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 08-29-2008, 05:46 AM #14
AnnBon AnnBon is offline
Junior Member
 
Join Date: Feb 2007
Posts: 64
15 yr Member
AnnBon AnnBon is offline
Junior Member
 
Join Date: Feb 2007
Posts: 64
15 yr Member
Default

Dear Allyeyator,

I am so sorry for all the pain and suffering your wife and yourself are going through and it is wonderful that you found a new pain specialist to work with her. Once she gets settled down with the proper meds. and feels a doctor is there for her she will settle down. I have had RSD for 4 and a half years and have worked with the same Dr. for the whole time and have seen many of his colleagues and fellows for additional consultations and have done some procedures some with success some not so successfull. The reason I bring this up one Dr. I worked with happen to be a graduate of Arizona University Medical School doing a fellowship on the East Coast maybe the Medical School has a pain program. I have found that these type of institutions have some very good pain programs and have access to the latest technology, just a suggestion.

I know how hard it is to deal with a person who goes from being normal one day then bang pain all over, that's how it happened to me. My husband had a back issue, but healthy, working so it's under control and I tell you if it was not that he has experienced bad back pain for long time periods I don't know how all this would be going he is very understanding or should I say understands. This is not a judgement on you but things will get better. Give her some time and yourself some time to adjust. I have felt desperate many, many times just as you and your wife do.

Good Luck and keep us posted.

Ann

Burnmyo,

Your post was possibly the best I have ever read and very constructive. Put perfectly.






Quote:
Originally Posted by Alleygator View Post
I got her into a new pain specialist who will keep her on her Methadone until they get her pain under control, put her on Lyrica and is going to set up her SCS trial so that is great news!

We tried Dragon Speak, but she can not speak clearly enough for the program to work right, hopefully if they can get her pain to a manageable she will be able to type and get on these forums to talk with other people with her condition.

Loretta – I would love to get information on your group; I think that would be great for the both us. We moved down here from Oregon about 3 years ago to try to get her better medical treatment, ironically, so it would be good for her to see people other than myself and her doctors. Her blood pressure usually sits a bit on the high side, but her doctors say it is normal with the amount of pain she is in. When they tried Clonidine out on her, it dropped it into the normal levels, but they pulled her off it when they switched her to the Methadone.

Lynns- I’m not even sure how to respond to that. I think you completely missed the objective of my post. If I intended to write this in the manner that you translated it, I would think that it WOULD need to be harsh. I would never let her kill herself, thus the part about removing anything in the house that she could use to do so.

In my 2nd post I stated that she was seeing a therapist and a psychiatrist and was doing well considering the circumstances. You stated that “Being a caretaker is difficult and can sometimes warp your point of view”, I completely agree. That is why I posted on here, to have some sort of a frame of reference on my “being selfish” by NOT considering her suicide as an option, to get a perspective of people that are going through what she is. I do not know what it feels like to go through what some of you do and will not discount her pain by pretending that I know how bad she is. If I was tied to a chair, covered with lighter fluid, lit on fire and was only given a misting bottle to help me put it out (that is how she describes it to me) and somebody told me that I was being selfish by wanting to die, personally I’d tell them to #%@& off.
AnnBon is offline   Reply With QuoteReply With Quote
 


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
You think you know your spouse. Blessings2You The Stumble Inn 32 07-14-2008 09:37 AM
Being Meish & Selfish buckwheat Reflex Sympathetic Dystrophy (RSD and CRPS) 12 10-14-2007 12:34 PM
Spouse of newly diagnosed MS patient LuckyTinkerbell New Member Introductions 4 04-13-2007 07:09 PM
Looking for thyroid advice for my spouse-- glenntaj Vitamins, Nutrients, Herbs and Supplements 2 01-08-2007 11:48 AM


All times are GMT -5. The time now is 11:36 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.