Our blog is all about our amazing son who was born with AMC. We speak about his struggles, triumphs and day to day life
I work at my church, this is a hobby and a way to keep family and friends informed about Luca’s progress.
Having a child with AMC (arthrogryposis) is something we didn’t plan or expect. We started blogging to show people the joys and trials of life with our amazing son
about a year
between 20-40
No
Any parent that has a child with disability. Family, friends.
about 20 minutes
It is a wonderful way to learn about AMC.
Write often. Write what’s on your heart. Be real.
This blog can be visited at http://borninseattle.blogspot.com
March 7, 2010
