Friday, April 22, 2011

Research Report: Vitiligo In Relation to Skin Disease

I posted about proper sun care a few weeks ago, and how the use of sunscreen is so crucial to keeping pigmentless spots safe from the sun. While it is true that these spots can get sunburned way worse than normal pigmented skin, it would seem that based off some of my research, people diagnosed with Vitiligo are not at higher risk of skin cancer. An article from the American Vitiligo Research Foundation says that the "results of two major studies showed that patients with Vitiligo do not have a higher risk to develop sun-induced skin cancer" but that "in the recent past an issue was put forward that PUVA therapy which is a frequently used treatment modality for vitiligo could be of potential risk to enhance the risk of skin cancer" [1].

A Health Buzz article from the US News even says that "Vitiligo may protect against skin cancer". Go figure. It says a "gene mutation linked to the skin condition Vitiligo ...may protect against melanoma" [3]. From what the article says, since Vitiligo is an auto-immune disease, your body is already fighting pretty hard against your skin cells, so you've got an added defense against melanoma. From what I also read in a BBC article, it seems to be a give take gene situation, it is a "common gene mutation that both increases the chance of Vitiligo and cuts cancer risk", and it says later that it helps against the "risk of malignant melanoma, the most serious form of skin cancer" [2]. But according to vitiligoguide.com, the "New England Journal of Medicine briefs that the pale skin patches are caused by Vitiligo which increases the risk of melanoma (skin cancer) due to the deficiency of the pigment melanin" [4].

So it is obviously still a heavily debated and researched concept, either way I say you should still be mindful of the sun and your skin. But it is still cool to think that the obvious reaction from everybody who thinks that no pigment means increased cancer risk could be the complete opposite. Alas, it still remains a mystery, as does the disease itself, perhaps we may never know everything about the disease.

Works Cited
[1] http://www.avrf.org/facts/sun.htm American Vitiligo Research Foundation. Date of access 4/22/2011

[2] http://news.bbc.co.uk/2/hi/8635844.stm BBC News. "People with vitiligo 'may have skin cancer protection'" Published 4/21/2010. Date of Access 4/22/2011

[3] http://health.usnews.com/health-news/family-health/cancer/articles/2010/04/22/health-buzz-vitiligo-may-protect-against-skin-cancer US News. Published 4/22/2010. Date of access 4/22/2011

[4] http://www.vitiligoguide.com/vitiligo-skin-cancer/ Vitiligo Guide. Posted 6/23/2010. Date of Access 4/22/2011

Podcast: Book Review

A simple book review of Turning White: A Memoir of Change by Lee Thomas. I couldn't figure out how to edit in a title, so it just kind've starts abruptly. Also keep in mind, that I don't like being filmed or watching myself on camera so sorry if I stutter a bit.

Research Report: Vitiligo and Your Diet

One of you who commented on my posts brought to my attention the concept of a Vitiligo diet, I became interested in this and decided to look into finding out more about it myself. One of the websites that was mentioned, antivitiligo.com, has a pretty good summation of what you should and shouldn't eat. Here is some of the list, taken straight from http://www.antivitiligo.com/vitiligo-treatment/vitiligo-diet.html 


  • Eat vegetables "Like Green Leaves, Beetroots, Spinach Broccoli, Brussels Sprouts, Cabbage, Carrots"
  • Eat fruits "Like Peaches and Apricots, Apples, Banana Mangoes, Black Dates"
  • Eat whole grains "Like porridge and whole wheat product are better than the highly refined carbohydrates like pasta"
  • Eat legumes "Chickpeas have recently shown in India to be very helpful in Vitiligo"
  • Eat protein "Vegetable proteins especially from Soya beans have been found useful for controlling the skin depigmentation. Animal proteins like meat and fish are however generally discouraged by herbalists"
  • Stay Hydrated! "Adequate hydration is an important component of healthy diet which should not be ignored" [1]
Apparently Blueberries "contain more anti-oxidants than any other fruit or vegetables", they also contain "powerful photochemical anthocyanins that not only protect the skin but boost brain efficiency including memory". Spinach "contains phytochemicals that help prevent degeneration and protect your skin" just as most nuts contain "protective photochemicals and 'good fats'" [3]. Another website says that you should avoid "cold and phlegm producing foods" which it later says are things like: "fish, beef, brinjal, heavy and light food mixed simultaneously" and "milk, curd, buttermilk" and other citrus type foods as well [5].

More on citrus and Vitiligo, an article from Life Force Homeopathy written by Dr. Rajesh Shah says that all "foods that are excessively sour should be avoided" and that "Vitamin C (ascorbic acid) is known to inhibit the production of melanin, the color pigment" [2]. Going along this same track, another site says that "stored sour things, junk food, tinned foods or drinks, chocolates, coffee or cocoa products should not be taken regularly" [4].

Overall, from the looks of things, if I were to completely undertake the Vitiligo Diet, it would pretty much be equivalent to becoming a vegan, because you're going to have to eat pretty much straight organic and no meats. While this is a bit too much for me to handle, I encourage anyone else out there with more will power than me to give this a shot. If it doesn't help with pigmentation, I guarantee it could help with your diet in general.

Works Cited

[1] http://www.antivitiligo.com/vitiligo-treatment/vitiligo-diet.html
[2] http://www.leucoderma.com/app/diet.asp
[3] http://www.vitiligoguide.com/vitiligo-diet/
[4] http://vitiligoleucoderma.com/
[5] http://www.wholisticresearch.com/info/artshow.php3?artid=270








Research Report: Stress In Relation to Vitiligo...

While dermatologists today seem to have a pretty good grasp on Vitiligo and its symptoms, what causes the onset of Vitiligo is still undetermined, but many researchers and physicians have proposed their own ideas on what the answer could be. One of the most prominent theories is a supposed correlation between stress and the onset/outbreaks of the disease. 

One such research experiment conducted by the  Dermatological Institute of Italy found that "vulnerability to Vitiligo is not increased by stressful events, except for many uncontrollable events" but that in fact, "insecure attachment and poor social support appear to increase susceptibility"[3]. This means that essentially it isn't the stressful event, but one's ability to recover and the support he receives in this process, which would make those who are struggling to make it on their own the most prominent demographic for a late on set of the disease. Another study, conducted by DR. A.K. Gupta, the Founder Director of Om Vidya Institute of Homeopathy and Allied Medical Sciences, showed that "80% of patients revealed that their white patches increase in numbers and size whenever they are mentally stressed". So this study refutes the some of the information listed in the first article, but it does list that they tested a broad range of subjects, "55% males and 45% were female and patients were of all age groups, the youngest being a 6 year old girl student and the eldest was a 74 year old advocate"[2]. While the patient information is not divulged in the first article, it's hard to say how the two compare in terms of subject broadness.

A page on vitiligosupport.org also had some interesting input, with little mention of normal mental stress on  the disease, but that perhaps "traumatic events" in someone's life may "trigger or exacerbate Vitiligo in those who are susceptible, though this has not been substantiated". It should also be noted that "surgery wounds or injuries to the skin have also been known to result in Vitiligo, which can spread." [4].

To take a brief repose from the conventional forms of stress, I found an article from Vitiligo Support International that tells about a different kind of stress that may contribute to the cause of Vitiligo. "Oxidative stress" which is "an over-accumulation of hydrogen peroxide in the skin" that is caused by a lack of the body producing "an enzyme called 'catalase'" that helps break it down into water and oxygen within the skin [4]. Not only could this cause Vitiligo, but Oxidative Stress could have a hand in many afflictions including, "atherosclerosis, Parkinson's disease, heart failure, myocardial infraction, Alzheimer's disease, fragile X syndrome, and chronic fatigue syndrome"[1]. So if you feel you may have Oxidative Stress, Vitiligo could be the least of your worries.

Works Cited



[1] http://www.news-medical.net/health/What-is-Oxidative-Stress.aspx. News Medical. Date of access 4/22/2011

[2]http://www.spiritindia.com/health-care-news-articles-530.html. Spirit India. Date of access 4/22/2011
[3]http://vitiligocover.com/does-stress-trigger-vitiligo/ Nathalie. 2004-2011. Date of access 4/22/2011
[4]http://www.vitiligosupport.org/faq.cfm Vitiligo Support International 2000-2008. Date of access 4/22/2011

FOR IMMEDIATE RELEASE:

Blog Regarding Vitiligo Takes Perspective Of A Student With The Disease

Richardson, Texas - April 22, 2011 - A 19 year-old college student attending The University of Texas at Dallas has constructed a blog about the skin disorder Vitiligo in accordance to a class he is currently enrolled in.

Griffin Marshall, a sophomore ATEC major, was diagnosed with the disease six years ago and felt that getting the blog assignment in his Writing for The World Wide Web class would be a chance for him to learn and teach others about the elusive disease.

The blog, which will contain posts on everything from potential treatments to brief histories, will be conveyed in multiple forms ranging from normal posts, to podcasts, and even guest entries.

It will also include interviews with some of Griffin's classmates, as well as a reputable dermatologist from the Austin area who diagnosed Griffin six years previous.

Contact:
Griffin Marshall
gkm090020@utdallas.edu
Ph # 512-289-4171

Guest Entry


(My name is Vincent Lo. Sophomore at UTD. Arts and Technology.)

The Two Basic Categories of Vitiligo
There are several types of vitiligo. Some of these types include focal, mucosal, acrofacial, vulgaris, universal, and mixed vitiligo. (1) That is a lot of different names! I won’t describe these in detail, but all these types can be organized into two basic categories: non-segmental vitiligo and segmental vitiligo. (2)
Non-segmental
Non-segmental vitiligo, or NSV, is more common than segmental. Two characteristics define NSV:
·       Generalized
·       Symmetrical
NSV is generalized, which means the patches of depigmentation appear anywhere on the body. Also, if these patches appear on one side of the body, it’s in the same place on the other side. For example, a person with NSV might have patches on both hands, both elbows, or both feet. (3) NSV also can appear at any age. (2)
Segmental
Segmental vitiligo, or SV, which isn’t as common as non-segmental, has two main characteristics:
·       Localized
·       Asymmetrical
SV is localized, which means the patches are limited to a particular area. And because SV is localized, it may only appear on one side of the body. SV appears more commonly in teenage years. (2)
NSV and SV can co-exist. This type of vitiligo is called mixed vitiligo. (3)

(1)  Different types of vitiligo. (n.d.). Retrieved from http://www.vitiligosupport.org/vitiligo/types.cfm

(2)  Vitiligo. (n.d.). In Wikipedia. Retrieved April 21, 2011, from

(3)  Pelletier, N. (n.d.). What is segmental & non-segmental vitiligo?. Retrieved from http://vitiligocover.com/what-is-segmental-non-segmental-vitiligo/

Wednesday, April 13, 2011

Interview With An Expert

This is a brief but concise email interview I conducted with Dr. Adrienne Feasel, a highly renowned dermatologist from Austin who originally diagnosed me with Vitiligo several years ago. Her bio and information about where she practices is provided here: http://www.laderaparkdermatology.com/physicians_feasel_bio.htm. If you live in Austin or nearby and have any questions regarding Vitiligo, I highly suggest getting an appointment with her.

GM: What is Vitiligo and what causes it exactly?

AF: Vitiligo is a skin disorder characterized by depigmentation of the skin, manifest as white macules.  It affects 0.5- 2% of the population worldwide.  Although the cause is unknown, there is a loss of functional melanocytes (pigment-producing cells) in the affected area.  While up to 30% of cases may be familial,  most cases of vitiligo occur sporadically.  Patients may be affected at any age, but many cases develop at 10-30 years of age. The majority of cases demonstrate depigmentation in limited areas (segmental), but the disease may become widespread in some individuals.  The course often progresses slowly, but may stabilize or rapidly worsen for some individuals.  The cosmetic appearance is often concerning for  patients and may be socially stigmatizing for others.

GM: What are the telltale signs of Vitiligo?

AF: The diagnosis of vitiligo is clinical, with obervation of sharply demarcated white areas of skin.  The observation of depigmentation may be aided by the use of a Wood's Lamp.  This may be paticularly useful in fair-skinned patients, where the descrepancy between light and white skin is not as apparent.  Biopsy demonstrates an absence of melanocytes in the affected area. 

GM: Does it have a cure?

AF: There is no single cure for vitiligo.   Most treatments attempt to repigment the skin, but response is variable among patients.  Topical therapies which may be useful  include corticosteroids, and immune modulators (tacrolimus ointment), and vitamin D derivatives.  Ultraviolet therapy with narrowband UVB,  and photochemotherapy with psoralen and UVA, often provide good clinical response. Excimer laser therapy is also useful for limited disease.Cosmetics (ie, Dermablend) help camoflauge affected skin during or in lieu of treatment. In rare, widespread cases, chemical depigmentation of the normal skin  may be employed. It is important to use strict photoprotection as the affected areas are easily sunburned. The discoloration also becomes more apparent  if the normal, surrounding skin is tanned.



Sunday, March 27, 2011

An Interesting Quote...

I was in the process of reading a book on Vitiligo that I plan on reviewing in a later blog post; and in the middle of the book, I found a quote from the author, Lee Thomas, that really jumped out at me as summing up the way I view Vitiligo now as opposed to when I first got it.

"The first speck freaked me out--- someone actually tried to wipe it off! You think the face is the definition of self, but I've formed a clearer picture. Now, I wear the mask of a superhero" [1]

When I happened across this quote, torn from the middle of a novel by Lee Thomas called Turning White: A Memoir Of Change, it immediately jumped out at me and I knew I had to share it with you guys. I don't think Lee could have summed up my feelings any better than he did here, because it's a feeling of comfortability that just happens. You'll know it when it does, because everything snaps into place, and you become comfortable with yourself. You begin to view Vitiligo as something that sets you apart from the masses in a positive way. Granted this may happen earlier on for some rather than others, especially depending on the seriousness of your individual case, but when it does you will feel so many days of self-consciousness quickly dissipate into history.

I hope this little post helps you out in some way, because I feel the gravity of that quote is very large, especially to those of us who have experienced the tougher times with Vitiligo. If you are feeling stressed out, alone, or are just looking for a good read, I suggest this book, Turning White: A Memoir Of Change. I just finished it, and can honestly say that it offers a lot of positive vibes. 


Works Cited

[1] "Turning White: A Memoir Of Change"Thomas, Lee. Published 2007. Read 4-3-2011

Treatment Review: Recouleur

Disclaimer:
Before you read, be sure to remember that this remedy is not a guaranteed cure, because Vitiligo is currently incurable. And while this product has a history of positive results, even the website says that "because people are different, this may not happen for everyone". [1]


For my entry this week, I've decided to review a Vitiligo treatment I've used for some time now. It is a dietary supplement that contains "a patented formula of vitamins and minerals helpful for vitiligo" and sells for $89.95 on http://www.recouleur.com/recouleur-vitamins.asp. [1] 




(I took these photos myself and photoshopped them together)


Why this treatment?
My parents and I originally bought this on a whim, as the result of several good reviews and a period of frantic searching for makeshift cures. The impulsive buy turned out for the better though, since this stuff definitely worked for me. After several months of taking one pill a day, I noticed that spots were disappearing. I was literally able to watch, day by day, as pigment appeared in the center of certain spots and gradually spread to the outer borders. Now obviously not all my spots filled in completely, but a lot of the little ones began to fill back in, and that alone was a huge morale booster.

What is it?
Recouleur is a multivitamin that contains "Vitamin B12, Folic Acid, Zinc, Vitamin C, Pantothenic Acid, and Copper", a concoction that is patented to aid patients with Vitiligo. [1] It is taken in pill form, once or twice a day depending on how strong of a dose you want, and after a few months time results should begin to show themselves.





Pros

  1. Very easy to use, simple maintenance.
  2. When it works, it really works.
  3. Helpful site, lots of support, it is a reliable treatment from a reliable source.
  4. You can choose your dosage, (within reason), if you want to take two in order to up the effects, you can.
  5. No known side-effects.


Cons


  1. While it works well, it is an expensive investment at $89.95 a bottle.
  2. It does not work for everyone, which in reality is kind of a given with diseases where there is no real cure, everybody sees different results.
  3. If you stop, you can potentially lose the progress you've made.


Overall
Before we go on, it should be known that I have a bias since I use this product, but I've done my best to keep the review straightforward so far. This being said, I will say that I believe everyone with Vitiligo or a similar pigment condition should give this product a try. Buy a bottle or two and use them until they are empty, depending on the results you get, you can gauge whether or not you'd like to proceed with this product. The only overwhelming con to this product is that it doesn't work for everyone, but the only way you're going to figure that out is if you try it. While a $90 price tag is a bit steep, it is well worth paying at least once because who knows, it may be your miracle cure.



Works Cited
[1] http://www.recouleur.com/ Supernatural Health 2011. Date of access: 3/27/2011

Saturday, March 26, 2011

How To Avoid Serious Sunburns During The Summer

Summer is an awesome time of the year, a brief repose from the likes of schoolwork and business, for kids at least. Either way, it can be a bit of a chore for those of us with Vitiligo because it is really easy to burn your depigmented spots in the hot summer sun. So I've prepared a set of tips and tricks to help you get the most out of the summer months while avoiding severe burns and increased risk of skin cancer.

Surviving Summer 101

Tip #1: Don't Underestimate Sunscreen
The first and most important thing to remember about keeping your skin safe during the summer season is to always use sunscreen, whenever you go outside carry it with you at all times. I feel like the easiest way to do this is to go to the store and buy a bunch of travel size sunscreen bottles, and make sure they have a high SPF, I typically choose 50 or 75. Put these bottles everywhere, to the point where it is nearly impossible to not have one on hand. I keep one in my car, my backpack, my swimsuit pocket, and sometimes in my pants pocket. If you're a girl, I'd highly suggest keeping one in your purse. Once you have these set up to your liking, the key is to use them as often as possible and reapply them every 2-3 hours. If you're like me and hate the feel/smell of sunscreen, I understand how it feels but doing it is well worth saving your skin in the long run. 

Tip #2: Don't Be Afraid To Take Breaks
While it is inevitable that you will spend lots of time outside in the summer sun, and believe me there is nothing wrong with this, you need to understand that regardless of sunscreen, prolonged exposure to the sun can be very damaging to affected spots of skin. So never be afraid to take a break and go inside for a while or spend some time in the shade, because the more often you allow your spots to recover from the sun the better. You should also seize these opportunities to reapply sunscreen as needed.

Tip #3: The More Clothing The Better
Now I understand that summer can be hot, I mean really hot, so the urge to wear shorts and a tank top is not without reason, but little changes in wardrobe can make a lot of difference. If you can stand it, wearing jeans pretty much eliminates all the worry for spots on your legs. Unless you apply lots of sunscreen to your shoulders, I would not recommend wearing anything more revealing than a t-shirt, but also don't go crazy and overheat yourself with something like a long sleeve shirt. The secret to skin safety is really about knowing yourself and applying this knowledge in the form of my last tip, listed below.

Tip #4: Be Aware
Regulate yourself as you see fit, don't do anything that is going to make you uncomfortable during the joyous days of summer. You've got to know that the more exposed your skin is, the more attention it will require in order to not get hurt. It is a matter of noticing when spots are getting pink, and knowing that it is a good time to take a break when this occurs. You've got to be aware of your body to be on top of countermeasures.

Interview with a Layperson

This is an interview that I conducted with a good friend of mine named Scott Easum. He is a Software Engineering Major and Sophomore here at UTD. I conducted this interview in his apartment living room on March 24, 2011.


(Photo used courtesy of Scott Easum)



GM: Thank you for agreeing to this interview, Scott.

SE: No problem, dude.

GM: Without further ado, let's get into this thing...

GM: Essentially, if I were to ask you what Vitiligo was, would you have any idea what I was talking about?

SE: Only because I know you. So no.

GM: Okay, so then you know that it's the spots on my skin right?

SE: Correct.

GM: What if I told you it was an auto-immune disease, where the pigment pretty much attacks itself, have you ever heard of anything like that before?

SE: Like AIDS?

GM:Yeah, like AIDS in the way that  your body is unknowingly hurting itself and there is no known cure, but nowhere near as severe. You can't die from Vitiligo.

SE: Is it transmittable?

GM: No, I don't thinks so. I'm pretty sure it's only hereditary.

SE: So wait then do your parents have it?

GM: No. I'm almost positive I'm like the only person in my family that has the disease. (laughs) Who's interviewing who here?

SE: (laughs) Sorry.

GM: No, it's alright.

GM: Have you ever seen anyone else besides me with this disease?

SE: Not where I knew it was a disease. I knew that they had spots on their skin.

GM: Okay. Well, then before you met me, did you know about this disease at all?

SE: Only for albinos.

GM: So you'd never heard of it through someone like Michael Jackson?

SE: I didn't know he had a disease, I thought he just did plastic surgery.

GM: Well the running thing is apparently he dyed himself white because he had Vitiligo.

GM: Well anyway, I'll cap this off with one more question and I'll let you go.

SE: Okay.

GM: Do you have any strange diseases or things that people don't normally have?

SE: I used to be allergic to like everything, including yeast. I couldn't eat at least 50 different foods.

GM: Really?

SE: Yeah. I also used to have chronic bronchitis.

GM: Okay, well that's all the questions I have for you, so thanks again for your time. And unless you've got any questions for me I figure we'll wrap things up.

Vitiligo in the news...

As far as I can tell from my research, Vitiligo does not get significant press coverage, but there is a collection of articles and entries on the New York Times website that focus on the disease. But I did find one:


While it is 10 years old, it is the most recent article I could dig up, and it still contains some very helpful information that I didn't know until now.

 The Ups and Downs of the Disease
This article written by Jane E. Brody details Vitiligo and the way it affects the social lives of both a woman, Loretta, and a teenager, April, who have the disease. Both of these women open up about the harassment they have endured because of their affliction and in April's case, how it has helped her grow and learn about herself and other people. While April experiences the harshness of schoolyard teasing, she also found a way to use her disposition as a way to teach others by making "cards to hand to the curious, in which she states that she is not contagious". [1]

Brody continues on to cover the basics of the disease and why it faces so much adversity from medical professionals who refuse to acknowledge it as a serious disease. She states that many She lets readers in on a list of facts about Vitiligo that many do not know, some of which are:

"Up to 30% of women with Vitiligo develop Thyroid disease".

"Vitiligo patients also have an increased risk of developing diabetes, pernicious anemia, as well as Addison's disease, an adrenal disorder".

"People with Vitiligo must protect their skin from exposure to the sun. Affected areas of skin can become seriously sunburned while the surrounding skin tans'. She also advises that those affected "be vigilant about wearing sunscreen with a high sun protection factor (30 or higher) on exposed skin year-round".

"Many insurers consider Vitiligo a cosmetic issue and do not cover treatment costs".

All of the above were quoted from source [1].

Potential Cures  
On the second page of the article, Brody goes more in-depth about various treatments that seem to have a higher success rate than others, but mainly focuses on a form of light therapy called PUVA. In this treatment, patients take a drug called psoralen that causes their skin to become more sensitive to light. Once this has happened, doctors expose affected spots to a special lamp that only shows ultraviolet A. While this treatment apparently has great results on the face and upper extremities, it does not work well on feet and hands. It also can be bad for you if done in excess, so extensive treatment can cause freckling as well as increase the risk for skin cancer. Researchers from Henry Ford hospital turned up some promising results in similar experimental light therapies that have successfully repigmented over 75% of two darker skinned african-american men. This, along with a synthetic enzyme called pseudocatalase that works similar to the PUVA treatments, means that scientists are slowly narowing their sights onto a true cure for Vitiligo.

Works Cited

[1] Brody, Jane E. "Personal Health; New Approach to a Discoloring Skin Disorder" July 3, 2001 Date of access: 3/26/2011

Thursday, March 10, 2011

A Brief Description and History of Vitiligo

In my last post, I gave a short introduction to who I am and why I am writing this blog, as well as a look into what I am going to cover in the posts that lay ahead. What I did not do was give any background information on the disease or its history, but that is where this post comes in to play. In the following two paragraphs I will briefly detail what scientists believe causes Vitiligo and Vitiligo's historical significance so far.

The Disease
Vitiligo is an auto-immune disease of the skin where "melanocytes (the cells that make pigment) in the skin are destroyed". "Proteins called cytokines" are the ones that "alter pigment-producing cells and cause these cells to die". This is the cause of the white skin discolorations that occur randomly on the body. It should be noted from my own experience and from the Vitiligo Article on medicinenet.com, that hair growing in these spots can sometimes be a white or blonde color. Vitiligo affects ".5 to 1 percent of the world's population, or as many as 65 million people" and "1 to 2 million" of that is in the United States alone. While doctors and researchers do not know exactly how the disease is acquired, "there is strong evidence that people with Vitiligo inherit a group of three genes that make them susceptible to depigmentation". All information quoted here was taken from medicinenet.com or source [1].



History
According to the History of Vitiligo page on www.vitiligoguide.com, evidence of this disease dates back to as early as 2200 BC. The page also says that the disease "has long been confused with leprosy" and the name Vitiligo is "derived from the Latin word 'vitelius' which means calf". [3] While Vitiligo certainly hasn't been dormant for all the years between then and now, it wasn't really reported on heavily until the 90's when it saw excessive media coverage due to Michael Jackson and Amitabh Bachan becoming affected. [3] But according to the article "Vitiligo in history: Henry Moss" on vitiligocover.com, a man named Henry Moss was a subject of much attention during the 18th and 19th century. Born in Virginia, Henry Moss was an African American man who had an onset of vitiligo at the age of 38. While it started on his hands, it eventually spread to cover most of his body and Moss decided to take advantage of his strange predicament. "He exhibited his body for a fee in taverns in the Philadelphia area as well as before the American Philosophical Society." He was dubbed the "man who was born 'entirely black' but after thirty eight years had 'become as white and fair as any white person'." [2] So there is evidence of publicity and coverage of the disease all the way back to the 18th and 19th centuries.

Works Cited

[1] http://www.medicinenet.com/vitiligo/article.htm . Government sourced.  1996-2011. Date of access: 3/10/11
[2] http://vitiligocover.com/vitiligo-in-history-henry-moss/ . Nathalie. 2004-2011. Date of Access: 2/28/2011
[3] http://www.vitiligoguide.com/vitiligo-history/ . 2008 . Date of Access: 2/28/11

Friday, March 4, 2011

About Me...

Hello readers,
First and foremost I would like to say thank you for coming and visiting my blog, but before we jump into things I believe I should let you guys know a little bit about me:

Who am I?
My name is Griffin Marshall, and I am a sophomore studying Arts and Technology at The University of Texas at Dallas (UTD). I love it here at UTD and plan on staying here, which is important seeing as I attended a new school each semester prior to this one. When I'm not studying or in classes, I enjoy hanging out with friends, playing music, and going on vacations.

Why am I writing this particular blog?
 I am creating this blog for the sole purpose of informing people about a relatively unknown skin disease I happen to have called Vitiligo. I was diagnosed with Vitiligo about 6 years ago, and having never heard of it before, I can say I was a little bit overwhelmed when first learning to deal with the effects of my new ailment. Now that I have had six years under my belt, I feel confident in my ability to pass on valuable information to those willing to listen. In the posts that will follow: I will give a historical background for Vitiligo, give reviews and recommendations for various treatments and other care related to the disease, and interview people, (both expert and laymen), about the disease itself. I sincerely hope that the end result of this process will be a successful first foray into the world of blogging for myself, as well as a significant learning opportunity for you and I alike.