I am grateful for the leadership and support @RepDeanPhillips has brought to the fight against ALS. Than you for being one of the #ALSChampions and taking it to the next level by joining the new bipartisan #ALSCaucus. #MN03
After lots of people dumped ice on their heads did you ever find yourself wondering, what the heck is ALS?
We did. And so did most Americans.
So we set out to answer this question in less than 60 seconds.
Watch. Share. Help kick some #ALS.
Our partners at @Google will be presenting our joint publication “Personalizing ASR for Dysarthric and Accented Speech with Limited Data” at the Interspeech 2019 conference. https://t.co/D98zVg3w3Y This exciting work presents an approach to improve ASR for people with ALS.
On July 24th, we held a groundbreaking meeting with @US_FDA and @BrainstormCell to discuss the potential breakthrough #ALS treatment, #NurOwn and efforts to speed treatment access to the ALS patient community.
Read more about the meeting results here:
https://t.co/8aMMzOW9zr
If you've been inspired by anything I've done in the past, I urge you to help me/us with this. It's time the @US_FDA delivers on its unmet promise.
I signed. I invite everyone to sign - everyone. Name, email, zip code. Read, sign, retweet. Let's get 10k Signatures by July 18th!
15 pALS and cALS wrote a letter to the FDA to hold them accountable for the long overdue ALS guidance document.
When we hand deliver this letter we want your name on it. This is all of our fight. Make your voice heard.
Read the letter and sign it here: https://t.co/9Tm8b5QdXj
Today, as we mark 80 years since Lou Gehrig announced his ALS diagnosis, we have one ask of you: Help us finally end ALS by sharing this video and tagging three of your friends. Ask them to join the fight by signing up: https://t.co/Kk8VD7VWdj
Thank you to the 38 Senators & 178 Representatives defending access to ventilators for people with #ALS! Congrats to all the advocates for mobilizing Congressional support. Did your member of Congress sign the letter? Find out: https://t.co/yKcnZHmqi3
#ALSAdvocacy#ChallengeMe
Lessons for #ALSTrials-this echos insights from Dr. Bedlack’s research @dukealsclinic on barriers for participation and why research offerings are a part of comprehensive care at ALS Centers of Excellence through @ALSA_MNNDSD https://t.co/hyPrIclJcy via @NYTimes
ALS. MS. Parkinson's. Alzheimer's. Huntington's. Frontotemporal Dementia.
They are all linked. They all have no cure.
We can change that. We will change that.
Cure one. Cure all. #CuresForAll
We are the ones we’ve been waiting for.