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Anonymous

Hi -- I contracted WNV in 2002 and as it was my experience that there were (and are) long-term sequelae, I've been following the research. There was a study done in North Dakota which interested me and I was able to contact one of the authors. He responded after a couple of weeks. There is a good chance he will have the answers you need. Information / links below.

The question I was trying to get answered - in order to get insurance coverage for it - was whether or not Provigil was actively being used to manage the fatigue of WNV (as it is used for the fatigue of MS). I didn't win the insurance battle, but it remains my experience that Provigil did more for the symptoms than anything else. (Persistent fatigue, word-finding difficulty, depression. My migraines also go MUCH worse for about 18 months then began to resolve back to normal). Anyway ... Contact info / links for Dr. Carson:

JournalWatch Abstract: http://infectious-diseases.jwatch.org/cgi/content/full/2006/913/1

Medline Abstract with Dr. Carson's email address at time of publication: http://www.ncbi.nlm.nih.gov/pubmed/16912946?dopt=Abstract

[email protected]

If you have any useful information to pass back, pls post here - am asking to be notified via em when this post is commented on.

GOOD LUCK to you and your patient. Nice to see an internist asking questions about this !!! Wish more would!

June 8, 2009 - 9:18pm

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