TR

#mecfs

72 clips from 30 authors · 9.8M total views. Every clip opens with its own counters and comments.

doing what i can and using the energy i have to beg for awareness befo — @rhymeswithdiva

5.3M2:21@rhymeswithdiva

i’ve been slowly working on a faq post for like a month and a half now — @angelfairer

1.4M@angelfairer

Betroffene sind teilweise arbeitsunfähig, werden pflegebedürftig und k — @5_sprechwunsch

640.5K1:05@5_sprechwunsch

This is a total game changer! Introducing the all-in-one Rollator and — @kaya.mieko

502.4K2:54@kaya.mieko

educational repost on PEM source: batemanhornecenter #mecfs #myalgicen — @angelfairer

371.7K@angelfairer

On today’s episode of “What the Hell?!” we have the BBC validating har — @drjoshuawolrich

311.3K5:05@drjoshuawolrich

It’s been 2 weeks now of being bedbound, but I have GOOD NEWS!! I do t — @faythegay

166.5K2:58@faythegay

Replying to @Emz #mecfs #chronicillness #invisibledisability — @me_lia88

160.2K8:01@me_lia88

I challenge you to make it through the entire video before commenting, — @faythegay

119.3K6:36@faythegay

Recommitting to pacing. Duh. I should know better. I guess I got a lit — @armond.needs.rest

71.1K1:29@armond.needs.rest

Quick Health Update on Dianna (Levi typing) Hey everyone, A few weeks — @thephysicsgirl

57.2K2:17@thephysicsgirl

Wenn Kleinigkeiten anstrengend werden. #mecfs #rettungsdienst #gesundh — @5_sprechwunsch

54.4K1:10@5_sprechwunsch

Replying to @Qv_411 what do i do for my husband? #mecfs #chronicillnes — @angelfairer

46.2K1:54@angelfairer

Poppy Coburn please never do journalism ever again. [VD - Armond is a — @armond.needs.rest

41.8K2:02@armond.needs.rest

I’ve had it since I was 14, far before people were speaking a lot onli — @faythegay

34.9K@faythegay

Sam Schofield passed away on 8/27/26 at 20 years old of Myalgic Enceph — @mind.body.problem

34.7K2:36@mind.body.problem

Watch for the routine, stay to fight ableism 💗 Curl products: Gel: @No — @faythegay

30.8K2:23@faythegay

I refuse to believe that your immediate instinct to see someone vulner — @faythegay

30.1K5:36@faythegay

I've been in a *very* bad flare the last couple weeks but I have felt — @soullesscreaturesoflight

28.7K0:48@soullesscreaturesoflight

This is probably the most vulnerable thing I’ve shared on the internet — @faythegay

24.4K9:59@faythegay

Thank you SO much to @Frankie Ray for traveling from Long Beach to my — @faythegay

21.7K2:37@faythegay

Equanimity and Grace available now on Amazon in my LTree! Coming to bo — @spoonfulofhannah

19.3K0:59@spoonfulofhannah

I never thought I’d be in this place, you may not think you will be ei — @faythegay

#chronicillness #epilepsy #mecfs #potssyndrome #disability — @spoonfulofhannah

19K@spoonfulofhannah

Best papa award 🥹🦋 For those concerned about the butterfly, butterflie — @faythegay

18.2K1:01@faythegay

Maybe I should film myself more when I’m in a crash? [VD - Armond is a — @armond.needs.rest

17.3K1:30@armond.needs.rest

Best merch ever??? Tysm @Planned Parenthood !! Ps. Friends, the little — @faythegay

17.3K3:43@faythegay

Finding joy and motivation in the darkness of severe illness is SO imp — @faythegay

16.8K1:15@faythegay

Rolling into this new era of life with @OAS Mobility in their OAS Air — @faythegay

16.8K1:01@faythegay

A full breakdown of living with ME/CFS with 10 hours of functional ene — @me_lia88

15.9K6:13@me_lia88

Having different ways of describing, even quantifying pain, disability — @littlemissdiagnosed

15.9K1:30@littlemissdiagnosed

“I know someone who—“ No, I don’t want some story about someone you cl — @spoonfulofhannah

15.9K0:06@spoonfulofhannah

New ME/CFS treatment being done in clinics around the country with a F — @autonomicdrama

15.2K1:38@autonomicdrama

2 months ago, my life completely changed. 1 month ago, we had an anniv — @faythegay

13.7K1:22@faythegay

if you want to keep your stem researching fuzzy little man peach and h — @thegoomanstem

11.3K@thegoomanstem

Being a spoonie (disabled by chronic illness) breakdown speed edition — @me_lia88

10.5K2:35@me_lia88

Only best content for you! I ate multiple things today!! 🫧🫧🫧🫧 Join me — @faythegay

10.4K0:11@faythegay

M.E. causes severe sensory sensitivity, so I’m limited in what I’m abl — @faythegay

10.3K@faythegay

blinds closed kind of day and i was in agonizing pain for multiple hou — @rhymeswithdiva

9.9K0:17@rhymeswithdiva

also the concept of 'i don't see it, therefore it doesn't exist' is wi — @bittergirlsclub

9.3K1:41@bittergirlsclub

If there’s one thing M.E. is going to do, it’s nuke you for basic ridi — @faythegay

Patients with severe Long COVID & Myalgic Encephalomyelitis can’t acce — @erinrackham

8.3K2:27@erinrackham

a rare fragile moment and an explanation for my absence <3 ty to every — @tullaia

Replying to @rbkah5202 My pacing tips! 1. Be gentle with yourself 2. g — @armond.needs.rest

7.2K2:02@armond.needs.rest

For so long, disabled people have been hidden from the world until oth — @spoonfulofhannah

7K0:06@spoonfulofhannah

I know I’ve been really quiet lately- partly because i’ve been going t — @kaylamae5500

5.2K1:05@kaylamae5500

Replying to @Sophie Kay language surrounding ME categories is specific — @rhymeswithdiva

4.4K0:05@rhymeswithdiva

Attn: ME/CFS Researchers, an open letter. ME/CFS is a very real physio — @autonomicdrama

4.1K6:37@autonomicdrama

I’m grateful and lucky to be in the “post”-trauma from my most severe — @erinrackham

3.9K2:56@erinrackham

ME/CFS is not a deadly condition according to ME advocacy groups.howev — @autonomicdrama

3.4K3:24@autonomicdrama

How can someone who might seem smart and quick-witted online have seve — @horriblemeanbadwoman

2.8K2:58@horriblemeanbadwoman

Being able to move enough to post and then spending the majority of th — @me_lia88

2.7K3:27@me_lia88

Things are really hard right now, but that’s real life. If you have to — @faythegay

2.4K9:55@faythegay

These conversations do the work necessary to further oppress all of us — @kendrawesomeness

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#chronicillness #epilepsy #mecfs #potssyndrome #disability — @spoonfulofhannah

2.1K@spoonfulofhannah

Myalgic Encephalomyelitis is an insanely damaging, life changing condi — @aspeninmaine

1.9K0:45@aspeninmaine

Pitching my new reality TV show idea ♿ Maybe the participants have to — @horriblemeanbadwoman

1.8K1:50@horriblemeanbadwoman

I’m genuinely grateful for all the knowledge I now have as a result of — @theendoagenda

1.8K0:06@theendoagenda

I need to know! I had a really bad reaction to propofol and if I decid — @joellefriend

1.6K0:17@joellefriend

It wasn’t until I started a dialogue and uncovered what my subconsciou — @amy_untamed

1.6K@amy_untamed