Hi, I'm Jo Moss, I live in Norwich, UK. I have a severe form of Myalgic Encephalomyelitis (ME), which was diagnosed in 2006, although I had been sick for many years before this. I started my blog ‘A Journey Through the Fog' to give myself a voice after years of being too sick to communicate. I write to educate, support, encourage, & raise awareness of this highly misunderstood illness, and to fight the discrimination and neglect with often face. I discuss all aspects of my health openly. I hope by sharing my experiences I can help others along the way, but most importantly, I want to let people know they are not alone. I'm also keen to show that, although life with ME can be tough, it can also be a life worth living. I love to read, and I'm passionate about music – I even started learning to play the guitar from my bed. I look forward to connecting with you.

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