Microcephaly Awareness Research And Education 

We are parents who were blessed with a beautiful little boy. Born early and weighed in at just a little over 3 pounds we were frightened, a few weeks latter we were told that our boy may have Microcephaly. We were sent to a specialist and the testing was started checking for Hydrocephalus (water on the brain) & Tumors MRI and CAT Scan showed nothing, Next off to Genetics testing and the doctor had no answers for us, no explanation as to how or why our boy has Microcephaly, test results were inconclusive. Special test were available but only for the most sever cases and a two year wait period. We researched for two years reading articles and test studies with very few answers. Everyone we talk to ask's the same question What is Microcephaly

That is what began our mission 

We started these pages for many reasons,

we want to bring awareness about Microcephaly and it's causes and effects on families to the public

We want to creat fundraisors and events throug-out the year and donate the proceeds to research

We are currently trying to raise donations for a no-profit state licence