ALS Association - DC/MD/VA Chapter

We are led by people with ALS, caregivers and loved ones, and are the largest private funder of ALS research in the world. Through our nationwide chapter network, we provide care and support to people with ALS and their families in every state and advocate for better public policies and more ALS research funding.

I Am ALS

We are a patient-centric movement revolutionizing how to end disease. We provide critical support and resources to patients, caregivers and loved ones. We empower advocates to raise awareness and lead the movement against ALS in driving the development of cures.

Robert Packard Center for ALS Research at Johns Hopkins

We have been on forefront of ALS research for the past twenty one years. Our approach to research is one where we facilitate intense scientific collaboration across institutional and administrative boundaries. Our aim is to provide innovative, promising, focused projects with researchers who understand that collaboration is a powerful catalyst in ending the disease.

ALS Association - Greater Chicago Chapter

We are led by people with ALS, caregivers and loved ones, and are the largest private funder of ALS research in the world. Through our nationwide chapter network, we provide care and support to people with ALS and their families in every state and advocate for better public policies and more ALS research funding.

I Am ALS

We are a patient-centric movement revolutionizing how to end disease. We provide critical support and resources to patients, caregivers and loved ones. We empower advocates to raise awareness and lead the movement against ALS in driving the development of cures.

Les Turner ALS Foundation

Our mission is to provide the most comprehensive care and support to people living with ALS and their families in Chicagoland so they can confidently navigate the disease, and advance scientific research for the prevention, treatment and cure of ALS.

Project Main St.

We strive to improve the quality of life for people afflicted with ALS. We help both low and middle income individuals and families. We are committed to helping those who are experiencing financial challenges as a direct result of ALS.

Team Gleason

Team Gleason Foundation was founded by former New Orleans Saints player, Steve Gleason, after his diagnosis with Amyotrophic Lateral Sclerosis (ALS) in 2011. Team Gleason’s mission is to improve life for people living with ALS by delivering innovative technology and equipment, as well as providing and empowering an improved life experience. For more information on how to help people living with ALS have the resources and the opportunities to not only continue living, but continue living productive, purposeful and meaningful lives, please visit www.TeamGleason.org.

ALS Association - Greater Chicago Chapter

We are led by people with ALS, caregivers and loved ones, and are the largest private funder of ALS research in the world. Through our nationwide chapter network, we provide care and support to people with ALS and their families in every state and advocate for better public policies and more ALS research funding.

Les Turner ALS Foundation

Our mission is to provide the most comprehensive care and support to people living with ALS and their families in Chicagoland so they can confidently navigate the disease, and advance scientific research for the prevention, treatment and cure of ALS.

ALS Association - Central & Southern Ohio Chapter

We are led by people with ALS, caregivers and loved ones, and are the largest private funder of ALS research in the world. Through our nationwide chapter network, we provide care and support to people with ALS and their families in every state and advocate for better public policies and more ALS research funding.

Playing Hardball Against ALS

The PHAALS Foundation exists to help fight for a cure for ALS—also known as Lou Gehrig’s Disease—and to enrich the lives of families affected by the disease.

ALS Association - Northern Ohio Chapter

The ALS Association Northern Ohio Chapter supports people living with ALS and their loved ones through services and education. We leave no stone unturned in the search for the cure of this progressive neurodegenerative disease. Our mission is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.

ALS Association - Rocky Mountain Chapter

The Rocky Mountain Chapter was founded in 1996 to serve the needs of those living with Amyotrophic Lateral Sclerosis and their caregivers. The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. The ALS Association covers all the bases — research, patient and community services, public education and advocacy — in providing help and hope to those facing the disease. The ALS Association National Office and the Rocky Mountain Chapter operate under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in the search for the cure.

Team Hilliard

Our family wishes to see the day when no other family has to go through this experience of battling ALS. We are committed to helping raise awareness and funding for ALS research. The ALS Therapy Development Institute and its scientists actively discover and develop treatments for ALS.

Team Gleason

Team Gleason Foundation was founded by former New Orleans Saints player, Steve Gleason, after his diagnosis with Amyotrophic Lateral Sclerosis (ALS) in 2011. Team Gleason’s mission is to improve life for people living with ALS by delivering innovative technology and equipment, as well as providing and empowering an improved life experience. For more information on how to help people living with ALS have the resources and the opportunities to not only continue living, but continue living productive, purposeful and meaningful lives, please visit www.TeamGleason.org.

ALS Association - Mid-America Chapter

The ALS Association Mid-America Chapter has been serving people with ALS for more than 40 years. With a wide array of services and programs, including five treatment centers, the Chapter serves Kansas, Nebraska and the western 2/3 of Missouri.

ALS Association - Orange County Chapter

The ALS Association (National Office and the Orange County Chapter) operates under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in the search for the cure. We work together to accomplish our mission. The Orange County Chapter focuses primarily on helping local patients and families live with ALS while the National Office focuses primarily on research and advocacy. The Chapter supports the National Office through revenue sharing and research contributions. The National Office supports the Chapters by providing up-to-date information and materials.

Augie's Quest

Augie’s Quest to Cure ALS is dedicated to changing the experience of people living with ALS. We raise the funds and awareness urgently needed to advance cutting-edge research, fast-track effective treatments and ultimately, find a cure for this devastating disease. Today, there is real hope, like never before.

Augie's Quest

Augie’s Quest to Cure ALS is dedicated to changing the experience of people living with ALS. We raise the funds and awareness urgently needed to advance cutting-edge research, fast-track effective treatments and ultimately, find a cure for this devastating disease. Today, there is real hope, like never before.

ALS Association - Wisconsin Chapter

The reason for a Wisconsin chapter is simple: a disease as devastating as ALS requires a localized level of care and resources. While we work closely with the National Office in sharing information and patient advocacy efforts, we’re largely an autonomous organization that relies on the financial and volunteer support of the local area. Our mission is to lead the fight to cure and treat ALS through global, cutting-edge research and to empower people with ALS and their families to live fuller lives by providing them with compassionate care and support.

ALS Association - Minnesota/North Dakota/South Dakota Chapter

The ALS Association (National Office and the MN/ND/SD Chapter) operates under a shared mission: To discover treatments and a cure for ALS, and to serve, advocate for and empower people affected by ALS to live their lives to the fullest. Our Chapter serves over 600 people living with ALS and their families across Minnesota, North Dakota and South Dakota through our equipment loan pools, caregiver respite program, support groups and more.

Project ALS

Project ALS identifies and funds the most promising scientific research that will lead to the first effective treatments and a cure for ALS. We recruit the world’s best scientists and doctors to work together—rationally and aggressively—to develop a better understanding of the ALS disease process and, in parallel, better therapeutic strategies.

ALS CURE Project

Stephen Piscotty and his father Mike Piscotty founded the ALS CURE Project in honor of Stephen's mother, Gretchen Piscotty, who passed from ALS in 2018. As a 501(c)(3) organization, the ALS CURE Project supports vital ALS research and organizes research collaborations to cure ALS. In 2020, the ALS CURE Project led an international symposium with 87 ALS researchers to create the first-ever "Roadmap to Cure ALS." The ALS CURE Project has funded novel research at Lawrence Livermore National Laboratory to identify the ALS disease mechanism using the second-fastest supercomputer in the world. The ALS CURE Project is a volunteer organization enabling 100% of donations to be applied directly to funding vital ALS research. The ALS CURE Project is turning up the Chatter around ALS. #ALSCHATTER

ALS Association - Greater Philadelphia Chapter

To discover treatments and a cure for ALS, and to serve, advocate for and empower people affected by ALS to live their lives to the fullest.

ALS Association - Western Pennsylvania Chapter

The ALS Association Western Pennsylvania Chapter’s mission is to discover treatments and a cure for ALS, and to serve, advocate for and empower people affected by ALS to live their lives to the fullest.

The LiveLikeLou Foundation

The LiveLikeLou Foundation is committed to making an impact on ALS research while it supports the children of families affected by ALS. Our impact is focused on facilitating learning amongst ALS researchers, supporting innovative research centers and giving children of ALS families life-enhancing experiences and financial assistance as they pursue higher education dreams.

ALS Association – Greater San Diego Chapter

We are led by people with ALS, caregivers and loved ones, and are the largest private funder of ALS research in the world. Through our nationwide chapter network, we provide care and support to people with ALS and their families in every state and advocate for better public policies and more ALS research funding.

Augie's Quest

Augie’s Quest to Cure ALS is dedicated to changing the experience of people living with ALS. We raise the funds and awareness urgently needed to advance cutting-edge research, fast-track effective treatments and ultimately, find a cure for this devastating disease. Today, there is real hope, like never before.

ALS Association - Golden West Chapter

Our mission is to discover treatments and a cure for ALS, and to serve, advocate for and empower people affected by ALS to live their lives to the fullest. The Golden West Chapter supports people living with ALS and their loved ones in 31 counties throughout California and the state of Hawaii. Everything we do advances the search for effective treatments and cures for ALS.

ALS Therapy Development Institute (ALS TDI)

We quickly discover and validate potential treatments for ALS. We are the world’s first and largest nonprofit biotech focused 100 percent on ALS research. Led by drug development experts and people with ALS, we understand the urgent need to slow and stop this disease.

ALS CURE Project

Stephen Piscotty and his father Mike Piscotty founded the ALS CURE Project in honor of Stephen's mother, Gretchen Piscotty, who passed from ALS in 2018. As a 501(c)(3) organization, the ALS CURE Project supports vital ALS research and organizes research collaborations to cure ALS. In 2020, the ALS CURE Project led an international symposium with 87 ALS researchers to create the first-ever "Roadmap to Cure ALS." The ALS CURE Project has funded novel research at Lawrence Livermore National Laboratory to identify the ALS disease mechanism using the second-fastest supercomputer in the world. The ALS CURE Project is a volunteer organization enabling 100% of donations to be applied directly to funding vital ALS research. The ALS CURE Project is turning up the Chatter around ALS. #ALSCHATTER

I Am ALS

We are a patient-centric movement revolutionizing how to end disease. We provide critical support and resources to patients, caregivers and loved ones. We empower advocates to raise awareness and lead the movement against ALS in driving the development of cures.

EverythingALS

We are a patient-focused non-profit bringing technological innovations and data science to support efforts -- from care to cure -- for people with ALS, by offering a open-data platform for direct engagement with patients, caregivers, researchers and drug companies.

Muscular Dystrophy Association

We remain committed to funding scientific and clinical research and care, to find treatments and cures for ALS, in addition to advocacy for ALS families.

Team Gleason

Team Gleason Foundation was founded by former New Orleans Saints player, Steve Gleason, after his diagnosis with Amyotrophic Lateral Sclerosis (ALS) in 2011. Team Gleason’s mission is to improve life for people living with ALS by delivering innovative technology and equipment, as well as providing and empowering an improved life experience. For more information on how to help people living with ALS have the resources and the opportunities to not only continue living, but continue living productive, purposeful and meaningful lives, please visit www.TeamGleason.org.

ALS Association - St. Louis Regional Chapter

The ALS Association St. Louis Regional Chapter improves the lives of people living with ALS and their loved ones in eastern Missouri and central and southern Illinois, through services and education. Our work covers all the bases — research, patient and community services, public education and advocacy — in providing help, support and hope to those facing the disease. The ALS Association and the St. Louis Regional Chapter operate under a shared mission— to improve the lives of people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search of treatments and a cure.

ALS Association - Texas Chapter

The ALS Association is the only national nonprofit completely dedicated to fighting ALS. The Texas Chapter focuses our resources on helping people across the state by addressing the entire ALS ecosystem: providing local care to support people who need help now, advocating for public policy that serves the needs of people with ALS and investing in research to find treatments and, ultimately, a cure.

Donate to support Texans with ALS, or donate in memory or honor of a loved one.

ALS Association - DC/MD/VA Chapter

We are led by people with ALS, caregivers and loved ones, and are the largest private funder of ALS research in the world. Through our nationwide chapter network, we provide care and support to people with ALS and their families in every state and advocate for better public policies and more ALS research funding.

I Am ALS

We are a patient-centric movement revolutionizing how to end disease. We provide critical support and resources to patients, caregivers and loved ones. We empower advocates to raise awareness and lead the movement against ALS in driving the development of cures.

Robert Packard Center for ALS Research at Johns Hopkins

We have been on forefront of ALS research for the past twenty one years. Our approach to research is one where we facilitate intense scientific collaboration across institutional and administrative boundaries. Our aim is to provide innovative, promising, focused projects with researchers who understand that collaboration is a powerful catalyst in ending the disease.