Little Miss Hannah
Our Fight against Gaucher's Disease type 2 or 3
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Why I Celebrate World Rare Disease Day
29
Feb
by
Carrie
~
Filed Under:
Rare Disease
In Hannah’s Memory
Hannah’s Fight
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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
Our 1st annual Tee up FORE Rare was a great success!
Meet Jenny Krshul, our New Executive Director!
Thank you Chuck and Judy Goodman!
Our Little Miss Hannah team is growing!
2018 Essay Scholarship Winner – Griffin Becker
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