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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Old 05-25-2016, 12:36 PM #1
St George 2013 St George 2013 is offline
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Default Hey Becca :)

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Originally Posted by Becca71 View Post
Has anyone here had a biopsy after having their CRPS? My GYN needs to do a uterine biopsy on me and I'm nervous. Because of course I've read that anything we do can cause a flare up or spread of the CRPS which is the last thing I want or need.
I know a biopsy is minimally invasive, so I'm hoping its low risk for causing problems?
If you are comfortable with your GYN I would go with the biopsy. Not sure what your symptoms are and I don't have RSD but I do know how very important a uterine biopsy is to rule out a number of problems.

Keep us posted.

Debi from Georgia
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Old 06-13-2016, 09:35 PM #2
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Well my pain doc says to just make sure my ob/gyn uses extra of whatever numbing agent she is using. So I hope that all will go well, but its still over a week away.
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Old 06-13-2016, 09:43 PM #3
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I will keep you in my thoughts...hopefully all will go well. Please keep us posted on how it goes.
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Old 06-13-2016, 11:18 PM #4
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Heart Hi Becca!

Hi Becca,

Very important question.

I understand your concern.
I do not know the answer to your question.
It seems your pain doctor and friends here gave reasonable advice.

You will see I have a recent thread which mentions a CRPS flare after biopsies.
I just want to be sure we all understand these were skin punch biopsies done on my foot and leg, which is where my CRPS is -- on both feet/ankles.

I tend to think, sometimes, we must weigh the potential costs/benefits and move forward, thinking positive and in our minds, picturing a very positive outcome.

I am guessing here, yet I think your GYN wants to do a biopsy to make sure you are okay? It's an important procedure, which could be life-saving for many people.

I wish you the best.

Love All Around,

DejaVu
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Old 06-14-2016, 02:01 PM #5
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Quote:
Originally Posted by DejaVu View Post
Hi Becca,

Very important question.

I understand your concern.
I do not know the answer to your question.
It seems your pain doctor and friends here gave reasonable advice.

You will see I have a recent thread which mentions a CRPS flare after biopsies.
I just want to be sure we all understand these were skin punch biopsies done on my foot and leg, which is where my CRPS is -- on both feet/ankles.

I tend to think, sometimes, we must weigh the potential costs/benefits and move forward, thinking positive and in our minds, picturing a very positive outcome.

I am guessing here, yet I think your GYN wants to do a biopsy to make sure you are okay? It's an important procedure, which could be life-saving for many people.

I wish you the best.

Love All Around,

DejaVu
I agree with my Doc that the biopsy is needed based on my symptoms. She needs to rule things out, so that she can then manage those issues in the best way possible. If I can get through this with no CRPS issues I will be so happy! If it does cause a flare, well, I'll manage that. I just really am scared of spread. I know it isn't common, but after my sympathetic nerve block wore off I had symptoms farther up my leg than before ... so yea. Plus, who the heck wants CRPS in the UTERUS???? I mean hell no!
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Old 06-14-2016, 03:34 PM #6
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Heart ((((( Becca )))))

So understandable!
I wish there were more clear answers.

I am guessing many women with CRPS have uterine biopsies. I wonder if any have written about any CRPS spread due to uterine biopsies?

I am hoping for the best possible outcome for you as well.

Love All Around,
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