Carrie Anna McGinn
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carriemcginn.bsky.social
Carrie Anna McGinn
@carriemcginn.bsky.social
Infection-associated chronic illness advocate | Life sidelined by #LongCovid #MECFS #POTS | #PatientPartner | MSc | Mom | She/Her | 🇨🇦 #Canada #Quebec

#CovidConscious #StillMasking
#MyalgicEncephalomyelitis #pwME #EMSFC
#CovidLongue #CovidLong #pwLC
🆘 Save Our Support Systems 👫
🆘 Save Our Science 🔬
🆘 Save Our Society 🌍

I am in solidarity with meactnet.bluesky.social protestors in DC & #pwME at home for #MillionsMissing 2025.

There are #NoTreatmentsNoCures for #MyalgicEncephalomyelitis & #LongCovid.

#DisabilitySOS #MECFS #MECFSAwarenessDay
May 13, 2025 at 1:54 AM
People with #MECFS need better clinical care and high-quality research to find treatments and cures and to get back to our full lives we miss so much.

Please mask up to avoid infections which put you at high risk of joining the #MillionsMissing from their lives due to ME.

2/
May 12, 2025 at 6:37 AM
May 12th is International #MEAwarenessDay.

Half of people with Long COVID develop #MyalgicEncephalomyelitis (ME)... including me.

Since the pandemic, millions of new people worldwide have developed #MECFS, a complex, chronic, multisystem and disabling illness with no treatments and no cure.

1/
May 12, 2025 at 6:37 AM