
Lorri Cavaliere
@lorricav
A mom in CT, fighting and advocating every day for the life of my 33-year old daughter, Alexandra, diagnosed with sporadic bulbar-onset ALS in July of 2020.
ID: 21973270
26-02-2009 04:58:57
789 Tweet
1,1K Followers
4,4K Following




Please take the few minutes to listen to Steve Gleason - "Live Impossible"’s acceptance speech, when receiving the Arthur Ashe Award for Courage. Bravo, Steve and Congratulations! ALS/MNDMamaBears Deb Bellina Kandy Simons Mitze Klingenberg BSN, RN BridgetRebecca ᴊᴀɴɪᴇ °.。·🫧.。 @Shines2017 Jan Mattingly


It would only be #BetterTogether if the The ALS Association joined forces with BrainStorm and helped to support and fund the Phase 3b trial. Without that, we are truly NOT #BetterTogether. That is all outlined in the lawsuit brought against them, by the 15 chapters that

Say YES to #onedrugadvocacy because right now, THERE IS NOTHING ELSE and yes, it worked on the children of my fellow MamaBears, as well as some of your friends. And please, don’t feel “left out” of our ALS/MNDMamaBears group. You don’t have children with ALS or any that died from

Ask not what #ALS can for you, ask what you can do to illuminate #ALS. Her ALS Story #33yearsold #ALSAwareness #Russia #Light 🌻




Happy New Year everyone….My wish for 2025 is that it will be THE year for newfound hope and long-awaited discoveries in the world of ALS/MND. I am anxiously waiting for the NurOwn Phase 3B trial to begin and I applaud the tenacity of C Lebovits and team at BrainStorm for not

My Daughter Deserves Better. The national The ALS Association recently released its financials, and the numbers tell a truly painful story. While they paid top executives hundreds of thousands of dollars (one receiving $500,000 in salary!), they also laid off 40 employees and saw 15



From everyone in CT affected by ALS, Thank you, ALS United Connecticut! ❤️