My DH has recently tested positive for BRCA2 mutation.
We were surprised to learn during our genetic counselling that we would be eligible for funded NHS to screen for BRCA2 mutations in embryos. This has given us a lot of food for thought about what the right thing to do is when trying for children.
DH had already floated before he had his tests about whether we should have genetic testing/IVF. I felt quite confident that IVF wasn’t the right option - the intrusion, artificial hormones, stress - also felt that with medical advances it wasn’t proportional to go down this route when cancer screening and treatment could look drastically different in a few decades time when our children are adults.
However learning that it is an option on the NHS (I had assumed it wouldn’t be!) has really made me think again about what the right thing to do is - will I be wracked with guilt and regret if we did have a daughter who ended up with cancer in early adulthood?
Would really appreciate hearing from others who have been through similar decisions - or what they feel now with hindsight if they didn’t have the option at the time 🤷🏻♀️