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  1. 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.

  2. The diagnosis of ALS suspended our dreams and cast a black cloud over our family.

  3. 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.

  4. www.iamals.org › stories › brian-wallachBrian Wallach - I AM ALS

    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.

  5. 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. Dec. 22, 2021, 8:52 AM PST. By Meghan Holohan. At night when the leg cramps struck, Leah Stavenhagen, then 26, jolted awake. While the cramps were annoying and made her feel old, she didn’t think...

  7. Together for ALS is continuing to collect stories to raise awareness, share the devastating consequences that people living with ALS and their loved ones face, and inspire others to feel empowered to share their stories as well.

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