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Emily's Story - HomeEmily Labrecque battles ATRT Childhood Brain Cancer
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Emily Labrecque battles ATRT Childhood Brain Cancer
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Emily Labrecque battles ATRT Childhood Brain Cancer
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Emily's Story - Emily's Blog
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Thank you everyone for the support you have shown us throughout this entire process! It has been a rough 11 months to say the least and still we're staying positive in hopes for a cancer free future for Emily! We encourage you to share your cancer stories with us no matter what age, form or outcome! Help raise awareness for all children battling cancer! Share your stories with us! Create a free website. Create your own free website. Start your own free website.
About ATRT - Emily's Story
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Mdash; a form of brain cancer. In the United States, three children per 1,000,000 or around 30 new cases are diagnosed each year (with cancer, about 3% of those children are diagnosed with AT/RT). Pediatric brain cancer is the second leading cause of death, just after leukemia. Because it is highly malignant, AT/RT has a high mortality rate." wrote Wayne Rivet of the Bridgton News. New radiation techniques that minimize damage to healthy tissue that surrounds brain tumor tissue are under investigation.
Wristbands - Emily's Story
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Hope 4 Emily - ATRT Childhood Brain Cancer. These wristbands represent more than just Emily's fight but all brain cancer (grey) and all childhood cancer (gold) and are a great way to help raise awareness about this rare disease and also help Emily at the same time! Made out of 100% Silicone. They are $2 each plus $1.25 shipping and can be purchased by mail or paypal. For PayPal purchases, please send your payment ($3.25 per wristband) to ericajl78@yahoo.com. The Emily Labrecque Fund. Sebago, Maine 04029.
Photos - Emily's Story
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Updates - Emily's Story
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February 11, 2011. February 9, 2011. Today is officially Emilys last day of Chemo Treatments! This has been such a hard long year for her filled with ups and downs. Today is such an exciting day for her and her family! Even though her battle is not far from over, This is an incredible Milestone to have achieved! Now she can begin her other therapies and hopefully be feeling better than she has! Thank you everyone for your continued support! January 28, 2011. January 14, 2011. Keep fighting little angel!
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Welcome - Hope For Eastern Hungary
How You Can Help. See the Millers' blog. Thank you for visiting the website of the IMB Eastern Hungary team and allowing us the opportunity to share with you about the Hungarian people group. Please take a few minutes to browse our pages and see what's new; learn how you can pray for eastern Hungary, and how the prayers of people here and around the world are being answered. Tiszafured church plant and friends from mother and sister churches. Look among the nations!
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Emily's Story - Home
Please see the Family Fun Night link on the left for more info about the upcoming benefit for Emily! 100% raised goes into her fun, The Emily Fund. Find us on Facebook under "Support Emily - ATRT Brain Cancer Awareness". Thank you everyone for the continuous support! Emily and her battle against brain cancer. Emily's mom, Erin, who is her lifeline, has no choice but to stay unemployed because of her daughters illness and the constant need for medical and emotional attention. She works full time takin...
Hope For Emma
Follow Emma's Journey at www.caringbridge.com/visit/emmagerman. Silent and Live Auction, Family Fun, and Dinner Belle Plaine Senior H.S. Saturday, February 12, 2011 4pm - 8 pm. Auction Items up for Bidding! Make a Card for Emma! For questions or more information! Please contact Maxine at Maxine.Hall@gmail.com. Monetary donations can be made to the. Hope for Emma Fund. C/o State Bank of Belle Plaine, 201 West Main Street, PO Box 87, Belle Plaine, MN 56011. Subscribe to: Posts (Atom).
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This Site Comes With Music! Do you want to hear the music? Please put in a valid email address. Please put in a valid email address. Please include a comment. We urgently need more medical reasearch towards a CURE. WE ARE HOPEFUL. Due to the small number of cases currently in the U.S., Diffuse Intrinsic Pontine Gliomas (DIPG) is not widely recognized; therefore, funding for its research is very lean. We plea for a prayer for every $ that you donate towards this cause. Thank you so much, and God bless.
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