The AISSG-USA was founded in 1995 and the first meeting was in 1996.

We hope to reach every AIS individuals and those with similar conditions so they can all come to the “table of support”, and get what they need, when they need it, so they can live their best life.

Take Eden (show above with her adopted son Ben), she was one of our earliest members, and today is out and proud of her Complete AIS status, and is an accomplished musician and is raising her son Ben!

We are here for you... whether you’re as “out” as Eden or the most private person in the world -- we’re here to provide information and support to people affected by androgen insensitivity syndrome (AIS), and similar conditions, including adults with the condition, parents of AIS children, and professionals working in the area of AIS.  Information and referrals, phone support, regional and national support group meetings, literature, advocacy and newsletters.

Snail mail:

AISSG-USA
PO Box 2148
Duncan, OK 75354-2148
 

E-mail:   aissgusa AT hotmail DOT com

On the web:

 www.aissg.org   (for UK) or

www.aissgusa.org (for US & Canada)

The Internal Revenue Services has approved our status as a "public charity" under section 170 (b) (1) (A) (vi). Contributions to AISSG-USA are tax-deductible, consult your tax preparer for additional details.

This web site was designed by Cindy in Indiana, and was updated in Sept. 2007
This web site at Indiana University is sponsored by
 The Kinsey Institute for Research in Sex, Gender, & Reproduction.
It is being published by the AISSG-USA Support Group.
You may contact Cindy, our webmaster, at this e-mail:  ais AT indiana DOT edu