MySpecialSpots.com

Welcome to
My Special Spots

Inspired by Leela's Special Spots, our mission is to help children and families feel seen, accepted, and understood.

Here you'll find educational resources, support, advocacy organizations, and inspiring stories from the vitiligo community — all created to encourage confidence, belonging, and self-acceptance.

"Our differences are what make us shine."

Every book purchased helps support our missionclick here to read our official giving policy and see how our net profits fund vitiligo awareness, advocacy, and research.

"We currently donate 100% of the net profits from every copy sold to tax-exempt 501(c)(3) charities dedicated to vitiligo awareness, advocacy, and research."

📖
Book
Discover Leela's story — a heartwarming tale about vitiligo, friendship, courage, and learning to love what makes you different.
Explore →
💜
Vitiligo
Learn what vitiligo is, who it affects, and why awareness and representation matter so deeply for children and families.
Learn More →
Author
Sonia K. Mehta was diagnosed with vitiligo at age five. Read her journey from childhood to the TODAY Show to published author.
Read Her Story →
🔗
Resources
Medical information, support groups, advocacy organizations, Facebook communities, children's events, and conferences — all in one place.
Find Resources →
🤝
Giving Back
Ways to support vitiligo research, donate to nonprofits, advocate for awareness, and give back to a community that lifts each other up.
Get Involved →

Leela's Special Spots

Front Cover
Back Cover
✦ Pre-Order the Book Learn More

✦ About the Book

Leela's Special Spots

Leela's Special Spots is a heartwarming picture book that helps children discover the beauty in what makes them unique.

When Leela begins to feel different because of the white spots on her skin, an unexpected friendship leads her on a magical adventure filled with wonder, courage, and self-discovery. Along the way, she learns that our differences are not something to hide — they are part of what makes us special.

Inspired by the experiences of those living with vitiligo, Leela's Special Spots encourages conversations about acceptance, belonging, kindness, and self-confidence. Whether a child is affected by vitiligo or simply learning to celebrate differences in others, this story offers an uplifting reminder that everyone deserves to feel seen, valued, and proud of who they are.

✦ The Book

Front & Back Cover

Front Cover

Front Cover

Back Cover

Back Cover

✦ Meet the Characters

The Heart of the Story

Leela
Meet Leela
A brave, curious girl with vitiligo on her face, hands & legs — learning to love every spot
The Visitor
Meet Nova
A furry purple alien covered in spots — who helps Leela discover that her differences are what make her shine

✦ What This Story Teaches

Big Lessons for Little Hearts

💜

Self-Acceptance

Learning to love what makes you uniquely, beautifully you.

Courage

Being brave enough to show your true self to the world.

🌟

Friendship

Finding unexpected bonds that change how we see ourselves.

🦋

Belonging

Every child deserves to feel seen, celebrated, and loved.

✦ Pre-Order — $12.99 / $19.99 Meet the Author →

✦ Giving Back

Make a Difference

Whether you donate, spread awareness, or share a book — every act of giving helps a child with vitiligo feel seen, valued, and loved.

📋 Our Giving Policy: We donate 100% of net profits to 501(c)(3) charities supporting vitiligo awareness, advocacy, and research. Read our full giving policy →

Donate to Vitiligo Research & Support

🔬

Vitiligo Research Foundation — Donate

Fund the search for a cure. 100% of donations go directly toward vitiligo research and patient education programs worldwide.

vrfoundation.org/donate
🇺🇸

American Vitiligo Research Foundation — Donate

Support the only U.S. nonprofit focused specifically on children with vitiligo. Funds awareness, counseling, and cruelty-free research.

avrf.org/donate
🌍

Global Vitiligo Foundation — Donate

Support patient education, annual conferences, and scientific symposiums that unite the global vitiligo community.

globalvitiligofoundation.org

Spread Awareness

💛

Join the #Lit4Vit Campaign — VITFriends

Every June 25th, buildings worldwide light up purple for World Vitiligo Day. Find your local event and share #Lit4Vit on social media.

vitfriends.org
📅

Attend a World Vitiligo Day Event — June 25, 2026

Find local or virtual events in 40+ countries and help make the vitiligo community feel seen and celebrated.

vrfoundation.org/events

Share the Book

Gift Leela's Special Spots to a Child Who Needs It

One of the most powerful things you can do is put the right book in the right hands. Donate a copy to a school, library, pediatrician's office, or family you know. Every book is a message: you are special exactly as you are.

Pre-Order a Copy ✦

✦ Vitiligo Awareness ✦

Understanding Vitiligo

Vitiligo is at the heart of Leela's story — and it's a real condition that millions of people around the world live with every day.

Vitiligo is a long-term skin condition where patches of skin lose their pigment (color), creating lighter or white spots. It happens when melanocytes — the cells that produce skin color — are attacked by the body's own immune system.

It can appear anywhere on the body, but commonly affects the face, hands, and arms. Vitiligo is not contagious, not painful, and not life-threatening — but for children especially, being visibly different can carry a real emotional weight.

Vitiligo touches people of every race, ethnicity, and age. The more we talk about it openly, the more we can replace stigma with understanding, empathy, and pride.

1–2%
of the global population has vitiligo
70M+
people worldwide are affected
50%
of cases begin before age 20
3.7M
Americans are living with vitiligo right now

✦ Common Questions

What people ask

No — not at all. Vitiligo cannot be passed from person to person through touch, sharing items, or proximity. It is an autoimmune condition that originates inside the body's own immune system.
Vitiligo occurs when the immune system mistakenly destroys melanocytes — the cells that give skin its color. Genetics, environmental triggers, and stress may all play a role, and researchers worldwide continue to study its exact causes.
There is currently no cure, but treatments like topical creams, light therapy, and newer medications can slow progression or restore some pigment. Many people with vitiligo choose to embrace their natural skin as part of who they are.
Vitiligo does not affect physical health or lifespan. Depigmented patches do have less UV protection, so sunscreen is recommended. The most significant impact is often emotional — especially for children — which is why stories like Leela's matter so much.
Use open, positive language. Read books like Leela's Special Spots together. Remind them that their spots are part of what makes them beautifully unique. Connect with vitiligo support communities, and most importantly — let them know they are loved exactly as they are.

✦ Why Representation Matters

Seeing yourself changes everything

When children see themselves in books, toys, and media, it tells them: you belong here. For a child with vitiligo, finding a character who looks like them can be transformative.

In 2020, Mattel released a Barbie doll with vitiligo — a landmark moment for the community. Sonia appeared on the NBC TODAY Show to share what that moment meant to her family.

Leela's Special Spots carries that mission forward — one page, one child, one story at a time.

✦ Read Sonia's Story
Sonia K. Mehta

✦ Meet the Author

Sonia K. Mehta

Author · Leela's Special Spots · Vitiligo Advocate

Sonia K. Mehta is a vitiligo advocate, author, and the founder of MySpecialSpots.com. Diagnosed with vitiligo at the age of five, she grew up navigating a world that rarely reflected her experience — explaining her skin to classmates, feeling the weight of curious stares, and wishing someone had told her that her spots were something to be proud of.

That experience became her purpose. Sonia has dedicated her life to raising vitiligo awareness and creating space for children and families to feel seen, understood, and celebrated. In 2020, she appeared on NBC's TODAY Show to feature the new vitiligo Barbie doll as part of Mattel's Fashionistas line — a milestone moment for the vitiligo community and for every child who had never seen themselves reflected in a toy.

She has also been featured on a billboard sponsored by the American Vitiligo Research Foundation (AVRF) at the Clearwater Marine Aquarium — honoring Nicholas, a dolphin with white spots who starred in the film Dolphin Tale. Through advocacy events and fundraising efforts across the country, Sonia has helped spread awareness and champion inclusion for the vitiligo community.

Leela's Special Spots is the book Sonia wishes she had as a little girl. Her hope is that every child who opens it — whether they have vitiligo or not — closes it knowing that what makes them different is exactly what makes them shine.

✦ Sonia's Journey

A story of courage & love

Age 5

Sonia is diagnosed with vitiligo. Patches appeared on her face, hands, and arms. A lifelong journey of learning to love her own skin begins. 💜

💜
Growing Up

Sonia navigates childhood and adolescence with vitiligo as a visible part of her identity — facing questions, stares, and moments of doubt, while building remarkable inner strength and resilience.

🐬
2016 — AVRF Retreat & Nicholas the Dolphin

Sonia was 7 when she met Nicholas at an AVRF retreat in Clearwater — one of the biggest moments in her journey. His healed burns left white patches on his skin, and seeing him helped her see her own spots in a whole new light.

📺
2020 — NBC TODAY Show

When Mattel unveiled a Barbie doll with vitiligo, Sonia was invited onto the NBC TODAY Show to share what this milestone meant for the vitiligo community and for families raising children who feel different.

✍️
Writing the Book

Sonia pours her entire journey — the questions, the stares, the growth, and the pride — into Leela's Special Spots. She writes the book she wished had existed when she was five years old.

Today

Sonia continues to advocate for vitiligo awareness and self-acceptance. Her book is a love letter to every child who has ever wished they could blend in — that your differences are what make you shine.

✦ As Seen On NBC TODAY Show

Sonia on national television

Sonia on the TODAY Show Sonia showing vitiligo on hands
TODAY Show segment thumbnail
Watch on TODAY.com
📺 NBC TODAY Show · February 2020

Barbie Gets a Makeover — And What It Meant to Sonia

When Mattel launched a new inclusive Barbie line featuring a doll with vitiligo, Sonia appeared on national television to share her personal story and what this moment of representation meant to millions of people living with the condition worldwide.

Watch the full segment ↗
Sonia holding the Mattel vitiligo Barbie doll

Sonia holding the Mattel vitiligo Barbie · NBC TODAY Show · 2020

✦ A Turning Point

AVRF's Impact on Sonia's Life

In 2016, Sonia attended the AVRF retreat in Clearwater, Florida — where she was surrounded by people who looked just like her. No stares, no explaining. Just belonging. It changed everything.

At the retreat she met Nicholas, a dolphin whose healed burns left white patches on his skin — a beautiful reflection of the vitiligo community. AVRF gave Sonia her first real sense of community, and she has never forgotten it. They showed her, in person, that her differences were always worth celebrating.

Sonia at the Nicholas dolphin exhibit at Clearwater Marine Aquarium, 2016

Sonia with Nicholas the Dolphin · AVRF Retreat · Clearwater, FL · 2016

📍 Clearwater Marine Aquarium · 2016

Meet Nicholas

At the 2016 AVRF retreat, Sonia met Nicholas — a dolphin whose healed burns left white patches on his skin, just like vitiligo. Standing next to him for the first time, surrounded by her vitiligo community, Sonia saw her own spots differently. AVRF adopted Nicholas and used his story to celebrate what makes each of us beautifully, uniquely marked.

Visit AVRF Retreats ↗
Front Cover
Back Cover

Leela's Special Spots

Coming Soon ✨

We're putting the finishing touches on something special.
Leela's Special Spots will be available soon in paperback and hardcover. Enter your email below to be the first to know when it's ready to order.

Paperback $12.99  ·  Hardcover $19.99

✦ Vitiligo Resources ✦

Find Help, Community & Information

Every link below is a real, accredited or verified community source. Click any item to visit the site directly.

💜

World Vitiligo Day is June 25th, 2026

Theme: "From Stigma to Strength." Events in 40+ countries — anchored in Chandigarh, India. Mark your calendar, find a local event, or join online to show your support.

See Events ↗
🩺

Medical Information

Accredited, doctor-reviewed sources
🏛️
UMass Vitiligo Clinic — Dr. John E. Harris
Led by Dr. John E. Harris, one of the world's leading vitiligo researchers and clinicians. The UMass Vitiligo Clinic provides cutting-edge treatment, research, and patient education on vitiligo.
umassmed.edu/vitiligo
Medical
⚕️
American Academy of Dermatology — Vitiligo Overview
The leading U.S. dermatology authority. Doctor-reviewed overview of vitiligo causes, symptoms, types, and all available treatments.
aad.org/public/diseases/a-z/vitiligo-overview
Medical
🏥
NIH — National Institutes of Health: Vitiligo
U.S. government health resource with clinical research, treatment guides, and links to active vitiligo trials for adults and children.
niams.nih.gov/health-topics/vitiligo
Medical
🔬
Mayo Clinic — Vitiligo: Symptoms, Causes & Treatments
Expert-written patient guide covering vitiligo symptoms, diagnosis, risk factors, and every current treatment option.
mayoclinic.org/diseases-conditions/vitiligo
Medical
💊
WebMD — Vitiligo Overview
Medically reviewed guide covering types of vitiligo, emotional impact, lifestyle tips, and latest FDA-approved treatments.
webmd.com/skin-problems-and-treatments/vitiligo-common-cause-loss-skin-pigment
Medical
📋
Healthline — Everything You Need to Know About Vitiligo
Medically reviewed deep-dive including photos, mental health resources, ruxolitinib (Opzelura) information, and daily skin care tips.
healthline.com/health/vitiligo
Medical
👨‍⚕️
AAD — Vitiligo Treatment Options
Doctor-reviewed guide to all available vitiligo treatments — from topical creams and light therapy to newer options like ruxolitinib (Opzelura).
aad.org/public/diseases/a-z/vitiligo-treatment
Medical
💬

Support Links & Online Communities

Websites, forums, and Facebook groups — real people, real support
🌸
Living Dappled — #1 Patient-Led Vitiligo Resource Hub
100+ vetted resources, personal stories, makeup guides, and a weekly encouragement newsletter. Founded by Erika Page, who lives with vitiligo.
livingdappled.com
Website
👥
MyVitiligoTeam — Social Network for Vitiligo
Dedicated platform connecting thousands of people with vitiligo. Share experiences, ask questions, and get real peer support.
myvitiligoteam.com
Community
🤲
Vitiligo Support International
One of the oldest online vitiligo communities. Forums, educational articles, and a welcoming space for individuals and families worldwide.
vitiligosupport.org
Forum
📘
Facebook Group — Vitiligo Support Community
An active Facebook group connecting people living with vitiligo. Share experiences, ask questions, and find peer support from a real community.
facebook.com/groups/141439573072656
Facebook
📘
Facebook Group — Ruxolitinib (Opzelura) Vitiligo Community
A Facebook group focused on vitiligo treatment with ruxolitinib cream — sharing experiences, updates, and support around this FDA-approved therapy.
facebook.com/groups/ruxolitinib-vitiligo-community
Facebook
📘
Facebook Group — My Life with Vitiligo
A welcoming Facebook community where people with vitiligo share their daily journeys, tips, stories, and encouragement with others who understand.
facebook.com/groups/MyLifeWithVitiligo
Facebook
📘
Facebook Group — Vitiligo Group
A large, active Facebook group for people with vitiligo and their families — open discussions, awareness posts, treatment updates, and daily support.
facebook.com/groups/vitiligogroup
Facebook
🗣️
Vitiligo Society — Virtual Support Group (Open Worldwide)
Regular Zoom gatherings moderated by The Vitiligo Society. Also runs a dedicated parents group for caregivers of children with vitiligo.
vitiligosociety.org/virtual-support-group
Support Group
📣

Advocacy Groups

Organizations driving policy change, visibility & rights
🌏
VIPOC — Vitiligo International Patient Organizations Committee
Paris-based NGO uniting 40+ patient organizations worldwide. Drives international policy, publishes the Vitiligo White Paper, and coordinates global campaigns.
vipoc.org
NGO
💛
VITFriends — International Vitiligo Advocacy Community
Organized the largest vitiligo rally in U.S. history at Capitol Hill. Leads the #Lit4Vit campaign, lighting 60+ global landmarks purple every June 25th.
vitfriends.org
Advocacy
🌍
Global Vitiligo Foundation (GVF)
International nonprofit hosting annual conferences, scientific symposiums, and patient education programs to unite the vitiligo community worldwide.
globalvitiligofoundation.org
Foundation
🔬
Vitiligo Research Foundation (VRF)
Solely dedicated to curing vitiligo. Funds research, hosts World Vitiligo Day globally, and holds Special Consultative Status with the United Nations.
vrfoundation.org
Foundation
🇺🇸
American Vitiligo Research Foundation (AVRF)
501(c)(3) nonprofit since 1995. Focused on children and families — awareness, education, counseling resources, and cruelty-free research funding.
avrf.org
Nonprofit
🇬🇧
The Vitiligo Society (UK)
UK charity that successfully campaigned for NHS vitiligo treatment coverage. Runs events, webinars, VitLife magazine, and active advocacy campaigns.
vitiligosociety.org
Charity
📢
VIPOC — How to Become a Vitiligo Advocate (Step-by-Step Guide)
Practical guide to advocacy — social media, working with doctors, influencing policy, and joining international vitiligo movements.
vipoc.org/from-awareness-to-action
Guide
👶

Children's Events & Family Resources

For kids, parents, and caregivers
🧒
AVRF — Children & Families Program
AVRF's core mission is supporting children with vitiligo. Education, peer support, family counseling, and pediatric research funding.
avrf.org
Children
🎒
AAD — Vitiligo Treatment Options
Doctor-reviewed guide to all available vitiligo treatments — from topical creams and light therapy to newer options like ruxolitinib (Opzelura).
aad.org/public/diseases/a-z/vitiligo-treatment
Parents
📘
Facebook Group — Vitiligo Support Community
An active Facebook group connecting people living with vitiligo. Share experiences, ask questions, and find peer support from a real community.
facebook.com/groups/141439573072656
Facebook
📘
Facebook Group — Ruxolitinib (Opzelura) Vitiligo Community
A Facebook group focused on vitiligo treatment with ruxolitinib cream — sharing experiences, updates, and support around this FDA-approved therapy.
facebook.com/groups/ruxolitinib-vitiligo-community
Facebook
📘
Facebook Group — My Life with Vitiligo
A welcoming Facebook community where people with vitiligo share their daily journeys, tips, stories, and encouragement with others who understand.
facebook.com/groups/MyLifeWithVitiligo
Facebook
📘
Facebook Group — Vitiligo Group
A large, active Facebook group for people with vitiligo and their families — open discussions, awareness posts, treatment updates, and daily support.
facebook.com/groups/vitiligogroup
Facebook
💞
Parents' Virtual Support Group — Vitiligo Society
Online group specifically for parents of children with vitiligo. Open to anyone worldwide — share experiences and support each other.
vitiligosociety.org/virtual-support-group
Parents
🎪
World Vitiligo Day — Children's Events & Grassroots Programs
Directory of children's activities and community events tied to World Vitiligo Day each June 25th worldwide.
worldvitiligoday.ca/grassroots-support
Events

⚠️ Important Disclaimers

Medical Disclaimer: The information on this website is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your dermatologist or other qualified healthcare provider with any questions you may have regarding vitiligo.

External Links Disclaimer: This website contains links to third-party organizations. These links are provided solely as a convenience. We do not endorse, control, or guarantee the accuracy, relevance, or safety of the content on these external sites.

Community Forums Warning: Some linked resources include peer-led community groups and forums. Peer recommendations found in these spaces — including home remedies, dietary changes, or product suggestions — are not vetted clinical treatments. Always consult a licensed dermatologist before making any changes to your care.

✦ Share the Story ✦

The best resource? A book that makes kids feel seen.

Leela's Special Spots gives every child with vitiligo a hero who looks just like them.

Pre-Order the Book Learn About Vitiligo

✦ Transparency & Giving ✦

Our Giving Policy

Thank you for supporting our mission! To ensure complete transparency under charitable disclosure guidelines, here is exactly how your purchase helps families navigating vitiligo.

Our Current Giving Commitment

We donate 100% of the net profits from every copy of Leela's Special Spots sold to tax-exempt 501(c)(3) charities dedicated to vitiligo awareness, advocacy, and research. Because we intend to expand our support to various organizations over time, we do not restrict our giving to a single group.

Our Charity Selection Criteria

We select recipient organizations based on the following strict standards:

  • They must be legally registered, tax-exempt 501(c)(3) nonprofits.
  • Their primary mission must support vitiligo medical research, family outreach, or public education.
  • They must have a proven track record of directly assisting children and families.

How "Net Profits" and Recouping Costs Work

Before donations are calculated, the author must first recover the actual out-of-pocket expenses required to bring this children's picture book to life. Net profits are calculated using this exact formula:

  • Gross Retail Price ($12.99) minus Amazon KDP or IngramSpark printing costs.
  • Minus platform/bookstore distribution fees.
  • Minus the author's initial setup costs (including illustration, professional formatting, and publishing tools).

Once these setup costs are fully recovered, every single penny of remaining profit goes directly to eligible causes. Because this policy lives on our website, the author reserves the right to adjust donation percentages or campaign parameters in the future to ensure the project's sustainability.

Specific charity names and dated donation receipts will be published transparently on this page as grants are made.

Please note: Purchases of this commercial book are not tax-deductible for the consumer.

Donation Receipts

As grants are made to qualifying 501(c)(3) organizations, the charity name, donation amount, and date will be published here for full public transparency.

No grants have been issued yet — check back after the book launches.

← Back to Giving Back Pre-Order the Book