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A Little More About Us: A Look Back at the Founding of PatientsLikeMe

“I got this call from my brother Stephen, and he said the news doesn’t look good. At that point, he’d been through enough processes to know what that meant – he had ALS. So I began this journey with my brother and my family…. We were thinking there had to be a way to make… Continue reading A Little More About Us: A Look Back at the Founding of PatientsLikeMe

Published July 21, 2011
Categorized as ALS, Chronic Fatigue Syndrome, Conditions, Epilepsy, Fibromyalgia, HIV/AIDS, Mental Health, Multiple Sclerosis, Organ Transplants, Parkinson's Disease, Patient Experiences, Rare Diseases Tagged About Us, ALS research, Ben Heywood, clinical trial matching, company history, David S. Williams, founding of PatientsLikeMe, health data, jamie heywood, lou gehrig's disease, medical data, MND, openness philosophy, patient community, patient social network, paul wicks, shared health data, Stephen Heywood, ventilator disconnect, video
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