We took Brady riding on the waverunners, for the first time today. He had a blast! He preferred to stand up the entire time, and was moving 100mph! He liked to ride slow, but loved to go fast, guess he takes after his mom,lol. When I was going to slow to suit him, he would reach up and push the throttle to make it go faster, he even tried to steer it a couple of times :) He waved at everyone on the shore and everyone that passed by us. I ended up having to ride with one leg wrapped around him, just to be sure that he didn't fall off. At one point he climbed onto the floor of the waverunner and was dragging his hand in the water. I think thats why he wanted to go fast, so that the water would splash him in the face. When I took him back to shore, he threw a fit, to get back on and ride some more, he did not want to leave. I told my hubby that I wouldn't even have exercise, since Brady gave me such a good workout while riding today. Anyways we had a blast, hope you guys enjoy the pics.
I am a happy healthy 5yr old little boy. I have Angelman Syndrome which makes me even more special. I bring joy to all those who meet me. Just because I am unable to speak, does not mean that I dont have lots to say. I make that very clear to mommy and daddy everyday!
Big Happy Tent is a homegrown non-profit organization started by Marcel Cairo and his family. Our mission is to take Angelman kids and their families camping, surround them with nature, water, music and fun, and let them soak in the wonder and joys of life.
This
downloadable Interactive Seizure Diary helps you track your seizure activity and medication routine. You can also record doctor appointments and notes about how you are feeling. Before a doctor appointment, print the information and share it with your physician.
The
Angelman Syndrome Foundation is a national organization of families,
caregivers and professionals who care about those with Angelman
Syndrome. It is also a member organization of the International
Angelman Syndrome Organization (IASO).
The AS Forum was created in April
2005 and provides an easy way for family members and carers of
people with Angelman Syndrome (AS) to exchange information with each
other.
