If you’re scrolling, PLEASE leave a dot . it's just a dot . gofund.me/62281c21

La même chose qui se produit tous les ans. Mais on va continuer d'entendre les fabuleux projets de ségrégation, de vacances "inclusives" entre handicapés, sans jamais remettre en question le modèle malgré les drames qui arrivent fréquemment

Je suis en train de mourir. Pas à cause d’une maladie. Mais à cause de l’État français. Je suis une personne handicapée, reconnue par la MDPH. Je détiens une CMI. Je vis légalement en France depuis 2021. Je suis marié à un citoyen français.

When she was just 26 Florence Merriam wrote the first guide to birding with binoculars in 1889. And she slipped in this incredible feminist gem:

of course sexism is connected to health issues in women, but it's almost always because misogyny has trapped women's medicine in the dark ages – not because we're more stressed or self-sacrificing or whatever

mainstream medicine: women's medical problems are mostly psychosomatic alternative medicine: women's medical problems are mostly psychosomatic 🌿

There's a huge myth that a ton of people are faking sickness for some social/financial benefit, but the reality is that most disabled/chronically ill people are actually pretending to be less disabled than they really are because that's what society wants.

Fighting for disability rights has to include fighting for people whose symptoms of their disability may make you uncomfortable. Some disabled people drool, some have tics, some yell, and they deserve rights too. Disability doesn’t have to be pretty.

Apparently, if you’re disabled, you’re supposed to eat gruel, rot in a silent room with no TV or entertainment, never go out (but also not get food delivered), have no life, no comforts, no basic necessities, no rights, and no help. No benefits, no support — just deliberate

Not all doctors are bad but everyone has probably had at least one really terrible experience with one and most chronically ill/disabled people have probably had multiple terrible experiences. Why that matters is it can be really traumatic and dehumanizing and make people

"Mind-body medicine" is the silent epidemic that is leading to mass gaslighting of chronic pain patients. Where there's pain, there's an underlying physiological problem that needs to be addressed. I was told my pain was psychosomatic/functional, when in reality I had

Pain management used to be a trusted profession where patients with lifelong chronic illnesses could find compassionate and worthy care.

Feminists actually talk about this. The unpaid labour that some men do such as helping someone with their car or fixing things around the house are rare, situational jobs. The unpaid work women do (cooking, cleaning, laundry, childcare) is daily, thankless and neverending.

Disabled and chronically ill people are allowed to enjoy things and do things they like (if they’re able) while still being sick and disabled. Yes, even if they aren’t employed. Hope this helps.

Non, le racisme n'est ni une pathologie, ni une maladie, ni assimilable de près ou de loin à la folie. Arrêtez de nourrir ce type de théories dépolitisantes.

Je vis avec une myopathie de Duchenne. Je ne marche plus. Je ne peux plus écrire. Je suis totalement dépendant des autres et j'ai besoin d'une assistance respiratoire la nuit et presque tout le jour... La proposition de loi sur « l’aide à mourir » m'inquiète, elle m'angoisse

Hugo 🧠 Baup Jean-Pierre Farandou Léa Salamé Dire "j’aurais préféré être sourd que d’entendre cette formule odieuse" c’est validiste. Ça véhicule une représentation négative de la surdité comme si c’était horrible d’être sourd mais qu’on "préférerait encore ça" plutôt que d’entendre cette phrase. Et vous niez aussi qu’il a

La salle Zen améliorait déjà un peu l'accessibilité des #Utopiales, mais avec les purificateurs d'air de l' Asso pour la Réduction des Risques Aéroportés (😴), c'est quand même mieux ! Utopiales, à quand un déploiement de ces mesures à l'ensemble du festival ?