The VP (Vulvar Pain) Foundation was established in 1992 as a non-profit organization to end the isolation of women suffering from vulvar pain and related disorders (fibromyalgia, interstitial cystitis, irritable bowel). The Foundation’s purposes are to give reliable information, hope, safety, and success to sufferers and their families, to advance the standard of medical practice in treating vulvar pain syndrome, and to promote scientific research.

An international organization, the Foundation publishes The VP Foundation Newsletter and The Low Oxalate Cookbook, sponsors research, and coordinates a network of personal support and other resources for its members. It also conducts a program of public education and outreach.

Your Membership Entitles You To:

~ The VP Foundation Newsletter

~ Discounts on educational resources
~ (back issues, books, videos)

~ Participation in the the VPF’s Support
~ Network and Support Group activities
~ and events (Network members only)

~ Opportunities to participate in research
~ studies and surveys (Network members
~ only)

~ Contact information for interested health
~ care professionals on request

~ Distribution of research and treatment
~ information to health care professionals
~ on request

~ Invitations to VPF seminars, workshops,
~ and conferences