
HOPE MORE, FEAR LESS, SMILE ALWAYS!
Working hard to help others while raising Histiocytosis Awareness.
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Working hard to help others while raising Histiocytosis Awareness.
Our team is committed to helping others! Whether it is helping others smile while dealing with a serious medical illness or raising Histiocytosis Awareness we do it with a smile!
Our daughter Taylor was diagnosed with Langerhans Cell Histiocytosis, a rare cancer, at the age of 8 so we found out first hand what it feels like to deal with a serious medical diagnosis. Raising awareness for this rare cancer and helping other ill children became very important to us!
We focus on making kids and their families smile so that they are reminded that they are not alone while they are dealing with a serious medical diagnosis, all while raising awareness for Histiocytosis and funds for research.
We have some new products for you to take a look at!
Since Taylor’s diagnosis we have been active in raising Histiocytosis Awareness and funds for research. A few years into treatment, probably around the age of 12, while in the hospital Taylor heard a couple of younger kids crying and she just kept saying why can’t we bring them toys or a fun gift to make them happy so they don’t feel so alone. This is when the idea of our own foundation started to take root.
Taylor's Hope was founded with the purpose of providing support to children who are ill from diseases, as well as raising awareness and funds for Histiocytosis research. We want to keep kids smiling during one of the most difficult times in their lives and provide support to them, their parents, and their siblings, who are also trying to deal with the magnitude of the situation. We want to show them that there are people that care, that understand and that want to help them.
Please check our Events page for more information on how you can help.
Your support and contributions will enable us to meet our goals and improve conditions. Your generous donation will fund our mission.
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