I am probably like many of you at my wits end with Doctors. My Doctor GP does not seem very knowledgeable although he does listen and try to help me with my symptoms. I would like to find a Dr. that has the most up to date information as well as knowledge and experience. I live in NY and there is a center in CT. I know they do not take insurance as well we all know how horrible insurance companies are nowadays. I have been to many Dr.s it seems they give me the old learn to live and bear it speech. Fibro fog cutting me off since I have a child calling for me and one climbing on me. Any good or bad stories please share. Where have you found most of your support medically.
Thank you.
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Permalink Reply by PVB Sandy on May 1, 2012 at 10:20pm
Permalink Reply by Tori on July 31, 2010 at 9:33pm
Permalink Reply by Tori on July 31, 2010 at 9:34pm Please don't waste your time and money on this clinic! I went to the FIbro and Fatigue Center in Atlanta, GA for a year and spent about $10,000 and saw no improvement! I got a friend to join after I started and unfortunately she got sicker and sicker. We both did the full treatment, vitamins, herbs, IV's with numerous ingredients, antibiotics, antivirals and hormones. Most doctors agree that their protocol is DANGEROUS! My friend ended up hospitalized with her hormones out of whack. They treat everyone's thyroid and prescribe cortisol for everyone. It permantly damaged my friends thyroid when it was normal before going to the clinic. They are very understanding and compassionate and that's what reels us in. I've never felt validated by a doctor until I went there. Trust me, it wasn't worth it. They're getting rich promising things they can't deliver. They told my friend and myself and had it in there literature that they had a 98% cure rate. They have since been sued and no longer tell that lie. I don't know anyone who got better while I was there.
Permalink Reply by Lynn on August 1, 2010 at 7:32am
Permalink Reply by Cindy Lou on June 11, 2011 at 11:48am Cindy Lou,
Sorry to hear about the fatigue. I have fatigue but it's not CFS. It is one of the worst symptoms.
I really think it is worth it and was not a waste of time trying the various things you have done. Since we each respond differently, we each have to be our own laboratory for experimentation.
I found out a few months ago that my fibromyalgia is caused by dysautonomia. It is a dysfunctional autonomic nervous system.
Not everyone with fibro has that but many do. There is a lot of research being done on it now in clinics around the US and around the world. Vanderbilt is one that is doing a lot of research.
I wrote up some information on my experience with dysautonomia. http://www.debdrake.com/dysautonomia.html
Tachycardia, blacking out when standing up, cold hands and feet, hot hands and feet, a mitral valve prolapse, blood pooling in the legs, over-reactions to stimulants... here's a list of symptoms: http://www.dinet.org/symptoms.htm
It may not fit your situation but since I found out about it everything makes so much more sense.
Deb
Permalink Reply by James Lee Barnes on July 29, 2011 at 12:35pm
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