Humans of ME/CFS

I have been ill with ME/CFS since 2010. I had so many hopes and dreams, but now they have had to change. My dreams are now to be well enough to enjoy being with my family and to have enough energy to look after my children. The little things have become the big things. I struggle to keep hopeful as the years roll by, but I do truly believe that one day a cure will be found. I want to live my life in a body that works properly, that doesn’t feel like I’m ill with the flu every single day.

I can’t get back the years that I have lost, but I hope for the future.