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 Flare-Up

 - UBBFriend: Email this page to someone!    
Author Topic: Interstitial Cystitis Flare-Up
MissVictoria
LymeNet Contributor
Member # 45232

Icon 1 posted      Profile for MissVictoria     Send New Private Message       Edit/Delete Post   Reply With Quote 
What helps you when you're having an IC flare-up that last for weeks or months? Have you found anything that ends the flare-up entirely?
Posts: 241 | From New Jersey | Registered: Jan 2015  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177

Icon 1 posted      Profile for Bartenderbonnie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, 100mg Gabapetin completely put my flares in remission.
Posts: 2977 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
If would be important to get a culture done by your doctor so you know if there is a particular pathogen as the cause.

This should be done before any kind of antibiotic or other antimicrobial Rx. see recent article in next post.

OXALATES can be a major player, with or without infection on board:

You might want to be sure you are eating a low-oxalate diet. For instance, avoid spinach, almonds and other things that are especially high in oxalates as they can be the problem -- or part of the problem with other things to consider.

A very low oxalate diet has helped me so much with bladder irritation and a similar issue of vulvodynia. Rinsing, too, a major help.

Facebook: Trying Low Oxalate - Susan Owens' group

&

https://sallyknorton.com/category/oxalates/

Sally K. Norton - Oxalate blog post

RINSE:

Also of help: with an clean empty squirt bottle rinse off uro-genital area each time after using the toilet, while still sitting on the toilet, though and then gently blot without too much force as you dry off with unbleached TP if you can find that.

Try to find a top that can aim right down and not go flying all around the bathroom.

Wear only full cotton underpants and no pantyhose or tights. If possible, try to wear a skirt rather than pants that can prevent good circulation of air.

Hope you feel better soon.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
This ignores some of the other things that I mention above -
and I find that annoying. However, this does emphasis two points:

Be mindful of raw poultry as that has been found to be problematic with e coli and bladder infections / UTIs

& the importance of always - always - getting a lab culture before starting any Rx as

the wrong Rx is so often used and that can make it worse if it is not matched specifically to the kind of microbe causing the infection -- if the UTI is from infection, and not due to other reasons.

https://www.nytimes.com/2019/07/13/health/urinary-infections-drug-resistant.html

Urinary Tract Infections Affect Millions. The Cures Are Faltering.

As the infections become increasingly resistant to antibiotics, some standard treatments no longer work for an ailment that was once easily cured.

By Matt Richtel - The New York TImes - July 13, 2019
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
https://www.healthline.com/health/d-mannose-for-uti#research

Can D-Mannose Treat or Prevent UTIs?

- Healthline - May 2019
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by Bartenderbonnie:
Yes, 100mg Gabapetin completely put my flares in remission.

Do you mean that 100 mg of gabapentin once a day got rid of it? Or several times a day?

Do you only have to take it when having a flare?

I have been meaning to ask you if you got over it, as it is so terrible. I know that it's connected with Lyme and Bart---or I sense that.

Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you, Keebler, for all of your information, and especially about a low oxalate diet. You are always so very helpful.
Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
dogmom2
LymeNet Contributor
Member # 23822

Icon 1 posted      Profile for dogmom2   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
marshmallow root has worked for me on 2 separate occasions. Upset my stomach after 1 week but didn't need it anymore by then.

Urostat for the pain while the m. root starts to work.

Posts: 857 | From northern california | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177

Icon 1 posted      Profile for Bartenderbonnie     Send New Private Message       Edit/Delete Post   Reply With Quote 
IC Pain is the WORST !
That was almost a deal-breaker for me. Waiting in the urologist's office, 2 hours, once a week, room full of patients, 20 trips to the bathroom, and in excruciating pain for months and months.

Urologist had me on hydroxyzine. Did nothing.
Weekly catheder treatments. Blow up bladder surgery.
Pain always came back.

I was also seeing a Neurologist at this time for chronic vertigo and chronic pain. He put me on Gabepentin. It did nothing for my vertigo and pain but it Miraculously cured my IC bladder pain.

I was so impressed, I told my urologist to please offer it to his other patients as it might help them.

I haven't had a flare in over a 1 1/2 year.. I do not take Gabepentin at all. But if I do notice any symptoms, like being unable to hold a teaspoon of urine in my bladder, believe me, Gabepentin will be the first line of defense.

Keebler is right on about getting a urine culture.
Primary's like the rapid urine test strips done in their office.
If you have symptoms, they will order an urinalysis.


But you need a culture done. This will let your sample grow for a few days to see if any visible bacteria or fungi grow. Of coarse you might get results like mine that said 'an unideniflied organism' present. I believe it was Bartonella or a BLO.

Sorry for your pain MissVictoria.

Posts: 2977 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
kidsgotlyme
Frequent Contributor (1K+ posts)
Member # 23691

Icon 1 posted      Profile for kidsgotlyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
MissVictoria, I am so sorry you are having a flare up. I hate it!! I am having a bit of one myself at the moment.

In the past, when I was in a constant flare and couldn't get rid of it, I swore up and down to my urologist that I didn't have a UTI. Turns out I did and I was so embarrassed for acting a fool in the office. I just wanted my bladder instill and for them to leave me alone but that was because I was in SO MUCH PAIN!

What I have found is watching my diet extra carefully when pain comes on because diet still does matter with IC. Since I've begun treating for bartonella, my flare ups have been doing so much better. Well...it was until starting Rifampin but I was expecting it.

Hydroxyzine helped me in the past but I quit taking it long term because of side effects. Elmiron helps...again quit taking it because my hair was falling out.

Marshmallow root was mentioned by someone else. That has helped soothe my bladder. Neurontin helps.

What made me worse was the D-Mannose. I know it is said to help others.

Uva Ursi is another herbal remedy that helps some. I have it but have never gotten the nerve up to try it. I have a real phobia about starting anything new.

Hope you feel better soon.

--------------------
symptoms since 1993 that I can remember. 9/2018 diagnosed with Borellia, Babesia Duncani, and Bartonella Hensalae thru DNA Connections.

Posts: 1470 | From Tennessee | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by Bartenderbonnie:
IC Pain is the WORST !
That was almost a deal-breaker for me. Waiting in the urologist's office, 2 hours, once a week, room full of patients, 20 trips to the bathroom, and in excruciating pain for months and months.

Urologist had me on hydroxyzine. Did nothing.
Weekly catheder treatments. Blow up bladder surgery.
Pain always came back.

I was also seeing a Neurologist at this time for chronic vertigo and chronic pain. He put me on Gabepentin. It did nothing for my vertigo and pain but it Miraculously cured my IC bladder pain.

I was so impressed, I told my urologist to please offer it to his other patients as it might help them.

I haven't had a flare in over a 1 1/2 year.. I do not take Gabepentin at all. But if I do notice any symptoms, like being unable to hold a teaspoon of urine in my bladder, believe me, Gabepentin will be the first line of defense.

Keebler is right on about getting a urine culture.
Primary's like the rapid urine test strips done in their office.
If you have symptoms, they will order an urinalysis.


But you need a culture done. This will let your sample grow for a few days to see if any visible bacteria or fungi grow. Of coarse you might get results like mine that said 'an unideniflied organism' present. I believe it was Bartonella or a BLO.

Sorry for your pain MissVictoria.

Bartender Bonnie,

Thank you for your response! I forgot to look for it until now (brain badly affected--arghh).

I gather that 1/ the gabapentin broke the cycle of the pain, 2/ I am presuming that treatment for Bart helped get over it, too. Is that correct that treatment for the Bart helped in the longer run?

When you did the 100 mg of gaba, did you take that 3 times a day?

Sorry for all the questions! I'm trying to figure out what might help. There are so many fronts to work on at once with TBD's!! It's overwhelming. Preaching to the choir, here.

Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177

Icon 1 posted      Profile for Bartenderbonnie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Totally understand you're overwhelmed Rumigirl.
My social calendar consists of nothing but healthcare provider's appointments.

My Bart is back.
But my IC Bladder is not.

Ive gotten Gabepentin scripts from Neuro's, pain management, primary, rheumotogist, they hand them out like candy. Not an opioid, low percentage of overdose or mis-use. They recommend a dose of 900mg daily, so they will order the 300mg tablet. You start slow, 1 300 mg per day and work your way up to 900 mg.

For me, the dose is too high. Side effects are drowsiness, severe dizziness, unable to drive, think, walk, unable to do daily chores. Even the next day, effects still linger.

So I requested the 100 mg capsule.
Neuro said that dose would serve no purpose but ordered it for me. It is the perfect dose. I take 1 capsule as needed, which is very seldom. Take at night. No side effects, no bladder pain.

For my wife-spread chronic pain, I take other pain relievers that cause less side-effects,

It's like wack-a-mole with this horrific disease.

Posts: 2977 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
lymenotlite
LymeNet Contributor
Member # 33166

Icon 1 posted      Profile for lymenotlite     Send New Private Message       Edit/Delete Post   Reply With Quote 
Here are some other ideas:

https://earthclinic.com/ailments/interstitial-cystitis/

Posts: 705 | From WA state | Registered: Jul 2011  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by Bartenderbonnie:
Totally understand you're overwhelmed Rumigirl.
My social calendar consists of nothing but healthcare provider's appointments.

My Bart is back.
But my IC Bladder is not.

Ive gotten Gabepentin scripts from Neuro's, pain management, primary, rheumotogist, they hand them out like candy. Not an opioid, low percentage of overdose or mis-use. They recommend a dose of 900mg daily, so they will order the 300mg tablet. You start slow, 1 300 mg per day and work your way up to 900 mg.

For me, the dose is too high. Side effects are drowsiness, severe dizziness, unable to drive, think, walk, unable to do daily chores. Even the next day, effects still linger.

So I requested the 100 mg capsule.
Neuro said that dose would serve no purpose but ordered it for me. It is the perfect dose. I take 1 capsule as needed, which is very seldom. Take at night. No side effects, no bladder pain.

For my wife-spread chronic pain, I take other pain relievers that cause less side-effects,

It's like wack-a-mole with this horrific disease.

Thank you, bartenerbonnie. I could never take gabapentin in the daytime, and my pain (CRPS, not just IC) is too great at night for gabapentin to cut it.

And yes, my social calendar is similar : - (

Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by lymenotlite:
Here are some other ideas:

https://earthclinic.com/ailments/interstitial-cystitis/

lymenotlite, looks interesting, I have to go back to read more. And the Zoloft causing IC---arghhh! The side-effect of all drugs, which doctors rarely quite aware of.
Posts: 3771 | From around | Registered: Mar 2008  |  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.