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August  7-10th-2

Get Ready: save the date

 

 

 

 

 

 

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#LittleAwesomeMoment

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sami

Born Brave: Tell us how you think your NF kids are brave! We love hearing from you.  info@littlesttumor.org

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Nuts

Please let us know your ideas for NF solutions! info@littlesttumor.org

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Such a GREAT year in our Advocacy efforts!

We rolled up our sleeves and got to work:

WI Model of Bipartisan Support for Nation

90 Congressional Representatives Sign on to support NF Research

10 Senators Sign on to support NF Research

 

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Our Commitment:

1  Building Awareness USE-2

 

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Summer Days: Our Favorite Green Juice

How to make Green Juice-3

 

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Unknown

NF Real Life: “Please still fund research! Both my children and I suffer with NF1, my daughter presents with the worst symptoms in our family. She has had 5 surgeries and is only 9. More surgeries are in her future. Tumors growing back and new ones are found. It’s a never ending battle. No child should have to live like this. “

Support NF Scientific Research Click Here!

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lillahipster

Never to Young: Meet the Crew

Young Hipster Lilla has been working for the NF cause since age 8. She has spoken to legislators, run/walk, cut off hair, and participated in most every event LTF has ever had.

Join her and volunteer today! Email us info@littlesttumor.org

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lilla_DC

Tell Your Legislators: tumors in children, we do not like them, we do not like them, WE DO NOT LIKE THEM

Pediatric medical research funding should never be sidelined by Congressional debate. Federal funding for Neurofibromatosis  (NF) needs continued legislative support.

We work on this all YEAR round!

Click here to sign for support!

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Yay!! Jack Black of Tenacious D performs at December Benefit for LTF.

jack black dec 2013 benefit

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nowThe opportunities for NF progress stand within our reach. Join us as we seize these opportunities and fulfill our vision: tumors in children, we do not like them. Donate now.

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tumors in children, we do not like them

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Check out our fundraising page!
 You can give a little to help A LOT.
You may ask yourself, how can I help the Littlest Tumor Foundation?
  1. Make a  $10 donation or start a campaign.
  1. Tell your family and friends–forward this email to inform them of how they can support the Littlest Tumor Foundation and make a difference in a child’s life.
  1. Join us on Facebook and Twitter to share our posts and help spread awareness.

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The Happiness List: Our List #100 Happy Days

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For us, connecting with our inner joy is working hard, taking the chances on the foundation that we do, and then seeing the impact it has on individuals and families. We try taking advantage of every opportunity and chance we have for the NF community.

What makes you happy? When someone offers you the chance to experience something new, bring your family together, or to just relax in the crazy times in life, do not be afraid to take it. Fill your life with happy memories and times that warm your heart because these are the moments we live for so why not experience more of them. Please share some things that make you happy!

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Our Mission

Increase understanding of Neurofibromatosis (NF), empower affected families, advance research of preventative therapies.



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