In my previous post, I talked about the struggles and challenges of living with an invisible illness Those that can't be researched on the internet, or advised by a doctor, because, unless you live with an illness/condition yourself, you'll never know. So,... Continue Reading →
There are many types of invisible illnesses, and we can all research the different variations, the definitions, the symptoms, the relief remedies (if any). But can we research what it's like living with an invisible illness? Can we research what... Continue Reading →
As all of you will know, I haven't posted in a while. Back in December, I decided to take a step back from blogging, in order to concentrate on my family over Christmas... It was a hectic one (something I'm sure... Continue Reading →
I have to admit, we've done well with the weather this year. October was pretty warm compared to usual and it didn't get that cold, in my opinion. This week, however, I got a bit of a shock to the... Continue Reading →
Well this post was supposed to be live a lot sooner than it has ended up being. Where I thought I had set a time for it to go live on my page, I apparently didn't (silly brain fog!). Sorry... Continue Reading →
Not my usual kind of post, nor is it the one I planned out. However, that being said, we've all, at one time or another, been affected by words that we shouldn't have to hear. Ones that come with the... Continue Reading →
With things being so hectic here and, of course, my brain fog to add to it, I forgot to update you guys on what's actually going on at camp and what I'm now doing. So if you have been following... Continue Reading →
I've officially broken my promise to you... I didn't post last month and therefore broke my promise about posting at least once every month. Most of you will know the reason why but if not... It's because I'm "over the... Continue Reading →
I'm currently writing this on the train so I won't promise how well my spelling will be, although I am in the spacious first class carriage so I'm not complaining too much at all. My free cuppa and soft drink,... Continue Reading →
Living with JHS 