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ALS Resources:
The following web sites are provided for your reference only. The ALS Hope Foundation does not endorse or recommend the agencies or organizations
listed, nor is this a complete listing of all of the websites available.
♦ International Alliance of ALS/MND Association:
- http://www.alsmndalliance.org
♦ Muscular Dystrophy Association:
- http://als.mdausa.org
♦ National Organization of Rare Disorders (ALS/MND):
- http://www.rarediseases.org
♦ The North East ALS Consortium (NEALS):
- http://www.alsconsortium.org
♦ National Institute of Neurological Disorders & Stroke (NINDS) - ALS:
- http://www.ninds.nih.gov
♦ American Academy of Neurology Foundation:
- http://www.thebrainmatters.org
♦ Society for Neuroscience:
- http://www.sfn.org
♦ World Federation of Neurology:
- http://www.wfnals.org
♦ ALS Association (ALSA):
- http://www.alsa.org
♦ Les Turner Amyotrophic Lateral Sclerosis Foundation:
- http://www.lesturnerals.org
♦ To read about ongoing trials in ALS:
- http://www.clinicaltrials.gov
♦ To understand clinical trials:
- http://www.clinicaltrials.gov
♦ The ALSconnection gathers information such as symptoms, symptomatic treatment, & access to care for all ALS patients in North America.:
- http://www.alsconnection.org
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