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New cities & service providers are now available on GatherMS.Choose City
National and local organizations providing information, programs and services to support people and families living with MS.
The Accelerated Cure Project for Multiple Sclerosis (ACP) is a patient-founded national non-profit organization dedicated to accelerating advances toward a cure for MS.
The Americans with Disabilities Act of 1990 (ADA) prohibits discrimination and ensures equal opportunity for persons with disabilities in employment, State and local government services, public accommodations, commercial facilities, and transportation.
Raise funds for MS research and treatment through cross country cycling trips.
The flagship four-day CAN DO Program is a four-day intensive educational program that teaches people with MS and their support partners how to take control of their life within the context of their MS.
Can Do MS transforms lives by delivering free health and wellness educational program for families with MS.
Can Do MS online resources include a library of MS articles, online Q&A and educational videos.
Can Do MS and the National MS Society brings together a collaboration of MS experts to help you build strategies to live your best life with MS. Each free webinar features two presenters with time for Q&A.
Caregiver Action Network (CAN) is the nation’s leading family caregiver organization working to improve the quality of life for the more than 90 million Americans who care for loved ones with chronic conditions, disabilities, disease, or the frailties of old age.
The Christopher & Dana Reeve Foundation is dedicated to advancing quality of life and discovering cures for spinal cord injury in the here and now.
To be the pre-eminent organization of Multiple Sclerosis health care providers improving the lives of those affected by Multiple Sclerosis.
Eldercare Locator is a public service of the U.S. Administration on Aging connecting you to services for older adults and their families.
Lotsa Helping Hands is a private, web-based caregiving coordination service.
The MSAA Networking Program is an online community of individuals with multiple sclerosis and their care partners who are interested in finding peer support and corresponding through email exchange.
Join over 25,000 people supporting one another and exploring the issues that shape your world.
MS Views and News (MSVN), is dedicated to the global collection and distribution of information concerning Multiple Sclerosis (MS). Through partnering relationships, MSVN provides education, advocacy and service to empower and enhance the quality of life of the MS community.
MSWorld is a website run by an all-volunteer team of people living with MS, in the process of being diagnosed or providing care to someone else living with MS.
Mr. Oscar Monkey is a MS advocacy group that supports children diagnosed with MS and their families by raising awareness of pediatric MS.
The Multiple Sclerosis Association of America (MSAA) is a leading resource for the entire MS community, improving lives today through vital services and support.
The MS Cure Fund is dedicated to raising awareness & educating patients through free programs.
The Multiple Sclerosis Foundation, known in the MS community as MS Focus, is a nonprofit organization focused on providing free services that address the critical needs of people with MS and their families, helping them maintain the best quality of life.
The National Alliance for Caregiving's mission is "Advancing family caregiving through Research, Innovation, and Advocacy."
The National Center for Assisted Living's mission is to improve lives by delivering solutions for quality care.
The National Multiple Sclerosis Society mobilizes people and resources so that everyone affected by multiple sclerosis can live their best lives as we stop MS in its tracks, restore what has been lost and end MS forever.
Everyone who wants to do something about multiple sclerosis can fuel progress.
Research breakthroughs continue to fuel the treatments and solutions that will stop the disease in its tracks, restore what has been lost, and end MS forever.
Pediatric Multiple Sclerosis Alliance (PMSA) aims to raise awareness of pediatric MS.
Shift.ms is a free social network for people living with MS to connect and share experiences.
The Home Wheelchair Ramp Project provides resources, including design and financial help, needed to get a ramp or steps built.
Local Resource Center
United Spinal Association provides support & services for the spinal cord injury & disease community.
Providing peer support and education about the special challenges and unique issues facing "well" spouses every day.
Local Resource Center
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