When I watched this video for the first time, I cried. As mothers we can all sympathize and understand how heartbreaking this must be on a family. I’d never heard of Gaucher’s Disease before since it is so rare but now I know enough to know that I want to help. Hannah’s mommy is not giving up hope and is reaching out to the blogosphere, sharing updates on Hannah and her family and is working hard to raise awareness about Gaucher’s Disease.. not only for Hannah but also for other children who have the same disease. Hannah’s mommy says that doctors are so close to having a GD2/3 mouse to test treatments on that could possibly save Hannah’s life! I think that is REALLY awesome news and a fundraiser can be found on their blog at LittleMissHannah.com to help support these medical treatment tests. They’re hoping to raise $10,000 by Hannah’s first birthday. So let’s help them; PRAY! Blog about it! Donate if you’re able. Give them support on their blog. Let’s just be there for them.
I’m praying for you baby Hannah!
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