Donate to ALS Organizations
Donate to ALS Organizations
Arizona Diamondbacks
ALS Association - Arizona Chapter
The ALS Association Arizona Chapter is dedicated to serving and empowering people living with ALS and their families. We provide free support, resources and education to Arizonans impacted by ALS, allowing them to endure their diagnosis with dignity, quality of life and hope for a world without ALS. Through family-centered care initiatives, we assess individual needs in terms of disease progression and equipment and resource needs. We invite families living with ALS into a community of supportive peers, ensuring them that they are not alone. ALS is a devastating, expensive disease that robs individuals of the ability to walk, speak, eat and eventually breathe. Your support directly impacts daily life for people facing this struggle, aids in the search for a cure and gives the gift of hope to all people affected by 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.
Gregory W. Fulton ALS & Neuromuscular Disease Center | Barrow Neurological Institute
Barrow Neurological Foundation’s mission is simple: to be the catalyst of our donors’ passion for transformation by providing the resources for Barrow Neurological Institute to achieve its mission of saving human lives through innovative treatment, groundbreaking, curative research and educating the next generation of the world’s leading neuro clinicians.
Donate to Barrow Neurological Institute
Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS and related neuromuscular diseases. For more than 70 years, MDA has led the way in ALS research, investing more than $173 million in innovations in ALS science and care. Thanks to MDA-funded research, tremendous leaps forward have been made in the understanding of the causes of ALS. MDA’s commitment to ALS includes support for a network of more than 150 multidisciplinary Care Centers at top medical institutions nationwide, including 48 designated MDA ALS Care Centers. MDA’s data hub, called MOVR, is the first-of-its-kind data technology hub, which collects clinical and genetic data from our network of Care Centers for neuromuscular diseases including ALS, serving as a valuable tool for accelerating therapy development. MDA’s advocacy efforts led to the passing of the ACT for ALS into law, which will accelerate access to treatment for the ALS community. To learn more visit mda.org and follow MDA on Instagram, Facebook, Twitter, TikTok and LinkedIn.
Atlanta Braves
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.
Hop On A Cure
John Driskell Hopkins (Hop), a founding and active member of Zac Brown Band, was diagnosed with ALS in December 2021 and immediately went into action by creating Hop On A Cure Foundation, Inc. Hop On A Cure is committed to supporting research to prevent, reverse and cure ALS while raising awareness, building a compassionate community and unleashing the healing power of hope.
Baltimore Orioles
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.
Brigance Brigade
The Brigance Brigade Foundation is a 501(c)(3) nonprofit organization with mission to equip, encourage and empower people living with ALS.
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.
Boston Red Sox
ALS Association of Massachusetts
The Massachusetts Chapter of the ALS Association was founded on Jan. 27, 1990, to serve the needs of those living with Amyotrophic Lateral Sclerosis and their caregivers. The Chapter provides no-cost services to ALS families which include support groups, home visits, insurance counseling, referrals to community resources, durable medical equipment loans, the Care Connection program, education and support.
Donate to ALS Association of Massachusetts
ALS One
Our Mission is to expedite treatments and ultimately find a cure for ALS while improving the care now for those living with the disease.
ALS Therapy Development Institute
The ALS Therapy Development Institute (ALS TDI) is the world's largest ALS-dedicated drug development organization. With 30 full-time, industry-trained drug development experts on staff, the nonprofit institute screens 25-30 compounds a year, and has screened over 300 since its inception in 1999. ALS TDI is internationally recognized for its work to optimize preclinical models of neurodegeneration for clinical translation, and has over 15 active partnerships with pharmaceutical companies and other biotechs from around the world. ALS TDI is funded by over 150 community grassroots initiatives, foundations, grants and bequests. Rated a four-star charity by CharityNavigator.com, more than 86% of each dollar raised is spent directly on the Institute's mission: to discover and develop effective treatments to end ALS.
Donate to ALS Therapy Development Institute
CCALS (Compassionate Cares)
CCALS is a nonprofit organization with a mission to support people diagnosed with ALS, their families, healthcare providers and communities as they navigate the complexities, both physical and emotional, associated with the disease. The organization provides resources including equipment, educational opportunities, insurance and Medicare assistance, guidance and awareness with regards to living with ALS, caregiving and exploring end-of-life when invited. CCALS offers an innovative approach to delivering support and services to our clients, which we tailor to the needs of each individual and their support network.
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.
Mass General Hospital: The Healey Center for ALS
The Sean M. Healey & AMG Center for ALS combines outstanding, multidisciplinary care with clinical and basic research informed by the needs of our patients. We are in the midst of dozens of innovative clinical trials that are accelerating the pace of discovery and making a meaningful difference in therapeutic options, even as we deliver compassionate care using age-old solutions, such as house calls, and new tools, such as telemedicine and digital monitoring tools. We believe strongly that every person with ALS should have treatment options and have built a clinical trial and expanded access program (compassionate use) to accomplish this mission. The Healey Center offers an Expanded Access Protocol (EAP) program, providing access to experimental treatments for people with ALS who are ineligible for clinical trials. The EAPs provide hope to people with ALS who need it most and allows scientists to collect safety and biomarker data that contributes to our understanding of these experimental agents in the later stages of ALS. Our goal is to raise $2 million a year to offer EAPs to 200 people each year across the US. We are determined to find the cures. Your support makes that possible.
Donate to The Healey Center for ALS
Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS and related neuromuscular diseases. For more than 70 years, MDA has led the way in ALS research, investing more than $173 million in innovations in ALS science and care. Thanks to MDA-funded research, tremendous leaps forward have been made in the understanding of the causes of ALS. MDA’s commitment to ALS includes support for a network of more than 150 multidisciplinary Care Centers at top medical institutions nationwide, including 48 designated MDA ALS Care Centers. MDA’s data hub, called MOVR, is the first-of-its-kind data technology hub, which collects clinical and genetic data from our network of Care Centers for neuromuscular diseases including ALS, serving as a valuable tool for accelerating therapy development. MDA’s advocacy efforts led to the passing of the ACT for ALS into law, which will accelerate access to treatment for the ALS community. To learn more visit mda.org and follow MDA on Instagram, Facebook, Twitter, TikTok and LinkedIn.
Donate to Muscular Dystrophy Association
Peter Frates Family Foundation
The Peter Frates Family Foundation is a 501c3 non profit established to financially assist ALS patients with the enormous financial burden of home health care. As the patient progresses on their ALS journey, these out of pocket expenses grow exponentially. Our assistance will help allow these patients to stay in their home surrounded by the love and support of their loved ones where they truly belong.
Chicago Cubs
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.
Donate to Les Turner ALS Foundation
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.
Chicago White Sox
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.
Donate to Les Turner ALS Foundation
Live Like Lou
Our mission is to create and connect communities to stimulate emerging ALS research and uniquely support families affected by Lou Gehrig’s disease.
Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is the No. 1 voluntary health organization in the United States for people living with muscular dystrophy, ALS and related neuromuscular diseases. For more than 70 years, MDA has led the way in ALS research, investing more than $173 million in innovations in ALS science and care. Thanks to MDA-funded research, tremendous leaps forward have been made in the understanding of the causes of ALS. MDA’s commitment to ALS includes support for a network of more than 150 multidisciplinary Care Centers at top medical institutions nationwide, including 48 designated MDA ALS Care Centers. MDA’s data hub, called MOVR, is the first-of-its-kind data technology hub, which collects clinical and genetic data from our network of Care Centers for neuromuscular diseases including ALS, serving as a valuable tool for accelerating therapy development. MDA’s advocacy efforts led to the passing of the ACT for ALS into law, which will accelerate access to treatment for the ALS community. To learn more visit mda.org and follow MDA on Instagram, Facebook, Twitter, TikTok and LinkedIn.
Cincinnati Reds
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.
Hop On A Cure
John Driskell Hopkins (Hop), a founding and active member of Zac Brown Band, was diagnosed with ALS in December 2021 and immediately went into action by creating Hop On A Cure Foundation, Inc. Hop On A Cure is committed to supporting research to prevent, reverse and cure ALS while raising awareness, building a compassionate community and unleashing the healing power of hope. For 2023’s Lou Gehrig Day, the Reds are hosting a Zac Brown Band Post-Game Benefit Concert 4-ALS, with a portion of the proceeds from every ticket sold for the game benefitting the Hop On A Cure Foundation.
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.
Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is the No. 1 voluntary health organization in the United States for people living with muscular dystrophy, ALS and related neuromuscular diseases. For more than 70 years, MDA has led the way in ALS research, investing more than $173 million in innovations in ALS science and care. Thanks to MDA-funded research, tremendous leaps forward have been made in the understanding of the causes of ALS. MDA’s commitment to ALS includes support for a network of more than 150 multidisciplinary Care Centers at top medical institutions nationwide, including 48 designated MDA ALS Care Centers. MDA’s data hub, called MOVR, is the first-of-its-kind data technology hub, which collects clinical and genetic data from our network of Care Centers for neuromuscular diseases including ALS, serving as a valuable tool for accelerating therapy development. MDA’s advocacy efforts led to the passing of the ACT for ALS into law, which will accelerate access to treatment for the ALS community. To learn more visit mda.org and follow MDA on Instagram, Facebook, Twitter, TikTok and LinkedIn.
Cleveland Guardians
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.
Colorado Rockies
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.
Detroit Tigers
The ALS Association – Michigan Chapter
The ALS Association Michigan Chapter has been committed to serving people with ALS and their families in the state of Michigan since 1988. Now, The Michigan Chapter has grown to support to the entire state of Michigan, including the Upper Peninsula. The Michigan Chapter provides help to people with ALS and their families; giving them hope for the future by providing no-cost services such as support groups, durable medical equipment loan closet, ALS Association liaison at affiliated ALS clinics, respite program, assistive technology program and education through literature and workshops.
Donate to The ALS Association – Michigan Chapter
ALS of Michigan
ALS of Michigan is a voluntary nonprofit organization, solely dedicated to the fight against ALS. Their mission is dedicated to helping pALS (people with ALS), their families and caregivers live life as fully as possible. We serve pALS and their families throughout the state of Michigan through a variety of programs, all offered at no cost to pALS. Some of ALS of Michigan services include Information, Referrals and Resource Guides, Workshops & Seminars, Equipment Loans, Augmentative & Alternative Communication Center, Home Visits, Peer Counseling, Support Groups and Respite Care Services (in certain areas).
I AM ALS
I AM ALS was created for patients, by patients. I AM ALS has set out to build a movement that connects patients, caregivers, researchers, clinicians, foundations, corporations and the public in their efforts because everyone has a part to play and are stronger when working together. I AM ALS empowers advocates to raise awareness and advocate for their community’ needs; increases federal funding for ALS research and revolutionizes the development of treatments and cures.
Muscular Dystrophy Association
A caring and concerned group of families started the Muscular Dystrophy Association in 1950. Today, they continue to relentlessly pursue their promise to transform the lives of people living with muscular dystrophy, ALS and related neuromuscular diseases through innovations in science and technology. MDA supports the largest network of multidisciplinary clinics providing best in class care at more than 150 of the nation’s top medical institutions. Their Resource Center serves the community with one-on-one specialized support, educational conferences, events, and materials for families and healthcare providers.
Houston Astros
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.
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.
Kansas City Royals
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.
Los Angeles Angels
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.
Los Angeles Dodgers
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.
Donate to the Golden West Chapter
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.
Miami Marlins
ALS Center | University of Miami (miami-als.org)
The ALS Center at the University of Miami effectively integrates comprehensive, coordinated care with groundbreaking research focused on developing effective treatments for patients with ALS.
The ALS Center is home to the largest multi-disciplinary clinic in the State, providing care for ALS patients in the South Florida community and beyond. Our research aims to advance ALS therapy development by identifying and filling knowledge gaps that have, in the past, hampered the development of effective treatments. As such, our research in highly collaborative, broadly inter-disciplinary, and seamlessly translational.
Our mission is to provide the highest level of care and multi-specialty support for patients and families living with ALS from the time of diagnosis to the end stages of the disease, while simultaneously advancing research to meaningfully impact the lives of patients with ALS. Our goals are for every patient and family to receive the best possible care, and to contribute to ending ALS through research.
Milwaukee Brewers
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.
Minnesota Twins
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.
New York Mets
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.
Oakland Athletics
ALS Association - Golden West Chapter
Our mission is to discover treatments and cures 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.
Donate to the Golden West Chapter
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 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% on ALS research. Led by drug development experts and people with ALS, we understand the urgent need to slow and stop this disease.
Donate to ALS Therapy Development Institute
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.
Philadelphia Phillies
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.
Pittsburgh Pirates
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.
San Diego Padres
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.
San Francisco Giants
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.
Donate to the Golden West Chapter
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% on ALS research. Led by drug development experts and people with ALS, we understand the urgent need to slow and stop this disease.
Donate to ALS Therapy Development Institute
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.
Seattle Mariners
ALS Association - Evergreen 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.
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.
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.
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.
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.
Donate to Muscular Dystrophy Association
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.
The ALS Therapy Development Institute (ALS TDI)
The ALS Therapy Development Institute (ALS TDI) is a nonprofit biotech and the world's foremost drug discovery lab focused solely on ALS. Our mission is to discover and develop effective treatments for ALS.
St. Louis Cardinals
The ALS Association
The ALS Association is the largest philanthropic funder of ALS research in the world. The Association funds global research collaborations, assists people with ALS and their families through its nationwide network of care and certified clinical care centers and advocates for better public policies for people with ALS. The ALS Association is working to make ALS a livable disease while urgently searching for new treatments and a cure. For more information about The ALS Association, visit our website at als.org.
Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS and related neuromuscular diseases. For more than 70 years, MDA has led the way in accelerating research, advancing care and advocating for the support of our families. MDA's mission is to empower the people we serve to live longer, more independent lives. To learn more visit mda.org.
Tampa Bay Rays
ALS Association - Florida Chapter
Established in 1987, The ALS Association Florida Chapter is fighting ALS on all fronts, or as we like to say, “Covering all the bases for people living with ALS in Florida." We provide patient programs, advocate on behalf of patients with our government leaders, create awareness of the disease and fund research. In addition, the Chapter provides financial support to our statewide multidisciplinary ALS clinics and research facilities, enabling them to increase patient care.
Texas Rangers
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.
Toronto Blue Jays
ALS Society of Canada
The ALS Society of Canada works with the ALS community to improve the lives of people affected by ALS through support, advocacy and investment in research for a future without ALS. Through the ALS Canada Research Program, we fund peer-reviewed research grants, foster collaboration and build capacity within Canada’s ALS research community, and participate in new areas of research where we are well-positioned to have an impact. Within Ontario, ALS Canada has a role similar to that of the provincial ALS societies providing services and support to help meet the needs of people living with ALS. Through advocacy federally and provincially within Ontario, ALS Canada gives voice to the collective experience of people living with ALS to help drive program and system changes for the ALS community. For information about or to support the ALS Society in your province, visit https://www.als.ca/support-services/other-provinces/.
Washington Nationals
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.
Brigance Brigade
The Brigance Brigade Foundation is a 501(c)(3) nonprofit organization with mission to equip, encourage and empower people living with ALS.
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.
National Organizations
ALS Association
The ALS Association is the only national non-profit organization fighting Lou Gehrig's disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.
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 Therapy Development Institute (ALS TDI)
The ALS Therapy Development Institute (ALS TDI) is the world's largest ALS-dedicated drug development organization. With 30 full-time, industry-trained drug development experts on staff, the nonprofit institute screens 25-30 compounds a year, and has screened over 300 since its inception in 1999. ALS TDI is internationally recognized for its work to optimize preclinical models of neurodegeneration for clinical translation, and has over 15 active partnerships with pharmaceutical companies and other biotechs from around the world. ALS TDI is funded by over 150 community grassroots initiatives, foundations, grants and bequests. Rated a four-star charity by CharityNavigator.com, more than 86% of each dollar raised is spent directly on the Institute's mission: to discover and develop effective treatments to end ALS.
Donate to ALS Therapy Development Institute
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.
Donate to Les Turner ALS Foundation
Mass General Hospital: The Healey Center for ALS
The Sean M. Healey & AMG Center for ALS combines outstanding, multidisciplinary care with clinical and basic research informed by the needs of our patients. We are in the midst of dozens of innovative clinical trials that are accelerating the pace of discovery and making a meaningful difference in therapeutic options, even as we deliver compassionate care using age-old solutions, such as house calls, and new tools, such as telemedicine and digital monitoring tools. We believe strongly that every person with ALS should have treatment options and have built a clinical trial and expanded access program (compassionate use) to accomplish this mission. The Healey Center offers an Expanded Access Protocol (EAP) program, providing access to experimental treatments for people with ALS who are ineligible for clinical trials. The EAPs provide hope to people with ALS who need it most and allows scientists to collect safety and biomarker data that contributes to our understanding of these experimental agents in the later stages of ALS. Our goal is to raise $2 million a year to offer EAPs to 200 people each year across the US. We are determined to find the cures. Your support makes that possible.
Donate to The Healey Center for ALS
Muscular Dystrophy Association
The Muscular Dystrophy Association is the world's leading nonprofit health agency dedicated to saving and improving the lives of anyone with muscle disease, including muscular dystrophy, amyotrophic lateral sclerosis (ALS) and other neuromuscular diseases. It does so by funding worldwide research to find treatments and cures; by providing comprehensive health care services and support to MDA families nationwide; and by rallying communities to fight back through advocacy, fundraising and local engagement.
Donate to Muscular Dystrophy Association
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.
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.
2023 Game Schedule
| Away | Home | Time | Location | |
|---|---|---|---|---|
| Brewers | Reds | 5:10 p.m. ET | Great American Ball Park | |
| Athletics | Marlins | 6:40 p.m. ET | loanDepot park | |
| Phillies | Nationals | 7:05 p.m. ET | Nationals Park | |
| Cardinals | Pirates | 7:05 p.m. ET | PNC Park | |
| Rays | Red Sox | 7:10 p.m. ET | Fenway Park | |
| Blue Jays | Mets | 7:10 p.m. ET | Citi Field | |
| Mariners | Rangers | 8:05 p.m. ET | Globe Life Field | |
| Angels | Astros | 8:10 p.m. ET | Minuate Maid Park | |
| Guardians | Twins | 8:10 p.m. ET | Target Field | |
| Rockies | Royals | 8:10 p.m. ET | Kauffman Stadium | |
| Tigers | White Sox | 8:10 p.m. ET | Guaranteed Rate Field | |
| Braves | Diamondbacks | 9:40 p.m. ET | Chase Field | |
| Cubs | Padres | 9:40 p.m. ET | Petco Park | |
| Yankees | Dodgers | 10:10 p.m. ET | Dodger Stadium | |
| Orioles | Giants | 10:15 p.m. ET | Oracle Park |