Events

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.

Alopecia Areata Awareness Month is a month-long celebration and recognition of all those affected by alopecia areata. During September, the NAAF community works to increase awareness, reduce stigma, and empower those living with alopecia areata locally and nationally.

There are several ways you can join in, raise funds, and spread awareness while having fun.

This support group is an ideal place to come and talk with other parents who have children living with alopecia areata. It is the place to gain knowledge from those with experience. With time comes the ability to deal and cope with hair loss of a loved one. We are very fortunate that so families 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 adult family members who attend.

2026 Virtual Support Meeting Schedule:

Thursday, September 3rd at 7:00pm Mountain Time

Alopecia Night @ The Rockies

September is Alopecia Areata Awareness month.  Join us for a baseball game and a portion of ticket sales will support NAAF research. 

Colorado Rockies vs. St. Louis Cardinals on Friday, 9/4/2026.

See attached flyer with QR code to purchase tickets.

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.

2026 Meeting Dates: 

November 17, 2026

2026 Support Meeting Dates:

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.

*Note:  If this is your first time attending, you must RSVP and fill out a form prior to attending.

Your Host:  Mary

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.

2026 Meeting Schedule:

October 19, 2026

November 16, 2026

December 21, 2026

The National Alopecia Areata Foundation’s (NAAF) 4th Annual Walk For Alopecia is the finale of Alopecia Areata Awareness Month, and it will once again bring the alopecia areata community of families, caregivers, friends, co-workers, and healthcare professionals together to help drive research for more treatments and a cure, increase support, advocate for change, and end stigma.

Join us to create hope, build community, and drive progress! Mark your calendar for the Walk For Alopecia today and plan to walk with us at one of our Flagship Sites in San Francisco and Philadelphia, community volunteer-led walk sites, or Walk Where You Are as a team or individual in your neighborhood.

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.

Meeting Schedule:

12/14/2026 – 6:30 pm