I never imagined that I would have a cleft effected child but I did.
I have learned so much during our on going journey and I want to inform other parents who might not know where to go for supplies, information or some basic knowledge.
This page is here to help you make decisions that are best for your family and situation.
Read all about our journey so far here…we still have a ways to go as this year Henry will start examinations for ortho as well as preparing for a Bone Graft Surgery.
- Henry is Born
- Journey to Surgery
- Changed Forever
- Nose Stents, Baptism and Family Vacations
- 3 Weeks until Palate Repair
- October – Surgery, Recovery and a little Partying
- Henry’s Journey
- Henry’s Smileversary
- 3 Years and 1 in 700
Support is crucial when dealing with a cleft. I am so thankful for the Facebook Group, Cleft Mom Support
These Moms and some Dads are supportive, kind and best of all understanding. This is a place for us to vent, ask questions or just to show off our little ones.
It’s very comforting to hear about the journey’s many parents of cleft affected children have gone through..the good, the bad, and the heart wrenching.