In fact, the nickname stuck so much that it is still used today and roses have become an unofficial symbol of CF. Fw-300 #ya-qn-sort h2 /* Breadcrumb */ #ya-question-breadcrumb #ya-question-breadcrumb i #ya-question-breadcrumb a #bc .ya-q-full-text, .ya-q-text #ya-question-detail h1 html[lang="zh-Hant-TW"] .ya-q-full-text, html[lang="zh-Hant-TW"] .ya-q-text, html[lang="zh-Hant-HK"] .ya-q-full-text, html[lang="zh-Hant-HK"] .ya-q-text html[lang="zh-Hant-TW"] #ya-question-detail h1, html[lang="zh-Hant-HK"] #ya-question-detail h1 #Stencil . In response, we’ve formed thriving online communities so that we can benefit from information sharing and support, but there’s no denying that virtual connections can never replace in person ones.For me, this is one of the hardest things about CF. CF and Tay Sachs are tied as the most fatal Jewish genetic diseases.People don’t doubt or question knowns, only unknowns.
I think many of us with cystic fibrosis (CF) have built up emotional walls around ourselves.
They don’t have to deal with that first tune-up hospitalization after you have been seeing someone new for two months and they feel uneasy or even panic, thinking there is something horribly wrong.
No, the average person doesn’t deal with these things.
We aren’t afraid to speak our minds and people like that. It’s about how our personalities and qualities align with someone else’s.
So I think dating with CF isn’t all that different from the way other people date.