#DiabetesAwarenessMonth life as a Type 1 diabetic is hard, trying to keep that A1C in a “normal” range. It’s like managing a 2nd job. This awesome kid of mine has been managing this since she was 8. Learn more 👇 instagram.com/reel/CzI5pX2IZ…

Would you like to participate in an ALS clinical trial & have been turned away? Are you interested in changing the trajectory of ALS? If so you may qualify for Prilenia Pridopidine expanded access program brought to you by #Act4ALS . Check this out 👇! Glen Rouse Garrett May

Here is another EAP brought to you by #Act4ALS . Thank you to the many ALS community members who fought diligently to pass this in Congress in 2021. If you don't qualify for an ALS trial you might be fortunate enough to get into this EAP. Learn more here. #EveryPointMatters

#Act4ALS is having a real impact on the ALS community getting drugs into bodies for those PLWALS who don't qualify for a trial. Here is 1/3 trials funded by the law that was announced at the NEALS conference today. Take a look!

reporter.nih.gov/project-detail…

Cathy why don't you lean in and help BrainStorm figure out this path if you think it would work?Remember they are a small bio-pharma country from Israel who I'm sure would appreciate assistance.I’ve worked on RTT & EAP & the FDA never mentioned this.Who has succeeded w/ it?

I am with you, Sandra, Brian & the rest of the community who would like to have the opportunity to try @BrainStorm’s #NurOwn .We need approval for a phase 4 trial.

Cost recovery doesn't work for cell therapy, where you must scale up. If BrainStorm’s #NurOwn is not approved & if the $ is found to do another trial w/out approval by the time that trial is complete, everyone living today & the next 2 generations will be DEAD!

Sandra, I 100% agree with you! Mike died waiting. Mike’s Mayo neurologist spoke at the ad com discussing its unprecedented benefits and yet it was voted down. ALS Advocacy please stop hurting the communities chances for #NurOwn .

I 100% stand with this statement! The PIs who have first-hand experience with patients receiving the treatment should carry more weight than the “experts” looking at numbers on a computer.

Thank you for sharing Kade's response to what he felt while receiving the therapy in the #NurOwn ad comm. You stated,'He felt good but needed to adjust to his new-found strength on his left side.'That is a good problem to have & not one a 'typical' ALS patient has. #NurOwn Works

Thank you, axeALSFoundation, for speaking out today regarding Eric's experience with #NurOwn stating that 'Without NurOwn, he has declined' and 'NurOwn enhances his quality of life.'

Thank you, Ajay Sampat, MD, for speaking at today's #NurOwn ad comm, and I believe the entire community will stand with your statement that 'Any preservation of function is clinically meaningful.' #EveryPointMatters #NurOwn Works

'We must work quickly to save the next ALS vintage & possibly some of us from this one. Please hurry! The waiting is deadly.' Sandy Morris Thank you, Joe, for your testimony for today's # NurOwn's ad comm; it was so powerful. 🌻🌻🌻 #NurOwnWorks #EveryPointMatters

Dear U.S. FDA please take into account this evidence in reviewing #NurOwn 'Progression slowed down and improved function' Smithstrongmom #EveryPointMatters #NurOwn Works

#EveryPointMatters thank you Mandi for representing the ALS community with a special note to those Veterans living with the brutal disease. #NurOwnWorks

This is exactly why NurOwn must move forward to slow down this turnstile of death. #NurOwnWorks

Dr. Windebank stated: I have never seen these benefits before... I want to see NurOwn move forward.