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26 results
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  • Article

A wheelchair in the world

| Jan GrueLinda Bournane Engelberth

Five years ago, Jan Grue, author of ‘I Live a Life Like Yours’, became a father. A wheelchair user since age eight, Grue explores how parenthood helped him reimagine his relationship with his wheelchair.

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How my wheelchair changed my life

| Natasha LipmanCamilla Greenwell

A young woman diagnosed with a disabling condition found her world shrank without the mobility aids she needed to get outside. Finally facing the stigma around using a wheelchair transformed her everyday life.

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Disabled musicians and the fight to perform

| Jamie HaleKirsten Irving

Music might be the universal language, but unfortunately it doesn’t come with universal access. London-based artist Miss Jacqui discusses the barriers to her career with Jamie Hale.

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“Disability is never an individual diagnosis”

| David ProudThomas S G Farnetti

As a 35-year-old man, I am sure that my fear of getting old is not uncommon. But for me, that fear goes deeper. I have spina bifida.

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Little feet on Pett Level Beach

| Penny Pepper

Poet and author Penny Pepper has vivid memories of childhood beach trips when her father was still alive, enthusiastically encouraging her curiosity and love of nature.

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Lying low for lockdown and beyond

| Liz CarrCarrie Ravenscroft

For Liz Carr the chances of catching Covid-19 are the same as for anyone else, but as a Disabled person she's at much greater risk of not getting the treatment she needs if she falls ill.

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Taking the piss

| Kevin CroweSteven Pocock

Council cuts have created public-toilet deserts across the UK, limiting journeys and days out for people whose medical conditions mean toilet access is essential. Campaigner Kevin Crowe highlights the issues.

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Adapting to life as a thalidomide survivor

| Ruth BlueHollie Chastain

Growing up as a thalidomide survivor meant coping with all the usual challenges of childhood and adolescence, while having to fit into a world designed for the able-bodied.

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Living with invisible illness

| Hannah TurnerMaryam Wahid

What happens when the signs of your illness are invisible to the rest of the world? Hannah Turner describes the daily struggles of living with invisible illness.

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Our Covid complicity

| Athena StevensCarrie Ravenscroft

Athena Stevens thought she had a cold that she tried to ignore, but it turned out to be Covid-19. Here she reflects on how we have all put ourselves and others at risk with the choices we’ve made during this pandemic.

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Walk, interrupted

| Caroline ButterwickKimberley Burrows

By listing all the things that get in her way, Caroline Butterwick wants to create an embodied experience of disability and convince you that inclusion is everyone’s responsibility.

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What writing myself has revealed

| Caroline ButterwickKimberley Burrows

Caroline Butterwick talks to two creators about how lived experience feeds their art, and reflects on her own year of writing about her life.

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How injury changed my brain

| Meg FozzardKathleen Arundell

Meg Fozzard, who experienced a brain injury in her 20s, writes about the huge impact it's had on her life, and talks to others with similar injuries.

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Public health campaigns and the ‘threat’ of disability

| Aparna Nair

By continuing to represent disability as the feared outcome of disease, public health campaigns help to perpetuate prejudice against disabled people.

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Vaccinating a community, saving lives

| Hannah DinesRobin Hammond

Doctor Jane Harvey always goes the extra mile to care for her patients, and in recent months that’s extended to huge efforts to save lives with her coronavirus vaccination push.

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An insider’s view of Play Well

| Gwendolyn SmithSteven Pocock

Curator Shamita Sharmacharja offers behind-the-scenes insights into an exhibition about the serious business of play.

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When a private pee is a public disgrace

| Lezlie LoweAdam Summerscales

The free pee is getting rarer. And the lack of suitably equipped disabled toilets is condemning people to lives cloistered away in their own homes. Discover how toilet access for all is part of an equal society.

  • Interview
  • Interview

Meet the climate emergency

| Gwendolyn SmithThomas S G Farnetti

Find out what led Yinka Shonibare to create the compelling artwork ‘Refugee Astronaut’.

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Words of hope and anger

| Penny Pepper

Author and spoken word poet Penny Pepper remembers her childhood dreams, and speaks out against the barriers society uses to prevent disabled people from fulfilling their potential.

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Rejecting shame and a decade of change

| Jess Thom

Jess Thom spent years trying to ignore and suppress the tics of Tourette’s syndrome. Read what happened when she decided to celebrate them instead.

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The search for a cure for endometriosis

| Jaipreet VirdiAnne Howeson

Discover how a white American doctor’s experimental operations on black female slaves laid the foundations for modern gynaecological surgery.

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A flat-packed forest

| Abi PalmerMaïa Walcott

The regular ritual of creating seasonally changing mini-forests for her indoor cats brought Abi Palmer a focus for reflection while the cats explored.

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Dementia playlists and musical memory

| Grace MeadowsSteven Pocock

Listening to the right music can provide both solace and pleasure for someone with dementia, helping them to reconnect with the world around them. Grace Meadows makes the case for more music in dementia care.

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  • Book extract

Sockets and stumps

| Dr Emily Mayhew

Historian Emily Mayhew has met soldiers who have survived the seemingly unsurvivable. Here, she explores the part prosthetics play in the process of military rehabilitation.

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‘Jessy’, a film about cerebral palsy

| Anthony McKay

How the 1950s British film industry portrayed this disease.