Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support.
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Brayden's Journey | braydenphillipson.blogspot.com Reviews
https://braydenphillipson.blogspot.com
Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support.
braydenphillipson.blogspot.com
Brayden's Journey: July 2014
http://braydenphillipson.blogspot.com/2014_07_01_archive.html
Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support. Sunday, July 27, 2014. Having fun this weekend at Sac County Fair! Area that is having problems. Brayden h...
Brayden's Journey: June 2014
http://braydenphillipson.blogspot.com/2014_06_01_archive.html
Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support. Sunday, June 29, 2014. Sunday, June 22, 2014. I have noticed the more these expanders weigh, the more it i...
Brayden's Journey: Surgery #11
http://braydenphillipson.blogspot.com/2014/10/surgery-11.html
Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support. Tuesday, October 28, 2014. The first night we got to hang out with our nevus friend, Brooklyn and her momm...
Brayden's Journey: Stitches are out!
http://braydenphillipson.blogspot.com/2014/07/stitches-are-out.html
Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support. Sunday, July 27, 2014. Having fun this weekend at Sac County Fair! Area that is having problems.
Brayden's Journey: November 2013
http://braydenphillipson.blogspot.com/2013_11_01_archive.html
Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support. Sunday, November 3, 2013. Good news.Brayden's back is finally healed! Happy 3rd birthday Brayden! One mont...
TOTAL PAGES IN THIS WEBSITE
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everybodylovesaustin.blogspot.com
Everybody Loves Austin: Garage and Bake Sale benefiting Nevus Outreach
http://everybodylovesaustin.blogspot.com/2012/09/garage-and-bake-sale-benefiting-nevus.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Sunday, September 23, 2012. Garage and Bake Sale benefiting Nevus Outreach. Please join us if you are in the area this weekend. We so appreciate all the support. Subscribe to: Post Comments (Atom). My son Austi...
everybodylovesaustin.blogspot.com
Everybody Loves Austin: July 2009
http://everybodylovesaustin.blogspot.com/2009_07_01_archive.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Friday, July 17, 2009. Subscribe to: Posts (Atom). E - Nevus Notes. Checking Back with Zac. Journey to Our lil Angel in China. The Wonderful World of Vance. The Sweet Life of Sophie. News from the Nagel's.
everybodylovesaustin.blogspot.com
Everybody Loves Austin: August 2009
http://everybodylovesaustin.blogspot.com/2009_08_01_archive.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Friday, August 7, 2009. I can't believe that my baby is turning 2 on August 24! We are so happy and thankful that we have made it this far! Subscribe to: Posts (Atom). E - Nevus Notes. Checking Back with Zac.
everybodylovesaustin.blogspot.com
Everybody Loves Austin: January 2009
http://everybodylovesaustin.blogspot.com/2009_01_01_archive.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Thursday, January 22, 2009. Subscribe to: Posts (Atom). E - Nevus Notes. Checking Back with Zac. Journey to Our lil Angel in China. The Wonderful World of Vance. The Sweet Life of Sophie. News from the Nagel's.
everybodylovesaustin.blogspot.com
Everybody Loves Austin: September
http://everybodylovesaustin.blogspot.com/2011/09/september.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Monday, September 26, 2011. Home after first shunt. In the hospital in critical condition. Subscribe to: Post Comments (Atom). E - Nevus Notes. Checking Back with Zac. Journey to Our lil Angel in China. If you ...
everybodylovesaustin.blogspot.com
Everybody Loves Austin: America's Giving Challenge
http://everybodylovesaustin.blogspot.com/2009/10/americas-giving-challenge.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Tuesday, October 13, 2009. Our cause just entered in America's Giving Challenge, which gives us a chance to win $50,000! Please donate today: http:/ www.causes.com/donations/select donation method? Journey to O...
everybodylovesaustin.blogspot.com
Everybody Loves Austin: Amazing 3 year old
http://everybodylovesaustin.blogspot.com/2010/09/amazing-3-year-old.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Monday, September 6, 2010. Amazing 3 year old. It's hard to believe but Austin just turned 3! There was an overwhelming feeling that day that a lot of earth shaking (at least to those in our world) information ...
everybodylovesaustin.blogspot.com
Everybody Loves Austin: Austin's 2nd birthday!
http://everybodylovesaustin.blogspot.com/2009/08/austins-2nd-birthday.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Friday, August 7, 2009. I can't believe that my baby is turning 2 on August 24! We are so happy and thankful that we have made it this far! Happy Birthday, Austin! August 24, 2009 at 6:12 AM. E - Nevus Notes.
everybodylovesaustin.blogspot.com
Everybody Loves Austin: Kindergartener
http://everybodylovesaustin.blogspot.com/2014/04/kindergartener.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Wednesday, April 2, 2014. If you cannot attend or would prefer to make a donation by credit card please visit our fundraising page at http:/ www.nevus.org/fundraiser-details id657.php? E - Nevus Notes. 2 Septem...
everybodylovesaustin.blogspot.com
Everybody Loves Austin: June 2009
http://everybodylovesaustin.blogspot.com/2009_06_01_archive.html
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Tuesday, June 2, 2009. Other families who need your prayers. Beautiful article about Austin. My mom wrote this article for US Catholic. It's about the day we found out Austin had hydrocephalus and decided t...
TOTAL LINKS TO THIS WEBSITE
39
Brayden Austin
This webpage tracks Brayden's progress. The videos have been placed in chronological order (the earliest video were posted first). Monday, July 28, 2008. Sunday, July 27, 2008. Brayden Having a Conversation. Wednesday, July 9, 2008. Heather and I can't believe it, but Brayden started talking the other day! Tuesday, July 8, 2008. One Month Old - June 28, 2008. Monday, July 7, 2008. Monday, June 16, 2008. Brayden and Papa Don. Friday, June 13, 2008. Subscribe to: Posts (Atom). Austin, TX, United States.
Brayden's First Blog
Brayden Patrick Fox, born 9-15-05; son of Jerry and Angela Folds Fox. Friday, November 20, 2009. Here I am with my friends Julius and Kiontez at last night's Predators game. I think I'm their biggest little fan. The Predators Foundation. Sponsors Against the Grain. Posted by Angela Folds @ 11/20/2009. Links to this post. Thursday, November 05, 2009. Posted by Angela Folds @ 11/05/2009. Links to this post. Brayden and Emerson (Okay, it's Emerson look-a-like Pumpkin! Posted by Angela Folds @ 11/05/2009.
Brayden Patterson
New and Exciting Information. Up on High Ground. Will air on CW/KPLR Channel 11 in St. Louis, MO (4 AM) as well as, Scranton, PA (5:30 AM) on October 25, 2014. Look for me in ". The Hunger Games: Mockingjay - Part 1. On November 21, 2014. Future Films to watch for me in. Premieres in October, 2015. The Hunger Games: Mockingjay - Part 2. Premieres on November 20, 2015. Hi, my name is Brayden Patterson and I am very glad to meet you!
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braydenphillipson.blogspot.com
Brayden's Journey
Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support. Wednesday, November 9, 2016. Brave Brayden turned 6 and his stitches are out! Monday, October 24, 2016.
brayden's blog
Mr Van Camp's Blog. Tuesday, March 30, 2010. Ann Coulter- Free speech. Is an American conservative social and political commentator, an author, and a syndicated columnist. She writes novels, writes a column for the paper and speaks to different crowds around the U.S.A and now just recently in Canada. Ann is the type of person that is not afraid to say what she is thinking. Monday, March 22, 2010. Wednesday, February 3, 2010. Going into the past. Subscribe to: Posts (Atom). Ann Coulter- Free speech.
Welcome | 360 The Band
Most people can't handle the awesomeness that is 360 The Band. If you think you are one of the elect few, click here. To book 360 The Band. Darr; Slide Down. Check out videos from Durham Bulls Stadium! Talk about 360 The Band. SQLSTATE[42000]: Syntax error or access violation: 1142 INSERT command denied to user 'dbo356539760'@'74.208.16.178' for table 'watchdog'. REQUEST: Array REQUEST URI: /.
Sydney Removalist | Castle Hill, Rouse Hill, Bella Vista & Kellyville
Removalist Services In Sydney and The Hills District. The Preferred Removalist In Sydney, Kellyville, Bella Vista, Castle Hill and Rouse Hill. Are you planning your next house move? We have used Wayne for both our office relocation and personal residential move. He and his team provide a first class experience with the proper equipment and experience in packing and moving everything from computers and work stations to delicate g. 8220;We hired Brayden Removals to move us from Richmond to Wahroonga. W...
