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 » Bladder / IC issues or Prostate?

 - UBBFriend: Email this page to someone!    
Author Topic: Bladder / IC issues or Prostate?
bcb1200
Frequent Contributor (1K+ posts)
Member # 25745

Icon 1 posted      Profile for bcb1200     Send New Private Message       Edit/Delete Post   Reply With Quote 
I know the majority of folks on here are women, but also know there are a few men lurking.

Again, I don't come around much anymore as life has more or less returned to normal, although I still have a few mild symptoms that flare from time to time. Specifically mild night sweats of head/neck, mild muscle twitching, mild tinnitus, etc.

Anyway...I was d/x'd in 2010 and have been in the 90% range since about 2012.

LLMD currently things what is left is either Brucellosis or Bart, Mold, Yeast, and/or Parasites (or some combination thereof.)

Anyway...back in April I started to notice that I had occasional, mild "bladder pressure." It was mild and I can usually ignore.

THis has come and gone over the past few months. Lately, when I've had it, I struggle to pinpoint exactly what the issue is. Is it bladder related? Is it Prostate related? Is it something else related to pelvic floor.

Here is what I experience now:
-Mild discomfort / pressure in the bladder/suprapubic area
-SOmetimes discomfort (mild burning) in the hip area
-Sometimes mild discomfort in the testicles or urethra.
-Occasional, mild feelings of needing to urinate, but these go away.

Here is what I don't have:
-discharge
-pain when urinating. (Feels pretty good actually)
-Pain when ejaculating (also feels pretty good [Wink] )
-BLood in urine / semen

I've read about Interstitial Cystitis (IC). It sounds horrible and while I may have the pressure / suprapubic discomfort, I don't have other symptoms.

I've read about Prostatitis, which seems like a closer fit. But then again, I don't have some symptoms listed.

I've read about bladder infection / UTI, but I don't have the discomfort when urinating, etc.

Right now it isn't bad...but I worry it will get worse. And I am worried because this is a NEW symptom for me. I haven't had a "New" symptom in years.

Anyone have any idea? Nothing has changed on my end except I was targeting Biofilms, Brucella/Bart (with Byron Why A-Bio), and parasites when this all started.

Thanks. I rarely get concerned about symptoms anymore...but am definitely concerned about this.

--------------------
Bite date ?
2/10 symptoms began
5/10 dx'd, after 3 months numerous test and doctors

IgM Igenex +/CDC +
+ 23/25, 30, 31, 34, 41, 83/93

Currently on:

Currently at around 95% +/- most days.

Posts: 3134 | From Massachusetts | Registered: May 2010  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
Mine was probably prostatitis from lyme, and bart, or what ever other bug might have been in there. Get the doc to check the prostate.

If it burns and hurts horribly, it is probably an infection. [Wink] My PSA levels were very low, but then again I am only thirty-five.

I had horrible hip pain, and trouble going when I needed to as it progressed, but the doc put me on an antibiotic that also happened to hit lyme.

This happened before I knew I had lyme. I got diagnosed with lyme two months later.

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  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 
For me (I have IC) .. it felt great while peeing ..but the minute I was through.. BAM! More pain.

If I have an infection, it HURTS to pee.

I'm doing much much better with my IC .. it flares when I eat foods high in salicylates or high in histamine. You may want to try avoiding at least the foods high in histamine to see if it's better.

Eating leftovers can also cause IC symptoms for me.

Also the IC sites tell you what other foods to avoid.

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
purplehaze
Member
Member # 40385

Icon 1 posted      Profile for purplehaze     Send New Private Message       Edit/Delete Post   Reply With Quote 
bcb1200,

I can totally relate, I have these same symptoms/issues for the past 16/17 months

Posts: 69 | From Ireland | Registered: Apr 2013  |  IP: Logged | Report this post to a Moderator
jackie51
Frequent Contributor (1K+ posts)
Member # 14233

Icon 1 posted      Profile for jackie51     Send New Private Message       Edit/Delete Post   Reply With Quote 
If you've ever smoked or been around smokers, get screened for bladder cancer. My urologist insists this is real.
Posts: 1374 | From Crazy Town | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
unsure445
LymeNet Contributor
Member # 15962

Icon 1 posted      Profile for unsure445     Send New Private Message       Edit/Delete Post   Reply With Quote 
I would get this checked out. Best not to assume that new symptoms are from Lyme and co-infections, especially if you have been feeling pretty good/stable.

My husband used to have Lyme and despite being cured he tends to think he is relapsing when he has a health issue. Each time he has had an issue it has not been a relapse/Lyme and co-infections.

--------------------
unsure445

Posts: 824 | From northeast | Registered: Jun 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.