I have had this pernicious retrovirus for almost 30 years. The first 10 weren't so bad, the last 20 have beena slow ride into total disability. My mother had this awful invisible illness. In the 1970's and on.
I understand the acronym FM/CFS is used recently. And a few people actually know what it means! Not most doctors, though. Some of them still don't believe fibromyalgia is as painful as it is. They have no clue about CFS treatment either.
I try to do everything I need to, but I get less and less done. I believe I've lost IQ points in the last 5 to 10 years. And with the lack of energy comes lack of interest, which makes me a very dull, uninteresting girl.
I'm indoors now due to Covid, which has already carried away a dear loved one. I'm mourning this, and waiting to see what the new president will do about this country, hope it's going to be low-key and effective.
Then a cure for FM/CFS.
.
- Location
-
California
- Reason
- DX FIBRO
- Diagnosis
- 03/1987
- Country
- US
- State
- CA
- City
- pleasant hill
- Occupation
- pain warrior
-
1
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