My experience of treatment

Treatment options for UK & Irish members; including VHI & HSE criteria for funding and E112 Applications etc.

My experience of treatment

Postby DeterminedLady » Sun Sep 24, 2017 12:54 pm

I was at rock bottom with overwhelming symptoms of pudendal neuralgia earlier this year that had taken over my ability to work and function as a carer to my children. The "pain management" route had not only failed to work, it had made the condition worse. I felt I couldn't go on. It was suggested to me that I try the chiropractic treatment route and I did.
I have been (and continue to) receive weekly treatment from pelvic pain specialists Sayer Clinics chiropractor and physiotherapist (as well as hormone therapy from London bioidentical hormones and important changes to my diet to address previously undiagnosed food intolerances). I have shifted from the downward spiral where I felt there was no hope at all, to a journey to recovery. I am continuing to make progress with my health, overall well being and my neuralgia symptoms are about 35% improved so far.
I have never "blogged" at all in my life but I am sharing this in case there's anyone else out there who is suffering like I was and who can learn from what I've been doing. I will post again when I get to my next goal - 70% - and share with you the next stage of my journey. Wishing everyone positivity and peace.
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Re: My experience of treatment

Postby Violet M » Mon Sep 25, 2017 4:38 am

Wishing you all the best with continued healing. ;)

Violet
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.
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