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Federal Funding for the study for a cure for the rare disease of NMO. Doctors are "flying by the seat of their pants" on this one. Basically they treat it with Chemo therapy periodically to kill the bad cells when they return which in my family is about every 9 months. This is not the answer for this very painful disease which paralyzed my family member and while their have been some gains in use of arms, the patient still cannot walk and it has been three years.

Submitted by None in Health Dec. 11, 2014, 12:58 a.m.
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#1946
45 votes

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