Primary dr, neuro, internist, opthamoligist, and finally the Rhumy who dx me.
Iv lost count of the number of gps, 1 rhumy app that was waited for 12 mths and lasted all of five mins, with go home nothink wrong with yu attatude, i have seen many other specialist when admited to a&e and still it draws a blanc, after given up on the medical professionals, i had a slight car accident and oh and by the way doc i have heat patches on my legs oh you have fibro....seen this gp lots of time so where he pulled this from i dont know..probably the same place he had been speaking out of for the past year!! so after all i did get a dx but only by accident???????
I started with
...... infectious disease doc (coincidence, he was my primary at the time)
......rhuematologist (gave me vioxx for arthritis that I didn't have, I'll never forgive him for that)
........neurologist (made me a topamax zombie, what happens to their brains after med school?).
.....endocronologist (he and a med student stared at my palm for a long time-what were they looking for?)
.......OB/GYN (included only because every year told her all my symptoms)
finally my non-medical friend suggested I go to her rhuematologist. He ran tests (a new experience for me) and made the diagnosis after two appts.
I was fortunate as I was diagnosed immediately after seeing a Neurologist in 2001. My insurance covers FM and that truly helps. My insurance that I have had since October 08 also just recently sent me a letter to call if I wanted to set up this Care Essentials program where a nurse manager will contact me regularly and coordinate with my doctors as well. Haven't started this process yet but it sounds like something beneficial.
I was one of the lucky ones. My Primary doctor sent me to a Rhuematologist because I also have Raynauds. The Rhuematologist diagnosed me after a couple of visits.
19 if I count right, and I haven't been officially diagnosed yet. That doesn't include urgent care and ER docs. Of course, at least half of those docs I wouldn't expect them to give me a diagnosis but the visits were symptom-related to everything I have dealt with.
I have been to so many doctors for the last 3 years and it wasn't until my pulmonologist asked me what were my main symptoms and when I told him, that if I could, I would stay in bed all day and sleep, that he sent me for blood work. I told ALL my doctors that, including my primary, my gyn, my gastro, cardio and pulmonologist. due to insurance reasons, I have a new primary. I think she would have listened initially. all my other doctors give me a pat on the head and say everyone is bloated and tired. Well, my bloating make me look 7 months pregnant and I am exhausted beyond belief. That is such a pet peeve of mine. I am 51 years old. I KNOW my body and when I say it is new or not normal for ME, they should pay attention. Ok, done ranting LOL
I was very fortunate as far as my doctors are concerned. I went to my internist/primary doc and he started the ball rolling. He then sent me to my Rheumy and he took over. They both are firm believers of Fibro/CFS and I was so happy that I wasn't going to have to search Houston all over to find a doctor. Our insurance covers all aspects of this disease. So I have been very fortunate since I became ill.
gentle hugs
Angel
10-15 ---- this is why I'm telling my health insurance company that they need to add fibromyalgia, CFS and lyme practitioners on their website ! It would save them a TON of $$$$$ too.