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 03-26-2013, 07:50 AM #1
Brambledog Brambledog is offline
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Join Date: Jul 2012
Location: England
Posts: 1,122
10 yr Member
Brambledog Brambledog is offline
Senior Member
 
Join Date: Jul 2012
Location: England
Posts: 1,122
10 yr Member
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Hi,

What Kymmie says is so true. My story is sort of similar to hers - I had a simple knee scope almost two years ago, they found acute PF osteo-arthritis, did the shaving and biopsies etc and closed up. I had terrible pain when I woke, no one understood why, I kept being told I shouldn't be in so much pain... After I had morphine things stabilised a bit and I went home after 3 days instead of my day surgery expected.

My initial symptom was pain. Horrible deep pain, no burning or sensitivity. Then after a month or so I noticed the cold skin, then blotchiness came, then heat, and burning and tacky skin, and hair and nail changes etc... My point is that this danged thing is both unpredictable and chaotic - everyone seems to have slightly different symptoms and they can change or be added to with time. There's a chart for CRPS symptoms as an aid to diagnosis, and it's all about fulfilling a criteria from each category - pain and temp changes can be enough for an experienced doc to diagnose it.

Over the almost two years, mine has spread to my foot and whole left leg, and now my left arm is symptomatic too and I have started physio on that as well. Pain, particularly when walking, is the main issue still.

My skin over my knee is still not that sensitive. My docs are always a bit surprised when they ask if they can touch my knee and I just say yeah go for it. But strangely, the skin over my knee almost feels numb now, yet where it spread to my foot, that is super sensitive. Both main areas act differently (my arm is sensitive but no heat yet), but its all CRPS. It's weird and it screws with your head

Get the best doc you can who knows CRPS, and do a lot of reading yourself, so that when you come face to face with that doc, you can tell whether they really know it or not. Always trust your own body and your instincts, and if they make you feel uncomfortable then find someone else who understands. It's worth fighting for that, because you need guidance with this, and fighting in the dark is no joke!

I'm so glad I found this place. You all get it. You know how we feel and we don't think each other is mad....well not much lol.

Take care of yourself, and good luck.

Bram.
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