Little Miss Hannah - Our Fight Against Gaucher's Disease type 2 or type 3

[orderedbullet]

I just want to say thanks for sharing this. I am 27 with gaucher type 1. I have been getting treatment since I was eight. My veins have been giving me a hard time and they are wanting to put in a port. I have been scared and depressed for a while now and even lost my fight and began missing treatment. I have to say that after watching this I feel so much better. Hannah has given me my fight back not only to fight for myself but for her and others like her. One day we will find a cure! T

[jjac31456287]

omg im cryin please God save this poor innocent lil gurl and all people that are diagnosed with this disease. its not fair to have to see people go through this. if u knew the answers to the world i would tell all so that no peoson would have to suffer from this.

[strachovie]

I was diagnosed last month but I am 18 I rly hope somehow Hannah and I can find a way to feel better and I appreciate this post to help awarness Thank You

[DelusionDispeller]

Please let us know how baby Hannah is doing. My cousin's son has a metabolic disorder too and I've been standing by her side through it all though I've never actually seen in person what her family goes through. My daughter has traits of the disorder as well, in the form of food intolerance.

[poeticpaul]

Hi little Hannah its took me a little while to find you and what a wonderful you smile you have bestowed this daddy I hope you dont mind me sharing you smile with my little Kevvy he lives in heaven now but he is watching over you and thinks you are wonderful

Night Night God bless sweet dreams little miss Hannah

[zanessacutie1000]

I'm praying for hannah

[txstoryteller]

Heartbreaking vid; God bless you! FIVE stars!

[zennnx]

omg this made me cry i feel bad if i know you guys i will give the money i got to find the best cure

[jessi09xx]

As a mother of three looking at this video really touches my heart i had tears...

I hope that all these big companies that are on the internet could help you out...

Such as you tube, google, facebook, yahoo, and many others.

I hope your beautiful daughter could live and see her children and her grandkids

Love always the Duquette Family

[LordOut16]

My Daughter has Gaucher 1

[LordOut16]

It's too bad we can't make a movie about rare genetic disorders to raise awareness. My prayers are with you.

[KroegerFan44]

Maybe with these YouTube videos we can get the word out and help find a cure for these aweful diseases. I wish you all the best.

[Petula1968]

Hi Mommy :)... I'm going to post the video on my blog. ... I'll try to post it on both blogs (I am still learning the other one.) TTYS

[momof42008]

My family and I will keep your daughter and ever1 else with this in our prayers. We hope for the very best .

[AddiCassiFund]

Hannah, you are beautiful and we love you so much.

Addi and Cassi

[IIIsychakIII]

I'll pray for your little girl. Such a touching video.

[violentlyhappywest]

Your daughter is BEAUTIFUL! I wish you the best and hope a cure can be found soon!