waysandbeing, to philosophy
@waysandbeing@mas.to avatar

🙌🏽🥳 Ahhh, the elation of simply not feeling absolutely terrible!

I dedicate this special moment (passing as it might be 😝) to folks out there also with (1 or 10+ of them 😂) 🤙🏽

You rock, even if / when you don't feel like it! 🤘🏽


@chronicillness @mecfs

ElleGray, to random
@ElleGray@mstdn.social avatar

deleted_by_author

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  • ChrisCPS,
    @ChrisCPS@mstdn.social avatar

    @ElleGray people every day

    Moby_MicroDick, to random French
    @Moby_MicroDick@piaille.fr avatar

    ♿ 🛏️
    C'est jusqu'au 6 avril,
    l'exposition "De la vie au lit",
    à Montréal, mais proposant des modalités de retransmissions web,
    et il s'agit du travail fondamental de l'excellente commissaire française Sarah Heussaff (qui est actuellement publiée dans le dernier Multitudes).

    Je suis profondément heureux de ce travail, il correspond notamment à plein d'échanges entre Sarah et moi, et la continuité de son travail pointu dans les Disability Arts / Arts Handicapés.
    C'est tout un pan de la culture handie & malades chroniques qui est étudiée via nos vies alitées puissantes. Nous existons allongé-es.

    Vive invitation à regarder.
    👉 https://galerie.uqam.ca/expositions/de-la-vie-au-lit/

    Moby_MicroDick,
    @Moby_MicroDick@piaille.fr avatar
    tomkindlon, to mecfs
    @tomkindlon@disabled.social avatar
    MikeImBack, to disabled
    @MikeImBack@disabled.social avatar
    SabiLewSounds, to random
    @SabiLewSounds@mastodon.social avatar

    I just want a fucking taco

    While my brain is overly swollen

    #migraine
    #ChronicPain
    #DisabledCreator

    scrappedbadnik, to transmasc

    I can't bind because of chronic pain, and trans tape isn't holding my tits because it's heavy, I can't do surgery either because it takes more than morphine for me to not suffer, what should I do? I'm lost.

    Desertdragon, to mentalhealth
    @Desertdragon@mastodon.social avatar

    Woke up for the third day with super bad back pain.

    It's making me cranky.

    Plus weird ass dreams.

    So cranky and tired.

    #MentalHealth #ChronicPain #disability

    MikeImBack, to random
    @MikeImBack@disabled.social avatar

    A story about one woman's decent into energy deprived . I can absolutely relate, but for me it's zapping my energy like you wouldn't believe. The best I can get out of life right now, is trying to live a normal life on the internet, as that just requires two thumbs. If I didn't have the internet, I may not even be alive today.

    Please take a second to read this very short article about an invisible life-controlling illness, so that the 'lazy' bias-ness can be killed ⬇️

    tomkindlon, to mecfs
    @tomkindlon@disabled.social avatar

    Mornings can be tough for people who have sleep problems, which are very common in ME/CFS as well as many other chronic illnesses and pain conditions

    @mecfs @longcovid
    @chronicillness
    @spoonies

    janetlogan, to actuallyautistic
    @janetlogan@mas.to avatar

    is really acting up today. pain is much higher than normal too. Thanks to the brain fog, I totally spaced on a group session earlier.

    @spoonies @actuallyautistic

    janetlogan, to spoonies
    @janetlogan@mas.to avatar

    Migraine aura beginning. I've already high dosed Tylenol. I hate headaches.

    @spoonies

    Neferure, to random

    Today is Rare Disease Day. I have a disease that is not particularly rare, but is considered so because it's underdiagnosed, misunderstood and some of the types are extremely rare.

    If there were more funding for research and more training for doctors, perhaps we wouldn't be considered rare any more. 🦓

    #RareDiseaseDay #RareDiseaseDay2024 #EhlersDanlosSyndrome #LeapYear #ShowYourStripes #ChronicIllness #ChronicPain

    Text "Je soutiens journée des maladies rares le 29 Fév 2024 #RareDiseaseDay rarediseaseday.org"

    tomkindlon, to disabled
    @tomkindlon@disabled.social avatar

    Got my postal vote for upcoming referendums in Ireland, so I thought I would remind people of this option for future votes (it's too late for the referendums).

    More Irish info here:
    https://www.citizensinformation.ie/en/government-in-ireland/elections-and-referenda/voting/registering-to-vote/#512d79

    Other countries have their own systems

    @chronicillness
    @spoonies
    @disability
    #Disabled
    #Disability
    #chronicillness
    #chroniclife
    #ChronicPain
    #Spoonielife
    #hiddenillness
    #invisibleillness
    #ChronicIllnesses
    #Spoonies
    #Spoonie
    #ChronicallyIll

    PLOSBiology, to Depression

    (STN) neurons are hyperactive in & ; this study shows that neurons projecting into the STN from the , which integrates pain signals with negative emotions, regulate STN neuron activity https://plos.io/3OOGHZB

    vlrny, to random
    @vlrny@disabled.social avatar

    In what should definitely be an event at the Spoonie Olympics, I just successfully gave myself an IM injection while having mild hand tremors and sketchy fine motor control.

    Announcer: ooooooh! That was shaky, but WHAT A LANDING!

    wild hiss of cheering crowd

    seb_tmg, to Meditation
    @seb_tmg@mastodon.cosmicnation.co avatar

    🦋 Love Your Love Muscle - Pain special

    Feb 26 @ 9pm UTC
    Join our live recording of the podcast "Love Your Love Muscle - Pain Special"! In this episode, we dive into the world of using meditation and self-regulation techniques for pain management. Tune in and learn how to find peace and empowerment through your pain. Don't miss out on this enlightening and transformative episode! - https://go.cosmicnation.co/TMGLive

    #Meditation #PainManagement #ChronicPain #TMGcommunity

    @meditation @consciousliving

    SabiLewSounds, to random
    @SabiLewSounds@mastodon.social avatar

    I'm missing my Dalilah so much this morning

    When I lost her I also lost my mom

    Dalilah was my mom's only companion when I was out working 13-14 hrs a day, a bulk of that was travel on 3-4 buses

    From 2015-2021 Mom only had Dalilah to talk with and she gave her so much joy and warmth

    Mom's not been the same since we had to say goodbye 03.11.22 Mom knew my bun was sick but didn't understand she wasn't going to wake up again that afternoon until it happened...

    Gray bunny laying on her side in front of a wooden box toy on a fluffy lilac blanket eating hay from a lime green plastic bowl in front of a large sliding glass door

    SabiLewSounds,
    @SabiLewSounds@mastodon.social avatar

    My new is warm and sweet but also rebellious - we can't free roam him the way we did with Dalilah

    This makes the days I have been from emotional exhaustion and and fatigue feel so much worse

    My makes these aspects of my physical health worse when I can't keep my family housed and safe and fed

    I can't afford to risk getting hospitalized to push my body and mind beyond their limits because my mother relies on me daily

    My too

    Elderly brown Latina Woman with long black hair sitting on a blue love seat with a medium sized brown bunny She's scolding him gently telling him where he can hang out but not on her table, she lovingly pets his back as he pokes his head up to investigate the area

    SabiLewSounds,
    @SabiLewSounds@mastodon.social avatar

    When I lost her two years ago I felt the weight of those negative beliefs pour onto me all over again, thinking it was my fault for the I've been fighting, being unable to take her to the vet in the early years I had her, thinking it was compounded damage from the years that I struggled to get her needs met because of my and fatigue and

    Even though in her last hours she wanted me at her side, more than food, more than water

    She wanted my my warmth

    image/jpeg

    tomkindlon, to chronicillness
    @tomkindlon@disabled.social avatar
    FiStitchWitch, to random
    @FiStitchWitch@mstdn.social avatar

    Morning folks, not a lot to say today. This low energy/high pain cycle is getting stupid now. Grumble, grumble, you know how this goes.

    Have a fab day folks, be good 😊

    kitwinter, to mecfs
    @kitwinter@dice.camp avatar

    Arthritis, fibromyalgia, and pain flares don't mix. If you can help out, please do! TIA

    https://www.gofundme.com/f/help-fund-a-power-chair

    feefifohannah, to random

    have you considered it might be all in your head?

    (That's a little / or just Being Female-Presenting With a Medical Problem joke for ya)

    tomkindlon, to mecfs
    @tomkindlon@disabled.social avatar

    Stigmatisation in medical encounters for persistent physical symptoms/functional disorders: scoping review and thematic synthesis

    Free fulltext:
    https://www.sciencedirect.com/science/article/pii/S073839912400065X

    "Patients with these conditions have to work hard in consultations to maintain their credibility"

    sebwhatever, to actuallyautistic

    @actuallyautistic

    What are you most proud of yourself today?

    MikeImBack,
    @MikeImBack@disabled.social avatar

    @sebwhatever @actuallyautistic I got out of bed three times by now. It's turning into a typical day, but with added in, a typical day is a glorious day

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