Managing Your Emotional Health With Vitiligo

Managing Your Emotional Health With Vitiligo

Managing Your Emotional Health With Vitiligo
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If you have vitiligo — an autoimmune condition that causes skin to lose color in patches — you likely know that it’s more than just a cosmetic problem. Although vitiligo isn’t contagious or fatal, it is a chronic condition that can have a psychological impact because it’s so visible to others.

People with vitiligo often experience emotional and mental health issues like low self-esteem or confidence, sleep problems, anxiety disorders, negative self-perception, loss of identity, and depression.

 Those with darker skin tones may also face stigmatization and discrimination due to their appearance.

However, while vitiligo can affect your well-being, there are ways to live confidently with the condition. Read on for tips on how to cope.

What Are the Symptoms of Vitiligo?

Board-certified dermatologist Andrew Alexis, MD, walks through some of the symptoms of vitiligo.
What Are the Symptoms of Vitiligo?

How Vitiligo Can Impact You

According to Mohammad Jafferany, MD, professor of psychodermatology, psychiatry, and behavioral sciences at Central Michigan University in Mount Pleasant, vitiligo is classified as a secondary psychiatric disorder, meaning that the psychological consequences of vitiligo affect those who have it as much as or even more than the physical consequences. Vitiligo can interfere with almost every aspect of a person’s life: career, relationships, identity, behavior, habits, and mental and emotional health.

“Some people just stop going outside or working to avoid stigma and meeting with people,” Dr. Jafferany says. As a result, they may experience loneliness, social isolation, and in more severe cases, suicidal thoughts and ideation.

In March 2021, the U.S. Food and Drug Administration (FDA) conducted a public meeting to hear how people with vitiligo and their caregivers experienced the condition. Many participants said it caused them to have anxiety, suicidal thoughts, low self-confidence, and a loss of identity. Due to the stigma attached to the condition, they also reported having difficulty growing friendships and relationships and meaningfully engaging in everyday and social activities.

About 75 percent of people with vitiligo say they have experienced psychiatric issues such as depression, anxiety, and stress, according to one study.

Cultural View of Vitiligo

The societal aspect of vitiligo should not be ignored, Jafferany says. In many cultures around the world, particularly in countries with people who have darker skin tones, those with vitiligo have a higher incidence of relationship breakups and divorces and may struggle to find a partner, he says.

Many people mistakenly think vitiligo is contagious. People with vitiligo are especially prone to experiencing discrimination, loss of privileges and opportunities, and difficulty progressing in different aspects of their lives owing to their appearance.

How to Feel More Confident With Vitiligo

Despite how disruptive living with vitiligo can be, you can take control of your experience and thrive with this condition. Consider these strategies:

Acknowledge Your Feelings

Vitiligo can make you feel self-conscious, which can be difficult. But rather than ignore these feelings, it’s better to own them, says Brett King, MD, PhD, a dermatologist at Yale Dermatology in Middlebury, Connecticut, and associate professor of medicine at Yale School of Medicine.

“Too often, people with vitiligo hear things like, ‘It could be worse,’ or ‘You could have cancer,’” Dr. King says. Although they might mean well, people who make such statements can dismiss your feelings. Rather than discounting yourself, acknowledge your emotions.

Learn About Your Condition

Understanding your symptoms and potential treatment options can make you feel more in control of the condition and overall health. “A basic understanding of what causes skin-color change in vitiligo is an essential step toward building self-confidence,” Jafferany says.

With more knowledge, you can become your own advocate, identifying and dispelling myths about vitiligo — including those that could affect your mood and confidence — and informing yourself about treatment options.

You can also help educate others. If you notice people staring at you, for example, King recommends saying something like, “I see you noticed the white spots on my skin. I have a condition called vitiligo, where the skin loses its color. That’s what causes those white spots. But I’m okay.”

Check out the Global Vitiligo Foundation, the Vitiligo Research Foundation, and the American Academy of Dermatology for information.

Rely on Your Support System

Although living with vitiligo can feel isolating, you don’t have to experience it alone. A solid support system, which may include family members, friends, and colleagues, plays a significant role in mitigating the many psychological impacts of vitiligo, according to Jafferany.

“Even if they don’t personally have vitiligo, connecting with others may help remind you that you are a valuable part of society,” he says.

Join Support Groups

It can be helpful to talk to others who know exactly what you’re going through. By participating in vitiligo support groups, you can meet people who can relate to you and hear how others are navigating life with the condition. In addition, interacting with people who make you feel seen can help you develop resilience, hope, and confidence.

Find support groups and other helpful resources through the Vitiligo Research Foundation, Vitiligo Support International, and Global Vitiligo Foundation.

Seek Professional Help

A study done in 2022 found that cognitive behavioral therapy — a type of talk therapy — can improve mental health symptoms, stress levels, and quality of life in people with vitiligo and other skin diseases.

If you’re experiencing overwhelming symptoms of depression, anxiety, or stress, Jafferany advises seeking professional counseling to learn coping skills and treat your symptoms. You may want to look specifically for a psychodermatologist — a therapist who works with people who have skin conditions — or another therapist who has experience working with people with chronic health conditions.

Practice Body Positivity

Learning to appreciate your appearance can help you live unapologetically with vitiligo. Start with being comfortable with yourself, advises Alex Dimitriu, MD, founder of Menlo Park Psychiatry and Sleep Medicine in California.

“This can be built on the core belief that appearances are only skin-deep, and your personality, kindness, intelligence, or other attributes you cherish matter far more than anything on the outside,” Dr. Dimitriu says. It might also help to realize that people who judge your color or appearance may not be the people you want in your life.

Consider Treatment for Vitiligo

Because vitiligo isn’t life-threatening or contagious, you can decide whether to treat it.

Medical treatments for vitiligo include:

  • Topical steroids, ruxolitinib, or calcineurin inhibitors
  • Light therapy
  • Depigmentation therapy
  • Procedures like melanocyte transplants, micro pigmentation, and skin grafting

Another option is to use special makeup to camouflage the white areas of skin. Your dermatologist can give you more information about how to use it and where to purchase it.

The Vitiligo Research Foundation has information about clinical trials researching treatments for vitiligo.

The Takeaway

  • People living with vitiligo often feel self-conscious about their skin’s appearance. This can result in mental health problems such as depression and anxiety.
  • Educating yourself and others about your condition can help you feel more confident.
  • Seeking support from friends, family, and support groups can help you feel less isolated.
  • Treating vitiligo is optional. If you decide you’d like to treat it, a dermatologist can help you understand available options.
EDITORIAL SOURCES
Everyday Health follows strict sourcing guidelines to ensure the accuracy of its content, outlined in our editorial policy. We use only trustworthy sources, including peer-reviewed studies, board-certified medical experts, patients with lived experience, and information from top institutions.
Resources
  1. Ezzedine K et al. Psychosocial Effects of Vitiligo: A Systematic Literature Review. American Journal of Clinical Dermatology. September 23, 2021.
  2. The Voice of the Patient: Vitiligo. U.S. Food and Drug Administration. December 2021.
  3. Nasser MA et al. Stress, anxiety, and depression in patients with vitiligo. Middle East Current Psychiatry. September 30, 2021.
  4. Raheel MF et al. Being female with vitiligo disease in traditional societies within North Africa. BioPsychoSocial Medicine. January 10, 2024.
  5. Geisler A et al. Importance of and instruction for starting a vitiligo patient support group. Dermatology Online Journal. November–December 2022.
  6. Revankar RR et al. Cognitive behavior therapy as dermatological treatment: a narrative review. International Journal of Women’s Dermatology. December 2022.
  7. Vitiligo: Diagnosis, Treatment, and Steps to Take. National Institute of Arthritis and Musculoskeletal and Skin Diseases.
Jacquelyn Dosal

Jacquelyn Dosal, MD

Medical Reviewer

Jacquelyn Dosal, MD, is a board-certified dermatologist practicing at The Dermatology House in Park City, Utah. Her areas of expertise include acne, rosacea, integrative treatments of inflammatory skin diseases, as well as laser treatment of the skin and injectables.

Dr. Dosal writes cosmetic questions for the certifying exams for the American Board of Dermatology. She is also the deputy editor for the American Academy of Dermatology's podcast, Dialogues in Dermatology.

Frances-Gatta-bio

Frances Gatta

Author
Frances Gatta is a freelance health and life sciences writer whose work appears regularly in Nature, Forbes Health, Healthline, WebMD, Yahoo Life, among other publications. She is based in Nigeria and holds a law degree from the University of Lagos. She has devoted her career to creating content that helps demystify health and science for the general audience.