This is topic Please help! in forum Medical Questions at LymeNet Flash.


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Posted by swimmeredurp (Member # 34305) on :
 
About a year and a half ago I started experiencing difficulty

sleeping because I always felt like I had to pee but never could

actually urinate. I talked to my LLMD about the issue and she

said that it most likely was not a UTI since I was taking

antibiotics at the time for treatment and she suggested

increasing my dosage of probiotics and she said also that

sometimes the Lyme bacteria can embed in the bladder to cause

that symptom. I am now a year and a half out and I am NOT

currently being treated--I am trying to figure out where to go, it

feels like the treatment has plateaued-- but I am still

experiencing some symptoms, however these symptoms are

unlike what I experienced at the beginning of my history with

Lyme. I now have arm tremors in my hands once in a while

whereas before I only ever had muscle twitches. Also, it feels like

the bladder issue is getting worse, but that could of course

perhaps be something else UTI, yeast? I also have been feeling

somewhat congested, short of breath, and extra tired fatigue;

however I do smoke a fair amount of marijuana so that could

account for those symptoms. I also have quite often bouts of

queasiness/nausea. I am currently moving and so having a very

hard time staying in really good touch with my doctor who is

very busy and I am trying to figure out where my Lyme treatment

should go without spending a fortune in doctor bills. If anyone

would like to help me with a few suggestions I'd be forever

grateful! Just private message me.
 
Posted by BoxerMom (Member # 25251) on :
 
Your Babesia is back. Take herbs while you figure out your next step.

Artemisinin, Cryptolepsis, Sida Acuta, Enula, Quina - all are good options.

My bladder spasms resolved with magnesium. I needed a ton of it. Mg relaxes smooth muscle. If you are deficient, the bladder always feels distended, but you can't pee. It's miserable.

I've also seen this symptom resolve with treatment for Lyme and co's. With no additional magnesium.

Good luck!
 
Posted by cozynana (Member # 34270) on :
 
I think my cycstitis that made me feel like I always needed to pee was fungus/bacteria driven. I am on Nystatin now and doing much better. Crazy as it sounds, when I started doing enemas I found the pain and irritation of the bladder got a lot better. Maybe I was cleaning out fungus/bacteria. The bowels and bladder seem to be closely conneted.
 


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