This section is for Triple-X girls or parents of Triple-X 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.
There is one Triple-X Syndrome mailing list for support and information:
There is a newly formed Triple-X Support Group:
Websites specific Triple-X information:
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Last update on June 29, 2014