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Join The TMA 20 for 20 Anniversary Campaign!

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Understanding Acute Flaccid Myelitis

Click here to read our blog posts by Dr. Benjamin Greenberg and Dr. Teri Schreiner

CDC guidelines for Treating Acute Flaccid Myelitis

 

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Join the TMA Walk-Run-N-Roll Awareness Campaign in your City!

Help the TMA increase awareness and funds for research and programs, such as our James T. Lubin Fellowship, and our research and education programs.

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TMA Family Camp at The Center for Courageous Kids

We are excited to announce that the dates for the 2015 TMA Family Camp are from July 21 – 25, 2015 at CCK in Scottsville, KY.

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…advocating for those with acute disseminated encephalomyelitis, neuromyelitis optica, optic neuritis and transverse myelitis

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The TMA advocates for those with rare neuro-immunologic disorders of the central nervous system.

Become A Member

Receive our publications, stay informed about your disorder, and stay connected to our community.

How To Help

Help support the TMA in our mission to advocate for those with rare neuroimmunologic disorders.

Our Mission

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Support and advocate for individuals and their families diagnosed with rare neuroimmunologic disorders of the central nervous system by promoting awareness through education and fostering clinician-scientists dedicated to these rare diseases through training and advancing new knowledge through supporting basic science and clinical research.

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