Recommended and Registered ALS/MND Organisations
The following online resources have been organized to help you quickly find the ALS organizations you need to get in touch with. If you find one of our resources outdated, not working, or no longer useful please take a moment to notify us. Please contact us if you feel we are missing a resource that you would like to see added.
International ALS or MND Organizations
The Motor Neurone Disease (MND) Association is the only national organization in England, Wales and Northern Ireland dedicated to the support of people with and those who care for them.
International Alliance of ALS/MND Associations - The International Alliance is the peak body for national organizations who support people living with ALS/MND.
North American Nonprofit Organizations
Are you looking for support groups and ALS clinics in your local town or city in the United States?. We've made it easy to find them, please visit our American directory ALS clinics & support groups.
|ALS Association - The ALS Association is the only national not-for-profit health agency dedicated solely to the fight against ALS through research, patient and community services, public education, and advocacy.
Signature Event: In 2005, the ALS Associations “Walk to d'Feet ALS” held approximately 150 walks nationwide and raised over $10 million in support of cutting-edge research and patient services programs (USD - reported 2006).
|ALS Society of Canada - mission is to fund research towards a cure for ALS and support provincial ALS Societies to provide quality care for those affected by ALS.
Signature Event: In 2005, the ALS Society of Canada's “Walk For ALS” raised over $1.7 million dollars for ALS Research and patient care services (CAD - reported 2006).
|ALS Therapy Development Foundation - The ALS Therapy Development Foundation is a nonprofit biotechnology company discovering treatments for patients alive today.|
|Ride For Life- mission is to raise public awareness of amyotrophic lateral sclerosis, assist research in finding a cure, support ALS patients and their families, and provide the ALS community with the latest ALS related news and information.
Signature Event: During the past 7 years the “Ride For Life” has seen ALS patients ride their wheelchairs from Yankee Stadium to Washington DC - raising over 1 million dollars (USD - reported 2006).
|Robert Packard Center for ALS Research at Johns Hopkins - The Robert Packard Center for ALS Research is non-profit organization that operates out of the Johns Hopkins School of Medicine in Baltimore and focuses solely on finding effective treatments for ALS, and ultimately, a cure. To ensure progress, the Robert Packard Center recruits only scientists of recognized merit, minimizing the often lengthy grant process typical of academic medicine. This international group of investigators meets once a month to share ideas and discoveries, a collaborative process that greatly speeds up the progress of research and understanding of ALS.|
Online Clinical Trial Resources
ClinicalTrials.gov - Provides regularly updated information about federally and privately supported clinical research in human volunteers.
Nonprofit Evaluators and Donating Recommendations
BBB Wise Giving Alliance - The BBB Wise Giving Alliance helps donors make informed giving decisions and advances high standards of conduct among organizations that solicit contributions from the public.
Submitting A Resource
If you have access to a useful resource concerning Lou Gehrig's Disease (ALS), motor neuron disease (MND) or primary lateral sclerosis please take a moment to submit it. We will review your submission for inclusion. Only registered organizations and verified resources will be published.