My visit to my PCP this week was a wash for lots of reasons. It is seriously time for me to move on. I am now on the waiting list to see a PCP who has experience with mindbody medicine as well as (supposedly) fibromyalgia and CFS/ME, but there are 80 people on the waiting list.
I did manage to find a clinic (3 hours away :banghead:) that takes my insurance and specializes in treating people with chronic illness using "integrated medicine" which is a catch-all term for mind body understanding. I had my first appointment on Wednesday. I liked the nurse and the place, but I'm still not sure they will actually be helpful to me (neither they nor my PCP was willing to do the assessment for orthostatic intolerance, which hugely frustrated me as it is so simple, but of course it takes time). I know I have this issue and that it is related to all my other issues, but I do not have an "official" diagnosis from an MD. Same goes for CFS/ME. Anyway, they took a dozen tubes of blood--retesting for many of the things I have been tested on before :sour:, but a few new ones that measure hormones. They seem convinced they will "find something"--I kind of doubt it, but it is my only recourse at the moment.
I need these diagnoses so that I can access the appropriate treatments for them. The treatments for fibromyalgia have just made me worse--the anti-depressants exacerbate my PTSD symptoms, and the exercise exacerbates the chronic fatigue. Can you hear me screaming? :arghh;. I want to :dead:. But I will not. Not yet. Not until I am certain that I am unable to get better than I am physically right now.
Now, to add insult to injury, my disability insurance company is requiring that I undergo a functional assessment with a physical therapist because my physician did not bother to write a letter telling them that I am not fit to return to full-time work. This assessment, of course, spells disaster because these tests are designed to assess physical injury or predictable and measurable physical issues--not chronic illnesses such as fibromyalgia or CFS/ME. I can never guarantee how physically functional I will be on any day or at any given time, but I am still pretty strong physically and can power through things when I need to--the crash comes later. Which, of course, will not get documented. :banghead::arghh;:banghead::banghead::banghead:. I won't lose my government benefits, thankfully, in any near-term time. But the small monthly income I get from my private insurance policy from my past employment is still a big deal thing to lose. And the terrible invalidation I feel is not helping my psychological state at all. But I am fighting back as best I can. Unusual for me, but it is just so wrong.
It's a rather new experience for me, feeling a righteous anger on my own behalf! Testimony, perhaps, to four years of psychotherapy.