Cleo 🦓♿️💙 @SpoonieTrees

Cat mum 🐾 Nature lover 🌱 Be kind 🥄 I follow back to engage 🫱🏼‍🫲🏽 RTs turned off ♿️ MECFS Fibro hEDS LongCovid MCAS POTS bsky.app/profile/ozgib.… South East, England Joined August 2018

Tweets

10K
Followers

2K
Following

1K
Likes

48K

Nick Reeves #RejoinEU #NAFO #FBPE @nickreeves9876

4 days ago

Here is the Sun's pitifully small apology for its lie about benefits tourism - a lie that was accepted as truth by millions and helped deliver Brexit. These lies are perverting our democracy. At a minimum, apologies should be published in the same location and size as the lie.

107 4K 5K 140K 178

Download Image

Patients with Power @PtsWithPower

4 days ago

#MedicalGaslighting is like taking a cracked mirror to be repaired, and instead being told, “No, the glass is perfect. It’s your self-image that’s distorted.” Instead of looking for medical causes, the doctor flips reality, making the patient doubt their own perception. #NEISvoid

0 4 7 212 0

Download Image

Cleo 🦓♿️💙 @SpoonieTrees

4 days ago

Or blame disabled people. Disabled people don't make your energy more expensive, triple to price of food, or increase mortgage rates. Blame the corruption of those in power and the politicians who enable them.

BladeoftheSun @BladeoftheS

5 days ago

744 2K 10K 191K 170

0 0 1 77 0

Olivia @oliviakarenn1

2 weeks ago

92% of people under 25, and 67% of people in the UK wish to rejoin the EU. RT if you are one.

1K 3K 6K 132K 27

Download Image

elle carnitine 🍉 @elle_carnitine

2 weeks ago

If you have ME, please please please take this survey on how you’d like illness severity to be measured. The research is led by the amazing Leonard Jason redcap.is.depaul.edu/surveys/?s=PY7…

15 102 172 12K 70

Anne Greensmith 💙 @snowleopardess

3 weeks ago

Farage exposing his total ignorance. “Your own GP is pressurised to put people on the disability register”. What register? There is no register. Benefits are awarded by the DWP after a harsh assessment by their own contractors. Your GP has no say in who gets benefits.

ITV News @itvnews

3 weeks ago

739 123 737 1.5M 116

Download Video

251 2K 8K 285K 211

Cleo 🦓♿️💙 @SpoonieTrees

3 weeks ago

Blood test to dx ME/CFS is looking positive and likely. "study found 116 “biomarkers” for ME in the blood of men and women with the condition" #pwME #MECFS #EDS #ChronicPain #ChronicIllness #BrainFog #Disability #Disabled web.archive.org/web/2025062002…

0 0 1 59 0

Sue J @SMpwrgr

3 weeks ago

Sarah Michelle Gellar today on Buffy set She prev had battle w- cvd: “it’s tough…those saying ‘it’s just a cold’...maybe 4 lucky people. But 4 this (relatively) young fit person who struggles w- asthma, it’s not my experience…I’ll 😷 in shower if it means I don’t get it again”

57 1K 7K 150K 588

Download Image

Nele @NeleHelena

4 weeks ago

People with severe chronic pain are experts in distracting themselves from it. Yet there's this idea that we only feel minor things in our body but just focus too much on it.

10 102 597 9K 48

Cleo 🦓♿️💙 @SpoonieTrees

a month ago

#LongCovid #Fibromyalgia #pwME #MECFS #EDS #ChronicPain #ChronicIllness #BrainFog #Disability #Disabled

0 0 2 87 0

Download Image

Y0ur_Neighb0ur @Y0ur_Neighb0ur

a month ago

It’s easy to love someone when they’re shining. The real test is when they’re breaking - when you have to hold them through storms & carry both their weight & yours. That’s love not just felt, but chosen. 💙 #MEcfs #severeME #pwME #Compassion #MentalHealth #UnconditionalLove

11 68 482 9K 13

Download Image

Erin Ekins (she/her) @QueerlyAutistic

a month ago

So much of societal ableism, and the way we culturally treat disabled people, comes from this fantasy abled people have that disability comes from failure and personal choice and they will never be disabled because they've done everything 'right'.

Simon @SimonHayes3196

a month ago

324 0 3 124K 23

15 329 1K 24K 80

Le Bleu Garcon @LeBleuGarcon30

a month ago

One of the wild things about having #MECFS is that I have friends who are well aware of my condition and have seen me degenerate over many years and still have no interest in the disease and don't ever want to hear about it from me

17 35 371 7K 19

Cleo 🦓♿️💙 @SpoonieTrees

2 months ago

Not really Sophie's Choice, is it? 😂

0 0 2 48 0

Download Image

Alethea Bernard @Tush27J

2 months ago

Parliamentary expenses surpass £15.5 million in just 14 MONTHS. Top of the leader board Kemi Badenoch. #BBCBreakfast #GMB #Expenses

520 3K 6K 380K 160

Download Image

The Good Grief Trust @goodgrieftrust

2 months ago

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 teeth; when I waited at the lights on the drive into work and as I heard the rain outside my window. I missed you as I ordered lunch and as I kicked off my shoes…

6 89 569 24K 113

Download Image

Cleo 🦓♿️💙 @SpoonieTrees

2 months ago

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.

0 8 65 966 4

Download Image

Han 🖤 @spoonfulofhan

2 months ago

I wish able bodied people understood that being forced to rest and lay around because of sickness isn't the same as them getting to rest. It's not enjoyable.

107 3K 16K 220K 484

Stef Benstead @StefBenstead

2 months ago

I get that charities can provide emotional support. And some of them give practical support. But I want my expert medical advice to come from my doctor. And I expect the govt to ensure the NHS has enough funding for there to *be* expert doctors in my condition(s).

Department of Health and Social Care @DHSCgovuk

2 months ago

139 34 50 115K 17

Download Image

25 64 219 6K 4

Lucy 🐾 @WildlifeLucy

2 months ago

Me, lying in bed, fantasising about a little note I’d like to send my GP surgery & the NHS’s offensively named “Chronic Fatigue Team” 👇 #pwME #MECFS #MedTwitter