There are many challenges on this trip for me. It is completely different from challenges with CF. With my cf lungs I needed to find a fridge, come up with a way to keep my medications cold while on the plane and of course lets not forget the fun of dragging my vest machine around the airport! Now I have pills to take at certain times, which was actually quite challenging trying to figure out when I should take them with the time change. (Add in my sleep deprived brain and it almost got me to tears I was so overwhelmed, I did figure it out and didn't miss any doses though!). I also have my immune suppression which makes finding food I can eat a challenge and riding on the moving petri dish (what some may refer to as the subway) is slightly terrifing. Luckily I have my mask and plenty of hand sanitizer!
So far I have seen most of the sights, Eiffele Tower, Louvre, Arc de Trionphe, etc, all from the safety of a double decker tour bus. One day we will be actually seeing the sights from the ground, hopefully they are much less crowded then they were as all I see when I see crowds is a bunch of walking germs and I'd kinda not like to be mixed into that. Well I'm off to bed, adios! (Being in a place where another language is all around has triggered my Spanish brain!)
Stumpy the Bird!
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