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Apert Syndrome
Advice
Advice of Apert Syndrome
Always Be yourself
by Lindy Franz
Ik ben een bikkel
by Mylene Kootstra
My son smile always make me feel better
by Mayssa
Cirurgia de descomprensão
by Raul de Paula Borges
Friends and family always there for support
by Torey
APAP/CPAP Therapy for moderately severe Sleep Apnea. ❤
by Cynthia Murphy- Craniofacial Awareness Advocate
Iam Just Human and Living This Life, Like Everyone Else.
by Lindy Franz
He is a fighter !!
by Mayssa
Fisioterapia, estimulação, fono e terapia ocupacional
by Raul de Paula Borges
I live a healthy life
by Torey
Meeting others within the craniofacial community who I can relate to in more ways than one. ❤
by Cynthia Murphy- Craniofacial Awareness Advocate
My Parents Treated Me, like A Human. not Special, Because I have This Rare Disease. They instilled in Me, That I Need to do My Best. Try New Things.
by Lindy Franz
He has a very soft heart
by Mayssa
Retirada da lactose
by Raul de Paula Borges
i learn everything about Craniofacial syndrome
by Torey
Advocating for the cause of craniofacial differences and involving EVERYONE in these efforts. We must raise awareness and enact change TOGETHER! ❤
by Cynthia Murphy- Craniofacial Awareness Advocate