The Pathfinder Outreach Network is designed to address these issues on a local basis and is overseen by the most important person on your child's cleft/craniofacial team...YOU! Become a Pathfinder!
While plenty of information is available about cleft lip and palate and other craniofacial conditions, getting that information out to those who need it...when they need it...can be a challenge. How many times have you thought, "I wish I had known about this website three years ago." Or, "If only I had someone to talk to after my baby was born...someone who understood what I was going through"?
The Pathfinder Outreach Network
You can make a difference!
Support "groups" are often associated with a monthly meeting at a particular time and location, and perhaps a special event once or twice a year. But we like the NETWORK approach much better! We want folks to realize that when a question comes up on a Tuesday night or a Saturday afternoon, they can call a local Pathfinder volunteer, or jump on-line to get a parent's point-of-view and words of encouragement and support.
The Pathfinder Program = Support NETWORK!
A program overview is available here!
This is NOT a traditional support group!
Vision without action is a daydream. Action without vision is a nightmare. Japanese Proverb
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