my fundraising group click on this to donate to wards my respite and they are really care
Hi SameDifference Community – Good Morning!
I have some wonderful news to announce to my community on here.
As you may all know, I’ve been fighting to get back into education for the next academic year. I have been accepted onto my Maths course starting in September and have an interview for my Health and Social Care, due to start in October but I will be enrolling in August!
I will update after my interview but I hope to tell you all that I have a place on Health and Social Care Level 2. Fingers crossed for me!
#Furthereducation #CerebralPalsy #Fightforaccesstoeducation #Wanttoqualify
Hastye Grace, very high standard cerebral palsy #FromRaising #HelpMeToGetToTheThousandPounds
You’ve probably seen one of the latest Twitter memes doing the rounds.
There’s black text – “click here” – on a white background. And an arrow pointing to the ALT image description label. Behind that, there’s a joke or a punchline.
Brands including McDonald’s (ALT: “Extra pickles life”) and Red Bull Gaming (ALT: “Ice cold Red Bull”) have jumped on the trend.
Just a bit of light-hearted content to make their followers laugh, right?
Well, alt text, short for alternative text, is a description of an image used by blind or partially sighted people to help them navigate social media.
So if you’re visually impaired, this joke’s not for you. And that’s got people upset.
‘A meme for sighted people’
Connor Scott-Gardner is blind and says alt text is so important to him because so much content posted online relies on images.
“There are entire social media platforms like Instagram, which are image-based,” he says.
“And we share a lot of information through images, whether that’s text or through memes, whether we’re making a joke or just through culturally significant things.
“So for me alt text gives me access to all of that content, and it means that I’m able to have an equitable experience on the web.”
So Connor, 29, says that the “click here” meme left him feeling “excluded on a very fundamental level”.
“It actually took sighted people calling out the meme for blind people to even know what it was,” he tells BBC Newsbeat.
“It’s very much a meme that is created for sighted people.”
Connor and other users hit out at some brands who’d jumped on the meme. McDonald’s Canada actually replied with an apology and deleted their post.
It took another company, Specsavers, to turn the trend on its head.
In a tweet that’s been seen millions of times, the company posted its own version of the “click here” meme.
But it used the alt text to make a serious point instead of cracking a joke.
It wrote: “Alt text is a hugely important accessibility tool designed to help people navigate the internet more easily, so it shouldn’t be used as a punchline.
“This is especially true if the Alt text doesn’t describe the image, leaving blind and visually impaired people out of the joke.”
‘Inclusive content is good content’
Becky Brynolf, who’s the head of social media at the Royal National Institute of Blind People (RNIB), agrees.
“Adding good alt text is such a quick win, I’m really surprised that more people don’t do it,” she says.
“Inclusive content is just good content. So you really shouldn’t be excluding anyone, especially not for a joke.
“If you wouldn’t take someone’s guide cane to show off how well you can twirl it about, you absolutely shouldn’t be misusing alt text for the sake of a joke.”
How to make your feeds more accessible
Becky says you can be really descriptive with your alt text, because you have 1,000 characters to play with.
“I’ve been really disappointed by all the tweets coming from the Met Gala, for example, that just say something like ‘Jeremy Strong attends the Met Gala’,” she says.
“But what is he wearing? What’s his facial expression? What’s the vibe like? Does he look happy to be there?
“Blind people want to hear about the fashion too. So don’t feel like people aren’t interested just because they can’t see the visuals.
“And just always think of accessibility as like a love note. Like it tells people we want you here as well.”
Connor says he’s especially annoyed that so many of the brands jumping on the bandwagon don’t use alt text in their other posts.
He says some have even posted things since without alt text.
“So it’s very clear that they have no interest in including blind people or giving us access to information,” he says.
“They’re only using that accessibility feature when it’s convenient to them and brings something to their sighted followers.”
Newsbeat contacted Twitter for a comment but it replied in the same way it does to all media, with a poo emoji.
Yay it’s Friday!
Happy Thursday! :)
You could be in for a chance of winning these prizes when you enter my raffle for respite care fundraiser!
Flavours of soap are:
Vanilla
Rose
Gardenia
Chamomile
Cherry Blossom
White Tea
To enter, please put the word “Raffle”, with your name (can be your real name or username) in the comments below this post in the comments. You will then receive a raffle number electronically.
Not quite sure when it will be drawn, details to be announced. Donate to my JustGiving or GoFundMe, linked below for a chance to win. Please use the same name to donate as the name in the comments.
I will put up a video to reveal who has won after I have announced the draw of the raffle, and the date and time of it. Thanks and have fun with this!
https://www.justgiving.com/crowdfunding/maya-richards


With many thanks to Benefits And Work.
Claimants are waiting over half an hour, on average, for PIP and DLA helpline calls to be answered, DWP minister Tom Pursglove admitted in a written parliamentary answer last week. But the minister now needs to come clean about how many callers never get an answer at all, because they are deliberately disconnected using a practice the department refers to as ‘call-blocking’.
Labour MP Beth Winter asked about waiting times for calls last month.
The response from the minister for disabled people was that the average waiting times for the PIP, DLA and AA telephone enquiry lines for the month of March 2023 were:
PIP – 37 minutes
DLA – 33.5 minutes
DLA65+ – 6 minutes
AA – 2 minutes
Clearly average waiting times of over half an hour for PIP and DLA are absolutely unacceptable, although many people who contact us have waited much longer without getting an answer at all.
But Pursglove’s response hides much more than it reveals. Because we also need to know about the number and proportion of calls that don’t get answered.
This would include claimants who hang up after waiting often for an hour or more.
And, crucially, it would include callers who are being deliberately and repeatedly cut-off by the DWP.
Back in March of this year a parliamentary question was asked about waiting times for the DWP Future Pension Centre. Call volumes had increased ten-fold as people tried to check their national insurance contribution record before a deadline.
The answer revealed that in March 443,000 calls out of a total of 517,00 had been blocked by the DWP – almost nine in ten callers. The practice is known by the DWP as ‘call-blocking’ and means that the DWP does not allow the call to enter the call waiting queue because there are too many people in it already. Instead, the line simply gets cut-off.
This sounds very similar to what has been happening to many callers to the PIP helpline, who report being repeatedly cut-off:
“Received PiP review form but my partner who it relates to is unwell in bed for last 3 days. Time scale for return quite short. Rang to get extension today. Keep getting cut off. Must have tried 10 times.”
“Been trying for Weeks to get through to change bank account details and it cuts off as soon as you go through all the automated talk. Three weeks ago got through the talk on the ‘make a new claim’ section only to hold for an hour and a half. I gave up without speaking to someone.”
“Ridiculous wait times, been trying to phone for 4 days now and each time it either cuts me off during asking for my details, or there is an hour 30 wait time and it cuts off. Only need to ask for an extension to my date as the forms only just arrived giving me 7 working days to reply back. I can’t even get an appointment with CAB in the next 2 weeks, let alone my doctors to request supporting documentation and they give 7 working days?”
In his written answer, the minister’s explanation for the long waiting times was:
“We are currently experiencing higher than forecast call volumes to the PIP and DLA telephony enquiry lines. We have recruited additional staff onto our telephony teams and have on-going recruitment to further increase resources.”
But, without knowing how many staff are being recruited and how many staff are already in post it is impossible to tell whether the extra staff are likely to make any real difference.
So, it’s good news that MPs have begun raising the issue of DWP call handling with ministers, but there are a lot more questions that need to be asked.
A picture of me dressed up from last night :)
A wheelchair user who crawled down metal steps from a plane when no-one could help him disembark has described the incident as “unacceptable”.
Adrian Keogh, from Wicklow in the Republic of Ireland, was told assistance would take an hour to arrive after his flight landed at Landvetter Airport in Sweden on Saturday.
Mr Keogh said cabin crew on the Ryanair flight told him he could crawl from the aircraft instead of waiting.
He has used a wheelchair since 2015.
The airport has apologised and Ryanair said it was looking into the incident.
Mr Keogh, who has a spinal injury following a construction accident, told BBC News NI he was not able to wait for an hour for assistance disembarking the plane as he was in pain after the flight and needed to use the bathroom.
He was travelling with his brother who offered to carry him down the stairs but Mr Keogh declined as he felt that would be too dangerous.
“They were steep, corrugated steel steps,” he said.
“If he fell we would have both been hurt so I had to bunny-hop down myself.”
Mr Keogh said air travel as a wheelchair user could sometimes be frustrating.
“This is not the first time I’ve been stuck on a plane after everyone else has disembarked,” he said.
“It’s unacceptable – all I ask for is to be able to travel with dignity.”
In a social media post, Landvetter Airport apologised, blaming busy flight traffic and a medical emergency for the delay in assistance.
BBC News NI has approached the airport for comment.
Ryanair said special assistance at Landvetter Airport was provided by a third-party service provider.
The airline said it was looking into the incident.
Similar issues have been reported at other airports, including by the BBC’s security editor Frank Gardner, who was left on a plane at Heathrow Airport.

How do you book (and complain) about airport assistance?
- The UK government recommends that passengers request assistance through their airline, tour operator or travel agent at least 48 hours before travel
- If a passenger has not pre-notified, assistance will always still be provided but you might have to wait longer to be helped
- If things go wrong and you’re unhappy, the Civil Aviation Authority recommends you take your complaint directly to the airline or airport
- If you remain dissatisfied, you can refer your complaint to an alternative dispute resolution body which provides alternative methods, such as mediation and conciliation, instead of going to court
Charities have paid tribute to an award-winning disability activist who has died aged 29.
Lucy Watts, MBE, who lived with her mother in Thundersley, Essex, sat on multiple NHS care committees and ran her own company for patient advocacy.
Her family said she died on Wednesday morning at Southend Hospital.
Toby Porter, chief executive at Hospice UK – a charity Ms Watts worked alongside – said she was “remarkable”.
“[She was] a true champion for hospice care and the rights of people living with disabilities and complex health conditions,” said Mr Porter.
“Lucy was for many years one of the clearest, most articulate and compelling voices across our entire palliative care community.”
Ms Watts was born with a life-limiting condition which included multiple organ failure and restrictive lung disease that eventually needed 24-hour care.
Influential
She attended the King John School in Thundersley and at 22 years old was appointed MBE for services to young people with disabilities.
She founded a stakeholder group in 2017 for people receiving palliative care – Palliative Care Voices – and in 2018 she set up her own advocacy company, Lucy Watts Ltd.
In 2019, she was named the ninth most-influential person in the UK in the Shaw Trust Disability Power 100 List.
She repeatedly spoke of the importance of talking openly about dying, and in a blog written in 2020, of which an extract was published by the BBC, she talked about shielding during the pandemic.
In a post shared on social media, her family said they hoped she was now “with her beloved” support dog, Molly, and grandparents “who adored her”.
A spokesperson for the Shaw Trust, a charity that advocates for people with disabilities in the workplace, said: “She will be very much missed by the disabled community for her work to effect change nationally and internationally.
“She leaves a powerful legacy behind – she was the change we all aspire to be.”
John McFall is the European Space Agency’s first ever para-astronaut, selected to study how feasible it is for someone with a physical disability to live and work in space. BBC News joined him on board a parabolic flight, where he experienced weightlessness for the first time.
One minute John McFall is lying on the floor of a plane. The next, he starts to float upwards, still horizontal, seemingly levitating towards the ceiling.
He looks astonished – everyone on this far-from-normal flight does, as they slowly rise into the air. The sensation of being weightless, no longer pinned down by gravity, is extraordinary.
You feel totally out of control – because you are. Any tiny movement against something solid sends you catapulting around the cabin, bouncing into walls and people. It’s like being in a slow-motion pinball machine.
A smile begins to form across John’s face – he starts laughing. “It’s brilliant, it’s amazing,” he says.
Then suddenly, the weightlessness is gone and he falls to the ground.
John is an astronaut candidate with a difference – he’s an amputee. When he was 19 he lost his leg in a motorcycle accident, and now uses a high-tech prosthesis.
He has now been recruited by the European Space Agency (Esa) to take part in a ground-breaking study assessing how to make spaceflight accessible to people with physical disabilities.
“I saw that the European Space Agency had announced that they were looking for an astronaut with a physical disability,” he says, “and I looked at the person specification and thought, ‘Wow, that’s me – I would love to give that a go’.”
John’s used to pushing himself to the limit. After losing his leg and learning to walk again with a prosthesis, he took up running – for fun at first, then competitively. He went on to win a bronze medal in the 100m at the 2008 Beijing Paralympics.
He then decided to become a doctor and is currently working as a trauma and orthopaedic registrar in Hampshire, but he’s had to pause his medical career – the opportunity to work with Esa was too good to turn down.
“I’m very much following my heart and I’m following my curiosity,” he explains, “and I’m following my passion for science and life.”
I’ve joined John on board a specially adapted aircraft to take a parabolic flight. As the plane flies steeply upwards, we experience extra gravity – about twice as much as usual – where your whole body is pressed down into the floor.
Then, as the plane gets ready to nosedive back down, there’s a moment when we become weightless for about 20 seconds. It’s not that gravity has vanished, we’re still bound by the laws of physics. Instead, we’re actually in freefall – as is the plane around us – but this reproduces zero-gravity conditions. The plane repeats this manoeuvre again and again.
https://emp.bbc.co.uk/emp/SMPj/2.49.2/iframe.htmlMedia caption,
Watch: The BBC’s Rebecca Morelle struggles during her first experience of weightlessness
There’s a reason parabolic flights are nicknamed “vomit comets” – it’s like riding on a mid-air rollercoaster.
Thankfully, I don’t feel sick, but it’s safe to say I’m not a natural astronaut.
I tumble, out of control, squealing, asking for help to come down. But I end up pinned to the ceiling – until the period of zero-gravity comes to an end, and I crash down like a sack of potatoes. Luckily the floor of this plane is well padded.
Meanwhile, John is faring much better, soaring around and gaining confidence with every period of “zero-gravity”.
The prosthesis John wears is technologically very complex, incorporating a microprocessor, hydraulics, a gyroscope, accelerometers and other force sensors.
“All those things together make the knee know where it is in space and how fast it’s bending or straightening,” John says.
He’s assessing how well his prosthetic leg is operating in this unusual environment, and the challenge comes when weightlessness kicks in.
“You’ll probably see I’m floating around with my leg out straight, because that gravity isn’t there,” he explains. “So it’s harder for me to turn quickly – because my leg doesn’t want to bend. I’m just getting used to that and working out how I can move myself in zero-g, but each parabola is a learning opportunity.”
John thinks that his prosthesis may be too high-tech for this environment, and a simpler one might fare better. And this is the whole point of his project with Esa: working out exactly what needs to be adapted for a person with a physical disability to spend time in space. It will cover everything, from pre-mission training, to looking at whether a spacecraft would have to be modified to accommodate John’s needs.
But he says everyday life in a microgravity environment is still the biggest unknown.
“Will I wear a prosthesis? And if I wear a prosthesis, will I have to have something that will accommodate variations in volume in my stump? Would I be able to run on a treadmill in space? Will we have to adapt a spacesuit for a spacewalk? If so, in what ways?” he wonders. “All these questions are things we do not have answers for.”
John is acutely aware that his disability is specific to him, and he needs to take that into account while he’s undertaking the study.
“I haven’t got a spinal cord injury, I haven’t got cerebral palsy, or spina bifida. So I’m thinking about how this applies to other disabilities as well – but we have to start somewhere.”
There’s a wider impact too. John hopes the project will redefine people’s expectations of what someone with a physical disability can do.
As the flight nears its end, John keeps working on and improving his zero-gravity skills. He’s now moving about easily and can even land standing up, while I continue to thwack down to the floor, every time.
When this project comes to an end, John isn’t guaranteed a mission to space, but as the plane starts its preparations for landing, I ask if this experience has whet his appetite for space, or made him have second thoughts about his new job.
“It’s given me even more hunger and excitement,” he says with a huge grin. “It’s just awesome – I can’t wait.”
bowling with wacky wheels 👩🏾🦽
memory of me at the cafe after going shopping two years ago.
Friday afternoon positive phone
making my own 24 for three years ago today during lockdown
PIP Points For Over-Eating
With many thanks to Benefits And Work.
An upper tribunal judge has held that over-eating can be grounds for scoring PIP points, if the problem is linked to a physical or mental health condition. Benefits and Work has been advising readers to claim points for this issue since PIP was introduced, but we will now be updating our PIP guide to include brief details and a link to the decision.
The case was brought by a former soldier who has anxiety, depression and post-traumatic stress.
In his evidence he explained that due to an incident while on active service abroad, he was unable to eat for two days. He now has difficulty in knowing when to stop eating. When he left the army, he was 15 stone and now he is 22 stone.
He relies on his wife to control his diet and eating habits. His wife monitors his food intake, making him packed lunches to ensure he is not overindulging whilst at work, and preventing him from taking cash so that he cannot buy ‘junk’ food.
The judge held that, depending on the circumstances, it might be correct to award 4 points for descriptor 2) d. ‘Needs prompting to be able to take nutrition’.
Although the claimant was able to take nutrition, because he took too much it might be the case that he did not take nutrition as often as reasonably required. Instead, he took it too frequently.
Alternatively, it might be found that he could not carry out the activity of taking nutrition to an acceptable standard if it was being performed repeatedly and to excess and in a chaotic way, though the judge considered this would be a harder case to make.
In some instances it might be that the activity cannot be carried out safely if food is eaten so quickly or compulsively that choking or serious vomiting risks arise, although that was not a factor in this case.
The judge sent the case back to a first-tier tribunal to be reconsidered.
It is worth noting that the success rate for claims where the primary condition is obesity is 78%, well above the average of 52%.
colour by number I did today with my support person
My fundraising link okay what’s up://www.justgiving.com/crowdfunding/maya-richards?utm_term=YdzA26Vzv for people would like to donate
British Vogue editor Edward Enninful has said working on May’s issue, which has five disabled cover stars, was “one of the proudest moments of my career”.
Titled Reframing Fashion, the edition focuses on 19 disabled people in total from fashion, sport and the arts.
The magazine’s cover stars include actress Selma Blair, who has multiple sclerosis, and model Ellie Goldstein, who has Down’s syndrome.
Enninful, 51, said he had “learned so much” from producing the issue.
“My tenure here at Vogue has always been about inclusivity and diversity, and people forget how hard it is for the disabled community,” Enninful told the BBC.
He revealed last year in his memoir that he had visual and hearing impairments and a blood disorder, which he said present “challenges” in his role as editor-in-chief at British Vogue.
“It was so important I could relate – I felt real pride that people can actually speak up about disabilities and not have to hide it and how it impacts them.
“I think this is one of the most incredible issues I’ve had the privilege of editing in my tenure.”
Other contributors to the new edition include racing driver Nicolas Hamilton and comedian Rosie Jones, who both have cerebral palsy, and Justina Miles, who is deaf and was the sign language interpreter at Rihanna’s 2023 Super Bowl half time show.
“What I loved about all of them is they all just speak up and champion their community by teaching the world to be more caring and understanding,” Enninful said. “Anybody like that deserves to be on a British Vogue cover.”
The May issue also features Sinéad Burke as a contributing editor and cover star. She runs accessibility consultancy Tilting the Lens, which has advised brands like Netflix and Starbucks on how to make their businesses more disability-friendly.
“Sinéad taught me that retail spaces are quite unfriendly to people with disabilities and that photographic studios are not designed to cater for them,” Enninful said.
“She has really opened my eyes and taught me that a whole group of people are being ignored.”
Burke spoke to the BBC’s Access All podcast about making sure all Vogue photoshoots for the issue were suitable.
“We surveyed every studio to learn what level of accessibility existed and then ensured the talent was set up to meaningfully participate,” she said.
“What makes this issue so different is the way in which we think about visibility and representation moving from something that is solely based on image and the cover, to being in the room where decisions are made so that it’s not a moment, it’s a movement.”
British Vogue said it hopes to represent some of the 16 million people living with invisible and visible disabilities in the UK, and show how the fashion industry can be more inclusive.
Enninful, who got the top job at British Vogue in 2017 and became European editorial director of Vogue in 2020, said he hopes to make the publication a more inclusive workplace.
“We want to carry this on and for people to see Vogue is taking that step… We’re not perfect, but we have to create this welcoming space,” he said.
It’s an issue that got some media attention earlier this year when Victoria Jenkins appeared on BBC show Dragon’s Den.
Having become disabled in her 20s, Jenkins discovered there were very few fashionable clothes on the market for people like her.
She founded her own brand Unhidden to cater for various disabilities.
I mentioned this to Enninful, and my own concerns as someone who has had inflammatory bowel disease for nearly 20 years and has had to resort to pyjamas and tracksuit bottoms during a flare-up or operation to feel comfortable.
“I always have conversations with designers and it’s something we’ll carry on with,” Enninful said.
“But I think the more you raise awareness of what people go through, the more people will start thinking how they can be more inclusive.”
Enninful said a big part of shooting this Vogue campaign involved making those involved feel like there was a place in the fashion industry for them.
Many people with both visible and hidden disabilities have not felt seen in the media, especially on the front of glossy and often airbrushed magazine covers.
“There were a lot of tears – a lot of them [models] didn’t think photoshoots were for them and couldn’t believe they were involved,” he replied.
“Ellie [Goldstein] said it was her dream to be on the cover of Vogue and she said, seven years ago people would have laughed at her, but there she is, and everybody deserves to be seen.
“When this issue comes out, I hope a lot of disabled people will look at it and say, not only can I see myself on the pages of Vogue, but also in fashion.”
are you Thursday saying :-) 😎💚👩🏾🦽
wishing you a successful Wednesday for all 🙂🙂😎😎👩🏾🦽👩🏾🦽👩🏾🦽
A theatre company in Hull is to give a presentation in Prague on creating productions which are accessible to people with learning disabilities.
Concrete Youth’s research into autonomous sensory meridian response (ASMR) was used in their 2022 touring production The Whispering Jungle.
The Prague Quadrennial is the world’s largest festival of scenography, theatre design and architecture.
The four-yearly event has been running since 1967.
Concrete Youth has specialised in creating inclusive theatre for people with profound and multiple learning disabilities (PMLD) and used its research into ASMR to give audiences a sensory experience during a 2022 tour.
Daniel Swift, Concrete Youth’s chief executive co-artistic director, said they were “thrilled” to have been invited to Prague.
“This is a huge moment not only for Concrete Youth, but also for our audience with profound and multiple learning disabilities, who are some of the most invisible members of society.
“This platform will spread international awareness of this community of people, the barriers they face and the lack of cultural provision that they experience daily.”
The company, which receives financial support from Hull City Council, began its ASMR project in 2020 and in 2021 expanded it to include work with hundreds of people with PMLD across the world, including specialists, carers and consultants in the UK, US and Singapore.
It was that work which would be included in the Whispering Jungle tour, which featured sensory play and sensory puppets in an immersive show.
Kath Wynne-Hague, head of culture at Hull City Council said their work was “incredibly valuable”.
“It provides the opportunity for people usually excluded from a typical theatre experience to not only participate, but experience something created specifically for them.”
Concrete Youth is the only touring organisation in the UK to have an exclusive sensory offer for people with PMLD in education and care settings and their talk in Prague will take place on 8 June.
A Barbie with Down’s syndrome is the latest doll to be released by Mattel in a bid to make its range more diverse.
The US toy giant had faced previous criticism that the traditional Barbie did not represent real women.
In recent years it has created dolls with a hearing aid, a prosthetic limb and a wheelchair.
Mattel’s goal was for “all children to see themselves in Barbie” as well as “play with dolls who do not look like themselves”.
The original Barbie doll launched in 1959 featured long legs, a tiny waist, and flowing blonde locks.
Academics from the University of South Australia suggested the likelihood of a woman having Barbie’s body shape was one in 100,000.
Some campaigners called for Barbie to represent a more realistic body image, while some people with disabilities said the dolls were not relatable.
In 2016 Mattel released Curvy Barbie, Tall Barbie and Petite Barbie, as well as a wide range of skin tones reflecting many different ethnicities.
Lisa McKnight, global head of Barbie & Dolls at Mattel said she hoped the new doll would help “teach understanding and build a greater sense of empathy, leading to a more accepting world.”
Mattel said it worked closely with the US National Down Syndrome Society (NDSS) to ensure its latest doll accurately represented a person with Down’s syndrome.
The doll has a shorter frame and a longer torso and its face is rounder with smaller ears, a flat nasal bridge and almond-shaped eyes which can all be characteristics of women who have the genetic condition.
The puff-sleeved dress is yellow and blue, colours associated with Down’s syndrome awareness.
The doll also has a pink pendant necklace with three upward chevrons representing the three copies of the 21st chromosome, the genetic material that causes the characteristics associated with Down’s syndrome.
It also wears pink ankle foot orthotics to match its outfit as some children with Down’s syndrome use orthotics to support their feet and ankles.
NDSS president and CEO Kandi Pickard said it was an honour to work on the project.
“This means so much for our community, who for the first time, can play with a Barbie doll that looks like them.
“We should never underestimate the power of representation. It is a huge step forward for inclusion and a moment that we are celebrating.”
British model Ellie Goldstein, an advocate for inclusion, visibility and understanding of people with Down’s syndrome, said she felt “overwhelmed” when she saw the doll.
“Diversity is important…as people need to see more people like me out there in the world and not be hidden away,” she added.
Ellie was revealed as one of five cover stars of the latest edition of British Vogue in what she said was her “dream”.
In 2016, Lego created its first young disabled mini-figure – a young, beanie-hat wearing wheelchair user – following a campaign by the UK-based #ToyLikeMe group.
The group had criticised the Danish firm for “pandering to disability stereotypes” because until then its only character to use a wheelchair was an elderly man.
The campaign was launched to create more toys to represent the 770,000 disabled children in the UK.































































































