Blogger, Artist and Nature Lover. Housebound with Severe Myalgic Encephalomyelitis (also called Chronic Fatigue Syndrome) since 2015. I am passionate about raising awareness of chronic illness, especially ME, since there is still so much stigma and misinformation attached to it. My goal is to support and encourage the community and to equip them to share their stories and raise awareness themselves. This is done through publishing their stories, creating informative posts as well as impactful graphics which they can share. I also manage various public and closed support groups on Facebook for people with ME and their carers. My hope is that people with ME will know they are supported, understood and not alone on this journey and to make sure that they have a platform where they are given a voice.
I’m a Patient Leader