Our journey
Cheese!!!
When you have a child who’s attention is shorter than you can say cheese, you take 100 photos and you finally get one to keep.
April 27, 2024
When you have a child who’s attention is shorter than you can say cheese, you take 100 photos and you finally get one to keep.
As parents of a child with special needs, my wife and I often encounter unique challenges that require unique solutions. Our son has Angelman syndrome,
Since 2019, we have traveled to 39 States but somehow we missed Utah when we did our West Coast route. This year, we are striking
As any parent can attest, the worst thing you ever want is to have to watch your child suffer. Unfortunately, we had no control over
We LIKE to be adventurous … ok, ok … pointing out the key word – like! We traveled to the Philippines in 2017 and it
We have been home since Saturday. I’m not a writer so it’s harder for my creative mind to write on the spot while we are
The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for
We are beyond grateful to Anker for their generous donation of the Nebula Mini Projector, and it has been a total game-changer for our family!
It is Mike’s 51st Birthday, he has never seen Niagara Falls so it was fitting to outline that we would be in the Niagara State
