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All Health A-Z Results: 1-5 of 5 Web Pages

Information designed to assist newly diagnosed patients with Epidermolysis Bullosa (EB), a group of rare, hereditary skin diseases. The page contains a brief description of EB, resources for patients... Details >

National Organization for Rare Disorders, Inc.  

Through the Society’s fifty-state network of chapters, assistance is provided to over a million people annually. Chapters encourage personal empowerment with employment counseling, family programs, vo... Details >

National Multiple Sclerosis Society  

The Sjögren's Syndrome Foundation sponsors nearly 100 groups located throughout the United States and Canada. These groups, run by volunteers, provide members opportunity to share advice and tips for ... Details >

Sjogren's Syndrome Foundation, Inc.  

There are currently 33 chapters of the Myasthenia Gravis Foundation of America. These chapters offer public education and patient services in cooperation with the Myasthenia Gravis Foundation of Amer... Details >

Myasthenia Gravis Foundation of America, Inc.  

This page offers a listing of Multiple Sclerosis Association of America (MSAA) support groups held in your state or geographic region. MSAA support groups provide safe environments where people, who h... Details >

Multiple Sclerosis Association of America