I’ve asked a few anti-mask, ‘covid is over’ people why they’re so sure the government lied about masks, vaccines, origin etc but can’t consider that the government may ALSO be lying when they say Covid is mild/over/only a threat to the vulnerable.
Today I got an answer. 🧵 /1
I was told - rather harshly - that the difference between right wing and left wing is that right wing people are busy living their lives while left wing are trying to tell others how to live. This is patently absurd - so I pushed back & asked them to take politics out of it. /2
I again asked if you distrust the government so much on ALL other things Covid related - why aren’t you distrustful now that they say it’s over? That we don’t need masks and that it’s become “mild”? /3
There’s new evidence coming out every day about how severe Covid really is & how damaging repeated infections are. The vaccines don’t prevent transmission. The economy suffered when people stayed home so perhaps there’s an economic reason to push the “it’s over” narrative? /4
The response I got at first was a lot more denial and anger. Typical replies such as masks don’t work, lockdowns ruined lives, we’ve got immunity debt etc. That only left wing virtual signallers care about Covid anymore. That we should “trust our immune systems.” /5
I pushed back & explained what we’ve learned about respirators & their effectiveness, that lockdowns were not “true lockdowns” & that immunity debt isn’t real. That people are getting sick more often after repeated Covid infections. That infection doesn’t have to be inevitable /6
They were somewhat accepting of this - but not enough to discuss making any changes. So they said “this doesn’t matter to me I’m young & healthy. Long Covid only impacts the vulnerable.” Cue my building anger & frustration. /7
I explained that there’s no real evidence to support that theory - that MANY people with Long Covid were young and healthy when they became ill. That initial infections can be mild & Long Covid can still debilitate. Their eyes started glazing over - they were tuning out. /8
So instead I tried explaining that many “vulnerabilities” are silent. You can have immune system or vascular damage and have no idea. It’s not like your immune system “hurts”. Oddly this seemed to be what got through to them. /9
They said “are you saying that since I have heart disease in my family I might actually BE vulnerable? I could get Long Covid?”. I said that’s exactly what I’m saying. We are ALL vulnerable and should all be taking precautions. Politics shouldn’t play any role in your health /10
It felt like we were having a lightbulb moment when they asked “how do I protect myself”. I responded with wearing a respirator, reducing indoor gatherings, using HEPA filters & testing regularly. /11
Unfortunately this was met with “that’s way too much work - I’m probably not THAT high risk.” This was a long & relatively engaged discussion that ended exactly where it started. In denial. I pleaded with them to reconsider /12
That’s when politics reared its ugly head again. I was told THIS was the “real” difference between the left & right wing. Left wing (me…apparently) trying to educate & change behaviour and right wing (them) just wanting to live their life. /13
I asked “wouldn’t you rather know these risks now while you can still DO something rather than later when you’re disabled & it’s too late?” Them: “Nope. Ignorance is bliss and I’ve got to live my life.” That was the end of the conversation. /14
It would seem that people are still willingly choosing to remain in denial rather than entertain even the smallest adjustments to their daily life. We’ve become a society incapable of change. Even if that change is necessary for our very survival. /15
We’ve politicized absolutely everything - and lumped people into groups (the left, the right, the vulnerable etc) to justify behaviour that deep down most people know is not justifiable. We know too much about the risks of covid (and its long term damage) to do nothing. /16
If you’re still doing nothing to mitigate spread because you need to “live your life”… you are contributing to the deaths and disability of millions of people. You may be able to ignore this - but some of us can’t. /17
Some of us are choosing to spend what limited energy we have on advocacy because we want to protect others. We believe ALL people deserve protection. It shouldn’t be about politics. It’s about caring for your fellow human beings. /18
You can still “live your life” and take precautions against Covid. We aren’t calling for lockdowns. We are calling for common sense measures. Wear a well fitted mask, open your windows & get a HEPA filter, test before large gatherings and isolate when you’re sick. /19
I know some people will say there’s no point trying to reach someone like this - they’ve made their bed so let them lay in it. I’m still trying because sometimes you DO connect & every heart and mind changed could be a life saved. /20
Also with airborne viruses - it’s not just the person who made the bed that lays in it. We must not forget about the children, elderly & vulnerable people who have no choice but to interact with people for care. They need US to protect them. So I try to reach whoever I can. /21
Covid doesn’t have to win. We’ve learned so much in the last 4 years & with collective effort & a desire to protect one another we could limit its spread. But we must put politics aside. The virus doesn’t care if you’re left or right. We are all people. Let’s work together. /end
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Just when I think things can’t get bleaker for disabled individuals - something happens to lower the bar further. Today it’s the people celebrating the possibility of banning medical masks. Saying we “deserve it” for making them wear masks at the beginning of COVID. 🧵 /1
I’m someone who masked before the pandemic. I’m immune compromised with severe allergies and chemical sensitivies - and masks helped keep me safe & lessen my symptoms. People never cared before the pandemic. Now? They yell, mock & threaten to remove it. /2
In hospitals HCWs would see my mask and intuitively put one on themselves. Now it’s a battle where I have to carefully choose my words to avoid being labelled as “anxious” or “difficult” and have my care compromised. /3
NC are proposing a bill to ban masks (including medical masks) in public settings. This is not only discriminatory - it’s dangerous. It’s removing the LAST tool we have to protect against COVID.
It also sets dangerous precedent & fuels damaging narratives about COVID. 🧵/1
The proposed bill would see all masks banned in public settings. If a person requires a mask - they would need to have a medical exemption. Disabled people are exhausted. We’ve been forced into dangerous situations for 4 years thanks to “you do you” COVID policy. /2
To now expect us to do additional work to procure a medical exemption just to be able to wear a respirator to help us prevent death or further disability? It’s unnecessarily cruel. Doctor’s appts & notes cost money. They’re not accessible to everyone. /3
Like most of us - I’m feeling hurt & betrayed by the knowledge that the WHO quietly upgraded their ventilation & air quality while pushing droplet dogma to the masses. They knew it was airborne & only protected themselves.
A 🧵on science, trust, trauma & how to move forward /1
Let’s face it - we’ve known for a long time that many governments and people in positions of power have been taking more Covid precautions than they publicly admit. They downplayed the risks to the average Joe while using as many layers of protection as possible for themselves /2
The World Economic Forum in Davos was perhaps the best example of this - where attendees had access to PCR tests and state of the art ventilation and filtration to lower their risk of Covid. Clean air for me but not for thee. /3
The pandemic has made accessing healthcare much harder. It’s not just the threat of infection - wait times have increased, staff are burned out & compassion is dwindling.
Recently I needed urgent care and encountered many frustrating hurdles. A 🧵 on accessibility /1
I had a bad fall a few months ago and needed relatively urgent outpatient care. I knew it wouldn’t be easy to arrange … but I was not prepared for how difficult it would be and how much it would exhaust my already sick & tired body. /2
When the injury happened I debated going to the ER - but it did not seem urgent enough to sit in a crowded waiting room risking Covid infection for 12-18 hours. I also have severe POTS and being masked for extended amounts of time impacts my extremely low blood pressure /3
10 years ago I moved across the country for a job opportunity in Calgary. It was a big risk - I didn’t know anyone outside of some folks from this app whom I had never met in person.
I had a medical emergency a few weeks after moving - and one of those people saved my life 🧵/1
His name was Tory and at the time I knew him only by his avatar and handle. But when I landed in Calgary he reached out via DM and offered me help and advice for getting to know my new city. /2
I told him I would take him up on that offer when I was more settled - but truthfully I was a bit leery about meeting a man I didn’t know in real life. So we exchanged messages here & there but did not meet up in person. /3
Toronto - ground zero for SARS1 (where patients are still suffering long term impacts of their infection) and the city in Canada where the sickest patients go…quietly dropped mask mandates in all hospitals. This will kill & disable people and we MUST push back 🧵/1
First off - it’s been a rough few weeks for disabled and chronically ill patients in Canada. We continue to see medically assisted death embraced & expanded, the financial assistance we were promised turned out to be inadequate & inaccessible and no one seems to care. /2
Now we find out that the same hospitals that dealt with the death & destruction of SARS1 have removed their mandatory masking policy. Disabled patients can’t choose to avoid hospitals. Many can’t mask. Mandatory masking kept them safe. /3