Alopecia Areata Treatment

Learn about alopecia areata treatment and remedies

Alopecia Areata Universalis

 

Alopecia Areata - Hair Loss Problem

Alopecia areata is a condition distressing humans, in which hair is lost from several or all areas of the body, usually from the scalp. Because it origin bald spots on the scalp, especially in the first stages, it is sometimes called spot baldness

Alopecia Areata UniversalisAlopecia areata is a malfunction of the immune system whereby the body begins to attack its own hair follicle. However it is very selective in which areas it attacks, so that circular / oval shaped bald patches develop. These are silky smooth to the touch, because all hair including vellus hair (soft downy hair) has been lost. Currently there is no medical explanation as to why the patches are selected in the manner in which they are. Accordingly there is no test that can be done to determine if the patches will stay contained in the given area or spread to another area.

What causes and origin alopecia areata? Less than 1% of the population suffers with alopecia areata with both males and females being affected. Children as well as adults suffer from the condition. There is a genetic link. Families that develop atopic allergies like asthma, psoriasis and eczema tend to have a greater incidence of alopecia areata. This would imply an inherited over-sensitive immune reaction. If you have an inherited tendency towards this disease, stress can cause the condition to start.

How do you confirm that you have alopecia areata? Due to the fact that the areas under immune attack are localized, it is not possible to confirm a diagnosis by blood tests. It follows that a punch biopsy (removing a section of the bald spot) is the only logical way to confirm an immune attack in such a localized area. However for most people this would be too invasive, so it tends to be diagnosed by the pattern of loss alone.

What treatments are available? At the initial onset it is common to see a spontaneous regrowth with no treatment. However it is common for it to spread rapidly and can result in total scalp hair loss. At this stage it is known as Alopecia Totalis. Further progression sees it spreading to the eyebrows and eyelashes and eventually affecting all body, scalp and facial hair. At this latter stage it is termed Alopecia Universalis and it is uncommon to see a spontaneous remission at such an advanced stage. As this disease has such an uncertain outcome it can have a big psychological effect. Doctors saying "do not worry it will probably grow back on its own", whilst it may have a high probability of being statistically correct, does very little to alleviate very real fear the patient has. That fear is based on the knowledge that it is also statistically correct that a lower percentage of sufferers will see it progress.

Most people fear that they will be the unlucky ones! Medical treatments are limited: With less than one percent of the population troubled by this problem, it is difficult from an investment standpoint to make a return on any investment into research work into a cure. However a pure investment returns approach sadly misses the fact that the disease is extremely upsetting to the sufferer. In western cultures it is common to see men lose their hair to alopecia androgenetica (male pattern baldness) so it is more socially acceptable to see a bald man. However that does not make the situation any easier for men. However women and children with hair loss are less common and attract much more unwanted stares and attention. Teasing at school can be very cruel as children tend to find patches of hair loss amusing.

Treatment types these tend to fall into broad categories:
Immune suppression like steroid creams or injections
Irritants like diphenylcyclopropenone.
Holistic approaches
Natural products like plant extracts and supplementation.

In many cases when a parent first approaches their doctor about alopecia areata, the doctor will refer the patient along to dermatologists. The very delay between seeing the doctor and dermatologist can be extremely stressful as the problem will usually be getting worse. Therefore many people seek alternative treatments via the web solely because they feel they at least they are being proactive and doing something that may benefit them.


What are the chances of alopecia areata universalis curing itself?
Just wondering.

Get the answers...


Question about medical insurance and what constitutes a prosthesis?
There is a disease called alopecia areata. It causes hair loss, and usually strikes women. It usually happens to women in their late teens, early 20's. There are two main forms of the disease. Alopecia areata totalis, and alopecia areata universalis. With alopecia areata totalis, the patient looses all the hair on their head (sometimes eyelashes and eyebrows as well). With alopecia areata universalis the patient looses all the hair on their entire body. This is the definition of a prosthesis in the dictionary: "an artificial device to replace or augment a missing or impaired part of the body" Insurance companies are required to cover breast implants for breast cancer patients (even the side that didn't have cancer), because the female breast is viewed as such a part of being female, and helps breast cancer patients recover emotionally and psychologically. So my question is, do you think that wigs for women with alopecia areata should qualify as a prosthesis under the insurance companies? Alopecia affects about 75% female patients, and 25% male patients. The disease does affect far more women than men. I'm also only speaking about women patients. Baldness is accepted, even found to be sexy in men, even very young men. So one person so far thinks a young woman can funcution normally in society, being bald, without a wig for a prosthesis. I'm finding it interesting that people don't think a wig should be covered as a prosthesis for women. I worked for a Dermatologist for almost nine years, and we saw a lot of patients with alopecia. The men, after the initial shock, adjusted well mentally. Not a single one of the women patients ever adjusted well. Every one of them was impacted in their social and working life. I remember one who was a public school teacher (in Seattle) who was tormented by her students (substitute teacher). She had to buy her own wig. A beautiful young lady who had long blonde hair. She couldn't afford her own wig, and eventually quit her job as a bank teller because of all the rude comments by customers. She had been bright, out-going, and funny. She became a completely withdrawn and negative person (despite medication). I saw the mental side effects in the women over and over again, and it REALLY impacted their lives. A quality wig is about $2000 and more. The insurance companies will not cover the wigs. They will however cover visits to Dermatologist, visits to therapists, and physchologists, anti depression medications, and all sorts of monthly expences incured with alopecia. Over a years time, the expences a patient racks up with the other costs far exceed the cost of a wig. That teacher who purchased her own wig didn't come in for a year. I though she'd moved. Nope, she just felt so much better about herself, and was able to function normally in public she stopped comming in for the alopecia.

Get the answers...


do people with Alopecia areata universalis have fingernails?
Alopecia areata universalis in a condition where you lose all of your hair everywhere, and I was wondering, do they still have fingernails?

Get the answers...

Related Alopecia-areata-universalis Videos


Next page: Alopecia Bald Spots


Bookmark/Share This Page:

ADD TO DEL.ICIO.US
ADD TO DIGG
ADD TO FURL
ADD TO NEWSVINE
ADD TO NETSCAPE
ADD TO REDDIT
ADD TO STUMBLEUPON
ADD TO TECHNORATI FAVORITES
ADD TO SQUIDOO
ADD TO WINDOWS LIVE
ADD TO YAHOO MYWEB
ADD TO ASK
ADD TO GOOGLE
ADD TO MAGNOLIA
ADD TO NING
ADD TO RAWSUGAR
ADD TO SPURL
ADD TO TAGTOOGA


Alopecia Areata Universalis News




NEW PSA Featuring Detroit Piston Charlie Villanueva

30 Apr 2010 at 2:24pm  youtube.com



Read more...




(no title)

12 Sep 2009 at 12:05am  youtube.com



Read more...




Alternatives to Wearing a Wig

22 Mar 2009 at 12:20pm  youtube.com



Read more...