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
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Don't forget to follow us and use the #spooniebloggers hashtag to be RT'd
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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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Spoonie Bloggers RT retweeted
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
26 Aug 2019
#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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Spoonie Bloggers RT retweeted
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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Spoonie Bloggers RT retweeted
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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Spoonie Bloggers RT retweeted
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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Spoonie Bloggers RT retweeted
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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Spoonie Bloggers RT retweeted
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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