Nicole O’Hara, a television reporter from North Carolina, woke up one morning feeling weak and without energy, thinking she had COVID or the Flu. She experienced symptoms like a pounding head, blurred vision, nausea, and shortness of breath lasting 4 days. A year later, she was diagnosed with Postural Orthostatic Tachycardia Syndrome (POTS).
TV Reporter Gets Life-Changing Diagnosis
After a fainting episode, Nicole sought medical help but was left without answers. She experienced recurring symptoms a year later, prompting a visit to the Mayo Clinic where she was diagnosed with POTS.
POTS affects circulation and the autonomic nervous system, leading to increased heart rate and symptoms during standing. Despite affecting millions, POTS is often undiagnosed or misdiagnosed, requiring specialized care for management.
Understanding POTS
Postural Orthostatic Tachycardia Syndrome disrupts blood circulation and autonomic functions, leading to symptoms like increased heart rate while standing. Proper diagnosis and management are crucial in addressing this condition.
Treatment and Management
While there is no cure for POTS, lifestyle modifications, medication, and adequate fluid intake can help manage symptoms. Consultation with healthcare providers is vital in creating a personalized treatment plan for individuals with POTS.
“For me, this is a challenging aspect of the condition — looking fine on the outside, but feeling like death on the inside. If I have a full face of makeup on and a smile, no one would know anything was wrong.”
Managing POTS involves understanding its impact on daily life and seeking appropriate medical advice for symptom management. Awareness and education about POTS are essential for better care and support.
Sources
- TODAY. Nicole O’Hara. September 9, 2022.
- Cleveland Clinic.
- Johns Hopkins Medicine.
- Healthline. Kathryn Watson. February 11, 2022.
