From Author and Vitiligo Advocate Sonia K. Mehta

Our Differences
Make Us Shine

Celebrating what makes every child unique.

Inspired by Sonia's experience growing up with vitiligo, Leela's Special Spots is a heartfelt picture book about courage, friendship, and self-acceptance. Beyond the story, My Special Spots connects children, families, and educators with accessible vitiligo information, reputable medical and research resources, support organizations, and opportunities for community connection.

Leela's Special Spots book
A story with heart. | Resources with purpose.

Our Mission

Through inclusive storytelling, accessible vitiligo education, and community outreach, My Special Spots helps children with vitiligo build confidence and self-acceptance while fostering empathy, understanding, and belonging within families and communities.

Meet Leela & Nova

Leela and Nova together

An unexpected friendship helps Leela discover a new way to see herself.

Leela
Nova

Leela

A kindhearted young girl whose magical journey helps her discover the beauty in what makes her unique.

Nova

A friendly, furry, spotted alien from another galaxy who helps Leela understand that differences are something to celebrate.

Free Coloring Pages
Download Leela & Nova coloring pages and fun activities!
DOWNLOAD NOW →
About Vitiligo
Kid-friendly information to help kids understand vitiligo.
LEARN MORE →
Giving Back
A portion of every purchase supports organizations dedicated to the vitiligo community.
OUR PARTNERS →
Resources
Books, videos, and tools for families, teachers, and caregivers.
EXPLORE RESOURCES →

✦ What They're Saying ✦

“Leela’s Special Spots is a truly inspiring story that will help children with vitiligo feel seen, embrace what makes them unique, and know they are perfect just the way they are. Its message of acceptance is one that children and adults alike can benefit from.”
Stella Pavlides
Founder, American Vitiligo Research Foundation (AVRF)
Sonia K. Mehta

About the Author

Sonia K. Mehta was diagnosed with vitiligo at age five. Today, she is an author, advocate, and speaker who is passionate about helping children embrace their differences and shine with confidence.

MEET SONIA →
Your differences make you
shine.
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✦ About the Book

Leela's Special Spots

Leela's Special Spots hardcover

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.

✦ 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
Nova
Meet Nova
A furry purple alien covered in spots — who helps Leela discover that her differences are what make her shine
Meet Nova — from illustration to real life!

✦ 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.

BUY ON AMAZON Meet the Author →
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✦ 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.

Buy on Amazon ✦
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✦ Vitiligo Awareness ✦

Understanding Vitiligo

Vitiligo is at the heart of Leela's story — and part of the lives of millions of people around the world.

Vitiligo is a chronic autoimmune condition that causes areas of the skin to lose pigment, resulting in lighter or white patches. It can affect people of any age, race, ethnicity, or skin tone, and every person's pattern and experience with vitiligo is different.

For many people, the physical changes are only one part of the experience. Because vitiligo is visible, it can also affect self-esteem, confidence, and emotional well-being — particularly for children and adolescents. Greater awareness and representation can help replace misconceptions and stigma with understanding and acceptance.

0.5–2%
of the global population has vitiligo
70M+
people worldwide are affected
20–30%
of people with vitiligo are children
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 usually does not make a person feel sick. It mainly changes the color of the skin. Because the lighter patches have less melanin, they can sunburn more easily and need extra protection from the sun. Some people with vitiligo may also develop another autoimmune condition, such as thyroid disease, but this does not happen to everyone. Vitiligo can also affect feelings and self-confidence, so emotional support is important, too.
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
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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 who appeared in Dolphin Tale 2 and whose severe sunburn left white patches on his skin.

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 K. Mehta with her book and hand-crocheted Nova plush

Sonia with Leela's Special Spots and her hand-crocheted Nova plush

✦ 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.

2018 — Brooklyn Bridge Vitiligo Awareness Walk

Participated with her family in the AVRF-sponsored walk-a-thon across the Brooklyn Bridge, raising awareness of vitiligo and supporting the organization through donations and community involvement.

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.

Creating the Book

Drawing on her experiences, Sonia wrote Leela's Special Spots and collaborated with illustrator Lauren Austin to bring Leela and Nova to life. She developed the project from its original concept through publication.

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 ↗
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Front Cover
Back Cover

Leela's Special Spots

Now Available on Amazon

Leela's Special Spots is here! Order your copy on Amazon and share Leela and Nova's story with the children in your life.

Buy on Amazon
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✦ 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

Conferences & Events

In-person and virtual — 2026 and beyond
World Vitiligo Day 2026 — Global Events Worldwide · June 25
40+ countries hosting events. Find one near you or join online. The VRF tracks and lists all global World Vitiligo Day events.
vrfoundation.org/events
June 25, 2026
World Vitiligo Day USA 2026 — Tampa, Florida
3-day annual GVF conference featuring dermatology Q&As, expert speakers, breakout sessions, and hundreds of vitiligo families.
globalvitiligofoundation.org
June 2026
GVF Annual Scientific Symposium — Denver, CO · March 26, 2026
Top vitiligo researchers present the latest science and treatment breakthroughs. Open to patients, advocates, and clinicians.
globalvitiligofoundation.org/events
March 26, 2026
Vitiligo Society — WVD 2026 Online Event & Year-Round Webinars
Global Zoom event on June 25, 2026 plus regular webinars, camouflage workshops, and monthly virtual support groups all year.
vitiligosociety.org
Online · June 25
WVD USA Conference Archive — VITFriends
Full history of every World Vitiligo Day USA conference since 2016 with past schedules, speakers, and how to get involved in future events.
vitfriends.org/events
Archive

✦ 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.

Buy the Book Learn About Vitiligo

✦ Medical Disclaimer ✦

The information and resources provided on this website concerning vitiligo, skin health, and related subjects are intended for general educational and informational purposes only. They do not constitute medical advice, diagnosis, or treatment and are not a substitute for consultation with a qualified physician, dermatologist, or other healthcare professional.

Always seek the advice of a qualified healthcare professional regarding any questions about a medical condition or treatment. Never disregard professional medical advice or delay seeking it because of information found on this website.

Links to outside organizations and resources are provided for general informational purposes. Special Spots Studio does not control and is not responsible for the content, medical accuracy, privacy practices, or availability of third-party websites.

Parents and caregivers should review website resources before sharing them with children.

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✦ 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 here for updates.

← Back to Giving Back Buy the Book
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✦ Free Download ✦

Free Coloring Pages

Enjoy all of Leela & Nova's printable coloring pages and activities — totally free for kids!

Leela's Special Spots Activity Pack

All 7 pages bundled into one printable PDF!

Activity Pack Cover
Activity Pack Cover
Color Nova
Color Nova
Our Differences Make Us Shine
Our Differences Make Us Shine
Create Your Own Alien Friend
Create Your Own Alien Friend
Design Nova's Planet
Design Nova's Planet
My Special Spots — Draw Yourself
My Special Spots — Draw Yourself
Maze: Help Leela Find Nova
Maze: Help Leela Find Nova
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✦ Legal ✦

Privacy Policy

Effective Date: June 2026

Special Spots Studio operates the My Special Spots website at myspecialspots.com. This Privacy Policy explains what information may be collected when you visit the website and how that information is used.

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✦ Legal ✦

Terms of Use

Effective Date: September 14, 2026

Welcome to myspecialspots.com, operated by Special Spots Studio. By using this website, you agree to these Terms of Use. If you do not agree, please do not use the website.

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This website provides information about Leela's Special Spots, its author, related educational resources, and the mission of My Special Spots.

The website's content is provided for general educational and informational purposes only.

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Unless otherwise stated, the text, graphics, characters, logos, photographs, illustrations, downloads, and other materials appearing on this website are owned by or licensed to Special Spots Studio and are protected by applicable copyright and intellectual-property laws.

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Please review our Medical Disclaimer for additional information.

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Nothing in these Terms excludes any rights or responsibilities that cannot legally be excluded.

Governing Law

These Terms are governed by the laws of the State of New Jersey, without regard to conflict-of-law principles.

Changes to These Terms

We may update these Terms of Use periodically. Changes will be posted on this page with a revised effective date. Continued use of the website after changes are posted constitutes acceptance of the revised Terms.

Contact

Questions about these Terms may be sent to:
Special Spots Studio
Email: info@myspecialspots.com

CONTACT PRIVACY POLICY TERMS OF USE
© 2025 Special Spots Studio

✦ Get in Touch ✦

Contact Us

We would love to hear from parents, caregivers, educators, librarians, community organizations, members of the vitiligo community, and the media.

For questions about Leela's Special Spots, classroom or community events, media inquiries, or general information, please use the form below or email info@myspecialspots.com.

Please do not send medical information or sensitive personal information. Special Spots Studio cannot provide medical advice or answer questions about individual medical conditions.

A Note for Children

If you are under 13, please do not send us your name, email address, photograph, or other personal information. Ask a parent or legal guardian to contact us for you.

This contact form is for adult use only

CONTACT PRIVACY POLICY TERMS OF USE
© 2025 Special Spots Studio