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BílýŠťastnýDrak
BílýŠťastnýDrak
@furchur.bsky.social
10 months ago
Chronický únavový syndrom | Blog drAka

Myalgická encefalomyelitida - odborný název pro Syndrom chronické únavy. Často bývá součástí fibromyalgie nebo LongCovid.
#MEAwarenessDay2025 #JustOneWish
Více o ME ⤵️
aukce.wz.cz/blog/single_post.php

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gardenia 🌱 on indefinite hiatus 🌿 pony enthusiast
gardenia 🌱 on indefinite hiatus 🌿 pony enthusiast
@stemmonade.bsky.social
10 months ago

resharing; monday, May 12, was #MEAwarenessDay2025 ! i missed posting about it day of bc of my ME lol, here is a thread talking abt my experience living with ME + a post at the end with info about it as well

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AQEM - Association québécoise de l'encéphalomyélite myalgique
AQEM - Association québécoise de l'encéphalomyélite myalgique
@aqem.bsky.social
11 months ago
Au milieu de l'illustration, il est écrit "12 mai. Journée internationale de sensibilisation à l'EM." Un ruban bleu clair est affiché sur un fond sarcelle avec le logo de l'Association québécoise de l'encéphalomyélite myalgique (AQEM) dans le coin inférieur gauche.

Au milieu de l'illustration, il est écrit "12 mai. Journée internationale de sensibilisation à l'EM." Un ruban bleu clair est affiché sur un fond sarcelle avec le logo de l'Association québécoise de l'encéphalomyélite myalgique (AQEM) dans le coin inférieur gauche.

#JourneeSensibilisationEMSFC #MEAwareness #MEAwarenessDay #MEAwarenessMonth #MECFSAwareness #MECFSAwarenessDay #MECFSAwarenessMonth #MEAwarenessDay2025 #MECFSAwarenessDay2025
#EncephalomyeliteMyalgique #EMSFC #PAEM #MyalgicEncephalomyelitis #MECFS #pwME

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Carrie Anna McGinn
Carrie Anna McGinn
@carriemcginn.bsky.social
11 months ago
Picture of a woman with long dark hair sitting outdoors in a travel electric wheelchair. She has sunglasses on her head and she is wearing a blue long sleeve shirt that says "Still sick, still fighting. There's a caption on the left half of the picture that says, "Half of people with Long COVID develop Myalgic Encephalomyelitis (ME)... including me. Since the pandemic, millions of new people worldwide have developed ME, a complex, chronic, multisystem and disabling illness with no treatments and no cure. We 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 catching unnecessary infections which put you at high risk of joining the #MillionsMissing from their lives due to ME."

Picture of a woman with long dark hair sitting outdoors in a travel electric wheelchair. She has sunglasses on her head and she is wearing a blue long sleeve shirt that says "Still sick, still fighting. There's a caption on the left half of the picture that says, "Half of people with Long COVID develop Myalgic Encephalomyelitis (ME)... including me. Since the pandemic, millions of new people worldwide have developed ME, a complex, chronic, multisystem and disabling illness with no treatments and no cure. We 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 catching unnecessary infections which put you at high risk of joining the #MillionsMissing from their lives due to ME."

#MEAwareness #MEAwarenessDay #MEAwarenessMonth #MECFSAwareness #MECFSAwarenessDay #MECFSAwarenessMonth #MEAwarenessDay2025 #MECFSAwarenessDay2025 #MyalgicEncephalomyelitis #MECFS #pwME

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Physiopedia
Physiopedia
@physio-pedia.com
11 months ago
Post image

🧠  This World ME Day (12 May), learn how rehabilitation professionals can help with pacing strategies instead of harmful exercise.

Explore Physiopedia's resources! #MEAwarenessDay2025 #JustOneWish

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