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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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Hi all,
I had meniscus repair surgery on 12/20 of last year. Im going through really bad pain and have been for awhile . Im taking upwards 4 1/2 750 Vicodin a day just to take the edge off. This is a work comp injury so I have to jump through hoops to get the right treatment. My current surgeon hasnt examined me once post injury and said that an injury received to my other knee was nothing and I was fine. So I took my xrays to another surgeon on my own insurance since work comp denied it and she said that I have dislocated my knee and my current dr must not have looked at my xrays. Anywho--she also looked at my left leg (surgical leg) and said it looks like i have RSD and that I should change drs asap. So Im in the process of changing drs, but because its work comp it takes forever! I thought I would post my pic to show the redness in my knee and the edema that abrubtly cuts off on the side, which ive read is a symptom of rsd. Here are my symptoms: Pain, deep aching pain, occasionally burning, but mostly deep throbbing, aching Pain especially bad when i move my leg or walk Redness in knee, leg seems a different color than normal leg toes are red and foot turns purple-even though i dont have much pain in my foot my pinky toe is curling in and i feel it contracting occasionaly swelling that doesnt go away stiff leg, wants to stay in one position cant walk without pain insomnia, forgetfullness depression I think thats it, but of course ive been super forgetful lately, maybe the pain meds. Feel free to take a look at my pic, bad lighting i know, but at least notice the swelling. Im now over 3 months post-op. I appreciate any input, opinions and suggestions.. I know RSD is a tough diagnosis and it seems most drs ive seen arent even looking for it, especially on work comp. Thanks all! Shan |
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#2 | |||
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Member
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Well, just to get the stuff said, we're of course not doctors here and anything we say is, of course, only our opionion based on what you've said. :-)
So, the swelling,color change,pain and burning are a part of rsd for sure. Have you noticed any temp change to the leg? Is the skin cold or hot? It can be either one and I've known some who it goes from cold to hot and back again. Work comp is definitely a big pain. I was there in 03, but thankfully settled and haven't had to deal with them anymore. There are many docs who have no clue what it is and, speaking from experience, work comp docs don't want to make that diagnosis because work comp will then begin to get nasty. My one and best piece of advice, be ready to get a lawyer!! In Florida, if work comp denies you even one little thing or doesn't pay you then a lawyer will take your case. In arizona I believe, work comp has to actually close your case on you completely before a lawyer will take you on. It would be worth finding out when lawyers in your state takes cases. I feel your pain and understand how wc does things. As far as I know, with wc lawyers you need no money up front or anything. They work your case and take their money out of your settlement with wc. As for you personally, do NOT use ice. It makes the pain worse with rsd and further constricts the blood vessels in the limb which is why we get color changes like that and temp changes to the skin. Your body still thinks it's injured. Physical Therapy will hopefully be forthcoming if you can get a doc. In the meantime, use the leg, don't baby it. At the same time, you need to take it slow and not overdo anything that would cause even more pain than you have now. I know...it's a hard balance to find. The saying for us RSD'ers is........If you don't use it, you WILL lose it! I'm figuring the contracture of your one toe is due to muscle spasms. I haven't had to deal with contractures so not entirely sure of the why. If you have any questions, feel free to ask. There is no such thing as a stupid question around here, only smart ones! ![]() Hugs, Karen
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Laugh until you cry, don't cry until you laugh. Living, loving and laughing with RSD for 14 years and counting. |
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#3 | ||
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Junior Member
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Oh yes, there is temp changes-forgot to add. Umm, sometimes my knee is cold and then other times its hot and sometimes its in between. It changes often. My foot does stay ice cold all the time, but my knee changes up. I recently got a work comp attorney, right after going to another dr on my own insurance and her "off the record" diagnosis of RSD. Now I just have to see if the work comp dr gets it tomorrow. Of course I hope to god it could be something else, but after hearing it from one dr and matching up my symptoms, it just makes sense. Therefore, I want to get this thing treated now, not 5 months from now in Work Comp time. But we will see, hopefully this physical medicine dr can give me some answers tomrrow.
I have been trying to keep up with my home exercises after work comp denied any more therapy for my leg-Agh they are crazy! I posted a pic in hopes that someone could see something that was something they had, as in a symptom, so that I would feel less crazy. Thanks so much for your support, I will keep you updated! Shannon |
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#4 | |||
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Elder
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www.rsds.org
Complex Regional Pain Syndrome (CRPS), also known as Reflex Sympathetic Dystrophy, is a chronic neurological syndrome characterized by:
Complex Regional Pain Syndrome Type I (RSD)
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My avatar pic is my beautiful niece Ashley! . Rest in Peace 3/8/90 ~~ 4/2/12
Last edited by Abbie; 03-23-2008 at 10:55 PM. Reason: taking wierd stuff out that somehow got in there... ??? |
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#5 | ||
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Junior Member
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First and foremost i am so sry for what u r going thru dear! i can tell you that what your knee looks like is what my whole left leg and hip looks like. And what Galena said is all i wood say 2 she took all the owrds rite oit of my mouth after i read your story i mean i didnt have work comp but i have had plenty of ppl in my life that have. I really hope you keep posting love 2 hear bout where this goes and how u r doing. I wish u all the luck there is and lots of pain free days!
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*~STACIE~* . |
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#6 | ||
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Junior Member
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Thank you all so much for your words of wisdom and support. I saw the physical medicine dr today and she said she wasnt sure if it was rsd because i dont have the barely touch pain, or pain when she barely blew on my leg. But Ive got the bad pain, especially over my incision site and below it. My foot turned a deep red while i was in there and she seemed torn over rsd and leaned more towards sapheanous sp? nerve injury from surgery. After reading everything about rsd and the swelling that stops abrubtly, im pretty sure rsd is the culprit, but of course im no dr, so who knows. She did prescribe me lyrica and she is looking to get me an mri and a tens unit for the pain.
Can rsd be diagnosed if you dont have the hypersensitivity to clothing or air blowing on your skin? I have the pain when she touched, moved, and examined, but she was unsure about the rsd.. well, at least with the nerve pain meds I know i am on the right track. .. Even if it turns out i get the dx rsd a little later than expected. Any thoughts? Thanks much Shannon |
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#7 | ||
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Member
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you do not have to have ALL the symptoms of RSD to have it.
I have been diagnosed with RSD by many docs, including at the Cleveland Clinic. I do not have sensitivity to wind, or light touch. I can wear **most** clothing. But let someone pat me on the arm or hug me, and I am miserable. Especially if I don't see it coming - such as someone coming up behind me and touching me. I also do not have the sensation of sunburn, or what I would call burning pain. I am sensitive to cold though. I can't hold a cold soda in the hand on the affected side. If I get chilled, my pain skyrockets. I have many other symptoms of it - skin shiny and red, fast growing ridged nails, hair changes on affected limbs, swelling, joint stiffness (my shoulder has been mostly frozen for close to 3 years now) EXTREME pain, lots of muscle spasms, temperature changes, etc etc This lack of sensitivity kept me from being diagnosed when RSD first hit my foot in 2001. Now, it's in my arm, shoulder etc. and I have gone to Dr.'s who knew more about RSD and recognized it as RSD. They tell me I may develop the sensitivity at any time. I am hoping you do not have RSD. |
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#8 | ||
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Junior Member
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Quote:
I'm a little late to this thread. My husband also developed rsd after a medial menisectomy in 6/05. He does not have the sensitivity to touch either. Never had it. Does have pain, redness and temperature changes. He started taking neurontin which helped immediately. Most of the pain management docs he's seen believe he has rsd. Dr. Oaklander, in Boston, however thought it was more likely the saphenous nerve. I wish you luck in finding a combination of treatment that helps you get your life back to functioning and pain free. |
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#9 | ||
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New Member
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I live in Iowa I had to be an idiot to move here , the med drs here are like
glorified vets, its rediculious and the arrogance is unbelieveable dont get me wrong im sure there are great docs somewhere in Iowa i just havent found any i used to live in mn and the docs there really know their stuff all i can recommend is get a doc that knows rsd and works with it on a regular basis, then you know your getting the best care ,as for me im moving back to mn, when i took myself to the docs here they acted confused & just scratched their heads , there is more than just taking pain meds all your life there has to be signed december |
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#10 | ||
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Junior Member
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December, sorry that you have to go through putting up with stupid drs. There must be more than taking pain pills and acting like a zombie all day, right? I would hope so for gods sake. Its getting old, however, I believe I have a life long left of pain pill taking.
Shan |
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