Microcephaly awareness day is tomorrow, September 30. Although we will never know the actual cause of Sarah's delays, her pediatric...

For the past couple of days, I have waited to go to the park with Sarah until the evening. She's on some medication that makes her skin ...

Lately one of Sarah's activities includes taking apart her toys. I mean she's taking the hair off her Playmobil people and disassemb...

Four years ago today I wrote this blog post .  This was the first day that I blogged about Sarah's delays, shortly after a speech asses...

I had recently read a blog that began like this:  If you had a magic wand that could "cure" your child's disability, would you...

It was on this day in 2011 when Doug and I sat in the pediatrician's office waiting to hear the results of Sarah's most recent MRI w...

May 16th marked the third anniversary of the day that "normal" was redefined for us. I blogged about that day HERE . Now I'm n...

Yesterday afternoon, I had the opportunity to meet with Sarah's pediatrician. By myself. Without my sweet (screaming) daughter. It was p...

Just the other day it kind of hit me at how much Sarah's speech has taken off. Lots and lots of words are coming from her. I'll admi...

On a daily basis I need to remind and encourage myself that it's alright that Sarah is not at a kindergarten level. Some days it's e...

Yeah, that about sums up what we've been going through lately. Of course, developmentally, all these things are appropriate since they u...

Day 1 Well, like most nights before a test or assessment, I didn't sleep very well on Monday night. The day dawned bright and early as...

The day dawned bright and clear for our quarterly pediatrician appointment.  Much to my dismay, the little patient woke up kind of "off...