HEALEY ALS Platform Trial
massgeneral.org
HEALEY ALS Platform Trial
Borrowing from successes in cancer drug development, the Healey Center and NEALS faculty are leading the first ALS Platform Trial.
Sep 25, 2019
Project ALS Research
While the scientists search for a cure .. and the big organisations fund research... At OPNMND we help people right now !! Building an OPNMND community of the diagnosed, their families, their carers and supporters. We will identify qualified experienced professionals who understand how their knowledge can fit into our project's development and we will make it relevant to specific area of motor neurone disease through working with families, carers and the diagnosed. Our content will not be the vo
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While the scientists search for a cure .. and the big organisations fund research... At OPNMND we help people right now !! Building an OPNMND community of the diagnosed, their families, their carers and supporters. We will identify qualified experienced professionals who understand how their knowledge can fit into our project's development and we will make it relevant to specific area of motor neurone disease through working with families, carers and the diagnosed. Our content will not be the vo
TikToktheopnmndproject
843 views3 weeks ago
Amyotrophic Lateral Sclerosis (ALS) Explained | Motor Neurone Disease | Pathophysiology Treatment | Deborah Osei-Sarfoh
Amyotrophic Lateral Sclerosis (ALS) Explained | Motor Neurone Disease | Pathophysiology Treatment | Deborah Osei-Sarfoh
linkedin.com
117 views2 months ago
✨ NEW SEATS ADDED ✨ A night to push ALS research forward while enjoying unique performances from Broadway legends such as Aaron Lazar, Andrew Rannells, Sara Bareilles, Kate Baldwin, Norm Lewis, Adam Pascal, Anthony Rapp and a guest appearance from Muniba Mazari. Mark your calendars for October 22nd at City Winery in New York City and be a part of creating a future free of ALS. Doors open at 6:30 PM. Join the experience today with tickets starting at $200: https://bit.ly/3ZdmnXY ALS is an aggress
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✨ NEW SEATS ADDED ✨ A night to push ALS research forward while enjoying unique performances from Broadway legends such as Aaron Lazar, Andrew Rannells, Sara Bareilles, Kate Baldwin, Norm Lewis, Adam Pascal, Anthony Rapp and a guest appearance from Muniba Mazari. Mark your calendars for October 22nd at City Winery in New York City and be a part of creating a future free of ALS. Doors open at 6:30 PM. Join the experience today with tickets starting at $200: https://bit.ly/3ZdmnXY ALS is an aggress
FacebookProject ALS
293 viewsOct 14, 2024
Top videos
1.3K views · 110 reactions | ALS drugs are near. Project ALS has...
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1.3K views · 110 reactions | ALS drugs are near. Project ALS has...
FacebookProject ALS
1.4K viewsOct 14, 2024
Jenifer Estess was a 35-year-old New York theater and film producer who was diagnosed—out of nowhere--with ALS. Her doctors told her to max out her credit cards and eat junk food—because they had no medicine to give her for ALS, a fatal brain disease. Jenifer made another choice. With her sisters, family and friends, she founded the non-profit Project ALS. Jenifer’s vision was to unite competing scientists to work together toward the first effective treatments. Project ALS built the world’s firs
0:15
Jenifer Estess was a 35-year-old New York theater and film producer who was diagnosed—out of nowhere--with ALS. Her doctors told her to max out her credit cards and eat junk food—because they had no medicine to give her for ALS, a fatal brain disease. Jenifer made another choice. With her sisters, family and friends, she founded the non-profit Project ALS. Jenifer’s vision was to unite competing scientists to work together toward the first effective treatments. Project ALS built the world’s firs
FacebookProject ALS
2.1K viewsMay 10, 2019
Join the Project ALS family and support critical research. Chris Combs, husband, father of 3, and former pitcher for the North Carolina State Wolfpack and Pittsburgh Pirates, was diagnosed with ALS in 2016. Watch his story and donate to Project ALS research now to bring us closer to a cure. | Project ALS
2:59
Join the Project ALS family and support critical research. Chris Combs, husband, father of 3, and former pitcher for the North Carolina State Wolfpack and Pittsburgh Pirates, was diagnosed with ALS in 2016. Watch his story and donate to Project ALS research now to bring us closer to a cure. | Project ALS
FacebookProject ALS
11.2K viewsDec 7, 2018
Project ALS Events
The making of " PROJECT ALS-ASENSO" is an ALS community garden in partnership of Toboso LGU headed by our Municipal Mayor Hon. Richard Jaojoco and the Department of Agriculture. It is located at Mabuhay 3,Brgy. Poblacion, Toboso (going to Senior High School and DRRM office). Please help us realize this project where our ALS learners grow not only plants, but life skills, livelihood knowledge, and environmental responsibility. Through partnership with the LGU, the project nurtures second chances,
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The making of " PROJECT ALS-ASENSO" is an ALS community garden in partnership of Toboso LGU headed by our Municipal Mayor Hon. Richard Jaojoco and the Department of Agriculture. It is located at Mabuhay 3,Brgy. Poblacion, Toboso (going to Senior High School and DRRM office). Please help us realize this project where our ALS learners grow not only plants, but life skills, livelihood knowledge, and environmental responsibility. Through partnership with the LGU, the project nurtures second chances,
FacebookMichelle Cabungcag Damaleri
406 views1 month ago
🎉 🎉 We are thrilled to announce that our 2026 ALS Canada Walk to End ALS events are now open for registration. Your participation matters! When you register, fundraise, and participate in the #WalkToEndALS, you are taking meaningful action in supporting people living with ALS in Canada and working toward a world free of ALS. Rally your friends, family, and colleagues and unite with the #ALS community. 💜 To register today, visit https://bit.ly/3wlNB2p. | ALS Canada
1:18
🎉 🎉 We are thrilled to announce that our 2026 ALS Canada Walk to End ALS events are now open for registration. Your participation matters! When you register, fundraise, and participate in the #WalkToEndALS, you are taking meaningful action in supporting people living with ALS in Canada and working toward a world free of ALS. Rally your friends, family, and colleagues and unite with the #ALS community. 💜 To register today, visit https://bit.ly/3wlNB2p. | ALS Canada
FacebookALS Canada
799 views2 weeks ago
projectvgg - Twitch
projectvgg - Twitch
Twitchprojectvgg
Dec 11, 2021
1.3K views · 110 reactions | ALS drugs are near. Project ALS has...
1:00
1.3K views · 110 reactions | ALS drugs are near. Project ALS has...
1.4K viewsOct 14, 2024
FacebookProject ALS
Jenifer Estess was a 35-year-old New York theater and film producer who was diagnosed—out of nowhere--with ALS. Her doctors told her to max out her credit cards and eat junk food—because they had no medicine to give her for ALS, a fatal brain disease. Jenifer made another choice. With her sisters, family and friends, she founded the non-profit Project ALS. Jenifer’s vision was to unite competing scientists to work together toward the first effective treatments. Project ALS built the world’s firs
0:15
Jenifer Estess was a 35-year-old New York theater and film produc…
2.1K viewsMay 10, 2019
FacebookProject ALS
Join the Project ALS family and support critical research. Chris Combs, husband, father of 3, and former pitcher for the North Carolina State Wolfpack and Pittsburgh Pirates, was diagnosed with ALS in 2016. Watch his story and donate to Project ALS research now to bring us closer to a cure. | Project ALS
2:59
Join the Project ALS family and support critical research. Chris Co…
11.2K viewsDec 7, 2018
FacebookProject ALS
2.2K views · 45 reactions | Three weeks ago, Project ALS had the...
6:30
2.2K views · 45 reactions | Three weeks ago, Project ALS had the...
764 viewsOct 14, 2024
FacebookProject ALS
Overview
Overview
Nov 19, 2022
lbl.gov
ALS-U Approach
ALS-U Approach
Sep 8, 2023
lbl.gov
Teens can get ALS too. Help us find out why. Project ALS met with 7 mothers nationwide who lost their teenage daughters to ALS. Watch their stories. Support crucial ALS genetics research now so we can end this disease - forever. Give now: https://fundraise.projectals.org/give/211906/#!/donation/checkout | Project ALS
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Teens can get ALS too. Help us find out why. Project ALS met with 7 m…
6.5K viewsDec 11, 2018
FacebookProject ALS
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12 reactions · 3 comments | Meredith met Project ALS in 2013 …
576 viewsOct 14, 2024
FacebookProject ALS
ALS Therapy Development Institute
Aug 29, 2019
als.net
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457 reactions · 54 shares | Just because ALS robs you of your spe…
16.2K viewsOct 14, 2024
FacebookProject ALS
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Project ALS on Reels | Facebook
27 viewsOct 14, 2024
FacebookProject ALS
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Project ALS on Reels
130 views3 months ago
FacebookProject ALS
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Project ALS was founded by three sisters, Jenifer, Meredith and Vale…
23.8K viewsDec 24, 2017
FacebookProject ALS
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5K views · 201 reactions | Meet Brooke Eby, a Her ALS Story mem…
5.1K viewsOct 14, 2024
FacebookProject ALS
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27 reactions · 5 comments | This holiday season marks twenty year…
771 viewsOct 14, 2024
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12K views · 341 reactions | In May, Project ALS brought together...
12.3K viewsOct 14, 2024
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1.6K views · 87 reactions | When Project ALS co-founder Jenifer...
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18K views · 123 reactions | A son continues his father’s legacy....
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Diagnosed with ALS at 28-years-old, A Langs Star is inspired by Sarah …
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Project ALS was founded by three sisters, Jenifer, Meredith, and Vale…
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327K views · 5K reactions | Christine Taylor & Ben Stiller want you to jo…
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What Brooke Eby said 👀 Create your fundraising page or donate here: …
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43K views · 11 reactions | Exciting news! We have partnered with...
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On February 4th, please join special guest Ben Stiller to learn how Jac…
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