I have not discussed this with any doctor because it scares me. However I have the question of whether this is to return the skin color and is it an ongoing treatment? Is it expensive treatment?

Thank you,
Martina.

I’m wondering what other conditions people got after being diagnosed with vitiligo. Or before for that matter. I’ve seen some discussions of psoriasis. What other conditions did you get? Did they come before or after the vitiligo?

If anyone would be so kind as to answer this question. I know everyone’s spots are different and unique, but was just getting a sense of an idea on what’s going on with my hands. Even though this can be different for everyone, this helps me get a bit calm in understanding how it happened to others, plus I LOVE hearing everyone’s story about how it started with vitiligo. This helps me not feel so alone with this next chapter of vitiligo.

I pray this doesn’t seem intrusive to anyone. So if… read more

I was told this by two doctors that Vitiligo is a fungus -I was also told by a dermatologist that is also associated and related to Hypo Thyroidism -Does anyone else have any information on this ? Are both Autoimmune issues too? Any feedback greatly appreciated

Kindly TL

So true first world problem....as part of a performance award in my corporate role, will get to go to a resort in Mexico. I ought to be thrilled. Yet, my anxiety over how to not be "the weird one" and avoid the sun on the beach while trying to be part of the group has me a bit stressed. Self imposed anxiety, right? Anyone else have universal vitiligo and try to "fit in" on a flipping beach? Lol...