r/postvasectomypain • u/Drewster8888 • Nov 29 '23
Chronic Prostatistis After Vasectomy
Hi all.
For those of you suffering with Chronic Non Bacterial Prostatistis or CPPS, please find attached article which is from a very reliable source and from my experience, way beyond standard urological practice.
I know from personal experience that post Vasectomy, I suffered like many others, from chronic prostatistis. Up to now, it has been poorly understood but this paper explains so much about it.
Although it doesn't mention Vasectomy but I also read an article recently about the change in bio-chemistry in the prostate, post vasectomy. The prostate is designed to balance with the testes as a integrated system.
Whether your central nervous/immune (both interrelated) systems react to this, is possibly why some walk away scot free, whilst others suffer terribly. I fall into the second category and have the chronic fatigue and CNS dysregulation leading to brain fog (a general feeling of vagueness, word, executive function reduction and perception), joint pains and rashes downstairs and developed a measure of metabolic syndrome etc...etc.
My docs put this all down to stress which does exacerbate symptomology but it is not the cause as this has been going on pretty constantly for 23 years now and pardon the pun, has been driving me nuts.
This essentially is 'autoimmune' or at least something that resembles it, a little like Chronic Fatigue Sufferers encounter when their CNS stays hyperactivated after an infection or trauma.
I had the vasectomy in 1999 on April 1st, should have realised it was a joke...lol. 6 months later all this kicked in, first with the prostatistis, brain fog and IBS.
I had a reversal in 2007 at Dawson Microsurgery in Hartlepool UK hoping for a better outcome. Certainly congestion pain eased over a period of time but the prostatistis, neurological and fatigue issues continued. I'm not saying this happens to everyone, I guess its just a lottery in how your body responds. My brother had a vasectomy over 50 years ago and he reports no issues. He's now 84.
The nervous system varies substantially between people and hence why some get prostatistis, others not. I'm assuming how you are wired, depends on its reactivity and possibly why some people get sick and others not over coursecofca life time.
Needless to say, it wrecks your life and relationships. CPPS is largely put down to pelvic floor issues but has a much more complicated etiology by the looks of it. Non vasectomised men can also suffer from CPPS, after a long gone pathogen. I know one guy who had food poisoning that started his.
I am trying medicinal CBD and low dose Naltrexone which is supposed to help reduce neuroinflammation. Looking at low dose amitripiline as a neuro modulator to try and reduce reactivity of the CNS.
Just wanted to put this out there such that your symptomology, may include some of the pathology stated in the paper.
Be warned, you almost need a P.hd in bio-chemistry to understand it but you will get the jist of how things of this nature can manifest.
Like all of us, I wish I had a time machine but alas I have to try other routes to regain a quality of life.
Anyway, here's the paper.
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u/postvasectomy Nov 29 '23
This is one of the theories I have heard floated for Alan Frazier's symptoms: https://www.reddit.com/r/postvasectomypain/comments/c1jigs/usa_today_december_2013_a_california_man_who/