Hi,
Finding this site was like finding a pot of gold at the end of the rainbow.
It brought me to tears to discover that so many people are experiencing the same symptoms that I have been experiencing for five years. It gave me such a sense of belonging to read your messages.
Thank you for allowing me to be here. I wish nothing but good days,( the best we can hope for on our individual journeys), to everyone struggling with Pudendal Nerve pain.
Hello and thank you
Hello and thank you
Last edited by KellyJane on Tue Oct 28, 2014 10:05 pm, edited 1 time in total.
Re: Hello and thank you
Welcome KellyJane,
So sorry you have had such a struggle but glad to hear you are having the courage to move forward. Your children I am sure are very glad you are searching for treatment. I feel some of your pain as it is a long road and hope you find some help soon. I am not a stimulator patient so I cannot give advice but wanted to welcome you. Best of luck.
Janet
So sorry you have had such a struggle but glad to hear you are having the courage to move forward. Your children I am sure are very glad you are searching for treatment. I feel some of your pain as it is a long road and hope you find some help soon. I am not a stimulator patient so I cannot give advice but wanted to welcome you. Best of luck.
Janet
2007-08 pelvic muscles spasms treated by EGS. 6/27/10 sat too long on hard chair- spasms, EGS not work Botox help, cortisone shots in coccyx help, still pain, PT found PNE & sent me to Dr Marvel nerve blocks & MRN, TG left surgery 5/9/11. I have chronic bunion pain surgery at age 21. TG gave me back enough sitting to keep my job & join in some social activities. I wish the best to everyone! 2019 luck with orthotics from pedorthist & great PT allowing me to get off oxycodone.
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stephanies
- Posts: 692
- Joined: Mon Oct 25, 2010 3:07 am
Re: Hello and thank you
KellyJane,
I am sorry you have been through so much. You seem to have a persevering attitude and I hope you find relief from your problems soon.
Sincerely,
Stephanies
I am sorry you have been through so much. You seem to have a persevering attitude and I hope you find relief from your problems soon.
Sincerely,
Stephanies
PN started 2004 from fall. Surgery with Filler Nov. 2006, Dr. Campbell April 2007. Pain decreased by 85% in 2008 (rectal and sitting pain resolved completely), pain returned in 12/13. Pain reduced significantly beginning around 11/23.
Re: Hello and thank you
Welcome KellyJane. That's major -- what you have been through. Have they ruled out any spinal nerve root problems as opposed to pudendal neuralgia?
PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.