She’s right. The school is wrong. It’s 2024 and we now know: 1) Covid is airborne 2) HEPAs lower transmission in schools 3) Covid harms children 4) a Covid infection can have long lasting effects on a child 5) 2 infections are worse than 1, 3 infections are worse than 2 ect

Εύχομαι σύντομα και στα δικά μας. Για κάθε κοινωνιοπαθές δίποδο που εγκλωβισμένο στη φούσκα του θεωρεί ότι ο κόσμος γυρίζει γύρω του. 4 μήνες είναι τίποτα για κάποιον που εχασε τη ζωή του, είναι μια αρχή. Να δω πόσοι θα συνεχίσουν να απαντάνε “φόρα μάσκα και στον ύπνο σου”.

From my perspective I don’t see the point in surviving day to day for decades dealing with such a horrific chronic illness. I’ve loss 2 years of my life, there is nothing positive to gain from this level of suffering. There is no reward at the end. Just pain and lost memories

It will be 3 years for me this December. I've lost my best years and I continue to lose them EVERYDAY living in this abusive household. I don't know how we can keep on going. #pwme #mecfs #longcovid

“I wish someone would talk more about the multitude of risk factors that cause one to be less impacted by Covid.” W H E R E. H A V E. Y O U. B E E N ? Plenty of people have talked about and studied the long-term effects of COVID-19. Years of research show that regardless of a

The suffering of #MECFS patients over the past decades could fill hell itself. And yet, we are still fighting for recognition and treatment. It’s incomprehensible and leaves me speechless every single day.

my childhood trauma didn’t make me stronger. it made me a people pleaser. it made me forgive way too much. it made me not speak when i’m supposed to. it made me an extreme empath.

Whatever happens to me (I know I won't make it) I just want to thank every single person who donated or keeps donating, has messaged me trying to show support even from far away. Thank you for being my 1% of hope. 🤍 #pwme #mecfs #longcovid

Please I need advice on how to talk to a psychiatrist with NO education about long covid or me/cfs to make them understand what in going through and help me with my abusive family situation. I can't think of any other way to get some help. #pwme #severeme #mecfs #longcovid

θα ήταν ωραία να ζούσα σε μια χώρα που δεν θα ήμουν αόρατη και η ζωή μου θα είχε αξία ✌️

My daughter Isla died in May, she had Severe ME. She was left to rot and die at home with no support from the NHS. She only received one home visit from her GP in her years of illness. Things have to change. #ThereForME #pwME #wesstreeting #severeME

received messages at shelters, edhi, & burney. All these people have been contacted by me, friends & psychologist from 2017 to 2023. Shelters don't want to be liable for disabled patients, organisations don't cater to our disabilities. Similar situation katiana is missing ❤️‍🩹🦠 #pwme #pmdd 1/

I talked to a national greek sos line for abuse yesterday. They told me "this is not abuse and we are not a line for disabled people". Being neglected and exposed to triggers that worsen you is not abuse I guess. #pwme #longcovidgreece #mecfs #longcovid

Well maybe some of those People Who Told You That Covid Isn’t A Problem are actually responsible for the permanent damage and/or death of other People Who TOLD You That Covid IS A Problem and acted as such but it didn't work out for them but hey we're all gonna die someday anyway

I don’t know how long I have left. Slowly being killed by #MyalgicEncephalomyelitis & neglect from medical, government, & family actively killing me. Need to rest. I can’t. It will kill me, if another Covid infection or any infection doesn’t. Govt offer counselling not help:

One of the hardest things to come to terms with in discovering that one’s partner is a narcissist/psychopath, is that you were not loved by them. That is gut-wrenchingly painful💔. They don’t have the capacity to love because of prefrontal cortex & amygdala brain anomalies.

#SevereME is a haunting. It is a horrifying presence that never leaves you, not at night or during the day. It torments you. Until many vanish. First, their personalities. Then, quite often - too often - their lives. #MECFS

If your joints including the neck snaps/pops/clicks/cracks/crackles, You have EHLERS DANLOS SYNDROME. You were made of the wrong material genetically. These patients are prone to Pots/ME/Fibro/Dysautonomia after a strong viral or vaccine trigger. #LongCovid #pwME #Pots #EDS