Project ALS identifies and funds the most promising scientific research that will lead to the first effective treatments and, ultimately, a cure for ALS.projectals.org New York, NYJoined January 2010
Today ONLY if you purchase any item from the website, a portion of proceeds from your order will go directly to @ProjectALSorg ! This is the second time this year we’ve had the awesome opportunity to work with them and help raise some money!
Discover the critical work shaping the future of Project ALS research at our Town Hall. Join us as we discuss emerging disease models, motor neuron rejuvenation, and the development of potential therapies for ALS.
Sign up for the virtual town hall today: bit.ly/497iCX8
Join us Nov. 14th at 11AM for The Alex and Jaci Hermstad Rare Disease Trailblazer Series. Hear from patients, families, advocates, and scientists working together toward a future free of ALS.
Register: bit.ly/3Uui0Vp
Join us on October 22nd at City Winery NYC for An Evening with Aaron Lazar—a night of music, laughter, and inspiration to benefit Project ALS Research. 🎤✨ Doors open at 6:30 PM!
Join the experience today: bit.ly/3ZdmnXY
Project ALS Core's Dr. Tulsi Patel is such a great example of women kicking some serious a**. Dr. Patel was at Gordon Conference, an international research forum, in Tuscany Italy this week repping Project ALS.
Get your @HerALSStory collab tee: bit.ly/46Czhk3
Project ALS recognizes the US Department of Defense for its critical ongoing support of ALS research. Did you know that service members are more likely to get ALS?
Learn more: cdmrp.health.mil
With no cure, it can be hard to have hope for a future free of ALS. Project ALS understands this frustration.
Our Director of Research, Valerie Estess, discusses the 26-year journey of Project ALS and what's next in our research efforts: bit.ly/3KQrwgr
Just 2 days left on this. Proceeds from each slab are benefiting @ProjectALSorg and thanks to your support our donation will be double last year!
Any and all shares would be AMAZING!
Cheers
Just 2 days left on this. Proceeds from each slab are benefiting @ProjectALSorg and thanks to your support our donation will be double last year!
Any and all shares would be AMAZING!
Cheers
21K Followers 4K FollowingWife to @bsw5020. Mama. Caregiver. CEO @synapticure providing medical care for Alzheimer’s, Parkinson’s and ALS. Co-founder @iamalsorg. EP @noc_film.
26K Followers 735 FollowingI AM ALS is the largest community movement made up of the very people living with, impacted by, and highly motivated to end ALS.
12K Followers 2K FollowingALS = Lou Gehrig's Disease Thought it had been cured by now? Still no known cause. Still no cure. Still no treatment. Still quickly fatal. Still outrageous.
4K Followers 5K FollowingAdvocate for Amyloidosis, ALS & Rare Diseases. Enviro Justice, Foster Care & Gun Safety. Love LA sports. @EndRareDiseases on bsky
9K Followers 573 Following40yo living with ALS on Life support. Author. Creative Director. Advocate. Dreamer. Public Servant. ALSFRS 1/48 https://t.co/vibJSKdIl4
13K Followers 558 FollowingDominating ALS one day at a time since 2018. Retired Police Officer. “Love the life you live and live the life you love” Go Royals! 💙#FightLikeAGirl
3K Followers 934 FollowingMarried to the love of my life. Christ follower. Mom of five. Mimi to 14! Entrepreneur. Diagnosed with Bulbar ALS 3/30/2020. Fighting to live.
4K Followers 761 FollowingAnesthesiologist -Johns Hopkins Hospital
Pain Management -UC San Diego
Now battling ALS & FDA regulatory rigidity for 100% fatal ALS
2K Followers 1K FollowingScott Craig. ALS Uncensored podcast. Digital Artist. AI Student. Typing with my eyes. Living Impossible! #ALSUncensored #ALS #EyeGazeArtist #AI #IWriteALS
2K Followers 873 FollowingLisa Stockman Mauriello fought for Expanded Access to an ALS treatment. Lisa passed away 8.4.21. Honor Lisa’s legacy by advocating for ALS.
4K Followers 375 FollowingWild & Wonderful WV. FSU grad. Married to @erika_poling , Father to Liam & Bayler, ALS Warrior & advocate. #EndALS
Founder of @project_seth
2K Followers 6K FollowingMAGA!!! 🇺🇸 Trump 2024 Victory !! America first! DOGE will cut the fat !!! Primary all RINOs !! Prosecute the traitors and criminals !!
0 Followers 8 FollowingWelcome To Dr Omole Herbal Home Of Cures,You Can Contact Me Through WhatsApp: https://t.co/pZmPBZ8Zcc Or Email; [email protected].
4K Followers 3K FollowingWorking on behalf of the residents of 3rd Hampshire in the MA House of Representatives. Over here now: https://t.co/brxPMdAj0e
65 Followers 170 FollowingA publicly traded (Nasdaq: MNOV) biopharmaceutical company that is developing novel therapeutics for disorders with unmet medical needs.
10K Followers 9K FollowingJoin us in heartfelt mission to build Sarah Memorial Neuro Hospital & Research Institute” a beacon for neurological care|Peace|Humanity |Trump 45/47 Psalm 23:1
21K Followers 4K FollowingWife to @bsw5020. Mama. Caregiver. CEO @synapticure providing medical care for Alzheimer’s, Parkinson’s and ALS. Co-founder @iamalsorg. EP @noc_film.
26K Followers 735 FollowingI AM ALS is the largest community movement made up of the very people living with, impacted by, and highly motivated to end ALS.
12K Followers 2K FollowingALS = Lou Gehrig's Disease Thought it had been cured by now? Still no known cause. Still no cure. Still no treatment. Still quickly fatal. Still outrageous.
4K Followers 5K FollowingAdvocate for Amyloidosis, ALS & Rare Diseases. Enviro Justice, Foster Care & Gun Safety. Love LA sports. @EndRareDiseases on bsky
9K Followers 573 Following40yo living with ALS on Life support. Author. Creative Director. Advocate. Dreamer. Public Servant. ALSFRS 1/48 https://t.co/vibJSKdIl4
13K Followers 558 FollowingDominating ALS one day at a time since 2018. Retired Police Officer. “Love the life you live and live the life you love” Go Royals! 💙#FightLikeAGirl
4K Followers 761 FollowingAnesthesiologist -Johns Hopkins Hospital
Pain Management -UC San Diego
Now battling ALS & FDA regulatory rigidity for 100% fatal ALS
194K Followers 291 FollowingNew Instagram - @stevegleasonofficial
Dad. Husband. Inspiring all people to live purposefully, despite tragedy. I tweet with my eyes. Embracing ALS.
2K Followers 873 FollowingLisa Stockman Mauriello fought for Expanded Access to an ALS treatment. Lisa passed away 8.4.21. Honor Lisa’s legacy by advocating for ALS.
24K Followers 188 FollowingHusband & Dad | Walking science experiment | Determined to beat ALS & win a Stanley Cup | Citizen of both 🇺🇸🇨🇦 | Assistant General Manager, Calgary Flames
4K Followers 375 FollowingWild & Wonderful WV. FSU grad. Married to @erika_poling , Father to Liam & Bayler, ALS Warrior & advocate. #EndALS
Founder of @project_seth
2K Followers 2K FollowingFighting for a cure for ALS/MND/ and it’s variants. Fighting daily for many years, for ALS drug access. Sod1 Gene carrier. Animals are my Love!!
4K Followers 1K FollowingALS advocate fighting for transparency, access to effective therapies, and ensuring ALS patients aren't victims of weak drug pharma gouging. YT: ALSNewsNow
21K Followers 12K FollowingSports artist for @MLB, @NHL and @TeamUSA / Member of @BaseballHall ⚾️/ Creator of the #MinimalistBallpark series & the #BallParkPrincess ⚾️👸
206K Followers 516 FollowingVery proud dad. ESPN's MLB/Little League/College World Series, College basketball play by play. #Pugpower and the Great Christino. IG ravech.karl
506 Followers 413 FollowingWife to a loving husband, Mom to 2 awesome young men, Mom to one adorable doodle fur baby, Anesthesiologist and a lucky daughter, sister, & friend #ALS Warrior
876 Followers 321 FollowingJacob Harper, 24, diagnosed with ALS in March, 2022! Fighting for a cure through a clinical trial at Ohio State University! "Genetic FUS-Gene Mutation" (P525L)
235 Followers 7 FollowingTim Miller, MD, PhD is a neurologist, neuroscientist with an interest in neurodegenerative diseases including ALS and dementias.
412 Followers 128 FollowingA user-friendly website where people living with ALS, caregivers, and professionals can find educational guides, expert video clips, resources, and more...
799 Followers 858 FollowingWorking hard to LIVE with ALS. Trying to Make Each Day My Best Day. Former Auburn Basketball player.
#maketodayyourbestday
#EndALS
51K Followers 5K FollowingHHMI believes in the power to advance science through research/science ed., making discoveries that benefit all. https://t.co/wRsmt29Bcs
23K Followers 837 FollowingVP/CSO @HHMInews & Head of #VosshallLab @rockefelleruniv Toward Excellent, Inclusive, & Open Science. See also @leslievosshall.bsky.social
2K Followers 154 FollowingWe are a group of women diagnosed with ALS before our 35th birthday who are challenging the stereotype that this is an old white man's disease.
1K Followers 3K FollowingSix people a day die with Motor Neurone Disease (#MND) / UK. @MHRAgovuk & @NICEcomms should conduct an Accelerated Review for existing treatments.
4K Followers 3K FollowingWriter, Veteran, & ALS Warrior.
Timeless Sisters available on Amazon now!
#FunFact - I type with my eyes.
#WritingCommunity #ReadingCommunity #Gratitude
3K Followers 47 FollowingOfficial Twitter account for the Director of FDA’s Center for Drug Evaluation and Research (CDER). Privacy Policy - https://t.co/gtX3WXfzSG
56K Followers 3K Following#NJ06 Congressman. Top Dem on @EnergyCommerce. Fighting to lower Rx costs, protect our shore, & hold corporate polluters accountable. Long Branch born & bred.
3K Followers 1K FollowingPlanting a beautiful garden in a pile of shit (ALS). Mama to 2 little loves, wife of @ebencathey. UIUC, VU & Peace Corps alum. Autism consultant @VanderbiltU
79K Followers 430 Following12 Year Streamer
Full Time Partner For @Twitch @Youtube @DeadByBHVR
I Have Terminal #ALS
Twitch https://t.co/Yz85kqPyLz
Youtube https://t.co/YlfqjwdfHm
Instagram https://t.co/kDyryLN0RT
553 Followers 249 FollowingQurAlis Corp. is a private clinical-stage #biotech driving #precisionmedicine breakthroughs for #ALS and other #neurodegenerative and #neurological diseases.
167 Followers 34 FollowingNon-profit enabling people w/ ALS to connect & communicate w/ family, friends & the broader world using assistive technology.
574 Followers 715 FollowingFather | Husband | Former Osler Marine | Interventional Cardiologist|ALS affected physician|Lover of National Parks|Sometimes artist
1K Followers 565 FollowingNon-profit discovering, developing, and providing personalized experimental ASO medicines to treat nano-rare patients — for free, for life
1K Followers 725 FollowingWe're Canada's first and only ALS patient-led nonprofit organization fighting to #EndALS forever. Join us!
Charitable organization BN: 791367204 RR 0001
1K Followers 923 FollowingMy Dad was diagnosed with #ALS in July 2018. Please join me in the fight to bring awareness to this disease and #EndALS @ALSAction
No recent Favorites. New Favorites will appear here.