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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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OMG my legs are refusing to work today! Both hips and knees keep locking up with added stabbing pain which sets off a cataplectic reaction and everything goes to Jell-O! Wow you mix RSD and arthritis with narcolepsy/cataplexy and it really sucks!
![]() I should add that I can't walk very well at all. My legs keep trying to buckle and it feels like every muscle in my body starts to spasm. Anyone ever experience that? What do did you do? Last edited by PhyllisJ; 11-14-2012 at 03:48 PM. |
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#2 | |||
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Elder
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I get the jello legs from time to time. Most of the times I've been lucky and have been at home or with friends who have been able to help me.
A couple of years ago, my Pain Doc decided I should use crutches when my jello legs happened right in front of him. I now use forearm crutches when I am outside of the house. My house is to small to use them inside. If I don't use them while walking I pay for it later....because my muscles have to fight to keep me from falling. Doc doesn't know for sure what causes this... only chalks it up to RSD. He has ran many tests and can't find any other reason. I wish you the best. Abbie
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My avatar pic is my beautiful niece Ashley! . Rest in Peace 3/8/90 ~~ 4/2/12
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#3 | ||
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Junior Member
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I've been using a cane since July when the RSD spread all over and attacked all the old injuries in my legs. I can't use crutches because my left hand (original RSD trauma site) doesn't work. Kind of scary stuff today.
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"Thanks for this!" says: | Abbie (11-16-2012) |
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#4 | ||
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Senior Member
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I've had a few falls in the past (thankfully with no big injuries!) with urinary incontinence with "jello legs" in the last few years. It was always when I was standing or walking for a few minutes, without any kind of support. I'm usually pretty sendentary/in the house. If I could catch myself and sit down, at least I didn't pee myself. Sorry if that's tmi folks !
![]() I stated a walking program in April (not suggesting that everyone can do that......I had support stating in March with a cortisone injection to my L hip bursitis, restarting Cymbalta, major increase in narcotic dosages, and the incentive that my mom broke her back/was dx'd with Parkinson's....and I, the family nurse, couldn't do much to help. I had quite a few issues when I started exercising, getting "stuck" when my legs just went to jello/overwhelming pain in both hips and knees (fibro issues, my RSD in L neck/arm). I just sat until I felt better. Had to make sure I had my cell phone with me, so I could call my 75 yo daddy to come rescue me if need be. Now that I'm more in shape (still have a loonnnggg way to go, but I am down 45 pounds and at least have some activity tolerance now), the jello legs happens much less frequently. I do know every rock to sit on and fence to lean on in my neighborhood and in my mom's neighborhood !
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. Gee, this looks like a great place to sit and have a picnic with my yummy bone ! |
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#5 | ||
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Junior Member
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That's great that you're able to walk better!
I keep trying to convince myself that it's "all in my head." LOL But my knees and hips argue the point when I try to walk "normal." Besides the pain, it's like someone put too much WD-40 on them...they almost swivel LOL |
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#6 | |||
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Senior Member
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Quote:
Do you walk with a walker at all? I have a rolling walker and it helps me a LOT with things like this. I have a much better walking gait with the walker than I do without. This was especially helpful when I was doing physical therapy to get walking "normal" again. Might be worth looking into. Without the walker, it would not be safe or possible for me to leave the house, be out in crowds, and away from a comfy couch to sit on. Also good is that the walker has a seat so if I DO need to sit down and rest while out there is always a chair with me. |
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