First hearing that you have vitiligo can be an overwhelming feeling filled with confusion on how or why it happened. We have information for the newly diagnosed or those who have lived with vitiligo for a long time. Click the button below for additional information.

Treatment Options

From topical and oral medication to phototherapy and surgical options, we have information on them all. Click the link below.


See what vitiligo events are happening in your area, or around the world.

Our Mission

To improve the quality of life for individuals with vitiligo through education, research, clinical care, and community support.

How we can help

You don’t have to do this alone. GVF is here to offer guidance, templates, and the opportunity for connection.

Support Groups

Support. Learn. Grow. Friendship.

Insurance and Reimbursement

Download forms and Read how-to info

Living Well with Vitiligo

Vitiligo is only part of who you are. Watch and Listen as professionals share valuable information on living well with vitiligo.

Education and Events

GVF Hosts events throughout the year both in-person and virtual events to support the ongoing needs and education of those with vitiligo. We also share information from support groups and other vitiligo organziations.

My Vitiligo Team

Vitiligo Social Network

My Vitiligo Team is the official GVF social network for people with vitiligo. GVF will be collaborating with MVT to bring important content to the MVT community.

Give Back

Clinical Research, Volunteer, Donate

We can’t do it without you.
GVF is a 501(c)3 nonprofit that thrives on the support of individuals like you.

A special thank you to our 2023 sponsors and supporters

Diamond Sponsor ($250K+)

Gold Sponsor ($50K – $99.9K)

Silver Sponsor ($25K – $49.9K)

Bronze Sponsor ($10K – $24.9K)