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The most interesting bit of my calls so far is that they say people should be treated equally which station, but only yesterday I was having to fight just to have my PE so I can’t normally would just my normal To go back to university or giving over a months notice that he was going to leave and has only just left last Thursday #DisabilityAndEquality #BrightonForDisabilityEqual

January 17, 2024

Who are the new followers? My name is Mirna. I am 24 years old and I have a sick guy procedure cerebral palsy. Apologies that I need respite Richardson funded by the local authority. At the present moment. So for my 2024 Aspire, oh The best In previous posts this morning, the link to my just giving for anybody that wants to do right now

January 17, 2024

Student card today I did health and social care assignment work. What did you do today? #Student #StudentAwareness #StudentsWithCerebralPalsyAwareness #Full-TimeWheelchairUser

January 17, 2024

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January 17, 2024

Rightly, cheerfully coloured flower, painting #Careful

January 17, 2024

A big and bold. Praying for you this morning to remind you of your productivity on the Wednesday morning/afternoon wherever you are in the world.

January 17, 2024

Girl, phone of the day I call you all with a colourful butterfly included in the sale of the

January 17, 2024

Floral and heart-shaped painting favourite painting of the day as I love flowers and all the different colours that are in this painting

January 17, 2024

From Grace zoom link provided by 2024, as I don’t have any funding from local authority for respite care at all I only get my day

January 17, 2024

https://www.facebook.com/share/p/Z8wB4UEpN1U4gv46/?

Part of her disability all experience with disability cerebral palsy and associated conditions. Are you love you get a prom with someone and take a personal assistant with you wherever you But the reality is 14 services for Berri’s personal assistant is really time-consuming and the pool

January 17, 2024

#CerebralPalsyAndDisability

it’s societal opinions and services It’s suicidal opinions and services that are you guys all set up to Care, but actually they do not show many disabled people with complex Sarah

January 17, 2024

When agencies and services for your disability, just want to make it awkward moon boot, you’ve been telling me to do for the last month how you

Hannah Cockroft ‘Scared’ To Be Disabled In Britain After Government Decision

January 17, 2024

    Seven-time Paralympic gold medallist Hannah Cockroft says disabled people in Britain are being “almost criminalised” in the way they are treated.

    The UK government downgraded the role of minister of state for disabled people to junior level last month.

    An open letter signed by 57 sporting bodies last week called for the role to be reinstated.

    “Britain is a really scary place to be as a disabled person right now,” Cockroft told BBC Sport.

    “Paralympians are almost seen as different to the rest of the disability community. We are shown for what we can do, and everyone else with a disability is almost criminalised for what they can’t do or struggle to do. I feel the statement puts us forward as one.”

    ParalympicsGB chief executive Dave Clarke said the downgrading of the ministerial role means disabled people “do not have a voice at the top level of government”.

    Wheelchair racer Cockroft says she faces great difficulties living her life in Britain, and praised the sporting organisations for challenging the government.

    “I still can’t catch a train if there is no-one there with a ramp, I still can’t catch a bus with my boyfriend, I still can’t enter a shop if it has a step to it,” Cockroft said. “Everything that affects disabled people in everyday life still affects me, no matter how quickly I push around a track.

    “Dave Clark, it is fantastic he felt confident enough and knew that voice was needed to push this forward and put it in the forefront of the government’s minds.

    “We have no-one to fight our corner, and that’s not a good place to be for six million people in the UK. We need someone voicing the things we need changing.”

    Mims Davies was appointed to the role in December within the Department for Work and Pensions as a parliamentary under-secretary of state – the lowest rung of the ministerial ladder.

    Davies’ predecessor, Tom Pursglove, was a minister of state when he held the job.

    Sporting organisations to sign the open letter included UK Athletics, British Cycling and the British Olympic Association.

    A government spokesperson told BBC Sport: “Minister Davies will build upon this government’s track record of supporting disabled people, having delivered millions of cost of living payments and helping over one million more disabled people into work five years earlier than planned.

    “The minister will help ensure there is always a strong safety net for the most vulnerable in our society, while tearing down barriers so that every disabled person can realise their potential and thrive.”

    For Cockroft, 2024 promises to be a life-changing year on and off the track.

    She is competing in two major championships for the first time, with the World Para Athletics Championships taking place in Kobe, Japan, in May, followed by the Paralympics in Paris between 28 August and 8 September.

    Cockroft, 31, has her eyes on increasing her haul of gold medals, but says that preparing for two major events in one year is a challenge unlike anything she has experienced before – albeit one she is welcoming.

    “I don’t understand going to a major championships and not wanting to win gold, that is definitely the aim in Paris,” she said.

    “But I have got a World Championships before then, so if I can add some more titles that would be a fantastic start to the Paralympic year. It’s the first time in my career that I’ve had two major championships in the same year so it’s a huge challenge to get everything right. Not just the training, but everything around that.

    “May and August sound really far apart, but if you don’t have the rest and recovery to get that right then things can quite quickly go wrong.

    “Right now things are the same as they usually are, but the difference I will really start to see as we go into the World Championships. Right now it more of a mental challenge than physical, but time will tell – it’s a completely new challenge, and 12 years into an international career you don’t normally have many firsts left. But I like a challenge.”

    Cockroft is hopeful that the atmosphere and excitement seen around the London 2012 Paralympics can be recaptured at Paris 2024, after two Games beset by problems.

    Rio 2016 was affected by budget cuts, while the Covid-19 pandemic forced the Tokyo Games to be postponed by a year to 2021 and eventually take place without fans.

    “I really think Paris has the potential to be bigger than London,” she said. “The time difference from Rio didn’t help us, then the lack of crowd, Covid, everything that happened around Tokyo really didn’t push Para-sport into the public eye.

    “Paris is only an hour apart from Britain. Coverage seems to be good, already so many companies and people, the things that were around before London seem to be coming back. It gives me great hope that it is going to be a big Games, and have the audiences we had in 2012.”

    On top of all this, Cockroft is marrying her fiancee, fellow Paralympic athlete Nathan Maguire, in October.

    “It’s a lot of pressure – the Paralympics, the Worlds and a wedding,” she said. “I’ve pretty much boxed off the things people do in a lifetime in one year, but if I get it right it could be the most incredible year ever.”

    Writing for support with cerebral palsy, going to college and the right personal assistance some professionals think you should be 18 before you’re actually 80 and live the life of the 18-year-old Photos over like me, but refuse to reply my favourite eight-year-old before we are 80 it is a constant battle. #PABTrostreDisabilityPersonalAssistanceOfGrandad Affects of Sarah because of it on easy. It is not with cerebral palsy. It is the system set up for the cerebral palsy and disability mean it’s not upset or disabled it makes make

    January 16, 2024

    Battling with Care, I didn’t see that is with my best friend. You are a young person with a disability and you just want to be a student or example, just like everybody Lower the weather like new list of getting the support you with your cerebral palsy is just ridiculous else that they do Do you know someone shocking and I’m sure people have been through this, who also have Why did buy for you to bring the sugar and the lights up at €80 even though we are 24

    January 16, 2024

    https://vm.tiktok.com/ZGe6Vc7Y9/Picture of the band performing on stage at the tiger mania concert on Saturday evening was totally amazing. #CommunityXXCerebralPalsyAwareness #ToPrimeWith#PersonalAssistantHasTokyo’sYay,Yay,Yay,GiveMeIndependent

    January 16, 2024

    Wolfram home, run the tailor, my new concept drawings of attending on Saturday. I really enjoyed it.

    January 16, 2024

    Who is it who is it who is playing of the day for you? All courtesy of creepy, Paula.

    January 16, 2024

    What’s the video to see a positive saying that of the day and to see more content from the concept that I went to answer

    January 16, 2024

    https://vm.tiktok.com/ZGe6VhN11/

    Joe concert content from the Taylor Swift Taylor mania, could put the time and every 24-year-old call time wheelchair user who likes concert and also is a Taylor Swift fan

    January 16, 2024

    https://vm.tiktok.com/ZGe64gEUN/

    Life With A Stoma: ‘It’s Not A Bag For Life, It’s A Bag For Living’

    January 16, 2024

      “I was terrified of getting it.”

      That was 24-year-old Stephen Blakely’s reaction to getting a stoma bag,

      He has now started to document his experience of living with a stoma on social media in a bid to bust myths and tackle stigma.

      Stephen, from Londonderry, became unwell in the summer of 2022, bleeding when going to the toilet and suffering severe pain. That year he underwent an ileostomy and now uses a stoma bag to collect waste products.

      He hopes his TikTok videos will help those with similar symptoms overcome any fear of getting help.

      “For me, whenever I got a stoma bag you always hear the myths and the rumours – there are plenty of them,” he told BBC Radio Foyle’s North West Today programme.

      “People thinking you are going to smell. That’s a terrifying thing to go through.

      “That was my most terrifying fear. I lay awake about that for days at a time, that I would go outside and people would think: ‘There’s an odour or smell coming off him.’

      “That’s never happened me once with a stoma bag – it’s very important that I get that across”.

      ‘A bag for living’

      Stephen has ulcerative colitis, a condition where the colon and rectum become inflamed.

      “I was going to the toilet 10 to 12 times a day at that time. I was in excruciating pain constantly,” he said.

      The ileostomy means he now lives with a stoma – an opening on the abdomen which connects to the digestive or urinary system and allows waste to be diverted out of the body and into a bag.

      “It doesn’t have to be a bag for life – it can be a bag for living,” he said.

      ‘I didn’t know anyone else with a bag’

      Stephen, who was active and healthy before he became sick, said he began to feel isolated after the surgery.

      When he left hospital he was visited regularly by specialist nurses but those visits became less frequent.

      “You are left dealing with it, struggling on your own. You have no-one else that can understand what you are going through – I didn’t know anyone with a bag when I got it,” he said.

      He said he went into “a hole” for two years while he tried to come to terms with how life had changed.

      Things are better now. He still struggles at times, but he’s socialising again, going out more often.

      He hopes his social media content will help others come to terms with life with a stoma and encourage anyone who is unwell to get help.

      “Since I made the TikTok account I have had people reaching out and contacting me. There’s more people than you would know with a stoma bag,” Stephen said.

      “If you are going through pain or bleeding, go and get checked out. It literally takes five minutes and could save your life.

      “There’s nothing a doctor or nurse hasn’t seen before. Yours isn’t the first backside they have seen.”

      my highlights of the trailer minute conversation yesterday #Highlights #TylerMaya #WheelchairUser #CommunityAccess #MollieCommunity #Concert#CerebralPalsyAwareness so posted to the my highlights to you is also orange read it because I was able to see music being through date and I was able to join in with his why disabil so important to the people that they say and help every single day this is why you’re right, the one I have for my disability should be paid more than I should be more career progression, #SpasticTo

      January 15, 2024

      Taylor mania concert last night that I went through with the help of my contacts, Louise personal assistant you see this picture of the stage, and please look on my page for the content to do with Phela mania

      January 15, 2024

      https://vm.tiktok.com/ZGe6mB3MC/

      tick-tock of me and my personal assistant having fun at the Taylor mania concert in the interval yesterday. Click on the video to see us having fun. Coser is local Vicky #AccessToMyCommunity #SupportWorkersMakeUpTheDifference #MeMySupportWorker #ReworkOnRepeat

      January 15, 2024

      https://vm.tiktok.com/ZGe6m2oBe/

      adventures with me and my cerebral palsy and associated complex late today me and

      January 15, 2024

      Post Office Horizon Software Originally Aimed At Claimants

      January 15, 2024

      With many thanks to Benefits And Work.

       

      The Horizon software at the centre of the current Post Office scandal was originally designed to save money and reduce fraud in connection with benefits and pension payments.  Even though the Benefits Agency dropped the software, there are disturbing parallels between the way sub-postmasters were, and claimants still are, treated.

      £700 million lost
      Horizon was a joint venture between the Post Office, the Benefits Agency (as the DWP was then called) and ICL, a subsidiary of Fujitsu.

      The intention was to create a swipe card system for benefits and pensions to be paid out at Post Offices, replacing paper payment books.

      The project began in 1996, but by 1999 the Benefits agency had lost all faith in the system ever working and pulled out, leaving the taxpayer with a massive £700 million bill with nothing to show at the end of it.

      In desperation, the project was repurposed to allow electronic bookkeeping to replace paper accounts in post offices.

      And the result of that is now playing out in the media, the courts and a public inquiry.

      Misuse of powers
      That the Benefits Agency pulled out of the Horizon system it so its credit. 

      But there are many alarming parallels  between the current DWP and the Post Office.

      Both have the power to conduct their own criminal investigations and both routinely misuse these powers.

      The Post Office threatened sub-postmasters with prosecution for theft unless they admitted wrongdoing and agreed to pay back all the money they allegedly owed.

      The reality was that the Post Office very often had no evidence that any theft had taken place and would not have been able to bring such a charge.  But sub-postmasters were never given the opportunity to examine the alleged evidence.

      Similarly, claimants interviewed under caution by the DWP are often told that if they end their claim and agree terms to pay back any alleged overpayment, they will escape prosecution for theft.

      Many claimants agree, without understanding that the DWP have failed to show them any evidence of the alleged overpayment.

      If such cases go to tribunal, rather than a criminal court, they are very often thrown out – or the alleged overpayment dramatically reduced – because of a lack of evidence.  The DWP has such poor systems that they often cannot actually show whether payments took place or how much they were for.

      In other cases, the claimant will insist that they informed the DWP of a change of circumstances but the DWP will be unable to supply a copy of the document they received from the claimant, even though there is evidence it existed.

      No legal representation
      Both sub-postmasters and claimants are routinely interviewed under caution without any legal representation being offered or provided.  This would not happen if prosecutions were being carried out via the police and the Crown Prosecution Service.

      The lack of legal representation allows the prosecuting body to mislead the people they are pursuing without any fear of consequences.

      Obsessive secrecy
      Both the DWP and the Post Office are obsessively secretive. 

      The Post Office’s often successful attempts to hide information from the courts and the current public inquiry are a scandal in themselves.

      In the same way, anyone who has attempted to obtain information from the DWP via the Freedom of Information Act will know the huge and very expensive lengths that the department will go to in order to keep evidence about their practices and procedures secret, even when it involves the death of claimants.

      And there are many examples of the DWP keeping evidence from inquiries, government committees and even coroners’ courts.

      Bonuses for wrongly recovering money
      Post Office investigators, it has now been revealed, were on a bonus system for any money they recovered by threatening and misleading sub-postmasters into repaying money they never owed.

      We don’t know if DWP investigators are also on a bonus system for recovering money from claimants.  But we do know that in the past the DWP has paid bonuses to teams for pushing claimants off benefits, including by way of sanctions.  So there is every possibility that fraud teams are incentivized in this way.

      Benefits and Work has made  a Freedom of Information request for any documents which deal with bonuses in relation to detecting fraud or recovering money from claimants.

      We don’t expect to get a genuine response anytime soon.

      Fears for the future
      The DWP have very recently been given powers to allow the mass surveillance of claimants’ bank accounts.

      But, as we revealed last November,  the DWP want to go much further than this.

      They are hoping to get the power to arrest claimants, search their homes and seize evidence.

      After what we have seen of the Post Office scandal, such a possibility is truly terrifying.  The opportunity for the department to disappear documents, including copies kept by the claimant which would establish their own innocence, do not bear thinking about.

      In the wake of the Post Office scandal, there is now a very strong argument for stripping the DWP of its power to prosecute claimants.  And there is an absolutely overwhelming argument for preventing them gaining any additional powers.

      But is there anyone who will effectively make that argument?

      You can read more about the connection between the Post Office Horizon system and the Benefits Agency in Alan Bates and Others vs the Post Office Technical Appendix to

      Judgment (No.6) “Horizon Issues”  and in the Private Eye special report Justice Lost in the Post

      Iron Age Infant With Down’s Syndrome Identified Using New DNA Testing

      January 15, 2024

        An infant with Down’s syndrome dating from the Iron Age has been discovered with a new method of DNA testing.

        The technique measures the amount of chromosomes in ancient human cells “more precisely”, said researchers.

        They have also identified the first prehistoric person with mosaic Turner syndrome, from about 2,500 years ago.

        The research was carried out by the University of York, the Francis Crick Institute, the University of Oxford and Oxford Archaeology.

        Down’s syndrome, mosaic Turner syndrome and other conditions the researchers identified all stem from chromosomal abnormalities.

        Most cells in the human body have 23 pairs of chromosomes and the conditions occur when a person’s cells have an extra or missing chromosome.

        Professor Ian Armit, from the University of York’s Department of Archaeology, said: “Ancient DNA samples decay over time and can often become contaminated.

        “A new technique was needed to help researchers overcome these challenges so that we could see just how far back we can trace these conditions, and we now know that they have been part of human history for a considerable period of time – more than 2,000 years in some cases.”

        The individuals tested with the new technology lived across a range of time periods, from the Iron Age 2,500 years ago up to the Post-Medieval period, about 250 years ago.

        Klinefelter, Jacob’s and mosaic Turner syndromes all involve abnormalities with sex chromosomes and the researchers found that the individuals with these conditions had delayed puberty.

        All were buried according to their society’s customs although no possessions were found with them, the experts said.

        Pontus Skoglund, group leader of the Ancient Genomics Laboratory at the Crick, said: “Our method is able to classify DNA contamination in many cases, and can help to analyse incomplete ancient DNA, so it could be applied to archaeological remains which have been difficult to analyse.

        “Combining this data with burial context and possessions can allow for a historical perspective of how sex, gender and diversity were perceived in past societies.”

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        January 14, 2024

        positive saying of the evening and stations this evening for more night out content

        January 14, 2024

        for any of my new followers please post it is for you. My name is Maya. I am 24 years old and I raise awareness about seeing me a bit messy in disability. Oh how do you live a life policy to play at the 20? Old with cerebral call Zoe home needs PAs, all personal assistance to help her with her. But I am not cerebral palsy. I am 24 I go to College. I am currently studying allergy awareness in health and social care. And level two functional skills maths so I am a student. I am a blogger I like to mate I like concert live I like seeing friends I get involved in lots of community volunteer work and have helped in Man U mobiles to organise things such as Christmas events, healthy, eating a Events and many more, are the service user engagement and staff training materials I’ve also been involved in lots of award ceremonies for the principal a my life. I would love to answer so put your questions down below in the comment because I’m all about an awareness of the time I have such is cerebral palsy and Florence neurology call unable to create no over awareness of how our lives or no different and how we live in Roberts or anybody else, but give me a different life because it’s the life we choose making allowances for a disability alarm in one

        January 14, 2024

        the winter positivity of the day is today. Courtesy of mini mouse join me for the adventures of a woman with cerebral palsy and other complex support name as I go to another concert with evening.#CommunityAccess##MyLifeCerebralPalsyAwareness #Functional

        January 14, 2024

        signing of the day, including peacock and a half. I chose this one as saying is also very pretty. I would like that is great that that would look lovely on the coffee table and

        January 14, 2024

        beach scene, painting with heart that huge and colourful and a centrepiece

        January 14, 2024

        link to my donation page for my 2020 for respite care due to the lack of respite from 0 to 25 together for a bit

        January 14, 2024

        https://www.facebook.com/share/p/j6i7GRbbWsFK2ta8/?

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        January 14, 2024

        colourful painting of the day

        January 14, 2024

        favourite paintings of the day

        January 14, 2024

        painting of a beautiful evening 30 for you that is very colourful, which is why I like it. I love the colours in paintings

        January 13, 2024

        favourite. How are you feeling for of the day call you this evening all my love

        January 13, 2024

        signing of the evening

        January 13, 2024

        Artwork

        January 13, 2024

        Joe nation page for those that want to contribute towards my respite of printing, printing tomorrow or no, is that man who might want to do, so please share as much as possible you Maya

        January 13, 2024

        https://www.facebook.com/share/p/G8Pv35F6u38WCsXP/?

        pictures of beautiful, colourful nature and animals of my favourite painting

        January 13, 2024

        https://vm.tiktok.com/ZGe6YDUf3/

        one year memory of me, yet to see a naughties with my PAMollie who has now gone onto a new

        January 13, 2024

        Amazon, affiliate first page of the day

        January 13, 2024

        turn off day for viewers of my flow

        January 13, 2024

        colouring book/activity book for Adam

        January 13, 2024

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        January 13, 2024

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        just additional needs adults in education and this morning Lisa Renner, I am proud to be at this moment a additional needs adult education, Dunkery Road, Maidstone, Paul are you still trying to? Is it 30 p.m. spreading awareness for the next I finish my

        January 12, 2024

        join me to find out what was called in my allergy awareness exam the other day as I get the results later on today. Also join me to see what schools I score in my maths test as a level one/level two functional skills, maths student who is working

        Tiktok

        January 12, 2024

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        January 12, 2024

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        elegant handbag for me use the link to purchase. Annemari is a picture included in this place for you to view it. You can also do it through the link if it is easier for you to rain in with you are

        January 12, 2024

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        notifying of the day for you for the early rises, and for those in England maybe just going to bed like me after a long day at college

        January 12, 2024

        🤨👩🏾‍🦽🌙 This is what it was like saying goodbye to my disability personal assistant today as she is going onto her career and I wish her luck that we will miss her and that did you get that I wish more people would use community hall for disabled as a understand it and paint under under under valued and underestimated how much independence, but I can bring to a disabled so therefore they are not paid the value and

        January 12, 2024

        Momentum Talk: Sustainable Development Goals- What Have We Achieved For Children With Disabilities?

        January 12, 2024

        Same Difference has been asked to publicise the following event by a friend of the site.

        The online event will be held on Zoom.

        no definite date open the Pinterest page before I go to bed. I have updated with a range Rover items so please go and have a look and see what you would like to purchase. Please tell me if there is the link of Amazon, yet that you would like to purchase and I will make this for you because there might be items to go for Finny yet to link that you would like to

        January 11, 2024

        good night time for everyone, followed by an Amazon

        January 11, 2024

        do you see her a woman with cerebral palsy and wheelchair-bound hide with her new kitten woman with cerebral palsy interacting with her to open your review that people who are wheelchair-bound search on Internet and play with #CerebralPalsy,Awareness text, District, I appreciate cerebral palsy #MyCerebralPalsyJourney#IAmAStudent #ThereIsMoreToMeThanMy

        January 11, 2024

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        January 11, 2024

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        January 11, 2024

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        January 11, 2024

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        January 11, 2024

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        January 11, 2024

        yes given from braising ring Rosa is that may choose to donate to my 2024/oh no someone who might want to give to causes like mine where there isn’t any respite from doing available local 0 to 25 together services for their disability. Do any of you know with charities that gave to Co-Ordinator like end friend respite for people like myself, thank you I’m sure I cannot be the only one and I’m sure that there are things that help with printing, at least some of a persons respite and the services that are supposed to support do not change to do is to make the decision for service isn’t essential that they do not live your life

        January 11, 2024

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        January 11, 2024

        the book, that is your own purchase of the day today for the book of the dissection of my block#BookOfTheDay

        January 11, 2024

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        first Amazon affiliate and the only one off today as I have already FaceTime afternoon so won’t be able to post an affiliate today she’s definitely get another one tomorrow

        January 11, 2024

        things for the cat, owners or cat lovers on my page, saying of the morning, especially for you who are cat lovers, Blastoise me and I love cats like there was a true word

        January 11, 2024

        positive morning, Sherry prime

        January 11, 2024

        first phone Move, the day and for painting of the day

        January 11, 2024

        Music Brings Trowbridge Mother And Disabled Daughter Together

        January 11, 2024

          A mother has said she is better able to communicate with her 14-year-old disabled daughter thanks to music.

          Emily Wadds’ daughter, Lydia, has a profound and multiple learning disability, is non-verbal, a full-time wheelchair user and has epilepsy.

          But after accessing the charity Soundabout, Mrs Wadds said: “I don’t think I’ve ever known her better.”

          Mrs Wadds, from Trowbridge, said that learning about Lydia’s expressions and noises has helped bring them together.

          The pair have been accessing Soundabout’s online music sessions for around four years.

          “Music has brought us much, much closer together,” Mrs Wadds, 52, told BBC Radio Wiltshire.

          “She’s non verbal, so she doesn’t talk, but just to hear her voice, I really can recognise her happy noises now – she does this little cluck.”

          Regular seizures meant that Lydia made little noise in her early years, but with music in Lydia’s life, Mrs Wadds said she has seen a real difference in her daughter.

          “We barely got any noise from her, she didn’t laugh for years,” she said.

          “Now she makes lots of different noises that she never did before and I think it’s given her confidence to make the noises, she’s exploring more with her vocal cords.”

          Mrs Wadds said that discovering Soundabout also gave her the opportunity to enjoy time with Lydia.

          “When she was little I was watching her all the time,” she said.

          “It was all about making sure she was safe, looking out for seizures, monitoring seizures, videoing seizures, talking about seizures – it was all health related.

          “Finding Soundabout, I watch her, but it’s for an enjoyable purpose – looking at her eyes and looking at her expressions, listening to her noises.

          “I think it’s one of the most important things in her life actually – music and food.”

          Rebecca Thomas has worked in special educational needs music for 15 years after studying music at Goldsmiths, University of London.

          She now works as a Soundabout family support coordinator.

          “Music is so universal, it connects people in so many different ways,” Miss Thomas said.

          “It doesn’t matter what language you speak or how you communicate – whether you communicate with vocalisations, without vocalisations, body language – music enhances all of those interactions.

          “It’s a way for us all to meet in the middle.

          “Lydia has all these incredible ways of communicating. I feel like music is just that tool to uphold all of the things she wants to tell us.”

          programmes, rocket shaped pillow, so the space love is in your life

          January 10, 2024

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          women’s travel hat for hot and cold drinks with a skull print on the front blue and pink multicoloured cup

          January 10, 2024

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          show blanket for children

          January 10, 2024

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          who won usual painting so unusual find them interesting so I have shared them now rather than tomorrow. Imagine if a dog painted like this and the woman walk round with flowers for the imagine what babes they would get from Coles in the traffic is a joke was saying and a woman was saying with flowers in her hair like that it’s very interesting and just imagine if that was something that was the Queen in real life have you where are is so interesting rendered if you’ve ever seen any of because it’s a it’s amazing how realistic these artists campaign, my pictures yet you know if the app and then we’ll life would be on new been something

          January 10, 2024

          on the TikTok video video to see me and the Green Day tribute band that I went to see on Saturday night because they are amazing. #LiveMusic #WomanWithCerebralPalsyInHerTwentiesThe show #

          January 10, 2024

          https://vm.tiktok.com/ZGejX3bYQ/

          bright, cerise pink sandals for those girls or women that like bright colours

          January 10, 2024

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