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Who we are, how to contact us and
how to contribute to the network

1. WhO We ArE

Who is Who in the Vaginismus Awareness Network Team Management

2. CoNtAcT uS

After years helping women and answering individually without asking for any type of fee and giving much of our free time away for the cause of women empowerment, beginning from the end of 2011 we will no longer answer personal e-mails and therefore this function has been removed. We received hundreds and hundreds of "thank you" emails, almost on a daily basis and we are very grateful we gave the help and support and encouragement we were able to but we can no longer keep up with the demand. We believe the information present on the website is enough to address most concerns so make sure you read it all properly, there's TONS of information! If you have any personal question re. your struggle or journey with vaginismus, or would like some support, the best course of action would be to join an online support group or check out questions posted on forums such as the Vaginismus1 forum on the web. If you too just wanted to say thank you to all the women who worked so hard to make this site possible and keep it alive, just please take a second to click on the poll on the homepage, bottom right. All the best with your great journey. And remember, vaginismus is so NOT the problem. The way society looks at it and the way you decide to look at it is, so have a different look :) V.A.N. Team

DISCLAIMER: This site is not designed to provide medical advice. All material is gathered from the experience of hundreds of women who experienced vaginismus but it is for information only and is not intended to be a substitute for professional or medical advice, diagnosis, and treatment. Please review the information contained on vaginismus-awareness-network.org carefully and confer with a health care professional specialized in vaginismus, as needed.