Friends

I am disabled with CFIDS/FMS. My mission to help people advocate for themselves and take control of their health challenges. My goal is to reach as many people as possible and share my own personal tips, tools, and pain management experience. I admire people that are able to deal with chronic illnesses. I also admire creative people that help inspire all types of people. I enjoy reading blogs,...

I am 31 years old, and I have had Chronic Fatigue and Immune Dysfunction Syndrome (CFIDS) -- also known as Chronic Fatigue Syndrome (CFS) and Myalgic Encephalomyelitis (ME) -- for my entire adult life. I am not alone. It is estimated that more than 4 million Americans (and countless others around the world) suffer from this disease. I currently work full-time at a great job and appear young and...

I have had CFS /CFIDS / ME for over two years but am getting to grips with it now that I have a diagnosis. I have always worked, somehow, though had to find imaginative and flexible options. I love the sun and the sea and making myself healthy. I am very lucky to have a supportive partner. I live in Australia and am exploring natural ways to restore my body to full health.

I have chronic Lyme and Chronic Fatigue Syndrome (also known as CFIDS and ME). I was diagnosed with Lyme 2 years ago and CFIDS/ME 9 months ago. I am also the mother of a hopping toddler boy. Learning to negotiate life and illness at the same time takes some balance that I'm still developing! I'm a health educator who works in the private sector. I've always been interested in helping folks...