Strongsville Patch. August 29,2011, by Gina Ragone.
Strongsville Teen Lives with Rare Disease.
Posted on: August 29, 2011
Categories: Families in the News
It has been seven years since DBA became part of our vocabulary. Our son’s diagnosis brought confusion, apprehension and despair. The discovery of DBAF is a stroke of serendipity. While even more tears were shed, these are now mingled with knowledge, understanding and, more significantly, hope. It will be through research that our son will be able to secure a brighter future.
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