Posts - Myalgic Encephalomyelitis Community | HealthUnlocked

Myalgic Encephalomyelitis Community

2,024 members • 634 posts

All posts for January 2024

Tired Tavern - Discord community for people with CFS/ME and/or Long Covid (PACS)

Hi guys, Tired Tavern is community server for people with CFS/ME and/or Long Covid. It's community where empathy, understanding and shared experiences...

Hi guys, Tired Tavern is community server for people with CFS/ME and/or Long Co...

TiredTavern

•3 months ago

1 Reply

Diagnosing ME/CFS

Just getting round to reading the Winter 2023 edition of the ME Associations magazine and they have a free booklet titled The Importance of an Early & Accurate...

Just getting round to reading the Winter 2023 edition of the ME Associations mag...

PortiaRose123

•3 months ago

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Tired Tavern - Discord server for people with CFS/ME and/or Long Covid (PACS)

Hi guys, Tired Tavern is community server for people with CFS/ME and/or Long Covid. It's community where empathy, understanding and shared experiences...

Hi guys, Tired Tavern is community server for people with CFS/ME and/or Long Co...

TiredTavern

•3 months ago

Be the first to reply

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New and need help

Hi all, I should say I haven’t been given a diagnosis however my GP has suggested that this may be the cause. I had a viral infection two months ago which...

Hi all, I should say I haven’t been given a diagnosis however my GP has suggeste...

Hatwindowwindow4

•4 months ago

16 Replies

A stab in the dark

What triggered your condition ? I’ve just finished my second course of antibiotics following a sinus/ ear infection and feel a bit washed out. I’ve started...

What triggered your condition ? I’ve just finished my second course of antibiot...

BabblingBrooks

•4 months ago

4 Replies

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Posts - Myalgic Encephalomyelitis Community | HealthUnlocked

Myalgic Encephalomyelitis Community

All posts for January 2024

Tired Tavern - Discord community for people with CFS/ME and/or Long Covid (PACS)

Diagnosing ME/CFS

Tired Tavern - Discord server for people with CFS/ME and/or Long Covid (PACS)

New and need help

A stab in the dark

Search posts

Pinned Posts

Latest poll

If ever been seen by UK 'CFS/ME' clinics what was your experience? Tick any that apply. (Will be more polls on this subject in future too!)

Topics

Archive