Little Miss Hannah
Our Fight against Gaucher's Disease type 2 or 3
Home
Meet Hannah
Hannah’s Foundation
In The News
Gaucher’s 2/3
If you have a child with GD23
GD23 Facts
GD23 Resources
GD23 Physicians
GD23 Research & News
How to Help!
donate
volunteer
Contact
@LMHF on Twitter
Surviving
Hannah’s Fight
LMH Foundation
Gaucher’s Disease
Rare Disease
Pics and Videos
Why I Celebrate World Rare Disease Day
29
Feb
by
Carrie
~
Filed Under:
Rare Disease
In Hannah’s Memory
Hannah’s Fight
Latest Comments
Mel
on
Few weeks to go
Cristina (Bertrand's mom)
on
The “Irrational” Stage of Grief
Milena
on
The “Irrational” Stage of Grief
Patty Taormino
on
Little Miss Hannah Goes to Washington!
Cristina (Bertrand's mom)
on
The Nightmares Return
LMHFoundation Blog
Latest Comments