I have found this aritcle (2011):
http://www.cam.ac.uk/research/news/gene ... identified
and this:
http://www.kcl.ac.uk/ioppn/depts/wolfso ... Peter.aspx
Here McNaughton contact:
peter.mcnaughton@kcl.ac.uk
I'm tryng to contact him...
Someone have news about some targeted therapy on the TRPV1 and HCN2 genes?
Thanks
HCN2 gene neurophatic pain
HCN2 gene neurophatic pain
2004 Urethral burnings, chronic prostatitis diagnosis, unuseful drugs. Lately added chronic pelvic contracture.
2011 Pudendal Neuralgia diagnosis, nerve blocks and oral drugs.
2013 Two neuromodulation surgeries.
2016 Possover negate Pudendal Neuralgia (no pain elicited on rectal exploration), says problem is more central but MRI- neurography show nothing.
2017 De Bisshop found Oedema/hyperpressure and neurological abnormal response on intrapiriform area, most on sx.
Failed injection blocks.
2011 Pudendal Neuralgia diagnosis, nerve blocks and oral drugs.
2013 Two neuromodulation surgeries.
2016 Possover negate Pudendal Neuralgia (no pain elicited on rectal exploration), says problem is more central but MRI- neurography show nothing.
2017 De Bisshop found Oedema/hyperpressure and neurological abnormal response on intrapiriform area, most on sx.
Failed injection blocks.
Re: HCN2 gene neurophatic pain
Haven't heard of it, Gabriel. Sounds promising though. Thanks for posting this info.
Violet
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.