Kelly Profile picture
Oct 29 12 tweets 3 min read Read on X
When I was first diagnosed with MCAS I thought “a condition I can control!”

I genuinely believed that since there were clear & obvious triggers - I could put in the work, overhaul my life and be free of attacks.

When a patient plans - mast cells laugh 🧵/1
I threw myself into research trying to learn how to adopt a low histamine diet, clean my air and change my body care and cleaning products.

I (falsely) assumed that if I made enough changes - sacrificed HARD enough - I wouldn’t have to deal with flare ups. /2
It was exhausting. Many of the changes DID help. A low histamine diet, cleaner air, a proper med and supplement schedule and non toxic cleaning products all helped to reduce my overall “bucket” so that my symptoms were less severe. /3
The problem was - I continued having attacks. From minor attacks to full blown anaphylaxis - no matter how much work I put in the attacks didn’t stop.

It was incredibly frustrating - and I began tracking everything I ate, used or did in an effort to find patterns. /4
In the end I realized that sometimes - there are no answers. “Putting in the work” doesn’t guarantee you won’t have attacks.

It’s a help - and we should do whatever we can to minimize our symptoms - but chronic illness (and especially MCAS) doesn’t care about your plans /5
I had to learn to let go. Constantly blaming myself, over analyzing every situation and trying to nail down exact triggers was exhausting me.

It wasn’t helping my physical health and was destroying my mental health /6
At a certain point - we have to accept that chronic illness can be wildly unpredictable - and flares are NOT our fault.

Setbacks happen - and the best thing you can do is give yourself grace and remember that the pain WILL pass. /7
This applies to Covid as well. I see far too many people who are covid cautious being blamed for their infections. Being grilled as to what their exact precautions were as people try and exploit a perceived weakness somewhere.

This isn’t helping. /8
If you’re masking and doing everything you can do to avoid covid - you’re doing a great job. If you got infected anyways - that’s the fault of our institutions and governments who’ve allowed the virus to run rampant and encouraged people NOT to take precautions /9
Just like we have to let go of trying to find every possible trigger for our chronic illness - we have to let go of the blame when people get infected with Covid.

Blame, shame and guilt aren’t helping anyone - and they aren’t good for your health. /10
To be clear - “letting go” doesn’t have to mean giving up. It doesn’t mean you stop trying to improve your health or stop mitigating for COVID.

It simply means you stop fighting the reality that you’re sick. You lean IN to the conditions and try and find ways to accommodate /11
It’s a difficult thing to do. I’m still having to work at it every single day. But it’s worth making the effort.

Society, HCWs and even friends & family can be cruel to those with chronic illness - we don’t need to be cruel to ourselves. /12

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More from @broadwaybabyto

Oct 28
A progressive male “friend” recently told me that he “only wants to date virgins” from now on. He’s 42.

I asked why - since he never cared in the past.

He said that “women are becoming too loose and it’s eroding family values. They should get married & procreate sooner” 🧵/1
I was shocked. This “friend” never even wanted marriage and children. He wasn’t conservative and balked at traditional family values.

Now he’s telling me that women need to get married younger so they don’t have the “chance” to become “loose.” /2
I asked whether he had considered how unlikely he was to find a virgin at his age - and he said he had but that just shows “how far we’ve allowed women to stray.”

That if they’re unmarried in their 40s - they should have the self control to “wait”. /3
Read 23 tweets
Oct 27
The early days of the pandemic were scary for everyone - but for many disabled people there were also rays of hope.

We saw the world become more inclusive seemingly overnight - providing services like telemedicine & remote work - which we had spent years begging for. 🧵/1
I also had hope that we were finally going to make real progress on chronic illness. That Long Covid would be “too big to ignore.”

That we would start being proactive with our health and work towards keeping people healthy and really HELPING those who were chronically ill. /2
I genuinely still can’t believe that 400 million people are suffering from Long Covid. The numbers are growing every day yet we do nothing.

No progress has been made on the comorbids either. I had POTS and MCAS before covid - and my treatments haven’t improved at all /3
Read 4 tweets
Oct 23
Misogyny in medicine is focusing more on what a man might WANT than what a woman NEEDS.

I NEEDED a hysterectomy and was told I wouldn’t survive pregnancy.

“Informed consent” for surgery looked like this:

“Don’t you want to be a Mom?”
“You may want BIOLOGICAL children”
/1 🧵
“What if you meet a man who wants babies?”

“What if he leaves you because you can’t bear his children?”

“Men went their OWN babies - what if you can’t do that?”

“You will feel like less of a woman.”

/2
Brought boyfriend in to try and change their minds. Them to him:

“Will you still love her if she’s BARREN?”

“Do you want kids?”

“What if you change your mind & want kids - will you LEAVE her?”

Him: “Save her life what I want doesn’t matter” (he understood the assignment) /3
Read 12 tweets
Oct 23
Many disabled and chronically ill people find themselves labeled “difficult” or “non compliant” simply because they’re advocating for what they need.

Some examples:

😷 you request staff wear a mask

🧵/1
😷 You decline to remove your mask (ie for oral temperature check that could be performed other ways)

😷 You decline a specific drug and/or treatment because you know it will harm you (example - fluoroquinolones are contradicted for EDS patients and not all doctors know this) /2
😷 You push for additional testing because you feel something has been missed

😷 You request a med be administered different way (eg- a slow drip over 30 min instead of pushed all at once - VERY important if you’re blood pressure is unstable and/or your prone to anaphylaxis) /3
Read 6 tweets
Oct 22
What happened to curiosity in medicine? Did it ever really exist?

A 🧵 contrasting two doctors appointments - one with a doctor willing to work collaboratively, listen and ask questions - the other lacking in curiosity and only interested in doing things “by the book.” /1
The first appt was for a strange infection that wasn’t responding to treatment.

Dr: “Have you been tested for HIV?”

Me: “It was negative.”

Dr: “You sure? Let’s test again.” It comes back negative again.

“That’s weird. Oh well. Best of luck.” /2
That was IT. No follow up. Zero curiosity. No testing to determine WHY I had an infection only seen in AIDS patients when I did not have AIDS. They wouldn’t run an immune panel to take a look at my CD4/ CD8 count. It was just “sorry about your luck but this is not my problem.” /3
Read 10 tweets
Oct 21
I remain stunned by how few men I see speaking out about Gisele Pelicot.

We NEED you to condemn this behaviour. To hold your fellow men responsible.

Too many men participated in these atrocities & what’s galling is of the men who declined … no one sought help /1 🧵
Not one of them went to the police - or even to Gisele herself - to let them know a woman was being repeatedly drugged, raped and assaulted and her HUSBAND was arranging it.
/2
They did nothing. They declined to actively participate and then patted themselves on the back for being “good men” /3
Read 5 tweets

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