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On the way to the I AM ALS Flag Event and Summit in DC. Look forward to remembering & honoring those we’ve lost to #ALS including Lisa Stockman Mauriello, Becky Mourey & Sandy Morris. Thrilled to share the work of Pat Dolan & The Mappers - the ALS Clinic Advisor.

An honor to welcome Blair Casey and Phil Green of Team Gleason to Apple Park. Thank you for your collaboration over the years, your tireless advocacy, and your commitment to supporting the ALS community through accessible technology. #ALSAwarenessMonth

The #ALS community is made up of some of the most incredible people that I have ever met🌻 made up of advocates that react to a devastating diagnosis by springing into action to enhance ‘ALS Land’ in their own unique ways. We are always #BetterTogether as we strive to #EndALS 💫

As a finalist for the 2023 Lou Gehrig Award, Mike Yastrzemski joined the Live Like Lou Foundation to present a scholarship to Elizabeth Duncan, an incoming college freshman, who has overcome the loss of her dad Jon, uncle Jeff and aunt Jennifer, all to ALS. #LouGehrigDay

'By the time that you watch this I will no longer be here' A poignant final message from the Leeds Rhinos legend and MND campaigner recorded before his death for a special BBC documentary 'There's Only One Rob Burrow' BBC One BBC iPlayer

Good to see my friends Osiel Mendoza & Corey Reich yesterday at Oracle Park to watch the New York Yankees vs SFGiants on #LouGehrigDay

Gosh I love my Greens!🌻 #LouGehrigDay Phil Green

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Amazing time at #ALSNexus meeting. So many important conversations! #EndALS ⁦Kylan Morris⁩ ⁦ALS Hope Foundation⁩ ⁦Terry Heiman-Patterson⁩

Two years without you doesn’t seem possible🌻 ours was (and is) a true and beautiful love story mama 💛⚡️Sandy Morris

Thinking of all those in ALS Land that are missing our OG Honeybadger Sandy Morris today. Thank you, Sandy, for inviting us all to sit at your crowded table ❤️

We are walking today to #EndALS with ALS Arizona Sandy Morris Kylan Morris BrainStorm

No more perfect way to spend a Saturday than at the ALS Network Walk & Roll for a Cure! ⚡️Grandma and I marched in memory of our person, 🌻Sandy Morris, & for all in this fight to #EndALS. We remain #BetterTogether✨ BrainStorm Marlene Seffern

Thanks Kylan Morris for shouting out on our behalf to the caregivers. We are #BetterTogether and let's do all we can to #EndALS #Phase3B

Exciting News! Next week, EverythingALS will participate in ALS ONE's 7th Annual ALS Research Symposium, a global gathering dedicated to advancing ALS research and hope. Date: November 13-15, 2024 Location: 100% virtual Cost: FREE x.com/alsone_officia…

juan Kylan Morris FDA Biologics The ALS Association While we understand the frustration many in the #ALS community feel, it's important to focus on the future and the potential of our Phase 3b trial. We're thankful for SPA agreement granted by the FDA and are committed to working closely with the FDA to ensure success of the trial

#ThankYouVeterans for your sacrifice. 🇺🇸 We honor the extraordinary strength of those who continue to battle an #ALS diagnosis, in addition to your service. Your resilience inspires our mission at @BrainStormCell to help end the suffering caused by #ALS. 🤝 #BetterTogether

This #VeteransDay, BrainStorm Cell Therapeutics recognizes Elizabeth Fassler, who served in the U.S. Army as a Tactical Control Officer for a Patriot missile battery. 🇺🇸 Elizabeth Fassler continues to serve others as a fierce advocate for the #ALS community by contributing to

Ron Faretra is a veteran living with #ALS who served 27 years in the U.S. Air Force. ✈️ Ron Faretra shares his tenacity with the #ALS community by helping to move the needle for the next generation of people that will be diagnosed. In the past two years, Ron played an instrumental

Mom loved her interactions with you, Pete! 🌻