Overview

Narcolepsy is a sleep disorder characterized by excessive daytime sleepiness, making individuals extremely drowsy during the day. People with narcolepsy struggle to stay awake for extended periods and may suddenly fall asleep at inappropriate times, significantly disrupting their daily routine.

Some individuals with narcolepsy experience a sudden loss of muscle tone, known as cataplexy, which can be triggered by intense emotions, particularly laughter. Narcolepsy is classified into two types; type 1 narcolepsy involves cataplexy, while type 2 narcolepsy does not exhibit this symptom.

Unfortunately, narcolepsy is a lifelong condition without a cure. However, symptom management can be achieved through medications and lifestyle changes. Support from family, friends, employers, and teachers can significantly help individuals cope with the disorder.

Symptoms of Narcolepsy

The symptoms of narcolepsy often persist throughout a person’s life, with daytime sleepiness being a prominent feature. Individuals with narcolepsy may experience:

  • Excessive daytime sleepiness, leading to sudden sleep episodes, even during activities such as working or conversing.
  • Decreased alertness and focus during the day, hindering daily functioning.
  • Performing tasks involuntarily while asleep, with no recollection of doing so upon waking.
  • Sudden loss of muscle tone, known as cataplexy, triggered by intense emotions, especially positive emotions like laughter.
  • Sleep paralysis, where individuals are unable to move or speak while falling asleep or waking up.
  • Visual hallucinations that may occur during sleep paralysis or as individuals fall asleep or wake up.
  • Changes in rapid eye movement (REM) sleep, with REM sleep occurring more quickly after falling asleep and potentially happening at any time of the day.

Additionally, people with narcolepsy may experience other sleep disorders such as obstructive sleep apnea, REM sleep behavior disorder, or insomnia.

Causes and Risk Factors

The exact cause of narcolepsy remains unknown, but research suggests that type 1 narcolepsy is associated with low levels of hypocretin (orexin), a brain chemical that regulates wakefulness and REM sleep. The loss of hypocretin-producing cells in the brain may result from an autoimmune reaction, where the body’s immune system attacks its own cells.

Genetics may also play a role in narcolepsy, although the risk of inheriting the disorder from a parent is low. Furthermore, exposure to certain viruses, such as the swine flu (H1N1 flu) or a specific H1N1 vaccine, has been linked to narcolepsy in some cases.

Typically, narcolepsy starts between the ages of 10 and 30, and individuals with a family history of the condition have an increased risk of developing narcolepsy.

Complications

Narcolepsy can give rise to various complications, including:

  • Public misconceptions leading to challenges at work or in personal relationships due to misconceptions of laziness or lethargy.
  • Strained intimate relationships as intense emotions can trigger cataplexy, causing withdrawal from emotional interactions.
  • Risk of physical harm due to sudden sleep episodes, increasing the likelihood of accidents and injuries.
  • Higher risk of obesity, as sleepiness symptoms may lead to weight gain.

When to Seek Medical Attention

If you experience excessive daytime sleepiness impacting your personal or professional life, it is essential to consult a healthcare provider for evaluation and appropriate management.

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Diagnosis of Narcolepsy

If you suspect you have narcolepsy, your healthcare provider may refer you to a sleep specialist for a formal diagnosis. The diagnostic process may involve:

  • A detailed sleep history, including filling out the Epworth Sleepiness Scale to assess your degree of sleepiness.
  • Maintaining sleep records for a week or two to analyze your sleep patterns and alertness.
  • Wearing an actigraph, a device that measures your activity and rest to indirectly assess your sleep patterns.
  • Undergoing a sleep study known as polysomnography, which involves monitoring brain waves, heart rate, breathing, leg, and eye movements during sleep.
  • Taking a multiple sleep latency test to measure how quickly you fall asleep during the day, with observation of rapid eye movement (REM) sleep.
  • In some cases, genetic tests and a lumbar puncture (spinal tap) may be performed to check for specific markers.

Treatment for Narcolepsy

While there is no cure for narcolepsy, symptoms can be managed with various treatments:

  • Medications: Stimulants that stimulate the central nervous system can help individuals stay awake during the day. Other medicines that suppress REM sleep may be prescribed to alleviate symptoms of cataplexy, hallucinations, and sleep paralysis. Sodium oxybate and oxybate salts are effective in relieving cataplexy and improving nighttime sleep.
  • Lifestyle Changes: Maintaining a consistent sleep schedule, taking short naps at regular intervals, avoiding nicotine and alcohol, and engaging in regular exercise can all contribute to symptom management.

Coping and Support

Dealing with narcolepsy can be challenging, but there are ways to cope:

  • Communicate with your employer or teachers about your condition and work with them to make necessary adjustments, such as taking naps during the day or breaking up tasks.
  • Practice safe driving by working with your healthcare provider to plan a safe trip, considering your medication schedule and taking breaks when feeling drowsy.
  • Support groups and counseling can provide emotional support and helpful coping strategies.

Preparing for Your Appointment

If you suspect narcolepsy, prepare for your appointment by:

  • Being aware of any pre-appointment restrictions.
  • Writing down your symptoms, personal information, and all medications you’re taking.
  • Bringing a family member or friend along for support.
  • Preparing a list of questions for your healthcare provider.

During your appointment, expect your doctor to ask questions about your symptoms, their frequency, and severity, as well as any family history of similar symptoms.

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