Jess has had Myalgic Encephalomyelitis for 10 years, she has also been diagnosed with Fibromyalgia and IBS with suspected POTS.

"I began my activism journey in July 2020.

I am excited to represent my chronic illness community and fight for intersectional equality."

Jess became unwell with Glandular fever at the age of 13 and she never got better. Myalgic Encephalomyelitis (M.E.) is a neurological condition that affects every single body system.

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"Instagram has allowed me to connect to people with similar experiences to me and has represented light in a lot of lonely darkness. I created my activism page with zero expectations but it has flourished into a beautiful and trusting community of wonderful people. My mental health has improved because of the connections I have made and the community I have built. I am honoured to be a part of the community!"