Established in 1983 as the first nonprofit organization in the United States to focus on pediatric brain tumor disease, the Brain Tumor Foundation for Children is a high touch organization committed to improving the lives of children and families who are affected.
http://www.braintumorkids.org/
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Brain Tumor Foundation for Children
Mary Campbell
6065 Rosw●●●●●●●●●Suite 505
At●●ta , GA, 30328
US
View this contact
Brain Tumor Foundation for Children
Mary Campbell
6065 Rosw●●●●●●●●●Suite 505
At●●ta , GA, 30328
US
View this contact
Brain Tumor Foundation for Children
Mary Campbell
6065 Rosw●●●●●●●●●Suite 505
At●●ta , GA, 30328
US
View this contact
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Welcome | Brain Tumor Foundation For Children, Inc. | braintumorkids.org Reviews
https://braintumorkids.org
Established in 1983 as the first nonprofit organization in the United States to focus on pediatric brain tumor disease, the Brain Tumor Foundation for Children is a high touch organization committed to improving the lives of children and families who are affected.
Thank You for Our Supporters!
http://www.kidscancersf.org/thank-you-for-our-supporters
August 28, 2016. Help Us Help Them Fight. Ways You Can Help! Founder’s Campaign Donors. Thank You for Our Supporters! You are here: Home. Thank You for Our Supporters! Thank You for Our Supporters! Angry Moon Cigars- Palm Beach Gardens. Atlantic Water Filter Corp. Best Buy – Wellington. Bonefish Mac’s Sports Grille. Cancer Alliance of Help and Hope. Capitol Carpet and Tile. Carrabba’s Italian Grille. Children’s Brain Tumor Foundation: Butterfly Fund. Children’s Wish Foundation. Friends for Life Foundation.
The Day Celebration - Giving Back
http://www.thedaycelebration.com/giving.html
We hope you will join the Fare Thee Well Foundation and share in the joy of The Day Celebration music festival. The Fare Thee Well Foundation, Inc. is a Georgia non-profit corporation, with the Federal Tax ID #26-0355008. The Fare Thee Well Foundation is proud to support the following quality organizations that richly deserve our blessing and support:. Brain Tumor Foundation for Children, Inc. For more information, please visit: www.braintumorkids.org. Georgia Coalition to End Homelessness, Inc. Most not...
People find a reason to believe: February 2008
http://meganandalyvia.blogspot.com/2008_02_01_archive.html
Feb 26, 2008. We are all sick! So for now we are laying low and getting lots of rest. (And it's an excuse to stay in our jammies all day long! Oh, and Livie has already had influenza once, and yes, she did have her flu shot. Apparently this year's flu shot hasn't been that proactive. I felt bad Livie's been so sick, so I gave her a "fun dip" (you know the lic-a-stix candy, I didn't even know they still existed.) She loved it. Posted by Megan and Alyvia. Feb 24, 2008. I was tagged again. 5 jobs I've had:.
People find a reason to believe: December 2007
http://meganandalyvia.blogspot.com/2007_12_01_archive.html
Dec 29, 2007. This is her pouty face. Christmas this year was a lot different than last year. Alyvia had C-Diff really bad and she was really agitated. She wasn't into opening presents at all. So we saved most of them and opened them when she felt better. She still has her good days and her bad days and Christmas was one of her not so good days. Posted by Megan and Alyvia. Dec 22, 2007. Alyvia is doing pretty good! Livie does, however, have C-Diff.yuck! I know that I have said Thank You, but I can't say ...
People find a reason to believe: November 2007
http://meganandalyvia.blogspot.com/2007_11_01_archive.html
Nov 30, 2007. Have to take the good with the bad. Alyvia had a great night last night, she was talking really well and we were singing nursery rhymes together, and she would kiss me and tell me that she loves me. It was great. (: I really miss those fun times we had together, its crazy how much I took those moments for granted. Posted by Megan and Alyvia. Nov 28, 2007. Thank you everyone for all the support and for all the prayers being offered up for sweet little Livie. Posted by Megan and Alyvia. So ye...
People find a reason to believe: October 2007
http://meganandalyvia.blogspot.com/2007_10_01_archive.html
Oct 30, 2007. She is able to swallow and protect her airway! Posted by Megan and Alyvia. Subscribe to: Posts (Atom). She really is our little miracle and has taught us the true meaning of love. View my complete profile. Brad, Shelley, and Noah. Breakfast With Santa 2014. Life in the N.C. Adam, Brittany and Andie Stevenson. Christmas Memories and Wishes. Quentin and Tara Woods Family. School Picture Mini Session. My Baby is 1! Please leave your email after the post. Keepin up with the Jones'.
People find a reason to believe: October 2008
http://meganandalyvia.blogspot.com/2008_10_01_archive.html
Oct 14, 2008. Minus Jojo and Logan, who is serving a mission). A couple weekends ago we had the opportunity to go to Lake Powell for a family vacation. It was sooo much fun! We had a really good time together, I'm so glad we were able to go. One year ago today, Livie was one of the sickest kids in the PICU at Primary's. Looking at her now, you would never know. Looking back at this past year helped me remember that I definitely have a lot to be grateful for! Posted by Megan and Alyvia. Life in the N.C.
People find a reason to believe: November 2008
http://meganandalyvia.blogspot.com/2008_11_01_archive.html
Nov 18, 2008. A little of this.a little of that. We have been tagged. 1Link to the person that tagged you and post the rules on your blog. 2Share 7 random and/or weird facts about yourself. 3Tag 7 random people at the end of your post and include links to their blogs. 4 Let each person know that they've been tagged by leaving a comment on their blog. Ok here we go, Tara. Cute little lizard we found at Lake Powell. Playing with Shayla's pet snake, Billy Bob. 5 Every night to get Livie to go to sleep (haha...
For patients
http://snip.stanford.edu/forpatients.html
The following support groups and organizations can help patients and their families and friends manage and cope with neurological disorders and diseases. National Institute of Neurologic Disorders and Stroke. The Stanford Brain Tumor Center. The American Brain Tumor Association. The Acoustic Neuroma Association. The Brain Tumor Foundation For Children, Inc. The Children's Brain Tumor Foundation. The National Brain Tumor Foundation. American Heart Association National Center. The Stanford Cyberknife Center.
TOTAL LINKS TO THIS WEBSITE
112
braintumorimmunologyfoundation.org
Brain Tumor Immunology Foundation - HOME
Brain Tumor Immunology Foundation. Brain Tumor Immunology Foundation. Is to help save the lives of those with Primary Brain Cancer with the hope that new research will eventually lead to successfully treating Metastatic Brain Tumors and children diagnosed with Pediatric Brain Tumors. We believe that the promising work of. May help to make the difference between a healthy life, and one cut short by Brain Cancer. An anonymous donor established the Brain Tumor Immunology Foundation so that brain tumor.
The Emily Dorfman Foundation for Children - The Interactive Brain Tumor Learning Center
The Interactive Brain Tumor Learning Center. The interactive Brain Tumor Learning Center was developed by The Brain Tumor Center at Duke University Medical Center. And funded by The Emily Dorfman Foundation for Children. This site uses colorful animations and audio clips to provide patients and their family members with information about brain tumors and their treatments. For visitors using a dial-up modem connection, animations will take approximately 1-2 minutes to load. I would like to learn about:.
The Emily Dorfman Foundation for Children - The Interactive Brain Tumor Learning Center
The Interactive Brain Tumor Learning Center. The interactive Brain Tumor Learning Center was developed by The Brain Tumor Center at Duke University Medical Center. And funded by The Emily Dorfman Foundation for Children. This site uses colorful animations and audio clips to provide patients and their family members with information about brain tumors and their treatments. For visitors using a dial-up modem connection, animations will take approximately 1-2 minutes to load. I would like to learn about:.
braintumorjournal.blogspot.com
Brain Tumor Journal
Sunday, March 16, 2008. EPILOGUE- How You Can Help Your Loved One. Blessed are you who. Understand that it is difficult for me to put thought into words. Understand that I can not speak when someone else is talking, because I have to have auditory-feedback. Take time to listen when I speak, in spite of my speech problem. Never ' hurry' me for often I need time more than help. Encourage me and praise me for continuing to try. Ask me for any help, for my greatest need is to feel needed. Every day was a str...
braintumorjourney.wordpress.com
Brain Tumor Journey | Taking on Glioblastoma
Bouncing Back Part Three: Facing Hardship with Grace. January 7, 2017. In October, I started a four-part blog post series that I call Bouncing Back. In this brain tumor-forced journey, we’ve endured unpredictable drops and turns, and yet somehow, hope and gratitude rise to the surface. I’ve enjoyed sharing my ponderings on this topic and am now ready to tackle part three. Featured at the North Carolina Museum of Art, part of the most extensive Rodin collection between Philadelphia and the West Coast.
Welcome | Brain Tumor Foundation For Children, Inc.
What Is A Tumor Trooper? The Georgia Chapter of the Pediatric Brain Tumor Foundation was established in August, 2014, when the 31-year-old Brain Tumor Foundation for Children united with the PBTF to create a louder voice and greater impact for the children served by both organizations. PBTF-GA is proud to be the first of numerous chapters that will be established around the country in the all-important effort to Cure the Kids. Join us at one of our 2015 Tumor Trooper Run/Walks! May 2nd - Birmingham, AL.
BUTTERFLY BLOG for the Brain Tumor Foundation for Children | You don't have to be a brain surgeon to help a child with a brain tumor.
BUTTERFLY BLOG for the Brain Tumor Foundation for Children. You don't have to be a brain surgeon to help a child with a brain tumor. Truly Inspiring: A Letter to Sophia. May 31, 2012. The Brain Tumor Foundation for Children. Aren’t you glad I didn’t say banana again? Remember how you loved to tell knock-knock jokes? How can it be that it has been over three years since we last were able to hold you in our arms? Would you be reading chapter books and talking about how boys are yucky? Sometimes it is hard ...
Cancer Care Center (702) 547-2273, Dr. Nav Sharda Brain Tumor Cancer Treatment Home
According to Dr. Nav Sharda. There are many different types of brain tumors, which are essentially masses of abnormal cells in the brain. While some brain tumors are noncancerous and others are cancerous, they don't necessarily have to begin in the brain. Some can start as a cancer in another part of the body and metastasize in the brain. These are called secondary tumors. And treatment really depends on what kind of brain tumor. A person has and how big it is. Says metastatic or secondary brain tumors a...
braintumorlife – Still-Life with Bob
A year with Bob. I have not been active with blogging in quite awhile and wanted to reach out to those of you who don’t know me personally or on Facebook. I have read so many incredible stories of perseverance, courage, and survival by connecting with other brain tumor bloggers. I have enduring admiration and hope for all of us. I count myself extremely fortunate to have not required surgery, chemotherapy, or radiation thus far, and have great optimism that the tumor on my brain stem will not grow. And I...
Brain Tumor Treatment - Welcome
Welcome to the Brain Tumor. Treatment website. We specialize in Gamma Knife. Treatment for patients with benign and malignant diseases of the brain. We are the only Gamma Knife program in the Twin Cities metro area. The Gamma Knife is a non-invasive, state-of-the-art technique that delivers a precise treatment to a specified target while protecting the surrounding normal brain tissue. To learn more about gamma knife and other treatment options, click here.
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