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