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
 

 An on-line community where those affected by ALS can share information and experiences as well as ask questions.
- http://www.patientslikeme.com/als/community