COVID-19 and Vitiligo Essential Updates
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I would like to find help with my vitiligo
You might find this new clinical trial education center useful. https://www.myvitiligoteam.com/resources/vitili...
Hello, Could Someone Please Tell Me How I Can Contact Or Directly Ask A Question To Dr. John Harris???
Thank you so much
I just noticed this message that you sent to me, right now.
I Was Told By A Health Provider To Take Vitamin D3 And Magnesium Glycinate To Slow Down The Vitiligo.
I have no insurance. And want some insite as to what I can use over the counter to fade the vitiligo spots? It's spreading everywhere faster than ever before. Is it something I am eating?
Mamabear4
Thank You for your advice and for reaching out to me. It's appreciated. I was told that stress is the main cause of this autoimmune deficiency. And to me it's difficult to handle everyday… read more
Any One Using Steroids To Treat Their Vitiligo? My New Derm Prescribed Demexadone (spelling). Too Many Side Effects For Me. Anyone Using?
What oral pill are you taking. I thought the pill was still in the final stage of clinical trial.
Those Taking Opzelura, Have You Experienced Any Increase Of More Serious Side Affects? I Am Fearful Of Being More Susceptible To Cancers!
Has Anyone Found An Alternative To Opzulera. I Received A Free Trial And It Worked Extremely Well And Very Quick On My Face.
I tried tacrolimus 0.1% ,clobetasol 0.05%
Alternating them weekly.
Unfortunately did not see any improvement
Anyone Interested In A Vitiligo Clinical Trial?
Please contact me if you are interested in participating. You maybe compensated for your time and travel.
(Phone number can only be seen by MyVitiligoTeam users)
(Email address can only be seen by MyVitiligoTeam users)
How did the trial go?
How Do I Find A Doctor In My Area Who Treats Vitiligo?
I Have Tried For 2 Years To Get My Insurance To Cover Opzelura With No Luck. Is There Anyway To Get It Covered?
I have had vitiligo for approximately 8 years. I am 63. In 2020 I was doing xtrac and light therapy. It brought back about 80% of my pigment. Then covid shut it all down. I am worse now then I was then.
I continue to use light treatment and only use Opzelura only on my hands and a few small spots on my face. The light treatment helped everywhere except my hands and face.
Anyone With Vitialgo Has Autoimmune Deficiency With IGA And IGM? My 7 Years Old Was Recently Diagnosed With IGA IGM Deficiency And Vitialgo
It seems that his vitialgo is getting worse and some red spots also showing. He hardly eat and lacks iron. Anyone with similar condition or has some info please share. I am sharing a photo of some of his spots.
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