How to be an Ally for chronically ill and disabled people
You would like to support your chronically ill/ disabled friends but are unsure how? Here are 4 ways you can show support. What is an...
A blog about my life with chronic illness
When I first learned about my diagnosis of ME/CFS, I knew nothing about it. I had to find my own way of navigating life with a chronic illness that almost nobody knows. Since then I learned many things that I now want to share with you in this blog. Hopefully some of the things I learned can help you along the way.
In 2011 my life changed forever. I graduated from Highschool, entered University and I also became very sick. I suffered from an illness called mononucleosis, caused by the infamous Epstein-Barr Virus.
My life was never the same again, because the illness never really went away. In 2019 I finally got a diagnosis- I have Chronic Fatigue Syndrome (ME/CFS). I heard about it for the first time just a few months prior. It was an illness I have never heard of before and I knew nothing about.
Since then I learned many things that I now want to share with you. I hope that one day my illness will be known much better and taken far more seriously.