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Medical Forum / Diseases and Disorders / Prostatitis / October 2003

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Nerver Damage

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Vince - 28 Sep 2003 22:37 GMT
Is it possible for a bacterial infection in the prostate to cause
permanent nerver damage. I have been battling ED problems ever since I
got this didsease 4 years ago. In the beginning it was certainly a
bacterial infection and abx helped quite well, but after it went
chronic. Is it possible that there have been som permanent nerve damage
?
ferrariboston@yahoo.com - 29 Sep 2003 13:30 GMT
> Is it possible for a bacterial infection in the prostate to cause
> permanent nerver damage. I have been battling ED problems ever since I
> got this didsease 4 years ago. In the beginning it was certainly a
> bacterial infection and abx helped quite well, but after it went
> chronic. Is it possible that there have been som permanent nerve damage
> ?

I don't know if it's permanent, but you could have nerve damage I've
heard of this and I think it can cause impotence problems,maybe it's
nerve irritation.  I was thinking of going to see Dr Shoskes and his
impotence partner Dr Hakim to help me with possible nerve
damage/prostatitis.  I also heard Dr Dimitrakov treats this condition.
Anyone with experience with nerve damage or with any of these doctors
could they reply!
Al - 02 Oct 2003 09:57 GMT
> > Is it possible for a bacterial infection in the prostate to cause
> > permanent nerver damage. I have been battling ED problems ever since I
> > got this didsease 4 years ago. In the beginning it was certainly a
> > bacterial infection and abx helped quite well, but after it went
> > chronic. Is it possible that there have been som permanent nerve damage

-------This sounds very similar to what happened to me. I fisrtly
developed an intensly inflamed prostate (red hot coal in rectum
sensation) and slowly developed the symptoms of CPPS during this time
(perineal pain etc). The red hot coal sensation was cleared up 2
months later when I was eventually switched to course of doxycycline.

I was left with chronic pelvic pain, (perineal pain; anal pain; pubic
pain; urinary frequency & hesitancy etc.) which was related to chronic
pelvic floor muscle spasm. From what I know, this is originaly a
protective 'splinting' response, but can then become the source of
chronic pelvic pain, even after the original cause (i.e. prostatitis)
has been treated.

I've improved by around 70% as a result of an ongoing course of
myofascial release/pelvic physiotherapy.

You might find these liks useful:
http://www.ic-network.com/guestlectures/rhondatranscript.html
http://www.pelvicdysfunction.ca/
http://www.pelvicdysfunction.ca/usd.htm
http://www.ic-network.com/guestlectures/weiss.html

This is an excellent article which discusses how damage to pelvic
organs can cause nerve damage resulting in a vicous cycle of increased
pain perception and muscle spasm. He also gives a good discription of
how these changes are reversible by creating a 'stimulation free
period', and uses the example of amputees and phantom limb pain to
illustrate this:

http://www.jmweissmd.com/article.htm

Hope this helps,
Al.
 
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