Events

Light refreshments will be served.

Please See Detailed program here>>>

You may RSVP for yourself and 2 additional people, with whom you would like to attend.

Your information will be forwarded to Robbie Baker, VP of Development, who will contact you with program event details.

Please note this program is an in-person, live event.
The program will not be recorded for on-demand viewing and tele-participation is not available.

This support group is an ideal place to come and talk with others about living with alopecia areata. It is the place to gain knowledge from those who have had years of experience. With time comes the ability to deal and cope with your own hair loss or that of a loved one. We are very fortunate that so many are willing to bring to the meetings their wisdom and advice to share in a direct but compassionate manner that reflects understanding and concern. The support group experience has its rewards for all who attend.

This support group is an ideal place to come and talk with others about living with alopecia areata. It is the place to gain knowledge from those who have had years of experience. With time comes the ability to deal and cope with your own hair loss or that of a loved one. We are very fortunate that so many are willing to bring to the meetings their wisdom and advice to share in a direct but compassionate manner that reflects understanding and concern. The support group experience has its rewards for all who attend.

What does it mean to be an advocate for alopecia areata? Join this webinar to hear from members of the alopecia areata community who have taken their advocacy to the next level!  Dermatologist Kristen Lo Sicco, MD,  along with founding members of the Alopecia Justice League and NAAF Legislative Advocates, Alison, Julie, and Lindsey, will talk about their advocacy work, key issues for the community, and the personal empowerment that comes from making a difference. 

Mary has lived with alopecia for over 25 years. She’s a psychotherapist experienced working with children, adults and families. This support group is aimed at providing those living with alopecia emotional support, material resources, and a place to share their experiences. This virtual support group is open to adults living with alopecia, children and their caregivers.

Dr. Caroline Mann of WashU Dermatology will be attending to answer questions about alopecia areata.

For Teen Girls Ages 12-17

This support group is an ideal place for teen girls who want to meet and talk with other girls their age about living with alopecia areata. Only teen girls will be allowed in this virtual support meeting.

Please Note:  You must RSVP to receive a link to this meeting.

This support group is an ideal place to come and talk with others about living with alopecia areata. It is the place to gain knowledge from those who have had years of experience. With time comes the ability to deal and cope with your own hair loss or that of a loved one. We are very fortunate that so many are willing to bring to the meetings their wisdom and advice to share in a direct but compassionate manner that reflects understanding and concern. The support group experience has its rewards for all who attend.

• Special guests and knowledgeable speakers will offer inspiration.
• Medical professionals will share valuable information and advice to better understand and manage alopecia areata.
• Expert researchers will detail the latest findings of recent clinical trials and soon to be approved drugs coming to market!
• Kids (5-17) will make new friends and wonderful memories at the Children’s Conference Camp.

2023 SPONSORS