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    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

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Anyone have prostatitis and ME?

Messages
20
ViaSwiss is there anyway you could share your cpps symptoms with me? If you dont mind, as Im a little confused by mine and dont know if its something else. Im getting a whole host of rectom, penis symptoms that are uncomfortable. Im also getting some tingly feelings.
My symptoms attributed to CPPS....

-Weaker urine stream
-Urinate more often
-Sometimes a dull ache in my perineum
-Sharp shooting pains about once a month
-Worsened erection quality
-Sometimes cold/numb penis (less sensitive)
-Sometimes a smaller, constricted (hard but not erect hard) penis
-Poor mind to penis connection sometimes

I've gone the testosterone route for years with the nations best endo. Did nothing at all.

It appears that the root cause is ANS dysfunction (overly sympathetic) and/or inflammation of the pudendal and sacral nerves...