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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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So I watched the movie 50/50 this weekend and thought to myself how wonderful would it be to have a “center” or a place to go and be treated that was solely dedicated to treating patients with RSD. I guess there is at least one in FL, but that might as well be half way around the world, for me anyway. Heck it would just be nice to find doctors who know about RSD.
(Here comes the rant…) So I have been without health insurance for about 20 months now. I have been self-employed for nearly 10 years and could no longer swing the premiums. I have become a part of a broken system. My husband was recently offered a job (after months of looking) that offers health insurance. I should be REAL excited about this… right?! And I was until I saw the nearly $11k per year premiums ![]() ![]() Let’s assume the premiums etc, were not a problem, there is still the problem of having to shop for a doctor that will work with me and do his or her best to try and help me. My condition was very bad when I was first Dx, then kind of plateaued for many years with slowed deterioration. The disease in recent years has advanced, and I am now desperate for the new health insurance just to try and keep pain under control so perhaps I can keep moving as much as possible, as to avoid a wheelchair. Well that’s it really, was just daydreaming about a WAY different scenario. Thanks for letting me share my random thoughts. ![]() |
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