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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
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    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

                    what time enjoying about my day today I am lying in bed making plans for the week ahead and watching Channel 4 or tails. Fox say wow, drinking tea as they do a lot of comedy cartoons and this is a box set of one of them, but I am enjoying watching hope you are enjoying your Monday. It’s not listen to kiss FM radio station and that is tearful for Monday

                    February 27, 2023

                    Over 400,000 PIP Claimants Should Be Protected From Punishment For Failing To Return PIP Form

                    February 27, 2023

                    With many thanks to Benefits And Work.

                    422,200 PIP claimants should be protected from losing their benefit if they fail to return a PIP{2 form.

                    Last month we learnt that 42,000 claimants lost their PIP award in 2021 because they failed to return their AR1 PIP review PIP form. 

                    We also revealed that claimants with serious mental health or cognitive conditions who have difficulty communicating or engaging with the PIP process, have their files ‘watermarked’ as Additional Support (AS), although they are not classed as vulnerable. 

                    These claimants should be asked to attend a PIP assessment even if they fail to return their form.

                    Now the DWP has published figures showing that the total number of current PIP recipients with an AS marker is 422,200.

                    If you or your client is refused PIP due to failure to return a form, it would be worth checking whether you have an AS marker on your file.

                    xxx

                    February 26, 2023

                    here is the link for those that might not of the earlier thank you, scientific community

                    The million pounds, you’re £1 million close. I can can you twerk million pound close and will update you on my opinions on it in tomorrow’s blog. Is there anybody else would rather than episode two because at the moment I’ve only got as far as episode two on series one, let me know your opinions on the million pounds you’re and whether you would like a yoghurt that is worth that much in your futures, if you had a great or whether you would like to live on one because I know if I was rich, I would and I would travel towards the Mediterranean countries to just eat Greek salad with feta cheese all day that would be my dream treble

                    February 26, 2023

                    because I will get up at 7 o’clock in the morning because it means that much to me Grandma I don’t get up at 7 o’clock for no reason, especially on a Sunday morning laugh out loud but me right now I got up that early to attend it. I thought Sundays were for being lazy but clearly Sundays in DBZ is 14. You be crazy. I think I think that every day is believe they arrange for us to study on a Sunday though and mustard mix if you can manage to donate just £1 that would mean so much to me mate, just giving Saturday evening everybody🙂 click🙂🤣

                    February 26, 2023

                    tomorrow my day is a lazy day because I got up at seven in the morning. How are you this morning to do Reidi’s tr

                    https://www.justgiving.com/crowdfunding/maya-richards?utm_term=4564P7nXd

                    because they were too slow. Hilarious photos when waiting for the teacher #SarahBecauseHeHasTackled #Cold #Don’tDoYouDoYouBeenTrainingInWinterAdvice

                    February 26, 2023

                    various photos that I took myself while waiting for this week

                    Believe how quiet the roads were in the countryside, they were almost deserted. This picture shows you how quiet it could be, if any of you don’t live in the countryside for I suggest you choose, the countryside as a holiday destination because it is peaceful and tranquil, unless you are next to the one road that they seem to run in and out so I found anywhere we saw a group of horses cantering and enjoying riding out in the countryside which you don’t see you in Hertfordshire, unless you are near the college which studies equine which I am so why do you see horses occasionally, but not being written out like that in groups and being encouraged to canter

                    February 26, 2023

                    old-fashioned cooking appliances, when camping we learnt how to put together a old-fashioned stove that has holes in it that look like a salad strainer to me in appearance we had to all learn how to construct it as it comes in different bits and part of it, you have to learn the history behind the old-fashioned cooking stove. It had a detachable handle with a saucepan and a frying pan.“ it looked like a bit of frying pan that we would use in the modern days, even though we haven’t been asked to use these in our qualifying, we have to know the history of them and to be able to identify the different bits of it confidently and be able to demonstrate that we can put one together if we really needed to, if we are we are stuck on top of the mountain although this was where we are not in the second world war we’re in 2023 this is my favourite part of the training so far as I learnt how soldiers may survive in the army using this tool although I don’t know how the food doesn’t taste metallic as every bit of it is metal and stainless steel. both of them that was probably a three add 13 was probably a luxury 100 years ago. it makes me realise how lucky modern countries are now as we can just use electricity when ever we want and put using proper gas mind or electric mines whenever we need to. Although it may cost a lot. It probably cost a lot because in all day and age, it is not a luxury, but it is classified as a modern necessity where is really for survival, unless we are severely disabled or disabled and rely on equipment, a person who is mainstream may not appreciate the cost of living because for them they can live without a bit of electricity or a bit of gas and heating. They just might have to put extra clothes on and it really made me think about why they might not appreciate the real necessity and the effects as well as teaching me. How are the people used to survive.😄

                    February 26, 2023

                    what a first lesson was on the school this morning

                    why your donations are so important to me through my just giving page it is important and means a lot to me. Please Read and Donate if this is a possibility for you and your financial situation Thanks a lot same, different community and beyond.

                    February 26, 2023

                    pictures of me in the woods on my training, just to prove that I am crazy enough to do it and to prove why your donation is so important for completion of this qualification because I am giving it 100% and I would love to complete it, and will complete it, because I am determined to do so

                    https://www.justgiving.com/crowdfunding/maya-richards?utm_term=yjq4xMBn8

                    pictures of the scenery today that I had to do my expedition training in for the expedition training day number two

                    February 26, 2023

                    pictures of the scenery on my diary President day today is the second one where more Boris says Reidi through the countryside, and would

                    https://www.justgiving.com/crowdfunding/maya-richards?utm_term=pdZxgQmZe challenge excepted link below calendar Sunday

                    February 26, 2023

                    do you accept my challenge of getting a lift to donations as a community or more by the time I return on Amazon, about seven tonight

                    show me support for my hard work, Roy Jerry Maguire, giving link or donating if you cannot afford if you cannot afford to donate that you can share with people make the decision if they want to doughnut telling to you guys get me at least two for my hard work by the time. I return home at about seven

                    February 26, 2023

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

                    ready and waiting for the Co-Ordinator to pick me up for my DV second training day. Here is a selfie of me already this morning.

                    February 26, 2023

                    donations of campaign equipment will be also appreciated if you cannot support financially

                    February 25, 2023

                    032 of questions do also feel free to donate any camping equipment that you can comment down below, if you want to donate temporary equipment for me to use for the duration of my GOV

                    students about fundraising goal if you have them before donating to my gift given

                    February 25, 2023

                    i it will be my pleasure to answer any questions you have about my fundraising girls, reporter uniting if you wish to

                    please see the picture below N please donate, ensure they just skipping even if you cannot tell Nan thank you to the community🙏🎼👩🏾‍🦽 and beyond

                    February 25, 2023

                    leaflet explain more about Michael Glaser

                    remind me tomorrow to call me Princess three-year-old woman with cerebral palsy o’clock. We’re not at home with my family but unfortunately social services will not my will not support this in my local area due to the fact that I do not need twins who were paid support when at home because my mum is at home with me and Keira❤️❤️ go on then I will to complete residential and travel a little bit so please donate to mine. Just Google

                    February 25, 2023

                    my just give however much you have a board

                    me the name https://www.justgiving.com/crowdfunding/maya-richards?utm_term=PYekK84wx ring Learning. Many thanks Maya, to the time difference, community and beyond.

                    scrapbook pages that I embrace it with my support worker

                    February 25, 2023
                    
                    
                    
                    
                    
                    
                    
                    
                    
                    					

                    Hey Goodafternoon same different community please remember that my just giving page is live if you would like to donate then please do and remember that every penny counts here is link for those that didn’t see it on my if you would like to donate feel free to do so important and feel generous enough to do so. Thank you, Maya#CerebralPalsy #Fundraising #SameDifferentCommunity #DoYouHaveAHashtagRespite #FestivalHasPassedYouLiveInA23-year-old do you know? That’s my friend. Sup England. Rosa is Reidi do you supposed to say? Good

                    February 25, 2023

                    https://www.justgiving.com/crowdfunding/maya-richards?utm_term=YAg72epv5

                    Shows I would like disable people represented in the first week of those that use mobility, aid search Walkers, walking stick and wheelchairs Love Island is the number one because I’ve only ever seen a deaf person in there but never anybody that uses a wheelchair in all the years it has been live streaming into a live with the rooms. I cannot believe that a wheelchair user has not because there’s people that have that have them in wheelchairs and also can you grow like myself who are born with complex disability, including more conditions. That mean we have to use a mobility aids, almost triple, mobility aids throughout all day and I tell me the price of the disabled wheelchair users to go on Love Island is on you Love Island with accept this record I didn’t zoom for me and other young, disabled women and men who Holman so facing disability, and having to face using a wheelchair or other mobility, aid or the voice yeah

                    February 25, 2023

                    ❤️❤️❤️❤️

                    February 25, 2023

                    how are you enjoying my morning of my Saturday we went to the harvester Florence where I had a salad board with pasta and beetroot which I love now we have come back home and will do some scrap booking and stick my art in to it that I made up the p my friend Mum bought me the other day using lots of different colours in lots of different shades it’s red hot Saturday definitely today I really enjoyed it immensely sofa happy Saturday so different

                    all the parts of the world that might be waking up right now in different countries

                    February 24, 2023

                    please don’t know if it all possible for you or anybody you know every little penny means a lot to me as this will continue to ensure that I reach my goal and ensure that I am able to share this brilliant news with you when the combo great, thank you

                    https://www.justgiving.com/crowdfunding/maya-richards?utm_term=2vkPgW8k5

                    fundraising update the time forgot to post earlier so that you can see what progress we are making from Moes that have been generous in into my just giving page in a small or a big it🎉

                    February 24, 2023

                    😗 ♥️🫶🏼♥️

                    happy weekend to everybody it’s a difference. Hope your partner in Holborn having a good Friday. Enjoy whatever you are doing in the scientific community.

                    February 24, 2023

                    what are did this week? my week this week was full of adventure including pancake, mix with scrapbooking painting choir, making a TikTok and many other adventures, including shopping for packed lunch for College on Sunday as I have a training day training today for my DNA which is the qualification, the {improve their support for

                    Help me reach my goal for the summer of 2023 and 2024. Please donate to my justgiving page if you can afford to, link below. Here is progress updates and photos down below as well. Thanks for the support for the course which is two years long. Please share if you are willing and able. https://www.justgiving.com/crowdfunding/maya-richards?utm_term=zn8DbyNZm

                    February 24, 2023

                    Lego Friends Launches Characters With Down Syndrome, Missing Limbs And Anxiety

                    February 24, 2023

                    Lego has released a series of new diverse Friends sets containing characters with disabilities, including one with Down syndrome.

                    Popular with young girls, Lego Friends was launched in 2012 and contains “mini-doll” figures which are the same size as traditional minifigures but more detailed and realistic.

                    The toymaker is striving to make its sets more inclusive and ensure that its characters represent all children across the world.

                    Lego’s new figures were announced in October 2022 and the sets went on sale in January 2023. They also feature in a new YouTube special that arrived this month.

                      Five Lego Friends sets contain the new characters

                      The new people will come in five different Lego Friends sets which are all available to buy on the Lego website now worldwide.

                      Here are the sets and prices:

                      • 41724 Paisley’s House (£39.99/$39.99)
                      • 41727 Dog Rescue Center (£54.99/$59.99)
                      • 41728 Heartlake Downtown Diner (£24.99/$29.99)
                      • 41730 Autumn’s House (£59.99/$69.99)
                      • 41731 Heartlake International School (£99.99/$99.99)

                      You can watch the TV special Lego Friends: New Beginning for free on the Lego YouTube channel now. It’s 44 minutes long and features all the locations in the sets.

                      The most exciting Lego release in 2022 was definitely the Eiffel Tower, which is the brand’s tallest set at a whopping 149cm tall.

                      Specifically designed for people aged 18 and above, it has 10,001 pieces, is ultra-realistic, and will set you back $629.99.

                        Lego Friends introduces character with Down syndrome

                        The characters show “multiple skin tones, cultures, physical and non-visible disabilities, and neurodiversity,” Lego says.

                        One of them has Down syndrome, whilst others suffer with anxiety, vitiligo, and have a missing arm. There is also a pet dog with a wheelchair.

                        Every year, 6,000 babies are born with Down’s syndrome in the US alone, the CDC reveals, making it the most common chromosomal condition in the US.

                        That means Down syndrome occurs in about 1 in every 700 babies in America, and those children will now feel represented by Lego.

                        The new toys will “explore and work to overcome modern challenges that they face, passions, obstacles, and differences, all while trying to create friendships”.

                        They will help children feel more represented

                        Lego says the “diverse” characters will “enable more children to feel represented during play” and celebrate “diverse friendships in the modern world”.

                        “At the LEGO Group, we understand that children want the characters they encounter to be more like the diverse personalities they meet in real life”, said Tracie Chiarella, Head of Product, LEGO Friends at the LEGO Group.

                        She added that they are continuously trying to evolve products so they are reflective of society today and are more authentic.

                        “We have chosen to evolve the LEGO Friends Universe and TV show to be more inclusive in order to give parents and kids more tools to navigate friendship and their emotions as they grow and learn.”

                        This comes as two rumored Lego sets have leaked for Disney’s 100th anniversary, including a celebration train and the house from the movie Up.

                          Five Lego Friends sets contain the new characters

                          The new people will come in five different Lego Friends sets which are all available to buy on the Lego website now worldwide.

                          Here are the sets and prices:

                          • 41724 Paisley’s House (£39.99/$39.99)
                          • 41727 Dog Rescue Center (£54.99/$59.99)
                          • 41728 Heartlake Downtown Diner (£24.99/$29.99)
                          • 41730 Autumn’s House (£59.99/$69.99)
                          • 41731 Heartlake International School (£99.99/$99.99)

                          You can watch the TV special Lego Friends: New Beginning for free on the Lego YouTube channel now. It’s 44 minutes long and features all the locations in the sets.

                          The most exciting Lego release in 2022 was definitely the Eiffel Tower, which is the brand’s tallest set at a whopping 149cm tall.

                          Specifically designed for people aged 18 and above, it has 10,001 pieces, is ultra-realistic, and will set you back $629.99.

                          heart shape hairstyles day 2, courtesy of my PA Mollie👩🏾‍🦽🫶🏼📺🌎 also going to watch transit plus the telly over the weekend. #Weekend #TellyTime #ScrapbookTime♿️

                          February 24, 2023

                          wheelchair user loving hairstyles. #CerebralPalsy #BeautifulAttackMeYeah I want to

                          heart shape hairstyles

                          Disabled Shopper Wins Fight Over Pavement Cafes

                          February 24, 2023

                          A disabled woman has won a legal battle with City of York Council after she accused the authority of breaking equalities law.

                          Flick Williams, a visually-impaired wheelchair user, found herself blocked from using dropped kerbs on a footpath while out shopping in York city centre in May last year.

                          On leaving a shop, she said furniture from a cafe had been put out while she was inside, covering the dropped kerbs on either side.

                          York City Council admitted it “got it wrong” about access for those with limited mobility.

                          The disability rights campaigner submitted a claim to York County Court for disability discrimination, with the council reaching an out-of-court settlement.

                          The council allowed York businesses to set up pavement cafes more easily under the government’s emergency Covid legislation in 2020.

                          But Ms Williams and others consistently argued that the way it was implemented in York broke equalities law, as many cafes did not leave the necessary 1.5m (4.9ft) width clear on the footpath to allow pedestrians to pass unimpeded.

                          Describing the incident, Ms Williams said: “This was an extremely distressing experience that put me into conflict with the staff of the business with the furniture out on the pavement,” the Local Democracy Reporting Service reported.

                          “They were busy justifying that they had a licence from the council, regardless of the fact that it had effectively prevented me from leaving.”

                          She said she had tried “repeatedly” to speak to the council but they defended their position on cafe licensing, with her believing “they were licensing unlawfully”.

                          A council spokesperson said it was “sorry” any individual had experienced difficulties with access issues.

                          “We recognise that we got it wrong, and are grateful that issues were brought to our attention.

                          “In working to meet our ambitions to deliver a more accessible city for all, we will continue to listen and learn from the lived experiences of disabled people.”