Links

1. What websites does this community offer?

1. This one, the new main site for English speaking patients.

2. The previous main site at pudendal.de, with group discussion. This was the most current of all the PN websites. It's forum was a greatly appreciated innovation, compared to the previous one on Yahoo. However due to problems we have had to create this new site.

3. The pn.jcon.org site, which pioneered the use of extensive thoughtful writing, high quality images, documents, and FAQs for PN patient self-education. It is being merged with the new site.

4. Dr. Ken Renney's site. This team, in Houston, Texas, is probably the best place in the US to go for diagnosis and treatment of PNE. Ken is unusually well qualified. He is a recovered PNE sufferer himself and is a great guy. As of October 1, 2003 they have completed over 40 surgeries.

5. A very old site at Yahoo, which is no longer used. This was the first forum dedicated to Pudendal Neuropathy. It helped many people and essentially crystallized the English speaking PN community.