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 ...

March is cerebral palsy awareness month. This term didn't mean much to me until the winter of 2011 when after an MRI showed that Sarah h...

My last posted blog was in October of 2016 - it's been almost a year since I last wrote anything here. All I was really doing was writin...

Facebook has this feature where it will show you previous posts and pictures that were shared. Some days I have none and others I have a few...

Today is Microcephaly Awareness Day. This is the diagnosis that I feel affects Sarah the most, even more so than the Cerebral Palsy. The M...

September brings with it a new school year, schedules and a return to routine. For us, it's also the month that Sarah has her 6 month fo...

Sarah turned EIGHT last month! Oh how the years have flown by and I can't believe how far she's come. I decided to do a bit of a rev...

Oh how the years go by Oh how the love brings tears to my eyes All through the changes the soul never dies We fight, we laugh, w...

March is cerebral palsy awareness month. This term didn't mean much to me until the winter of 2011 when after an MRI showed that Sarah h...

I recently was a reading a book and one of the questions asked was "What is my duty before the God who loves me?" This took me a w...

I have been waiting for this birthday for quite some time. I'm not sure if I think something great and wonderful will happen or wha...