Hi! I'm Logan. Welcome to my Gift Shop!
|Langerhans Cell Histiocytosis is an extremely rare
disease that can be deadly or cause life-long disabilities. It affects
mainly children, and I'm one of them. Since the disease is so
rare, it is classed as an "Orphan Disease," and receives no government
funding for research.
Mommy, Daddy, and my brother Erik and I
have opened this Gift Shop to:
- Raise funds for Histiocytosis research
- Raise awareness about Histiocytosis
Proceeds from every Gift Shop item benefit Histiocytosis research.
And every item sold has our special logo on the back. You can see the
logo in the upper left corner of the screen. We call it "A Family
United." It's each of our hands, and we're all wearing our blue
Histiocytosis arm bands. When Histiocytosis strikes one family member,
it affects all family members. The logo signifies that we're all in
the battle together!
When you send one of our Gift Shop items, you're raising awareness!
Click here to learn more about Logan's battle with
Twenty percent of the purchase price of Gift Shop items is donated to Histiocytosis
research (10% to the Histiocytosis Association of America, and 10% to
Dr. McClain's research on genes active in Langerhans Cell
Histiocytosis at Texas Children's Cancer Center).
I don't want
another child to learn the word "Histiocytosis."
Help me send Histiocytosis "To
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