Please help us to support people with ME/ CFS and their families.

Chronic Fatigue Syndrome (CFS) is something that has affected me for the past 4 years since I received a diagnosis in 2020. I would therefore like to fundraise for the ME association to hopefully help the other 250,000 people in the UK who also have CFS. There is currently no known cure but hopefully with additional funding this can be explored to help those that suffer with fatigue, muscle aches and pains and brain fog. Many people experience disruption to their studies and work due to CFS and can sometimes not even leave their houses!

Please help if you can!