A few weeks ago, I told my therapist that I wanted to do something like bake cookies and deliver them to my friend’s front porches, but the

Redmond is free! On December 19, 2019, we were able to remove the g-tube permanently.

My inconsistent January of 2019 meant that it was the last two days of the month before I determined what I will work on this year.

I have a guest post today over at the awesome Down syndrome blog, https://www.cedarsstory.com/5-tips-for-moms-of-gtube-babies/

I was able to test out my healing from PTSD through an unexpected challenge recently.

Plans. I’m beginning to wonder why I bother to make them at all.

I was warned every time of the high, higher, and highest likelihood of birth defects in my babies.

I’ve been working hard on my health for about a month now.

My son has been the one in the hospital. But I've been the one breaking.

When I did my internship in 2005 with the women’s minister at a large, urban church, I asked her for some book recommendations.

I’ll never forget my shock on that first day in the NICU with Redmond

One year ago this week was the most terrifying and awful time in my life.

My son, Redmond, is 11-months old and thriving.

There’s a famous poem about Down syndrome called “Welcome to Holland.”

I never considered the possibility that a traumatic birth and subsequent stay in the NICU with my baby could lead to a diagnosis of PTSD.

As of November 13, there are NO tubes on his face.

Rick and I are so happy to let you know that Baby Wyse #3 is on the way!

I decided that my new year’s resolution is to BE AWESOME.

The last several weeks have been difficult for me.