averyspecialcase.blogspot.com
A Very Special Case.My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences.
http://averyspecialcase.blogspot.com/
My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences.
http://averyspecialcase.blogspot.com/
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A Very Special Case. | averyspecialcase.blogspot.com Reviews
https://averyspecialcase.blogspot.com
My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences.
averyspecialcase.blogspot.com
A Very Special Case.: July 2014
http://averyspecialcase.blogspot.com/2014_07_01_archive.html
A Very Special Case. My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences. This amazing boy was born 12-21-10 at a whopping 2 pounds, 13 ounces due to an unknown syndrome and Inner-Uterine-Growth-Restriction. His doctors didn't expect him to live but living life to the fullest is what he does! This Is his story:. He suffers from Failure to Thrive and extreme short stature. About a year ago, he passed out i...
A Very Special Case.: A Beautiful Year. A Beautiful You.
http://averyspecialcase.blogspot.com/2015/01/a-beautiful-year-beautiful-you.html
A Very Special Case. My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences. This amazing boy was born 12-21-10 at a whopping 2 pounds, 13 ounces due to an unknown syndrome and Inner-Uterine-Growth-Restriction. His doctors didn't expect him to live but living life to the fullest is what he does! This Is his story:. He suffers from Failure to Thrive and extreme short stature. About a year ago, he passed out i...
A Very Special Case.: August 2014
http://averyspecialcase.blogspot.com/2014_08_01_archive.html
A Very Special Case. My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences. This amazing boy was born 12-21-10 at a whopping 2 pounds, 13 ounces due to an unknown syndrome and Inner-Uterine-Growth-Restriction. His doctors didn't expect him to live but living life to the fullest is what he does! This Is his story:. He suffers from Failure to Thrive and extreme short stature. About a year ago, he passed out i...
A Very Special Case.: April 2015
http://averyspecialcase.blogspot.com/2015_04_01_archive.html
A Very Special Case. My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences. This amazing boy was born 12-21-10 at a whopping 2 pounds, 13 ounces due to an unknown syndrome and Inner-Uterine-Growth-Restriction. His doctors didn't expect him to live but living life to the fullest is what he does! This Is his story:. He suffers from Failure to Thrive and extreme short stature. About a year ago, he passed out i...
A Very Special Case.: October 2014
http://averyspecialcase.blogspot.com/2014_10_01_archive.html
A Very Special Case. My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences. This amazing boy was born 12-21-10 at a whopping 2 pounds, 13 ounces due to an unknown syndrome and Inner-Uterine-Growth-Restriction. His doctors didn't expect him to live but living life to the fullest is what he does! This Is his story:. He suffers from Failure to Thrive and extreme short stature. About a year ago, he passed out i...
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TinySuperheroes: Super Casen
http://tinysuperheroes.blogspot.com/2013/02/super-casen.html
Empowering TinySuperheroes one cape at a time! Wednesday, February 27, 2013. Today, on Rare Disease Day, it is our pleasure to introduce you to Super Casen - an Extraordinary TinySuperhero living with a Rare Disease. Super Casen is six years old, hails from Texas, and is a big Texas Longhorns fan! A few days before his third birthday. Casen proceeded to go through every test you could think of and several seizure medicines without any results as to what was causing the seizures. By this time, Casen's...
TinySuperheroes: Super Owen
http://tinysuperheroes.blogspot.com/2013/02/super-owen.html
Empowering TinySuperheroes one cape at a time! Saturday, February 23, 2013. This stud is Super Owen. When his parents chose his name, they didn't know its meaning, but Owen means Young Fighter, and this TinySuperhero has definitely lived up to his name. Owen was born on April 2, 2012. By birth he had already proven that he was indeed a young fighter and stubborn! 39 hours and a C Section later, Super Owen came into our world! After surgery, Owen spent his first month and a half in the hospital recovering.
TinySuperheroes: Super Mabel
http://tinysuperheroes.blogspot.com/2013/02/super-mabel.html
Empowering TinySuperheroes one cape at a time! Wednesday, February 27, 2013. I know that Mabel is a super hero. She has the ability to change this world tucked inside of her little frame. Her spirit is so pure and she is full of ease. She has changed lives of those around her from the very moment she was born and continues to do so every single day.". This is Super Mabel, an Extraordinary TinySuperhero who, alongside Super Casen and Super Elijah. Is living with Batten Disease. Daughter. This isn't a ...
TinySuperheroes: Rare Disease Day
http://tinysuperheroes.blogspot.com/2013/02/rare-disease-day.html
Empowering TinySuperheroes one cape at a time! Wednesday, February 27, 2013. Today is Rare Disease Day. Last year, I didn't even know Rare Disease Day existed, and today I feel connected to dozens of families to whom this day holds great importance. For every one family I've met, I know there are hundreds more. Today, think of the TinySuperheroes we have introduced so far who are living with a Rare Disease: Super Brenna, Super Evan, Super Case, Super Wyatt, Super Elijah, and Super Esmé. We know there are...
TinySuperheroes: March 2013
http://tinysuperheroes.blogspot.com/2013_03_01_archive.html
Empowering TinySuperheroes one cape at a time! Tuesday, March 5, 2013. Please head over to. And check out our new blog, new store,. And new Extraordinary TinySuperhero! Subscribe to: Posts (Atom). 160;Please head over to www.tinysuperher. Become a Hero: Buy One, Give One. View my complete profile. Awesome Inc. template. Powered by Blogger.
TinySuperheroes: February 2013
http://tinysuperheroes.blogspot.com/2013_02_01_archive.html
Empowering TinySuperheroes one cape at a time! Wednesday, February 27, 2013. Today is Rare Disease Day. Last year, I didn't even know Rare Disease Day existed, and today I feel connected to dozens of families to whom this day holds great importance. For every one family I've met, I know there are hundreds more. Today, think of the TinySuperheroes we have introduced so far who are living with a Rare Disease: Super Brenna, Super Evan, Super Case, Super Wyatt, Super Elijah, and Super Esmé. We know there are...
Precious And Priceless Kids: June 2013
http://www.preciousandpricelesskids.com/2013_06_01_archive.html
Precious And Priceless Kids. To raise awareness and support for the families and children with chronic and terminal illness. Facebook www.facebook.com/preciousandpricelesskids stop by and like the page please :). Wednesday, June 26, 2013. Traven's Battle With Craniopharyngioma. This young guy has been through so much! Traven also has diabetes insipidus , http:/ www.mayoclinic.com/health/diabetes-insipidus/DS00799. I'm looking forward to seeing Traven handling all the obstacles that come his way with ease!
TinySuperheroes: Super Gabriel
http://tinysuperheroes.blogspot.com/2013/02/super-gabriel.html
Empowering TinySuperheroes one cape at a time! Tuesday, February 26, 2013. He's pretty much the coolest kid in the world. He saved my life, that's for sure. His story is one of happiness. At only 2 years old, he has overcome more than I have in my 22 years of life. There's only one name for a person so strong.Hero.". In August 2010, an Extraordinary TinySuperhero was born in Louisiana to a superhero mom and dad. Meet Super Gabriel! Super Gabriel was pretty lucky to be born to superhero parents. His m...
TinySuperheroes: January 2013
http://tinysuperheroes.blogspot.com/2013_01_01_archive.html
Empowering TinySuperheroes one cape at a time! Wednesday, January 30, 2013. He brought this family to a new normal and has shown us how special, special needs really are. He has taught us to live in today and deal with tomorrow when tomorrow comes. He is our blessing, our lesson and our tiny teacher.". We are so excited for you to meet Super Case - a true TinySuperhero. You know the saying "the best gifts come in small packages"? Well, Case is proof. One of Case's biggest struggles has been with eating&#...
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Some are born great, some achieve greatness, and some have greatness thrust upon 'em." And some of us would settle for mediocrity. Tuesday, December 20, 2005. Subfile under "Obvious, Restating the", along with "East, Sun rises in"; "West, Sun sets in"; "Sun, Earth revolves around"; and Monsieur Jourdain, a character in Moliere's The Bourgeois Gentleman. Who discovers that he has been speaking prose all his life and didn't even know it. Judge rules against ‘intelligent design’. The ruling was a major setb...
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A.Very Special Breakfast
The best start to your morning. Wednesday, October 7. Mushroom and miso broth poured over Prickly Sow Thistle and lacto-fermented tomatoes roasted with thin slices of garlic. Prickly and Perennial Sow Thistle wilted with kimchi topped with poached eggs. Sunday, October 4. Crab Apples and Cheddar on toast with Chickweed and mushroom vinaigrette. Giant Puffball and Blackening Russula with Sea Beet on toast. Wednesday, September 30. Saturday, September 26. Wednesday, September 23. Subscribe to: Posts (Atom).
A Very Special Breed
A Very Special Breed. Products and gifts for those that give love, time, comfort, money and a chance at a beautiful life to those that dont have a voice! A website created by GoDaddy’s Website Builder.
A Very Special Case.
A Very Special Case. My husband and I have four Children. Our fourth is a little boy named Case Daniel. This is his story and the lessons he's taught through his differences. Sunday, January 7, 2018. Hello My Name Is. Hello my name is warrior. I am fierce and strong. I fight battles I never dreamed I would have to fight. I am fearless even when I'm afraid and fight until the battle is won. I run on love, adrenaline and coffee. Hello my name is Momma Bear. Hello my name is Dreamer. Hello my name is Mom.
Home Page | A Very Special Christmas
These holiday classics bring joy to the world and help people with intellectual disabilities through the power of sports. The grants generated by the A Very Special Christmas albums have an enormous effect on Special Olympics Programs around the world. Around the world, people with intellectual disabilities are living better lives, thanks to AVSC and Special Olympics. A fascinating documentary about the music that changed the world, with interviews and live performances, hosted by Vanessa Williams. Creat...
A Very Special Collection - Tissue Paper Foundation Patterns
A Very Special Collection. PO Box 2243, Yorktown, VA 23692 .
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A Very Special Day. It's easy to get started creating your website. Knowing some of the basics will help. What is a Content Management System? A content management system is software that allows you to create and manage webpages easily by separating the creation of your content from the mechanics required to present it on the web. In this site, the content is stored in a. The look and feel are created by a. Brings together the template and your content to create web pages. The boxes around the main conte...
A VERY SPECIAL DAY | WEDDINGS & EVENTS
A Very Special Day | Your dream wedding, come true.
A Very Special Day. Your dream wedding, come true. A Very Special Day’s Slow Motion Video Lounge at the Venetian Hotel in Las Vegas. In Slow Motion Video Lounge. Asymp; Leave a comment. P a href=” http:/ vimeo.com/107887221″ The. Knot Party at The Venetian Hotel in Las Vegas at the Wedding MBA – Slow Motion Video Lounge at Club TOA /a from a href=” http:/ vimeo.com/avsdpro” avsdpro /a>. On a href=” https:/ vimeo.com” Vimeo /a>. A Very Special Family. August 28, 2014. Continue reading →. August 7, 2014.
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