This section is for XXX girls or parents of XXX girls who are looking to talk to others of a similar variant.

I can only imagine what you go through and feel when you find out this news.  Since I know how it felt to find out my XXY diagnosis, I would expect it to be somewhat similar.  Here you have the opportunity to meet others and to connect to those that have dealt directly with this situation.  Some of those who have been in this situation, are listed below with their e-mail address and other information.  Feel free to contact them.

If you would like your information added to this section or if you have any questions for me, please e-mail Stefan.

There are two XXX mailing list for support and information:

• http://groups.yahoo.com/group/raregeneticdisorders/

• National Organization for Rare Disorders
• Triplo-X Syndrome
• The Triple-X Support Group
• Triple-X Females: An Orientation
• Triple-X Syndrome
• Triple-X in Dutch  
• University of Michigan Health System: Triple-X Syndrome
• National Institute of Mental Health (NIMH) 

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Last update on March 3, 2007.