Tomorrow, the House Appropriations Committee (@HouseAppropsGOP, @AppropsDems) votes on research funding legislation that will help determine the future of ALS research.
People living with ALS can't wait. Congress needs to hear from you TODAY.
Post at your Member of Congress in under 60 seconds:
https://t.co/ZTkNaotbkr
#ALS #FundALSResearch
As Supers start tomorrow let’s not forget where the “Tarps Off” movement started! On top of a garage off of Tway Way next to Jim Patterson Stadium! 😜🐔⚾️ #GoCards#TarpsOff#garageparty@SFAClubBsbl
As ALS Awareness Month comes to a close, we want to take a moment to say thank you to all of you for helping us accelerate the cure. ALS moves fast. You can move science faster.
But just because May is ending doesn’t mean the work is done. We are more determined than ever to continue because every 90 minutes, someone is diagnosed with ALS. That is why we are continuing to put every dollar you donate directly research.
Our fight continues with urgency. And there are still so many ways you can help accelerate the cure.
Your contributions fuel our mission, providing funds needed to support families and investments in research, alleviating the many challenges today and looking for treatments and cure of the future. Make a donation today! https://t.co/awkxydx3zN
Did you know that military veterans are more likely to be diagnosed with ALS than people who have not served in the military? In recognition of Military Appreciation Month this month, we are highlighting the ways that you can join us in supporting veterans living with ALS and their families.
Discover ways that you can support ALS veterans: https://t.co/ttBOoAcLLB