The Bailiwick Project: One in 88

The Project...of an author and mother.

We are at a crossroad in our lives. Things are changing and we can either follow the road to where it takes us. Or, we can take the path that has been silently waiting for us.
Nathan has been diagnosed with classical autism, congenital heart disease, PVL (brain damage), apraxia, growth delay and a rare chromosomal mutation.
Chase has been diagnosed with classical autism, complex partial epilepsy and apraxia. Chase has also been diagnosed with a chromosomal mutation that falls in line with his autism diagnosis.
This project is to bring accountability to my days. It is so easy to let yet another day slip by. But, I can't. I need to find my 'Bailiwick' and my family's 'Bailiwick'. What works for us. Then we need to work it! Take time to follow along with us. And, discover your own 'Bailiwick' too.
(As you follow along please take time to search for all the links often placed discretely in that day's entry.)

The Bailiwick Project

Pages

Friday, March 30, 2012

One in 88

No comments:

Post a Comment

About Me

Blog Archive