Cystic fibrosis dating other people with cystic fibrosis
Stagg was diagnosed at the age of 14, much later than most cases, which are identified in the first few years of life.
It was around the time medical authorities discovered that gatherings of CF patients put them at risk, bringing an end to summer camps for children with the disease and other group activities.
Unfortunately, that has held true even in my dating life. Add a genetic disease to the mix and it can become impossible at times.
Being single into my late 20s, I've done my fair share of dating while managing the daily life of a person with CF.
But I would be remiss if I didn't acknowledge that CF complicates finding “the one” beyond what the majority of my friends have had to deal with.
I can't think of a single stage of any relationship that I've had where this disease hasn't played a major role.
Mother Zoe Elliott has to separate them because both her children have cystic fibrosis, which means they are prone to picking up bugs and infections.
A social network launched by the non-profit Cystic Fibrosis Canada will help them find one another and converse via video-chat, instant message or online forums.“It’s the kind of thing the community really needs,” says Carly Stagg, 31, of Calgary, a CF patient who was actively involved in planning and designing the new portal.They could relate to violent coughing attacks and what it feels like to be drowning.They had spent more time in children's hospitals than in school.Brian shared his good fortune: Eight years after a double lung transplant, he was doing fine.But like anybody with cystic fibrosis, he knew you can't take anything for granted. It didn't matter that Brian, at 25, was seven years older. In November, Brian's lungs failed and he landed in the emergency room at a hospital near his home in West Palm Beach.