So today you have two posts from me because I didn't want to start making all my posts turn negative.
Also wanted to say that there are some lovely people at my new school and I'm so grateful to know them!!!!!
Anyway I wanted to address something else...
Having Cystic Fibrosis is a life long battle and I just feel as if people should be more educated on this illness.
People always comment saying that we don't 'look ill' or that we have it easy being in bed all day when we are off school but the reality is so far off.
On days that we may look well, inside we are fighting. We can hardly breathe walking up stairs and getting too out of breathe causes mass coughing fits.
I know that this illness differs from person to person but I wish people would appreciate all we go through.
I find it horrible seeing my CF buddies go through pain. Cicely is in hospital for a six week admission and is being so brave about it. I think everyone who reads this should send her loves to cheer her upppp!!!!
Updates...
So I went for clinic last week and my lung function still isn't great. They took a cough swab and some bloods to try and get to the bottom of what was wrong. After getting the results they found I had a throat infection and that my bloods where fine.
I'm going for an appointment on Monday to hopefully kill this infection as it's causing me to have chest pains and I'm finding it hard to walk anywhere.
Today my colomycin ran out, meaning that I can finally stop using me eflow and move onto my ineb (which is charging right now) I'm actually super exited because it means that my treatment time each day should be reduced.
Well that's all for today guys, sorry if my posts are not well structured I just write what comes to my mind.