Sunil,
Congratulations on your efforts to help fellow PNE sufferers in your country!!!
This is awesome and I wish you the best of luck... please keep us updated on how things proceed.
Sincerely,
A's Mommy
ACT Pudendal nerve treatment capital to be!
Re: ACT Pudendal nerve treatment capital to be!
Daughter grew completely on left side of pelvis
Multiple uterine surgeries to fix uterine adhesions, septum, and endo
Had all the conservative workups done, 3Tesla (Potter), recovering from L sided TG (Hibner) 11/10, Botox 6/11 failed, bilateral anterior PNE decompression (distal Alcock's/perineal branch), Aszmann, Vienna, 10/11; dx'd with CRPS Type 2, 12/11, Ketamine @ CCF 2/12, doing 75% better PRAISE JESUS!
http://fighting-pne.blogspot.com
http://www.thepelvicmessenger.org
Multiple uterine surgeries to fix uterine adhesions, septum, and endo
Had all the conservative workups done, 3Tesla (Potter), recovering from L sided TG (Hibner) 11/10, Botox 6/11 failed, bilateral anterior PNE decompression (distal Alcock's/perineal branch), Aszmann, Vienna, 10/11; dx'd with CRPS Type 2, 12/11, Ketamine @ CCF 2/12, doing 75% better PRAISE JESUS!
http://fighting-pne.blogspot.com
http://www.thepelvicmessenger.org
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catherine a
- Posts: 291
- Joined: Sat Sep 18, 2010 4:46 am
- Location: Perth Western Australia
Re: ACT Pudendal nerve treatment capital to be!
Sunil,
I'm so happy to hear you're setting up a support group. Ours starts on 9th April. I'll let you know how it all goes. Good on ya Sunil!! Your support in the ACT is much needed. Hope you're feeling better too.
Catherine (WA)
I'm so happy to hear you're setting up a support group. Ours starts on 9th April. I'll let you know how it all goes. Good on ya Sunil!! Your support in the ACT is much needed. Hope you're feeling better too.
Catherine (WA)
2004 PNE following vag. hysterectomy and A & P repair. 2007 TIR surgery France. severe entrapment at Alcocks canal & SS ligaments . Have my life back. 90% cured.No longer have medical appts.or physio.Some pain remains but is tolerable. 2012 Flew from Australia to the UK without pain flare. Very manageable. Almost back to normal. Now hold support group meetings at KEMH Subiaco Perth WA. Every 2nd Sat. of the month. Still pace my activities. PN doesn't dominate any more.