MEpedia – Our Future

What is MEpedia? MEpedia is a project founded by MEAction, powered by the patient community, and built by volunteers including patients, students, and researchers. The team at MEpedia are crowd-sourcing a knowledge base on the history, science and medicine of ME, CFS, and related diseases. But they need your help. http://me-pedia.org/ Imagine a website where Read the full article…

Thoughts from within a Depressive Episode

I wrote this piece while I was experiencing a particularly bad (for me) depressive episode. Thankfully it didn’t last long but I needed to write my thoughts down (somehow I found the motivation to do this) in an attempt to make sense of them. So I apologise in advance for how, well depressing, this post Read the full article…

Guest Post: ‎Sefik Villasante‎ – My Story

My Story of overcoming the dark and desperate times is one that I hope can show others that there is a way out to the other side ! It was Sept 2016 and after 12 years of striving and seriously hard work and sacrifice I achieved a promotion within a huge U.S Multinational Company . Read the full article…

Why do so many people still refuse to believe Myalgic Encephalomyelitis (ME) exists?

I would like to start by saying a big thank you to everyone who has left kind and encouraging comments, your support means so much to me. The last 48 hours have been exhausting and a real eye opener. I didn’t realise sharing my story about the realities of living with severe ME would stir Read the full article…