posted
Sorry, the inital di not go through. As saying I am taking lev 500(9weeks now) day and Zith 5oo2day (jsut started) I still ahve that feverish felling. In Spril this year I had an mri with the balloon (wow was that unpleasant)and everything looked fine. Most symtoms went away and in Late september they came back. The pain in the tip area and urinary tract infection was bad for 3 weeks. I still have that feverish feeling, but I notice after lots of walking yesterday and having relations this morning, It hurts in the anal area inside when using the bathroom sitting down. It almost feels like the muscles are hurting. then after a few minutes it seems to have a reocurrring pain for one second. the same place kinda on the inner wall. I had some pain a few weeks ago when using the bathroom in the muscles around the opening but they went a way. Today it really hurt. Anyone else have these symptoms? Sorry about the sitting down analogies.
-------------------- bc Posts: 327 | From Tampa.Florida,usa | Registered: Jun 2002
| IP: Logged |
posted
I have heard of many with lyme that develop unusual prostate symptoms. Usually nothing can be found with testing except an enlarged prostate. Being on abx (ceftin I think) helped my prostate issues.
The pain you are describing happens to be right where the prostate is, and if it's inflamed what you are saying makes sense.
Sorry I can't help more. Good luck..
Posts: 413 | From nj | Registered: Nov 2005
| IP: Logged |
valymemom
Frequent Contributor (1K+ posts)
Member # 7076
posted
If you do a search of "carnivora", Marnie has a post about quercitin (sp) and there is info that it helps prostrate pain/problems.
Sorry I can't be more specific but I just saw it today on a past thread when reading about the carnivora.
Posts: 1240 | From Centreville,VA | Registered: Mar 2005
| IP: Logged |
This is all very interesting as I have an elevated PSA and a little problem with urination at night now..all discovered and happening after being treated for lyme disease with doxycyclene. Anyone?
Posts: 1 | From randolph, nj | Registered: Sep 2006
| IP: Logged |
gwb
Frequent Contributor (1K+ posts)
Member # 7273
posted
bcox, I've got similar problems and have been having a discussion about this on another thread this evening. There's some great information on this thread that I think you'll find very helpful.
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,
NJ08534USA http://www.lymenet.org/