Joined February 2016
- Tweets 1,294
- Following 493
- Followers 1,952
- Likes 259
967 Photos and videos
Jun 11
Last month, Target ALS CEO Manish Raisinghani traveled to San Juan to speak at the Fifth Annual ALS Symposium hosted by UPR's Recinto de Ciencias Médicas, sharing insights on our research efforts to expand diversity in clinical research.
Learn more: ow.ly/9Q4X50Z9z1e
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Jun 9
From the West Coast to the East Coast, our team has been on the move, connecting with the brightest minds in #ALSResearch and neuroscience.
We're proud to be at the table, breaking down barriers and accelerating progress to build a world where Everyone with ALS Lives.
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Jun 5
We are honored to share that Target ALS Founder and Chairman, Dan Doctoroff, has been named a recipient of the FNIH Partnership Award. Congratulations, Dan.
Read the press release: fnih.org/press-release/fnih-…
#ALS #ALSResearch #EveryoneLives
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Jun 5
Our ALS Global Research Initiative is growing, and we're excited to welcome Malaysia as our newest participating region in the Target ALS Global Natural History Study.
Learn more and get involved in making #ALSResearch more inclusive and impactful: targetals.org/global-natural…
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Jun 4
In our latest story, Adam Crystal reflects on ALS through the lens of an oncologist and son of someone who was affected by the disease.
Get a candid look at genetics, drug discovery, and the importance of this moment in #ALSResearch: ow.ly/mnlO50Z6nlq
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Jun 2
Lou Gehrig was a Hall of Famer whose name became inseparable from #ALS, and whose legacy continues to drive our fight.
Join us as ballparks across the league pause to honor #LouGehrigsDay:
🏟️ Yankees: 6/2: ow.ly/3sA550Z6mQn
⚾ Mets: 6/10: ow.ly/yw3B50Z6mQo
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Jun 1
A major update to the Target ALS Data Engine is here — expanding scale, harmonization, and usability for multi-modal ALS research.
Explore the new features: ow.ly/o8WK50Z6mJ9
#ALS #OpenScience #Multiomics #Neurodegeneration #ALSResearch #Genomics #EveryoneLives
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May 31
This #ALSAwarenessMonth, we asked our community to go #ALLIN for ALS research.
The response was overwhelming. Every face you see here represents someone who is ALL IN and, for them, we are ALL IN to build a world where Everyone with ALS Lives.
Go #ALLIN: ow.ly/1Bjt50Z5o2B
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May 30
Kama is #ALLIN for her niece, Ashlee, a nurse, wife, and mom of three, who was diagnosed with ALS at 43.
Ashlee's story, and so many like it, is an urgent reminder of the work that must continue, so no other family has to carry this weight.
Go ALL IN: ow.ly/ynJj50Z5nX4
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May 30
ALS doesn't take one person at a time. It takes families. Communities. Generations. Meet three people who know that truth firsthand.
They are ALL IN. Join them: ow.ly/whYC50Z5nWo
#ALSAwarenessMonth #ALSResearch #ALS
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May 29
Cathy is #ALLIN.
She has taught K-5 for 34 years and was diagnosed with ALS in 2022. However, she is still teaching us about strength, about support systems, and about how to show up for change.
Join Cathy and go ALL IN: ow.ly/j03Y50Z5nMM
#ALSAwarenessMonth #ALSResearch
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May 29
ALS research is only as strong as the people it represents. Our ALS Global Research Initiative (AGRI) is closing gaps in research and making participation possible for communities that ALS research has too often left behind.
See how AGRI is #ALLIN: ow.ly/B41x50Z5nO8
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May 28
Tiffany is #ALLIN for her dad, who passed away from ALS.
In a letter to him, she writes about the man he was and the promise she's made to carry his story forward, honestly, without softening what ALS is: ow.ly/349450Z5n6l
#ALSAwarenessMonth #ALSResearch #ALS
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May 28
Eric Dane joined our Board of Directors just a few months before he passed. He didn't have time to do the work he wanted to do with us.
But he chose us and fought for people living with ALS.
Eric's fight is our fight. In Eric's memory, go #ALLIN: ow.ly/7Pvy50Z2v96
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May 27
Kristie, a doctor and 4th-generation C9 carrier, is #ALLIN. She was diagnosed with #ALS in 2025 and is showing up for the science she believes will change what ALS means for the next generation of her family.
Go ALL IN: ow.ly/iQYI50Z4ULV
#ALSAwarenessMonth #ALSResearch
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May 27
Brooke is #ALLIN to fight for research in honor of her mother, who passed away from #ALS. Join her:
🎭 Attend her cabaret fundraiser in NYC: ow.ly/LLo150Z4UiH
🔬 Donate to her fundraiser: ow.ly/1RaG50Z4UiI
🔥 Start your own fundraiser: targetals.org/fundraise-for-…
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May 26
Brenda White was a college senior when her father was diagnosed with bulbar ALS. He died just three months later, and it took nearly four decades and three more family diagnoses before testing revealed answers.
Read Brenda's story and why she's #ALLIN: ow.ly/spcl50Z4p0s
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May 23
When former Senator Laura Woods was diagnosed with ALS, she chose the one thing she could control.
"The best gift I can give to my children, grandchildren, nieces, and nephews is to be involved in research for a cure."
Share your #ALLIN story: ow.ly/YYvK50Z2rRK
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May 22
A group of Dan Doctoroff's high school classmates went #ALLIN to raise $100,000 for Target ALS and succeeded.
Together, they crossed the finish line, exceeding their goal and fueling progress toward new ALS treatments.
Start your own fundraiser: ow.ly/jU2l50Z0men
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