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Pictures!
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Pictures!
Considering the fact all of these young people are living with Huntington's Disease every day of their life, either by having the juvenile form of HD, being at-risk for it, or having a parent with HD it does a heart good to see them smile!  That's what being able to attend an HDSA National Convention does for them....the love, support and understanding they receive there can be seen in their faces!!  For a few days each year they can be themselves, surrounded by people who understand and care.
 
 
2005 Atlanta
If you have a link to pictures taken of young people at an HDSA National Convention
you would like linked here, please email the URL to Jean Miller-NYA Adult Advisor

nyaflyerpic.jpg

 "If you have no where to go,
look for me and I'll give you a way out.
If you need support,
I'll be right there on the sidelines,
cheering for you until I lose my voice.
If you ever need me, but don't know
where I am, look behind you;
I'll be there ready to push you back up
if you start to fall behind."
~Rachel Turner