One of the biggest obstacles for me when i was learning to live with my Ehlers Danlos Syndrome diagnosis was working out what i was now allergic to in terms of skin and hair care. Many of the staple products i had relied on for years were suddenly leaving me with awful flaky scalp, itchy rashes, or dry skin, so I realised it was time to go back to the drawing board and change the products i was using. Please bear in mind every single person is different when it comes to work for them, but these are recommendations and it might give you a place to start.Read More
Online, people see my life as magical, where I never have to go to work, have an incredible boyfriend and a crazy cat called Moo. Where books seem to flow out of me in a torrent of unstoppable words. But what aren’t you seeing?
Well… I’ll tell you.Read More
I talk to a lot of chronic pain sufferers, whether that’s because I’m looking for advice, or they’re looking for advice from me. However, I always seem to end up seeing the same thing both externally and internally and it got me thinking.
Chronic pain sufferers struggle with self-worth.
Why is that?
Is it because we are worthless?
Is it because we lose our worth to these diseases?
Absolutely not.Read More