Alopecia Areata Treatment

Learn about alopecia areata treatment and remedies

Alopecia Areata Totalis

 

Alopecia Areata

A hair loss disease.

Alopecia Areata TotalisInformation about Alopecia Areata, a hair loss disease.

Alopecia Areata
(al-oh-PEE-shah air-ee-AH-tah)

What is Alopecia Areata?

  • Autoimmune skin disease. Affects integumentary system.
  • Immune system attacks hair follicles by mistake.
  • Results in loss of hair on scalp and other body parts.
  • What triggers immune system is unknown (could be virus or genetics). Note: 1 of 5 people with A.A. has a person in their family with it.
  • Any hair-bearing site can be affected alone or with scalp.
  • Besides hair loss, people with A.A. are usually in good physical health.
  • Lack of societal understanding of disease leads to psychological issues.
  • Not life-threatening
  • Disease is unpredictable:
    • Sudden onsets
    • Recurrent episodes

Symptoms

  • Usually starts with one or several small bald spots on scalp and can progress to:
    • Total loss of hair on scalp (alopecia totalis)
    • Total loss of hair on entire body (alopecia universalis)
  • Can last for varying amounts of time.

Who gets A.A.?

  • Affects 1.7% of world population
    • Over 4.7 million of all Americans currently living will be affected during their lifetime.
  • Occurs without regard to gender, age or race
  • Begins most often during childhood

Treatments

  • No cure.
  • Re-growth can occur without treatment.
  • Cases where less than 50% of scalp hair is lost
    • Cortisone injections into bare skin. If hair will grow again, it will take four weeks.
    • 5% topical minoxidil solution applied twice a day. May grow hair.
    • Anthralin cream (synthetic, tar-like substance applied to bare skin and washed off after an hour). If hair will grow again, it will take eight to twelve weeks.
  • Cases where more than 50% of scalp hair is lost...
    • Cortisone pills. Much stronger than injections.
    • 5% topical minoxidil solution applied twice a day. May grow hair.
    • Topical immunotherapy. Chemicals are applied to scalp to produce special allergic reaction. 40% of patients will grow scalp hair. Must continue treatment to keep hair.
    • Aesthetic aids: Wigs, headscarves, removable eyebrow tattoos, bandanas, hats

Works Cited

http://my.webmd.com/hw/health_guide_atoz/tp22285.asp
http://www.naaf.org


CURE FOR ALOPECIA AREATA?
is there anything that works on alopecia areata/totalis?

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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.

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Alopecia Areata Totalis News




"We're not an oddity; we're just bald"

16 Jul 2009 at 3:24am  youtube.com



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