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Treacher Collins syndrome
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Treacher Collins syndrome
Advice
Advice of Treacher Collins syndrome
I never let my disability stop me
by Amanda
ver que mi hija es fuerte
by Isa
Coisa 1
by Thiago
APAP/CPAP Therapy for moderately severe Sleep Apnea. ❤
by Cynthia Murphy- Craniofacial Awareness Advocate
My family has always backed me up
by Amanda
que m demuestre dia a dia lo valiente q es
by Isa
Coisa 2
by Thiago
Meeting others within the craniofacial community who I can relate to in more ways than one. ❤
by Cynthia Murphy- Craniofacial Awareness Advocate
I know i can do anything i want
by Amanda
q nada ni nadie podra hacerla sentir menos
by Isa
Coisa 3
by Thiago
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