When I was diagnosed with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) in 2012, my life changed overnight. I went from being a 16-year-old just starting college, making new friends, enjoying my independence, and planning for the future, to being bedridden, unable to go anywhere without help, and feeling a complete sense of loss over my body and mind. Over the years, I have also lived with other conditions that affect me both physically and mentally. Together, these conditions shape my daily reality and often leave me balancing pain, fatigue, and brain fog against my work and personal life.





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