familieswithccd : families with CCD

Share with other people who have cleidocranial dysplasia also known as cleidocranal disostosis.

Hello to all I've lived with ccd for almost 57 years and the only problem I had was with my teeth. Had them out at 18 and got dentures which have giving me no problems. Posted - Fri Apr 14, 2006 6:25 am	lucy372 Offline Send Email
Re: Hello Yvonne, I cannot seem to contact you directly through e-mail. I want very much to be friends. Please write me at anitak1982@hotmail .com (no spaces) Do you Posted - Sat Feb 11, 2006 1:55 pm	Anita anitak1982 Offline Send Email
Re: [families with CCD] Hello My 2 1/2 year old son also is the first in our families to have it (Spontaneous gene mutation). He has no collarbones and is petite framed. He has the pot Posted - Sat Feb 11, 2006 12:55 am	Shelley Flores spray76 Offline Send Email
Re: [families with CCD] Hello Yvonne, Did you mean to write to this group or the Cleidocranial_Dysplasia one? This one hasn't had any activity in a while and from reading the words in your Posted - Fri Feb 10, 2006 10:45 pm	Anita anitak1982 Offline Send Email
Hello Hello to everyone on this great site. I have been a member for a long time but never get the chance to post. I'm 32, live in the NE of England and my 4 year Posted - Fri Feb 10, 2006 9:05 pm	why2shy4beni Offline
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