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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index

thanks for your reply hun, as far as nerve blocks go, I cannot get them anymore cause they provide me only about a day or two of relief, so right now the only option is the nerve blocks, they have discussed with me about the SCS but I am a little nervous about it because I never had anything like this before so the thought of having something in my back makes me a little nervous, but I know it will be a great benefit for me as far as pain goes and will ease the pain a whole lot.

But I am afraid it will fail or I will have issues with it which makes it a little more scary, but if this is the only way I can get pain relief now, so be it. I can hardly take pain pills now as I fear the RSD advanced into my stomach and making it hard for me to keep them down, if they don't make me vomit, it makes me nauseous and lightheaded.

The nerve blocks are very effective and I think you should try them, I got up to about 4 months of relief, but I don't know why all of a sudden it failed this time around which makes me nervous, but remember just cause it failed for me after some time doesn't mean it will for you, I would give it a try.

I go back in about two weeks to Charlottesville probably for another treatment, but I don't know what they are gonna do, if they can even do another nerve burn this early, they may jump straight to a SCS trial, I am not sure

I am dreading the cold weather cause its gonna be brutal on my foot and leg until I get treatment, and I am now getting sick which makes things worse, I am basically bed bound curled up in blankets wishing for the sickness and pain to go away :(

please pray for me!

thanks for all the care and concern.

We just all have to stay strong and hope for a miracle of a cure :)

take care hun!

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