Post

Avatar
Avatar
Avatar
I’ve heard from a number of people on Spiro that their symptoms can be a lot like POTS. Some of the most understanding people I’ve met without POTS have been trans women who had a rough time with spiro.
Avatar
yeah Spiro is def in that space where if it works for you then it’s fine, but if it doesn’t then the side effects can be exhausting.
Avatar
if you need a t-blocker see if you can get your insurance to cover either bicalutamide pills or ideally Lupron (leuprolide) injections. not all insurance covers Lupron, but it is a puberty blocker that you get every 3 months & it suppresses testosterone production.
Avatar
bica has its own issues with potential liver failure, but iirc that’s largely due to it being tested primarily on elderly cis men already dying of cancer. as always, do your own research. i’m on Lupron currently. ❤️🏳️‍⚧️🫡
Avatar
those tests were also how they figured out that bica has the side effect of inducing breast tissue development in patients. growing boobs is not an ideal side effect for elderly cis men, but it definitely is for most trans women lol
Avatar
thank you for the info Sage, I'll bring all of these up when I have my next PP visit (also going to entertain the idea of injections so… 👀)
Avatar
Interesting, I think one of my doctors is very anti-Lupron because of bone density issues (but I might be mis-remembering)
Avatar
I’ve had Lupron recommended to me as a cis woman with endometriosis, but lots of cis women I know who have been on it said it was ROUGH on them. I turned it down. I hope it’s easier on trans women.
Avatar
interesting! i’ll need to look into this further. i’ve personally had good results so far, so fingers crossed🤞☺️
Avatar
I truly don't understand how, but my understanding from reading the packet is that Lupron effectively blocks either testosterone or oestrogen produced by the body and doesn't do the same to exogenous hormones. So I can see how it would be very rough for a cis woman not taking any hrt, but less so-
Avatar
Bicalutamide is cheap enough that insurance coverage doesn't really matter. You just have to convince a doctor to prescribe it.
Avatar
I had no idea that meds I’ve even been on caused this!
Avatar
same, I knew there were some potential side-effects for spiro but didn't realize this was one of them…sucks I can't drop them entirely yet but I'll see if I can reduce my dosage
Avatar
Ugh I’m so sorry this is affecting you! I missed 11:11 or that’d be my wish today to magically have it stop 💜
Avatar
Avatar
(but also diagnosed with POTS a bit later, it just had made it so much worse) bsky.app/profile/cher...
my first experience with that was me saying "yeah, everything feels great!" and my doc replying "you just told me you almost pass out every time you stand up" before taking me off spiro and changing stuff that took another year and a half to balance out levels
bsky.app
Avatar
The only spiro I'm on is bu-spiro-ne, and that seems to be fine in most weather.
Avatar
Oh! Thanks for mentioning!
Avatar
damn, I've been on citalopram for five years and I heard it here first
Avatar
Avatar
Avatar
Avatar
::Me gulping down water ::“Can confirm!”
Avatar
Huh. I’ve been on sertraline for years and never knew this. Thanks!
Avatar
Maybe that is why I was dripping sweat and soaking my shirt through on a 1.5 mile walk. Well, that I have gained weight being on high dose steroids for almost 3+ months. And I'm badly out of shape.
Avatar
Avatar
Avatar
Not sure what all those are but that's why I'm trying to get my apt accessible & safe. Health issues, diabetes one of them, keep me in & I'm 70.
Avatar
Em what? Depression and anti-depressants have been part of my life for a quarter of a century and I have *never* heard this before. Are you sure it’s real and comes from a reputable source?
Avatar
Avatar
Thank you! Down the rabbit hole I went (nearly an hour); Increased sweating may occurs in maybe 1 in 6 anti-depressant users. But its seems that increased risk of heat stroke is assumed based on that and I found no data that anti-depressant users are treated for heat stroke more than anyone else.
Avatar
Being well-informed is hugely important but we also know that there is a lot of scaremongering out there regarding anti-depressants that scares people away from helpful or even life-saving treatments. Let's not make it needlessly worse.
Avatar
I've been on them for a decade. This is the first year I've been cautioned about it by my new psychiatrist as she was prescribing. I also was never told to avoid decongestants due to serotonin syndrome and found that one out the hard way.
Avatar
I don't know a way to ask this that doesn't come across as rude, so please don't take it that way, but, do you have a source for this?
Avatar
It's not rude to ask for a source, don't worry.
Avatar
Avatar
Avatar
Thanks. I see the first article describes SSRIs and TCAs, but not SNRIs, and the Mayo article doesn't say anything about heat sensitivity. Rather, that SNRIs can cause excessive sweating. It's all autonomic dysfunction, and can certainly all cascade in heat, but I'll have to do more reading
Avatar
As someone who has the 'excessive sweating' side-effect of SNRIs - the problem isn't heat stroke, it's the dehydration and electrolyte imbalance. I've given myself what is basically exercise-associated hyponatremia more than once - you need fluids that replace the electrolytes, not just water.
Avatar
Yes, that's what caught my attention originally. I'm on an SNRI, and I live in Phoenix, the home of heat stroke, so I want to understand the mechanics. I'm already on constant lookout for sales of liquid iv!
Avatar
Avatar
So, it’s not just my hot flashes!!!
Avatar
Avatar
Not just overheating and dehydration though; more people are likely to develop sun poisoning from prolonged sun exposure, develop skin blisters, etc. when they get sunburns. Please, if you’re taking these medications, wear sunscreen and drink lots of water!!
Avatar
When I started on ADHD meds (Elvanse) I was on 225mg of venlafaxine as well and I was basically melting constantly it was so grim.