Our family has decided we would like to do the Congenital Heart Walk in memory of Silas. It will be held on May 21, 2016 in Indianapolis.  We wanted something our whole family could participate in to remember Silas and to raise money and awareness for CHDs.  There is still so much research that needs to be done to help these babies survive to birth and thrive.  It will be an honor if our family can be a small part in helping families who have been touched in some way by CHDs.  I feel we have to do our part now that we are no longer “ignorant” to these defects.  I wish there had been enough research done to have saved my Silas.  It is also not just about the fundraising, but it is important to Boyd and I that our other children remember Silas and what his journey was about.

If you would like to donate or come walk with us go to https://shar.es/1CGe3j

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