me and my padre. He didnt even know his computer had a webcam.
my bracelet says i am a "fall risk"
X Marks the spot! My doctor drew an x on my chest so he would know where to cut...how hard could it be....
Here is a picutre of me and my mom in the waiting room.
1 comment:
Hi Rebecca, nice blog. I found the link on valvereplacement.com I'm the mother of a 6 year old with PVS, AV canal defect, Noonan Syndrome and a few other goodies. I could totally relate to your not being able to sleep. On the days leading up to my son's OHS I am an insomniac and have difficulty functioning. I'll bet your parents do too. Just wanted to wish you well and to encourage you to keep writing. It really helps those of us who are raising kids with CHD to see how it goes for adults with CHD.
Best wishes for a smooth, speedy recovery!
Theresa in Virginia
Mom to Idrees with CHD, Noonan Syndrome, etc....
Post a Comment