newish and getting dramatically worse.
Posted: Thu Oct 24, 2013 2:46 am
Hi I'm Lanny,
I've posted on here once before but I need more advice and didnt know where else to ask. I gave my history on that post but here it is again. I am 19 but have had pudendal nerve pain since I was 13 after multi-level surgery. I am under the care of Natasha Curran and Andrew Baranowski at UCL I've only had 1 appt but based on that they found I have pelvic floor dysfunction as well as a tight with painful trigger points in bilateral Obturators inturnus I also have both Pirofomis pain which is treated else where but when it is treated does not help the pudendal pain ad it is injectd every 6 months with botox and steroids, I was also told that the Pudendal nerve itself is being irritated. My only treatment so far was done in January of this year and the following month where I had 2 CT guided steroid injections into the OI, I was very happy with the relief I got but I have not gotten any relief for months and the pain is now worse then ever, I'm now on the edge of tears with the pain...call it teenage dramatics but these pains I get in both my clitoris - almost all the time and after orgasm, deep inside my vagina - not constantly but a good amount and rectum - before during and after a bowel movements (which sitting on the loo helps with for both rectum and vaginal pain) ...are some of the worse pains I have ever had.
I have called UCL a number of times left countless messages and sent them a letter and I am getting no where. I just need some help for the pain to stop its all I've known my whole teenage life. I'm about to turn 20 and I would love for it to be reduced before another era of my life. I know it may never be gone, I have neuropathic pain in my knees as well as cerebral palsy I'm okay with a life of pain but just maybe not this much pain if I can help it.
What should I do about UCL what can I do about my pain.
Thank you for reading this.
Lanny. x
I've posted on here once before but I need more advice and didnt know where else to ask. I gave my history on that post but here it is again. I am 19 but have had pudendal nerve pain since I was 13 after multi-level surgery. I am under the care of Natasha Curran and Andrew Baranowski at UCL I've only had 1 appt but based on that they found I have pelvic floor dysfunction as well as a tight with painful trigger points in bilateral Obturators inturnus I also have both Pirofomis pain which is treated else where but when it is treated does not help the pudendal pain ad it is injectd every 6 months with botox and steroids, I was also told that the Pudendal nerve itself is being irritated. My only treatment so far was done in January of this year and the following month where I had 2 CT guided steroid injections into the OI, I was very happy with the relief I got but I have not gotten any relief for months and the pain is now worse then ever, I'm now on the edge of tears with the pain...call it teenage dramatics but these pains I get in both my clitoris - almost all the time and after orgasm, deep inside my vagina - not constantly but a good amount and rectum - before during and after a bowel movements (which sitting on the loo helps with for both rectum and vaginal pain) ...are some of the worse pains I have ever had.
I have called UCL a number of times left countless messages and sent them a letter and I am getting no where. I just need some help for the pain to stop its all I've known my whole teenage life. I'm about to turn 20 and I would love for it to be reduced before another era of my life. I know it may never be gone, I have neuropathic pain in my knees as well as cerebral palsy I'm okay with a life of pain but just maybe not this much pain if I can help it.
What should I do about UCL what can I do about my pain.
Thank you for reading this.
Lanny. x