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Patient and Family Resources
Motor neuron diseases
Amyotrophic lateral sclerosis (ALS)
ALS Association
provides patient education, services and research.
Spinal muscular atrophy (SMA)
Cure SMA
offers support, services, education and research.
SMA Support Inc.
provides grants and resources to families.
SMA Foundation
aims to accelerate the development of a treatment for SMA.
Muscular dystrophy
Muscular
Dystrop
hy
Association
pursues innovations in science and care to help those with neuromuscular disease.
Myotonic Dystrophy Foundation
provides education, support and research.
Parent Project
offers education, advocacy, support and research on Duchenne muscular dystrophy.
Young Adult Transitions Program
provides resources, programming and community connections for young adults with neuromuscular diseases.
Facioscapulohumeral (FSH) muscular dystrophy
FSH Society
provides education and research.
Limb-Girdle muscular dystrophy
Kurt and Peter Foundation
funds research to produce drug treatments.
Jain Foundation provides a Limb-Girdle 2B and Miyoshi myopathy patient registry and research foundation.
Limb-Girdle Research Fund
provides grants for those developing treatments.
Limb-Girdle MD offers a
Fukutin-related protein registry
.
Congenital muscular dystrophy
Congenital Muscle Disease International patient registry
.
Cure CMD
provides advocacy and education.
Metabolic diseases of the muscle
North American Mitochondrial Disease Consortium
offers patient support and research.
United Mitochondrial Disease Foundation
provides patient support and research.
Myopathies
A Foundation Building Strength
offers nemaline myopathy advocacy.
Joshua Frase Foundation
provides myotubular myopathy education and research.
Neuromuscular junction disease
Myasthenia Gravis Foundation of America, Inc.
offers patient support, education and research.
Myasthenia Gravis Foundation of California
funds research and education and accepts volunteers.
Neuropathies
Friedreich’s Ataxia Research Alliance
supports scientific research leading to treatments for FA.
Peripheral neuropathies
Charcot-Marie-Tooth Association
is devoted to developing new drugs, improving quality of life, and finding a cure.
Resources for teens living with neuromuscular conditions
Young Adult Transitions Program
provides resources, programming and community connections for young adults with neuromuscular diseases.
In this Section
Brain and Behavior
Neuromuscular Diseases Clinic Overview
Conditions We Treat
Spinal Muscular Atrophy (SMA)
Muscular Dystrophies
Pompe Disease
Charcot-Marie-Tooth (CMT)
Our Services
Pharmacological Treatments
Electromyography (EMG)
Our Care Team
Research & Innovation
Contact & Location
Patient & Family Resources
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(650) 507-0457
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