Two years ago I lost my baby at 24wks. He had Trisomy 13. Emmanuel had multiple physical deformities as well as other conditions. I was just wanting to hear from people who have been through similar experience. I have just found that when I tell people about my baby and his condition they seem to treat me like some sort of freak for having a baby with such deformities. It's hard enough going through the loss of a baby but when you say the word "deformities" their attitude changes. How do you cope with people's reactions?
Regards,
Dianne