Here are links to You tube. Pelvic Pain Awareness Day. 2008. Gynaecological Awareness Information Network. GAIN Inc. Australia.
http://www.youtube.com/watch?v=juAve2pNxws
http://www.youtube.com/watch?v=JyCjxtRMoMs
http://www.youtube.com/watch?v=KMu1xby_d74
http://www.youtube.com/watch?v=aqj6Qrzar7E
http://www.youtube.com/watch?v=FEErRW0e1RI
http://www.youtube.com/watch?v=eJUNKmurUoA
http://www.youtube.com/watch?v=5E2LjVRO-OA
Eric Bautrant:
http://www.youtube.com/watch?v=HVz89RCT_to
http://www.youtube.com/watch?v=ZbLlCLsO0AE
Video footage on PN You Tube
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catherine a
- Posts: 291
- Joined: Sat Sep 18, 2010 4:46 am
- Location: Perth Western Australia
Re: Video footage on PN You Tube
Sunil,
This interview was done by a women's gynaecological support group called GAIN Inc. As you are male, if you have time or are interested, you could seek out a similar group who support men. Women are more often likely to form groups where they can discuss their problems more so than men. Perhaps Australia would have a 'Chronic Pain Society' that you could approach and get them to be involved with issues of PN. Maybe even ask Prof. Vancaillie & Peter Dornan to give a talk. (They both treat males for PN issues.) Someone would have to initiate the first step and it could be yourself. This particular interview was initiated by myself. I found the support group in Perth, and asked Prof. V if he would give a talk at one of GAIN's awareness days. both he and Dr. Pavy (my pain management doctor.) agreed. I just googled http://www.chronicpainaustralia.org/ Would be a good place for you to start. The more people we have taking the first step the more help and information will be available. You would be a great source of information and support to other men who are suffering but have nowhere or no-one to turn to for advice. I would be willing to also get in touch with Chronic Pain Australia. Between us we could see what could be done. I was hoping that one day we could have ABC or SBS do a documentary but I don't know where to start. I looked at the TV channels online but their application for ideas only seem to be for people in the media.
Maybe someone in the media might see this website and help us get started.
Catherine.
This interview was done by a women's gynaecological support group called GAIN Inc. As you are male, if you have time or are interested, you could seek out a similar group who support men. Women are more often likely to form groups where they can discuss their problems more so than men. Perhaps Australia would have a 'Chronic Pain Society' that you could approach and get them to be involved with issues of PN. Maybe even ask Prof. Vancaillie & Peter Dornan to give a talk. (They both treat males for PN issues.) Someone would have to initiate the first step and it could be yourself. This particular interview was initiated by myself. I found the support group in Perth, and asked Prof. V if he would give a talk at one of GAIN's awareness days. both he and Dr. Pavy (my pain management doctor.) agreed. I just googled http://www.chronicpainaustralia.org/ Would be a good place for you to start. The more people we have taking the first step the more help and information will be available. You would be a great source of information and support to other men who are suffering but have nowhere or no-one to turn to for advice. I would be willing to also get in touch with Chronic Pain Australia. Between us we could see what could be done. I was hoping that one day we could have ABC or SBS do a documentary but I don't know where to start. I looked at the TV channels online but their application for ideas only seem to be for people in the media.
Maybe someone in the media might see this website and help us get started.
Catherine.
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.