The Reflection Of Living With Alopecia Aerate

My cheeks were flushed from the sun and excitement of the day spent exploring Phillip Island. I could see my curls caught in the wind and moving

I don’t quite know how to explain what happened next. It was like being in a sensory deprivation tank, but I could feel—no that's not right—I could sense something different was moving toward me.

Touch, as we walked thru the forest I touched many amazing things. The first thing we came across was the rough texture of a rock. Half of the rock had green moss on it and the other side had nothing but rock on it. Another thing I touched was a snake. The snake was surprisingly smooth but at the same time very scaly.

“Open your eyes…” A voice whispered. I lifted an eyelid, feeling a warm breath on my neck.

Alopecia Areata is a common autoimmune skin disease that attacks the hair follicles and causes hair loss in places like the scalp, face, and sometimes other places on the body. Alopecia is very common because it affects about 6.8 million people in the United States alone and can affect people of all ages, genders, and ethnic groups.

I could feel it in my fingertips, the ends of my hair, and everywhere in between. It stretched inside of me like a coiling snake, ready to lash out.

Alopecia Areata is a disease that causes loss of hair on the head, face, or body in patches and speckles. The regions of this hair loss could range from very small to very large. It is not only found on the scalp, but is found in areas of facial hair or even body hair. This disease is found in both men and women even though men are more common. Alopecia Areata is the only name given to the disease, though there are different names for different types of the illness. This disease is not confirmed to be genetic, but if a family member has the illness there is a higher chance for another family member to acquire it. It is in fact a polygenic disease. The National Alopecia Areata Foundation reports, “unlike a single-gene disease, both parents must

When your child is diagnosed with alopecia, you probably have scoured the web for relevant information about the disease. Even if you know everything you know about hair loss, nerve-wracking to meet this guy has such a serious topic. The first step is to have a chat child will learn how to think through. How old is your child? O when that day will be the most open to talk to? Style of speaking for him or her what to rage around? Which ones to help him or her to stay calm and collected?

A cold breeze continued to blow as I looked around, hearing my neck make a loud pop that made me question

I was the last girl to walk on the floor and hit my starting spot. I felt a wave of heat as I walked into the

I had the terrifying sensation of knowing that all the bones inside my body were dissolving, as a hard, fingernail—like crust covered me all over.

It was as if my whole world dissipated, many emotions rapidly sped through my head, most of which were unregistered except anger and sadness.

My heart pumped quicker as goose bumps invaded my limbs, and my fingertips rang as a stark volt of electricity ventured up my spine, prickling my skin, and I dropped it.

The jump seemed a mile long. It touched my toes with only the slightest bit of warmth. It reached for my knees and grabbed onto my waist. It rushed up as if it was trying to kill me in it depths. Yellow liquid reached my head and seemed to pull me down under.

Then on my feet I felt water going past my feet. Then I looked behind me and there