Julia Ranney battles debilitating condition following COVID-19 infection
Toronto, ON – Julia Ranney’s life took a drastic turn after her COVID-19 infection earlier this year. Diagnosed with postural orthostatic tachycardia syndrome (POTS), Ranney now faces a daily battle against the debilitating condition.
POTS is a condition that causes a variety of symptoms when transitioning from lying down to standing up, including dizziness, fatigue, and a rapid heart rate. While most COVID patients recover within weeks, Ranney’s symptoms only worsened over time.
“I knew something was wrong when one day I almost blacked out in the shower. I felt dizzy, nauseous and my feet turned a deep purple in colour,” said Ranney, describing her initial symptoms.
After consultations with various specialists, Ranney received the diagnosis of POTS. Also known as postural orthostatic tachycardia syndrome, this condition disrupts the body’s autonomic nervous system, causing a lack of balance in blood pressure and heart rate.
Individuals with POTS may experience blood pooling in their legs, leading to changes in the color of the feet and legs. POTS can be triggered by infections, diseases, or disorders such as COVID-19, diabetes, Lupus, or Lyme disease.
Ranney’s symptoms included extreme fatigue, lightheadedness, and a constant feeling of dizziness. Basic tasks became a challenge, and her mental health was severely affected. However, her concerns were initially dismissed as anxiety.
Determined to seek help, Ranney joined Cornerstone Physiotherapy’s online Long COVID clinic, which specializes in POTS. Through various tests, including monitoring her heart rate, Ranney’s specialist confirmed her suspicions of having POTS.
Ranney’s case is not unique. A recent international survey indicated that approximately 30% of COVID long-haulers qualify for POTS, with roughly 67% experiencing some form of nervous system dysfunction after infection.
The impact of POTS on Ranney’s life has been significant. Daily tasks now require careful planning, as she must manage her fatigue and limit her calorie burning. Standing for long periods of time is not possible, and even simple activities like making tea or doing hair and makeup require breaks or adjustments.
Heat also triggers Ranney’s symptoms, causing her to miss out on outdoor activities during the summer months. However, she remains hopeful and is supported by a strong medical team and an understanding network of family, friends, and colleagues.
“I’m more than my condition. I’m more than my health. And I won’t let POTS take over my life,” Ranney emphasized.
Ranney’s story sheds light on the impact of POTS following a COVID-19 infection and serves as a reminder of the importance of proper medical care and support for individuals dealing with long-term effects.
This article is for informational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Contact a qualified medical professional before engaging in any physical activity, or making any changes to your diet, medication, or lifestyle.
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