top of page

This site was designed with the

website builder. Create your website today.Start Now

Raising Awareness for Apert Syndrome

Dawsons Journey

Every life matters

Every life matters

Every life matters

Something this apert family/community doesn’t know about us is, Dawson has several siblings in heaven. I have had multiple discussions...

dwsjourney

Oct 22, 20222 min read

32 views

0 comments

Fall trip

Fall trip

Fall trip

Quick weekend getaway to Nanas house! Daws has never been able to go do these fun things with Nana and really enjoyed this fun time! )...

dwsjourney

Oct 18, 20221 min read

17 views

0 comments

Recovering

Recovering

Recovering

Recovery is FULL of ups and downs! But I’m thankful he’s on his feet for the most part! Even if there is very little sleep going on...

dwsjourney

Sep 28, 20221 min read

18 views

0 comments

Headed HOME

Headed HOME

Headed HOME

Y’all!! We’re on the way home!! Dr.F showed up this morning and was beyond impressed at how Dawson is bouncing back!! Labs are amazing,...

dwsjourney

Sep 24, 20221 min read

37 views

1 comment

Dawson

This is a blog about Dawson, who was born at 34 weeks gestation and stayed 37 days in NICU. He has been diagnosed with a rare syndrome; Acrocephalosyndactyly type I (ACS1), otherwise known as Apert Syndrome. Please follow along with us on this new adventure we call life. We will not only be updating on his journey, but will also do our best to raise awareness for Aperts.

bottom of page