This Is What Inclusion Looks Like... Josh and Dave hang out. A lot. They talk about everything. They're coworkers and they've known each other over t…
Louie’s differences Louie was born with achondroplasia, the most common form of dwarfism. He’s a little person. This is a random RARE genetic mutation (1 in 40,000). We …
My Netflix Role and Company I Started Hi! I am Sammi Haney, I’m 9 years old, and I play #Esperanza on the #Netflix Series #RaisingDion and I also started my own t-shirt company www.disabi…
SMA Farah is a sweet 2.5 year old baby girl that is fighting a condition called Spinal Muscular Atrophy type 1 (SMA). Farah was born a typical kiddo but …
Trauma Met Me Early Tragedy met me at a young age, 5 years old to be exact. I’m a victim and a survivor of childhood sexual abuse by the hands of three of my mother’s br…
My story with Lymphatic Malformation I was born with a Lymphatic Malformation. (also known as Cystic Hygroma). LM only affects 1 in every 4000 births. Lymphatic Malformations are rare no…
It was just a normal day In June of 2018, I suffered a stroke causing paralysis on my right side. I have since regained most of my arm function back but my leg has had no imp…
Keeping A Smile with Ehlers-Danlos Syndrome (EDS) I’m Josie and I’m a 25 year old wife and mother with Ehlers-Danlos Syndrome (EDS). EDS is a degenerative genetic condition that makes my collagen def…
Golden Har Syndrome & Vater’s syndrome My name is Rasheera Dopson. I’m 28 years old and I was born with two rare diseases: Golden Har Syndrome and Vater’s syndrome. Both of these condition…
Our Miracle Baby: Colton Colton was born at 3:08 PM on November 30, 2014, after a very hard labor with several health complications. We spent six days in the NICU, due to swe…
BY CREATING AN ACCOUNT YOU AGREE TO THE TERMS OF SERVICE ANDPRIVACY POLICY.
