Post #10 - Posts from last year about solo travelling, that I forgot to post...
Solo Travels: Parts 4, 5 and 6 - PART 4 - On the Monday I made my way over to the Anne Frank museum, turned up and managed to go straight...
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This is my story.
Hi, I'm Louise and I have Cystic Fibrosis.
CF will be a frequent feature in my posts because it features heavily in my life! But this blog is about all aspects of life, daily routines, dreams and aspirations, failures and funny stories.
I love to laugh and I'm very chatty so this will probably be quite informal. I hope you enjoy and let me know any feedback you have :)
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Post #9 - Solo Travels: Part 3
My first full day exploring!
Post #8 - Solo Travels: Part 2
The day before...
Post #7 - Solo Travels
Take a look into my newest adventure...
Post #6 - Returning to freedom
TRIGGER WARNING: I talk about the side effects I had from my Covid vaccine, they weren't pretty but I wouldn't change the fact that I had...
Post #5 - Shielding
How do you even start to explain shielding to someone who hasn't experienced it first hand? March 2020: I saw my family on the first of...
Post #4 - A day in my life
An insight to a day in my life!
Post #3 - Catching up
Hello! So if you remember me starting my blogging journey in June 2020, then you're probably wondering where I've been? If I'm completely...
Post #2 - My hospital admissions
Find out what it's like to spend time as an inpatient on a Cystic Fibrosis Ward!
Post #1 : An Introduction
An insight into my life so far, with a stunning picture of my favourite place #IOS
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