HI I've been recently diagnosed with late onset cah . My husband and I have so many questions regarding our future plans for a family. Whenever I ask my Endocronologist I only become more confused.I feel like my doctor is cautious about the information that she gives me . Reading the messages on this site I have only discovered today I am empowered by the wealth of experience and courage of the fabulous women who have share their stories on this site and would appreciate any communication offered to me.

I am wondering if the same precautions need to be taken during pregnancy for locah as cah?

Is it less likely to be passed on if my husband is not a carrier?

Do female children born with masculine features require surgery or is hormonal therapy sufficient?

Can parents with locah produce children with cah ?

I am suffering from constant flu symptoms and respiratory problems could this be related to locah? (not yet medicated)

Has anyone experienced anxiety or mood disturbances related to cah? 

Thanks again for providing a means for venting my many concerns. Looking forward to hearing any comments.

meg .