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#chronicillness

60 posts31 participants1 post today

People don’t “get” chronic illness until it happens to them or someone they love.

The same goes for preventative health measures. Folks take unnecessary risks believing they’ll be the exception.

When the worst happens, do they adapt?

Some do. But the parents of a Texas child who died of measles don’t fall into that category.

They lost their child and are still recommending parents don’t vaccinate their children. The reason? The other 4 kids had “mild” cases

This is ghastly.

independent.co.uk/news/world/a

The Independent · Parents of unvaccinated 6-year-old killed by measles in Texas speak out. They still are anti-vaxBy Gustaf Kilander

#medical #ChronicIllness #health

I appreciate my doctor's efforts to help me with my ongoing complex health issues ... but if he tells me one more time to “just hang in there" when I tell him I'm struggling, I swear I'm just going to start breaking things.

It's not normal to be housebound 80% of the time.
It's not normal to need to rest in bed for days after spending just 2 hours 'out in the world doing things.’
It's not normal to have doctors tell you to 'just hang in there' when you say your combined disability is severely affecting the quality of your life and ability to work, study, and participate in society.

Normalize treating complex, disabled patients.
Normalize prioritizing our well-being.
Normalize hearing our self-advocacy.
Normalize advocating for us.

Guidelines about accommodating people with disabilities are being scrubbed from the Justice departments website in an effort to … reduce the cost of groceries.

Once again disabled people are targeted because the government assumes no one will speak up for us.

Speak up. We need you.

Spoiler alert… this will not actually lower the cost of groceries. It will lower the quality of life for people like me though!

theguardian.com/us-news/2025/m

The Guardian · Justice department removes disability guidelines for US businessesBy Lauren Aratani
“You might be a hypochondriac!” 😑
“That isn’t pain, it’s just sensation!” 🙃
“We won’t treat your pain, or we might not know what’s causing it!” 🤡

Medical professionals, I’m begging you, make it make sense.

Luna, like so many of us, has dealt with every variation of medical gaslighting. Doctors dismissing pain, questioning reality, and prescribing a whole lot of nothing—while ordering tests that don’t even make sense. If you’ve ever had a doctor make you question your own body, you are not alone.

💬 Drop the worst medical advice you’ve ever received in the comments.
(Or just scream in solidarity, that’s valid too.) 🫠🫂

#MedicalGaslighting #ChronicIllness #DisabilityAwareness #PainIsReal #ButYouDontLookSick #HealthcareStruggles #MedicalTrauma #HealthCareSystem #TrustPatients #ADayInTheLuna