Fibromyalgia Support Group
You're not alone in your pain. Fibromyalgia is a condition that can be difficult to diagnose and manage. If you're trying to cope with pain throughout your body, sleep problems, general fatigue, or other common fibromyalgia symptoms, you're in the right place. The community is here for you to talk about therapies and share your challenges.
What I learned in my Nolo's Book for Social Security Disability is that if one has a chronic pain problem that is not listed on their schedule of impairments (is FMS by now? ) then they can't approve you for it. But, if you have a chronic pain condition and you are in constant treatment for it as it is an ongoing problem, they have to consider it - or should consider it.
Did you have a lawyer?
My advice is to keep your claim active, do what you can with work and keep getting treatment. If it is shown you cannot hold on to or keep pace at a regular full-time job, they will either help you with services to find the right job or consider you disabled. But unfortunately, you will have to a hearing at this point, which could be beneficial to you whichever way it goes.
If they won't approve you, then ask to be referred to voc rehab services. I am going myself because I don't like being disabled and struggling at a part-time job from home that doesn't exactly make the best use of my real abilities.
Yoga has been helping me greatly but I still have big energy crashes and my mental disabilities have gotten worse over time so if I am not hit with pain and fatigue, I'm hit with periods of profound mental depression. But I'm working at getting as well as possible.
I need to be able to make more money in life and on SSDI, I am only able to make so much extra and it's not enough. I want a career again.
Good luck to you! Keep going for treatment and if you develop depression or already have, go get treated for that as well.
I simply cannot keep the same pace as everyone else I know. I thought I was doing okay for a few days but then suddenly I had a fatigue crash and ended up on the couch for three days. For what it's worth, my brain just shuts down at times and I am sure the FMS and the meds have something to do with that.