My story Hi, my name is Mariano Landa, I'm 38 years old and I have Friedreich's ataxia. It's a rare disease, basically, I have less coordination, les…
Meet Ayla Meet Ayla! She's two years old.😇 This beautiful strong girl was diagnosed with spina bifida and hydrocephalus, as well as a club foot, in August 201…
Dance For Life Jermaine Greaves I (@jermainegreaves) am originally from Georgetown, Guyana and migrated to New York City when I was 9 years old. Dancing makes me happy I…
A rising star falls I was born with arthrogryposis multiplex congenita and scoliosis. Since my tiny years I have been singing, acting, dancing, and putting on shows for …
Graduation: A Reflection on why my disability doesn't make me different I want to say it was a success. It was, but it wasn’t. You see I am a dancer, but a dancer alone is not at all who I am. Through my dancing experienc…
My Story: Living with Scoliosis Hi! I am Nova, I am 18 years old and living in the Netherlands. I have a dysplasia and luxation in my right hip. At 12 years old, I was also diagnose…
Nothing Can Stop Her Today, it seems we live in a culture of “yes.” Skim any lifestyle blog or self-help book, and you’ll find a new list of 15 ways to transform your lif…
Life is good with Muscular Dystrophy I was born in 1974, and I have had Becker's muscular dystrophy since I was 13 years old. I walked a lot while I was a child, but the diseas…
Introduction to Transverse Myelitis My name is Sarah Todd Hammer (I go by Sarah Todd) and I'm fifteen years old. When I was eight, I became paralyzed from the neck-down due to a ra…
Never give up Hello, I am Daniele Magrí Wana. I am from Italy and I am 28 years old. 3 years ago I had many problems with my back which lead to a spinal cord injur…
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