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RFA of knee, anyone had one?
Hello, I'm kinda new here. I haven't logged in since 2012 until earlier today. I've enjoyed lurking over the years, but as my RSD has progressed and spread to my left leg and knee after knee surgery in 2014, I'm ready to jump in to help support others, and hopefully find support too.
My RSD spread 48 hours post op, and my pain doc retired shortly after leaving me no one to help. I finally got a new pain mgt dr 5 months later and he's been a huge resource for me! I didn't get my first lumbar block until 6 mo post op. I've had 3 since and they have me great leg coverage, but no knee coverage. I had a diagnostic genicular block in June on my knee and it was successful in covering the nerve pain. I'm scheduled Nov 2rd for my RFA (nerve ablation), and I'm wondering if anyone else has had one? I'd love to hear from others and their experiences. Thanks in advance. |
Welcome!
Hi Redraidermommy,
I have not had a nerve ablation. I just want to say hi and welcome! Warmly, DejaVu |
Hi and Welcome back!
I hope you had a successful procedure and get good pain relief. Let us know how it went. I don't know how many of us have tried a peripheral nerve RFA or might even be a candidate for one (my nerve that is troublesome is too near motor branches). We will all want to know how this works out for you. Hopefully stellar! Sending hugs and healing love, :hug: |
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Yeah! It sounds like it went well. Good to hear you have no nerve pain. I hope it stays quiet!
As we know, ice is no good with CRPS but I find gel packs kept in the fridge instead of the freezer to be nice for swelling. And of course lots of elevation. It might not be a bad idea to hit 500 mg of Vit C daily for a month like you would for a regular surgery. Sending thoughts for quick recovery, :hug: |
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These are rarely done for CRPS since they can actually cause more damage. I'm glad it worked for the OP thus far, but anyone considering the procedure should do lots of research first and get a second opinion by a CRPS specialist.
I had one performed years ago which exacerbated my CRPS significantly and permanently. It's the medical procedure I regret the most after developing CRPS, and I even had surgery in the area of my original CRPS site without complications. http://www.rsdinfo.com/html/crps-sympathectomy.html |
I think it's important to note that I did not have a sympathectomy. A sympathectomy is the permanent surgical cutting of the sympathetic nerve and/ or removal of that nerve, and is not reversible. It is important to differentiate the two so people are not misinformed/miseducated, and that genicular RFA can be a wonderful temporary solution to a very painful problem.
I had a genicular nerve ablation via RFA (radio frequency ablation) on the genicular nerves in my (RSD affected) knee, in the joint. Nothing was cut surgically or removed. Perhaps this can clear the air about my procedure and what was performed. http://strykerivs.com/resources/radiofrequency-ablation http://ainsworthinstitute.com/genicular-neurotomy/ I wanted to post an update, and let everybody know that I'm about 80% pain-free in my left knee and leg! The flare ups are minimal, but it does flares up due to aggravating factors like vigorous exercise, cold weather/fast barometric weather changes, long periods of standing on my feet, or not wearing the correct shoes (dress boots versus my tennis shoes or uggs). It's not a cure of course, and I was not expecting it to be, but it has made a significant difference in my pain levels, and I Don't have to use my pain meds as much as I did before. PT is much more tolerable too. The color in my knee also seems to better and the allodynia has improved. I still do precautions like double layering, not working too hard at the gym, keeping it propped up when I'm at my desk, and elevating at home. The recovery was painful, but it was definitely worth it! |
hi red and welcome. i haven't had a nerve abalation either but if i were you i would research it as much as you can before you get it done to make sure it is not going to aggravate your rsd. i am not a dr and its just what i would do before any new procedure for rsd. i hope all goes well and you start getting some relief from your rsd pain soon whatever you decide to do. soft hugs.
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