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Alopecia Areata Support Network

Women With Alopecia Areata Support Network Blog

Thea Chassin

Thea Chassin is the founder of Bald Girls Do Lunch. She has had alopecia areata (universalis) since 1997 and has extensive experience as a health professional. She feels passionately that no woman should ever feel alone with any form of alopecia.
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Recent Posts

10 Tips for a Visit to Your Dermatologist or Other Health Providers

September 6, 2023 at 2:33 PM

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Topics: alopecia areata advice

Let's Do Lunch for People with Alopecia Areata in Pennsylvania

April 18, 2023 at 3:08 PM

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Topics: women living with alopecia, alopecia support, alopecia areata, talk about alopecia, alopecia support in Pennsylvania

Giving Tuesday Match Extended! Donations have 2X impact until December 5!

December 1, 2022 at 9:23 AM

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Topics: alopecia areata

It’s September! Alopecia Areata Awareness Month

September 22, 2022 at 9:41 AM

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Topics: alopecia month, alopecia awareness, alopecia areata

An Alopecia Areata Story: Mother and Daughter Speak Out!

June 21, 2022 at 5:32 PM

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Topics: alopecia areata, alopecia tips, alopecia areata advice, alopecia areata in girls, talk about alopecia, hair loss in children, children with alopecia areata, alopecia advice, alopecia areata in children, kids with alopecia areata

Alopecia Areata Teenager: Hannah’s Story

November 16, 2021 at 10:35 AM

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Topics: women living with alopecia, stories of women with alopecia, talking about alopecia, volunteers

Meet Alopecia Areata Volunteer, Hannah

November 16, 2021 at 10:34 AM

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Topics: women living with alopecia, stories of women with alopecia, alopecia areata, volunteers

URGENT: Global Dermatology Research Survey

January 25, 2021 at 5:30 AM

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Topics: alopecia research, alopecia areata

New Alopecia Research Opportunity. Thank you, participants! Recruitment is now closed.

May 18, 2020 at 9:06 PM

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Topics: alopecia medical resources, research for alopecia treatment, alopecia research, alopecia areata

“I Take My Lead From Becky”

February 11, 2020 at 7:10 PM

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Topics: coping with alopecia, women living with alopecia, stories of women with alopecia, talking about alopecia, alopecia awareness