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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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#21 | ||
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Magnate
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Mike,
I also still respond to steroid packs. I can get 3 or 4 really good days (when I'm at the highest dosages) so I use them as part of my bag of tricks for flares and travel. Is this another case of them only working for certain RSDers? Certain types or length of onset, etc. I'm only able to do 3 cycles of steroids or so per year. I remember coming across something you wrote about a longer course of steroids and meant to do more research and then forgot all about it... Memory issues of course. If you have any new info on either the longer course or just using in the regular way, it would be appreciated. I'll do a search on your old post when I'm having a good day! ![]() I didn't mean to imply anyone could undergo blocks to the same area for months or years on end. Even though I was getting relief, my doc said that scar tissue would build up after a short while. (Another reason to make sure you're getting the best block available, they aren't all equal IMHO...) I think I maybe had 4 with him, and since it was clearly only giving me short term relief he stopped. Perhaps even when responsive, after a certain period, remission is just not possible--hardwiring of the spine, etc. That being said, it seems unfair to not be given the chance for remission, even if the chance is slight, even if someone is 2 years post onset. ![]() |
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#22 | |||
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Junior Member
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Wow...I don't know where to start, I think just giving you a BIG hug Mike. Thank you so much for all of your input and knowledge. I am super frustrated with just about everything having to do with my RSD right now. I am going to call my PM doc today and make an appt to see him and talk about not doing more blocks and changing my new ER type pain meds. The ER pain meds he just put me on are making my heart race and pretty much put me in a coma like state. So, along with the blocks not working I am also having major issues with my pain meds. Sheesh...but, I do have a wonderful support system (my husband, Lit Love, and my family.) Again, thank you so very much for taking so much time to help me and give me clear answers to all my questions. Really can't thank you enough for listening and giving me such fantastic input.
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"Thanks for this!" says: | fmichael (10-04-2011) |
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#23 | |||
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Junior Member
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#24 | |||
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Member
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Were these just diagnostic blocks? They usually don't last long.
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#25 | ||
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Quote:
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"Thanks for this!" says: | fmichael (10-04-2011) |
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#26 | |||
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Member
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Sometimes, depending on what was in the injection, it can take 3-5 days for you to feel the full effect. Some have lidocaine which you would notice right away, and depo-medrol which would take longer for you to notice the results. I am always told to go home and put the heating pad on my injection site, and not do any thing strenuous for 36 hrs or so.
Hope you are feeling better.
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"Thanks for this!" says: | Karen67 (10-05-2011) |
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