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Diagnosed at 38. Her ALS Story represents only a fraction of young women with ALS. We are honored to highlight others that never got the chance to officially be a part of our group. <3. Alex H.
- About HAS — Her ALS Story
Her ALS Story strives to educate the public that ALS does...
- 10 Lessons from 10 Years with ALS — Her ALS Story
Your ALS journey is unique. Everyone hears this early on in...
- About HAS — Her ALS Story
The diagnosis of ALS suspended our dreams and cast a black cloud over our family.
21 Μαΐ 2024 · Your ALS journey is unique. Everyone hears this early on in their diagnosis, but it’s worth repeating. I went from completing a 70.3-mile half Ironman triathlon to walking with a cane (and slurred speech) in 6 months.
6 Μαΐ 2022 · My general practitioner offered a priority list of possible diagnoses: a mild stroke, a neurological issue, something ENT related, or something else. The head scan proved there was no stroke, a huge relief at the time. Because of the pandemic, getting an appointment with a neurologist was nearly impossible.
90% of the people diagnosed with ALS have no family history of ALS. 90% On average, they will live 2 to 5 years after being given this diagnosis. So this story, my story, is actually our story—because if ALS can affect anyone, curing it takes everyone.
Brooke Eby shares her Lou Gehrig’s disease, or ALS, diagnosis at age 33 and details her outlook on life after getting a terminal prognosis in her 30s.
24 Μαΐ 2023 · After her ALS diagnosis, Andrea Peet set an impossible goal — 50 races in 50 states. Read the inspiring story of one woman’s fight against the odds.