#Support Groups Flagstaff, AZ In-Person Support Meeting Flagstaff, Arizona Monday, April 27, 2026 | 6:00 PM, MST 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.
#Support Groups Sterling Heights, MI In-Person Support Meeting Sterling Heights, Michigan Thursday, May 14, 2026 | 7:00 PM, EDT 2026 Support Meeting Dates: July 14 September 16 November 17 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.
#Support Groups Cleveland, OH Virtual Support Meeting Virtual Event Monday, May 18, 2026 | 7:00 PM, EDT 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: July 20, 2026 September 15, 2026 November 17, 2026
#Support Groups Teen Girls, Virtual Support Meeting Virtual Event Monday, May 18, 2026 | 7:00 PM, EDT *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: June 15, 2026 July 20, 2026 August 17, 2026 September 21, 2026 October 19, 2026 November 16, 2026 December 21, 2026
#Support Groups Colorado Virtual Children’s Support Meeting Virtual Event Tuesday, June 2, 2026 | 7:00 PM, MDT 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: Wednesday, September 2nd at 7:00pm MST Thursday, December 3rd at 7:00pm MST
#Support Groups Boston Parents Virtual Support Meeting Virtual Event Monday, June 8, 2026 | 6:30 PM, EDT 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: 8/10/2026 – 6:30 pm 10/5/2026 – 6:30 pm 12/14/2026 – 6:30 pm
#Support Groups Maine/New England – Virtual Support Meeting Virtual Event Monday, June 15, 2026 | 6:15 PM, EDT 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. Upcoming Virtual Meetings: August 17, 2026 October 19, 2026
#Support Groups Teen Girls, Virtual Support Meeting Virtual Event Monday, June 15, 2026 | 7:00 PM, EDT *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: July 20, 2026 August 17, 2026 September 21, 2026 October 19, 2026 November 16, 2026 December 21, 2026
#Conference 41st Annual NAAF Conference Orlando, Florida Thursday, June 25, 2026 | 12:00 AM, EDT Join us for the 41st Annual NAAF Conference in Orlando, FL, on June 25-28. Complete the interest form to be the first to know when registration opens at a special discounted rate. More details coming soon!
#Fundraiser #Awareness 4th Annual Walk For Alopecia Kickoff Lunch Orlando, Florida Saturday, June 27, 2026 | 12:00 PM, EDT 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.
