Skip to content
A personal blog about my experience of living with the illness Myalgic Encephalomyelitis (ME)
About. And Some Useful ME Resources.
Post One. Intro.
Post Two. My Sigur Rós Payback.
Post Three. From Healthy To Not Healthy.
Post Four. Tonsillitis.
Post Five. Music & Dad & ME.
Post Six. Update, Tonsillitis Still.
Post Seven. Symptoms.
Post Eight. Sweet Potato Cinnamon Rolls.
Post Nine. Why I Write This Blog.
Post Ten. What’s My Future?
Post Eleven. From Healthy To Not Healthy.
Post Twelve. How You Can Help.
Post Thirteen. My Mum’s Birthday/Fundraising Party for Invest In ME.
Post Fourteen. ME And Me, By Amelia.
Post Fifteen. Employed To Unemployed.
Post Sixteen. Wheelchair Or Not?
Post Sixteen Continued… Wheelchair Or Not. An Afterword.
Post Seventeen. The PACE Trial Scandal.
Post Eighteen. Crowdfunding My Wheelchair.
Post Nineteen. Time For Unrest.
Post Twenty. Thank You For Funding My Wheelchair!
Post Twenty One. The Wheelchair Has Arrived.
Post Twenty Two. Reblog. An Interview with Dr David Tuller.
Post Twenty Three. Wheelchair’s First Holiday.
Post Twenty Four. Unrest In Peebles.
Post Twenty Five. General Update – The Last Three Months.
Post Twenty Six. How Having ME Has Affected My Mental Health.
To find out more, including how to control cookies, see here: