page. If you can afford to or would like to every little bit is appreciated immensely but if you can’t don’t worry, just please share the link as much as possible to gain publicity of my page. https://www.justgiving.com/crowdfunding/maya-richards?utm_term=848dYZBMx

                          March 1, 2023

                          My day out shopping in Luton with the most normal PA i’ve ever heard of to get an outfit for my night out to see Grease on Friday.

                          March 1, 2023

                          pictures of men celebrating Saint David’s day with our two years ago

                          March 1, 2023

                          beautiful my physical section of the UV2 years ago virtual dammit, Jim addition

                          March 1, 2023

                          Energy Prices: People With Disabilities Raise Concerns Over Cost

                          March 1, 2023

                            A seriously ill man said he is concerned about a possible rise in energy costs.

                            Stephen Walker from Leeds uses a powered feeding line to keep him alive, which he runs up to 15 hours a day.

                            Mr Walker said he is now paying more than four times as much for electricity, compared with last year.

                            A spokesperson said: “Government support will continue to help households with their energy bills”.

                            Bills are expected to rise because the government’s energy price guarantee, which subsidises the cost, becomes less generous in April.

                            “Without it I wouldn’t be here, because that’s what’s keeping me alive,” he said.

                            “It takes up about a third of my income, probably more. If the [price] goes up in April there is nothing left in the reserves.”

                            “The price cap is non existent for me,” he added.

                            The amount companies can charge households for energy has been cut by regulator Ofgem, but bills will still rise in April as government help eases.

                            Ofgem’s announcement itself does not directly affect what customers will pay for gas and electricity but it reduces the costs faced by government.

                            The typical household bill will rise to £3,000 a year in April.

                            Disability campaigner Jan Sergeant, who has Parkinson’s, said her energy bill in January was almost £400.

                            “It was cold,” she said.”I can’t function if I’m cold. My body seizes up, I can’t move, I suffer incredible pain, that is the impact of the cold on people with Parkinson’s.”

                            Mrs Sergeant has spoken to a group of MPs about the impact of rising energy costs on people with disabilities.

                            A Department for Energy Security and Net Zero spokesperson said the Chancellor had announced cost of living payments for people with disabilities and a rise in benefits in line with inflation from April.

                            “We know this is a difficult time for families, which is why the Government has covered around half of the typical household’s energy bill this winter, and by the end of June the Energy Price Guarantee will have saved a typical household in Great Britain around £1,000 since it began in October.

                            “The cost of energy has already been falling and we expect this to drop further over the coming months, which we fully expect suppliers to pass onto their customers.”

                            Glow in the dark

                            February 28, 2023

                            😂🤣🤣🤣🤣

                            Mario princess, 30 I am off to help young will be leaving school and will become adult likes me. #Community #SpecialNeedsSchoolCommunityEvenAnAdult #CommunityForever #LongDoes Life #Memories #AtSchool #ForeverGratefulForMyHeadteacherAndCommunityIbuprofenAtTheSchoolBreakthroughForever and will always over them to remind Brandom, not in a manic present. That’s what I want. That’s so good for me while and feel honoured that they still take me to give me this opportunity because they’re not known as my Grumman, I known as Maya would 23 study and hold the in one of their independent learning for living four days a week on independent schools, right loading a washing machine cooking going shopping like in independent and turn off the can and cannot delete and when you asked for help and went to try and be as well now I am on Main Street student who honestly couldn’t that she would be a mainstream student when she first finished her time at school, but because of my girls termination of where is my iPhone I have now been doing special needs school shoes for I have now finished special-needs courses and doing my history for about 2 1/2 years and I am forever. Grateful for those that supported me in my nightmares to make me the person I am today I am also Independence #HeadteachersThatBullyABullyAndYouWillLetYou

                            February 28, 2023

                            special needs school, Anderson

                            and my girl, how do you social care level two extended certificate to go to not leverage in August to go to the Popworld Mencap club night as I have never been to pop round and would love to go for more time volunteering. I have been offered an opportunity to Lonsdale which is where are used to go to school today adulthood conference to explain what I don’t like as someone who used to be alone. So cool, but now has been out of school for four so I am excited to do that alongside my headteacher and some of the support staff that used to support me as a child at school I feel honoured to take on this opportunity complete my silver do you me this summer so that I can move onto the final level of POV this next two years. #Joe #SarahBecauseHeHasTakenHerToGoToPurchasePrice to school with younger #PreparingForAdulthood #8 pmCall #LondonNow

                            February 28, 2023

                            what programs are would love to go on is Alan Titchmarsh love your garden my mum would love that too. Has anybody else been on that? #HowDoYouGetOnAtTesco? #AlanTitchmarshLoveYourGarden

                            February 28, 2023

                            just giving link to help raise money for my dear Dave/respite care

                            February 28, 2023

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

                            Miranda from one year ago, I love this picture is this this is one of my favourite photos from last year

                            February 28, 2023

                            making walk down from and giving a reason to get out of bed during a very unstructured time, otherwise

                            February 28, 2023

                            activities that I did it virtual learning through leisure two years ago years ago. Yesterday I helped run and suggest some of these activities. This is just for most of them that we used to do during lockdown.

                            One year memory of meeting up with where am I? XPA for a catch up and a coffee look at this lovely photo Grapher5

                            February 28, 2023

                            Picture of me, enjoying virtual Rickmansworth (Gateway) two years ago yesterday🥰😍😍🥰😍🥰🥰🙃🙃😍😇🥹

                            February 28, 2023

                            happy Tuesday saying different. Hope you enjoy your day today and have enjoyed my content this month on Friday. I will be going to see Grace so you have have more /Joe content coming out on thank you and also here is the link to my just giving page as I am still fundraising

                            February 28, 2023

                            https://www.justgiving.com/crowdfunding/maya-richards?utm_term=RNKGbmjW7

                            I’ve managed to get in £10 so far so carry on helping me reach that girl. Thank you

                            go bright David Learning for laser virtual day service two years ago yesterday to raise money for muscular dystrophy UK. This is the national day where they are bright colours and use bright colours in at exit the app to raise for the rare disease, muscular dystrophy in particular Duchenne, muscular dystrophy for eight the disease as well. They even do things to help the people with the disease find me a and with the employment

                            February 28, 2023

                            New Sanction Trap For UC Claimants With £250 Incentive For DWP Staff

                            February 28, 2023

                            With many thanks to Benefits And Work.

                             

                            Universal credit (UC) claimants are to be faced with a new sanction trap disguised as help to move into work. The scheme has been condemned by the DWP staff union who say the government is “hellbent on making it more difficult for people to claim benefits”, even though jobcentre workers stand to gain from a £250 ‘incentive’ if their office tops a league table.

                            UC sanctions are already at a record high. Over 98% of all sanctions are for failure to attend an interview, with over half a million claimants being sanctioned for this reason last year.

                            Yet, under the new Additional Jobcentre Support scheme claimants are being forced to attend  a jobcentre 10 times over a two week period.  In these obligatory sessions they will have “work search conversations” and “support sessions”. Missing a single session is likely to lead to a sanction.

                            The scheme has been tested in 4 jobcentres is now to be rolled out to a further 60 across England and Scotland.

                            According to DWP secretary of state Mel Stride, the DWP will also be offering a bonus “to recognise and reward jobcentre teams who furthest exceed their aspirational targets.”

                            The reward is a £250 voucher for each member of staff in  the best performing jobcentres.

                            No explanation of what “aspirational targets” consist of or whether they include getting people off benefits, sanctioning claimants or solely getting claimants into work. 

                            The PCS union, which represents DWP staff has no doubt, however, that the main purpose of the Additional Jobcentre Support pilot scheme is to make life harder for claimants and “the incentivisation of placing others into a more vulnerable situation.”.

                            Martin Cavanagh, PCS DWP Group President, said:

                            “Our members will see through this pilot for what it is – a government hellbent on making it more difficult for people to claim benefits and which will increase the risk of poverty for those customers who fall foul of this pilot. Asking more customers to travel more often into jobcentres does nothing to help our staff or their workloads and does nothing to help the customers find the work that they need.”

                            The PCS also revealed that there are no additional staff to deliver the extra work, which is likely to mean poorer service for all jobcentre users.

                            The pilot is aimed at claimants who have been in receipt of UC for more than 13 weeks.  It will not include claimants who are:

                            • Awaiting a Work Capability Assessment;
                            • Required to undertake less than 20 hours a week of work search activity;
                            • Who are Gainfully Self-Employed;
                            • Who have no work related requirements;
                            • With an easement in place; and
                            • On a full-time provision offer.

                            The scheme has already been running in Coalville, Crawley, Partick and Pontefract Jobcentres.  The new pilot began on 27 February in  n 60 jobcentres across Central Scotland, Surrey & Sussex, West Yorkshire, Leicestershire and Northamptonshire.

                            Benefits and Work would be happy to hear from anyone involved in this scheme.

                            You can read Mel Stride’s statement on the Additional Jobcentre Support pilot here

                            You can read the PCS union’s statement here.

                            Prepayment Energy Meters, Are You Due Compensation?

                            February 28, 2023

                            With many thanks to Benefits And Work.

                             

                            Energy suppliers have been told by Ofgem this week to pay compensation to customers wrongly forced to have prepayment meters.  Other customers may have the right to have their prepayment meters removed, even if they don’t get compensation.  We would like to hear from Benefits and Work readers if you have been affected by this growing scandal.

                            According to Ofgem rules, suppliers can’t legally force-fit a prepayment meter under warrant for people in very vulnerable situations if they don’t want one. Nor can they legally use warrants on people who would find the experience very traumatic.

                            Yet it has become increasingly clear that suppliers have been forcibly fitting meters unlawfully with virtually no scrutiny by courts, who simply took the suppliers word that all the necessary checks had been made.

                            T get a warrant, energy companies’ representatives swear an oath that they have complied with their supply licence.  This licence stipulates that they must not seek a warrant to enter the homes of vulnerable people in order to fit prepayment meters.

                            The Magistrates Association now says that energy companies “cannot be safely relied upon to ensure that those for whom warrants are sought are not vulnerable, but only that they are not known to be”.

                            In other words, magistrates now suspect that energy companies have not been bothering to check whether someone is vulnerable before forcing their way into their home.

                            People who count as vulnerable include those who have a physical or mental health condition which makes it hard to use a prepayment meter.  This could include problems with reaching the meter, reading the meter, adding credit or getting to a shop where they can buy credit.

                            People who have an illness that affects their breathing or which is made worse by being cold will also be classed as vulnerable, as will people who rely on medical equipment that needs electricity such as a stairlift or dialysis machine.

                            There’s more information about this on the Citizens Advice website.

                            Energy suppliers have now been told to stop forcibly fitting meters until 31 March, when it is expected that new guidance will be issued.

                            But, according to a report in the Guardian, Ofgem has told energy suppliers they should uninstall prepayment meters that were wrongly forced on customers and pay compensation now, rather than wait for the new guidance.

                            You can find more about Ofgem’s rules on prepayment meters here.

                            If you agreed to a prepayment meter being installed you may have done so under duress, with threats to disconnect you.  Under these circumstances, if you are a vulnerable person, you can still ask for the meter to be replaced and may be entitled to compensation. 

                            Even if you agreed without duress, if it’s no longer safe and practical for you to use a prepayment meter, your supplier has to do one of the following:

                            • move your meter to a place where you can get to it
                            • replace your meter with a standard credit meter
                            • adapt your meter or payments so they become safe and practical
                            • arrange for you to pay in a different way

                            Rosie Jones: ‘If I Went On Question Time Again, I’d Shut Twitter Down’

                            February 28, 2023

                              Comedian Rosie Jones seems to be everywhere these days from Casualty to QI. But as she prepares to begin her first solo stand-up tour she’s also battling against her own feelings that she doesn’t belong.

                              “I’m excited about the tour,” Rosie says, with just a few days to go. “I’m a little bit scared, but I’m excited to go out and meet people.”

                              At just 32, Rosie seems to have achieved everything when it comes to “media” – acting in long-running dramas, publishing several children’s books and writing for the Netflix hit, Sex Education.

                              She’s also fronted Trip Hazard, her own travel show, appeared on Live At The Apollo and got all political on Question Time (more on that shortly), but she says people are surprised to learn she hasn’t toured before.

                              “I’ve really only been doing comedy for six years, and two of those were wiped out by a pandemic,” she tells Access All, the BBC’s weekly disability and mental health podcast.

                              Her tour – Triple Threat – will examine the idea of dealing with new fame and whether she actually deserves it, a topic which sees art mimic life.

                              Starting on 3 March she has 35 fully accessible venues booked with many performances including British Sign Language (BSL) interpretation.

                              She knows she can’t be seen to drop the ball on this.

                              “I was absolutely determined to make sure every room was accessible,” she says, aware the disabled community would be particularly critical of her if she messed up.

                              “My production company had to ring up every venue and say ‘what can you do?’ And any venue that said ‘we can’t do that’ they said ‘Rosie won’t go’.”

                              Although she is excited about her tour she feels nervous. Being a gay disabled woman, she explains, brings on imposter syndrome.

                              “I go in thinking of the comedian stereotype which I grew up with which was male, non-disabled, straight, loud and talking really quickly.

                              “When you come to see me, you don’t get fast-paced jokes but I guarantee you laugh a lot.”

                              Rosie has cerebral palsy. It affects her speech and walk and she says she’s “constantly fighting internalised ableism”.

                              Ableism is discrimination that favours non-disabled people above disabled people.

                              Internalised ableism, a phrase we’re hearing a lot more of especially on social media, is when a disabled person absorbs the discrimination they face and think that way about themselves, too.

                              “Being a woman and being gay means that every time I’m on TV I’ll get a comment about what I sound like, my disability, my weight, my teeth, my hair. So every single level is a way to abuse me.

                              “Because of that I’m in therapy. I’m really dealing with a lot of internalised ableism and things that I probably painted over with a joke,” she says.

                              Trolling and ableism are on her mind at the moment. As well as preparing for her tour, she’s filming a Channel 4 documentary about society’s attitudes towards disabled people which is due to be aired in May.

                              She says: “Every single day I get some form of ableism online or in real life and I think in order to eradicate that, in order to face the abusers I’ve got to come here and go ‘you know what, it’s not Ok’.

                              “We absolutely need to call ableism out in order to eradicate it.”

                              When Rosie appeared twice on BBC One’s flagship debate show, Question Time, social media lit up with seriously unpleasant comments about her which made headlines.

                              “Both times I started trending on Twitter from all the abuse I was getting,” she says.

                              “[They were saying] that I should be in a cage, I shouldn’t be on TV, I should die.”

                              Stars like TV presenter and author Richard Osman, who himself is visually impaired, came out in support and it prompted a national debate about the way society viewed disability.

                              BBC reporter Alex Taylor summarised it at the time saying: “Society is used to disability being discussed, but not so much disabled people making their own voices heard.”

                              It has been two years since Rosie’s last appearance on the late night politics show and she has had time to reflect.

                              “I think Question Time is brilliant but it attracts a lot of angry people and not only being female, disabled and gay I am also, surprise, surprise, extremely Labour-leaning. So when I went onto that show and said ‘here’s what I think’ a lot of right-wing people didn’t agree with me and the easy thing to get me for was my disability.

                              “Would I do it again? Yes. But I would go in there more prepared and I’d probably shut my Twitter down for a few weeks.”

                              The experience rocked her but she says speaking out for what she believes in is more important.

                              “I will always champion diversity, but it’s hard and it’s exhausting when I expose myself to so much abuse.”

                              Despite that experience Rosie’s career has continued to rise. Her series of children’s books about The Amazing Edie Eckhart, who has cerebral palsy. have brought her legions of young fans and she is currently the go-to girl when it comes to booking a female, disabled comedian.

                              “Selfishly I like that because it’s bought me a lovely house, ” she jokes. “But I don’t think I’m taking jobs from other disabled people.

                              “We’re still, unfortunately, at a stage where they’re getting either me or another white straight non-disabled person.”

                              She says appearing on as many different shows as possible might “encourage more disabled people to come into the industry”.

                              Her “ultimate dream” is to appear on a panel show which just happens to feature several other disabled comics at the same time.

                              It’s something she got close to recently when she fronted Rosie Jones’s Disability Comedy Extravaganza – an online event showcasing 10 disabled up and coming comedians for UKTV Play and Dave TV’s YouTube channel.

                              One of the comedians who performed was Dan Tiernan who talks about being dyspraxic in his stand-up routine. He has gone on to win both the BBC New Comedy Award and British Comedian of the Year, demonstrating the strength and mainstream appeal of the acts.

                              Rosie appreciates that with her recently found success, she can help to change the industry.

                              “I’ve got this platform, and it’s about how we bring up a load of brilliant disabled comics with me,” she says.

                              As Rosie gets ready to head to Birmingham for opening night she acknowledges, “I’m really proud of myself”.

                              Just like a rockstar, she has a non-negotiable rider that she expects to be provided at every venue.

                              “This is the most embarrassing thing. I wish I was a packet of fags and bottle of whiskey gal. But it’s just a bit of Yorkshire Tea.”

                              appreciation for the guys that might decide to ignite to my drafts giving platform link to my just giving page if you want to. Donate it is Anthony, please donate so that I can throw complete my room and manage summer. #Girls #CerebralPalsy #Annemari #PleaseDonate #HoweverBigOrSmallItDoesn’tMatter,IHadToTakeEveryPennyMoveEverything

                              February 27, 2023

                              https://www.justgiving.com/crowdfunding/maya-richards?utm_term=5bYyQPXz8

                              Picture of my cat, he thinks he’s a princess princess minute

                              February 27, 2023

                              volunteer job from September 2023. I will be working with the diabetes to help run training sessions for DNA and to help the invoice for those students that have not completed. What the fuck was that Mum is that okay pardon yeah I want to take turning it down but it keeps turning is it open I don’t know how is the disabled do you have a student #Student #DOB #IWillCompleteMichael

                              February 27, 2023

                              everybody you have a good first day at work for the week or there volunteering if there is also I am sharing ring who know I’ve seen

                              February 27, 2023

                              😆😁😁

                              https://www.justgiving.com/crowdfunding/maya-richards?utm_term=2RmA26r9w

                              virtual disco approximately please go with (Gateway)

                              February 27, 2023

                              volcano making picture from my employability skills course that I studied and finished studying halfway through lockdown two years ago. This was one of my creative time projects that are able to video to my college teacher. I just find it amazing how time flies and those

                              February 27, 2023

                              four years ago in my first ever year in school in college and not in school, any more it’s amazing how time flies

                              February 27, 2023

                              Picture of me city with the College Peacock

                              of doing my course record age, which at the time I was studying employability skills and this would run my creative time project that I completed. Can you set my teacher 🥰🥰🥰video what I had based on her timetable that she sent me

                              February 27, 2023

                              two year memory from lockdown

                              happy Easter to work and wait for them to open education. Hope you have a good week at work. All you prune Perry Rose in that this week is good for you as I know that Monday is Tenby miserable my alarm for eight

                              February 27, 2023

                              please donate to my just giving me know if you wish to share it if you cannot afford to donate, share, share and share some more pleasehttps://www.justgiving.com/crowdfunding/maya-richards?utm_term=3yV3Qgdw2 time difference

                              February 27, 2023