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)


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 11-13-2016, 02:40 PM #5
Sophie0513 Sophie0513 is offline
Junior Member
 
Join Date: Nov 2016
Posts: 94
5 yr Member
Sophie0513 Sophie0513 is offline
Junior Member
 
Join Date: Nov 2016
Posts: 94
5 yr Member
Default Thank you

Quote:
Originally Posted by Shay08 View Post
Sophie, I really feel your emotional pain right now. I have a tendency to worry and stress out over the decisions that need to be made regarding treatments. Stress overload tends to worsen our pain. I try to deal with it using mindfulness exercises and by preparing in writing every question or comment I have to address with my doctor(s).


"SHould I talk to my PM doctor about the MN? I told him about it at our first meeting but he didn't see to concerned about it. Or should I wait and see how I respond to the sympathetic nerve block on Wednesday and the gabapentin? I will search the threads again about blocks but I did watch (forget his name-Dr chop raps video) and he said nerve blocks really don't help. I just have this nagging feeling that my left foot/mortons neuroma is coming into play in all of this or it could have been the cortisone shots. All I know is that it is creating a lot of painful burning
"

I believe you should address all of these issues with your doctor. Whether you do that before or after your nerve block is up to you. If I am not mistaken, you had nerve blocks with your first encounter with CRPS and you eventually went into remission. Be prepared with a written list and listen closely to the doctor's responses. Leaving issues unspoken will only add to your stress.

Try to think positively. You went into remission before and you can do it again!

I will keep you in my thoughts and prayers. Remember we are here for you and care.

Shay
THank you Shay ! I am trying to stay positive however my fear gets the worst of me! I know I went into remission once. I had basically forgotten what that whole experience felt like but wow it's pretty much the same thing with the exception thAt I could at least walk! I think that not being able to walk, stand for more than 5 mins or wear any kind of shoe has kind of sent me over the edge! I'm holding on and glad that I found this site!!!!
These kind of sites were not around when I first got RSD! Thank you again
Sophie0513 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Littlepaw (11-13-2016), Shay08 (11-14-2016)
 

Tags
crps, feet, foot, podiatrist, started


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
your input please jeanb Parkinson's Disease 8 09-27-2011 08:28 PM
I really need your input!! MelodyL Alcoholism, Addiction and Recovery 15 07-22-2009 09:54 PM
Still Need Your Input, Please Virginia Therese Parkinson's Disease 11 01-30-2008 07:47 PM
Please...I need your input Virginia Therese Parkinson's Disease 5 01-28-2008 03:27 PM
Tell it like it is - Need your input! pegleg Parkinson's Disease 35 04-29-2007 08:15 AM


All times are GMT -5. The time now is 12:12 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.