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Film Review: Spider-Man Far From Home

Spider-Man: Far From Home (2019) Director: Jon Watts UK rating: 12A Length: 129 minutes Cast: Tom Holland, Zendaya, Jake Gyllenhaal If you know anything about me, you’ll know that I am a massive Marvel fan. I would happily sit for hours watching the films or tv shows, they’re that good! With that in mind, I may be biased. However, in my opinion, Spider-Man: Far From Home is the film to beat this year.  I was able to go see the first showing of Spider-Man: Far From Home in Odeon at midnight which is always a fun thing to do as you’re usually surrounded by other mega fans of the franchise. The screen we were in was actually quite empty and basically silent throughout the film which was kind of sad but I think I reacted enough for everyone in there to be honest! There’s so much to talk about with this film that I honestly don’t know where to start. Please be aware that there will be spoilers in this post! Don’t read unless you’ve seen the film! I have to begin wi...
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What it's Like Being a Friend to Someone with CF (GP)

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How & When We Met: I met Shannon in comprehensive school, we were in the same form class, so met in year 7. We didn't really interact until year 8, this is when we started becoming friends, I questioned why sometimes she was in the little meeting room in form and why she got to stay inside some days and she explained that she had cf. Of course, I'd never heard of this so when I got home that day I did a little research on what that was. Becoming Friends: We started off as mutual friends with Amy, I'd known Amy from primary then Shannon and Amy became friendly and of course, we became friends too. We had sleepovers and went out. As me and Shannon became closer Amy became more distant. We were all still friendly with each other and still are. Shannon and I seemed to share more interests. My Understanding of CF: To my understanding, CF is a genetic disease that 1 in 25 people are carriers of and don't even know it. It is described as an "invisible illn...
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Cystic Fibrosis and Mental Health (GP)

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My name is Siobhan Coles and I would first of all like to start off by thanking Shannon for the opportunity to be featured on her Blog for Cystic Fibrosis Awareness Month! I am here today to talk about my own experiences of life with Cystic Fibrosis and its effects on Mental Health, all too often Mental Health is pushed to one side and not always considered as being important when it comes to our physical health and the effects that Cystic Fibrosis is having on our lungs. Our clinical teams are constantly looking at numbers and test results and trying to find the best solution to treat the chest infections that we grow in our lungs. Friends and family tend to only notice when we are coughing more, when we become more tired and possibly less motivated to do everyday tasks, like getting dressed for example. In the last three years my Cystic Fibrosis and Mental Health have had a huge impact on me as a person specifically when I started college and had to start taking...
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