An awareness can be done singlehandedly, but there is much to say about solidarity. Our family can be fully transparent about our challenges but having
I have been in the US for 26 years, lived here a lot longer than I have lived in my native country the Phillipines. Every
Today, we are officially on our 1ST DAY launching our Angelman Syndrome Awareness Camper Campaign across the US and to attend ASF’s Family Conference in
This little boy never ceases to amaze us. Right as we were pulling away from our house he started saying “GOD” and held his hands
Trek donated two amazing bicycles and helmets so that we can ride around different places we stop. Burley donated this awesome trailer that we can
One GREAT thing about working for such an amazing company is the opportunity to fill-in for my wife and work from home, when needed. Today
This is audio of Matthew and Mommy doing their nightly routine. After reading a book, they then pray and prepare for a good nights sleep.
We can’t thank Lettering Express in Oklahoma City enough for their donation of a wrap for the back of our travel trailer. I know that
Just because Matthew has limitations doesn’t mean we also stop living life. We love to travel — at least that is what my husband I
Our youngest son, Matthew, was born with a rare genetic disorder called “Angelman Syndrome.” Our family is always looking for ways to educate others on