October is Dysautonomia Awareness Month: Understanding Autonomic Disorders
Every October, Dysautonomia Awareness Month shines a spotlight on disorders of the autonomic nervous system (ANS), which regulates involuntary bodily functions like heart rate, blood pressure, digestion, and temperature control.

This month-long campaign aims to educate the public, support patients, and advocate for research into conditions such as Postural Orthostatic Tachycardia Syndrome (POTS), neurocardiogenic syncope, and multiple system atrophy. Lee’s Summit Tribune+5Healthline+5Medical News Today+5
- What is Dysautonomia?
- Types of Dysautonomia
- 1. Postural Orthostatic Tachycardia Syndrome (POTS)
- 2. Neurocardiogenic Syncope (NCS)
- 3. Multiple System Atrophy (MSA)
- 4. Familial Dysautonomia
- Prevalence and Impact
- Dysautonomia Awareness Month Activities
- Living with Dysautonomia: A Personal Story
- Frequently Asked Questions
- Conclusion
What is Dysautonomia?
Dysautonomia refers to a group of medical conditions that result from a malfunction of the ANS. When the ANS doesn’t work properly, it can cause a range of symptoms, from mild to life-threatening. Common symptoms include: Town of Collingwood+1Medical News Today+1Healthline
- Dizziness or fainting
- Rapid or irregular heartbeat
- Fatigue
- Digestive issues
- Temperature regulation problems
- Visual disturbances
- Shortness of breathTeen Vogue+3National Day Calendar+3Town of Collingwood+3Awareness for POTSies+3Town of Collingwood+3Healthline+3
These symptoms can vary widely among individuals and may fluctuate in severity.
Types of Dysautonomia
There are several types of dysautonomia, each with distinct characteristics:
1. Postural Orthostatic Tachycardia Syndrome (POTS)
POTS is characterized by an excessive increase in heart rate upon standing, leading to symptoms like lightheadedness, palpitations, and fatigue. It predominantly affects women between the ages of 15 and 50.Teen Vogue+6Wikipedia+6Medical News Today+6
2. Neurocardiogenic Syncope (NCS)
Also known as vasovagal syncope, NCS is the most common cause of fainting. It occurs when the body overreacts to certain triggers, such as stress or prolonged standing, leading to a sudden drop in heart rate and blood pressure.Medical News Today+2Lee’s Summit Tribune+2Healthline+2
3. Multiple System Atrophy (MSA)
MSA is a rare, progressive neurodegenerative disorder that affects multiple systems, including the ANS. Symptoms may include muscle rigidity, coordination problems, and autonomic dysfunction. Healthline
4. Familial Dysautonomia
This genetic disorder primarily affects individuals of Ashkenazi Jewish descent. It impairs the development of the ANS, leading to issues with blood pressure regulation, temperature control, and digestion. Healthline
Prevalence and Impact
Dysautonomia affects millions worldwide, yet it remains underdiagnosed and misunderstood. The following table summarizes key statistics:
Statistic | Value | Source |
---|---|---|
Estimated global prevalence of dysautonomia | Over 70 million people | Healthline |
Estimated number of Americans with POTS | 1–3 million | Wikipedia |
Percentage of POTS patients who are female | Approximately 85% | Lee’s Summit Tribune |
Average diagnostic delay for POTS patients | 4–7 years | Teen Vogue |
These figures highlight the need for increased awareness and education about dysautonomia.
Dysautonomia Awareness Month Activities
Dysautonomia Awareness Month, observed every October, offers various opportunities for individuals and communities to get involved:
- Wear Turquoise: Turquoise is the official color representing dysautonomia awareness. Wearing turquoise clothing or accessories can help spark conversations and show support. Medical News Today
- Participate in Events: Attend or organize local events, such as walks, fundraisers, or educational seminars, to raise awareness and funds for research.
- Light Up Landmarks: Many landmarks and buildings participate by lighting up in turquoise during October. Encourage local establishments to join this initiative.Town of Collingwood+3potsuk.org+3Healthline+3
Living with Dysautonomia: A Personal Story
At 17, a young woman suffered a concussion that led to the development of POTS. For seven years, she experienced debilitating symptoms, including dizziness, fatigue, and migraines. Despite numerous medical consultations, her condition remained undiagnosed until a specialist at the Mayo Clinic identified POTS as the underlying issue. Now, she manages her symptoms through lifestyle changes and advocates for others affected by dysautonomia. Her story underscores the importance of awareness and early diagnosis. Teen Vogue
Frequently Asked Questions
Q: What causes dysautonomia?
A: Dysautonomia can result from various factors, including genetic mutations, autoimmune diseases, viral infections, and traumatic injuries. In some cases, the exact cause remains unknown.
Q: Is there a cure for dysautonomia?
A: Currently, there is no cure for dysautonomia. However, treatment focuses on managing symptoms through medications, lifestyle modifications, and physical therapy.
Q: How is dysautonomia diagnosed?
A: Diagnosis involves a combination of medical history, physical examination, and specialized tests like tilt table testing, blood tests, and autonomic function tests.
Q: Can dysautonomia be life-threatening?
A: While many forms of dysautonomia are manageable, some types, like multiple system atrophy, can be life-threatening. It’s essential to seek medical attention for proper diagnosis and management. Healthline
Conclusion
Dysautonomia Awareness Month serves as a crucial reminder of the challenges faced by individuals with autonomic disorders. By educating ourselves and others, supporting research, and advocating for patients, we can contribute to a better understanding and improved quality of life for those affected. This October, let’s wear turquoise, share information, and stand in solidarity with the dysautonomia community.