Hannah Mollie Stimell Welcome to our web page for our 7 month old daughter Hannah. It has been provided to keep people updated about Hannah and her condition. Hannah was diagnosed on July 16, 2004 with a rare genetic disease called Niemann Pick Type A. There is currently no effective treatment or cure for this and our only hope is a cord blood transplant. Hannah is now undergoing intense Chemotherapy and is scheduled to receive her transplant on August 21. Please sign Hannah's guestbook so we will know you have visited.
Journal
Monday, February 2, 2009 9:14 AM CST i can't believe today is 4 years that hannah passed away in my arms.i can't believe we have not physically seen or held hannah for that length of time it seems so incomprehendable!!. not a day goes by that hannah is not thought of or spoken of. not a day goes by that she does not make a difference in the way i think and feel and who i have become .i am the most proud to have been hannahs daddy and i know jill is most proud to have been the greatest mommy to hannah. we miss that beautiful little girl. and wonder what hannah would be like now over 5 years old. i just felt the need to write today how much hannah means to us and how much we miss you hannah. none of it makes any sense zero!!!!!!! just the fact that you are free from all the pain and tubes , medication that you had to endure that no child should ever have to deal with never!!!!!!!!!! hannah we love and miss you sooooo much... but those are words that never have to be written because it's beyond words. loving you, missing you ,and thinking about you today and everyday. we love you always mommy and daddy
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Hospital Information: Fairview-University Hospital 420 Delaware Street S.E. Minneapolis, MN 55455 612-672-6000
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