Managed a post on #MEAwarenessDay.
Must nap now!

Help me escape #abusers & have a chance at life. Dying of abuse/neglect - running out of time.
$250wk negotiable for rent, room, land for caravan/cabin- anywhere safe & accessible. On #DSP can’t afford much. #Community help needed. Can you spare a room? Land? Time? Know someone who can?

Info & help with costs:
(I either write too much or not enough depending on who you ask so further info in fund & Canary article link)

💸Fund: https://www.chuffed.org/project/161937-help-anna-escape
☕️BMaC: https://www.buymeacoffee.com/Halcionandon
🎁AmazonAU: https://www.amazon.com.au/hz/wishlist/ls/1B9A74NSROTQZ
ᯓ➤Beem: Halcionandon
🗞️Article: “Nearly a year on and severe ME patient Anna is still trapped in life-threatening domestic abuse”https://www.thecanary.co/global/world-analysis/2025/04/01/anna-severe-me-cfs/

#mutualaid
#MECFS #PWME #SevereME #MyalgicEncephalomyelitis
#MEAwarenessweek

@mecfs
@mutualaid
@DisabilityJustice
@[email protected]

No fancy post for #MEAwarenessDay

Help me escape #abusers & have a chance at life. Dying of abuse- running out of time.
$250wk negotiable for rent, room, land for caravan/cabin- anywhere safe & accessible. On #DSP can’t afford much. #Community help needed. Info & help with costs:

💸Fund: https://www.chuffed.org/project/161937-help-anna-escape
☕️BMaC: https://www.buymeacoffee.com/Halcionandon
🎁AmazonAU: https://www.amazon.com.au/hz/wishlist/ls/1B9A74NSROTQZ
ᯓ➤Beem: Halcionandon

#mutualaid
#MECFS #PWME #SevereME #MyalgicEncephalomyelitis
#MEAwarenessweek

@mecfs
@mutualaid

A little beauty hidden out of sight in the dark ditch wild area behind the shed at the end of the garden. #MEAwarenessWeek #MEcfsEgress #BloomScrolling DailyNaturePics 20

ME Research UK

For ease of access, we have collated all our symptom postings from ME Awareness Week into one article:
https://www.meresearch.org.uk/what-makes-me-cfs-so-debilitating/

#MEAW2024 #MEAwarenessweek #Myalgicencephalomyelitis #mecfs #MyalgicE
#MEAwareness #PEM #pwME #MECFS #MyalgicEncephalomyelitis

ME Research UK
Beyond core symptoms, people with ME/CFS may experience an array of symptoms e.g. pain, gut issues, and dizziness. Individuals often have comorbidities e.g. POTS, and fibromyalgia.

Read why ME/CFS is NOT a psychosomatic illness: https://www.meresearch.org.uk/research-shows-that-me-cfs-is-a-biological-illness-so-why-do-some-people-still-think-it-is-psychological-in-nature/

#MEAwarenessweek #MECFS
@mecfs

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME

ME Research UK

“People with ME/CFS often report waking up exhausted and feeling as if they haven't slept at all—no matter how long they were actually asleep.” https://bit.ly/4b8cDBq

Read more about sleep in ME/CFS: https://www.meresearch.org.uk/world-sleep-day-2024/

#MEAwareness #MEAwarenessweek #pwME #sleepdysfunction @mecfs
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME

Unrefreshing Sleep May Be the Reason Why You Are Exhausted After Rest

Learn what unrefreshing sleep is, how it's tied to chronic fatigue syndrome, and what treatments are available.

Verywell Health

ME Research UK

Cognitive dysfunction ("brain fog") cannot be equated to occasional forgetfulness and lapses in concentration experienced by healthy individuals, rather it is a complex and distressing symptom.

Read more: https://bit.ly/MEbrainfog2

#MEAwareness #MEAwarenessweek #MECFS #brainfog @mecfs

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME

ME Research UK:
Post-exertional malaise (PEM), the cardinal feature of ME/CFS, is the worsening of symptoms following minimal physical and mental exertion.

Read about the experience of PEM: https://www.meresearch.org.uk/the-experience-of-post-exertional-malaise-part-2/

#MEAwarenessweek #MECFS #Myalgicencephalomyelitis #postexertionalmalaise #PEM @mecfs

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME

Ich habe die Ablehnung des Antrags zur Verbesserung der Lage #MECFS-Betroffener durch die Regierung als Thema für die Lage der Nation vorgeschlagen. Korrigiert oder ergänzt meinen Vorschlag gern.

#LongCovid #MEAwarenessWeek

https://talk.lagedernation.org/t/regierung-lehnt-aus-parteitaktischen-gruenden-antrag-ab-der-versorgung-fuer-nicht-behandelbare-krankheit-me-cfs-long-covid-fordert/20150

Regierung lehnt aus parteitaktischen Gründen Antrag ab, der Versorgung für nicht behandelbare Krankheit (ME/CFS & Long Covid) fordert

ME/CFS und Long COVID ME/CFS (Myalgische Enzephalomyelitis / Chronisches Fatigue Syndrom) ist eine schwere neuroimmunologische Erkrankung, die häufig im Anschluss an Infektionskrankheiten auftritt und mit einem hohen Grad an Behinderung einhergeht. ME/CFS beginnt häufig auch im Anschluss an milde COVID19-Verläufe (Scheibenbogen et al. 2022). Sehr lesenswerte Artikel über katastrophale Lage der Erkrankten: Martin Rücker: Anna und das Biest Martin Rücker: Mit Pfefferminzöl bin ich dein Arz...

Talk der Nation

Our pal (Street Wolves consultant and future Forever King artist) Badgers wanted me to share that it's #MEAwarenessWeek.

Thousands of people suffer from this debilitating chronic illness. Myalgic Encephalomyelitis, also known as Chronic Fatigue Syndrome.

Let's work together to raise awareness and support those who are affected by ME/CFS.

To learn more or to donate check out https://solvecfs.org/

Home - Solve ME/CFS Initiative

Solve M.E. is a non-profit org focused on myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid and other post-infection diseases.

Solve ME/CFS Initiative