I am just over half way through my 2 week course of IVs, it has already made me feel A LOT better, I have lots more energy, and want to be able to do things.
The only thing I don't like about it is I can't join in properly at Cheerleading or go out with my friends much as my Ivs are every 8 hours, 8 in the morning, 4 in the afternoon and then midnight.
CF clinic.
So today, Wednesday 31st July, I went to Cystic fibrosis clinic, everything went well, I put weight on, I grew a little, and my lung function stayed the same, I will have another lung function in just less than a weeks time (onTuesday) to check my lung function after my Ivs, so I'm hoping it will go up and won't be in the 80's. My normal lung function is usually between 90%-97% so it's usually pretty good!
Social networking sites.
Also if you have a Facebook page please follow my journey at 'Emily's journey with Cystic Fibrosis'
Or if you have Instagram please follow me there on @emilyrscheer or @cf_fighter_
Thankyou x
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