Events

Join us for the 4th Annual Walk For Alopecia Kickoff Lunch at the 41st Annual NAAF Conference! Attendees will enjoy a complimentary lunch, hear from inspirational speakers, and learn about the impact Walk For Alopecia fundraisers, donors, sponsors, and partners have on the nearly 7 million Americans living with this autoimmune disease. There may also be an exciting surprise or two!

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.

Additional details, including the exact time and location, will be provided soon.

You must be registered for the 41st Annual NAAF Conference to attend the 4th Annual Walk For Alopecia Kickoff Lunch.

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.

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:

August 17, 2026

September 21, 2026

October 19, 2026

November 16, 2026

December 21, 2026

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: 

September 15, 2026

November 17, 2026

Colorado Children’s Alopecia Group Family Fun Event!

All are welcome to join our Colorado Children’s Alopecia Group Family Fun event!  Group members are hosting a BBQ and will provide hamburgers, hot dogs, condiments and drinks.  The reserved picnic area is in the Snowberry Pavilion, near the splash pad.  You are welcome to bring all your family members and friends.  Bring your swimsuit and change of clothes to enjoy the park water features and picnic. If you plan to attend, please email the contact listed below with your RSVP and we will provide a sign-up link if you would like to bring a “side, drink or extra” to the event. 

Contact Patti McLaughlin, pattimcl@yahoo.com

Alopecia Awareness Game – Detroit Tigers at San Francisco Giants

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:

10/5/2026 – 6:30 pm

12/14/2026 – 6:30 pm