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It's Time to CoppaFeel with Y Salon

You may have spotted on my Instagram a few weeks ago I had the honor to attend the CoppaFeel event at Y Salon in Newcastle. I was really looking forward to this event, knowing how important this cause is. It was such an inspiring event, I feel like I've learned so much about Breast Cancer and the CoppaFeel charity. I've decided to share it on my blog, because I think it's something that everyone should be aware of. 1 in 2 people will be affected by cancer, so it's important we do what we can to find it and stop it as soon as possible.

About the Salon The event was held in the Y Salon, who work with the Kevin Murphy brand. Kevin Murphy are committed to natural ingredients and being kind to the environment. They have so many amazing products, which we all got to have a look at during the event, which are all cruelty free and full of natural ingredients. In this day and age, it's so important we start making these changes, so it was really great to get to know what Ke…

The Fibro Diaries | Reflecting


This is one of those posts that actually has absolutely no point, it's simply me having a ramble about what life with fibro is like. My posts like these are really going to be short and sweet, but it might give a little insight into life with fibromyalgia.

Lately I've been thinking about what my life was like when I was first experiencing fibromyalgia symptoms. I wasn't diagnosed until September 2015, but really it all started when I first moved to Uni in 2012. A lot of people think that fibro can start with big personal events etc, and the move to Uni was a big thing for me, so I think this may have been where it all started. Of course, when you start uni, your life revolves around eating your body weight in takeaways, constantly drinking and having the most horrendous sleeping patterns, so it was difficult to tell if what I was experiencing was just typical student life taking its toll or if it was something more. It wasn't until my second year when I found that I was really struggling to make the walk to lectures and my concentration levels just completely dropped that I thought it might have been something more.

It took me quite some time to get my diagnosis but really, I need to give a huge shoutout to Teesside University, I'm so surprised I managed to come away with a degree but I had some really great support so I will always be thankful for that.

Basically, the early days of fibromyalgia can be so tough. It's completely invisible and there's so many things that the doctors have to rule out before they can start thinking about fibro. I'm lucky that it really only took me about 2-3 years to get my diagnosis, I know some people it takes so much longer! But the timing of it all for me made it difficult to even know myself if anything was wrong! I instantly noticed an improvement in my health when I moved back home, so clearly the student life isn't the best for fibro warriors out there, but I still have days where I genuinely wonder whether I'll make it out of bed.

If you've been diagnosed with Fibromyalgia or another chronic condition, how did the diagnosis go? Or are you still waiting for your diagnosis? I think it's crazy how different everyone's experiences are!

Abbey xx

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