Showing posts with label disability. Show all posts
Showing posts with label disability. Show all posts

Monday, August 17, 2026

BRITAIN'S FIRST DEAF-BLIND DOCTOR

Daily Mail

 

I'm Britain's first deafblind doctor... here's why my disabilities have made me better with patients

By OLIVIA ALLHUSEN, FOREIGN NEWS REPORTER

Published: 14:18 EDT, 16 August 2026 | Updated: 16:52 EDT, 16 August 2026

 

Britain's first deafblind doctor has revealed how the disabilities she was told would stop her becoming a medic have instead made her a better one.

 

Dr Alexandra Adams, 32, says her heightened sense of touch has helped her find veins after other medics had failed.

 

She also uses a Bluetooth stethoscope linked to her hearing aids, which has even enabled her to pick up a subtle heart murmur missed during a consultant ward round.

 

But she believes her greatest strength comes from years spent as a patient herself.

 

The newly qualified doctor said that experience helped her realise an elderly woman thought to be refusing treatment simply could not hear because her hearing aids had been left in a cupboard.

 

After fixing the hearing aids and putting them back in, the woman was able to hold a normal conversation with medics and discuss her wishes for the end of her life.

 

'She wasn't not being cooperative. It was because nobody had thought, "Oh, maybe this patient's just deaf",' she said.

 

'If anything, because I have a lot more insight over eyesight. I use my empathy as a tool to help make patients feel more comfortable.'

 

Dr Adams said her own experiences in hospital had fundamentally changed the kind of doctor she wanted to become.

 

'What I do know is that it absolutely sucks to be stuck in a bed have all your independence and your dignity taken away from you.

 

'I understand all the holistic stuff and the psychosocial elements of being a patient. So I try wherever I can to really take that into consideration when I'm working with patients.'

 

Dr Adams, who last month began work in Dorset, was born deafblind and has just under five per cent central vision in her left eye alongside severe to profound hearing loss.

 

She said her sight loss has sharpened her sense of touch, helping her perform procedures that rely more on feel than sight.

 

'As someone with sight loss, my sense of touch and feel is naturally heightened,' she said.

 

'I've had a number of occasions where multiple people have attempted to get a cannula into a really unwell patient who's obviously really swollen and difficult to cannulate.'

 

Dr Adams said her Bluetooth stethoscope connects wirelessly to her hearing aids, allowing her to adjust the volume, replay recordings and display a visual representation of heart sounds on her phone.

 

She said it had even helped her identify 'a really subtle and faint murmur that the consultant ward round hasn't picked up".

 

Before pursuing medicine, Dr Adams was a promising para-swimmer who trained with the Great Britain swimming team towards the London 2012 Paralympics.

 

But her sporting ambitions were cut short after complications from what should have been routine stomach surgery left her in hospital for more than a year when she was 16.

 

As she recovered, one doctor's compassion transformed the course of her life.

 

'She asked me probably the three most important words anybody wants to ever hear. And they were, "Are you okay?"'

 

The doctor then lifted her top, showed Dr Adams a scar across her abdomen and said: 'I know how you feel.'

 

'Perhaps empathy was going to be my superpower and my tool to be able to help other people in the future,' she said.

 

Her resilience was tested again during the Covid pandemic when she spent 17 months in hospital suffering multiple pulmonary embolisms, aspiration pneumonia and sepsis.

 

She described the ordeal as 'horrific' and said: 'The trauma from that is something that will probably stay with me for the rest of my life.'

 

Despite the setbacks, she never abandoned her ambition of becoming a doctor.

 

'I don't think I've ever lost hope because I've always been. I've been very lucky to always have self-belief,' she said.

 

Her journey to becoming Britain's first deafblind doctor was not without prejudice.

 

On her first clinical placement, she said a consultant approached her and, before introducing himself, asked: 'Imagine you're a patient. Would you want a disabled doctor treating you? Absolutely not.'

 

She said she was then sent home.

 

'At the end of the day, it wasn't my disabilities that were the obstacle. It was the perception of other people,' she said.

 

Now beginning her NHS career, Dr Adams hopes her story will encourage others to challenge assumptions about disability.

 

'I really do hope that my story will change attitudes open minds a little bit encourage people to be a little bit more innovative and stand up for themselves,' she said.

 

Although she has now achieved her lifelong ambition, she admits it still feels surreal.

 

'As a writer, I have no words,' she said. 'I'm proud of myself.'

Wednesday, July 29, 2026

OLYMPIC HOPEFUL WHO BECAME PARALYSED FINDS NEW PURPOSE REVIEWING RESTAURANTS FOR WHEELCHAIR ACCESSIBILITY

PEOPLE

 

Olympic Hopeful Who Became Paralyzed Doing Flip Finds New Purpose Reviewing Restaurants for Wheelchair Accessibility (Exclusive)

By Jordan Greene  Updated on July 27, 2026 03:36PM EDT

 

When Taylor Lindsay-Noel enters a restaurant, she notices details that many other diners might overlook.

 

She looks at whether the entrance has steps, if there is enough room between tables to maneuver her power wheelchair and whether the bathroom is truly accessible. Then, she shares what she finds with her followers through Access By Tay, her social media platform dedicated to reviewing restaurants and public spaces through the lens of accessibility.

 

For Lindsay-Noel, 32, the work is deeply personal. Nearly two decades ago, she was a Canadian national gymnast training for what she hoped would become an Olympic career. Then, one attempt at a new skill changed the trajectory of her life.

 

On July 15, 2008, the Toronto athlete arrived at the gym for what she expected to be a routine day of training. Instead, she says her longtime coach asked her to perform a skill she had never seen or attempted before.

 

“It was something that we definitely fought about back and forth over the course of an hour,” Lindsay-Noel tells PEOPLE exclusively. “But because of the dynamics in our gym and me appreciating and respecting authority, I eventually broke down.”

 

Lindsay-Noel says her coach assured her that other gymnasts around the world were performing the skill and told her she needed to trust him.

 

“I couldn’t fathom that somebody who was an Olympic-level coach would lie about something so serious,” she recalls. “Even though I was telling him over and over again that I didn’t really believe him, he was telling me that I was being a silly girl and that I was letting my fear cloud my judgment.”

 

“When you are a gymnast, you are very connected to your body,” she explains. “I knew instantly in the air that something really bad was going to happen because I was lost. I had no idea where I was.”

 

She landed headfirst, breaking her neck and becoming instantly paralyzed.

 

Lindsay-Noel never lost consciousness. As she lay on the mat, she remembers hearing her coach repeatedly tell her to get up and try again.

 

“I took a deep breath to get up, and when I tried, nothing moved,” she says. “That was terrifying because, as a gymnast, you fall all the time, but you always get back up.”

 

After several unsuccessful attempts to move, Lindsay-Noel told her coach something was wrong. He came over and began touching different areas of her body, asking her to say when she could feel something.

 

“He had the most icy blue eyes, and they kind of glazed over,” she recalls. “He said, ‘I’ve been touching you this whole time, and you can’t feel it?’ ”

 

It wasn’t until he brushed her chin that Lindsay-Noel felt his touch. An ambulance rushed her to Toronto’s Hospital for Sick Children, where she underwent emergency spinal surgery.

 

Still, it would take weeks for the severity of her injury to fully sink in.

 

“The doctors in the ICU were telling me, ‘You will never walk again,’ and it’s a very jarring thing to hear,” she says. “However, I had always been an athlete, and I’m like, ‘They just don’t know me. I’m going to bounce back, and it’s all going to be fine.’ ”

 

After seven weeks in the hospital, Lindsay-Noel was transferred to Holland Bloorview Kids Rehabilitation Hospital. There, as she learned more about the spinal cord and the extent of her injury, she began confronting the possibility that she might never walk again.

 

She spent 19 months in rehabilitation, relearning how to navigate everyday life. When she first arrived, she couldn’t lift her arms and could barely sit upright without fainting. Tasks that had once been effortless suddenly required assistance.

 

“I hated people seeing my body when I couldn’t take care of myself to shower,” she says. “I hated having to ask for help to go to the bathroom.”

 

To cope with the grueling physical work, Lindsay-Noel drew on the mindset she had developed as an elite athlete.

 

“I started treating my everyday physiotherapy like training,” she says. “That mindset of being an athlete really helped me get through some of the most difficult parts of physical rehabilitation.”

 

Her earliest goals were seemingly small but significant: sitting upright without feeling faint, no longer needing her legs wrapped daily to maintain her blood pressure and eventually completing a bicep curl.

 

One of her biggest breakthroughs came when she received her first power wheelchair and learned how to maneuver it independently.

 

“That power wheelchair gave me a bit of freedom back that I didn’t have,” she says. “I was able to move about rehab by myself. When I was comfortable, I was able to navigate back into the community and go out to a mall.”

 

“That was my first step into feeling like, ‘Okay, this is going to be different. Life is going to be strange, but when I’m in my chair, I can be independent,’ ” she adds. “That is huge to me.”

 

Although Lindsay-Noel made progress physically, she says the emotional toll was far more difficult to navigate.

 

“People think that being disabled is just a physical journey, but it’s a mental journey as well,” she says. “I struggled in silence.”

 

Lindsay-Noel describes herself at the time as “a functioning depressed person.” Already overwhelmed by the ways her body had changed, she worried that sharing her emotional pain would become too much for her loved ones to bear.

 

“I hid it from a lot of people for a very long time,” she says. “It brought me to a really dark place that I was scared I would never get out of.”

 

Throughout that period, her mother became her fiercest advocate. She slept beside Lindsay-Noel on a pullout chair every night during rehabilitation, retired early to care for her full-time and oversaw the construction of a fully accessible home for her daughter.

 

“She gave me a voice when I didn’t have one for myself,” Lindsay-Noel says. “I would not have been able to get through this experience without her.”

 

Returning home, however, brought a new set of challenges. Lindsay-Noel had grown comfortable at Holland Bloorview, where she had around-the-clock support and was surrounded by other young people facing difficult circumstances. Outside the hospital, she struggled as she watched her friends experience teenage milestones she feared she might never have herself.

 

Eventually, she began rebuilding her identity beyond the sport that had once consumed her life. She joined clubs at school, became involved in morning announcements and was elected student council president during her final year.

 

“Student council was a big part of me rediscovering who I was as a person,” she says. “Not Taylor the gymnast or Taylor the future Olympian, but just Taylor.”

 

After high school, Lindsay-Noel studied radio and television arts at Toronto Metropolitan University with hopes of becoming an entertainment reporter. She interned with Entertainment Tonight Canada and Global News but says she soon realized the industry was not yet designed for someone with a disability to easily thrive.

 

She ultimately created her own opportunities, first launching the interview podcast Tea Time with Tay. When a major tea company did not respond to her sponsorship request, she decided to launch a tea company of her own, Cup of Té.

 

The gamble paid off. In 2020, Lindsay-Noel received an email from Oprah Winfrey’s team asking her to submit products for consideration. Convinced it was spam, she initially deleted it.

 

The timing only made the message seem more unbelievable: It arrived on July 15, the anniversary of her accident.

 

“On top of this being the worst day of the year, I get this really horrible spam email suggesting that Oprah wanted to try my teas,” she remembers telling her mother.

 

Her mother encouraged her to investigate, and the email turned out to be real. Cup of Té was selected for Oprah’s Favorite Things list that year and again in 2024.

 

“It changed the trajectory of my business,” Lindsay-Noel says. “As an entrepreneur, that is one of the holy grail signs that you’re doing something right.”

 

During the COVID-19 pandemic, Lindsay-Noel began thinking about another problem she had repeatedly encountered. Whenever she and her friends went to dinner, they tended to return to the same few restaurants because those were the places she knew she could safely navigate.

 

“I thought, ‘Why do people with disabilities have to worry so much about where they go?’ ” she recalls. “It’s because we don’t have accurate information about the places in our city.”

 

Once it became safe to dine out again, Lindsay-Noel began filming detailed accessibility reviews of restaurants, event venues and other public spaces around Toronto. Through Access By Tay, she shows viewers what it is actually like to navigate each location in a wheelchair.

 

The platform quickly found an audience far beyond what Lindsay-Noel anticipated. Along with wheelchair users, her followers include older adults, caregivers and parents looking for places they can navigate with strollers.

 

“I thought my audience would only be disabled people, but to this day, I get messages from able-bodied people saying, ‘Thank you for opening up my mind. I didn’t even think about this before,’ ” she says.

 

Her first viral review documented a disappointing birthday dinner at a restaurant Lindsay-Noel had been told was wheelchair accessible. Although she could enter through the front, she says the interior was difficult to navigate and the bathroom could only be reached using stairs.

 

“It was a horrible experience,” she says. “I shared my experience, and I was very honest about what had happened, and it blew up. It reached millions of people.”

 

For Lindsay-Noel, one message in particular demonstrated the impact of her work. A fellow wheelchair user told her she had become afraid to leave her home following a spinal injury. After eight years, the woman used one of Lindsay-Noel’s reviews to select a restaurant and ventured out again.

 

“Because of how detailed my reviews were, and just seeing my joy navigating the city, for the first time in eight years, she left her home and went to a place that I had suggested,” Lindsay-Noel says.

 

The woman has since begun visiting more of the places featured in Lindsay-Noel’s videos.

 

“To know somebody has gotten out of the house when they were almost paralyzed by fear of it because of my videos is beyond,” she says.

 

Lindsay-Noel now hopes to expand Access By Tay internationally, bringing the accessibility conversations she has helped foster in Toronto to cities around the world.

 

She has also maintained her love for gymnastics, though she hopes her story reminds young athletes that they have the right to speak up when something feels unsafe.

 

“Make sure that they feel and understand that they have a voice that matters, that their body is theirs and they should never do something that they don’t feel comfortable with, even if a person in authority is telling them to do so,” she says. “No sport is worth that.”

 

Nearly two decades after the accident that upended her Olympic dreams, Lindsay-Noel says her life may not look the way she once imagined, but it remains rich with meaning.

 

“Even if life throws you the most horrible hand of cards, you’re still able to live a really full life,” she says. “I feel and am very happy. I have the most incredible people in my life.”

 

“There’s so much life after tragedy,” she adds. “I hope that’s what resonates with people.”

Thursday, July 9, 2026

A LOVE LETTER TO MY HOMETOWN

I currently reside in my hometown, having moved here when I was five from a farm near another small town just seven miles away. Though over the years I've thought of moving, I am now content with the fact where I'm living is home.

 

Some people have suggested I move to Toronto. However, these people don't realize the fact a disabled person gets the same amount of government financial assistance per month no matter where they live. I'm just sort of managing to live where I do now on the 1400 dollars I get from the provincial government. I can't imagine what it would be like trying to make out on that amount in the city. There'd be plenty of things to do, but I couldn't afford to eat, let alone partake of the plethora of fun and enriching events.

 

Additionally, I once ran into a young woman who had a brother who was also blind and lived there. She related how he had fallen in the hole of a construction sight while the workers just stood there watching. She also told how her brother had given someone a twenty dollar bill so the person could buy cigarettes for him, only to be told the bill her brother knew to be a twenty was actually a ten and that her brother owed the person ten more dollars.

 

Contrary to moving to a bigger centre, a disabled person living in a small town as I do just has to adapt to and embrace a few things.

 

First of all, though there isn't the range of activities as in a city, there's always something to do, or at least this is the case in the town in which I reside. There may be only one concert in the park or card party at the Legion you can get to, but if you're flexible enough and are willing to go along, you'll have fun, meet people you know and have some good conversation into the bargain.

 

Second, there isn't public transit, but it's a matter of building connections with folks who are willing to give you a ride. I often joke my small town does have public transportation. Start walking in the general direction of whereever you wish to go. After a while, a friend, acquaintance or even a stranger will pull up beside you and ask where you are going and if you want a ride. Once you reach your destination, odds are you will meet a similar person there who can give you a ride home.

 

Just as in any human love relationship, my hometown is far from perfect, but the positive traits about it are what cause me to do anything but make plans to leave. 

Friday, June 12, 2026

WICKED STAR MARISSA BODE CLAIMS SHE WAS DENIED BOARDING FLIGHT OVER HER WHEELCHAIR

Page Six

 

‘Wicked’ star Marissa Bode claims she was denied boarding flight over her wheelchair: ‘Do f—ing better’

By Adam Silverstein

Published April 25, 2026, 1:40 a.m. ET

 

“Wicked” actress Marissa Bode claimed she was denied boarding her Southern Airways flight because she uses a wheelchair — and she’s not holding back after calling out the airline.

 

The 25-year-old, who has been confined to a wheelchair since being involved in a car crash at age 11, took to TikTok on Thursday, claiming, “I was denied boarding a flight because I’m disabled,” describing the experience as “awful.”

 

Bode said the interaction occurred during a layover flight while she was traveling to a speaking engagement in Pennsylvania.

 

She said her first flight on United Airlines went smoothly, but things took a turn when she approached the gate for her connecting flight with Southern Airways — which serves only eight states in the US.

 

“I got to the gate and was like, ‘Hey, could you help me locate my boarding pass?’” she said.

 

“And the two people at the gate look at me and they’re like, ‘Can you stand?’ And I said, ‘No.’ And they said, ‘I’m sorry, because of that we’re gonna have to deny you boarding.’”

 

Bode said she was stunned by the explanation that followed.

 

“They proceeded to tell me all the planes within this airline have stairs to get on the plane. Wild. Never heard of that before … You’re telling me none of the people who have flown on your plane before are disabled?”

 

She went on to call the situation “blatant segregation,” adding that staff also raised concerns about her 35-pound wheelchair.

 

The actress said her team had already coordinated with the airline before the trip.

 

“My manager spoke to them beforehand and they fully assured that I would be set for my flight,” she said, suggesting the denial came despite prior arrangements.

 

“It is always something when I’m flying,” she said. “It is very rare that I’m flying and there isn’t a problem with my chair or I’m not talked down to.”

 

She added that the situation went beyond a simple mix-up.

 

“It’s so much more than bad communication,” she said. “It’s so much more than a mistake. These are our lives. This is our entire existence you’re talking about. My wheelchair is my freedom.”

 

Bode also addressed how she felt reacting in the moment.

 

“And of course when I’m crying out of frustration and talking to the people at the gate very firmly, I look like a crazy person,” she continued. “I look like the one that’s in the wrong.”

 

Ultimately, she had no choice but to make the trip by car instead.

 

“I had to drive three and a half hours to get to my destination,” she said, before blasting the airline directly: “You should be ashamed of yourself.”

 

“And airlines as a whole, once again, do f—ing better,” she added.

 

Under the Air Carrier Access Act, airlines are prohibited from discriminating against passengers with disabilities and are required to assist, including help with boarding and connections.

 

However, Southern Airways’ contract of carriage states that passengers “must be able to ascend and descend several steps” due to the design of its smaller aircraft, which typically carry fewer than 30 passengers.

 

The airline notes that it is not required under federal law to provide mechanical lifts in those cases, though ramps may sometimes be available.

 

The incident comes as Bode continues to gain visibility following her role as Nessarose in “Wicked.”

 

After the original film’s release in 2024, she faced backlash online tied to her character, with some viewers criticizing Nessarose as a “bad sister” to Elphaba — commentary that spilled into hateful comments about her disability.

 

“Aggressive comments and jokes about Nessa’s disability itself is deeply uncomfortable, because disability is not fictional,” Bode said at the time.