Maylee Jacob’s Journey with Raynaud’s: A Common Condition Often Overlooked

by drbyos

Living with Raynaud’s: Understanding and Managing a Common Cold-Related Condition

Maylee Jacob, like many others, has lived with “frozen fingers” for as long as she can remember. “In the wintertime, or even in an overly air conditioned room, the tips of my fingers would turn white and go numb,” Jacob describes the discomfort.

After years of self-diagnosis via the internet, Jacob received a professional diagnosis of Raynaud’s syndrome from her doctor.

MIKE DEAL / FREE PRESS


Maylee Jacob has been dealing with frozen fingers for most of her life and several years ago received a diagnosis of Raynaud’s.

What is Raynaud’s Syndrome?

Raynaud’s syndrome is a complex neurovascular condition that causes small blood vessels in the extremities to momentarily constrict in response to cold temperatures or stress. This constriction significantly reduces blood flow to the fingers, toes, ears, nose, and sometimes even the tongue, causing them to turn white or blue. The return of blood can trigger pain, swelling, and redness.

“It’s basically an overreaction to the cold,” Dr. Annaliese Tisseverasinghe, a rheumatologist and assistant professor of medicine at the University of Manitoba, explains. “It’s the body’s way of protecting the heart and brain by shutting off blood supply to less crucial areas.”

Recognized since 1862 by French physician Maurice Raynaud, this condition predominantly affects women, with a gender ratio of four to one. Despite often being dismissed as mere cold intolerance, Raynaud’s can significantly impact daily life.

Primary vs. Secondary Raynaud’s: Understanding the Difference

February marks Raynaud’s Awareness Month, highlighting the prevalence of this condition during the colder months. Primarily Raynaud’s occurs independently, without an underlying cause. It often appears between the ages of 15 and 30, and while symptoms can be uncomfortable, they typically don’t impair quality of life severely.

Conversely, Secondary Raynaud’s is a symptom of connective tissue disorders or autoimmune diseases like arthritis or lupus. It usually develops later in life and can be more severe.


NIKLAS D / WIKIMEDIA COMMONS
Raynaud’s typically affects the fingers and toes.

NIKLAS D / WIKIMEDIA COMMONS


Raynaud’s typically affects the fingers and toes.

Woman like Marion Pacy, diagnosed with systemic sclerosis (scleroderma) and secondary Raynaud’s at age 40, vividly understand the severity. Pacy’s career as a Winnipeg Transit bus driver was compromised due to frequent vasospasms triggered by busdoor activity. “The Raynaud’s got so bad with Winnipeg’s cold winters that I couldn’t handle it anymore,” she recalls.

Living with Raynaud’s: Coping and Management

For patients like Maylee Jacob, managing Raynaud’s involves a combination of medication, behavioral changes, and protective measures. Jacob receives a daily calcium channel blocker, essential during winter months. Additionally, she wears warm mittens, uses hand warmers, and avoids prolonged exposure to cold.

Lisa Merkeley, another woman living with the condition, retreats south annually to escape the frost. “It’s freeing; you don’t have to think twice about going outside,” she mentions from a Mexican balcony. “Back home, my fingers can turn white just by opening the fridge, so I spend most of my time indoors, hiding from the cold.”

The Impact on Daily Life

Frequent Raynaud’s episodes can lead to social isolation and missed opportunities. Activities like tobogganing with grandchildren or watching hockey games in winter may be curtailed. The severity of symptoms varies widely among individuals. Some experience mild discomfort, while others face life-changing consequences.

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MIKAELA MACKENZIE / FREE PRESS 
Dr. Annaliese Tisseverasinghe is a rheumatologist who treats patients with Raynaud’s syndrome.

MIKAELA MACKENZIE / FREE PRESS

Dr. Annaliese Tisseverasinghe emphasizes the importance of self-monitoring for proper diagnosis and management. Comparing Raynaud’s symptoms to a “heart attack for your fingers,” she underscores the necessity of recognizing its significant impact on well-being.

Recent Developments in Raynaud’s Research

Scientific advancements are shedding light on potential treatment options. A landmark study in London and Berlin identified specific genetic markers linked to Primary Raynaud’s, providing insights into its causes and potential therapies.

Published in Nature Communications, this study revealed that variations in adrenaline receptors and DNA-binding proteins play pivotal roles in causing blood vessel contractions. These findings indicate possible new drug targets, offering hope for better management of symptoms.


MIKE DEMBECK / THE CANADIAN PRESS
Michelle Richard has Raynaud’s disease, which causes her fingers and hands to transform colour from completely white, to blue and then red after exposure to a sudden change in temperature.

MIKE DEMBECK / THE CANADIAN PRESS


Michelle Richard has Raynaud’s disease, which causes her fingers and hands to transform colour from completely white, to blue and then red after exposure to a sudden change in temperature.

Treatment Options and Lifestyle Adjustments

Managing Raynaud’s often involves a combination of lifestyle changes and medical interventions. The primary treatment focuses on warming strategies:

  • Wearing layered clothing, mittens, and heat producing accessories.
  • Avoiding exposure to cold areas, including refrigerators.
  • Engaging in stress-reducing activities.

Dr. Tisseverasinghe recommends using photos during episodes to document changes for medical consultation.

Medical treatments include:

  • Calcium channel blockers and angiotensin receptor blockers, common blood pressure medications.
  • Topical creams and patches.
  • Antidepressants to manage stress.

Specialized surgical procedures like sympathectomy are reserved for severe cases.

The Role of Support Groups

Support groups play a crucial role in the lives of Raynaud’s sufferers. Organizations like Scleroderma Manitoba provide resources, forums, and connectivity for individuals.

“People need to talk to others experiencing similar challenges: how they handle it, medication suggestions, and product tips.” – Debbie Robitaille, Support Group Coordinator

These groups offer much-needed support, understanding, and coping strategies essential for navigating daily challenges.

Conclusion: Facing Winter with Raynaud’s

Living with Raynaud’s requires a proactive approach to manage symptoms and enhance quality of life. While challenges persist, support systems and medical research continue to improve outcomes.

“Most people think, ‘Oh, your hands are just cold,’ but it’s kind of like having a heart attack for your fingers,” Dr. Tisseverasinghe highlights.

For Maylee Jacob, the journey involves medication, meticulous self-care, and strategic lifestyle adaptations.

Ultimately, understanding and managing Raynaud’s enables individuals like Jacob to lead fulfilling lives despite winter’s challenges.

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