I am a physician-scientist who focuses my clinical and research efforts on vitiligo, and therefore I think about this disease a lot – all the time, in fact. Therefore I thought it would be helpful to share my thoughts with others who are interested in vitiligo as well, particularly the patients who suffer from it and their loved ones. I want to make clear that while I am affiliated with many vitiligo organizations, my comments in this blog are my own, and do not reflect the opinions of those organizations. In addition, my research is largely focused on finding new treatments, and ultimately a cure, for vitiligo. This work is supported by a number of sources, including pharmaceutical companies, which by definition creates potential conflicts of interest. In full disclosure, here is a list of our vitiligo research supporters. Please know that, to the best of my ability, all of my comments are unbiased reflections of my understanding of vitiligo as both a physician and scientist. I do not permit advertisements on my website, and do not endorse companies or products that may advertise on other sites that may be referenced here.
This has been a tremendous year for us in the Vitiligo Clinic and Research Center at UMass Chan Medical School. It’s fun to reflect at this time and to think about the hard work done for vitiligo and its potential global impact! I am currently on a much-needed vacation with my wife’s family near Chicago, and I’m using some of my downtime to think and write this summary about the year. There were some ups and downs, but mostly ups, and next year promises to bring even more excitement. Read more...
This blog post in response to multiple exciting and generous requests to help support our research effort to find a cure for vitiligo. I have been touched by the unsolicited outreach by readers all over the world who are just as passionate as we are about improving the lives of tens of millions with vitiligo. In response, we have set up a user-friendly and safe method to donate to support our work. At the end of the blog post there is a link to do just that. I’ll also outline what we have done so far with donor support, and tell you where we’d like to go in the future if we have sufficient resources to do it. You can help!
We recently published our research study in the journal Science Translational Medicine in which we found a new immune pathway that could be targeted as a treatment for the disease. You can read the actual article hereif you’re interested, although it’s pretty dense reading. For those who would like a lighter summary of what we found, you can read the rest of this blog post.
Happy New Year! A lot has happened in our lives in 2017, and the vitiligo community is no exception. While I have become more and more busy since I started this blog, I do recognize its importance to those who read it, and heard the requests for updates on vitiligo research and clinical care. So here is one, looking back at 2017 and forward to 2018!