A teenager has been left struggling without his wheelchair after it was lost on an easyJet flight from Edinburgh to Paris.
Michael Cloke, 17, had to borrow wheelchairs at landmarks in Paris when the airline told him they could not find it after the flight on Tuesday.
His family tried seven organisations before they were able to hire a chair on the fourth day of the visit.
EasyJet apologised and said it was “doing all possible” to locate it.
Michael needs the chair for a heart condition which causes severe fatigue.
His mother Gillian, a book editor from Edinburgh, said the loss of the chair was having a “major impact” on the family’s visit to France.
She said she checked-in the wheelchair as hold luggage at Edinburgh Airport, but it did not come out when they landed in France.
She said: “It takes a lot of planning going on holiday with someone who is disabled. To lose a crucial bit of kit completely derailed our plans.
Mrs Cloke said visiting The Louvre art gallery as a “complete nightmare”, because taxis could not get the family close enough for Michael to walk to the entrance without a chair.
She said she struggled to contact easyJet for help as the automated systems were set up for people with lost luggage instead of wheelchairs.
She added: “We have done everything we can which involves sitting, the river tour, buses.
“It is beautiful and sunny and it’s Paris and we’re trying not to be ungrateful considering everything else that is going on here.”
Gesture of goodwill
There has been four nights of riots in France after the fatal shooting of a 17-year-old boy during a traffic check by police near Paris.
EasyJet said it was investigating with its ground-handling partners at Edinburgh and Paris and the airport’s special assistance provider.
A spokesperson said: “We are doing all possible to try and locate it and fully understand the inconvenience this will have caused them which we are very sorry for.
“The family have advised us they have been using a temporary replacement wheelchair and we have been in contact with them since Tuesday to ensure Michael’s wellbeing and see how we can assist them further.
“We will also be offering a gesture of goodwill to apologise for their experience and the delay in reuniting Michael with his wheelchair.”
evening Prime for Sunday evening
ring Elsie oh no
happy disability pride month for all disabled community. This is a month where we celebrate, disabled or differently abled people. It is for my whole of July for the Alison. Don’t celebrate it might be coming across my blow this disability pride is this month it’s very important to me as a disabled person who challenged perception of what is being disabled actually means really, it’s not much different to those that are not disabled
You’re phone Paula, call yourself today evening from me to you as my viewers and the whole of the Moon from different
my fundraising page for those that may want to donate as
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evening :-) who all the members of the community?
Second setting of the day for Friday
Community Friday, saying all my viewers 🤣🤣😹
measuring up bro, open mediaeval festival four years ago and me in the crown. The crown may be there 💕💕♥️
Tributes have been paid to the co-founder of a wheelchair dancing charity who starred on Britain’s Got Talent.
Paula Moulton, part of Strictly Wheels alongside dance partner Gary Lyness, died in hospital on Monday, the charity said in a statement. She was 52.
“Her passing was unexpected, making the loss all the more saddening,” it said.
“She will be deeply missed by friends and family and everyone within the international wheelchair dance community.”
Ms Moulton and Mr Lyness started dancing together in 2010 and founded Strictly Wheels six years later.
The charity provides wheelchair dance classes and workshops in Manchester.
They appeared on Britain’s Got Talent in 2012 and reached the semi-finals, wowing audiences by dancing to a version of Alicia Keys’ Empire State of Mind.
The couple remained undefeated across Europe as Amateur Combi Latin Champions for three years and competed for Para Dance Sport Team GB in 2016.
‘Positivity’
Paying tribute, Mr Lyness said: “Paula always focused on the positive things in life, her disability was never a barrier.
“As well as an avid dancer and Team GB competitor, Paula was a champion for disability rights, speaking at many events and conferences.
“She should be remembered for all the positivity she brought into the many lives she touched.
“Her passing will leave a huge hole in my personal and dance life and so many others in the wheelchair dance community. “
another nice illustration for your night
for Tuesday night for all the community 🙂🙂🙂
he’s here if you want to come with you ♥️
how are you before years ago today? 🥰 when I went out for cocktails four years ago today photo
The signed up project is complete. Who is the last picture of a Projects that I completed yesterday evening? ❤️🙂💕
An 11-year-old with Tourette’s syndrome has written to Lewis Capaldi lending his support after the singer struggled to finish his Glastonbury set.
James Craven was diagnosed with the condition on Friday – a day before watching the Scottish star, who also has Tourette’s, perform at Glastonbury.
The youngster, from Teesside, wrote: “I like that you have Tourette’s and you keep going with it.”
Fans sang along with Capaldi after he fought to complete his set on Saturday.
On a sheet of A4 paper, James wrote: “Whenever I see you struggling but continue going, it brings a smile to my face”, adding “you are a role model to everyone with Tourette’s and it shows them that they can be successful”.
Speaking to BBC Radio Tees, James said: “I know how he [Capaldi] feels, especially when he’s ticking a lot. I look up to him.”
‘Collective voice’
His mum, Kate, said she was “proud” of her son’s actions.
“He sat down at the kitchen table and wrote it based on what had happened to us over the weekend – with James’s diagnosis on the Friday – and watching Lewis’s performance.
“James has followed Lewis Capaldi for a long time. It was lovely to see him feel inspired and also, like a lot of the country, having compassion for his situation.
She added: “It’s been really lovely [to see the reaction online]. I think it was the innocence and rawness of the letter [that has touched people].
James’ dad, Joe, said: “I had a tear in my eye when I read it. It was lovely that he was thinking of someone else.
He said the family had received “lots of comments” from people with Tourette’s on social media, who “recognise and understand” the singer’s struggles.
“It’s a collective voice with people feeling able to talk about it and that’s a very healthy thing.”
https://www.justgiving.com/crowdfunding/maya-richards?utm_term=qRnwQqym7 my phone is running for anybody that Sarah wishes to
Down’s Syndrome Campaigner Speaks At UN Conference
A Devon woman with Down’s syndrome has spoken at the United Nations about challenges for people with disabilities.
Emma Bishop, 44, was speaking as a self-advocate at the biggest meeting on disability in the world, in New York.
She gave two presentations to officials about what could be done to to improve inclusivity.
She said: “When I did my speech, I felt power building inside me like a volcano.
“I am so happy about reading my speeches and speaking up for people like me, who don’t have a voice.”
Ms Bishop spoke at the annual Conference of States Parties (COSP) to the Convention On The Rights Of Persons With Disabilities.
Her first presentation was about the need for everyday information to be made accessible for everyone.
Her second presentation was about voting, which she said “feels good inside and makes me happy about something I’ve done.”
The chair of the panel, Charlotte McClain-Nhlapo, a human rights lawyer from America, congratulated her for “knowing and using her power”.
Emma was asked to attend the conference by the Down’s Syndrome Association (DSA), as a member of their self-advocacy group ‘Our Voice’.
It is a team of people who have Down’s syndrome who meet with DSA staff each week to discuss various subjects.
Whilst at the conference, Emma also had a meeting with the Minister for Disabled People, Tom Pursglove, as well as networking with other self-advocates from across the globe.
Speaking on her return, she said it was an “amazing trip” and her first time in New York.
“It was fantastic and I am so happy about reading my two speeches and I am so proud of myself.”
The DSA, which accompanied Ms Bishop, said Down’s syndrome is a genetic condition caused by the presence of an extra chromosome, affecting around 40,000 people in the UK.
evening, Simon ❤️😀😆
your afternoon Grace and please pass illustratios 🤣
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hello morning saying you everybody in this ♥️
Actress Rose Ayling-Ellis is calling for sign language lessons to be made freely available to those who need them – such as the parents and guardians of deaf children. The current funding for sign language tuition has been described as inconsistent and insufficient.
“Being deaf is not something that you overcome, it’s something that you embrace,” says Rose Ayling-Ellis.
The 28-year-old Olivier-nominated star made history when she became the first deaf actress to play a regular character on EastEnders and won Strictly Come Dancing in 2021.
But as a British Sign Language (BSL) user, she says she cannot believe that some parents and guardians of deaf children have to pay for sign language tuition.
“It’s a shame that you have to pay to communicate with your own child,” she told the BBC.
British Sign Language is taught in levels – from one to six. Some basic or taster courses can be free, but the cost of accredited courses can vary from about £200 to £700, depending on the level and the provider.
Martin McLean, senior policy advisor at the National Deaf Children’s Society (NDCS), says funding earmarked by local authorities for BSL tuition is insufficient, “meaning that most parents wanting to learn BSL to any meaningful level will have to fork out hundreds, sometimes thousands, of pounds in tuition fees”.
He adds that the funding model is inconsistent – so while some local authorities provide funding, others don’t, leading to a “postcode lottery”.
“Amid the cost of living crisis, it is wrong that families may have to choose between learning a language that is vital for their children, or simply paying their electricity bill,” says Mr McLean.
Rose mostly lip-reads and uses her hearing aid, but she says she misses a lot of what is being said, so also uses a sign language interpreter on occasion.
Sign language is not just about the gestures made with your hands, it also involves facial expressions. It has its own grammar, vocabulary and regional variations.
After her appearance on Strictly, learning to sign became a real trend, Rose says, but this hasn’t always been the case.
When Rose was a child, her parents were discouraged from teaching her sign language – other family members had received advice from a professional who said it would stop her from learning to talk. But research has shown that rather than hinder speech development, sign language may actually encourage it.
Rose’s mother says she knew how important it was to communicate, and found the money for sign language tuition.
“As she learnt, she taught me,” says Rose. “I found talking difficult, so having some basic sign language really helped.”
More than 90% of deaf children are born to hearing parents, who are less likely to have experience of BSL. The British Deaf Association (BDA) says that language acquisition in the first five years of life is essential – and inadequate access to any form of language can lead to life-long consequences for a child’s cognitive development and wellbeing.
Katie Littlejohns, whose two-year-old son Alvie is deaf, set up a petition calling for the government to fund free BSL classes for all parents and guardians of deaf children.
She says she felt overwhelmed when she found out, when he was seven weeks old, that Alvie was deaf – as there was so much she had to learn.
“He was fitted with his hearing aids at 10 weeks and I asked if we would need to learn sign language, but we were told, ‘Oh no, don’t worry, you don’t need to.'”
Hearing aids are amazing says Katie, but there can be certain situations where they might not work as well, such as loud and busy environments, so she decided to learn to sign. But she was shocked that, in many cases, families were having to pay for the courses.
“I have a friend, her little boy is completely deaf, he can’t wear hearing aids or a cochlear implant,” says Katie. “She’s managed to secure some funding. Her son will only be able to use BSL and her family has spent thousands – he’s two. Everybody needs communication and why does it have a price tag?”
A spokesperson for the Department for Education in England said: “Many local authorities will already fund sign language lessons for parents of deaf children, and we provide funding for a range of British Sign Language qualifications through our adult education budget and advanced learner loans.”
A spokesperson for the Scottish government said work was under way to develop a new BSL national plan, adding that it provided annual funding to the NDCS which has supported opportunities for families to learn the basics of BSL.
A Welsh government spokesperson said BSL was included in the curriculum for Wales alongside Welsh, English and other languages and there is “guidance for supporting progression in BSL for deaf BSL users as well as allowing schools to introduce BSL to other learners”.
In Northern Ireland, the Department for Communities said it was committed to introducing sign language legislation which includes “provision of free family sign language BSL/ISL (Irish Sign Language) classes to deaf children, their parents/guardians, siblings and grandparents”. But it added that executive approval was required for the legislation to pass – and the executive is not currently functioning.
When the music fell silent in the middle of her couple’s choice dance on Strictly Come Dancing, Rose wanted the moment to encapsulate how joyful it is to be deaf.
Since her victory, and the visibility of her interpreter on screen alongside presenters Claudia Winkleman and Tess Daly, attitudes towards sign language have been changing.
In 2022, the British Sign Language Bill was passed, recognising BSL as an official language of England, Scotland and Wales. The Department for Education in England says it is working towards a new BSL GCSE qualification, which will be available in schools from September 2025.
A spokesperson for the Scottish government has also said that the General Teaching Council is working with the University of Edinburgh on the development of an undergraduate degree in Primary Education and BSL, which “would lead to graduates qualifying as primary teachers with enhanced BSL skills”.
In February 2023, Rose was nominated for an Olivier award for her creative signing in a production of Shakespeare’s As You Like It in the West End of London.
“I never overcame my deafness and I’m so glad I didn’t, because I don’t think I would be at the Oliviers if I didn’t celebrate my identity,” she says.
“It is amazing to have this recognition, but more needs to change, sign language should be a right not a privilege. Society needs to accept that this is our language and it should be freely available to all who need it.”
Watch Rose Ayling-Ellis: Signs for Change on Monday 26 June at 21:00 BST on BBC One. Or catch up afterwards on BBC iPlayer
your second saying of the day I’m meeting you, hopefully community is enjoying their members
Rose Ayling-Ellis: Signs For Change
Rose Ayling-Ellis fronts an exciting and groundbreaking film, challenging perceptions of the deaf community and putting audiences at the heart of the deaf experience.
Following the news that, as of April 2022, British sign language has been officially recognised in law, this documentary follows Rose on a personal journey as she speaks to those closest to her, as well as the people pushing boundaries within the deaf community. Exploring whether society is adapting fast enough to allow equality amongst the deaf and hearing worlds, Rose challenges the perception of deafness as something that needs to be cured, and highlights the beauty of sign language and the deaf experience.
Filmed over a period of time that sees her performing in Shakespeare’s As You Like It and reflecting on her time as the first regular deaf character in EastEnders and deaf contestant and winner of Strictly Come Dancing, Rose explores whether attitudes towards the deaf community are capable of changing.
Prior to joining Strictly, MP Rosie Cooper, whose parents were both deaf, had introduced a bill into Parliament asking for BSL to be legally recognised. Rose meets with her to discuss the misconceptions and attitudes that many faced then and now. Rose reflects on what it meant for her to grow up deaf, in discussion with her parents, the advice given to them from diagnosis, and questioning if anything has changed for those growing up deaf now. Rose meets deaf language expert Dr Kate Rowley and tests her own language abilities, raising questions about the role of sign language in her formative years. She is introduced to Katie and her son Alvie, who were advised not to learn sign language and who has since started a petition to encourage the UK government to make it more accessible.
She also meets a charity that teaches deaf children to speak. Rose explores how technology plays a role in the lives of deaf people and asks whether the hearing world focuses too much on technological fixes and too little on encouraging sign language.
Throughout the film, Rose explores her deaf identity, peering into her personal world and who she is when surrounded by friends and family, as well as the Rose we see on screen and stage.
me at the mediaeval festival in St Albans four years ago
romantic person saying of the day-good-night-quotes-images-for-girl-friend.jpg 579×328 pixels
Romantic Good Night Quotes and Messages
Romantic good night quotes and messages are text messages that you can send to your friends and love partner to wish them for the good night. These romantic good night quotes are very lovely and sweet messages. These romantic good night quotes which make your love partner or friend make happy and feel good about you. You can send these romantic good night quotes via messages, sms or social share. Simply copy any of the best romantic good night quotes from the below list.
Romantic good night quotes for friends, girlfriend, wife, husband or boyfriend
Romantic quotes for good night
As long as they are about me and you, I wish that all your dreams come true. Good night.
The moon is angry at me and jealous of you because I said that no one can light my nights up like my girlfriend. Good night.
I wish moon always be full & bright and U always be cool & right. Whenever U go to switch off the light, Remeber that I’m wishing U …Good Night!
Everyday I spend with you is the new best day of my life. Can’t wait for the morning. Good night baby.
Love is the simpler feelings, I dream every night abut you I want to capture your heart… I love you.
Sun is upset and moon is happy, because sun is missing u, and the moon is gonna be with u for the rest of the night, have a wonderful night.
A day is going to end again. It is nice to have someone like U making everyday seems so great. Thank U my love and may all the angels guard you this night!
I think of you as soon as I wake up and then again before I fall asleep. You see, you’re never out of my thoughts. Have a Good Night!
Touch your heart, close ur eyes. Make a wish, say goodnight. Sky so wide, stars so bright, off the lights, sleep so tight.
Also Read: GOOD NIGHT LOVE QUOTES AND IMAGES
Also Read: GOOD NIGHT QUOTES FOR HER
During the day I keep myself busy and sometimes time passes. But at night, I really miss you.
I wish we could cuddle all night long… and fall asleep after watching the sun rise together. Good night.
I have never felt so lonely like this, all I can think about is giving you a kiss. Such is the blissful effect of our love on me, that all I do is miss you dearly. Good night.
I wish I could come over quickly, I wish you would kiss me. I wish we could cuddle the night away, I wish it would never turn into day. Good night.
Do you know why the moon is shining so brightly tonight? Because it is trying to be as beautifully radiant as you are. Good night.
These are some of the best romantic good night quotes and romantic good night messages that you can send to your love partner, friend, wife, husband, girl friend or boyfriend. These romantic good night quotes will surely make them feel happy and loving for you.
Also Read: Falling in love quotes for her
Related Searches: Romantic good night quotes, romantic good night messages, romantic quotes for good night, romantic night quotes, romantic good night quotes and messagesFunny good night text messages – Funny messages
Images you’re saying Friday evening for all the community wishing all of you are very good and hope you feel we can
A university engineering student born with missing fingers has invented a prosthesis designed to fit any hand, young or old.
Luke Cox, 26, from Grantham, created it for his final-year project at Staffordshire University.
Its design means it could be worn throughout childhood, he said, unlike many others, potentially saving families thousands of pounds.
Mr Cox said he felt “proud” to have made something that could help others.
The student was born with Ectrodactyly, which means he has missing fingers on his right hand.
While he does not use a prosthesis himself, he said he was inspired to develop one by the cost and limitations of existing devices.
“Knowing what it’s like to grow up with a disability, you [have] that empathy,” he said.
“Top end prostheses, with electric devices that use muscle signals, can cost around £100,000. Even the more basic body-actuated models can be up to about £4,000.”
Mr Cox’s 3D-printed model cost him £19.97 to produce.
Since his design is mouldable in hot water it can conform to any size of hand. The finger modules are removable and can be upgraded to a larger size.
“Children have to update their devices two times a year, which is quite expensive and it’s also quite wasteful,” he said.
“If you’ve got one prosthesis you can have throughout your whole childhood, that’s going to make a big difference.”
The final prototype has received positive feedback from industry experts, Mr Cox said, adding he planned to seek advice on pushing it to market, though did not know how much the device might retail for.
“I’ve made something physical could help people in the real world and knowing that I’ve made something like that does make me feel quite proud, I suppose.”
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“Good Evening” is probably the most general greet we can tell to our friends, colleagues, family ones and loved ones. But somehow saying “Good Evening” will not connect to strangers. So it is committed to closed ones. Whenever you met the person in the evening times it common to say Good evening. Even at night times, if you meeting a person you should say Good evening not good night. It’s because Good night is the last greet what we make to others.
When to Say “Good Evening”:
From 4:00 PM to 7:00 PM: “Good EVENING”
It’s always confuse people whether to greet “Good Evening” or “Good Night” if they them in the dark. If you are meeting a person at 9:00 PM, even though it’s darkening, you need to say “Good Evening”. Because you starts the conversation with that greet.
Cute Good Evening Wishes and Sayings
We are share with you best and amazing collection of Good Evening Wishes and Sayings, Photo, Greetings & Wallpapers to share with your family members, relatives, friends and loving ones on Facebook, Whatsapp etc.
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Teenager Arrives At Berkeley Prom With Bike Convoy
An autistic teenager, who once struggled to fit in, has now had her prom dream come true.
Lia Filby from Gloucestershire, who defied her doctor’s predictions by finishing all her GCSE exams, had wanted to arrive at the event escorted by a convoy of motorbikes.
“I want to impress people. My friends are going in cars, but I want a whole motorcycle escort,” Lia said.
“I want all the popular kids to go,’Wow!'”.
Lia is about to leave mainstream schooling after her studies, something her family might never have believed was possible.
At the age of three, when she was non-verbal, they were told she would require life-long care.
But after undertaking speech and language therapy, she proved her doctors wrong.
“She has done amazing,” Ms Filby’s mum Linsey said.
Lia has also faced many other challenges – she lost her dad at a young age and at the age of 10, she developed alopecia from stress.
“In year seven, I had to hide who I was, and I wanted to be normal,” Lia said.
“Until I was like, ‘I am so bored, nothing interesting goes on in my life, let me just turn into actually myself’.
“Since then, everything has gone uphill, I’ve got a lot more friends now, it seems like being myself as gained me popularity.”
As she arrived at the prom, Lia was greeted by her best friend, before joining the evening’s celebrations.
#AdultServices, #Daylightclub #Mathschampion #Socialisation #cerebalpalsy #Outinmycommunity
Swavesey Boy, 7, Leads Fundraising Campaign For Hero Arm
A boy who was born without a right hand has been leading a fundraising campaign for a robotic arm, so he “can do stuff other children can do”.
Seven-year-old Louie Morgan-Kemp, from Swavesey, Cambridgeshire, said the so-called “Hero Arm” would “make me have more confidence”.
The 3D-printed prosthetic limb, built by Open Bionics, costs £13,000.
Louie’s mother, Hannah Morgan, said: “I suppose it’s stuff we don’t think about that we take for granted.”
Ms Morgan, 32, a teaching assistant, said Louie wanted to be able to pour his own drink without spilling it, to carry objects in two hands and not have to balance items against his chest.
“He’s always been really resilient and he’s made most things work one-handed or he’s found his own way to do things, but he was meant to be right-handed,” she said.
“When he went to reach for things, he went with his right hand which obviously he hasn’t got.”
She said they had tried “loads of different prosthetics, NHS ones, charity-funded ones”, but none worked for him.
“The NHS one was like a mannequin hand that didn’t do anything and the charity ones were quite heavy for him,” said Ms Morgan.
She told how Louie was “amazed” after seeing the Hero Arm at a roadshow last month.
It features multi-grip functions and wrist rotation, with special superhero sleeve covers for children.
The family enquired about the arm when Louie was two years old, but were told he would not qualify until the age of seven.
Ms Morgan said: “He [Louie] said, ‘I’ll be able to hold two things with two hands and be able to do stuff that other children do’.”
Football fan Louie, who supports Ipswich Town and Tottenham Hotspur, also plays for a local team, coached by his father Scott Kemp.
More than £2,000 of donations have been pledged since the “Lend Louie A Hand” GoFundMe campaign began on Friday.
this evening, saying for Tuesday evening🥰
May your Evening be filled with joy and peace
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Good Afternoon Everyone Images
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Disability rights campaigner Heidi Crowter has set a world record for identifying the most celebrity birthdays in three minutes.
The 27-year-old recalled 70 in under 180 seconds, from Queen Victoria to pop star Shakira.
Her achievement came under a Guinness World Records initiative allowing reasonable adjustments for attempts to better include those with a disability.
Ms Crowter said she had been “writing a birthday list and practising a lot”.
Under the rules, her mother Liz would call out names from a randomised list of 100 celebrities and she was asked to identify the correct birthday – day and month.
Ms Crowter said she loved “sharing my joy of birthdays with people” and was “feeling very proud of myself”.
“If I can set a world record, I know that means I can do anything I set my mind to,” she said.
The records organisation announced her achievement at the start of Learning Disability Awareness Week.
Ms Crowter’s record – the most celebrity birthdays identified in three minutes (II) – was achieved under Guinness World Records’ new impairments initiative, developed alongside Mencap, in the intellectual impairment (II) category.
The charity said she recalled the birthdays, “from Queen Victoria and Margaret Thatcher to Brad Pitt and Shakira, without hesitation”.
She was described by Guinness World Records as a Mencap “myth buster” who wanted to challenge misconceptions about learning disability and to campaign for change.
Last month, the 27-year-old, who has challenged legislation allowing foetuses with Down’s syndrome to be aborted up until birth, said she was taking her case to the European Court of Human Rights.
In November last year judges at the Court of Appeal decided the Abortion Act did not interfere with the rights of the living disabled.
Under legislation in England, Wales and Scotland, there is a 24-week time limit for abortion, unless “there is a substantial risk that if the child were born it would suffer from such physical or mental abnormalities as to be seriously handicapped”, which includes Down’s syndrome.
Ms Crowter said she was taking her case to the Strasbourg court “because it is downright discrimination that people with disabilities are treated differently”.
Hundreds of volunteers are sought for a major summer sporting event for blind and partially sighted athletes.
The 2023 International Blind Sport Federation (IBSA) World Games runs for 10 days from 18 August.
Organisers expect the games, held in venues across the West Midlands, to be the largest ever UK sporting gathering of its kind.
“[It] has the potential to be a real watershed moment,” said Sallie Barker from British Blind Sport.
“This event will not only help provide the stage for the world’s best blind and partially sighted athletes to showcase their talents, but it will also inspire other blind and partially sighted individuals to take advantage of the pathways into sport and opportunities to volunteer,” she added.
About 1,250 competitors from 70 countries will participate in sports such as archery, powerlifting and tennis, with judo, football and goalball tournaments being held as qualifying events for the 2024 Paralympics.
The summer event marks the first time the World Games has been hosted in the UK.
More than 400 volunteers are needed for tasks such as helping with classification, assisting athletes and spectators, and creating media content.
Venues are primarily Birmingham-based, including the University of Birmingham’s Edgbaston campus, but athletes will also compete at Coventry Building Society Arena, the University of Wolverhampton’s Walsall Campus, and in Warwick.
“Birmingham is a proud sporting city as we saw when it successfully hosted the Commonwealth Games last year, and there are so many volunteering opportunities for people in the community to be part of another great festival of sport,” said Ms Barker.
Power of People Ltd, which is managing the volunteer programme on behalf of Sport Birmingham, said it was looking for volunteers available for six shifts or more throughout the duration of the event.
