CFS Patient Advocate

Sunday, October 25, 2009

The Abstract and the Real

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All this viral research and treatment is heady stuff, riddled with uncertainly. On a daily basis the Patient Advocate has to deal with much ...
3 comments:
Saturday, October 24, 2009

Lisa Nagy

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When this Patient Advocate was attending the CFS conference in Ft. Lauderdale in 2007, he met a very interesting gal. Her name is Lisa Nagy...
Wednesday, October 21, 2009

Dr. Dale Guyer

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In the pursuit of his daughter's betterment, this Patient Advocate has written about a number of CFS/ME doctors. The PA admires many re...
Wednesday, October 7, 2009

Vegetable Juicing

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The Patient Advocate first learned about the potential benefits of vegetable juicing from the Prohealth Boar d. Rick Carlson wrote a short p...
2 comments:
Thursday, October 1, 2009

Viruses

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Trying to figure out whether viruses are involved in my daughter ’s illness is a nightmare. She came down with this neuro-immune illness fol...
1 comment:
Tuesday, September 29, 2009

Gut Dysbiosis (again)

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At times stories emerge of individuals gaining betterment from one particular treatment. For instance MATN recovered from her illness with a...
4 comments:
Wednesday, September 23, 2009

Dr. Derek Enlander

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Dr. Derek Enlander has a practice in New York City. His office is in midtown NY, on 69th and Fifth Avenue. Dr. Enlander has been treating C...
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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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