Cleo 🦓♿️💙
@SpoonieTrees
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Following
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Cat mum 🐾 Nature lover 🌱 Be kind 🥄 I follow back to engage 🫱🏼🫲🏽 RTs turned off ♿️ MECFS Fibro hEDS LongCovid MCAS POTS
South East, England
Joined August 2018
RT @Y0ur_Neighb0ur: It’s easy to love someone when they’re shining. The real test is when they’re breaking - when you have to hold them thr….
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RT @QueerlyAutistic: So much of societal ableism, and the way we culturally treat disabled people, comes from this fantasy abled people hav….
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RT @LeBleuGarcon30: One of the wild things about having #MECFS is that I have friends who are well aware of my condition and have seen me d….
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RT @Tush27J: Parliamentary expenses surpass £15.5 million in just 14 MONTHS. Top of the leader board Kemi Badenoch. #BBCBreakfast #GMB #Ex….
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RT @goodgrieftrust: I missed you quietly today. So quietly that no one noticed. I missed you as I climbed out of bed and as I brushed my t….
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Omg. Maeve's mum was just on @BBCBreakfast talking and ADVOCATING for those of us with ME/CFS. She says all the right things & I'm bawling. 😭. Watch it on iPlayer catch up from 7.13am.
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RT @spoonfulofhan: I wish able bodied people understood that being forced to rest and lay around because of sickness isn't the same as them….
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RT @StefBenstead: I get that charities can provide emotional support. And some of them give practical support. But I want my expert medical….
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RT @WildlifeLucy: Me, lying in bed, fantasising about a little note I’d like to send my GP surgery & the NHS’s offensively named “Chronic F….
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RT @Emma_h_mua: My UC which I get bc I'm disabled & bedbound most days is about £9k a year. She's claimed over triple what I'm forced to li….
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Keir Starmer voodoo doll .Because you're worth it .💅🏻🩸. #Labour #benefits #TakingThePIP #WelfareNotWarfare.#LabourLiars #giftidea #etsysale.
etsy.com
This Goth & Horror Dolls item by SpoonieTrees has 2 favorites from Etsy shoppers. Ships from United Kingdom. Listed on Jul 28, 2025
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RT @QueerlyAutistic: My favourite thing about this country is that 'you can't take money from millionaires, they might leave' is considered….
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Wow. 18% of doctors with long covid can no longer work. They have also been abandoned by the healthcare system. If they can't get help, what hope is there for the rest of us?! .
bmj.com
Almost one in five doctors (18%) with long covid who responded to a survey said that they were no longer able to work, and fewer than one in three (31%) were working full time, compared with more...
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RT @Beesy1001: @ChasingGlimmers @leicesterliz It disturbs me to see so much bias aimed at pensioners, the sick and disabled. Yet I see noth….
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Read in the news about an ultra rare condition that went from discovery to cure in 12 years due to life expectancy being approx. 40. How can we gain attention about the life expectancy of some ME patients & poor quality of life? It seems our research isn't a priority. 🤔.
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Worth bookmarking this long thread & read it in chunks as it explains PEM within the body. #pwME #MECFS . "More energy spent creating an inflammatory response means less energy for exertion, and *dire* consequences".
Ok, so after that (unintentional) cliffhanger, let's talk about energy production infrastructure and post-exertional malaise (PEM) in people with infection- and exposure-associated chronic illnesses (IACIs) such as #LongCOVID, #MECFS, chronic #Lyme and more. Let's start with 1/.
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Stick some lego in the shoes & I'll stand there and yell "you're too young to need all that help".
EVERY doctor and nurse should have to do this before they can tell me what I should or shouldn't be doing daily
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RT @goodgrieftrust: Tomorrow is the deadline to sign this Petition. Please take a look, as there is currently no legal right to paid berea….
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Yep, there's "my" MP Bayo Alaba. That'll explain why he ignores my emails. I may print this out and staple it to his head if he ever knocks on my door again canvassing for votes.
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