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#mecfs

56 clips from 26 authors · 8.9M 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 — @rhymeswithdiva5.3M2:21@rhymeswithdivai’ve been slowly working on a faq post for like a month and a half now — @angelfairer1.4M@angelfairerThis is a total game changer! Introducing the all-in-one Rollator and  — @kaya.mieko488.7K2:54@kaya.miekoeducational repost on PEM source: batemanhornecenter #mecfs #myalgicen — @angelfairer371.7K@angelfairerOn today’s episode of “What the Hell?!” we have the BBC validating har — @drjoshuawolrich311K5:05@drjoshuawolrichIt’s been 2 weeks now of being bedbound, but I have GOOD NEWS!! I do t — @faythegay166.5K2:58@faythegayReplying to @Emz #mecfs #chronicillness #invisibledisability — @me_lia88160.2K8:01@me_lia88I challenge you to make it through the entire video before commenting, — @faythegay119.3K6:36@faythegayRecommitting to pacing. Duh. I should know better. I guess I got a lit — @armond.needs.rest71.1K1:29@armond.needs.restWenn Kleinigkeiten anstrengend werden. #mecfs #rettungsdienst #gesundh — @5_sprechwunsch54.4K1:10@5_sprechwunschReplying to @Qv_411 what do i do for my husband? #mecfs #chronicillnes — @angelfairer46.2K1:54@angelfairerPoppy Coburn please never do journalism ever again. [VD - Armond is a  — @armond.needs.rest41.8K2:02@armond.needs.restI've been in a *very* bad flare the last couple weeks but I have felt  — @soullesscreaturesoflight28.7K0:48@soullesscreaturesoflightI’ve had it since I was 14, far before people were speaking a lot onli — @faythegay26K@faythegayThis is probably the most vulnerable thing I’ve shared on the internet — @faythegay24.4K9:59@faythegayWatch for the routine, stay to fight ableism 💗 Curl products: Gel: @No — @faythegay21.8K2:23@faythegayEquanimity and Grace available now on Amazon in my LTree! Coming to bo — @spoonfulofhannah19.3K0:59@spoonfulofhannahI never thought I’d be in this place, you may not think you will be ei — @faythegay19K@faythegay#chronicillness #epilepsy #mecfs #potssyndrome #disability — @spoonfulofhannah19K@spoonfulofhannahBest merch ever??? Tysm @Planned Parenthood !! Ps. Friends, the little — @faythegay17.3K3:43@faythegayMaybe I should film myself more when I’m in a crash? [VD - Armond is a — @armond.needs.rest17.3K1:30@armond.needs.restRolling into this new era of life with @OAS Mobility in their OAS Air  — @faythegay16.8K1:01@faythegayA full breakdown of living with ME/CFS with 10 hours of functional ene — @me_lia8815.9K6:13@me_lia88“I know someone who—“ No, I don’t want some story about someone you cl — @spoonfulofhannah15.9K0:06@spoonfulofhannahHaving different ways of describing, even quantifying pain, disability — @littlemissdiagnosed15.9K1:30@littlemissdiagnosedBeing a spoonie (disabled by chronic illness) breakdown speed edition  — @me_lia8810.5K2:35@me_lia88Only best content for you! I ate multiple things today!! 🫧🫧🫧🫧 Join me  — @faythegay10.4K0:11@faythegayBest papa award 🥹🦋 For those concerned about the butterfly, butterflie — @faythegay10K1:01@faythegayblinds closed kind of day and i was in agonizing pain for multiple hou — @rhymeswithdiva9.9K0:17@rhymeswithdivaalso the concept of 'i don't see it, therefore it doesn't exist' is wi — @bittergirlsclub9.3K1:41@bittergirlsclubPatients with severe Long COVID & Myalgic Encephalomyelitis can’t acce — @erinrackham8.3K2:27@erinrackhama rare fragile moment and an explanation for my absence <3 ty to every — @tullaia8K1:15@tullaiaReplying to @rbkah5202 My pacing tips! 1. Be gentle with yourself 2. g — @armond.needs.rest7.2K2:02@armond.needs.restFor so long, disabled people have been hidden from the world until oth — @spoonfulofhannah7K0:06@spoonfulofhannahI know I’ve been really quiet lately- partly because i’ve been going t — @kaylamae55005.2K1:05@kaylamae5500Replying to @Sophie Kay language surrounding ME categories is specific — @rhymeswithdiva4.4K0:05@rhymeswithdivaFinding joy and motivation in the darkness of severe illness is SO imp — @faythegay4.2K1:15@faythegayI’m grateful and lucky to be in the “post”-trauma from my most severe  — @erinrackham3.9K2:56@erinrackhamBeing able to move enough to post and then spending the majority of th — @me_lia882.7K3:27@me_lia88Things are really hard right now, but that’s real life. If you have to — @faythegay2.4K9:55@faythegayThese conversations do the work necessary to further oppress all of us — @kendrawesomeness2.4K3:54@kendrawesomeness#chronicillness #epilepsy #mecfs #potssyndrome #disability — @spoonfulofhannah2.1K@spoonfulofhannahMyalgic Encephalomyelitis is an insanely damaging, life changing condi — @aspeninmaine1.9K0:45@aspeninmaineI’m genuinely grateful for all the knowledge I now have as a result of — @theendoagenda1.8K0:06@theendoagendaI need to know! I had a really bad reaction to propofol and if I decid — @joellefriend1.6K0:17@joellefriendIt wasn’t until I started a dialogue and uncovered what my subconsciou — @amy_untamed1.6K@amy_untamedLong covid and an immune system that sucks led to pots, mecfs, mcas, a — @askdrmom1.5K1:35@askdrmom#chronicillness #epilepsy #mecfs #potssyndrome #disability — @spoonfulofhannah1.4K0:06@spoonfulofhannahWhat should I name my butterfly? #mecfs #myalgicencephalomyelitis — @faythegay1.4K3:49@faythegayI need to hire a cleaning lady. 😐 I was trying to clean, but my heart  — @joellefriend1.3K0:11@joellefriendAs May is Fibromyalgia and ME/CFS Awareness Month, I wanted to share t — @itsnangemagro1.2K@itsnangemagroMan my body is not enjoying healing a broken bone at all #spoonie #mec — @me_lia881.1K2:40@me_lia88Sometimes the person you’re grieving is you. I’ll always miss the vers — @lilith_unleashed928@lilith_unleashedA conversation we need to have! #disability #disabilitypride #chronici — @ilana_jacqueline7682:23@ilana_jacquelineLDN has quite a few studies behind it touting it as the “wonder drug”  — @catsmeowcrafts6621:34@catsmeowcraftsI know it’s called stand‑up, but I’m chronically ill so I sat down… an — @itsaliceella5162:45@itsaliceella

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