Sure, Shawn's conditions affects 1 in 35 million children, but congenital anomalies affect 1 in 30 children. We have also recently found a study by the Center for Disease Control that shows congenital anomalies are the leading cause of infant deaths (http://www.cdc.gov/nchs/data/nvsr/nvsr60/nvsr60_04.pdf). That fact became all too real when we saw Liam lose his 18 month battle with a congenital heart defect.
I hope that I am never insensitive to any other organization that helps raise awareness for other conditions. We have all been touched by cancer, diabetes, autism, etc. I am happy that there are thousands of organizations out there that help raise awareness for these conditions, but I am also a little envious of their success. Maybe it is just because of my own impatience to bring more awareness to what we now has been proven to be HUGE issue that has received very little attention. It has led me to sound like a broken record to those that are close to me or have been following this journey from the beginning, but I do this because I am reminded daily by someone's comment that they don't truly understand the real Shawn's Anomaly mission to provide education, hope, and help to families dealing with congenital anomalies. They think that all of this is about my son.
Everything has a beginning, and Shawn was the start of Shawn's Anomaly, but it has now grown into something far greater than my family. The #SIM365USA Challenge is designed to tell the greater story of the 1 in 30 children that are affected by congenital anomalies.
Our first story that we are highlighting is about the Pratt family. I recently had the opportunity to sit down with Amy Pratt to find out more about her family. Please see below the 4 part interview:
HELP us by sharing this post and donating to the #SIM365USA Challenge. Phase 1 ends on October 31st and important payments need to be made to secure that the challenge will happen. This is your chance to change the lives of families just like the Pratt family.