LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Interstitial Cystitis

 - UBBFriend: Email this page to someone!    
Author Topic: Interstitial Cystitis
chaps
LymeNet Contributor
Member # 25286

Icon 1 posted      Profile for chaps     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've got a friend who has had lyme for 17 years and has interstitial cystitis.

She's not well enough to post on here, but I was wondering if anyone here knows of anyone who has been able to overcome this painful and persistent condition which is lyme-induced and can send me an IM with the name of the physician that helped them get through it, the methods, etc.

This person is really suffering with this. It's very painful. She can't eat anything, it only makes the pain worse.

--------------------
-chaps
�Listen to the bell, Borrelia. It tolls for thee!�

Posts: 631 | From A little place called, "we'll see." | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
Treating bartonella helped me immensely.

When my bart relapsed, the bladder issues returned.

Things that helped me immensely (aside from bart treatment),

1) Avoidance of any sodas, aspartame drinks. One glass of diet soda now is like an instant IC flare.

2) D'mannose. 4 capsules 4 times per day for 4 days (to load), then 2 capsules 3 times per day.

3) Avoiding cranberry juice

4) Vaginal Probiotic. Such as Fem Flora by New Roots (a probiotic suppository)

5) Oral probiotics made for female system. RenewLife VS formula 50 billion cfu in the pink box.

I was a regular with a urologist before I started the above.

Sorry your friend is going through this. It is the more annoying and life disturbing symptoms of TBDs.

[group hug]

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Greta has a good list there. Mine is much much better after Lyme and babesia treatment nearly 10 years ago. I was dxd with IC in 1992.

Tell her to also avoid sugar like the plague. I think candida/yeast makes it worse. A few months ago I began eating sweets and was eating foods high in salicylates and histamine.

When I stopped doing all 3 of those, my IC symptoms went back to "normal."

IC no longer controls my life like it used to.

One thing that some people have used is a product called "Aloe Fields" .. She could also try George's Aloe. It does not have any citric acid in it. She needs to be SURE to avoid citric acid LIKE THE PLAGUE.

www.ic-network.org
www.ichelp.org

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
chaps
LymeNet Contributor
Member # 25286

Icon 1 posted      Profile for chaps     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for your replies. I'll pass it on to her.

--------------------
-chaps
�Listen to the bell, Borrelia. It tolls for thee!�

Posts: 631 | From A little place called, "we'll see." | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
Dogsandcats
Frequent Contributor (1K+ posts)
Member # 28544

Icon 1 posted      Profile for Dogsandcats     Send New Private Message       Edit/Delete Post   Reply With Quote 
Private message sent.....

--------------------
God will prepare everything for our perfect happiness in heaven, and if it takes my dog being there, I believe he'll be there.

Billy Graham

Posts: 1967 | From California | Registered: Oct 2010  |  IP: Logged | Report this post to a Moderator
bla
Member
Member # 42361

Icon 1 posted      Profile for bla   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ditto what GretaM said. I've had IC for 12 years. I'm much better now than I was the first couple years with it.

Avoid acidic foods/drinks, for sure. My treatment was three months of abx. I herxed terribly, but the last week of treatment was like a miracle, the symptoms lifted, and I felt like a new person.

Sadly, once the treatment was stopped, my symptoms returned. I was not being treated for Lyme at the time. So, getting an abx for a period of three months was an achievement in its self. My symptoms came back [Frown]

Also, my experience with the diagnostic procedure called laproscopy was somewhat different than others'. I was put to sleep for the procedure, and what they did was fill my bladder with a solution, stretching it to the max, and used a tiny camera to look at inside of bladder wall.

Something about the stretching of my bladder, I think, but the procedure was therapeutic for me. I didn't have any IC symptoms at all for about a week after, and my symptoms never went back to pre-procedure levels even after a week.

I've been doing much better since. Not everyone has this experience with the laproscopy, though. I've read that it made some people feel much worse.

Other than that and long term abx, plus managing acid levels, I don't know what else there is. I feel for anyone suffering with IC, knowing how horrible it is first hand.

Oh yeah, don't take ibuprofen. It makes the bladder flare something terrible. Some people don't know that and take it thinking they're remedying their painful bladder when they are actually doing the opposite, making it feel worse. Good luck.

--------------------
bla

Posts: 59 | From Pennsylvania | Registered: Oct 2013  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Chaps...

Hyperbaric Oxygen is showing positive results for IC:

http://www.ncbi.nlm.nih.gov/pubmed/15183555

Posts: 1885 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by bla:


Also, my experience with the diagnostic procedure called laproscopy was somewhat different than others'. I was put to sleep for the procedure, and what they did was fill my bladder with a solution, stretching it to the max, and used a tiny camera to look at inside of bladder wall.

Something about the stretching of my bladder, I think, but the procedure was therapeutic for me.

-
Yes, that procedure (not called a laparoscopy) is supposed to be "therapeutic"... It helped me the first time but when we repeated it a year or so later it made me so bad I had to quit teaching. I think the correct term is "bladder distension" but of course that is not the technical term.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
Right! Excellent point bla! The ibuprofen does make the bladder sting! I haven't taken it in so long I forgot!
Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.