Burberry Scarf


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Comments for VITSAF http://www.vitsaf.org Vitiligo Support and Awareness Foundation Sat, 31 Dec 2011 14:57:07 +0000 hourly 1 http://wordpress.org/?v=3.2.1 Comment on Share Ur Story by VITSAF http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-488 VITSAF Sat, 31 Dec 2011 14:57:07 +0000 http://vitsaf.org/blog/#comment-488 Hello kenny, I am sorry replying this late, I had replied before, but guess it didnt upload possibly due to network issues. I sent you an email as promised but yet to read from you. One thing I can tell you is that you should try and think and worry less about Vitiligo because the more you think and worry about it the more it gets. Let your daughter understand what Vitiligo is, start educating her as much as you can. Believe me people are actually not staring at you that much, you are only calling their attention to it by your carriage and way of living with it. I believe you got my sms, let me know how you are today and how you are feeling now. Welcome to 2012! Hello kenny,
I am sorry replying this late, I had replied before, but guess it didnt upload possibly due to network issues.
I sent you an email as promised but yet to read from you. One thing I can tell you is that you should try and think and worry less about Vitiligo because the more you think and worry about it the more it gets. Let your daughter understand what Vitiligo is, start educating her as much as you can. Believe me people are actually not staring at you that much, you are only calling their attention to it by your carriage and way of living with it.
I believe you got my sms, let me know how you are today and how you are feeling now.

Welcome to 2012!

]]>
Comment on Share Ur Story by VITSAF http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-487 VITSAF Sat, 31 Dec 2011 12:50:55 +0000 http://vitsaf.org/blog/#comment-487 Thoughts on Managing Vitiligo Naturally Dr. Ben Kim story Posted By Dr. Ben Kim http://www.drbenkim.com/vitiligo-natural-management.htm My experience with vitiligo started when I was nineteen years old. I was in my second year of university, struggling to meet academic expectations, and unhappy with my relationships at home. Ultimately, trying to meet my parents' expectations for my academic career and failing to reconcile the mixed feelings that I had about being a pastor's kid of a new church created more pressure than I was capable of handling. During this angst-filled time, I distinctly remember days when I would lie face down in bed and wish that I could get sick in some way so that there would be less expectations for my life. I guess on some level, I thought that if I became ill, my parents would feel sorry for me and show me that it was okay if I didn't fulfill their hopes for my life. After several months of constant stress, worry, and self-pity, I woke up one day and noticed a small patch of white skin under my right eye. I didn't think too much of it until a few days later, I noticed another white spot on my neck. A few weeks and several new spots later, a visit with our family doctor and a dermatologist led to a diagnosis of vitiligo. Over the next several years, unaware of how my diet and emotional stress were causing steady progression of my vitiligo, I went on to lose about 25 percent of my skin color. Fortunately, my studies led me to a field of promoting health via healthy living called natural hygiene. Over time, I came to an understanding of autoimmune illness, which helped me formulate a plan to address vitiligo through natural means. Here's what everyone with vitiligo should know: Your melanocytes (pigment-producing cells), unless irreversibly destroyed, are always ready and willing to restore pigment to your skin. In order to restore color to areas of your skin where your melanocytes are still functional, the key is to make sure that your diet and lifestyle (including emotional stress) don't continuously undo the re-pigmenting work that your melanocytes are constantly engaged in. If you read through my articles on the root causes of autoimmune illness and natural ways to prevent and reverse autoimmune illness, you'll have the knowledge you need to follow a diet and lifestyle that minimize the inflammation that characterizes the loss of skin color in people with vitiligo. To briefly summarize these dietary and lifestyle measures, they are: Eat a plant-centered diet - the bulk of your food choices should be vegetables, fruits, legumes, and whole grains that your body doesn't have trouble digesting. Ensure adequate intake of vitamin B12 and DHA (an omega-3 fatty acid that strict vegans tend to be deficient in). Ensure adequate vitamin D status through diet and sunlight exposure and supplementation if necessary. Avoid intake of dairy products and flesh meats. If you choose to eat some animal products, stick with small amounts of organic eggs and wild fish. Closer to raw is best. Lightly cooked is acceptable. Strive to be emotionally balanced. Work at being a master of managing emotional stressors. Get high quality sleep as often as possible. For most humans, nine to ten hours of restful sleep every day is an optimal amount. These measures give your melanocytes all the support that they could ask for to produce pigment in areas that need it, as well as to minimize new bouts of inflammation that can create more loss of skin color. But there is one other essential stimulus for re-pigmentation: sunlight exposure. Your melanocytes produce pigment (melanin) in response to sunlight exposure, as melanin serves to protect your skin against burning. The trouble with this requirement for re-pigmentation is that for someone with vitiligo, sunlight exposure is hard to tolerate physically and emotionally. On a pure physical level, the challenge is avoiding sunburn because areas with no pigment are unprotected against ultraviolet rays. For this challenge, I recommend being ultra conservative with sunlight exposure - just a few minutes at a time - and increasing intake of red beets, carrots, and dark green vegetables - these pigment-rich vegetables appear to provide some level of natural protection against sunburning from the inside-out. Just be careful not to overdo it with the beets and carrots if you have a problem with your blood sugar-regulating mechanisms, as these root vegetables are rich in natural sugars. Emotionally, sunlight exposure can be challenging because it leads to greater contrast between areas that still have pigment and areas that have lost pigment. And because some melanocytes in de-pigmented areas may no longer be functional, there's no guarantee of full re-pigmentation with sunlight exposure, which means that getting lots of sun can help stimulate some re-pigmentation, but at the cost of having the vitiligo that remains to be more noticeable. As someone who has lived with vitiligo for almost 20 years, I know full well that the emotional component of living with vitiligo can be a huge challenge; it's not an exaggeration to say that it can be crippling. Because you look different, particularly if you have darker complexion to begin with, having your vitiligo be more noticeable with sunlight exposure increases the number of stares that you get on the street. It can affect what you wear, your confidence level, and how you interact with others. Because everyone's situation is unique, I don't think there are any sure-fire ways to deal with and overcome the emotional challenges of living with vitiligo. My belief is that all of us have to create our own journeys and make choices and realizations on our own timetables. Though my vitiligo has been relatively stable for many years now and I do experience some re-pigmentation here and there during the summers, I would be lying if I said that I never feel self conscious about it. At the same time, I can say that I'm deeply grateful for all of the experiences and realizations that I've had because of my vitiligo. Developing vitiligo was the main stimulus that caused me to learn about experiencing optimal health through healthy living - I'm grateful in knowing that I'm coming close to accessing my full health and life potential because of my daily choices. Having vitiligo has deepened my capacity to empathize with others who suffer with anxiety about their appearance or any other perceived disability. Having vitiligo has given me the gift of being able to almost instantly identify and appreciate people who have extra compassion for others. I think it takes especially kind souls to treat others with vitiligo or some other unique physical trait as though nothing stands out. I'm not writing about being apathetic to another person's appearance at first glance. Rather, I'm thinking about this special gift that some people have, this gift of communicating warmth, acceptance, and genuine care through their friendly gaze. And I believe that living with vitiligo has developed my radar for such people. Really, I could write many pages on how having vitiligo has made me feel more human. It's forced me to mature in ways that I may not have without it. During the first few years, I remember being humiliated whenever someone asked me about my vitiligo. For example, one day while having lunch with a good friend and Matt, my friend's adorable toddler son, Matt suddenly paused his chewing, looked at me intently with cupcake icing covering his lips, and asked, "what are those white spots around your mouth?" Matt's question, perfectly innocent and appropriate for an inquisitive 3-year old, paralyzed me. I was too embarrassed to answer. As the years went by and I grew to accept that I shouldn't be ashamed of my vitiligo, I realized that people who ask about vitiligo - especially young kids - just want to know more about it; rarely is there intention to cause embarrassment. These days, whenever children ask me about my white spots, I typically ask them if they know of any animals that have white spots, say, those that emit "moos" or dogs that live at fire halls. As soon as their eyes answer yes, I explain that I'm the same way, that I have white spots here and there, but that they don't hurt, that that this is just the way that I am, just like some animals. And as soon as they understand this, I see in their eyes that I am nothing unusual to them - I'm just Ben, Joshua and Noah's daddy. Adults really are the same as children in this regard. Even those who stare at first and appear to be a bit uncomfortable, wondering if what I have is contagious - once they see that I'm comfortable with who I am, it seems that they become more comfortable with who I am. When I was younger and not as comfortable with my vitiligo, I think that others could feel my self consciousness, which may have contributed to them being extra conscious of my unique appearance. I suppose my point here is that natural management of vitiligo should go far beyond nutritional considerations. In almost all cases, even those involving young children, my belief is that there is a significant emotional component. To work at curing vitiligo without taking time to consider the many life lessons that it presents is to miss out on some serious marrow, I think. Which brings us to one final life lesson that I've learned from living with vitiligo, one that I'll end this post with: "...there is nothing either good or bad, but thinking makes it so." Thanks to my good friend, Chet Day for putting good old Shakespeare back into my head this morning. :) If you would like to share any thoughts on vitiligo or anything related to the main themes in this post, please feel free to add to this discussion via the comments section below. http://www.drbenkim.com/vitiligo-natural-management.htm Thanks for reading. Thoughts on Managing Vitiligo Naturally
Dr. Ben Kim story

Posted By Dr. Ben Kim
http://www.drbenkim.com/vitiligo-natural-management.htm

My experience with vitiligo started when I was nineteen years old. I was in my second year of university, struggling to meet academic expectations, and unhappy with my relationships at home.

Ultimately, trying to meet my parents’ expectations for my academic career and failing to reconcile the mixed feelings that I had about being a pastor’s kid of a new church created more pressure than I was capable of handling.

During this angst-filled time, I distinctly remember days when I would lie face down in bed and wish that I could get sick in some way so that there would be less expectations for my life.

I guess on some level, I thought that if I became ill, my parents would feel sorry for me and show me that it was okay if I didn’t fulfill their hopes for my life.

After several months of constant stress, worry, and self-pity, I woke up one day and noticed a small patch of white skin under my right eye.

I didn’t think too much of it until a few days later, I noticed another white spot on my neck.

A few weeks and several new spots later, a visit with our family doctor and a dermatologist led to a diagnosis of vitiligo.

Over the next several years, unaware of how my diet and emotional stress were causing steady progression of my vitiligo, I went on to lose about 25 percent of my skin color.

Fortunately, my studies led me to a field of promoting health via healthy living called natural hygiene. Over time, I came to an understanding of autoimmune illness, which helped me formulate a plan to address vitiligo through natural means.

Here’s what everyone with vitiligo should know:

Your melanocytes (pigment-producing cells), unless irreversibly destroyed, are always ready and willing to restore pigment to your skin.

In order to restore color to areas of your skin where your melanocytes are still functional, the key is to make sure that your diet and lifestyle (including emotional stress) don’t continuously undo the re-pigmenting work that your melanocytes are constantly engaged in.

If you read through my articles on the root causes of autoimmune illness and natural ways to prevent and reverse autoimmune illness, you’ll have the knowledge you need to follow a diet and lifestyle that minimize the inflammation that characterizes the loss of skin color in people with vitiligo.

To briefly summarize these dietary and lifestyle measures, they are:

Eat a plant-centered diet – the bulk of your food choices should be vegetables, fruits, legumes, and whole grains that your body doesn’t have trouble digesting.

Ensure adequate intake of vitamin B12 and DHA (an omega-3 fatty acid that strict vegans tend to be deficient in).

Ensure adequate vitamin D status through diet and sunlight exposure and supplementation if necessary.

Avoid intake of dairy products and flesh meats.

If you choose to eat some animal products, stick with small amounts of organic eggs and wild fish. Closer to raw is best. Lightly cooked is acceptable.

Strive to be emotionally balanced. Work at being a master of managing emotional stressors.

Get high quality sleep as often as possible. For most humans, nine to ten hours of restful sleep every day is an optimal amount.

These measures give your melanocytes all the support that they could ask for to produce pigment in areas that need it, as well as to minimize new bouts of inflammation that can create more loss of skin color.

But there is one other essential stimulus for re-pigmentation: sunlight exposure.

Your melanocytes produce pigment (melanin) in response to sunlight exposure, as melanin serves to protect your skin against burning.

The trouble with this requirement for re-pigmentation is that for someone with vitiligo, sunlight exposure is hard to tolerate physically and emotionally.

On a pure physical level, the challenge is avoiding sunburn because areas with no pigment are unprotected against ultraviolet rays.

For this challenge, I recommend being ultra conservative with sunlight exposure – just a few minutes at a time – and increasing intake of red beets, carrots, and dark green vegetables – these pigment-rich vegetables appear to provide some level of natural protection against sunburning from the inside-out. Just be careful not to overdo it with the beets and carrots if you have a problem with your blood sugar-regulating mechanisms, as these root vegetables are rich in natural sugars.

Emotionally, sunlight exposure can be challenging because it leads to greater contrast between areas that still have pigment and areas that have lost pigment.

And because some melanocytes in de-pigmented areas may no longer be functional, there’s no guarantee of full re-pigmentation with sunlight exposure, which means that getting lots of sun can help stimulate some re-pigmentation, but at the cost of having the vitiligo that remains to be more noticeable.

As someone who has lived with vitiligo for almost 20 years, I know full well that the emotional component of living with vitiligo can be a huge challenge; it’s not an exaggeration to say that it can be crippling.

Because you look different, particularly if you have darker complexion to begin with, having your vitiligo be more noticeable with sunlight exposure increases the number of stares that you get on the street. It can affect what you wear, your confidence level, and how you interact with others.

Because everyone’s situation is unique, I don’t think there are any sure-fire ways to deal with and overcome the emotional challenges of living with vitiligo. My belief is that all of us have to create our own journeys and make choices and realizations on our own timetables.

Though my vitiligo has been relatively stable for many years now and I do experience some re-pigmentation here and there during the summers, I would be lying if I said that I never feel self conscious about it.

At the same time, I can say that I’m deeply grateful for all of the experiences and realizations that I’ve had because of my vitiligo.

Developing vitiligo was the main stimulus that caused me to learn about experiencing optimal health through healthy living – I’m grateful in knowing that I’m coming close to accessing my full health and life potential because of my daily choices.

Having vitiligo has deepened my capacity to empathize with others who suffer with anxiety about their appearance or any other perceived disability.

Having vitiligo has given me the gift of being able to almost instantly identify and appreciate people who have extra compassion for others. I think it takes especially kind souls to treat others with vitiligo or some other unique physical trait as though nothing stands out. I’m not writing about being apathetic to another person’s appearance at first glance. Rather, I’m thinking about this special gift that some people have, this gift of communicating warmth, acceptance, and genuine care through their friendly gaze. And I believe that living with vitiligo has developed my radar for such people.

Really, I could write many pages on how having vitiligo has made me feel more human. It’s forced me to mature in ways that I may not have without it.

During the first few years, I remember being humiliated whenever someone asked me about my vitiligo. For example, one day while having lunch with a good friend and Matt, my friend’s adorable toddler son, Matt suddenly paused his chewing, looked at me intently with cupcake icing covering his lips, and asked, “what are those white spots around your mouth?”

Matt’s question, perfectly innocent and appropriate for an inquisitive 3-year old, paralyzed me. I was too embarrassed to answer.

As the years went by and I grew to accept that I shouldn’t be ashamed of my vitiligo, I realized that people who ask about vitiligo – especially young kids – just want to know more about it; rarely is there intention to cause embarrassment.

These days, whenever children ask me about my white spots, I typically ask them if they know of any animals that have white spots, say, those that emit “moos” or dogs that live at fire halls. As soon as their eyes answer yes, I explain that I’m the same way, that I have white spots here and there, but that they don’t hurt, that that this is just the way that I am, just like some animals. And as soon as they understand this, I see in their eyes that I am nothing unusual to them – I’m just Ben, Joshua and Noah’s daddy.

Adults really are the same as children in this regard. Even those who stare at first and appear to be a bit uncomfortable, wondering if what I have is contagious – once they see that I’m comfortable with who I am, it seems that they become more comfortable with who I am.

When I was younger and not as comfortable with my vitiligo, I think that others could feel my self consciousness, which may have contributed to them being extra conscious of my unique appearance.

I suppose my point here is that natural management of vitiligo should go far beyond nutritional considerations. In almost all cases, even those involving young children, my belief is that there is a significant emotional component. To work at curing vitiligo without taking time to consider the many life lessons that it presents is to miss out on some serious marrow, I think.

Which brings us to one final life lesson that I’ve learned from living with vitiligo, one that I’ll end this post with:

“…there is nothing either good or bad, but thinking makes it so.”

Thanks to my good friend, Chet Day for putting good old Shakespeare back into my head this morning. :)

If you would like to share any thoughts on vitiligo or anything related to the main themes in this post, please feel free to add to this discussion via the comments section below. http://www.drbenkim.com/vitiligo-natural-management.htm

Thanks for reading.

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Comment on Share Ur Story by Kenny http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-434 Kenny Tue, 29 Nov 2011 22:07:58 +0000 http://vitsaf.org/blog/#comment-434 Am kenny 4rm ogunstate and av been living with vitiligo since 2002 and am now 23yrs, although it is nt in al my body but it is on my lips d edge of my nose, my 2harms my hand, my breast my knee, my leg. I use to think in 2yrs tym it wil spread al over my body. Pls it seems am d only 1 living with dis vitiligo in ogunstate and pple do look at me as if there is sheat on my body atimes i get scared of going out becus i use to feel dat i wil be d television 4 people to watch. Is getting worse evryday. So many times my daughter use to ask me dat , mummy wat is dis in ur hand and i wil say it is natural but inside me i use 2 feel sad. Pls anytin to use atleast if nt al wil go i expect little of it to go Or wat to use to stop dis disease becus 2 me is a disease. Pls somebody shuld advice. Thanks Am kenny 4rm ogunstate and av been living with vitiligo since 2002 and am now 23yrs, although it is nt in al my body but it is on my lips d edge of my nose, my 2harms my hand, my breast my knee, my leg. I use to think in 2yrs tym it wil spread al over my body. Pls it seems am d only 1 living with dis vitiligo in ogunstate and pple do look at me as if there is sheat on my body atimes i get scared of going out becus i use to feel dat i wil be d television 4 people to watch. Is getting worse evryday. So many times my daughter use to ask me dat , mummy wat is dis in ur hand and i wil say it is natural but inside me i use 2 feel sad. Pls anytin to use atleast if nt al wil go i expect little of it to go Or wat to use to stop dis disease becus 2 me is a disease. Pls somebody shuld advice. Thanks

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Comment on Welcome to our Blog, Be Positive, Be healthy!!! by VITSAF http://www.vitsaf.org/welcome-to-our-blog-be-positive-be-healthy/comment-page-1#comment-382 VITSAF Sat, 10 Sep 2011 08:06:40 +0000 http://vitsaf.org/blog/?p=5#comment-382 Thank you Ikechukwu, again I appreciate your kind words, but want you to know that this is an advocacy, concerned about needs of persons living with Vitiligo and the disfigured. I refer to your caution 'note that we are on earth to experience', sure we are and some experiences are not even understood and been misunderstood for ages like in the case of Vitiligo where people cant get employed, get into a relationship of their choice or even go about Social events freely, rather the society gives it names such as spiritual, a curse , nemesis et cetra..... I believe there is absolutely nothing God cant do and that's why we have Churches and Mosques, ordinarily we can get our Bibles and Quaran and study bu ourselves. What the Churches and Mosques does to people is what we are to ourselves. Its always easy for us humans to settle the case with words till we find ourselves close to it. Thank you Ikechukwu, again I appreciate your kind words, but want you to know that this is an advocacy, concerned about needs of persons living with Vitiligo and the disfigured.
I refer to your caution ‘note that we are on earth to experience’, sure we are and some experiences are not even understood and been misunderstood for ages like in the case of Vitiligo where people cant get employed, get into a relationship of their choice or even go about Social events freely, rather the society gives it names such as spiritual, a curse , nemesis et cetra…..

I believe there is absolutely nothing God cant do and that’s why we have Churches and Mosques, ordinarily we can get our Bibles and Quaran and study bu ourselves. What the Churches and Mosques does to people is what we are to ourselves.

Its always easy for us humans to settle the case with words till we find ourselves close to it.

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Comment on Share Ur Story by VITSAF http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-375 VITSAF Thu, 25 Aug 2011 17:21:59 +0000 http://vitsaf.org/blog/#comment-375 Thanks so much Gloria for sharing, when you say you don't want to recount all you went through looking for a cure.....I can only imagine, truly anyone who as not worn this shoe will hardly understand how and where it pinches.I am glad you are confident now and living your life to the full. Thanks for that advise to all...'Just be Optimistic about Life!!! Thanks so much Gloria for sharing, when you say you don’t want to recount all you went through looking for a cure…..I can only imagine, truly anyone who as not worn this shoe will hardly understand how and where it pinches.I am glad you are confident now and living your life to the full.

Thanks for that advise to all…’Just be Optimistic about Life!!!

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Comment on Share Ur Story by Gloria samson http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-374 Gloria samson Tue, 23 Aug 2011 20:24:14 +0000 http://vitsaf.org/blog/#comment-374 I am also one of us.I jt woke up one mornin nd saw a large white patch under my right eye in 2003 after d birth of my 1st daughter and it has bn spreadin ova my body. I dont want 2 recount all i went tru lukin 4 a cure. Though i am nw confident abt me,at a time i almost lost it completely.My family were wondaful nd dat was my savin grace. God is d giver of streangth 2 all of us wit vit,jt b optimistic abt life. God bless u OGO 4 dis vision. I am also one of us.I jt woke up one mornin nd saw a large white patch under my right eye in 2003 after d birth of my 1st daughter and it has bn spreadin ova my body. I dont want 2 recount all i went tru lukin 4 a cure. Though i am nw confident abt me,at a time i almost lost it completely.My family were wondaful nd dat was my savin grace. God is d giver of streangth 2 all of us wit vit,jt b optimistic abt life. God bless u OGO 4 dis vision.

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Comment on Share Ur Story by VITSAF http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-369 VITSAF Sun, 07 Aug 2011 23:19:51 +0000 http://vitsaf.org/blog/#comment-369 Hello Omua, Thanks so very much for sharing, I truly appreciate your kind words and prayers.... Please join us as much as you can in Vitiligo Awareness especially as we campaign and advocate for World Vitiligo Day for June 25th. Please sign our petition http://www.vitsaf.org/world-vitiligo-day-june-25 to that regard, please invite your friends and family to do same. Thank you Hello Omua,
Thanks so very much for sharing, I truly appreciate your kind words and prayers….

Please join us as much as you can in Vitiligo Awareness especially as we campaign and advocate for World Vitiligo Day for June 25th. Please sign our petition http://www.vitsaf.org/world-vitiligo-day-june-25 to that regard, please invite your friends and family to do same.

Thank you

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Comment on Share Ur Story by VITSAF http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-368 VITSAF Sun, 07 Aug 2011 23:16:22 +0000 http://vitsaf.org/blog/#comment-368 Thanks for sharing Adele, really reading all the stories gives me hope that we shall all conquer someday....... Together we can Adele, yes lets get on with vitiligo Awareness ....please sign our petition for Campaign and Advocacy for World Vitiligo Day http://www.vitsaf.org/world-vitiligo-day-june-25. Thanks once again and please come around here often. Thanks for sharing Adele, really reading all the stories gives me hope that we shall all conquer someday…….

Together we can Adele, yes lets get on with vitiligo Awareness ….please sign our petition for Campaign and Advocacy for World Vitiligo Day http://www.vitsaf.org/world-vitiligo-day-june-25.

Thanks once again and please come around here often.

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Comment on Share Ur Story by Adele Bimbai http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-367 Adele Bimbai Sun, 07 Aug 2011 17:20:16 +0000 http://vitsaf.org/blog/#comment-367 I was diagnosed with Vitiligo when I was 8 years old. I have a small patch of it around the corner of mouth. When you have a condition like this at such a young age, living in the U.S., it's hard to accept or even understand what you truly have and what you will go through in your life connected with this disease. I had UV treatments as a kid that allowed my skin to re-pigment by about 65% or higher. It was really successful but there's still that small patch that refuses to go away ;) During my teens and early adulthood, I fought depression, thoughts of suicide, self-loathing, feeling alone, and hating myself over my vitiligo. Even though as a female, many people have told me that I was beautiful and many guys have wanted to date me, I never believed that I was beautiful. I used to think people were lying to me to make me feel better. I refused going out with friends, participating in sports, or doing anything that would put me in the public eye. I used to hate large crowds of people because I knew they would stare. When I was 21, I started using cosmetics to cover it up, and while it game me temporary relief, I felt like I was lying to myself and the world by covering something up that I didn't ask for. After a year, I threw the makeup away. It did more harm than good for me. I am now 25 years old and have realized that having Vitiligo has actually made me a much stronger person and more confident than most people. I feel like I attracted this disease because I am supposed to help with raising awareness about it and helping society understand that it affects a lot of people in the world. I am beautiful inside and out, no matter what others may think. I will not let my skin keep me from living my life to the fullest and taking pride in my self-worth or self-esteem. My Creator designed me perfectly in His/Her own image. It has been an extremely long journey to get to this point and in no way has it been easy but I am proud that I am who I am and that I look the way I do. I am no longer a sufferer and am now a survivor! I was diagnosed with Vitiligo when I was 8 years old. I have a small patch of it around the corner of mouth. When you have a condition like this at such a young age, living in the U.S., it’s hard to accept or even understand what you truly have and what you will go through in your life connected with this disease. I had UV treatments as a kid that allowed my skin to re-pigment by about 65% or higher. It was really successful but there’s still that small patch that refuses to go away ;)

During my teens and early adulthood, I fought depression, thoughts of suicide, self-loathing, feeling alone, and hating myself over my vitiligo. Even though as a female, many people have told me that I was beautiful and many guys have wanted to date me, I never believed that I was beautiful. I used to think people were lying to me to make me feel better. I refused going out with friends, participating in sports, or doing anything that would put me in the public eye. I used to hate large crowds of people because I knew they would stare. When I was 21, I started using cosmetics to cover it up, and while it game me temporary relief, I felt like I was lying to myself and the world by covering something up that I didn’t ask for. After a year, I threw the makeup away. It did more harm than good for me.

I am now 25 years old and have realized that having Vitiligo has actually made me a much stronger person and more confident than most people. I feel like I attracted this disease because I am supposed to help with raising awareness about it and helping society understand that it affects a lot of people in the world. I am beautiful inside and out, no matter what others may think. I will not let my skin keep me from living my life to the fullest and taking pride in my self-worth or self-esteem. My Creator designed me perfectly in His/Her own image.

It has been an extremely long journey to get to this point and in no way has it been easy but I am proud that I am who I am and that I look the way I do. I am no longer a sufferer and am now a survivor!

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Comment on Share Ur Story by Omua http://www.vitsaf.org/vitiligo/my-vitiligo-story/share-ur-story/comment-page-1#comment-364 Omua Tue, 26 Jul 2011 12:01:59 +0000 http://vitsaf.org/blog/#comment-364 Hi guys, All your stories are very touchy and inspiring. I have had this white patch on the left side of my forehead as long as i can remember. I will be 37 in December and i noticed it when i was like 6 years old. It came as a very white patch on my head and then i was told mayb i ate raw cocoyam. My father thank God was wide travelled so he went to India and got this very short bottle wit liquid in it which i had to apply on the patch every night before going to bed. But we all saw that the place became darker and it never spread more than were it was. I have always had positive feelings about myself so i never did feel bad when people stare at me then and some will ask is it fire burn, did u have an accident all i say and stil say is that i just saw it coming or Na birth mark. Though my vit. is just a small patch but i pray that a cure shud come up fast for those who have it all over so they can live life without inferiority. But i say to you.. You are the only one responsible for your happiness and to. Ogo i say Kudos to you for the good work you are doin and May Godly richly bless you and grant you the strenght. Peace, Omua. Hi guys,
All your stories are very touchy and inspiring. I have had this white patch on the left side of my forehead as long as i can remember. I will be 37 in December and i noticed it when i was like 6 years old. It came as a very white patch on my head and then i was told mayb i ate raw cocoyam. My father thank God was wide travelled so he went to India and got this very short bottle wit liquid in it which i had to apply on the patch every night before going to bed. But we all saw that the place became darker and it never spread more than were it was. I have always had positive feelings about myself so i never did feel bad when people stare at me then and some will ask is it fire burn, did u have an accident all i say and stil say is that i just saw it coming or Na birth mark. Though my vit. is just a small patch but i pray that a cure shud come up fast for those who have it all over so they can live life without inferiority. But i say to you.. You are the only one responsible for your happiness and to.
Ogo i say Kudos to you for the good work you are doin and May Godly richly bless you and grant you the strenght.
Peace,
Omua.

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