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The problem with this is how many doctors write off as anxiety. I had to see 4 doctors before one would take me seriously and its so upseting because not everyone has just has magic funds to blow on doctors who refuse to even listen before finding one that does.

I've had three dr. try to put my daughter who has pots on birth control 😢 Apparently if your in childbearing years, birth control is the dr. answer for EVERYTHING! 😮😡

Thanks. By the way, I find you beautiful 🤩 ☺️

You conveyed it well. It’s like a 🧩

I have had vovid and then i had all the symptoms in this video

I have to disagree personally i find silence causes my anxiety and depression to become worse. I listen to audio bks. Always

i can't do cardio at all but can do limited weight exercise and i always wonder why thank you

I've never been diagnosed but I'm certain I have pots. I too get lightheaded especially in the morning hours, and have occasionally passed out. Think I need to pursue a diagnosis for the explanation of why I feel so very depleted at times.

I have POTS Diagnosed 2 years ago.. now in last 6 months i have been facing reactive hypoglycemia as well. Is it POTS which is triggerring Reactive hypoglycemia? Or otherway ?

Fairly sure I developed pots after mono but chemo made it 100x worse due to the nerve damage I sustained. At least I'm here though. 👍

My worst hypoglycemia happens around 5am. Is this reactive hypoglycemia? It also happens throughout the day, but gets worse the longer I go between meals.

I’m guessing this may be what I have. Ever since I got sick my life hasn’t been the same. Now I’m constantly dizzy when I stand and my heart rate goes from 80 to 130 in seconds it’s crazy. How do I deal with this? It’s ruining my life.

Shower time is hell especially on the days. I have to wash my hair and shave my legs.

I have the surges and then tremor! It’s awful

This seems to answer a couple questions I have 😮 Thank you! I need to talk to my doctor now 😊

Hi there, I keep trying to download your masterclass and it never sends anything to my email. How do I get this sent over? Thank you so much!

I’m also type 1 diabetic! Would love to connect.

This is so me😢

Check all… since covid infection in 2022. Doctor said it’s psychosomatic. Yeah right tell that to the millions of people suffering.

POTS is heterogeneous and viral infections are known cause of Dysautonomia. Great work spreading the word!

Thank you for smart reminders!

Sad but true

I figured this out the hard way because I was constantly eating junk food because I always felt like I was starving so over the years I’ve gained about 30 pounds but now I’m trying to eat better.

My period ❤️

Hi loana. I guess any good electrolyte drink is ok? I've used Recuperol + previously. I'd appreciate your thoughts. Cheers

Uhmm… guysss

I feel lightheaded when I get up fast, but I’ve never fainted, is that just normal?? Or is it just a really mild version of

if your dr blames it on anxiety go see another dr

I just experience POTS symptoms for several months and I'm now in remission but so worried to experience again and I got after a EBV infection and I was 45 years old.

How do people get diagnosised i have almost every symptom ???????????????

This was really helpful thanks!!!

I have the neurological symptoms and some of the cardiac ones. Inside I feel like I’m dying most days and look perfectly fine on the outside. 3years this October. I’ve come along way though!! 🙏🏼

if a dr says it's anxiety, which most do, go to another dr. don't stop till you get answers!

I had the pots Syndrome since I was 17 years of age and have been treated like an hypochondriac all my life, I almost taught of giving up, they my friend from Africa recommended me to a Nigeria herbal doctor on RUclips, who help me solved my problems with adding to it, he was one amazing soul I ever came across during the treatment process I will say he was my therapist. GOD bless #drobaedo on RUclips. ❤❤

Beta Blockers do not work if you have a normal BP the side effects will make your qualtiy of life much worse. The fatigue gets worse and constantly trying to stablize your BP was not worth it.

I have been on midodrine and ivabradine for 3 years. It has really helped my pots symptoms, but I don't want to be on them forever. I'm currently coming off. It's not easy - headaches, insomnia, digestive troubles and random pains. Hoping it will ease soon 🙏

I'm a man and I got pots after COVID, the second time I got COVID I developed orthostatic hypotension. However made those viruses can kiss me where I crap. This has been linked to COVID. There are a few other men I know that got pots after COVID.

I have orthostatic intolerance & dysautonomia of the sympathetic NS

I have recently got pots and just want a few tips on how to controll my pots while in school, when I play tennis, and how to explain to my teachers what is happening.

This is so great, thank for sharing!

This is great, thanks for making this. I have pots and I've come to realize me repressing trauma and repressing my emotions has caused my pots.

My son, me, my sister & my nephew all got covid back in 2020. Ever since we all have cardiac issues. My sister & nephew were diagnosed with Pots Then i was diagnosed with tachycardia with possible afib off of a ekg. They havent done a tilt test on me and now my son is experiencing same symptoms as me. I think we have pots too

I’ve had pots my whole life

I'm not sure why 🤷

Honestly try gaba theanine. {Act as beta blockers.} and iron pills and just doing your research. You can run the tests at home. I would only foot the bill if your symptoms are chronic and completely disabling.

Where is the link that she mentioned ? The one with the 3 day video on healthful eating for POTS.

Is there any more symptoms? I think I may have this. I feel lightheaded and have feel general weakness and have problems walking.

I have POTS. When I stand my heart goes from 90 to 170 and even two hundred bps😅

Thank you for this but don’t mean to be rude you are very fast talker you should be a little slower for people like us that English is second language ❤

So for most with pots it's a low carb high salt high electrolyte diet.