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That's correct, I will be traveling 8,000 miles to bottom of the Earth to battle 40 foot seas, 30 Mph winds, and sub zero temperatures to show that with dedication and persistence a cure for NF is within our grasp.
What Drew and thousands of NF families go through on a daily basis is more than a test of strength. It is a battle of attitude and endurance to see the light at the end of this tunnel. So what's the good news? The good news, is money raised by the TUMORNATORS has directly funded research on mice with Schwannomatosis. We are firmly on the path to treatment and YOU have funded the initial steps for a cure! There is still much work to be done, and a long road at home with more questions than answers, but with your continued support I know we can make it.
If you have not seen the slide show and would like to learn more www.TUMORNATORS.com .
The Children's Tumor Foundation is a nonprofit organization dedicated to finding a cure for NF including Schwannomatosis. .
To learn more about NF and Schwannomatosis, a very common genetic disorder check out this link for information on Neurofibromatosis and current research CLICK HERE FOR CTF.org.
We cannot thank each and everyone of you enough for your help and support. You truly mean the world to Drew and our family, thank you.
Sincerely,
Chad, Ben, & Drew Leathers
Fran & Jon Cone & The Entire TumornatorNation!
FOLLOW THE
TEAM'S PROGRESS HERE
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Total Donations Collected:$52,796.00
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| Goal: $100,000 |
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Below is a video from the Children’s
Tumor Foundation that demonstrates how your support benefits nearly
2 million people worldwide that are affected by Neurofibromatosis. I
hope you’ll please take a few minutes to watch the video and perhaps
be as motivated as we are to support The Children’s Tumor
Foundation.

Adobe Flash Player is required to view
video.
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CLICK HERE to follow the NFE Antarctica BLOG
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Sorry.
Fundraising has ended.
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