Finally , accessible information on the #c9orf72 repeat expansion that speaks to the people impacted. Proud to share this well cited article: endthelegacy.org/c9orf72

Let's do this! #NurOwn #ALS ir.brainstorm-cell.com/2023-11-20-Bra…

Tonight, I want to share the incredible story that ran on CBS Sunday Morning 🌞. The story is both a reminder of how fragile life is and a reminder of how people can do the most extraordinary things. Thank you for watching and for sharing. Good night moon. cbsnews.com/video/fighting…

Thanks so much for your ongoing support. We are on the way to the meeting. #NurOwn #ALS

Check out this article healthandpharma.net/als-treatment-…

It's not uncommon to find 15, or even 50, different organizations dedicated to a single rare disease. This is without a doubt holding the rare disease community back. The reality is that compared to more common diseases, rare diseases already face significant hurdles in

"dawn comes after the darkness" CONGRATULATIONS! You and the wonderful teams I AM ALS so much deserve this. Keep up the good work! #ENDALS

Here we go!

Thanks Stacy Lindborg !

The FDA has agreed that the design of a Phase 3b trial is generally adequate to back a potential regulatory application for NurOwn for ALS. alsnewstoday.com/news/fda-oks-p…

The 3rd Annual #ALS Drug Development Summit took place in Boston this week. Stacy Lindborg, PhD delivered a presentation on new #biomarker data from the NurOwn Expanded Access Program (EAP) along with data from the Phase 3 trial.

This is why we fight! "For Love and Life" tells a powerful story of love, determination & the fight against ALS. So grateful for Brian & Sandra Wallach's advocacy & the dedicated ALS community. Watch it on Prime Video & join the fight! #Love #Determination #ALS #BetterTogether

Sara Feldman, PT, DPT, ATP has been the Physical Therapist and Assistive Technology Professional at the MDA/ALS Center of Hope in Philadelphia since 1994. In addition to her clinical work, Sara Feldman is the Clinical Evaluator for #clinicaltrials and is passionate about

SO well deserved!!!

Please join us in asking Congress to pass the Elizabeth Dole 21st Century Veterans Healthcare and Benefits Act. Our Veterans with ALS need help THIS YEAR so they can remain at home with their families for their care. iamals.org/action/elizabe…

We're excited to welcome Dr. Haro Hartounian as our new EVP & COO! His expertise in cell & gene therapy will be instrumental in advancing #NurOwn for #ALS patients. #neurology #celltherapy BrainStorm ir.brainstorm-cell.com/2024-06-20-Bra…

#BetterTogether

Indeed #BetterTogether

$BCLI #NurOwn #ALS Phase 3B Trial preparations are progressing well. We're meticulously laying the groundwork for a successful launch. #BetterTogether Your support fuels our determination to make a difference.