Vitiligo Foundation of India: Advocacy & Patient Support
I co-founded the Vitiligo Foundation of India to build a community where patients, researchers, and dermatologists can connect, learn, and find real support.
This is the incredible group of over 200 delegates who participated in our inaugural Vitiligo Foundation of India CME & Workshop in New Delhi. The energy and enthusiasm to learn and collaborate were truly inspiring.
The core team of the Vitiligo Foundation of India, celebrating a successful inaugural event. I am so proud of what we have built together to support the Vitiligo community.
This slide shows the mission of the Vitiligo Foundation of India: to bring together dermatologists, researchers, and patients. As a founder member, launching this initiative on World Vitiligo Day was a dream come true.
A slide from our VFI conference illustrating our research strategy, which focuses on the seamless integration of clinical, translational, and basic research to find better solutions for Vitiligo.
During our VFI event, we were honored to have a virtual presentation from Dr. John Harris, a leading Vitiligo researcher. This slide shows his team and highlights the global collaborations we are fostering.
An artwork I shared for World Vitiligo Day. The theme "Looking into the Future" is fitting, as recent years have brought approved, effective treatments and promising research, offering real hope.
About Vitiligo Foundation of India: Advocacy & Patient Support
One of the most valuable resources we offer is our dedicated patient Q&A sessions, where we bridge the gap between academic research and your everyday concerns. Instead of searching for answers online, you can engage directly with experts who understand both the medical science and the emotional reality of living with vitiligo.
Our Mission at VFI
When I helped launch the Vitiligo Foundation of India, my goal was to create a space that looks beyond the clinic walls. For too long, the medical community and patients have operated in silos. My work here focuses on bringing together dermatologists, researchers, and families so that information is not just accessible, but understandable.
Why Support Matters
Living with vitiligo often involves more than just finding the right topical medication or phototherapy routine. It involves navigating the social and psychological aspects of pigment loss. Our foundation hosts regular workshops and forums where we discuss:
- Latest Research: Translating complex studies into practical knowledge you can use.
- Treatment Realities: Honest discussions about what procedures like melanocyte transplantation or JAK inhibitors can realistically achieve.
- Family Guidance: Resources for parents and partners to help them support their loved ones effectively.
Bridging the Gap
I believe that when you are better informed, you are more empowered in your own treatment journey. Through our conferences and CME (Continuing Medical Education) workshops, I invite leading experts to share insights on everything from surgical techniques to new therapeutic avenues. This isn't just about sharing academic papers; it is about ensuring that the advancements being made in labs across the globe eventually reach the patients in my clinic in Andheri West and beyond.
If you have been feeling overwhelmed by conflicting information or simply want to be part of a supportive, knowledgeable community, I encourage you to join our efforts. We are constantly updating our resources to provide you with the clarity you need.
Madhulika Mhatre
I started the Vitiligo Foundation of India because I realized my patients needed more than just a prescription. I am here to bridge the gap between complex research and your daily life, ensuring you never feel alone in this journey.
Find resources and related support
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