CFS Patient Advocate

Patient Advocate

The job of Patient Advocate came upon me uninvited. I did not apply for this job, nor did I have any qualifications for it. I am a sculptor, not a doctor or a researcher. My daughter became sick with a mysterious fatigue illness and I was the obvious person to fill the job. Learning the job of a PA unfolds over time and there is no instruction manual. Certain ideas and thoughts can be transferred from former jobs and former lives, but much has to be learned from scratch. It is helpful in doing the PA job if you have a lot of time and a lot of money, as the solution to this disease takes a great deal of both. It would also be helpful to have an education in bio-chemistry, of which I have none. The most important qualification that a Patient Advocate needs is persistence and discipline. A PA also needs to remain objective and detached, even under the most extreme conditions. Every Patient Advocate has a patient. My patient is my daughter. The objective of this particular Patient Advocate is to make his daughter better. How to set about it is another matter, and turns out to be a complex and sustained set of illusive problems. While most doctors look at a broad and confusing set of symptoms and try to attach treatments to an entire cohort of partially differentiated patients, the PA’s problem is slightly different. The Patient Advocate, by job definition, is obliged to help one person - in this case, his daughter - his patient. Thus the PA is looking at one narrow and confusing set of symptoms, which makes his problem slightly easier.

  • Health Rising
    Did a Lab Study Just Uncover a Craniocervical Instability Subset in ME/CFS?
    5 days ago
  • CFS Remission
    Discussion with a Long COVID patient on using Microbiome Prescription
    1 week ago
  • THE NICEGUIDELINES BLOG
    Care providers use the knowledge gap about ME/CFS as an excuse for indolence
    5 years ago
  • Quixotic: My M.E. Blog
    I'm now treating with Cromolyn for Mast Cell Activation Syndrome
    6 years ago
  • LOOKING AT LYME DISEASE - MSIDS
    SECRET HISTORY OF LYME DISEASE AND A BIOWEAPONS LINK.
    6 years ago
  • Living With Chronic Fatigue Syndrome
    My Experience with Rituximab for ME
    6 years ago
  • The Self-Taught Author
    Which heart rate monitor for ME/CFS?
    7 years ago
  • Onward Through the Fog
    Telebriefing on NIH Research - November 28, 2017
    7 years ago
  • Thoughts About ME
    Standing Up to Coyne and Against Unfair Treatment of ME Advocates
    9 years ago
  • the corner room
    A Move
    12 years ago
  • CFIDS Watch
    MTHFR Resources
    12 years ago
  • Advanced Techniques For Overcoming CFS, FMS and GWS
  • BetterHealthGuy.com: A Site Dedicated to Lyme Disease

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      • Interview with Dr. John Chia
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Christopher Cairns

Christopher Cairns

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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Monday, October 25, 2021

Interview with Dr. John Chia


 

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