And click here to view our family portraits from Disney World.
Monday, February 1, 2010
Friday, January 29, 2010
I know that I haven't posted in a while and I am very sorry. Zoe is doing wonderfully well. We double her nutritionals so that she receives 4 ml per day now instead of 2. We have seen marked improvement since we started that. She almost has her third tooth and she is learning to stand. She claps, waves bye, patty cakes, high fives, and laughs whenever she sees cats. Today, we began to teach her sign language as a way to help her communicate before she can talk and to help her with her verbal and reading skills as she gets older. You can find out more about babies and sign language by clicking here. She currently says mama, dada, and no, and the other day she actually said "my dada" a few times.
We took her to Disney over Christmas and she turned 1 year on January 8, 2009. I promise to have pictures posted soon!
Tuesday, December 15, 2009
I just wanted to let everyone know that Zoe's MRI on the 3rd went very well. There was no change at all in the mass. There are still no enhancements, which is unique in Zoe's case. The neurosurgeon said today that he is "pleasantly baffled," and her oncologist stated that she looks "amazing." Thank you all for your thoughts and prayers. Please continue to think of and pray for Zoe!
Thursday, December 3, 2009
I just wanted to let you all know that Zoe did have her MRI this morning. Everything went well. Sadly, they had to prick her 4 times before they got her IV started!! Poor girl got her Daddy's difficult veins :-( But she did really well and we are just waiting to hear from the doctor about the results. Thank you all for your thoughts and prayers and please continue to pray for her.