To commemorate ME/CFS Month and ME/CFS Week, which was last week, Open Medicine Foundation conducted an interview with me about living with the illness for two decades. You can find the full interview here on OMF’s website. I hope you check it out! Below you find a snippet. Love,Sandra
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?
Sandra Postma 