UK fundraiser seeking your ME stories

Ellie Rushton, Birmingham UK, is setting out on a rather unique fundraising adventure.

For the next six months (September to February) she will be attempting to do 1000 reps of bodyweight exercises every, single, day. Ambitious indeed! But what does it have to do with ME?

I had never heard of ME until I met my sister in law, Hattie. I was shocked to learn through her that there is so little medical understanding of such a debilitating condition. That countless health professionals don’t believe it even exists. That the only treatment available on our national health service makes over 60% of patients worse.

 I wanted to raise money for #MEAction by using my body and the privilege that comes with it in a way that I know people with ME are unable to do. This is for all the patients who have been told that they need to exercise more. We all know that’s bullsh*t – so I’ll do that exercise instead.

I’ll be attempting to get 1000 bodyweight reps done in half an hour every day. I’m sure most of the time I won’t even reach half that number in that time, but you can follow my progress on my instagram page. Wish me luck!

Ellie will also be blogging about her fundraising on Medium, and she would like to use that platform to tell the stories of people with ME all over the world.

If you’d like to share your experience, email Ellie on [email protected] with the subject ‘ME blog’. Please keep your stories under 500 words.

Ellie hopes to raise £3000 in 6 months. You can help her do so by donating!

[maxbutton id=”22″ url=”https://www.meaction.net/start-an-meaction-fundraiser/1000-reps-a-day-for-meaction-eleanor-rushton/” text=”Donate now!” ]

 

Facebook
Twitter
WhatsApp
Email

Latest News

a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.

Severe ME Artists Project 2024

Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by

Read More »
Light blue square with rainbows in the top left and bottom right corner. In the middle are the words, -Pride is Valid- No Matter How One Celebrates or Experiences It. #MEAction Board Member, Jennifer England, shares her views on Pride. The #MEAction logo in the top right corner.

Pride Is Valid No Matter How One Celebrates or Experiences It

In honor of Pride Month, #MEAction is sharing a heartfelt message from our board member, Jennifer England, about what Pride means to her and her wife who lives with severe ME. My wife and I have both been queer our whole lives, but in the 70s that was the quiet part you didn’t say out

Read More »

Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

Read More »
Scroll to Top