Yesterday I entered my new home for the next 3 months during self isolation, a large open farmhouse style apartment with dark wooden beams lining the ceiling and open sky lights bringing the outside inside. It is my cozy sanctuary. The corner sofa has a mountain of pillows to drown in and a soft but… Continue reading Relying On Myself
Today I’m sharing my first ever guest post! Written by a blogger with EDS. Naomi is the author of http://www.diaryofazebra.com where she writes about chronic illness and features guest bloggers. If you’d be interested in having a guest blog on my site email me email@example.com The emotional toll of being chronically ill is huge.… Continue reading The Emotional Toll Of Being Chronically Ill
In honour of U.K. Sexual Health Week September 16-22nd, I am writing a few posts discussing the barriers people with disabilities face to intimacy - not just sex but general relationships. There’s many things that complicate intimate relationships as disabled people so here’s some, please check my blog again later in September to see the… Continue reading Barriers To Intimacy With Disabilities
Change hope and uncertainty are scary things that come up a lot during life as a chronically ill person. So let’s talk about it.
COMPACTCATH review I was recently sent some free catheters to try & review. The brand is called compact cath and they make well, compact catheters. These catheters are different to other designs I’ve seen since they come in this kind of disc shaped spiral which makes it super small and flat in your bag or… Continue reading Review: COMPACTCATH
Let’s be honest, showering when you have chronic fatigue is rough. It becomes a dreaded chore. I know for me, I don’t shower as much as I’d like to because I sleep through the times I’ve planned too, someones not always around to help, and just generally too exhausted. But friends, I have a life… Continue reading Nilaqua Body Wash review
I love YouTube and decided to write a list of Youtubers with chronic issues because representation is important.
Even though I’m blind I’ve always loved doing art, but now sitting up hurts too much to do art. I miss doing it so much!
“I can see but I can’t SEE” In today blog post I explain what my vision is like.
Showering with a chronicnillness is one of the hardest tasks we don it’s just so exhausting. But it’s mandatory. Here’s some tips to help you.