Meet Mike Winston. This is a short documentary about him, a 24-year-old young man living with ALS, also known as Lou Gehrig’s disease. In the film, you get to glimpse the life he lived directly after being diagnosed and compare that to how he lives 6 months after his diagnosis.
Social Clips
ALS Diagnosis Inspires Family To Live ‘Magical Year’
In this 2013 video, meet Susan. Award-winning journalist Susan Spencer-Wendel was in her prime when she got a devastating diagnosis: ALS, sometimes known as Lou Gehrig’s disease. Knowing she only had a few years to live, she and her family started tackling all the items on her bucket list.
“In an effort to top last year’s wildly successful #ALSIceBucketChallenge, the ALS Association reviews a new batch of Bucket Challenge alternatives from Neil Patrick Harris, JK Simmons, Martha Stewart, and more.” Learn more about ALS here: https://bit.ly/ALSNewsToday…
Last Week’s Top-3 Most Read Posts On ALS
Read the Articles Here: Dysfunctional ALS Patient Skin-Derived Muscle Neurons Rescued by Kenpaullone ALS and Other Neurological Disorders May Benefit from Prions Created in Lab Genervon’s GM604 May Slow Disease Progression in ALS Patients…
Want to learn more about GM604?
Stay updated with all the latest GM604 news here: https://bit.ly/1RdVESt…
What is ALS?
“Everybody knows about the Ice Bucket Challenge. But what do you know about the disease behind this challenge, known as ALS or MND? Watch this video to learn about it.” Learn more about ALS: https://bit.ly/ALSNewsToday…
Recent Posts
- FDA puts injection therapy COYA 302 on fast track for treating ALS
- ALS Association invests $3M to bring access to care closer to home
- Protein recycling system may be treatment target in ALS
- New AI matchmaker pairs ALS patients with clinical trials in seconds
- How my husband and I try to teach our children well in life with ALS