DID YOU KNOW?
1 in 6 ALS patients is a veteran.
I didn't until I spoke with @ALS_USMC4Life.
Marine Roger Brannon served our country for almost three decades, not realizing he would be starting the fight for his life in 2016.
He's has very powerful insight. (1/3)
@alsassociation
Project ALS co-founder Jenifer Estess was initially told that she couldn't have ALS—that her symptoms were all in her head—because she was a young, apparently healthy woman. Two decades later, this false narrative persists. It's time to change that. #InHerALSShoes
The inaugural Lou Gehrig Day will be held this year on Wed., June 2 to celebrate the HOFer who continues to inspire the movement to end ALS. We look forward to working with our Clubs and @LG4Day to continue baseball's support of the ALS community
The inaugural Lou Gehrig Day will be held this year on Wed., June 2 to celebrate the HOFer who continues to inspire the movement to end ALS. We look forward to working with our Clubs and @LG4Day to continue baseball's support of the ALS community
This may have the impetuous to catapult this horrible disease to the national stage. Way over due, let's fill stadiums with pALS! https://t.co/2HkK6rX6Qw
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THIS. IS. HAPPENING!!! There will be a Lou Gehrig Day in baseball this season! Thanks to @MLB and all 30 teams for making this happen and thanks to YOU all for your support of #LG4Day! Read more here: https://t.co/5zqFfNjFzC
Not only is @shellyhoover a key member of our Veterans Affairs team and an amazing advocate, but she’s also a talented author!
Check out Shelly’s new book In Ruby’s Shoes: https://t.co/8Z15fjBIEX
Meeting with stockholders first then a week later a meeting with the participants in the study? Priority should goto the participants not the stock holders! By the way I am a stock holder and ALS patient!
We are grateful to each of the Phase 3 trial participants. Next week, we will host a meeting to share topline results and answer your questions. Your clinical trial site will be reaching out to you with details. #EndALS
I have ALS. It’s a terminal illness so there is no “normal” for me because normal means I would have died already. Instead, everyday I walk, talk, and breathe, rock a @alextoussaint25 ride or push forward the fight for cures I am living proof that Nothing Is Impossible.
My son is a 5 tour combat vet. My husband is vet w/ALS. I stay in the fight to beat ALS for all veterans. Unless we have a cure my husband will die because he served. He deserves better & so does my son & all of those that serve. We #EndALS 4 those who serve thats the endgame
Teresa (@sauceyredhead02) taking over! Veterans with ALS! The quickest and easiest way to apply for disability and compensation benefits with the VA is through your nearest Paralyzed Veterans of America (PVA) representative. https://t.co/ncWFx5iw5i