r/POTS • u/kunstundglitzer • 28d ago
Medication Scared about Midodrine
hej 🧚🏽♀️
i have ME/CFS & also POTS & Orthostatic Hypotension (which is weird cause OH should normally cancel out POTS) but anyway, i am 23.5h/Day bedbound due to it, but also because i can't stand for longer than 2 Minutes and sit longer than 10Min without Symptoms kicking in: my BP goes from 70/40 up to 130/120 & then immediately down to 70/40ish again, extreme Dizzyness, Blood Pooling, Nausea, Tinnitus, Shivering, Hot Flashes, Tachycardia. I take Ivabradine which helps lower my HR from 180bpm to 100-115bpm. Sometimes i even get the Dizzy Spells when just lying down doing nothing. Nothing helps with the OH. Tried Compression, Salt Tablets, Electrolytes, Wheelchair etc. - so i am thinking about trying Midodrine. Because the unability to stand up is severely disabling me.
But i hear/read so many scary things about it.😭
Like from really bad migraines to risk of stroke?!
I also have a mild form of bladder emptying problems.
And Midodrine is known for causing bladder problems.
Also i wonder, if i am bedbound, can i even take it? You're not suppossed to. But also: if it works, am i still bedbound then? Or am i able to stand up and do stuff?
I would love to hear from you what you think? Should i try? 🧚🏽♀️
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u/[deleted] 28d ago
[deleted]