I have two sons with CF and while I’m not going to say you should or shouldn’t date this man I hope I can give you a realistic picture of what life is like with CF.
With the new medications CF is not the death sentence it once was. I now believe my sons to have a normal life expectancy. Obviously there will be exceptions to this and it would also depend on the level of organ damage prior to starting the medication.
Before starting Kaftrio five years ago they were both on IV antibiotics every three months but haven’t needed any since.
Neither has had a sick day for CF related illness in that time.
A bigger concern would be the impact on daily life. So while the burden of treatment has reduced greatly they still have to do nebulisers, physio and take a lot of medication.
They attend regular clinic appointments at the hospital. I’m lucky that they are seen locally but some people would have to travel further for this. There are also appointments from time to time for liver scans, bone density scans and blood tests.
There is at least a 95% chance they are infertile so fertility treatment would be likely if you wanted more children. Also if you are a carrier there is a high likelihood any children would also have CF (3 in 4 chance).
They can’t mix with other people with CF due to cross infection risks and need to be really careful around mixing with people with coughs, colds etc.
There are some activities they can’t do because of risks of infection eg. No hot tubs or jacuzzi.
Everyone with CF will be making their own risk assessment as to what is acceptable for them.
Recently we have had supply issues with some of their meds which has been stressful and time consuming to locate supplies.
On the positive side they are both great at looking after their health - no smoking, vaping, drinking and plenty of exercise.
I hope you will find this useful.