For all #spoonie bloggers (bloggers with chronic illness, any genre) Follow & include #spooniebloggers for a RT. Run by @whentaniatalks and @chronic_hopeful

Joined July 2015
Spoonie Bloggers RT retweeted
Next in my active user wheelchair series, I'm talking about the different options when it comes to backrest heights! whentaniatalks.com/active-us… #disabledbloggers #spooniebloggers @LovingBlogs @wetweetblogs
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Spoonie Bloggers RT retweeted
Information overkill about #braininjury is daunting. Do I want to know more? It makes me scared & worries me. Is knowledge power or is ignorance bliss? #jumbledbrain #tbi #anxiety #brain #neuroscience #spooniebloggers jumbledbrain.com?p=1478
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The #EffectsOfME Campaign: featuring quotes from people with M.E. For details, visit chronicallyhopeful.com/m-e-a… To see the entire gallery, visit: chronicallyhopeful.com/effec… #pwME #MyalgicE #SevereME #CanYouSeeMEnow #MEcfs #SpoonieBloggers #BloggingBed
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Spoonie Bloggers RT retweeted
#bookbloggers #chronicillnessbloggers #mecfsbloggers Hi I'm looking for lovely #spooniebloggers to help me spread the word about my novel, Little Eden, which is due out in paperback next month. I have #mecfs & so does my fictional heroine, can help me shout out about it?
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Want to know how you can help the #MillionsMissing? I'm sharing loads of great advocacy / fundraising ideas and resources here: chronicallyhopeful.com/how-t… #MyalgicE #ActsOfKindness #Advocacy #SpoonieBloggers #BloggingBed #DisabilityRights #pwME #NHS #caregivers
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A summary of the treatments that have worked best for my sons & I over the years - we now function fairly well & live active lives again. livewithcfs.blogspot.com/p/m… via @livewithmecfs #MEcfs #pwME #ChronicIllness #SpoonieBloggers #MillionsMissing
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Want to help the #MillionsMissing? Quick and easy ways to get involved and show your support. Many of them won't even cost you a penny: lifeofpippa.co.uk/2018/05/01… via @lifeofpippa_ #MyalgicE #pwME #BloggingBed #SpoonieBloggers #Healthcare #ActsOfKindness #ChronicIllness
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This #illness is always with us. Even on our “good” days we have to be cautious & always, thinking: Am I doing too much? Will I pay for this? Is it worth it? When can I rest? Am I pacing enough? notjusttired.com/2018/09/24/… via @Not_Just_Tired #pwME #MillionsMissing #SpoonieBloggers
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Spoonie Bloggers RT retweeted
A new YouTube video has just gone live on my channel! Most of it is about the latest issues with my wheelchair, including a brake not being fitted properly! youtu.be/lPYzz8uAiUw #disabledbloggers #spooniebloggers @UKBlogRT @LovingBlogs
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Looking back can be a very positive experience. There's always something we can learn, even from the most negative circumstances. chronicallyhopeful.com/refle… #pwME #ChronicIllness #Housebound #StayPositive @SpoonieBloggers @FemaleBloggerRT #bloggerstribe
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Spoonie Bloggers RT retweeted
Managed to pull together my notes & ramblings on the DWP/PIP debacle so far w/out turning the air too blue 😉 "surely in doing work that will actually impact people’s lives, wellbeing & finances everyone should pay attention to detail?" #PIP #pwme #rheum singlerheum.com/?p=439
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Chronic Illness Spotlight: Ankylosing Spondylitis featuring Nicole Loffler bit.ly/2TZKvYS #ankylosingspondylitis #Awareness @SpoonieBloggers @BloggingBed
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Get Your Own Personalised #MillionsMissing Poster For ME Awareness Month! Share your story, raise awareness, show others they're not alone. Can be anon. #pwME #MyalgicE #SevereME #CanYouSeeMEnow #SpoonieBloggers #BloggingBed chronicallyhopeful.com/get-y…
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