COVID-19 gave me POTS disorder — here’s what the illness is like

COVID-19 gave me POTS disorder — here’s what the illness is like

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4 years after COVID-19 was declared a world pandemic, Yahoo Canada spoke with a number of folks nonetheless living with long COVID. Learn their tales HERE.

This text is for informational functions solely and isn’t an alternative choice to skilled medical recommendation, prognosis or therapy. Contact a professional medical skilled earlier than participating in any bodily exercise, or making any adjustments to your weight loss program, treatment or life-style.

Julia Ranney was diagnosed with POTS, a debilitating condition, after her COVID-19 infection earlier in 2023. (Photo courtesy of writer)Julia Ranney was diagnosed with POTS, a debilitating condition, after her COVID-19 infection earlier in 2023. (Photo courtesy of writer)

Julia Ranney was recognized with POTS, a debilitating situation, after her COVID-19 an infection earlier in 2023 result in lengthy COVID. (Picture courtesy of author)

When most individuals hear the phrase “POTS,” they may take into consideration what they’ll cook dinner for dinner. However I affiliate the phrase with trauma, anxiety and a medical situation I battle every day.

It began when I contracted COVID-19 in early 2023. Whereas nearly all of COVID sufferers resolve their signs in a matter of weeks, mine acquired worse over time. I knew one thing was fallacious when in the future I virtually blacked out within the bathe. I felt dizzy, nauseous and my toes turned a deep purple in color.

After a slew of docs, cardiologists and rheumatologists, I used to be instructed I had POTS.

It has been practically 4 years since March 11, 2020, when the World Health Organization declared a global pandemic. In response to Well being Canada, lengthy COVID also referred to as post-COVID-19, impacts everybody in a different way and there have been reviews of over 100 signs. Many, like myself, have been recognized with new sicknesses as a consequence.

However what’s POTS, and the way does it have an effect on my life? This is every little thing you’ll want to know.

POTS, or postural orthostatic tachycardia syndrome, is a condition that causes a variety of symptoms when transitioning from lying down to standing up, including dizziness, fatigue and rapid heart rate. (Photo via Getty Images)POTS, or postural orthostatic tachycardia syndrome, is a condition that causes a variety of symptoms when transitioning from lying down to standing up, including dizziness, fatigue and rapid heart rate. (Photo via Getty Images)

POTS, or postural orthostatic tachycardia syndrome, is a situation that causes quite a lot of signs when transitioning from mendacity right down to standing up, together with dizziness, fatigue and speedy coronary heart fee. (Picture through Getty Photos)

What’s POTS?

POTS, or postural orthostatic tachycardia syndrome, is a situation that causes quite a lot of signs when transitioning from mendacity right down to standing up, resembling dizziness, fatigue and speedy coronary heart fee.

Usually, your physique’s autonomic nervous system balances your blood strain and coronary heart fee to maintain your blood flowing correctly all through your physique, it doesn’t matter what place you are in.

However you probably have POTS, your physique doesn’t routinely stability your blood vessels and coronary heart fee. Consequently, blood strain and coronary heart fee can dramatically change.

“I knew one thing was actually fallacious when in the future I virtually blacked out within the bathe. I felt dizzy, nauseous and my toes turned deep purple.”Julia Ranney

Since blood will not be being correctly pumped to your mind, it might additionally pool in your legs, causing your feet and legs to change colour.

You will get POTS after getting an an infection, situation or illness like COVID, diabetes, Lupus or Lyme. It may additionally develop after contracting the rest that assaults your autonomic nervous system.

A rapid increase in heart rate when transitioning from lying down to standing up is a key indicator of POTS. (Photo via Getty Images).A rapid increase in heart rate when transitioning from lying down to standing up is a key indicator of POTS. (Photo via Getty Images).

A speedy improve in coronary heart fee when transitioning from mendacity right down to standing up is a key indicator of POTS. (Picture through Getty Photos).


My prognosis amid lengthy COVID

Aside from practically blacking out whereas showering, my first main signs of POTS have been excessive fatigue and lightheadedness. I used to be basically couch-ridden, and each time I attempted to face up, I might get a head rush and the room would spin.

Fundamental duties like cooking or making my mattress grew to become a problem, and my mental health grew to become severely affected. My physician instructed me my signs have been simply anxiousness, however I knew it was one thing extra.

As a determined try to hunt assist, I joined Cornerstone Physiotherapy’s online Long COVID clinic, which additionally makes a speciality of POTS within the Higher Toronto Space.

“When transitioning from mendacity right down to standing up, my coronary heart fee would improve by not less than 50 beats per minute. For context, the typical particular person’s coronary heart fee ought to improve by solely 10-15 beats.”Julia Ranney

My specialist suspected I had POTS because of my predominant signs. To verify, he had me take a look at my coronary heart fee whereas mendacity down after which standing up with my Apple Watch.

When transitioning from mendacity right down to standing up, my coronary heart fee would improve by not less than 50 beats per minute. For context, the typical particular person’s coronary heart fee ought to improve by solely 10-15 beats. To qualify for POTS, your coronary heart fee has to extend by not less than 30 beats per minute when transitioning from mendacity right down to standing up.

I used to be despatched to a rheumatologist to test my autoimmune system, after which a heart specialist to look at my coronary heart. From these appointments, it was clear that I had COVID-induced POTS.

A recent international survey indicated that roughly 67 per cent of COVID long-haulers have some type of nervous system dysfunction post-infection, and 30 per cent qualify for POTS.

Approximately 67 per cent of COVID long-haulers have some form of nervous system dysfunction post-infection, and 30 per cent qualify for POTS. (Photo via Getty Images)Approximately 67 per cent of COVID long-haulers have some form of nervous system dysfunction post-infection, and 30 per cent qualify for POTS. (Photo via Getty Images)

Roughly 67 per cent of COVID long-haulers have some type of nervous system dysfunction post-infection, and 30 per cent qualify for POTS. (Picture through Getty Photos)


How does POTS have an effect on my life?

Every case of POTS is completely different, however for me, on a regular basis life now requires group and planning.

Resulting from my fatigue and signs, alongside my therapy plan, I am solely allowed to burn a certain quantity of energy per day, and I can’t stand for lengthy intervals of time.

Contemplating this, I can not make tea, do my hair and make-up or eat breakfast all whereas standing up within the morning. I both have to sit down right down to do these duties, or take breaks in between. If I’ve a social occasion to go to, I’ve to relaxation the day earlier than, the hours earlier than the occasion and all the day after.

At the moment second, I’ve to lie down for not less than quarter-hour each hour, eat not less than 5,000mg of salt per day to maintain my blood strain up, drink virtually three litres of fluids per day to extend blood quantity and put on compression pants to stop blood pooling.

“I am greater than my situation. I am greater than my well being. And I will not let POTS take over my life.”Julia Ranney

Warmth can even set off my dizziness, so I’ve spent a lot of the summer season inside. That is extraordinarily irritating when all of my family and friends are out having fun with the solar and collaborating in enjoyable actions with out me.

However regardless of my heartbreak, I am attempting to stay hopeful. Many individuals with POTS can see signs come and go over time. I’ve an amazing medical workforce behind me, and changes in weight loss program, bodily exercise and drugs can enhance my high quality of life.

Most significantly, my help system, together with household, pals and colleagues, helps carry me up on down days and jogs my memory that I am greater than my situation. I am greater than my well being. And I will not let POTS take over my life.

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