# What celebrities have been diagnosed with POTS syndrome?

Paige Thornton · August 4, 2026

> Postural Orthostatic Tachycardia Syndrome (POTS) is part of a larger category of disorders known as dysautonomia, which affects the autonomic nervous...

Postural Orthostatic Tachycardia Syndrome (POTS) is part of a larger category of disorders known as dysautonomia, which affects the autonomic nervous system responsible for regulating involuntary bodily functions such as heart rate and blood pressure.

Symptoms of POTS can include dizziness, fainting, heart palpitations, and fatigue upon standing, which can significantly impact daily life and activities for those affected.

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POTS predominantly affects young women, with studies indicating that approximately 80% of diagnosed individuals are female, often between the ages of 12 and 50.

The exact cause of POTS remains unclear, but it is believed to be related to various factors, including blood volume abnormalities, neuropathic issues, and hyperadrenergic states, where the body has an increased level of norepinephrine.

Olympic swimmer Katie Ledecky has publicly shared her struggles with POTS, illustrating that even elite athletes can be affected by this condition, which challenges the stereotype that chronic illnesses are only faced by non-athletic individuals.

Celebrities such as Tori Moore, a former volleyball player, and Bethenny Frankel, a television personality, have also been open about their experiences with POTS, contributing to greater awareness of the syndrome.

Bella Hadid, a well-known model, has discussed her diagnosis of POTS alongside Ehlers-Danlos Syndrome (EDS), highlighting the overlap between POTS and other connective tissue disorders.

Research indicates that individuals with EDS are more likely to develop POTS due to the impact of connective tissue abnormalities on blood vessel function and blood flow regulation.

The prevalence of POTS may be underreported; some estimates suggest that it could affect up to 1-3 million people in the United States, yet many cases go undiagnosed due to a lack of awareness among healthcare providers.

POTS can often coexist with other conditions, including Mast Cell Activation Syndrome (MCAS) and autoimmune disorders, complicating diagnosis and treatment for affected individuals.

Treatment options for POTS typically include lifestyle changes such as increased salt and fluid intake, wearing compression garments, and medications that can help manage symptoms and stabilize blood pressure.

The autonomic nervous system's dysfunction in POTS can lead to an exaggerated response to stress, resulting in symptoms that may mimic anxiety or panic attacks, further complicating the clinical picture.

Studies suggest that exercise can be beneficial for POTS patients, but it must be approached cautiously, as overexertion can exacerbate symptoms.

The relationship between POTS and COVID-19 has garnered attention, with some patients reporting post-viral symptoms that resemble POTS, leading to research into long COVID and its implications.

POTS can be diagnosed through a tilt table test, which measures changes in heart rate and blood pressure upon standing, helping healthcare providers confirm the condition.

Some individuals with POTS may experience a phenomenon known as "brain fog," which includes cognitive difficulties such as trouble concentrating and memory issues, stemming from reduced blood flow to the brain.

The pathophysiology of POTS is complex and multifactorial, with ongoing research exploring genetic predispositions and potential environmental triggers.

Public figures like Carrie Ann Inaba and Jameela Jamil have used their platforms to raise awareness about POTS, emphasizing the importance of understanding chronic illnesses and reducing stigma.

The condition can significantly impact mental health, as the unpredictability of symptoms can lead to anxiety, depression, and social isolation for those living with POTS.

Ongoing research is aimed at better understanding POTS, developing targeted therapies, and improving diagnostic criteria to enhance care for individuals affected by this often-misunderstood condition.

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