Dysautonomia explained

Have you heard about dysautonomia? This condition affects many people who have recovered from COVID-19 and can cause a range of symptoms including fatigue, dizziness, and heart palpitations.
Checkout our full episode on post-Covid Dysautonomia here:
• From COVID-19 to Dysau...
In this episode, you'll hear from those living with dysautonomia and their experiences managing symptoms and seeking medical help.
By listening to these stories, we hope to raise awareness about dysautonomia and inspire more support and research for those affected.
Please these videos with your followers and help spread the word about this important issue. Let's work together to support those living with post-COVID dysautonomia. #DysautonomiaAwareness #PostCOVID #SpreadAwareness
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[@cochiefemeralds3616]

I have had it since early childhood, but I was diagnosed when I was 28 years old and my form of it is called POTS, which stands for postural orthostatic tachycardia syndrome

[@SurvivorDiariesOfficial]

Thanks so much for sharing! I’m sorry you’ve had to go through all of that. We actually did a whole episode on POTS. You can check it out here: Post-Covid POTS | Covid-19 Survivor Diaries Episode 10 kzbin.info/www/bejne/j5LTYZ-tnNtmnqc

[@seratonin7004]

I've just been diagnosed with Dysautonomia, query POTS. I'm trying to get my head around it, but I struggle with brain fog, so short segments like this are helpful.

[@YourNewBestie828]

I've had Dysautonomia my whole life! I'm 27. I only got a diagnosis at 16-17 years old

[@SurvivorDiariesOfficial]

Wow! Any recommendations for others?

[@acrad7187]

This explains a lot!

[@SurvivorDiariesOfficial]

Thanks for watching!

[@marinalessismore4206]

I have dysautonomia since the vaccine, Covid long exists and vax long too. good luck to every body, it is an awfull desease

[@OceanBaby813]

I wanna know if it’s hereditary too

[@happytyphi]

the geneticist said there are 2 form- 1 is genetic and another is caused by severe illness.