ATTENTION MEDIA & OTHERS SEEKING INTERVIEWS!
If you represent a media company, are a student writing a report or anyone interested in interviewing our visitors, please seek permission (see email address at the bottom of the page) before posting your requests or emailing solicitations for any talk show, magazine, thesis, census or other interview on any message board on this site. If not, your posts WILL be removed. Please respect the privacy of our members.
I am 25 and have CAH. After quite a few different (incorrect) diagnosis, I was diagnosed with CAH when i was about 16 as i did not begin my period and was quite often unwell as a child.
I have only just found this website and seen what an inspiration and help it has been to mothers of children with CAH and was wondering if there was anyone out there in their 20's (or younger/older) that wanted or needed to chat to someone about their issues with this. I have had trouble growing up with coming to terms with this, but know NO-ONE with anything even similar to i suppose 'appreciate' what i go through. I suppose the thing i really need to see is, is there anyone out there that was afraid to have children knowing they have CAH and knowing that this is hereditary?
