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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Old 05-03-2015, 05:15 PM #11
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Originally Posted by pathfinderjd View Post
Hello. I am new here. I have been stalking this forum off and on for months now. I come. I read. Somtimes I leave inspired. Some times I leave in tears. Knowing we are not alone brings happiness and sadness. I am happy to have a community to fall on. But so heartbroken that anyone has to deal with this.... I have a 10 year old daughter who has had CRPS for 8 month, 2 weeks....not that we are coounting. ;-) We have seen othro, pain, PCP, osteopath, accupuncturist, OT, PT... I think that covers it. We now homeschool. She has been on steroids, gabapentin, and pain medication. For the first 10 weeks, she did not sleep. The gabapentin did give her some help with that. However, over time it became clear the side effects were not worth that benefit. Nothing else seems to help. The first PT folks we saw were with a children's hospital. I expected great things. They told her it was all in her head and to stop "burdening" me with the fake pain. So, I lost it on them and we left. The ortho and the accupucturist both told us they could do nothing else for us. Ortho sent us to a surgeon. I cancelled that appointment. Did research and decided that was of no use. Saw a new doctor. He had the audacity to tell her she would live with this forever. So, now she is depressed. Getting OT now. Was getting it 3 times a week. Saw improvement. But insurance will not cover that much. Now down to 1 time a week and that seems to be making it flare back up. Other kids her age don't undertsand, so she is isolated. Pain seems to be getting worse. Cries herslef to sleep at night. We are working on getting in to an inpatient rehab program. (Looking forward to fighting with the insurance on that one. NOT!) Looking into options for CBD oil. Cannot find a safe, monitored place to get it for a child. Anyone have anything to share in this area? Willing to travel within continental US. We are currently in the southeast US. We are a stronger family than we were 8 months ago...but man life is so different. There are things I took for granted.
Hi, I'm so sorry you & your daughter are going through this! It's hard enough at my age, I just can't even imagine at hers, or worse, it being my daughter. Oh, I'm so sorry. The good news is, children have the best remission rates.

I'm not sure where in the SE you are, but there are two absolutely amazing dr's in FL. I haven't been to either personally, I'm in NJ, but I am very active in support groups and have heard nothing but rave reviews. There's also a great Dr in MA, and of coarse, my Dr in South Jersey.

Finding the right therapist is so very difficult (sorry). It's taken me 2 years. Of coarse I'm note driving the extra distance to the one my dr recommends. What a HUGE difference! His philosophy is "no extra pain" & he's teaching me to control the pain & work worth it instead of against it. My dr kept saying ours not like normal therapy, the whole "push through the pain", nope, uh uh. So, just a suggestion, look for that philosophy & ask around... Interview. It's your money.
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