Mia Barbara Burke was born on December 10th, 2015.  She was the light of our life.  She was such a happy baby with the best belly laugh.  Sadly, just 5 short months after being born, Mia fell asleep at Daycare and never woke up.  As her parents, we have struggled to come to terms with having a child pass due to what is believed to be SIDS.  There are very few answers when it comes to SIDS.  We have very few answers.  

We were made aware of the Robert's Program through a support group.  Dr. Hannah Kinney and her team have been responsible for the last 2 major SIDS research breakthroughs and are so very close to even more.  We have spoken directly to Dr. Kinney. We believe in this program so much, that we have donated Mia's medical records, brain and spinal cord to Dr. Hannah Kinney's team for research.  

We have created this page to allow family and friends make a direct donation to this program if they choose to do so.  ALL money donated is sent to this program.  Our hope is to someday have answers and the hope that no more families have to live this incredible nightmare.  Please consider honoring our Mia with a donation.

Love,

Lauren & Mike