Forum

I'm certain I'm not alone in wishing to know what methods of treatment others have tried and with what success, where they live, when they were diagnosed, how old they are, what they eat, how much sun exposure they have had, what their thyroid levels are, and on.

Log-in to the database should record IP address, but otherwise should only record a number, not our names or any other identifier about us.

This research can be used by us, but more importantly by the medical community.

We are living it and can tell our story, by facts, better than anyone else, doctor or otherwise.

With the existence our columnar data, we and our researchers can sort based on diet, age, nationality, thyroid levels, genetic predisposition based on parents and siblings having Vitiligo, contagion based on spouses having or not having Vitiligo, and on.

How about it, Steve, or others?  Does anyone see the value in this, and can we get it going?

Thanks,

Tom