My father is threatening me because I talk about the abuse I get on the Internet. I'm really afraid. He threatens to sue and harm people who care about me, believe me and want to help me. I don't have anyone. I'm all alone. Please help.

#severeme #longcovid #mecfs

Lying flat, doing absolutely nothing. With a HR of 215. However, Alice has been awake for OVER 140hrs, could this be making it worse? 🤪😭 #VerySevereME #PoTS #vasculardysfunction #pwME #NEISvoid #insomniac #tachycardia #hEDS #severeME

1) Having #severeME and being homebound often feels like a prison. You're locked up in your home and your body, away from society, your loved ones, from the life you desperately yearn to live.

Most years, I see maybe one or two people, and many years I

youtu.be/yLRateIQdzc?si…

This is my 1st year of #MECFS vs now, nearly 3 years later with very severe ME. It doesn't matter how healthy you were, once you get #severeME your life as you know it is over. I'm bedridden and unable to speak at 25. WE NEED TREATMENTS NOW #WorldMEDay #MEAwarenessDay

#InternationalMEawarenessDay #severeME

#pwME
#MyalgicEncephalomyelitis
#MEAwarenessDay
#MillionsMissing
#SevereME

Gastrointestinal symptoms are common in people with #ME , whether the disease is mild, moderate, or severe.
#ME AwarenessDay
#EndMalnutritioninME
#SevereME

#MEcfs #MyalgicE #MyalgicE ncephalomyelitis #pwme #severeME #verysevereME #MedicalScandal #MedicalCorruption #MedicalNeglect #MedicalAbuse #iatrogenesis #DisabilityDenial #Gaslighting #ScienceNotStigma #PsychAbuse #PsychologisingIllness #ExposeMEnow #DontletMEdie #MillionsMissing

A patient with #severeME uses hand signals on her mattress to communicate with her carers.

For many with Long COVID and ME, this is what life looks like.

#MedTwitter you don't see these patients because they can't come to your clinic.

#UniteToFight2024

#WorldMEDay
#ExposeMENow
#MyalgicEncephalomyelitis
#MEAwarenessDay
#VerySevereME
#BringMillieHome
#SaveCarlasLife
#SevereME
#MillionsMissing
#DontLetMEDie

#LearnAboutME
#severeME

Update about Millie

Petition
change.org/p/save-millie-…

#MillieSevereME #SevereME #pwME #saveMillie #BringMillieHome #DontLetMEDie #ExposeMENow

Help me. This is me everyday not only #MEAwarenessDay . I need a safe place to stay. Where I don’t have to fight for basic needs like food from the people supposed to care for me. I have nowhere to go. Help me please. 🙏

#SevereME #May12
#pwME #MECFS #PWLC #LongCovid

#MEAwarenessDay #WorldMEDay #ExposeMENow #VerySevereME #SevereME #MyalgicEncephalomyelitis #SaveCarlasLife #BringMillieHome #CareForKaren

#MEAwarenessDay #WorldMEDay #ExposeMENow #VerySevereME #SevereME #MyalgicEncephalomyelitis #SaveCarlasLife #BringMillieHome #CareForKaren

We're severely chronically ill in a way society doesn't know and doesn't believe exists. That's scary.

#severeME #severePOTS etc

I can’t remember ever seeing much about a difficulty with swallowing in the symptom lists of #MyalgicEncephalomyelitis but it is a symptom that many people with #ME especially #SevereME experience.

#ME AwarenessDay
#WorldMEDay
#MillionsMissing

I don’t really have any words other than that you should really watch this.

It shows the reality of #SevereME . The prison of ME. When will the prison sentence end?

Teared up at the bit where Anil was able to witness the seasons changing again.

#MEAwarenessDay #MEAwarenesss

#WorldMEDay
#ExposeMENow
#MEAwarenessDay
#MyalgicEncephalomyelitis
#MillionsMissing
#SevereME
#VerySevereME
#DontLetMEDie

ME symptoms can lead to nutritional problems, particularly in #SevereME .
#MEAwarenessWeek #EndMalnutritioninME