dylanhartung.blogspot.com
Everything's Possible<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> An Australian boy's fight against Neuroblastoma, a lethal childhood cancer
http://dylanhartung.blogspot.com/
<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> An Australian boy's fight against Neuroblastoma, a lethal childhood cancer
http://dylanhartung.blogspot.com/
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Everything's Possible | dylanhartung.blogspot.com Reviews
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<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> An Australian boy&#39;s fight against Neuroblastoma, a lethal childhood cancer
dylanhartung.blogspot.com
Everything's Possible: Latest Media
http://dylanhartung.blogspot.com/2012/08/latest-media.html
160; An Australian boys fight against Neuroblastoma, a lethal childhood cancer. Tuesday, August 21, 2012. Here is a a link to Channel Nine who did a short story on our up coming return home. Click. Related blogs I follow. How can I keep from singing? Support For Christi Thomas. Welcome to Erin's Home. Ellie Skees - A new day. Safe in HIS Arms. Dad's Diary - a journey through childhood cancer. Madelyn Bell's Status Page. Prince Liam the Brave. Laura Stiles a gentle spirit. Shania's Sunflower of Hope.
Everything's Possible: FB takes over blog! Noooooo....
http://dylanhartung.blogspot.com/2013/02/fb-takes-over-blog-noooooo.html
160; An Australian boys fight against Neuroblastoma, a lethal childhood cancer. Thursday, February 7, 2013. FB takes over blog! I am so relieved. A full baseline work up will be done in the next 4-8 weeks allowing time for Dylan to settle into school, as the work up will mean 4-5 days off school. Up early, showered, teeth brushed and lunch made! Then I realized that I could tell he really did want to do the homework but he didn’t know how. But it was so simple, how could he not know how? School has...
Everything's Possible: 6 weeks to go
http://dylanhartung.blogspot.com/2012/07/6-weeks-to-go.html
160; An Australian boys fight against Neuroblastoma, a lethal childhood cancer. Friday, July 27, 2012. 6 weeks to go. Related blogs I follow. How can I keep from singing? Support For Christi Thomas. Welcome to Erin's Home. Ellie Skees - A new day. Safe in HIS Arms. Dad's Diary - a journey through childhood cancer. Madelyn Bell's Status Page. Prince Liam the Brave. Laura Stiles a gentle spirit. Shania's Sunflower of Hope. XinXin Battle Against Neuroblastoma. Hannah's Circle of Friends.
Everything's Possible: TheTruth 365
http://dylanhartung.blogspot.com/2012/08/thetruth-365.html
160; An Australian boys fight against Neuroblastoma, a lethal childhood cancer. Friday, August 17, 2012. Please read and support: http:/ thetruth365.org/. The following is from their website Facts most of us do not know but should.Please make sure you sign the petition page! Cancer claims the lives of more children each year than AIDS, asthma, cystic fibrosis and diabetes combined. It is the leading cause of death by disease in children and adolescents. About one in 500 young adults is a childhood ...
Everything's Possible: First hospital admission since arrival home to Australia
http://dylanhartung.blogspot.com/2013/04/first-hospital-admission-since-arrival.html
160; An Australian boys fight against Neuroblastoma, a lethal childhood cancer. Sunday, April 14, 2013. First hospital admission since arrival home to Australia. Related blogs I follow. How can I keep from singing? Support For Christi Thomas. Welcome to Erin's Home. Ellie Skees - A new day. Safe in HIS Arms. Dad's Diary - a journey through childhood cancer. Madelyn Bell's Status Page. Prince Liam the Brave. Laura Stiles a gentle spirit. Shania's Sunflower of Hope. XinXin Battle Against Neuroblastoma.
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The Granny Blog: November 2009
http://thegrannyblog.blogspot.com/2009_11_01_archive.html
Tuesday, November 24, 2009. So now it is time for us to care for her. In October, it was discovered that she had 4 brain aneurysms. Yes 4! I added the picture of my son Scott and his deer. You can see he really looks like a happy hunter. Later that morning he came back with the boys for a few minutes. Jayden and Bryce were so excited to tell me that Daddy got a big deer! I love the excitment in their little voices. But who can resist those huge chocolate brown eyes! Links to this post. Days in the life.
Toby Pannone: August 2009
http://tobypannone.blogspot.com/2009_08_01_archive.html
Monday, August 10, 2009. Thankful for every day. Toby's summer has been full of sunshine, beach days, hot dog cookouts, puddle jumping, bike rides and ice cream. He's doing really well, finishing up his 10th cycle of ABT-751, with clean MiBG CT scans and clear bone marrows. We are so very, very lucky. And yet, shouldn't this be the norm? Recently relapsed and is spending his third summer battling neuroblastoma. He is all of 5 years old. Sweet Evan. Subscribe to: Posts (Atom). Blood and Platelet Drive.
Toby Pannone: Walk
http://tobypannone.blogspot.com/2010/05/walk.html
Wednesday, May 5, 2010. During the year that hospital became home, Toby spent most of his waking hours in bed. Moving was difficult. So we used a wheelchair to get to surgery, radiation and countless middle-of-the-night emergency scans. And we carried Toby everywhere else: to the bathroom and the IV room, to look out the window as the world spun madly on. And we cried as his body withered, his little bones pushing through skin. After a year Toby began to walk again. My gosh, Toby! Thank you for posting&#...
Toby Pannone: December 2008
http://tobypannone.blogspot.com/2008_12_01_archive.html
Thursday, December 4, 2008. In the 20 months since Toby got sick, Stephen and I have watched 30 children die. They are children we shared rooms with and children we came to love through their parents’ writings. Their names are Gus, Jack, Max, Katie, Lillie, Lucas, Penelope, Brody. Their parents cope with unfathomable grief. We think about death a lot, over here. It is forever knocking at our door, lingering in corners, forcing us to ask, “is today the day? But we also focus on the joy of each day. We...
Toby Pannone: March 2010
http://tobypannone.blogspot.com/2010_03_01_archive.html
Friday, March 12, 2010. When I started this blog almost three years ago, I spent most nights in a pit of fear, adjusting tubes, cleaning vomit and watching my child waste away. In between terror and tears I searched constantly for "neuroblastoma blog" online, in desperate need of finding others like Toby. They each lived so large—running, laughing, overcoming every obstacle with pluck, determination and joy. In less than 2 years, four of these five children have died. Sam died today. Liam I miss you.
Toby Pannone: January 2011
http://tobypannone.blogspot.com/2011_01_01_archive.html
Wednesday, January 26, 2011. Good-night, sweet Prince. I loved Liam before I ever met him. In April 2007, after Toby was diagnosed with stage IV neuroblastoma, after we saw the scans of his body filled with metastatic cancer, and after our doctor told us that Toby might die from the baseball-sized tumor in his abdomen, a parent from Toby's preschool sent me a clipping from Cookie magazine. "Maybe you've seen this," she wrote. "This boy has cancer too.". Imagine if Liam was your child. Imagine adminis...
Toby Pannone: November 2009
http://tobypannone.blogspot.com/2009_11_01_archive.html
Monday, November 2, 2009. It's all so good around here. And it seems I've forgotten how to write. Mostly I drink the beauty of normal. We ride our bikes to soccer in the park, we read chapter books. and we have regular tooth fairy visits. Not a day goes by that we don't count our blessings. An empty one has been hanging out with the bath toys, but surely that can't be it. "Toby, do you remember what these are? Thanks for dropping in. Subscribe to: Posts (Atom). Blood and Platelet Drive. Liam I miss you.
Toby Pannone: Financial Support
http://tobypannone.blogspot.com/2007/04/from-rabbi-carie-carter-at-park-slope.html
Monday, April 23, 2007. Contributions can be made in two ways:. To make a tax-deductible donation to Toby via Park Slope Jewish Center, please make your check out to "Rabbi's Discretionary Fund" and put "Toby" in the memo. All funds raised will be put aside specifically for Toby and his family to pay or reimburse medically-related expenses. All contributions to this fund are tax-deductible. Park Slope Jewish Center. Brooklyn, NY 11215. For account reference numbers. New York, NY. Bank swift code- WMSBUS66.
The Granny Blog: 6 Degrees of Seperation
http://thegrannyblog.blogspot.com/2011/05/6-degrees-of-seperation.html
Monday, May 16, 2011. 6 Degrees of Seperation. Wow look at how long it has been since I wrote on this blog! Shame on me. The picture is Laura reading to me one night a couple of months ago. There has been so much happening recently. Laura has relapsed with her neuroblastoma and the chemo does not seem to be working. We have so many people praying for us that we feel completely surrounded by love. Sure enough, here was a poster of Laura! Kara Lynn has organized a fund raiser for Laura at the Grand Ledge P...
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Dylan Hart Photography
Welcome to Dylan Hart Photography. For more information, contact Dylan Hart: (360) 319-5043, or email me at: dylan@dylanhart.com.
Dylan Hartas
Do not fill in this field. Join Mailing List for Free Download Too Wrong. Dylan Hartas Featured in Australian Musician. Dylan recently sat down with Australian Musician to chat about his life long love of music and guitar, discussing equipment, inspirations and a life dedicated to playing in the Australian music scene. Check out the full interview here. ON SALE Signed CD only $15 postage paid. New Toy 4 string cigar box guitar.
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Dylan Hart Photography
Welcome to Dylan Hart Photography. For more information, contact Dylan Hart: (360) 319-5043, or email me at: dylan@dylanhart.com.
Everything's Possible
160; An Australian boys fight against Neuroblastoma, a lethal childhood cancer. Sunday, April 14, 2013. First hospital admission since arrival home to Australia. Thursday, February 7, 2013. FB takes over blog! I am so relieved. A full baseline work up will be done in the next 4-8 weeks allowing time for Dylan to settle into school, as the work up will mean 4-5 days off school. Up early, showered, teeth brushed and lunch made! So I looked at the questions again, read them twice over, then it hit me!
Everything's Possible
Welcome to Dylan Hartung's Web Page. It was first created to keep friends, family and supporters of Dylan's campaign up to date. Dylan is an Australian boy who was diagnosed with Stage IV Neuroblastoma on 26th July 2004 when he was 5 years old. Dylan's cancer fight led him to New York for treatment for almost 8 years. Dylan is now back in Australia, after he was given 2-12 months to live by Australian doctors in 2004. Click on the links to follow his journey and learn more about Dylan.
dylan harvey con/scam/rip off
Dylan harvey con/scam/rip off. Wednesday, 4 March 2009. Do not buy from these fraudulent. If you have put any money in but can still get out - do it before it's too late. Every single transaction will prove to be worth approx. 30% less when the truth comes to light. They con in differing ways and prey on people where they possibly can - usually through your weakness. Most DH customers are lovely people and TW. Often it is not apparent. Another con is that you believe that you have parking and suddenly th...
dylanharveypropertydepositpetition.blogspot.com
Dylan Harvey Property Deposit Petition
Dylan Harvey Property Deposit Petition. A site petition blog for investors who want their deposit back. Sunday, 23 November 2008. PETITION TO DYLAN HARVEY. ALL VISITORS TO THIS SITE ARE LEAVING COMMENTS ON THIS BLOG TO PETITION FOR THE REFUND OF THEIR DEPOSIT PAID UPFRONT TO DYLAN HARVEY. PLEASE SHOW YOUR SUPPORT TO ENSURE DYLAN HARVEY FULLY REFUND THOSE CUSTOMERS WHO FEEL THAT THEY HAVE BEEN MISLEAD, SCAMMED AND RIPPED OFF. PLEASE POST ALL COMMENTS HERE* *. Subscribe to: Posts (Atom).
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