Our Fight against Gaucher's Disease type 2 or 3
July 4th is coming up… To me, it marks one year since Hannah was able to enjoy her last holiday with us. She was still smiling, still very interactive, and she was very intrigued with the fireworks in the sky. Just a couple of months later, her health would deteriorate so horribly. To […]
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The countdown begins until the launch of our Little Miss Hannah Foundation on July 25th. July 25th, what would have been Hannah’s 4th birthday. We have been putting SO much work into the development of our foundation — from incorporation to nonprofit status to licenses and permits and all of the other business end of […]
[Continue reading...]My handsome boy, now a middle school kid. He was the student speaker for his class, and his speech was absolutely amazing ~ well, from what I heard at the beginning. He talked about his school memories, the fun times, and his friends. He shared about Hannah and how supportive the school was after she […]
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(be sure to bring the event flyer on June 7) Vegas friends, Celebrate the last day of school with us and help us raise money for the Little Miss Hannah Foundation! 20% of all food purchases will go towards LMHF. June 7th – 11 am to 1:00 am – ALL DAY! Many of our LMHF […]
[Continue reading...]It is coming up on six months since Hannah passed away. June 4th looms on my calendar ~ even though the day is blank, I know what that date represents. I found a few places online for grieving mothers, but only one really speaks to me. It validates how I am feeling. It sends […]
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SAVE THE DATE! July 25th, 5:30 pm to 9:00 pm – District at Green Valley Please come out on July 25th to celebrate our kick-off event for our Little Miss Hannah Foundation. It would mean so much to our family to have our friends come join us in this celebration – which is also Hannah’s […]
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