Hi all,

I’m sorry if this subject is upsetting for anyone. I’ll be 14 weeks next week. NIPT came back low risk for Downs and related disorders, and our 12 week scan looked great, but I just found out I am a carrier for cystic fibrosis and another very rare disorder. Now my husband goes in for testing and we wait. This is our first pregnancy.

Anyone else have stories of hope after finding out you’re a carrier? I know the chances of our baby having CF are still low, but I was devastated by this news. I can’t stop crying.

Thank you in advance xx