Looking for Hope
As parents/caregivers of a child with a rare disease, physically visible anomaly, or hidden anomaly, we often need someone, or something, to carry us through moments of despair – discouragement – disbelief – disappointment – and/or dispression.
Please allow these videos to inspire within you, the strength and empowerment to pick yourself up and continue moving forward.
REMEMBER: We’re all a little rare; but, when we fall into mutual rareness…We call it a family!
Courtesy of Rare Disease Day 2015
Courtesy of Vascular Birthmarks Foundation