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my symptoms have been getting so much worse over the last few months. lately, every other day or so I wake up in enough pain to cry. being in the same position for five or more minutes has become torturous, i have to move and shift constantly, and often i won't even feel how bad it's gotten...

has anyone here managed to get on disability for fibro? or while you're still young? I'm in my mid 20s. I've probably had fibro since I was young, progressing more and more until dx'ed at 19. I've had people straight up tell me I can't have it because I'm too young, I've had so many doctors call...

I've been having trouble feeling like there's any hope for me as someone poor with fibromyalgia from a young age. especially with the american economic climate. i've given up on ever owning a house, leaving the country, going to college, having any sort of career, etc. I'm only 25 but most of...

In the first half of this year I was redoubling my efforts to get on disability. I wanted more records, more concrete proof, and read some advice for people with more visible conditions and mistakenly took it to heart: get a functional capacity test. they measured how much i could move around...

last year i had work exemption for food stamps. this year my doctor decided she "wouldnt lie" and marked that i could work with restrictions- the "restrictions" just being an attached functional capacity report i should've never had done because all it does is show i dont have hard measurable...

I'm 24. I think I've had fibro at least developing since i was 14 - lots of time lost to pain brought on by stress. The symptoms only got worse until I was diagnosed at 19. even though it's a diagnosis of exclusion, and my family's reaction ranged from doubt to mockery, i looked for everything I...