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Great things happen

We’re developing support for XXY’ers in New Zealand

What is XXY and Klinefelter’s Syndrome?

If you have googled it you might be as horrified as we were too. It is hard finding out something new especially when the public information doesn’t at all match the reality that we live with.

We are making it part of our mission to share our stories – hopefully this will help parents, family and friends as well as new XXY’ers – understand what it is and what it is not.

There are a lot of great resources – let us guide you to some.

Experience life with us

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Discover stories

Sam talks about his experience being diagnosed with Klinefelters Syndrome (XXY)
Many people over the years have helped increase the awareness of XXY in New Zealand. Thank you to all involved.