Cystic Fibrosis carriers
My husband and I have been talking about trying for our 3rd. We found out we are carriers for cystic fibrosis. I was really excited to try and grow our family again but now I’m really apprehensive. We have 2 little girls who are fine. My husband wants to try still and I do but I kind of feel like we’d be pushing our luck kind of thing? Like we already have 2 healthy kids so I feel like we got so lucky so if we try again would that be wrong knowing we have a 25% chance of giving a little one this disease. I know medicine is far better these days and people with CF are living long full lives but I would just like some opinions if it would be completely wrong as we know we are carriers. Please only nice comments as this has been weighing on me for a while now and I feel so stressed and anxious about it.
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