ingarrettsmemory blogspot.com

Garretts House

to promote awareness and offer education about a rare genetic skin condition called Epidermolysis Bullosa.

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LINKS TO WEB SITE

Biancas Adventures

The dance of life must go on, no matter how much the tune of the music changes. Thursday, August 25, 2016. A Summer of Firsts 2016. In January I will be running a 10K in honor of my. Please consider sharing or donating to this wonderful event! 2017 Walt Disney World Marathon Weekend - Sally Contreras. Saturday, February 28, 2015.

Four busy bees and two little butterflies

Four busy bees and two little butterflies. Sharing the happy, funny, crazy and sometimes sad moments of our lives. Wednesday, February 11, 2015. The 10-year mark was MUCH harder than I even imagined it would be. Ten-year, an entire decade; does not seem possible it has been that long. That day was a very busy day for us! She participated in a program after school called Girls on the Run! Links to this post.

Raquel Bella

We are a small family unit within a large caring and supportive community of friends, family and health care professionals that are doing their best to keep Raquel as comfortable and growing till we can beat EB. Friday, August 7, 2015. Her style of it anyway and is jogging anytime she gets out of the house. Raquel in her typical jog trying to track down her cousin.

This Little Light Capturing your little light shining

Tripp lost his fight against EB on January. 14th 2012 in the arms of his loving mommy. He does however continue to shine in the thousands of lives that he has touched. It is my hope that this journey does not end here. That this is only the beginning. I am committed to help in the effort of spreading awareness, being a voice for these precious children and eventually finding a cure to EB.

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Our parsers identified that a lone page on ingarrettsmemory.blogspot.com took six hundred and thirty-one milliseconds to come up. We could not find a SSL certificate, so our crawlers consider ingarrettsmemory.blogspot.com not secure.
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Garretts House

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to promote awareness and offer education about a rare genetic skin condition called Epidermolysis Bullosa.

CONTENT

This web page ingarrettsmemory.blogspot.com states the following, "To promote awareness and offer education about a rare genetic skin condition called Epidermolysis Bullosa." We saw that the webpage said " A Guide for New Families." It also said " The Proof it works! The proof blended diet works! We started blended diet around age 2. At the time he has been on formula since birth. At 18 months he weighted 24 pounds 50 and was 32 50 tall and his EB was still very severe; about 60 of his body had open wounds. We had blood work on in the fall of 2012 and here were the results."

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