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Old 10-08-2008, 07:55 AM
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Join Date: Jul 2007
Location: Yorkshire, UK
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ali12 ali12 is offline
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Join Date: Jul 2007
Location: Yorkshire, UK
Posts: 2,463
15 yr Member
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Quote:
Originally Posted by Gymjunkie View Post
So far there has been no suggestion of using any drugs to treat the movement problems I have. I am slightly surprised because Baclofen is the screamingly obvious drug to try here but I have been wholly unimpressed by all of the medical "care" I have had so far so its no great shock!! In spite of all of the problems and the pain, I have gone back to work full-time and I doubt that I could continue in my job if I started to take a drug like Baclofen or diazepam. If I had to choose, I'd rather have my job and remain mentally sharp than try to medicate the movement problems and then struggle to maintain my cognitive abilities.

Unfortunately, I seem to have had the experience of falling into the "too hard" pile for the doctors I have seen and they all know little or nothing about CRPS. Instead of making my case unusual and interesting to them, it has the opposite effect - they can't get rid of me fast enough because it exposes their own limitations!!! I suspect it has been hampered by the fact that my treatment was all done privately initially so I was seeing docs who are more motivated by making extra cash on the side rather than academic or research clinicians who are motivated by seeing interesting cases. I think its also different when children are involved with difficult medical conditions - doctors seem to be more interested and responsive than with adults, especially in a specialist children's hospital like GOSH.

I am seeing a new PM doc soon so it'll be interesting to see what he has to say. The previous one told me that he wasn't aware of CRPS being associated with movement problems so that didn't fill me with much confidence (especially since when I first started to get the thumping great tremor in my right leg, he said that often happened with CRPS and he was confident that it would "go away"!!!). My neuro has never seen or treated CRPS and neither had the orthopaedic surgeon who did the surgery that kicked it all off (and he has just retired in his 60's). Great huh!!?
I really hope that your appointment with your new PM Doctor goes well and that he gives you some answers and is able to treat you. I know how scary it is having Doctor's that don't know what to do or how to treat you.

My Doctors also have No clue on how to treat me, they are basically just trying EVERYTHING they can think of and hoping that something will work eventually. I feel like a guinea pig as everything is "trial and error" and it's "We will try this but it might not work". I think because the Doctors have never seen anything like my condition, they just don't have a clue on what to do that might help. It took me nearly 18 long months to finally find a Doctor who wanted to try and help me. I don't want to be on meds either but I was told that it was the best chance at getting the spasms to reduce.

You are not alone, I also have some of the symptoms you have. Like I said, if you ever want to talk I am here

Alison
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