It’s M.E Awareness Week 2018!

You’ve seen the first blog post of M.E Awareness Week yesterday, about how bad M.E can get. You’ll get to see a more humourous blog post next Sunday, all about the ridiculous theories I have encountered concerning the cause and treatment of M.E.

What else am I doing for M.E Awareness Week 2018?

Donate

That’s 25% of ALL donations, not just profit. I should also clarify that I will be donating 25% of the money donated BEFORE PayPal take their cut. If you donate £10, $2.50 goes to the M.E Assocation. Click on the donate tab in the menu to proceed!

Find out more about the M.E Association here: http://www.meassociation.org.uk/

Q&A

You can send me your questions via social media, through social media private messaging services, or by going to the contact tab in the menu above. I am willing to answer anything about living with M.E, so submit your questions! The video will be posted on here on Saturday!

Author: diaryofadisabledperson

When I was 14, I suffered viral meningitis, and as a result I contracted a disease called Chronic Fatigue Syndrome (CFS), which is sometimes called Myalgic Encephalomyelitis (M.E). Over 7 years on I use a powered wheelchair to get around, and I'm hoping that this blog will give people an insight into life as a disabled person.

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