Welcome

Landen has been (and is) such a priceless and eternal blessing to our family since his arrival. As you can tell, he's absolutely adorable and happy. We simply can't get enough of him!
As of August of 2013 we added another addition to our family, Brigit Nicole. She is missing part of her 3rd chromosome. We are still learning every day new things about her disability. We have a total of 4 kids and couldn't be happier!



The purpose of our site is to reach out to others who have Angels with Spina Bifida (or other special needs) for a supportive bond.

Please feel free to contact us @ ronandtosh@comporium.net



Wednesday, May 2, 2012

Landen's Walk N Rollers

On Saturday, May 5th, our team, Landen's Walk n' Rollers, is participating in a walk to benefit the Spina Bifida Association and All proceeds are used for programs and services for people living with Spina Bifida.

Spina Bifida is the most common permanently disabling birth defect in the US. An average of 8 babies every day are born with Spina Bifida or similar birth defect of the brain and spine. The majority of these babies, like Landen, experience major back surgery within the first few hours of birth.

When we started Landen's team a few weeks ago, our goal was to raise $300.  We didn't have enough time to raise alot of money so we didn't want to make our goal out of our range. We are VERY pleased to say that within 2 weeks of started our team, we have raised over $1200. We are soooo very excited to turn in all that money this Saturday!

Here is a picture of the shirts we designed for Landen's Walk n- Rollers!



1 comment:

  1. We are so excited to be a part of this!! The shirts look awesome:)

    ReplyDelete