CEO Brainstorm $BCLI

Joined February 2013
27 Photos and videos
C Lebovits retweeted
We are so grateful to new FDA Commissioner @FDA_KyleD and the entire agency for their commitment to regulatory flexibility and progress. It was an honor to be in the room with other rare disease leaders to recommend concrete changes and advance therapies.
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C Lebovits retweeted
Here’s to The Iron Horse. ⚾️
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C Lebovits retweeted
Lou Gehrig's story is part of our history. People living with ALS are fighting for their future. Scientific progress is advancing rapidly. People living with ALS deserve every opportunity to benefit from it. @RCJAPH bit.ly/4dXu22y #LouGehrigDay #StrikeOutALS
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C Lebovits retweeted
We have exciting news! Thanks to our generous sponsors, virtual registration for #ALSNexus is now FREE for people living with ALS and their caregivers! We're grateful for the support that makes this possible and hope you’ll join us. Register today to attend ALS Nexus: alsnexus.org
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C Lebovits retweeted
A Citizen Petition was submitted to the FDA requesting a new review of data supporting NurOwn®. We remain focused on advancing the ENDURANCE Phase 3b trial and exploring pathways that could bring meaningful options to people living with #ALS. Here: bit.ly/4nArET5
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C Lebovits retweeted
Have you registered for the 2025 NEALS Annual Meeting? 🧠
 📅 October 7–10 2025
📍 Clearwater, FL Join us in person or virtually for four days of collaboration, science, and community in ALS research. 🔗 Learn more & register today: meeting.neals.org/
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C Lebovits retweeted
I’m excited to speak again tomorrow on the National Mall at the @iamalsorg ALS Community Summit in front of 6,000 blue flags, including one with my mother’s name on it. #EndALS #ALSisHere #SoAreWe
7 May 2025
Today, we’re here on the National Mall, steps from the White House & the Capitol, to be visible & spread awareness. We’re planting 6,000 blue flags to represent the 6,000 people diagnosed with ALS each year. #ALSisHere, but #SoAreWe – & we’re not going anywhere until we end ALS.
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C Lebovits retweeted
Support isn’t always loud—but it can change everything. When Tony Rosello’s family was overwhelmed, one friend stepped in and stayed. This #ALSawareness Month, we’re honoring moments of quiet strength. #MomentsThatMattered #BetterTogether #ShowUpForALS #SupportIsStrength @RealBlundetto
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5 May 2025
Wendy Hendrickson joined an #ALS trial and found something deeper than treatment—purpose. She was contributing to research, pushing progress forward—for herself and others. #MomentsThatMattered #ALSawareness #BetterTogether #ClinicalTrialsMatter #SupportIsStrength @ALSHF @HeimanPatterson @saritaapril
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C Lebovits retweeted
“When I was diagnosed with ALS, I chose not to stay silent.” Wendy Hendrickson shared her story to raise awareness—and found purpose in the process. #MomentsThatMattered #ALSawareness #BetterTogether #ShowUpForALS #SupportIsStrength
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C Lebovits retweeted
🗓️🌟May is ALS Awareness Month! Join us as we highlight the latest in ALS research, honor those affected, and work together to accelerate treatments. Follow along and help spread awareness. #ALSawarenessMonth #NEALSforALS #ALSawarenessMonth #NEALSforALS
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1 May 2025
Powerful stories for #ALSawareness Month. These "Moments That Mattered" underscore the urgency as we move towards our pivotal Phase 3b trial. Stay tuned. #BetterTogether #ShowUpForALS #SupportIsStrength
This #ALSawareness Month, we’re sharing real stories from people living with #ALS and their loved ones—moments of strength, love, and showing up when it mattered most. We’re in this together. #MomentsThatMattered #BetterTogether #ShowUpForALS #SupportIsStrength
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1 May 2025
Reposting with immense pride! The "Breakthrough Science" recognition for our NurOwn® data at #ISCT2025, especially the #UNC13A findings in #ALS, fuels our drive as we move towards our pivotal Phase 3b trial.This validates the potential of our MSC-NTF cell therapy to change lives.
Exciting news! Our NurOwn® data has been selected as "Breakthrough Science" for #ISCT2025, emphasizing the role of the #UNC13A genotype in ALS treatment response. A significant stride in neurodegenerative disease research. Read the full press release here: ir.brainstorm-cell.com/2025-…#ALS #NeurodegenerativeDiseases #MSCCellTherapy #ISCT2025 #BrainStormCellTherapeutics
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26 Feb 2025
Determined & hopeful on #RareDiseaseDay. Crucial Phase 3b preps are ongoing. Every day counts for ALS patients. Join us in supporting research. #ALS #HopeThroughScience #NurOwn
As Rare Disease Day approaches, let’s shine a light on the over 300 million people worldwide living with a rare disease including the 500,000 people globally living with ALS. For those living with ALS and other rare diseases, every day is a fight for time, treatments and hope.
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C Lebovits retweeted
4 Dec 2024
Absolutely true
🇺🇸 STEVE JOBS: THE BEST MANAGERS ARE GREAT CONTRIBUTORS... WHO NEVER WANTED TO BE MANAGERS "At Apple, we thought hiring professional managers would make us a big company. It didn’t work—most were bozos who could manage but couldn’t do anything else. The best managers? Great individual contributors who never wanted the job but took it because they knew no one else could do it as well." Source: BusinessX on IG
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Don’t quit. Don’t give up. Persevere. It pays off!!! @BrainstormCell #NurOwn #ALS $BCLI
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