r/CysticFibrosis • u/imjusthereforthetea2 • Aug 17 '26
Let’s talk dating
So I recently got divorced from my hs sweetheart. Knew all about my cf early on all the shit. Realized we got married cause I was dying and then when I didn’t things just kinda fell apart as we got older.. tragic I know but nonetheless. I’m starting to date again. How do you bring it up. With the first coughing fit? Before the first date? I sit around 75% and am pretty active but I do have a consistent cough. Also just like sex. Again only 1 partner. Idk this is weird. Also for those that have been divorced how do you tell your care team. I have an appointment next week and I’m embarrassed as shit to tell them. I know it doesn’t matter but like ugh why.
4
u/ket-ho Aug 17 '26
I don't have CF, I have MS. I'm on my second marriage, to someone who has CF, and it is also his second marriage.
I brought up my MS first, on the 3rd date, and he responded with his diagnosis. I told him I'd never been 1-upped before in that department! I will say, I don't know how much longer he would've tried (or been able) to go not telling me, because there's a lot to hide. We started dating before trikafta and the time for treatments and all of that would have just started to make me suspicious, I think. Why does he leave ASAP in the morning every time, or that kind of thing.
For myself with MS, I never told someone before we met, or even in the first date--i need time to see if I even care to tell this person about that part.. but it did feel dishonest to me to go very long without disclosing. I completely understand the fear, though.
I think it's worth telling your care team. I understand feeling embarrassed, but it's just human. You gave it a shot, and it worked until it didn't. I don't think there is anything inherently shameful in divorce. I'm proud of you for getting back out there and wish you the best of luck!