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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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Ok.. for the past few weeks to mos my joints have been getting steadily worse and I dont know if its my RSD spreading of something else..so thats where i need your guys' help!!
Soo here are my symptoms... I have joint swelling in fingers nad wrists so i can even make a fist , hurts to move my wrist. i cant barley ring out my hair after i get out of the shower Elbows kill with joint pain and my good foot (i have RSD in my right foot and ankle and leg) i have nasty swelling where it looks like i have a belly roll that comes from the leg and hits the top o my foot. not too bad but i notice it and never was there bfore and that foot kills me even after walking around the house!! My back has kicked in too so i cant even twist around to put sometihn be hind me and my knee is swollen too and i cant barely bend it to get it out of the shower and drags over the top of the tub bc i cant get it up and thats also new.. and it also kills me with pain. Now all this is all new and cant remember what it was like when the RSD set into my right foot and leg bc its been 5 years and now im just used to that pain in there but now that its in other areas.. its acutally makin me cry at nite and during the day i find my self not using my hands alot bc it does hurt... I dont want to jump to that all this is RSD spraeading and going full body and i havent called my PM yet either but this is just drivnin me nuts and not sure if i shold go to my PM or my pcp?? i havent done anything that would trigger this like pulled my back out or carried to much or anythng stupid.. its just steadily getting worse ... HELP! What was it like for you all when it spread and or went full body on you?? Ok gotta stop.. my fingers are telling me to stop and take a rest... Ohh yea.. my pain meds dont even take this away either so that makes me think it is RSD..?? grrr Thanks guys!! I appreciate it sooo much! ![]() ![]() |
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#2 | |||
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Magnate
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My thought would to see your PCP and have him send you to an othopedic Dr. to see if you might have pinched nerves in your hands and arms. It could be something such as Carpal, cubital, radial, ulner or triggerfinger syndrome going on. I have all of these along with RSD and it's hard to tell them apart. I knew when I had rotator cuff problems besides the RSD. Since I hurt my middle finger last week, I have no doubt I have problems in the palm of my hand which most likely is the triggerfinger syndrome coming back alive. I had shots a year ago but with this injury, I have some of it going again.
Also, you could have arthritis setting into your back, hips and knees. I would have all of this checked out before I came to the conclusion of the RSD spread. It is possible but if you just treat the RSD then you aren't going to be able to calm down anything else. With the nerve impingments, I can tell you right now, the meds aren't going to do a damn thing for the pain from them either. I have delt with that all week from this finger I messed up. it could be arthritis setting up in your fingers also. With injuries this happens. I hope you start feeling better and get some answers soon. Ada |
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#3 | |||
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Hi,
I have full body RSD and it spread full body over a 6 month period from when the RSD started. I reckon it is worth making appointments with both the PCP and the PM doctors - as if you are crying from pain during the day and waking crying at night then it's definetly worth getting it sorted out!!! I agree with Ada (and you!) that you shouldn't jump to the conclusion that it is RSD - it could be other auto immune issues, or an infection or all sorts of things. When mine spread I would literally get aches for two or three days and then BAM! black leg, agony, couldn't stand anything or anyone near me or touching me, shaking, etc etc etc Do you use crutches? Just if you do it could be nerve damage from using crutches. I know several people who have had similar symptoms and it's because of overusing crutches and the other leg. Really hope that you get some relief soon and that it isn't RSD!! Love and pain free hugs Frogga xxxxxxx |
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#4 | ||
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Member
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Amber,
The first symptoms I had before the spreading to each new area was muscle spasms and cramping. Then the symptoms would spread to that area: color/ temp changes, PAIN, hair loss, nail changes, etc... Also, I had the spreading to each new area a few weeks apart. So every few weeks the symptoms and PAIN would spread... ugh!! It stinks having it full body... sounds like it could me going that route for you! ![]() You are in my thoughts and prayers!! I hope things start looking up soon!! ((hugs)) ![]() ![]() |
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#5 | |||
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Member
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Hi Amber!
I had carpal tunnal surgery and got this demon ![]() ![]() ![]() ![]() ![]()
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I Will Always Believe in Poems, Prayers And Promises Love, Desi . |
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#6 | |||
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Co-Administrator
Community Support Team
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When you mentioned joint pains - It made me wonder about rheumatoid arthritis?? I would for sure get an appt to have this checked out.
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Search the NeuroTalk forums - . |
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#7 | ||
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Junior Member
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Hi.
I have had CRPS in my left leg since 2003. I developed arthritis in my right knee in 2005. Recently my hands, fingers and wrists have become very painful and during my doctor visit a couple of weeks ago he confirmed my suspicion that arthritis has likely attacked these joints now. Arthritis causes a lot of pain and swelling. I am considered young to have this disease and it is not part of my family's medical history. I have an xray appointment coming up. I don't know if there is a connection between these two illnesses, but there is no doubt that I am afflicted by arthritis. I too suffer from low back and hip pain. I also have difficulty with raising my arms above my head. Showering is really hard and sometimes I have to wait for my hubby to help me because I just can't do it myself. I hate this. I was dx with myofascial pain syndrome (by the pain specialist) last year. Resting my arms and massage are the only things that have helped resolve some of the pain and mobility problems. Take care, Miss Irie Last edited by miss irie; 07-16-2007 at 02:02 AM. |
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#8 | |||
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Member
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Thanks for all the replies.. I cant get in to my PM .. or rather his frreekin secratary is being a ..... and not doing her job.. have to call his nurse and tattle on her .. yet again.. any hows
I got in to see my PCP today and he said that its not RSD spreading .. that he thinks right now.. which is good.. but then it can be one of 3 things... my thyroid is back outta wack, or Rhumatoid arthritis, or lupus. Its so bad that he can see the swelling in my face... which i noticed too,.. but its been there awhile so he thinks that the likely choice is gonna be RA or lupus.. Im already on a strong thyroid pill so it doesnt make sense... SO i have to have bld work done on thurs morning and then i will have to wait to prob mond. mornig or soo. He said that he cant treat me with out knowing what it is .. so i have to go on all blown up .. hahahh Its soo bad that when he walked into the room and instantly said who put you on the steroids bc my face is soo puffy... Im not on any either sooo.. And he would notice too bc i was his nurse for 7 years before i got this soo.. Ok.. i have to stop but wnated to give ya alll an update.. thanks again!! ~Amber |
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