Story
Thanks for taking the time to visit our JustGiving page.
Three years ago, I (Em) was diagnosed with ME/CFS after having Glandular Fever. I went from Lifeguarding for the RNLI and being really fit, to not being able to walk for 5 minutes without pain and fatigue. I very quickly lost my fitness and my normal life. I continued to struggle for more than two years, with little to no explanation from doctors as to why I could no longer do anything. At bad points, I wouldn’t be able to leave bed and there was no treatment available.
After two and a half years of struggling with my health, and massive lifestyle changes, I have made huge steps in recovery, and some days I still struggle. I never thought I’d be able to walk long distances again, let alone run. It’s a huge privilege to be able to do this, for such a worthy cause.
Thousands of people (mainly women) are diagnosed with ME every year. There is no medical cure, for a condition that can, at times, leave people bed bound. This has become even more prevalent after COVID, with lots of people suffering with post-viral symptoms. The ME association are undertaking vital research into a syndrome which is not understood.
We are running 44 miles on the Cornish coast path, from the Lizard to Lands End (22 miles each), for the Endurance Life Classic Quarter Relay Pair trail race, some of the toughest trails in the country. Thank you very much for your donation, it’s beyond appreciated.
Event link: http://www.endurancelife.com/classic-quarter.