The American Association for Klinefelter Syndrome Information and Support (AAKSIS) proudly joins the world of XXY/Klinefelter syndrome e-mail lists.

Hypogonadism2

This is the best list of its kind that I have found. Expect a LOT of well-informed expert mail. The list is very good for anyone who identifies as male and wishes to explore, understand, and use Tesosterone Replacement Therapy. To subscribe, please click here.

Intersex-Androgynous

A place for support and education about and for persons with an intersexed and/or androgynous physical appearance.  Together we will survive androgyny.  Please click here for more information.

To cling to the pathological definitions that have been imposed on us is not the purpose of this group. On the contrary, this group has as its mission to allow us to investigate all the facets of our identity, not only the body or our trauma. Please click here for more information.

Klinefelterxxy

A list for people 18 years of age and over, who have the karyotype 47, XXY+ / Klinefelter Syndrome and who identify in all sexualities, though current members are predominantly gay. Non - XXY'rs who have an interest in the subject either for personal and / or medical reasons, may apply for membership giving details of your interest. This list is intended as a community for support and education. Many here are experts on the subject of XXY, from having a deep knowledge of living with XXY. Subscribing information

KS&A offers a number of e-mail lists for different childhood age groups and for adult XXYs. "These discussion support lists have been created for you to exchange any ideas, information, news, comments, gripes, fears, or whatever, related to XXY and its variants. The lists are a place to discuss issues, to give and receive support, and to post information about the syndrome and how to live with it." Please click here for more information.

Join this group if your child has any variation of Klinefelter Syndrome other than XXY.  This group will provide parents with support and understanding from other parents with similar needs.  Please click here for more information.

Discussion list for XXYs, only, any age, living in Denmark, Iceland, Finland, Greenland, Norway, and Sweden.  Click http://lists.kanalen.org/mailinglistor.html or write xxy@telia.com for more information.

A list to help Canadian XXYs, family members, and parents pool information, resources, and support in Canada.  Click here to subscribe, or contact 47xxyorg@gmail.com for more information.

XXY-hb2 is an e-mail list for for adult people, born with XXY or variable, more commonly known as Klinefelter Syndrome, who are also homosexual, bisexual, intersexual or androgynous.   This is for ongoing discussion and support of this sex chromosome anomaly.   No moms, pops of youngsters or heterosexual people will be admitted.   Owned by Bill Bucar.  Click here for subscription information.

This unmoderated list is owned and operated by an XXY.  This list is not a support list, but rather for information and discussion, and often gets quite rowdy.  Click here for information on subscribing.

This moderated support list is owned and operated by Robert Grace, 47,XXY, from northern California.   Click here to subscribe.

This is a list for mothers of XXY sons, expectant XXY mothers, or other sex chromosome anomalies.  Learning about the anomaly and supporting each other is the goal.  It is a restricted list and members must be approved by the moderator.  Please click here to join.

A Discussion/Support List for Moms and/or Dads whose son's genetic signature is XXY(or a variation thereof) and whose son's age is between onset of puberty through adulthood.  It is a restricted List which means that the List owner/moderator must approve each person's subscription request.

To subscribe, please click here.

This list is for wives and girlfriends of XXY men for support and sharing information.  It is a private list and subscribers must be approved.  Click here to subscribe, or for more information, click here.

This is a web-based message board whose mission is to provide a professionally hosted website that we can share information, ideas, and just simply communicate with one another for those who are either XXY themselves (or some variant) or keenly interested in XXY (Klinefelter Syndrome). Click http://www.xxytalk.com/fusionbb/portal/index.php to join

The XXYY parent network has been established for parents of sons with the karyotype 48,XXYY and gives them a place to talk with each other about issues specific to this karyotype.  This is a moderated list and by subscription ONLY to those parents who have an XXYY son.   Click here to subscribe.