With one more week to go on my fundraiser to fund research into the condition myalgic encephalomyelitis (also ME or chronic fatigue symdrome), I wanted to share some other articles with you on the reality of this illness for others. People Magazine dedicated an article and video to the story of Whitney Dafoe, a once … More ONE MORE WEEK TO DONATE TO MY FUNDRAISER FOR ME/CFS RESEARCH
There are two weeks left on my fundraiser for research into the illness Myalgic Encephalomyelitis/Chronic Fatigue Syndrome – also known as ME/CFS – for Open Medicine Foundation (to donate go HERE) and I wanted to give an update on the things I have been sharing over on my Instagram for the past several weeks. On … More My ME/CFS Fundraiser: My Life With Chronic Illness
We are halfway through my fundraising campaign for Open Medicine Foundation, an organisation that raises funds to help and stimulate research into Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (also known as ME/CFS) and other complex illnesses such as fibromyalgia and Lyme Disease. For more on my reasons to fund for this non-profit, do read my previous blog! … More Halfway Point of My Fundraiser for ME/CFS Research
Today is an incredibly exciting but also scary day for me. Because today I am launching a fundraiser in partnership with CrowdChange and Open Medicine Foundation to raise money for research into Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)! That’s right! I’m organising a fundraiser! This month means 20 years of living with ME/CFS for me. To … More MY FUNDRAISER FOR ME/CFS RESEARCH
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome is a very long and confusing term for an illness that is itself still shrouded in a lot of mist. Many of us deal with similar symptoms, such as fatigue, headaches, muscle aches and what we call brain fog, but a biological cause is yet to be found and a clear … More MY ME/CFS FUNDRAISER: What is ME/CFS?