Browsing Category: Cystic Fibrosis

Body Image

Following on from my CF related posts, I wanted to talk about something that is a very touchy subject with me. So, I have thought that this week I will discuss Body Image and how it’s affected me over the years. To start things off, I wanted to say how difficult this is for me […]

My Medication

Following on from my previous post about my treatment, I’ve decided it would be easier if I wrote about my medications separately. Throughout my life I have taken so many tablets – it actually blows my mind. So on a daily basis I take 79 tablets and this isn’t including antibiotics or steroids. That works […]

My daily treatment

As there is no cure for Cystic Fibrosis, we get given numerous amounts of treatments and medications that we have to do everyday and this will last for the rest of our lives. I thought I would share some more information on the certain steps that I have to do daily, now this varies for […]

My story

This week is Cystic Fibrosis week and I have decided that each day I will upload a new blog post related to CF. Each post is going to be a different aspect of Cystic Fibrosis. So I thought my first post will be my own story with CF. When I was 2 years old I […]

What has happened recently?

“Sometimes it’s okay if the only thing you’ve done today is breathe” Majority of you would already know that I have Cystic Fibrosis but not everyone does and that’s purely to the fact that this condition isn’t always visible. I want more people to understand that living with a hidden disability has its positives and […]