VITILIGO Friends "VITFriends" 

A Vitiligo Support Community of FRIENDS

What FOLKS are saying:





Your Thoughts: (Ask about our Life Coach packages or visit our President's page)


....Share your Thoughts.... 


January 2016

My name is Kim Mitchell and I have had vitiligo most of my life.  I am a 48 year old woman I can't tell you when it started.  I was a preteen when I first noticed my first spots early all my vitiligo was concentrated to areas of my body that I was able to hide in the last 10 years my vitiligo has gotten more aggressive and has spread over a large portion of my body.

I'm looking for Support.  I'm trying to learn how to get comfortable living in my new skin.  I appreciate your time listening to my story.  I live in Long Beach California and I am looking to connect with a local support group.  Thank you!


January 2016

I am Rev. Dr. Wallace Henry, III and was originally diagnosed with Vitiligo in April of 2013.   I was initially very shocked and had a million questions for my doctor about how and why did this show up in me. Unfortunately very few were answered so I began my own research.  After an unsuccessful response from topical creams I began using more homeopathic treatments and had minimal results.  In the fall of 2014 I began ultraviolent treatment that showed some success with re-pigmentation however it was limited.   In terms of an emotional response, I initially saw it as just a skin issue that was going to go away before the diagnosis.   Once diagnosed, I soon began using a cover foundation that was a summer nightmare and a lot of work.  After holding a meeting with my staff one day I looking in a mirror I discovered that my “makeup” had ran and that everyone already saw and knew something was going on, so I said oh well enough of that.  That was the last time I wore a cover regularly.   I was slowly beginning to accept the reality that I may lose my skin color.  I think the journey to accepting this change in my life was slow and once I got over the fear I began to live beyond it.

 As an Assistant Pastor I was very open with my congregation and struggle with the changes I was experiencing.   I am thankful to God for the peace and the strength to deal with the deck I was given.   One of the things that made me seek out VITFriends was the need to share my struggle with those who also were experiencing it.  Unfortunately I did not find a support group here in DC and so my goal was to start one.   I previously ran a HIV support group in Atlanta and now I want to take my experience and help others connect and advocate for themselves around Vitilogo.




September 2015 

I am fine.I have had vilitigo for near 30 years now. Started with patches on my arms, I thought at first they where scars from a horrible accident I had when I was in my teens when my hand went right through some glass. The little white areas grew. As of today 45% of my body is covered. I was seeing a specialist about a liver disease when he spotted The things people listen to and believe wow. I am not ashamed of my vitiligo. In fact one day a man was picking on some African males in front of a bar. I said I have parts about me that you like and dislike all at the same time. I showed him. I said see, you can pick a color on me that you like or dislike. The man had nothing to say. The males thanked me for standing up for them.  I live in Windsor Ontario Canada, and I have found no support group in Canada that supports Vitiligo. I would love to be a part of a support group. I know how each one feels having it. I can send pictures of my vitiligo. I am white so the vitiligo is not as pronounced as someone with darker skin. I am a person that likes more to personality than color of skin I think this is why it does not bother so much. I do hope you accept me into your group even though I am Canadian, even though you are USA based. I am working on my own stuff about vitiligo and get more Canadians aware of it, other than promotions for products that suppose to help it. We need more awareness. Others out there need to know they are not alone. I have heard of others but never got the contact. I will keep working at it.

- J Gallant


Hello: Education/Awareness is important. Today, I took my mother to a meeting

about her health care coverage. It was cold inside of the auditorium, so

I stepped outside to get a jacket out of her car and also to move the car closer

for her. As I am walking back in, a college student was walking by, but she

stopped and started staring at me. The first thing that comes to my mind, Oh

here, we go, again, the strange looks/stares. But this time it was different, kind

of, I asked her was she alright? She had a puzzled/surprised look on her face. It

took her a minute, then, she said she thought I was hurt and it looked like I had

blood on my face(she did have sunglasses on) I said no, that I have vitiligo,

which is a skin condition that turns the melanin in my skin white. She still

didn't understand, then I said it was the same thing Micheal Jackson has. Then

she said, oh yeah, he bleached his skin, right? Then she asks does it hurt? she

was sorry I had vitiligo, and asked does it itch and is it contagious. No, that is not what happened, I googled "vitiligo" for her and showed her photos of people with

vitiligo and my photos of when my skin changed. She seemed to understand and

apologized for staring because, that was rude. I accepted her apology and when



- C. Brooks, Middle Georgia




June 2015

Introducing Shazaad Games our Brooklyn, NY - VITFriends Co-Leader:



My name is Azlin, and i am about to try my best to tell you my story as brief as i can. And honestly, i have been wanting to tell my story to someone so bad.Thank you. I was born perfect until the age of 28. I was one of the popular girl in school. I was smart, beautiful and had countless admirers. That was my past.

May 2007, in the first year of my wedding, i spotted white patches between both side of my legs. I thought it was some kind of temporary skin problem and just applied some skin cream on it. I gave birth to my first child on 2009 and ever since, the patches just keep spreading all over my body. I surfed the internet, and i did spend all my life saving to a specialist dermatologist to help me. I i was confirmed to have a vitiligo and there is no cure. I suffered the psychology breakdown effect of vitiligo, and i can't deny that I had thought of suicide. I had even asked my husband to just divorced me and start his life all over again with another woman and take care for our son. I felt as if i am done living, hopeless and useless.

The society i came from and living in currently thought "vitiligo" is some kind of cursed from God. My parents are Malaysian. Any child would turn to their parents when they are feeling down, am i right? I was not that lucky. I told them and showed them my vitiligo patches. My dad warned me about how my husband and my son would disgust with my condition. My mom, until today, warned me to hide myself, or cover my white patches whenever our family members came to visit. My younger sister and brother were my coolest buddies. Not much they can do but at least they never treated me as a "contagious" person. It hurts.

My husband's family was another challenge. His family especially my mother in law put "beauty appearance" above anything in order to be part of his family. She was a party-goer and as the daughter in law, i am expected to tag along. Only God knows how hard it was for me to live under the thick make up and worrying about my patches being noticed by anyone. My marriage will be devastated if any of my in law discover my condition. I find excuses after excuses to avoid seeing any of them. My mother in law was so pissed at me and started to bring up her "niece" drama up. "Niece's drama" was her broken dream. She had arranged for my husband to marry her niece whom she always praise as " supermodel" when my husband was 9 years old. However, her son had fallen in love with me and married me instead. Since then, she has been trying to poison me, ruin my marriage with untrue gossips, uses black magic on me and many more. She successfully stained my wedding day. For the respect i have for her, i keep hold on to this eggshell relationship.  So, just imagine if she find out that i have " vitiligo"?

My career was jeopardized because if vitiligo. I was one the number one Customer Service and Sales Rep in a company run by "not nice" middle eastern people. The General Manager prefer good looking girl over qualification. In the beginning i was promoted every 4 months. The moment the spots started to attack my both hands and fingers, and face, i felt as if i was demoted. From salary , i was put to hourly at a very low rate compare to my 10 years been working with the company. My income was too low and yet i have family to support. I begged for more hours and they granted it but my overtime hours was never counted at the overtime rate. October 2013, the employer promoted an illegal worker, a good looking girl who came from the same country as they are to take over my position. I was terminated without paperwork. I fought, and a few days after termination i received a threat called from the employer claiming that i had committed a fraud. They threaten to throw me in jail and to ruin my five years old son's life. I sort legal help and the threat stops. But, i never felt safe since then.

I try looking for another job, and so far 25 interviews has turned me down. Each interview i went to would end their interview questions informally with a question, " Where do you get those scars on your hand?" , which actually refer to my spotty hands and fingers. I am just able to throw them a silent smile. I am jobless until today. My husband is doing his best to support us three.

I don't see doctors when i am sick fearing that the doctors and the nurses would find me contagious. I don't go to hair saloon, beauty saloon or any social facilities fearing the same reason. I love to swim, and that too i wasn't able to enjoy it anymore.

So, tell me my dear vitFriends...what do you think so far about my experiences with vitiligo? It took me 2 years to recover from this suicide thought. I had to fight the thought using my last option, be close to God. Too many tears, i shared only with God. I have heard the verse that "God love us not by our appearance, but He love the "beauty" inside us"- and I made this as the reasons for me to continue living. I strive everyday to please God and not to please other people. Everytime the "breakdown" hit me, God send me a reminder. A reminder that tells me not to be frustrated with my condition , but be grateful as they are many others that are facing way more sad condition than i am. My husband loved me no matter how hard i have rejected to be with him. He loves me unconditionally. My five years old son love me dearly beyond his age.Every night i heard him whisper in his prayer to God, " God, please make my mom live long, happy and take away her white clouds ( he refer to the patches) that always make her upset.Amen."

2015 marks the 8th years of me living as a vitiligan. I am a stronger person with a positive thinking. I see boundless hope and opportunity in my future. I have discover those who are important in my life and those that i should care less. i talked openly about my condition to anyone who asked and curious about it. I see doctors when i am sick. I still exclude myself from the beauty parlors , because i don't feel they can do much. Lol. I believe God is giving me a second life, an amazing experience, and most important of all God is making me see His Everlasting Blessing.




March 2015

Luis Narváez - I have Vitiligo, I have never attended a meeting in my country Colombia, I would like to someday share with people like us around the world from an association I'm getting ahead, I hope I collaborate to establish the association in my country and more than especially in the city of Cali..donde reside and in which there are many of person in this condition.

Tengo Vitiligo, nunca he asistido a una reunion en mi país Colombia, me gustaria algún dia compartir con gente como nosotros de todo el mundo a partir de una asociación que estoy sacando adelante, espero me colaboren para fundar la asociación en mi país y mas que todo en la ciudad de Cali..donde resido y en la cual habemos muchas persona en esta condicion.





December 2014

Renee Rose - 12-31-2014: Hello and happy new year to you. I've had vitiligo for 12 years and I live in Nairobi Kenya. At first it was difficult living with vitiligo especially during my teen years but the love and support of my family made me strong and I was able to overcome it all. I've tried many treatments and am currently undergoing one for now. For me, it's only around the eyes, mouth and partly on my hands and neck.


October 2014:

From VITFriends:  Hooorah to our Jaeden

From Jaeden's MOM:  I am so happy to have learned about your site.. I, myself , do not have
Vitiligo. My 7 year old son Jaeden has Vitiligo. He has had vitiligo since he
was about 2 years old. His body is about 30 percent depigmented. His vitiligo is
in rapid movement these days. Not sure if it is because of summer and my son
being in our pool constantly, but it is moving fast.. My son has embraced his
and always seems to keep his wonderful smile on his face. I am so
grateful for your site. It allows me to educated my son about Vitiligo and gives
me a sense of support! Thank you for all you do!    J. Rodriguez


September 2014

I have taken photos since the diagnosis of Vitiligo, only to be asked this question..."where is your smile? Why aren't you smiling?

Like my husband would always say..."only who feels it...knows it." This simply means only those who are experiencing a certain thing...knows the pain...knows the cost of the thing.

Some days it is hard, it's painful to smile, but as time goes by, it gets easier and it gets better.

So, Do you think that Vitiligo has hindered, even slightly, your once enormous Smile?



July 2014

We WELCOME Michele Hanson from New Jersey. She is one of our newest fb friends and we love her take on vitiligo, so we had to share it with you

"To my VITFriends Vitiligo Support Group friends all over this world. Thinking about us this morning and I ask that you not only be encouraged, but think of your skin change as the transformation of the caterpillar/butterfly. It's very hard walking this out and many pray that God would restore your pigment, I know because I do too. Yet in the waiting and walking this out I've realized, that the transformation, like the butterfly happens on the inside first! The caterpillar wraps himself in a cocoon and within that cocoon a beautiful process happens, it's called change. I don't know if you know it, but many of us who are walking with vitiligo have undergone not only an outside transformation, but an inner one too. This walk has made me more compassionate, humble, loving, less complaining, more understanding and patient...along with many other things (think about what has changed for the good for you). So as you go through life with vitiligo and wait for either a cure or re-pigment, think of how beautiful God made you and how He believed that you were the right person for this cocoon experience in order to have an awesome transformation, inside and out!"






December 2012

Pakistan - Hello and Hi everybody,

Am really Glad to be a member of this association for the people having the Vitiligo, i have had already take part of this society, though am not in the position to Donate this Association for the people having Skin disorder, but my feelings goes towards all of them, i think there is no difference of color , but all is about our way to live our Minds, We must love ourselves and in the same ways we must give love to our next.
I actually do not have lot to ask or to make questions here, but to appreciate this association to make more success and to give only some tap on shoulders to make more efforts to gather and to collect all of the people having this kind of skin disorder,
I would like to know if i can Join personally to the incoming Conference in next year , which will be holding on Boston.
Kindly let me know if You really can send me the Non objection paper for Visit for the people living abroad. I would be grateful to You.
i want to participate and start frequenting thoroughly all of it's conferences , Functions or celebrations or Parties and i want to make feel good my self and other people with Vitiligo by participating these parties.
Hamed Amin.

December 2010  -  To: Valarie - From: Kerusha - South Africa says:

Hello my frend i hope u well:-)Wud lyk 2say the following. You r a wonderful woman and amazing human being!Thank you 4the support u give 2ppl in general, u alwayz have g0od warm thoughts and such lovely words 2say.Thank u once m0re.U tk care:-)much love 2u.


April 22, 2009 - Sabrina, Chicago, IL 

Hi  Valarie,

Girl it is ok to vent, let it out! Just know that you are beautifully made. And I now think that everything happens to us for a reason, sometimes the reason is just not obvious. Let me share something with you, when I first got the diagnosis, I felt myself going into a deep and dark depression. Now this is from a woman that LOVES the LORD with all my heart, I was raised in a God fearing home, the whole 9yrds. I did not understand why this is happening to me. I felt like this was somehow my fault, or punishment for something I did in my past. I questioned God as to why he placed this burden of all things, on me. And I was almost at the point of giving up.

Valarie the day before I wrote my very first email to you, I wrote out my suicide note and my last will and testament. I had decided that if this disease got to the point that I could not take it, then I would take the easy way out.(I was ready to commit the ultimate sin) I felt my quality of life was more important, and with vitiligo I saw it as a death sentence. This was my thought process almost a month ago to the day. I was scared, confused, angry, angry, angry, hurt, sad, scared, scared and scared!

Then I found your website and met YOU! And Valarie I don’t know if you have a direct link to GOD but whatever you did or said in your prayer for me worked a miracle. You pulled me off the edge of the cliff, just as I was ready to jump. Your encouraging words were proof that LIFE GOES ON WITH VITILIGO! You encouraged me to hang in there a little while longer! To be strong and know that GOD is in and will always be in control. When I saw your picture on the internet I saw a beautiful woman, living and doing great things with vitiligo. I feel stronger because of YOU. (I HAVE TO STOP NOW BECAUSE I’M AT WORK AND I’M STARTING TO CRY. (SO NOT SEXY) lol. I just wanted you to know that, and I understand that it’s hard not being able to do the things you use to do, or the way you use to do them, but think of all the new and wonderful things that you can do as a result of this disease. Take solace in knowing that vitiligo helped you save a person’s life. MINE!

Love you!





Feb. 23, 2009 - Robert (London, England)

Dear Valerie,

My name is Robert, I have recently been using the social networking site ‘Facebook’ as a forum, I created a group on there which has in excess of 300 members who all join in discussion about vitiligo and their own personal experiences. Having vitiligo myself I know that being able to talk to someone else who understands and realising that I wasn’t alone was great help. It was through Facebook that I saw the note from your Son about I have looked at your site and can I say that you have done an amazing job getting everything set up.

If I can I would like to give you some background on myself. I first developed vitiligo at the age of 2; it was presented as a small triangle above my belly button. It remained as that for 5-6 years. It was then that I was really affected. I lost 70% of my pigment in a very short space of time. I was here that I learn something that a child shouldn’t really think ‘Life can be cruel’. I was lucky that my Medical Practitioner knew (only a small amount) some information on vitiligo and I was referred to a specialist.

From here I was given some Topical Steroids to use. These had no effect on my vitiligo, however they did cause my shins to bleed a lot during football (soccer). So on my next visit 4 months later I was taken off those creams and tried on another cream (a trial cream) which my mum gave permission for me to use. Once again no results. By now I was around the age of 8 or 9, I had been on holiday and was devastated by the way people including adults reacted to my skin (for the next 5 years on holiday I would wear long trousers and a long sleeve top, even on the hottest of days) My confidence had gone completely and I was heading downward in a destructive spiral. I began to stop communicating with people, I bottled everything up inside. I cried myself to sleep for a number of years.

I think the worst part for me was trying something I believed would make me better, and then seeing that nothing worked. The next recommendation for me was a treatment known as PUVA which I am sure that you are aware of. I went for the consultation and they then showed me the goggles that I would have to wear 24 hours after treatment. Straight away my answer was NO. I was only about ten at the time. I said to my mum, people look at me enough already why would I want another reason for them to do so. Once again another possibility taken away from me. My hopes were finally crushed.

The next major event that was coming up in life was my 11+ Exams to move on up to secondary school. Unfortunately the night before those exams I attempted to commit suicide. As you can probably guess my exams did not go that well. However from here onward was slowly the start of a change in my life. I went to a group called ‘Changing Faces’ where I received one on one sessions, creating my tool box on how to deal with people who don’t understand.  In theory it was great however in the real world things aren’t always as simple. I did gradually adapt these to my own personality and way of thinking. They did tell my mum about a group called the ‘British Red Cross’ who are a free service offering camouflage. This was something that I went to and initially liked. I saw a normal leg and torso when I looked in the mirror. I felt a brief moment of happiness. The next years holiday I wore the camouflage, for 2 days. I woke up the third morning and I said to my mum, I don’t want to do it. I said why should I have to cover up. It’s not me with the problem I am fine its them. To this day neither me or my mum know what changed in me that night. But as they say it was the start of the rest of my life. From that day on vitiligo and treatment were never mentioned in the same sentence.

Then when I was 15 my friend Harry invited me away to Florida with his dad. Of course I accepted. It was here that I finally decided I know what I’ve been told by doctors, about the risks involved with sun. I decided no they were wrong. Everyday I was in shorts and no top. I wore no sun cream. I admit my patches went a rose colour. But something happened. I repigmented to 40% in 2 weeks. Not to mention the confidence I had. That hole holiday, I would talk to pretty girls on the beach. Which taught me something else, vitiligo doesn’t make someone ugly unless they let it. I would chat away and if any asked about my vitiligo, I explained what it was and they were fine with it. That holiday changed my life, I got home and my mum was amazed to see the difference in pigment and in me. I was smiling and not just one day, but all the time. She was also amazed at the clothes I had bought. I bought a bright yellow pair of combat trousers (which I still own and to this day remain my favourite piece of clothing) and many other weird and colourful clothing.

I had finally fully embraced my vitiligo as a part of me, I actually thought to myself. I like the attention I get, people staring at me. This is where the clothes came into play. So that even when I’m covered up people still stare. For a 15 year old I think that was quiet an achievement. My confidence then went through the roof. I was no longer afraid to expose myself. I stared to get into relationships with girls, I would play football in just shorts. I even began to volunteer at the Vitiligo Society taking part in a DVD we produced about vitiligo.

Since then over the years my mum would take me away to hot places and gradually my vitiligo is still getting better, I am now only 20% covered (if that). I am now 20 years old, just over a year ago I proposed to the woman that I love, and she said yes. Not only that but we also now have a 4 month old baby boy. Throughout my life even after having accepted my vitiligo I was still worried that no one would want to settle down with me and have children. I was wrong, she supports me in everything that I do and I could not ask to blessed with anything more beautiful than my son, he is such a happy baby always smiling and playing. He even sleeps through the night. Even after those days that go on, I get home and one smile from him gives me such a boost. And the best thing about my life is, I wouldn’t change having vitiligo if I had the chance to. I honestly believe that my vitiligo has given me the compassion and love that I have for all things, I have not one nasty bone in my body, and I also believe that my vitiligo has given me the confidence that I have. All my friends and Family tell that I am Vein and that I Love myself. I say to them back ‘and’ I do love myself I think I am beautiful and I think that everyone else is beautiful. And the only thing in my life that I can put all that down to is my vitiligo.

I now work for the society and I hope to eventually be able to talk to (not council because I don’t agree with the term) young people with vitiligo, I want to be able to relay my experiences to them so that they know it’s not the end of the world, there is a very small percentage of people out there who are genuinely nasty people, everyone else is quiet accepting. I want them to know that they can find love. But it is all about believing in yourself. As long as you see your vitiligo as a good thing then it doesn’t matter about other people.

I am sorry for having typed so much, I hope you took the time to read it as I like to be able to share my experiences. I was mainly writing to start correspondence, I believe that eventually we will be able to get a forum going, which is accessed by members of vitiligo groups etc from around the world. On facebook alone there are 4 groups. If there was one big forum, with different topics obviously. Could you imagine the potential in that. I believe so many people would feel better about themselves and their lives with vitiligo.

Thank you for taking the time to read this, and I hope to hear form you soon,

Kindest regards,



December 30, 2008 - Crandall (Kansas)  "I am Blessed!  All I have had to deal with in my life is VIT, which started @ the age of 9 yr old. It was Tuff as Hell in school to deal with in them Days.  It was also very hard to get jobs. Val it has been good to talk to you ,  the Chief in command ! I feel so good you took time to talk to Me, just a person ,  thank you my forever friend... Crandall"


July 10, 2007 - Vera - My Vit is getting worse on my face, my arms are almost completely white, my legs half brown, half white and my torso almost completely white.  I've almost gotten to the stage that I'm going to stop wearing make-up on my face.  It doesn't last all day and what the heck, the rest of my body is white. My grandson and I went to Ravinia with our "Grandparents raising grandkids group" saturday and he said he noticed people staring at me.  I guess that's the first time he noticed it.  He's 13 years old.  He said to me why do people stare at you?  How would they feel if people stared at them? He loves me unconditionly and that's all that matters.




Moressa - St. Thomas, United States Virgin Islands

I am so glad that I took the time to visit your website. I never really knew much about this condition, but now I know. God is good and God is great and he WILL take care of you. I Love you always no matter what you are my sister.

Rev. Mark Williams - New York, NY

It was interesting and informative to visit the website. Know that it doesn't matter to me what you look like, you will always be loved by me and our family. You can count on loving support from your cousins in New York cause girl you are the bomb.


Herman - Boston, MA  (Bank Director)

"The ultimate measure of a man(WOMAN) is not where he/SHE stands in moments of comfort and convenience, but where he/SHE stands at times of challenge and controversy." --Dr. Martin Luther King, Jr.


Betty - Paducah, Kentucky    "We Might as Well DANCE"

Life may not be the party we hoped for, but while we are here we might as well dance..... 

"In the end, it's not the years in your life that count, it's the life in your years."  - Abraham Lincoln




Our GOAL is to Educate and to ADVOCATE......




Well known recording artist Mary J. Blige, in an interview with Essence magazine in August 2010 made this statement:


"You're all you have. If you don't think you're beautiful, no one else will." 






Please read this story and share your thoughts with us:






BIG....NEWS!!!!! - 1 Samuel 16:7

For the LORD seeth not as man seeth; for man looketh on the outward appearance, but the LORD looketh on the heart. Amen!

Live GODS perfect will for your Life    ...He knows what that is     ...So, you just....LIVE!


Take a moment, look in the mirror and Say......"Today, I declare that I am BEAUTIFUL!"


If King David in the Holy Bible said it...I can say it too....... and so can YOU!    This is what he said.......Psalm 139:14  "I praise and thank you GOD because I am BEAUTIFULLY AND WONDERFULLY made."


Also Remember that  - GOD does everything well!

If the world can't see our outward BEAUTY - Let's make sure they see the inward BEAUTY!

We are special to GOD....

If God had a refrigerator, your picture would be on it.  If he had a wallet, your photo would be in it. He sends you flowers every spring and a sunrise every morning. Whenever you want to talk, He WILL listen. He can live anywhere in the universe, but HE chooses your heartÂ…Face it, VITfriend - God is crazy about you.


Live your best life NOW.....Just like our Vitiligo Friends of North Carolina.....June 2011.




Be Blessed!

Someone will always be prettier.
Someone will always be smarter.

Some of their houses will be bigger.
Some will drive a better car.

Their children will do better in school.
And their husband will fix more things around the house.

So let it go, and love you and your circumstances.

Think about it! The prettiest woman in the world can have hell in her heart.
And the most highly favored woman on your job may be unable to have children.

And the richest woman you know, may have the car, the house, the clothes~~~~
but maybe lonely. The BIBLE says, "If I have not Love, I am nothing."
So, again, love you. Love who you are.

Look in the mirror in the morning and smile and say,
"I am too Blessed to be Stressed and too Anointed to be Disappointed!"

REMEMBER: "Winners make things happen~~ Losers let things happen."
"To the world you might be one person,
but to one person you just could mean so much."

Be "Blessed"



Dorothea  -  Boston, MA (College Professor)

Good motto to live by ...."Life should NOT be a journey to the grave with the intention of arriving safely in an attractive and well preserved body, but rather to skid in sideways, Champagne in one hand - strawberries in the other, body thoroughly used up, totally worn out and screaming WOO HOO - What a Ride!"

From:  Lucy

I love this site. You have found an outlet for your pain and you use poetry. I to have vitiligo and are seeking on-line friends to talk to. So if any one wants a new friend just e-mail me at the above address and I will get back in touch. Lets stick together and help each other until a cure is found. One kind word or smile can brighten some one day.


From:  Sterlena Williams

Thanks for this site. I too have had vit for 53yrs I am completly white , I completed my turn when iI was 50yrs old no medicine just the Lord Jesus Christ. I am 66 yrs now.


Patricia Rossy

Hello to my new Vit Friends. I am glad to be apart of wonderful group of people. A unique people. God is about being creative and we are the canvas in which he does his work. God\'s Got It.


your website is very interesting, I love to read every single page in here. I am 33 live in Boston, MA, married and have 1 daughter. I got vit when I was 12.


From:  Glow

I am a 32yr old F. with Vit for about 4 yr. Mine started with a little patch in one finger and has prograssed a lot since.Part of my career intails drawing blood so it was difficult getting it on my hands. Some people ask if I got burned because I am brown P.R. I guess I have come to terms with it cause I have no choose but it can still be embarassing and makes me depressed at times. It is a comfort to know I am not alone in this feeling. Thank u for sharing all your stories. Maybe God will bless us with a cure soon!

FROM: Hunnee (Pat)

Great site Val. We can't let vit get us down. I try to keep an upbeat positive outlook . I notice people tend to look past the spots and patches because I am very open, approachable and most of all happy. I have been blessed in so many ways by the Almighty. I give thanks every day for my life, my friends and family. If anyone wants to vent, rant or just talk please feel free to email me.  LIVE LIFE LIKE YOU MEAN IT!!!



I live in Northern MA. on the east coast. I am interested in getting together some time. I hope in the near future. I have had Vit for 18 years now, and only recently 2-3 years it has taken over like wildfire. I am going to see a Dr. Bigby at Beth Isreal in Boston. I am thinking of depigmentation. I hope you can find sometime to keep in touch. your new friend Elvy.
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