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- #AtoZChallenge Three-year participant
To read what I wrote, A to Z, for each year's challenge, click that year's fun badge, below! Learn about the annual challenge. 



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that meant a new post on writing by me and the others in the group on the first Wednesday of the month. (Click the photo for my posts; click here for the group website).

Category Archives: advocacy
#MEAwareness: Guest Post “Send My Apologies”
dSavannah note: I’d like to introduce y’all to my friend Alice Ballinger, a #ChronicIllnessWarrior and poet, who publishes her work on Facebook on her Green Goat Poetry page, and who is raising funds for a desperately needed wheelchair. (Also, please … Continue reading
Help Me Help Others!
Dear readers, no, your eyes do not deceive you. It’s not the 15th, the day I promised to publish a blog post every month this year. It’s the 5th! (I actually meant to publish this on Monday the 1st, but … Continue reading
Being ‘brave’ (actually, I’m angry)
So, last month (May) was #MEAwareness Month, and I did what I could by publishing two posts (instead of just one): May is #MEcfs Awareness Month • #MillionsMissing (on the 1st), in which I included photos of how my illnesses … Continue reading
#MEAwareness: Guest Post on waking up to severe m.e.
dSavannah note: So, as I said in my January post, I plan to publish a blog post the 15th of every month this year, come hell or high water. Well, I published a post on the 1st of this month … Continue reading
May is #MEAwareness Month • #MillionsMissing
Dear Readers, No, your eyes do not deceive you. I have indeed published my May post on the 1st of the month, instead of the 15th. (Will there also be a blog on the 15th? That remains to be seen, … Continue reading
Just one thing
Once again, I am changing my blog post topic at the last minute (okay, a week before publish date, which as I’ve mentioned, is now “last minute” for me), so you’ll just have to wait longer to read my thoughts … Continue reading
i’m tired
dSavannah note: This post probably isn’t complete. It likely doesn’t make sense. That’s Myalgic Encephalomyelitis (MEcfs) for you. As my friend, who has had ME since he was 3 years old in 1984☆, said: “please help all of us find … Continue reading


