Cystic fibrosis dating other people with cystic fibrosis

Oli: If I wasn't 100% sure about a date, I wouldn't tell them about my condition.

It was easy for me to hide it because I had my transplant at an early age, so I don’t show any obvious symptoms.

Sure, the things we go through are sometimes extremely different; he’s fighting his body while I’m fighting my mind. We’re just two people trying to fight the parts of our body that aren’t willingly co-operative. And most of all, dating someone with CF has changed my perspective on hospitals.

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I had no idea what cystic fibrosis (CF) was until I met my boyfriend on Bumble in September 2016. Afraid of getting close to someone just to lose them again.

We talked online for a week before actually meeting in person. Having no idea what CF was, I immediately went online and started researching it, trying to understand what it meant. The first thing I felt was sadness – some of my worst memories were in a hospital. But I knew that you can’t control if and when you lose someone. Like I have to make room in my purse for his medication.

I have spoken to a few people with CF throughout my life, from a distance, and sadly most of them have died.

In spite of this, I would absolutely encourage those with CF to connect with others in the same position as it can be enormously helpful and comforting.

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Since then I’ve been reluctant to make friends with other people with CF.Mahi: People tend to take it one of three ways when I tell them I have CF.They either go and do research on it, googgle everything about it.I used to be quite self-conscious about it, but I find it best to be open and up front about everything, because it is a big part of my life.Also there are things that I do that others don’t when I’m on a date.

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