Press

Showing my true self to the world with alopecia: "I wanted to be free, I feel liberated"

By Aziza Shuler on September 14th, 2023 PHILADELPHIA (CBS) -- A member of our CBS News Philadelphia family, weekend anchor Aziza Shuler,...

AJL Takes on PIX11

Last Tuesday, two AJL co-founders - Alison Lee and Dr. Kristen Lo Sicco - were interviewed live on PIX 11 regarding the recent FDA...

New Hair Loss Treatments for Teens with Alopecia Comes After Years of Limited Options

By Adrianna Rodriguez on June 23, 2023 Alison Lee felt a slight tug at the back of her head. Her dark wig slipped off in an instant,...

The Bald Pack Journals (S2): Alison Lee

AJL Co-Founder Alison Lee recently appeared on the Those Bald Chicks Podcast. Make sure to listen to the episode and follow their account...

Durable Medical Equipment and Medicare Reform

Since I was very young, I have lived with alopecia areata which has stripped me of all my hair. Because of my autoimmune condition, I...

Wigs Aren’t Mandated Under Medicare, But I Want To Change That

By Alison Lee on October 18, 2022 I've had alopecia areata — a condition which sees the immune system attack hair follicles, resulting in...

10 Things I’ve Learned About Dating with Alopecia

I was diagnosed with alopecia areata, an autoimmune disorder that causes your hair to come out, at the age of 2 and just celebrated my 30th

SK(IN) DEPTH Advocacy

The extent of the problem: 25.2% of patients living with alopecia areata (AA) describe a serious economic burden, and 18.2% indicate...

Alison Lee and the Alopecia Justice League Are Teaming Up to Change the World

“Because everyone has hair, it is challenging to grasp life without it,” Lee says. “It is even more difficult for individuals to empathize w

Alison Lee on the Alopecia Justice League & Never Being Too Young to Implement Change

Very Nearly Almost | April 22, 2022 The teen years can be some of the toughest to face having alopecia, but Alison Lee has taken her...