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Press Release for Glam Polish - Alopecia Awareness Fundraising

Press release to share Glam Polish's Alopecia Awareness Fundraising Shade

"Bad Hair Day" Alopecia Awareness Fundraising Shade.
For the month of September we are raising funds and awareness for Alopecia all funds donated will go to Alopecia Areata Association of Australia Foundation Inc. to help fund wigs for children with alopecia and aid in educating against bullying.

We will also be accepting donations from our gofundme fundraising page, all proceeds will go to the Alopecia Areata Association of Australia. To donate please visit:

Launch Info 

Our Alopecia Awareness Fundraising shade "Bad Hair Day" will be launching from our website at the following times:

USA Launch Time: 6pm EDT Friday September 4th.

Australian Launch Time: 8am AEST Saturday September 5th.

A small amount of "Bad Hair Day" will also be available from some of our International Stockists in September.
Bad Hair Day - Navy blue scattered holographic with navy, ocean blue and silver ultra holo microglitter, a special shade made to help us raise awareness and funds for Alopecia Areata, this shade was named by Natalia Voss a 13 year old girl with Alopecia Areata, some days it can be very hard covering up patches of missing hair or even looking at your hair in the mirror when you have Alopecia Areata so we thought this was the perfect name for our fundraising shade, we are donating $7.00 AUD from the purchase of each bottle to the Australia Alopecia Areata Foundation Inc.
Information and Facts About Alopecia

There are over half a million Australians and around 6.5 million americans living with Alopecia - a condition where people lose their hair from all areas of the body including the scalp, for which there is currently no known cure.

Approximately 60% of people diagnosed are under the age of 20, and for children especially, hair loss can have a negative impact on their self-esteem, which in many cases is linked to anxiety, depression, impaired academic performance and lack of social inclusion. To support children affected by the condition, Australia Alopecia Areata Foundation & Variety grants wigs - helping children gain their confidence and feel more comfortable amongst their peers.

* Alopecia (al-oh-PEE-shah) is a HAIRLOSS Condition, that can cause round patches of baldness, or total body hairless.

* There are 3 Main Types of Alopecia: Alopecia Areata - round patches / bald spots, Alopecia Totalis - complete Scalp baldness and Alopecia Universalis - total hair loss from body and scalp.

*Alopecia Areata is a believed to be a AUTOIMMUNE disease: the immune system mistakenly attacks the body (hair follicles) instead of defending it.

*Alopecia Areata affects MEN & WOMEN equally.  It can occur at ANY AGE, often begins during childhood or early teen years.  It does not discriminate on race.

*Alopecia is NOT Contagious.
AAAF Foundation Information.

Australia Alopecia Areata Foundation Inc. (AAAF), is established to be the national Australia body supporting research to find a cure or acceptable treatment for all forms of Alopecia Areata, support those with the disease and their families, and inform the public about all forms of Alopecia Areata.

Our Service philosophy is to give each person the best chance of managing their alopecia journey positively, the whole family and each individual needs to be supported to manage their unique experience. By reducing the financial and emotional stress and enabling children, young people, adults and their support networks to develop their strengths and skills, AAAF assists the whole family to achieve that positive journey.

Photo Credit to @lylynails


  1. What an amazing cause! I thought for a long time I was suffering from Alopecia but it turned out to be terrible hair lose caused by Dematitis. These are horrible problems that take away your confidence and makes you feel awful all the time. Because is it something very hard to fight against and so noticeable.

    1. I'm glad to be able to spread the word and help Glam raise some awareness and hopefully she can make some money to donate to help find a cure. They are both sad and hopefully people are made aware of them both and can do what they can to help the on-going research for cures. Thank you for sharing <3


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