FAQ/Help |
Calendar |
Search |
Today's Posts |
|
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) |
Reply |
|
Thread Tools | Display Modes |
|
10-22-2012, 07:12 PM | #1 | ||
|
|||
Junior Member
|
Hi, I've had RSD for over a year now, and I am only 17. I have had pain blocks in my spine and been through vigorous PT and medication but nothing helps. I am now using acupuncture weekly to help subside some of the pain, but it never goes away. I can barely walk and do anything by myself. What is my next step?
|
||
Reply With Quote |
10-22-2012, 07:48 PM | #2 | ||
|
|||
Junior Member
|
I have RSD, I am in soo much pain right now, on some websites they say not to use ice on the affected limb, is that true?
|
||
Reply With Quote |
10-22-2012, 08:39 PM | #3 | ||
|
|||
Junior Member
|
People argue about the ice thing. I never use ice because my leg is generally so cold as it is. We did use ice on my leg during PT before knowing I had CRPS.
Are you seeing a pain management doctor? They should be giving you an idea of what steps to follow next. What meds have you tried? I was 17 when diagnosed so I know how devestating this is during your teen years. I felt like my world was crumbling. Please PM me if you ever feel like chatting about that. (I'm 25 now.) |
||
Reply With Quote |
"Thanks for this!" says: | ginnie (10-23-2012) |
10-22-2012, 08:46 PM | #4 | ||
|
|||
Guest
|
No Ice No Hot and cold water contrast therapy.
see picture |
||
Reply With Quote |
10-22-2012, 10:36 PM | #5 | ||
|
|||
Member
|
|
||
Reply With Quote |
10-23-2012, 03:38 PM | #6 | ||
|
|||
Junior Member
|
Yes I am seeing a pain management doctor but not as often as I should due to bills that we can't afford. They have me on tylenol and ultram or vicodin for pain, flexeril for my muscles and voltaron for swelling. *(I know those might now be spelled correct). What really just made everything worse is that the mri showed bruised bone as well, so they want to cast me or i have to be on crutches at all times. I go to college half day and my high school he other half. I don't know how I will manage that.
|
||
Reply With Quote |
10-23-2012, 07:26 PM | #7 | ||
|
|||
Member
|
The only thing i think alot of us do is just try and manage the pain. Unfortantly there is no cure and there is no real treatments for it. Im in my young 20s and its crap, its in both my arms, chest and neck. Im looking into diffrent things that MAYBE i could try. But for the last 4 1/2 yrs its just been a matter of managing my pain the best we can.
|
||
Reply With Quote |
10-25-2012, 12:48 AM | #8 | ||
|
|||
Junior Member
|
Quote:
|
||
Reply With Quote |
12-12-2012, 01:06 AM | #9 | ||
|
|||
Member
|
Quote:
Hope you feel "better" soon |
||
Reply With Quote |
10-25-2012, 03:02 AM | #10 | ||
|
|||
Member
|
Quote:
I've had RSD since I was 14 (I'm now just shy of 21), so I understand where you're coming from. For me, I kind of went down the same path it seems like you described. My RSD started in my right foot, but then it slowly spread to include all of my limbs, trunk, neck, and back. I did a nerve block (ick) and intense PT/OT. The best I can say in what helped me the most were PT and OT. However, I would find a PT/OT place that has successfully dealt with RSD before. It is definitely painful, but since you have age on your side, you may have some success. I was in a day-treatment program for 40 hours per week for about 4 months or so. I did have to go on home-bound with my school because of it, but I went to an in-patient and out-patient facility that had worked with a few RSD patients before. The one who got discharged right before I started had RSD in her left foot and was about 12 or 13 I think...Either way, she went through the same program as well and is now back dancing. Ultimately, I did learn how to walk again, though I definitely wasn't able to return back to gymnastics since it's such a high-impact sport. Sorry, I just realized I rambled a bit...I guess what I'm trying to say is that you should (1) get a general doctor who you trust (on top of the PM doctor) and who is familiar with RSD...I know this might get expensive, but you don't have to see him or her frequently...it's more of a safety precaution so that you know you have a doctor who is familiar with you every step of the way...it also helps in regard to referrals in case you wind up needing one in the future; (2) don't get anymore pain blocks...if it didn't work the first few times, it more than likely won't work in the future; and (3) find a PT/OT place that's successfully dealt with RSD patients. ps: Oh, no on the ice. Definite no. pps: If you ever want to pm, just feel free to send me a message. I had RSD all through high school...I'm now in college and managing RSD on top of that, so I can definitely sympathize with you. |
||
Reply With Quote |
Reply |
|
|
Similar Threads | ||||
Thread | Forum | |||
Neuropathic pain step by step | Peripheral Neuropathy | |||
Lost my step dad ten years ago, today he'd have been 88 | Bipolar Disorder |