Conflicting views on Prostatitis symptoms
Posted , 7 users are following.
Hi all,
Brief history of story: 2 years ago was diagnosed with Epididymitis after receiving oral sex from someone. The pain went from the head of penis into extreme testicular pain. I was diagnosed with chronic prostatitis about a year ago. I have had all sexual checks at GUM clinic (clear) and all urine, bloods and semen culture clear and no sti. I have had camera inserted into urethra twice and also clear.
My symptoms are: very red tip/opening of penis, clear colored discharge, pain after urinating/ejeculation, slow flow and pelvic/stomach/back pain.
My Urologist states that there is nothing more they can do to help me as I have had all antibiotics and I should live with it.
My doctor feels symptoms such as red tip and discharging are not signs of prostatitis and should be investigated further?
I have just ordered a kit online to test for Mycoplasma and Ureaplasma as I am so anxious. I don't understand how it would be any of these things as I have taken numerous courses of antibiotics that eliminate them.
Are my symptoms found in prostatitis? Should I push the urologist to support me more? I am at a loss of where to turn or where to go to sort this mess out. I know Prostatitis can be life long and not asking for a cure....just a way of managing the pain.
Thanks in advance
Danny
0 likes, 13 replies
joe98530 daniel76051
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daniel76051 joe98530
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But what STD could it be If I have been cleared of everything through numerous test methods? I was at the sexual health clinic again last week for more tests as it is constantly nagging me and desperate for something to come back but again tests were all negative?
Surely the urine, swabs, bloods and semen culture that I have had would have flagged an STD?
Cheers
daniel76051
Posted
as12829 daniel76051
Posted
When doctors say there is no more they can do, it is not anything you should accept. I would do some research and find what doctor is best at this kind of thing, and go see him or her. Maybe have to travel, but no more expensive than suffering pain week after week. I don't mean just pick another urologist to see, but search for the best of the best. Sometimes these places are called a center of excellence.
I guess you've had all the work ups and blood tests you care to even talk about, but there are likely things out there for which there are no tests, maybe rare things that most doctors would not be aware of in the first place. But the key is to not give up and do not accept that nothing more can be done.
daniel76051 as12829
Posted
Thanks bud,
I will do some digging and research. It's just such a nightmare. I have a new job starting next week...second baby is due to drop any minute....time is very scarce for travelling around but I guess I am going to have to prioritise. I feel this is holding me back from so much
john_14065 daniel76051
Posted
Then I went to see my 15th or 20th physical therapist. He was out in the country, not at a big time city clinic. But he understood my body and he cured me without drugs.
I urge you to keep researching and knocking on doors.
daniel76051 john_14065
Posted
Thanks John.
I will keep on trooping. As I mentioned I have just paid £100 for a test online for other STD related issues (Mycoplasma Genitaliem and Ureaplasm). I just can't believe I have been pushed from sexual health clinics as having 'nothing sexual related' and then on to Urology...1 specialist laughed and told me the symptoms were all in my head and prescribed me antidepressants...The second got to work with Cipro, Doxy and all sorts but has given up now and told me to exercise and drink water.
There will be someone out there. I just can't live with this pain much more, it is driving me mad.
Thanks again
as12829 daniel76051
Posted
I am wondering if it is not nerve damage? Do you ever notice any numbness or tingling?
daniel76051 as12829
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Funny you say that.
I read on another forum of a user who couldn't find answers to his prostatitis diagnosis/pains. He had a lower back injury. After all of the antibiotics etc he was sent for an MRI which showed it was his nerves that was causing all of the pelvic/groin/leg pains.
Around the time I started experiencing symptoms I was diagnosed with Lumbar Spondylosis which showed my discs were crumbling in lower back. For the last 2 years I have been experiencing very bad pain in my lower back, random pins and needles in my right arm and leg and tingling in my thighs. I went to the doctor this morning and have been referred to Osteopathy for an MRI but this will probably take time.
I couldn't imagine nerve damage would be behind the tip of my penis being red and the discharge? I also read somewhere that the discharge may be irritating the opening which is causing the redness. But it's another lead I guess.
daniel76051
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dcooperxyz daniel76051
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richard25210 daniel76051
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justin18892 daniel76051
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