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A lot of people are having trauma responses, and they don't even know it. Now trauma isn't a free pass to be an asshole, but one of the ways it can manifest is through 'over controlling'. They're scared, trying to push down that fear by attacking everyone around them.


Now, trauma doesn't make you a racist, but being a racist does inflict trauma.
When you're triggered and vulnerable (and being vulnerable feels unsafe), this can lead to fear. In a desperate attempt to avoid that fear, and lack of control, people can try to control everything.

Someone disagrees with you and threatens what you're using to make sense of the universe? You attack, because it feels like an attack on you, and what you think is keeping you safe.

It doesn't mean there aren't things you should be critiquing, or that you can't have discussions, but it does mean you can and should be mindful of how your vulnerabilities are interacting with the ways you are trying to make sense of the world.

The good news is, the Government has funded 20 sessions of Medicare, so hopefully everyone can go to therapy and figure out a way to navigate a world that has changed forever.
All my random ass behavior threads in one place🥲


On power and power


Why we're weird about


Empathy and petty dick gifts


Hypocrisy and
Minister @DrZweliMkhize committs to uploading MAC Vaccine ADVISORIES by end of briefing. Commits to urgency and expediting availability.

#Vaccines
#nocovidmonopolies

#1Country1Plan


Aim for 67% of population. First HCWs, then elderly and those with co-morbidities.

Mainly COVAX. Balance of funds being secured from govt. when 'COVAX delivers'.

Aiming for earlier date than COVAX. Depends on bilat negotiations with phrma. No DRUG Company has CONFIRMED.

Medical schemes being included and through PMBs (amending reg.ns), public-private initiatives being set up. Task Team/s set up for medical schemes and govt and priv sector (BUSA).
I don’t know how to make the world understand what it’s like to live with longterm illness. To wake up each day never knowing if you’ll be ok, to have your dreams and plans constantly disrupted. What it’s like to never feel rested and to always be in pain


I have EDS. 79.5% of people with Ehlers-Danlos have significant fatigue (Anne Krahe, 2017, Systemic Manifestations and Health- Related Quality of Life in Joint Hypermobility Syndrome/Ehlers- Danlos Syndrome-Hypermobility Type)

“Chronic pain has been documented to affect up to 100% of individuals with a diagnosis of JHS/EDS-HT, while 85.7% report experiencing progressively worsening pain.” (Ibid.)

I am just...so sorry for all the people who survive COVID-19 trying to find condition management that doesn’t exist or is unaffordable. I’m so angry at all the hooks and lures set out by shills and charlatans that’ll cause so much iatrogenic harm

I want you to know that you won’t be the same person after you become chronically ill. It changes you and forces you to find new ways to live. Embrace that transition but know it’s ok to grieve for what you’ve lost