That’s bullshit, there is no pudendal nerve damage, i don’t understand how a top Dr. can tell you this bullshit. I can smash his theory in 5 minutes with facts, and i bet there will not be any decent reply from dr.'s side.
I researched so much for last 4 years, this dr. make me laugh.
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Agreed 100%.
I used them all at one point but Prozac was the last one
Hi
What do you mean exactly that it’s BS and it’s not nerve damage? I’m just trying to see what you’re alluding too
Thanks
Hey. I am another PFS patient who went serious side effect and had wishes for death because the period was just way too hard. And I can relate to you how you feel. Right now I am recovered, although I had blurred vision, severe cognitive disfunction and sexual disfunction as well. I got them all back.
Although I may not be a medical expert, I am in college studying chemistry and biology & I have clinical experience as well while serving in the military. I assume although the tests may show your nerves functioning not properly, it may be only the signals not transmitting properly since we took medications that inhibits hormones, which basically are signals.
Sadly, I also agree that although Doctors are respectable for their time dedicated and their IQ, Ive seen many doctors not truly caring about the patients, and they only know what they learnt from textbook and conferences. Ive seen them make a lot of wrong judgements, minor or major.
Sorry about your condition, but believe it’s recoverable as many of the people here did. My prayer goes out to you tonight brother. Sincerely.
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Awesome how you recovered happy for you! You should tell your story in the recovery thread! Thank you for coming here and giving us hope!
I think you and the doctor should have gotten it clear whether he meant temporary neuropathy or damage. When it is really cold or you have been sitting in the wrong position maybe you lose sensation for a bit. It doesn’t mean your nerves are “damaged”. Likewise we may just have inflammation or something that impairs nerve function and isn’t “damage”.
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Exactly. I couldn’t think of a way to explain it any better than this.
Just because there’s lack of sensation doesn’t mean it has to be permanent nerve damage.
Please take Goldsteins diagnosis with a grain of salt. He seems to over exaggerate everyones diagnoses. I received very different reactions from his urologist in the office than him. He approaches his tests from the perspective of “if its not perfect, then you are fucked.” Try to remember that we are prone to believe the words of any doctor who recognizes this as a condition. Hes one of very few. It may be true what he tells you but I guarantee it is made out to be more extreme than it is.
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Have you thought about writing Goldstein to clarify whether he meant temporary neuropathy or irreversible neuropathy? It seems that distinction might not have been made or communicated.
It’s permanent in most cases unfortunately 
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Jesus 
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Thats terrible news - had he continued to get worse
Prayers for him and his family
He wasn’t doing good.
What test did they do to confirm inhibited dopamine?
What procedure are they talking about for the spine ?
Jesus did not read this thread in its entirety. I’m sorry man . If it’s true that you are no longer with us I hope you are in a better place and that justice is eventually served here
Cómo has mejorado ? Gracias 
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Yeah I am very curious about this as literally everything for over a year via MRIs, EMGs, all blood work, spinal tap etc was ruled out for me except pudendal nerve damage. One day on finasteride after 1.5 years my dick and balls just became numb, except it extended through to my tailbone, and then into pelvic organs causing urinary retention, difficulty with BM, severe muscle atrophy. What do you think that could possibly be other than pudendal nerve damage? Only symptoms I have ever had were in direct innervation of that nerve and its gotten worse and worse over 15 months.
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I’m really sorry to hear that brother
Unfortunately I’m going through similar circumstances and it’s very rough
How are you coping?
I’m really hoping done of the moderators it just someone who knows ANYTHING can chime in on this issue please
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I am starting at the bottom and trying to use several outlets to accomplish an overarching treatment goal, basically to take the knowledge gleaned from what I have seen work for people online consistently, but mostly that I can integrate and develop through various medical specialists. So, I am seeing a whole health (integrative medicine) doctor to gather bloodwork specifics and establish baselines, an endocrinologist to delve further into the hormonal aspects of it all and ensure achievement and sustained balance, a doctor that is DUTCH test certified to help me interpret what results of that truly indicate and can mean moving forward/ how to achieve these desireable levels and to focus on specific dietary regimens and exercise methods, a physical therapist specializing in pelvic floor therapy, and lastly a neurologist who has a lot of experience in pudendal nerve issues and potentials for understanding underlying neuro-response mechanisms to the integrated treatments to ensure proper feedback and results desired.
I am a pharmacy student and I refuse to live like this for a second longer. I donate to the PFS to move things along, but in the meantime I feel that I have resources to utilize and in turn hope that I find something that works as well as possible for me and to share this with others if so. I research a lot and IMO there is never a better idea than getting multiple perspectives and integrating several synergistic approaches to maximize advances.
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