VITILIGO Friends "VITFriends"

A Vitiligo Support Community of FRIENDS

NEWS and Updates...

Minnesota's Upcoming meeting

 Saturday September 8th 2018


Sheridan Park

2801 W 65th St Richfield 


 Proud Sponsors of Minnesota VITFriends




Alicia's Presentation

at Mayo Clinic in Rochester Minnesota





Our group was recently featured on Twin Cities Live.


Minnesota's first annual Vitiligo Picnic

 Alicia's appearance on Fox 9  


Saturday, September 8 at 11:30 AM - 2:30 PM
Sheridan Park
2801 W 65th St, Richfield, MN 55423

WELCOME Minnesota!

 Meet our Leader - Alicia Roufs of New  Prague, MN


Alicia Roufs reports... that I has had vitiligo since I was three months old.   I have never known myself without vitiligo.  It has shaped who I am, and how I am. What’s underneath my spotted exterior is what matters most to me and others.  I’m not gonna lie and tell you everything was wonderful growing up.  Having vitiligo at such a young age was very hard.  Kids are very cruel and I was called every name you can imagine.  It definitely made me a stronger more outspoken person.   I wasn’t going to let a silly little skin disease rule my life.  I learned to be the class clown and make jokes.  I figured if they could laugh with me, it was stopping them from laughing at me.


The doctors have linked my vitiligo to my mother developing hypothyroidism before she was pregnant with me.  I guess auto immune diseases run in my family.  My sister also has hypothyroidism, and I have diabetes on both sides.  I have developed Graves’ Disease which is also an auto immune disease.   It’s amazing to me how so much is linked together.  I have never used make up or tried any treatment for my vitiligo.  I have just used my self-confidence to get me through it.   I wouldn’t say I have given up hope for a cure, but I think I have come to the realization that trying to cure an auto immune disease isn’t probably going to happen in my lifetime.  

I am married to an awesome man Dominic Roufs, who is a huge supporter of my vitiligo awareness efforts.  I also have one son named Herbie who thinks that vitiligo ROCKS!!  We live in a small town in Minnesota in our home with our dog Bob.  We are very blessed people and are very lucky for all we have. 



My goal with our group here in Minnesota, is to bring everyone together and let them know that there are so many people with vit just like them.  I would have given anything growing up to know someone else with vitiligo.  I also want to be a link between doctors and dermatologist for patients with vitiligo who feel they have nowhere to turn.  I also want to help educate the medical community on vitiligo since many people who work in it have never even heard of vit. 


I am proud that I can sit here and say I have vitiligo.  I have no problem educating those around me and informing what I have.  I have been truly blessed to have such a supportive and loving family to lean on during tough and unsure times.  I have loved meeting fellow vitiligo people via FaceBook and offering advice and a shoulder to lean on.  It has given me a much greater purpose.  I know that God doesn’t make mistakes.  He gave me this disease because he knew I could handle it and help others.  I am glad he did.  Because really, those who mind don’t matter, and those who matter don’t mind.  


Be sure to check out our local Minnesota Support page on






You Tube 


For details email: 






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