Fifty-seven percent of long-term COVID patients develop moderate to severe autonomic imbalance. Some medical conditions can cause autonomic nervous system dysfunction.
Freemont, Michigan-Fifty-seven percent of long-term COVID patients develop moderate to severe autonomic imbalance, according to early data from Stony Brook University and Stanford University. Including POTSAccording to Lauren Styles, President of Autonomic Imbalance International.
Autonomic Imbalance International, 501 (c) (3) Nonprofit Organization, It deals with different forms of autonomic imbalance, a comprehensive term used to describe several different pathologies that cause autonomic nervous system dysfunction. The more common known variations of autonomic imbalance are: POTS-Postural Tachycardia Syndrome, NCS-Neurocardiogenic Syncope, and MSA-Multiple System Atrophy.
Although dysautonomia is not uncommon (70 million people worldwide suffer from dysautonomia), it is not always easy to diagnose. Rachel Miller, primary care manager, said it was usually not a quick response time.
“The average diagnostic period is four years,” Miller said. “But for me, she was a very nice advocate because my mother was on top of it. I was diagnosed in three months.”
She said that some people recovering from COVID may develop POTS. Syndromes can affect the body in a variety of ways, but some of the more prominent symptoms include elevated heart rate, brain fog, malaise, and sometimes fainting.
Miller said you need to keep an eye on your health. Talk to your doctor if your symptoms do not go away after dealing with COVID.
“You know your body. You know what’s normal and what’s not normal for your body, and you have to trust it,” Miller said. ..
She was diagnosed with POTS 15 years ago. Her brother was diagnosed a year later, but he grew up from it, it’s possible.
But Miller has lived with the syndrome for years. Unfortunately, last year her family joined a new club that no one wanted to be a member of and became infected with COVID.
“I got it first, then my mother got it, and then my dad got it,” Miller said. “Unfortunately my mother couldn’t survive it.”
Unfortunately, six weeks after her mother died, she lost both her grandparents to illness.
Rachel knew her POTS diagnosis, so she realized how strongly she was affected by the survival of COVID.
“We are adjusting the drug and going back to physiotherapy and trying to readjust my body from fighting COVID,” Miller said.
However, she said it was a medical problem that should be checked by a doctor for those who continue to have COVID symptoms after fighting the virus.
To help with this growing problem, Dysautonomia International has funded the University of Toledo with $ 100,000 in research to investigate immunity and platelet abnormalities in patients with POTS and long COVID. This study is led by Dr. Blairgrab, an internationally recognized POTS expert. Click here for more information.
Chronic COVID symptoms can be a sign of further illness
Source link Chronic COVID symptoms can be a sign of further illness