Please lend a hand and help me raise funds for the Children's Tumor Foundation!
I will be running in my undies this February so kids like Eva can grow up happy and healthy. You may ask why this is important to me. Eva is my 6 yr old daughter. She was diagnosed with NF1 at age 4. As an infant she had many Cafe au lait spots but no other symptoms. By age 4 she was diagnosed with NF1 at her 4 yr. old check-up. She has a tumor on her foot, back of her neck, small one on her hand and an optic glioma (tumor on optic nerve). She has many visits throughout the year at Duke.
Next time you think you’re having a bad day; think about Eva and other kids who have this incurable illness. If you’d like to help you can do so by donating or joining our team of undie-clad runners. Your donation will ultimately fund the research to find a cure for NF.
Together, we can be the difference in the lives of children like Eva and help #endNF.
The Children's Tumor Foundation funds clinical trials to find treatments and a cure for neurofibromatosis (NF), a genetic disorder that causes tumors to grow throughout the nervous system at a rampant pace, often manifesting itself during adolescence and causing deafness, blindness, paralysis, severe pain and so much more.
Whether the gift is $5 or $500, all donations are tax-deductible and will have great impact on those in need!
DONATE HERE: https://my.cupids.org/BradStikeleather
I greatly appreciate any and all assistance in this fundraising endeavor, and more importantly it means the world to the 2 million worldwide who battle NF on a daily basis!
My sincerest thanks to those on the board that have given early on. You will never know how much that means to me and my family. If you can't give that is understandable also. I would ask for your prayers for not only Eva but all the kids with this illness. Thanks again!
GTHC! and GO DUKE!!!
I will be running in my undies this February so kids like Eva can grow up happy and healthy. You may ask why this is important to me. Eva is my 6 yr old daughter. She was diagnosed with NF1 at age 4. As an infant she had many Cafe au lait spots but no other symptoms. By age 4 she was diagnosed with NF1 at her 4 yr. old check-up. She has a tumor on her foot, back of her neck, small one on her hand and an optic glioma (tumor on optic nerve). She has many visits throughout the year at Duke.
Next time you think you’re having a bad day; think about Eva and other kids who have this incurable illness. If you’d like to help you can do so by donating or joining our team of undie-clad runners. Your donation will ultimately fund the research to find a cure for NF.
Together, we can be the difference in the lives of children like Eva and help #endNF.
The Children's Tumor Foundation funds clinical trials to find treatments and a cure for neurofibromatosis (NF), a genetic disorder that causes tumors to grow throughout the nervous system at a rampant pace, often manifesting itself during adolescence and causing deafness, blindness, paralysis, severe pain and so much more.
Whether the gift is $5 or $500, all donations are tax-deductible and will have great impact on those in need!
DONATE HERE: https://my.cupids.org/BradStikeleather
I greatly appreciate any and all assistance in this fundraising endeavor, and more importantly it means the world to the 2 million worldwide who battle NF on a daily basis!
My sincerest thanks to those on the board that have given early on. You will never know how much that means to me and my family. If you can't give that is understandable also. I would ask for your prayers for not only Eva but all the kids with this illness. Thanks again!
GTHC! and GO DUKE!!!