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Η κοπελα μου πηγε στις διαδηλωσεις για την Παλαιστινη στο Συνταγμα, και γυρισε σπιτι ετσι. Τους την επεσε μια Διμοιρία Δέλτα απο οτι καταλαβα. F the police. Μητσοτακη γμς #gaza #antireport #FreePalestine #Παλαιστίνη #σύνταγμα

What I’ve learned from opening up beyond my anonymous acc. is that strangers often care the most. People I thought forgot about me never did. And those I thought were closest… weren’t. So many are silently suffering, waiting for someone to ask. #MECFS #chronicillness #LongCovid

My right side of face is barely moving. My right eye is droopy and crying on its own. I can’t smile in that side and when I try I’m having spasms. All these 4 years every time a neurologist tested me I told them I don’t feel anything on that side. No help though. #mecfs #pwme

This is SO ACCURATE. I went two years with an undiagnosed hernia because nobody would do a bloody exam or send me for proper imaging.

Grieving myself everyday. Covid-19 destroyed my connective tissue and nervous system. #pwme #mecfs #severeme #longcovid

It may be hard for people to admit that some of us are just genetically predisposed to this shit and others can continue on with their lives as normal. And even if they have lingering issues in years, they have those years. Some of us were young, in our 20s, fucked immediately

Awesome collaboration finds 2 distinct ME/CFS clusters: "Instability & obstructions at the craniocervical junction may contribute to impaired movement & production of CSF, in turn altering MMP or cytokine levels in either cluster." academic.oup.com/jimmunol/advan… #mespine #longcovid 1/

It was never my family and me, together, against my disease. It was family against me, personally. Me being sick was a personal failure on my part, and like a direct attack on them. That’s what it’s like being sick in a dysfunctional family. No love. #chronicillness #cptsd

Two days ago, my dad William “Bill” Cowern passed away somewhat unexpectedly. I flew last minute to Hawaii to be with him and my family for his last days. I feel incredibly lucky to be healthy enough I could finally see him after years of missing him. My dad was joking, and

Ah, the ubiquitous image of well-groomed middle class white lady with hand on head, the misnomer of 'chronic fatigue' when it's ME (Myalgic Encephalomyelitis)...when we've known there's clearly distinct physiological markers but no one wants to spend funding on research.... When

Yeah, breakups are hard, but have you ever been told that you have an incurable illness that will make you suffer for your entire life?

Welp unfortunately I also need help Too I am surviving off your Donations as I only get $480 from winz and they still haven’t reinstated my disability support 3 months on, are intentionally paying me less than the other two girls here for accommodation (50 vs 100)

Y’all, I know people are desperate, I am too, but people have got to stop recommending random drugs-du-jour (especially buying them online/overseas) to people whose medical conditions and histories you do not even know in depth. It’s seriously going to hurt someone one day.

The Medical Misogyny Toolkit: - Pelvic floor therapy - Fibre - CBT - Something about your weight - “Stress” - Anxiety - Ibuprofen - Nortriptyline - SSRI - The pill - Drink water What am I missing?

I’m tired of being punished for wanting to be alive. It’s the least punishable offense in human history. And we face one of the worst punishments for it in human history. #MECFS #LongCovid. .

Tomorrow is my 3 year anniversary and I cannot believe how much time I already lost while the whole world moves on …. I’m in dept, no friends, no future, 24/7 pain and fatigue. I hate my life #mecfs #longcovid #pots #covid gofundme.com/f/unterstutzun…

Me few weeks before, and now 3 years in. COVID SUCKED THE LIFE PUT OF ME. I’m 27 and look like a grandma compared to my healthy body before #mecfs #longcovid #pots. Can’t even take photos anymore and I cannot do anything about it. Happy 3y anniversary

I just can’t accept the fact that my life stopped a random day back in 2021 and all my efforts, studies, dreams collapsed and now I’m living like inside a medieval torture machine every day. #mecfs #pwme #longcovid