tinysuperheroes.blogspot.com
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.blogspot.com
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.
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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.blogspot.com
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.blogspot.com
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.blogspot.com
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&#...
tinysuperheroes.blogspot.com
TinySuperheroes: Super Sophia Joy
http://tinysuperheroes.blogspot.com/2013/02/super-sophia-joy.html
Empowering TinySuperheroes one cape at a time! Sunday, February 24, 2013. On October 22, 2010 a very special, Extraordinary TinySuperhero was born named Sophia Joy. At five days old, she was diagnosed with Down Syndrome. Then, in 2012 she was diagnosed with Leukemia. Super Sophia Joy is fighting for her life as we speak - and our support, thoughts, and prayers can really help to strengthen and renew her incredible super powers. Sophia in October 2012. Photo from Sophia Joy's Facebook Page. Yesterday we w...
tinysuperheroes.blogspot.com
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.
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TinySuperheroes
http://tinysuperheroes.blogspot.com/2013/03/new-website-head-over-to-www.html
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