Joined May 2012
Grateful for the opportunity to share new insights into the impact of longer treatment with NurOwn on NfL and to be surrounded by passionate individuals dedicated to finding treatments for ALS. Can’t think of a better way to spend the morning.
Replying to @StacyLindborg
@StacyLindborg what a great presentation. Wonderful feedback from the community. Now we’re going to listen to @MaryKayTurner1 and @KylanMorris1 together with @layneo5 about patients experience with selecting clinical trials.
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Congratulations Lloyd …. Inspiring, simply inspiring.
Massive congratulations to Lloyd!!
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Replying to @MaryKayTurner1
Never!
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The @US_FDA granted $BCLI a positive Special Protocol Assessment (SPA) for this trial and formally agreed that the design and planned analysis for our phase 3b trial adequately address the objectives necessary to support a regulatory approval. ir.brainstorm-cell.com/2024-…
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Largely unreported, SEC has made an unannounced policy shift where they treat many Reverse Mergers like "shell" deSPACs (not as typical mergers), which hampers ability of newly public co to finance & locks up affiliates far longer. May materially change +/-'s for Reverse Mergers
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Great coffee, Great cause!
This Post is from an account that no longer exists. Learn more
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I AM ALS will host a town hall with BrainStorm Cell Therapeutics on November 7th at 1pm ET to hear directly from BrainStorm about next steps, clarify any questions or uncertainty about their process with the FDA, & learn about the path forward for NurOwn. iamals.org/action/brainstorm…
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A study in CONTRAST… The first two images are what a @Google search for Down syndrome generates. I challenge you to find another group of humans in @Google search results so inhumanely, callously and erroneously labeled by “medical experts.” The last image? The last image is what our LIFE and EXPERIENCE with Iron Will has generated. The DIFFERENCE? The @Google search results are clinical, “medical diagnoses” that dehumanize, reinforce negative stereotypes, and generate fear and false limitations. The LAST image - the product of our family’s extensive, actual interaction with Iron Will - is the REALITY. What we KNOW. It’s a list of characteristics that recognizes his INTRINSIC PERSONHOOD and WORTH, captures the infinite JOY and VALUE of his very presence, and PRESUMES COMPETENCE in ALL that he does. Relentless. Forward. Advocacy. #IronWill #DownSyndrome #TeamIronWill #SmashingTheNarrative
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I got off to a very late start raising money for CCALS. With less than a week to go I’m about half way to my goal of $1,500. For the next week I’ll match all donations that come in. Anyone want to help me achieve this goal and contribute to an amazing organizaiton?
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I’m running the Falmouth Road Race to raise $ for Compassionate Care ALS. The generosity they provide to navigate the complexity of this disease is truly amazing. Please help me support people fighting this disease: raceroster.com/events/2023/7…
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Another step forward for people living with ALS.
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ASK ME: Advocacy in ALS - Why Your Voice Matters is on Thursday, June 22, at 5 pm PDT/2 pm HST. Join us for an informative evening, where you will learn how advocacy efforts benefit the #ALS community and how you can become involved. Register today at bit.ly/2023-06-AskMe.
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