Bring Back The Juvenile Huntington's Disease Award In Honor Of Kelly Miller
49 Comments
B
Barbara Sipes
10 years ago
Please bring back the JHD award. I would like to be allowed to nominate a young lady for the 2017 award.
K
Kendra
10 years ago
Its sucks haVing juvenile huntingtons disease
H
Holly renee
10 years ago
For Jacey ❤
J
jane mervar
10 years ago
Featured
PLEASE PLEASE PLEASE keep the jhd award in honor of kelly miller! Every year it is not awarded begins to feel like even the HDSA has abandoned our kids and there are many families and young people doing wonderful things in support of this battle and many children who need to know that their lives matter ...
M
Marie kovach
10 years ago
Signed.
V
Vicki Owen
10 years ago
this will keep raising awareness...which is very needed in this community
B
Barb Hanshaw
10 years ago
Prayers for all with this disease.
M
Mark gazlay
10 years ago
Rip karli.....
A
Astra Glover
10 years ago
I hope everything works out to your favor! Sending love and happy thoughts.
J
Justin Mukka
10 years ago
Signed
V
Vanessa B Carriere
10 years ago
This shouldn't have been discontinued in the first place! Lets bring it back!!
B
Ben lamoreau
10 years ago
I think this would be a wonderful idea and such an inspiration to whom ever may win it. Let's do it
D
Dave Hodgson
10 years ago
Apparently Kelly Miller's name was NOT taken off the award. The award was not given out this year. I stand corrected.
W
Wendi Lutz
10 years ago
Bring back the award!
D
Dave Hodgson
10 years ago
Featured
Bring this award back! Why was it discontinued? After ALL the work Jean Miller did to establish the NYA along with Susie Hodgson, it's a shame Kelly Miller's name was taken off the award.
L
lisa ethridge
10 years ago
This needs to be addressed
S
Stacey Sargent
10 years ago
I agree with a comment above, " If the committee didn't feel like they had enough info on a nominee, they should have taken it upon themselves to learn more about that child! Sounds to me like someone took the lazy way out or didn't like who was nominated!" These kids are often disabled at a young age, unable to participate in sports or activities where trophies are awarded, this is something that they look forward to, and for one brief moment, makes them feel like a "normal" kid. HDSA needs to start recognizing JHD more, and the families more. I want to see HDSA contribute to JHD studies and research! Maybe it is time for a new leadership team?!
C
Cindy Moore
10 years ago
Why would they stop something so important. Boggles my mind. This should be awarded every year without any hesitation!!
C
Cindy Moore
10 years ago
Featured
I live in Canada, but I will support JHD until the last breath I take, This is very important that we recognize this horrible disease and do everything we can to find a cure. My daughter also suffers from this horrible disease labelled as the worst disease known to mankind.
Please bring back the JHD award. I would like to be allowed to nominate a young lady for the 2017 award.
Its sucks haVing juvenile huntingtons disease
For Jacey ❤
PLEASE PLEASE PLEASE keep the jhd award in honor of kelly miller! Every year it is not awarded begins to feel like even the HDSA has abandoned our kids and there are many families and young people doing wonderful things in support of this battle and many children who need to know that their lives matter ...
Signed.
this will keep raising awareness...which is very needed in this community
Prayers for all with this disease.
Rip karli.....
I hope everything works out to your favor! Sending love and happy thoughts.
Signed
This shouldn't have been discontinued in the first place! Lets bring it back!!
I think this would be a wonderful idea and such an inspiration to whom ever may win it. Let's do it
Apparently Kelly Miller's name was NOT taken off the award. The award was not given out this year. I stand corrected.
Bring back the award!
Bring this award back! Why was it discontinued? After ALL the work Jean Miller did to establish the NYA along with Susie Hodgson, it's a shame Kelly Miller's name was taken off the award.
This needs to be addressed
I agree with a comment above, " If the committee didn't feel like they had enough info on a nominee, they should have taken it upon themselves to learn more about that child! Sounds to me like someone took the lazy way out or didn't like who was nominated!" These kids are often disabled at a young age, unable to participate in sports or activities where trophies are awarded, this is something that they look forward to, and for one brief moment, makes them feel like a "normal" kid. HDSA needs to start recognizing JHD more, and the families more. I want to see HDSA contribute to JHD studies and research! Maybe it is time for a new leadership team?!
Why would they stop something so important. Boggles my mind. This should be awarded every year without any hesitation!!
I live in Canada, but I will support JHD until the last breath I take, This is very important that we recognize this horrible disease and do everything we can to find a cure. My daughter also suffers from this horrible disease labelled as the worst disease known to mankind.
Please bring back the jhdkids award