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
Reply
 
Thread Tools Display Modes
Old 07-12-2013, 05:07 PM #1
Nanc's Avatar
Nanc Nanc is offline
Member
 
Join Date: Jan 2011
Location: VA
Posts: 975
10 yr Member
Nanc Nanc is offline
Member
Nanc's Avatar
 
Join Date: Jan 2011
Location: VA
Posts: 975
10 yr Member
Default interstitial cystitis and RSD

Hello all! So I have been having some bladder issues for a while now. It has gotten much worse recently. I went to my family doctor this morning and she mentioned interstitial cystitis. I looked it up online and I saw that it is a form of RSD. I have read some posts on here about it also. Forgive me if I am repeating previous questions...those of you who have this, what do you do for it? Do you take the same meds as you do for RSD elsewhere?

Thanks!
Nanc
Nanc is offline   Reply With QuoteReply With Quote

advertisement
Old 07-12-2013, 06:26 PM #2
Vrae's Avatar
Vrae Vrae is offline
Member
 
Join Date: Apr 2011
Location: Denver
Posts: 703
10 yr Member
Vrae Vrae is offline
Member
Vrae's Avatar
 
Join Date: Apr 2011
Location: Denver
Posts: 703
10 yr Member
Default

Quote:
Originally Posted by Nanc View Post
Hello all! So I have been having some bladder issues for a while now. It has gotten much worse recently. I went to my family doctor this morning and she mentioned interstitial cystitis. I looked it up online and I saw that it is a form of RSD. I have read some posts on here about it also. Forgive me if I am repeating previous questions...those of you who have this, what do you do for it? Do you take the same meds as you do for RSD elsewhere?

Thanks!
Nanc
I have many of the symptoms. My OBGYN wants to do hysterectomy due to prolapse and then some mesh thing to help hold up my prolapsed bladder. He told me what a MAJOR surgery this would be. He also said I was in the driver's seat and we'd do it when I was ready. Let's see I think that was 3 years ago. I am scared of the surgery even though I know that some day I will more than likely do it. Sorry that your having trouble hon. I wish I had some good advice. Perhaps someone else will.

Last edited by Vrae; 07-12-2013 at 09:36 PM.
Vrae is offline   Reply With QuoteReply With Quote
Old 07-12-2013, 07:25 PM #3
Nanc's Avatar
Nanc Nanc is offline
Member
 
Join Date: Jan 2011
Location: VA
Posts: 975
10 yr Member
Nanc Nanc is offline
Member
Nanc's Avatar
 
Join Date: Jan 2011
Location: VA
Posts: 975
10 yr Member
Default

Quote:
Originally Posted by Vrae View Post
I have many of the symptoms. My OBGYN wants to do hysterectomy due to prolapse and then some mesh thing to help hold up my prolapsed bladder. He told me what a MOJOR surgery this would be. He also said I was in the driver's seat and we'd do it when I was ready. Let's see I think that was 3 years ago. I am scared of the surgery even though I know that some day I will more than likely do it. Sorry that your having trouble hon. I wish I had some good advice. Perhaps someone else will.
Hi Vrae. Sorry about the issues you are having. I have had RSD since '91 and I had a hysterectomy and o-rectomy in '96. I figured I would develop some bladder issues in time...these are not the issues I expected

I knew nothing about RSD back then, no one really did! The things I have read about RSD in the past few years explained a lot about stuff I experienced that no doctor could explain.
Nanc is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Terristie (09-17-2013)
Old 07-12-2013, 09:46 PM #4
Vrae's Avatar
Vrae Vrae is offline
Member
 
Join Date: Apr 2011
Location: Denver
Posts: 703
10 yr Member
Vrae Vrae is offline
Member
Vrae's Avatar
 
Join Date: Apr 2011
Location: Denver
Posts: 703
10 yr Member
Default

Quote:
Originally Posted by Nanc View Post
I knew nothing about RSD back then, no one really did! The things I have read about RSD in the past few years explained a lot about stuff I experienced that no doctor could explain.
I know what you mean. Granted you are an RSD veteran, but when I was told just a few months after the surgery that rendered me RSD back in 2004, there wasn't much on the internet that I found back then either. I so wish I had known the things to do that MIGHT have got me any time in remission.

I am having a hell of a night tonight. Oh I hate when it flares , then I cry b/c pain, which I try to keep in check b/c it only makes it worse. I am getting to where both my feet are so involved I am concerned about how much longer I will be able to use them. Just a short trip to the bathroom tonight is agonizing. Sorry to complain. It just is what it is I suppose. I hope you're feeling better!
Vrae is offline   Reply With QuoteReply With Quote
Old 07-13-2013, 11:41 AM #5
Nanc's Avatar
Nanc Nanc is offline
Member
 
Join Date: Jan 2011
Location: VA
Posts: 975
10 yr Member
Nanc Nanc is offline
Member
Nanc's Avatar
 
Join Date: Jan 2011
Location: VA
Posts: 975
10 yr Member
Default

Quote:
Originally Posted by Vrae View Post
I know what you mean. Granted you are an RSD veteran, but when I was told just a few months after the surgery that rendered me RSD back in 2004, there wasn't much on the internet that I found back then either. I so wish I had known the things to do that MIGHT have got me any time in remission.

I am having a hell of a night tonight. Oh I hate when it flares , then I cry b/c pain, which I try to keep in check b/c it only makes it worse. I am getting to where both my feet are so involved I am concerned about how much longer I will be able to use them. Just a short trip to the bathroom tonight is agonizing. Sorry to complain. It just is what it is I suppose. I hope you're feeling better!
I was lucky that mine was discovered and treated right away back in '91, I was in remission for many years. I bit a rock that was in my food at a restaurant. Lost my three back bottom teeth after failed root canals, then ended up with dental implants. This is what caused the RSD in my face. The hospital's pain clinic I was treated at said this was the first time they had ever seen or heard of it in someones face. They wanted my dentist (who got me to the pain clinic) to submit my case to the medical journal. He didn't do it because of fear of being "laughed at" since it was so unheard of. I sued the restaurant to cover the $13,000 spent on my mouth/face. I didn't get much more than that. Had I known what RSD was back then I would not have settled! Even when I came out of remission, my flare-ups were manageable. I hurt my right hand in 2009 and developed RSD there...then it spread with a vengeance. I learned so much more about it when it started spreading. I completely understand you concern about having it in both feet, mine are both affected too. We went to the store yesterday to pick up new meds and a few groceries. I hit my little toe on the cart when checking out, and oh the pain! By the time we left, I could barely walk.

I am sorry you are having such a hard time. No need to apologize for complaining, it is completely understood and acceptable!!! Thankfully I did sleep better last night, which is great considering I didn't the night before because of this new bladder pain...so frustrating! I hope you are having a better day today.

Nanc
Nanc is offline   Reply With QuoteReply With Quote
Old 07-13-2013, 12:05 PM #6
Vrae's Avatar
Vrae Vrae is offline
Member
 
Join Date: Apr 2011
Location: Denver
Posts: 703
10 yr Member
Vrae Vrae is offline
Member
Vrae's Avatar
 
Join Date: Apr 2011
Location: Denver
Posts: 703
10 yr Member
Default

Thanks Nanc. Yep, much better, mornings are always better for me. Although I'm not looking forward to the night. It always seems to be worse at night. Anywho, thanks again Nanc! Have yourself a wonderful day!!
Vrae is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Nanc (07-13-2013)
Old 09-17-2013, 07:53 AM #7
Nanc's Avatar
Nanc Nanc is offline
Member
 
Join Date: Jan 2011
Location: VA
Posts: 975
10 yr Member
Nanc Nanc is offline
Member
Nanc's Avatar
 
Join Date: Jan 2011
Location: VA
Posts: 975
10 yr Member
Default

Well, I had the series of tests and was officially diagnosed with interstitial cystitis. Due to allergies, I cannot take the meds normally prescribed for IC. I am trying the IC diet, but there is so much conflicting info online. One list will show something is "IC friendly" while another list will show it as an "avoid"! So confused!! This is difficult for sure...already gluten free and have many food allergies, now this. Trying to determine what I can eat is a challenge.

Any advice would be appreciated!
Thanks!
Nanc
Nanc is offline   Reply With QuoteReply With Quote
Reply


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
Interstitial Lung Disease and my meds dog lover Myasthenia Gravis 16 01-28-2010 09:41 PM
Interstitial lung disease PMCPMC Myasthenia Gravis 4 01-16-2010 07:40 PM


All times are GMT -5. The time now is 05:13 AM.

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.