The Mission of Dylan’s Quest for the Cure, which was started in May, 2010, is to promote disease awareness for Krabbe Disease and other forms of Leukodystrophy, to help raise money for research, and to help find a cure for these deadly killers.
Also, Joyce and I enjoy meeting other Krabbe families, to share stories and exchange memories. We have already traveled the path that you are on, and we know the heartache and sorrow that you are feeling, and that which is yet to come. To those families that choose to meet with us, we offer our “Blanket of Love” to each child, a small token from Dylan’s Quest to you. We are always eager to talk to any and all families that come to Pittsburgh, and all calls and e-mail’s are welcome anytime! Remember, YOU are NOT alone!!!
All are invited to join and share any and all Leukodystrophy topics,stories or pictures!
We Thank You for visiting our page, and hope that you leave a comment or two.
Joe, Joyce & Joe Jr.
Co-Founders, Dylan’s Quest For The Cure
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