Guys I have pressure in my ractum to anus area, feel like I have to push like poo. I have constantly burning sensation in my urethra,fell something giving pressure in my base of penis and urethra. Sometimes I have penis burning sensation. No doctor help me. Our Bangladeshi doctor have no idea what kind of deases it is. I have no STD and UTI prob. Please somebody help me...I from Bangladesh. Problem started while I was setting for eating a tingling sensation come to my perenium..
After 2 days of this incident all problem arises 1by 1.
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Anik420
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Maybe you have bladder infection. Did doctor test urine specimen. Sorry you are suffering, there are a lot of us with persistent burning , it’s very distressing.
Sorry Anik I could not possibly guess. You really need to be examined by a doctor. Did any of the doctors examine you?
Did anything happen just before the symptoms started? You say that you just sat down to eat a few days ago and this happened?
Did you have a fall just before?
Did you lift anything heavy?
Did you feel anything strain or 'pull' unusually as you sat down?
I am not medically qualified (no one is on here ). I do not know about pudendal neuralgia. Am not sure what that is.
I do have pelvic floor dysfunction.
I think mine was caused by severe constipation and made worse by a bad fall which injured (strained) my left groin. So I have total Pelvic Floor Failure and severe prolapse of pelvic organs snd severe bowel conditions which have resulted in bowel dysfuncion.
This is why I asked if you have good bowel function or any recent constipation problem?
Are there any other local doctors or hospitals near enough that you can go to? Or have you considered going back to a doctor you saw first and saying - this problem is not getting better - please help me ?
I have visited 3 doctor...they just gave me medicine... nothing told what's that...but now I have pressure in ractum area like something is pushing or I have to go to toilet...I Never had constipation problem before this...but the bowl movement is not same as before..my urehta burns 24/7.... something got vanished for few moments..also the pressure....now am taking Serta and clonium.
I am sorry to hear yet another person on here, but my immediate thought was pudendal nerve. This is what I suffer with every waking moment. A burning sensation like constant sun burn when it feels bruised where it is so bad. I live in NZ and really not a lot is known about it...o I struggle on. I’m sorry for you
Hi. How long have you had this pain and sensations? I would suggest that you see a pelvic pain specialist, if you can find one. If you’ve had the pain for more than a few months, it might be to do with the pudendal nerve, but you would need to be examined. Physiotherapists who specialise in pelvic pain can also be very helpful. One thing I did was to print off information about pudendal neuralgia and take it to my doctor, who had never heard of the condition, but referred me to a pelvic pain clinic. There are several books that you might find helpful, including Healing Pelvic Pain, A Headache in the Pelvis and Teach us to Sit Still. I find that a combination of gentle yoga, walking and meditation helps me to manage, as well as medication. I wish you luck in finding someone who can help you.
I am suffering from last 2 month.. sometimes the pressure and burning urethra has vanished for some moment. in Bangladesh there is no pelvic pain clinic...I m trying some pelvic floor loosen exercise from YouTube and taking homeopathic treatment.
Try doing the yoga Child’s Pose. Also lie on your back, pull your knees to your chest, then spread your knees wide like out to your shoulders. Hold that for several minutes. It stretches the entire groin area. The problem you have with PN is that your muscles are too tight around the pudendal nerve. You need to do exercises to loosen (not tighten) the muscles.
I do like him and his assistants (PAs). I was mostly better when I got to him but had a feeling of fullness in my rectum. Physical therapy helped tremendously.
I had PN pretty bad for several months. It was after at least 6 months of pain and then discomfort when I finally found him. I iced a lot, prayed a lot and had many people praying for me. I swear I thought I might be dying.
I realized I was holding my torso and groin tight most of the time and I tried to increase my awareness and relax my groin whenever I caught myself holding it tight. Stretching exercises help too as well as the PT, icing and vaginal dialator. My PT was a woman named Bharti at Northside Rehabilitation in Franklin on International Dr.
Pain can wear on you and affect everything else. Wishing you the best!
I put ice in a baggie and held in my crotch around my perineum and rectum, while I watched tv. Jarnagan didn’t do tests because I got to him when I was almost better. I was treated for Trigonitis and I don’t think I had it honestly. I think it was PE the whole time. My perineum started aching and it grew more and more intense. Urinating hurt and I couldn’t feel my bowels. I had to look in the toilet to see if I’d gone. It was awful for 3 months or so and gradually started getting better. They did MRIs and a flex sig to see if I had something wrong with my bowels and nothing showed up. Just recently it flared up because I carried a heavy suitcase. I really have to be careful of heavy items and squatting. I hope you get some relief.
It does sound to me like you could have pudendal neuralgia. Many times it is brought on by a fall, constipation or heavy lifting. I'm not a man but I've read many posts on this sight by men who have PN. I have it and the symptoms you list fit the condition. Physical Therapy (pelvic pain specialist) and medications like amitryptoline, gabapentin or Lyrica are the prescribed for nerve pain. Im very sorry for your pain. Its difficult going to docs who have no clue about this very painful and real condition. I would go to pudendalhope.com and print out info to take to your doctor.
Don’t give up! I’m female but have Pudendal Neuralgia. I saw numerous doctors including a urologist who all failed to diagnose it. Do NOT get constipated...it definitely makes it worse. Definitely find a “pelvic pain specialist”. Try an ice pack on your groin when It feels hot/swollen. See if you can get physical therapy for the condition. It’s what finally helped me. No heavy lifting, squats or lunges for exercise, can aggravate it too.
I had IBS in the past but hadn’t had many issues for years until the PN started. The IBS was so bad that I wondered if I had a parasite. I’m not sure they ever tested for one. My bowels were messed up for a couple months...maybe even 3. I think it’s possible the IBS and PN could be linked. I don’t think people’s symptoms necessarily present in the same way. When I had the initial PN it was so painful to sit on a toilet seat. The pain ran down the back of my thighs. I was uncomfortable sitting at all and told the scores of doctors I saw that I felt I was sitting on little water balloons. They all just scratched their heads. I now think It was that the pudendal nerve was that inflamed/entrapped. Definitely DO NOT let yourself get constipated. It definitely makes it worse. I’m really good now since physical therapy but if I get the least bit constipated, I can feel it again. I would also try to avoid sitting a lot. I walk and hike for exercise and it helps a lot.
I am however, I recently did yard work...lots of squatting and lifting. I woke up the next day and my groin was on fire. I kept trying to figure out what happened...then I remembered how many times I had squatted the previous day. I took care not to exert too much, iced my groin and used my vaginal dialator to stretch the muscles around the nerve and was better in 2-3 days.
Are you from Tennessee? If so, I am too. I would like to ask you some questions about the Pudendal Neuralgia. I was diagnosed as having Levator Aani Syndrome. Wanted to know the difference between the two .
Yes, I’m from TN. I know both conditions are pelvic floor issues. Not exactly sure of the difference except I think PN specifically deals with the nerve and often entrapment of the Pudendal Nerve and I believe the other deals with the muscles. It’s all together in the groin so I imagine there can be some overlap in symptoms. I’m sorry I’m not more help. I think treatment for Levator Ani is more heat application like soaking and for me with PN, icing helped because the area was inflamed and swollen. You’d have to do some research online or ask your doctor to be sure.
This is how I feel, please try to be positive. Although everyday I grieve for the loss of me. I was damaged whilst I was in surgery. Treatment injury. If I had done this to myself I’m sure I would be coping better. Lipoic Acid and High doses of vit b and b12 but I guess you have enough of that in your sunshine. Good luck, it’s hard I feel we are being tested for something, maybe to make us stronger people
Oh God last night while I was sleeping suddenly I woke up by erected penis with urethral burning....and a pressure in my left butock .....I am dying with this discomfort.....
Just from what i been through with pelvic floor dysfunction i would suggest same or pudendal nerve problems!
See a dr or a physio that deals with that problem... i see a great pelvic physio who was only person after all specialists that got the diagnosis right!!
Yes i see a physio that specialises in groin/pelvic area as there are loads around now a days as it seems to b more recognised and three months down the line i am alot better i have bad days but no where near like i did... i had pain all time....
u can google “ pudendal nerve or pelvic floor exercises” and u get some good strengthening exercise that will help u.
Also i dont eat any gluten dairy and spice as it seems to aggravate my stomach then if i have poop problems that will inflame it... and NEVER GET CONSTIPATION.. thats what gave me it in first place
non bacterial prostratis aka chronic pelvic pain syndrome maybe?? that’s what mine turned out to be, amitriptaline is the only thing that helps with mine, and avoiding rich tomato based foods, curries and things like that (i used to eat them every day, was heartbroken) and caffeine seems to aggravate it too
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