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Revised presymptomatic testing protocol
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Acknowledgement and Disclaimer

Young People's Page

Please contact Jan if you have submissions for this page.

This is a section for young people in New Zealand who are affected by HD in any way. Please make contact if you have any suggections for making this area useful and interesting.

Huntingtons In My Family
A story told by Jenny Taylor (17yrs) about her HD family

The Courage To Go On
A story told by Sara Duncan (14yrs) about her HD father and how she feels about HD.

The Juvenile HD Caregivers Club (USA) is available on Yahoo.
For a fuller description of this group, see the Links page.



Appreciation and thanks must go to Judy Lyon for compiling the wealth of information available
on this site, and to Graham Taylor for maintaining the original site for so long.
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