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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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#1 | ||
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Hi Karma. I'm a newbie too. I developed CRPS following surgery in Dec 2012. I am sorry you have had such a tough time with doctors. I was really lucky because my surgeon recognised it right away and referred me to an experienced pain specialist. I am still seeing both of them along with a physiotherapist.
I'm in London so I don't know of any doctors in your area. Sadly, there are lots of people on here who have been dealing with this disease for a very long time and I'm sure they will have plenty of helpful advice for you. I'm still trying to figure this thing out myself. One thing I have figured out, though, is that the people on here are wonderful. Their support is priceless. |
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Senior Member
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Hi Karma, welcome
![]() ![]() I'm UK as well, and always feel so sorry for you folks dealing with insurance companies and workman's comp on top of dealing with this horrible condition, which alone is another to drive us all a bit loopy. Sadly, it's not easy for any of us to find a good doctor that is willing to both work with us, and learn themselves to understand a condition very few really know about. It's a rough time finding someone, but it will be worth the fight, so keep at it until you can feel more confident with someone on your side. Good luck wi the search. I'm sorry you're feeling so rough, I would say that after feeling really crappy for the first 4-6 months with this, I did very slowly start to feel a bit more human again. A lot is to do with learning to cope better with the things it throws at you, but also I think the disease settles down a bit after initially going berserk. I have good and bad patches now, but more good at the moment. I hope yours eases off a bit, must be a frightening time. The sweating/body temp issues are fairly common I suspect. I don't deal well with heat or cold now.. Brain issues are also common, there is a thread at the moment discussing the weird things that go on for many of us - slurring speech, not being able to find words, losing focus, all manner of frustrating and scary things. Hang in there and keep believing that you can find a way through this to a full life again ![]() Best of luck, Bram.
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CRPS started in left knee after op in Aug. 2011 Spread to entire left leg and foot, left arm, right foot. Coeliac since 2007. Patella femoral arthritis both knees. Keep smiling! . |
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