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A personal blog about my experience of living with the illness Myalgic Encephalomyelitis (ME), by Phoebe Boag.
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 and Dad and 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.
Post Twenty Seven. No, I’m Not Tired.
Post Twenty Eight. Disbelief About The ‘Afflicted’.
Post Twenty Nine. How A Cat Taught Me Just How Bad My ME Is.
Post Thirty. General Update – The Latest On My ME.
Post Thirty One. A Blog Post (Mainly) About My Blog – Looking Back & Looking Forward.
Post Thirty Two. Some Things I’d Like My Visitors To Be Mindful Of.
Post Thirty Three. This Is How We Become The #MillionsMissing – A New Project For 2019.
Post Thirty Four. Planning For A Future With Severe ME.
Post Thirty Five. Scottish Borders Council ‘Disability Tax’.
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