i am 30 years of age and have c,l,p
i want to share my exp and help others
offcourse because it's so hard ppl wanting to understand
but they don't.
i have been to multi clinics in sheffeild, Manchester and now Swansea
i can appreciate the difficulties involved, as the mouth is a major human appearance
if I can get support in understanding, I reckon at early age I should I have studied
into procedures and help.
Now I'm mentally able to just cope in silence.
hope I have not offended any one and please feel free to email me on
as I am very concerned for others in the uk, that are suffering alone.
i just want you to know, I'm here for you, thanks to the World Wide Web and thanks to this website.
Hi, I was born with a bilateral cleft lip and palate and in the past 21 years that I've been on this planet, I've never considered reaching out to others who were born with our condition until now. I'm positive that our experiences, as well as perspectives, on living with this condition set us apart from one another and unite us. I am here because I would like to know more about our community.I...
Hi everyone, I am new to the forum. My name is Mariam, and I was born with a cleft of the hard palate. I had two surgeries, one at four months and one at eight years. My cleft was the result of teratogens in my mom's environment, which cause the timing problem during my embryological development. And.... walah! A cleft.Because I don't have a cleft lip, my cleft is "invisible". However, I...