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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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Junior Member
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Nope, no ACE inhibitors.
So, I'm not sure what to think or do. Today is horrible! My whole body burns! Thank you for any input. I'm a mystery! ![]()
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Kymmie67 |
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#2 | |||
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Member
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Certain narcotic medications can put hot spots on your body. If that doesn't apply to you, I apologize. RSD in general gives me hot flashes/hot spots. Face included.
As long as the sensitivity stays away, you should be ok. Prickly skin, the tingly/electric feeling coming on in an area is a sad sign of spread
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Synthetic right hamate hook. Rsd type 2 |
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#3 | |||
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Junior Member
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Well, I am taking methodone every twelve hours and Percocet for breakthrough pain. I'm sure, between the two of them, I'll get my fair share of hotspots!
Today, however, it's not just hotspots all over my body. As you were describing spread, Morgan, I realized that I'm feeling only the hotspots in certain areas....but others, like the tops of my feet....have started to be sensitive and tingly/prickly. Oh dear! Just what I don't need! Thank you!
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Kymmie67 |
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#4 | ||
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Senior Member
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Kymmie,
Breathe girl, don't let this danged thing panic you ![]() ![]() My CRPS started in my left knee after a minor op, and stayed there for about 10 months. Then I started getting symptoms in the toes of my left foot. It gradually spread to my whole foot and ankle, and up my thigh to my buttock. I also have it in the first two toes of my right foot now, and that scares me witless. In the last three months I have been having symptoms in my left arm, not awful, but in that insidious way it seems to work. One day you think it's ok, the next omg its bad and you can't ignore it. Sometimes I think I'm going a bit crazy. I've also had electric shock pains over my whole body, including my face, and I quite often have flushes on the left side of my face, normally in the morning. The left side of my face often feels as though I have slight sunburn. I am at the moment having problems with body temp, sometimes I feel freezing and shiver, other times I feel burning hot...and it can change within a minute. I get tingles, prickles and little stabby pains all over me at random times. More on those bad days of course. I've done a lot of reading about this thing, like most of us I think lol, and CRPS can affect so many things.... I'm convinced this type of stuff is the CRPS playing nasty little games. The only way I can deal with this stuff is by trying to pretend its not happening and distract myself and my body. It does settle in the end. I don't think it means your CRPS spreading everywhere. Really good luck, it is scary sometimes, and it's tricky to try and get on with life when things like this are going on and you feel anything but normal. You're not alone with this, and I hope it calms down for you soon. Bram. Last edited by Brambledog; 03-21-2013 at 12:21 PM. Reason: Forgot a bit! |
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"Thanks for this!" says: | reluctant@thetable (03-21-2013) |
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#5 | |||
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Junior Member
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Bram....you are totally and completely describing me exactly! That is kind of scary!
I am almost positive it all has something to do with this CRPS. At times I am pretty calm and have the "whatever will be, will be" attitude and other times I'm scared out of my skin!(oh how I wish that were true sometimes!😁 ![]() But, I am in line for a spine stimulator, the trial worked well for me. So, hopefully that helps with other parts of my body and not just the right leg that the trial covered. I have to be somewhere all dressed up (difficult all by itself), in a room where it would be completely conspicuous to get up and leave, and sitting....not up and down, but in a sit up type chair. How am I going to deal with that? I am burning all over today. I don't like this one little bit! Thanks for the words of wisdom....gotta run.
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Kymmie67 |
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