CFS Patient Advocate

Saturday, November 23, 2013

Mt. Sinai ME/CFS conference – November 20, 2013

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The second conference at the Mt. Sinai ME/CFS Center was held on Wednesday, November 20, 2013. (The first conference was t...
12 comments:
Wednesday, November 13, 2013

Yellow Soup

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There was another fantastic and interesting article on Dr. Alexander Khoruts today. It appears in City Pages, is entitled The Forgotten Org...
Thursday, October 31, 2013

Mount Sinai ME/CFS conference - November 20, 2013

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Dr. Derek Enlander is chairing an ME/CFS treatment conference at Mount Sinai in New York City on Wednesday, November 20, 2013. This one day...
4 comments:
Thursday, October 17, 2013

ILADS/San Diego

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I am heading to San Diego for the ILADS conference on October 18-20. ILADS is a four-day conference on Lyme disease, its diagn...
4 comments:
Wednesday, September 11, 2013

Blue Skies in MN (NK cell function)

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I was pleased to receive the DVD of the Invest in ME conference. The Invest in ME conference was held in London in late May ...
3 comments:
Friday, August 16, 2013

Striker drugs or terrain modulation?

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Here in Minnesota, I try to escape the role of a patient advocate for a few hours and recapture my own reality. Often I go into the ...
7 comments:
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About Me

consuegra
I am the patient advocate of my 40-year-old daughter. She is housebound in St. Paul MN with CFS/ME. This blog presents reports from several lectures or conferences. It also attempts to define, in my own way, the role of a Patient Advocate. The premise is simple. I make my observations in hopes that they might be beneficial to others, in the same spirit of generosity that so many others' comments have been useful to me. These entries are presented for information only purposes. In no way should they be taken as medical advice. I am not a doctor and I do not want to be one.
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