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Neuropathy Foundation Websites

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American Autonomic Society
Coping with the symptoms of Autonomic Neuropathy is a reality for thousands of neuropathy patients. Besides providing patient resources, the American Autonomic Society has been established to bring together individuals from diverse disciplines who share an interest in the structure and function of the autonomic nervous system and in the pathology, treatment, and prevention of its disorders. The Society sponsors annual meetings and provides a point of contact among the many interested clinical and basic scientists who wish to communicate across disciplinary lines.
Foundation for Peripheral Neuropathy
The Foundation for Peripheral Neuropathy works to educate the public and healthcare professionals, provide state-of-the-art treatment for patients with peripheral neuropathy, and aspires to be the catalyst for advancing innovative therapeutic developments and accelerating a cure for painful neuropathies.
GBS/CIDP Foundation Int’l
The GBS/CIDP Foundation began over 30 years ago as a support group for patients and families impacted by Guillain-Barré syndrome, chronic inflammatory demyelinating polyneuropathy (CIDP) or any of the variants that exist.
Hereditary Neuropathy Foundation
The Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization which raises awareness, funds scientific research, and educates the medical community as well as the general public about Charcot-Marie-Tooth disease (CMT). HNF is committed to providing support to people living with CMT and their families.
Neuropathy Action Foundation
The Neuropathy Action Foundation (NAF), a 501(c)(3) non profit, is dedicated to ensuring neuropathy patients obtain the necessary resources, information and tools to access individualized treatment to improve their quality of life. The NAF increases awareness among physicians, appropriate institutions, the general public and public policy officials that neuropathy can potentially be a serious, widespread and disabling condition, which may be treatable when appropriate medical care is provided.
Neuropathy Alliance of Texas
The Neuropathy Alliance of Texas works together with national and local health care organizations to ensure that people with a peripheral neuropathy and their caregivers in the Central Texas region have the latest information on treatments and research into cures.
Neuropathy Support Network
Neuropathy Patient Questions can be submitted via the website. Questions are always answered with medical sources noted and/or reviewed by a Neuromuscular Neurologist. Website contains information on all subjects related to Neuropathy along with Resources. Neuropathy Support Group listings with self edit capability by support group leaders. Physician Listings with links to websites such as WebMD and Health Grades for further information and reviews. The NSN publishes the Neuropathy Journal, the premier internet magazine written for those suffering from Neuropathy by Neuropathy Patients, Neurologists and Neuropathy Medical Specialists.
The Neuropathy Journal
Sjogrens Syndrome Foundation
Sjogren’s Syndrome (a rare type of neuropathy) is a chronic autoimmune disease in which a person’s white blood cells attack their moisture-producing glands. Today, as many as 4 million Americans are living with this disease. Although the hallmark symptoms are dry eyes and dry mouth, Sjögren’s also causes serious complications throughout the entire body.
Western Neuropathy Association
The Western Neuropathy Association is a California non-profit, tax-exempt corporation. Their mission is to provide hope through caring, support, research, education, information, and empowerment to the million + individuals in California who suffer from with peripheral neuropathy and those who care about them. They help inform and connect with the health care community and support research in peripheral neuropathy treatments.