Community Events

Our calendar of events keeps our supporters informed of support group meetings, fundraisers, walk-a-thons and more! We are happy to list your meeting, walk-a-thon, Tortoise & Hair run/walk, Links for Locks golf tournament, bowl-a-thon, etc. The possibilities are endless. If you can think of it, you can do it.

We are here to help you make your specific event a success. Let us know what we can do for you, be it providing you with materials to disperse, targeting a specific demographic for a mailing, or notifying the NAAF community on your upcoming event.

Send your event details to us at to be included on the calendar. If you know of other events that would be of direct interest to NAAF supporters please let us know about them as well. If you are just getting started and don't know what kind of event to host, please contact Laura Ralph at 415.472.3780 or via email at

NOTE: The National Alopecia Areata Foundation’s Support Group and Telephone Support Contact information is provided solely for personal use. It is intended for people with alopecia areata and their loved ones to easily find services in their area. This list, or any part of this list, may not be downloaded, republished, or duplicated in whole or in part for commercial purposes. Additionally, contacting individuals on this list directly to engage in commercial activities of any kind, is strictly prohibited. 


Super Power Challenge - Alopecia Areata Awareness Month

Sep 01, 2018, 12:00AM PDT to Sep 30, 2018, 11:00PM PDT
Alopecia areata is an autoimmune skin disease that affects as many as 6.8 million people in the U.S. Although no cure currently exists, progress in treatment has been made thanks to the countless heroes who empower and advocate for those living with the disease. This September, in celebration of Alopecia Areata Awareness Month, NAAF invites you to join the Super Power Challenge, a fundraising and awareness campaign that unites the powers of heroes like you to avenge the forces of alopecia areata that try to keep us down. Every superhero has a unique and special power. What’s yours?Read more

Team Up with the Washington Nationals

Sep 21, 2018, 7:00PM EDT
Team Up with the Washington Nationals on Friday, September 21!Read more

Team Up with the St. Louis Cardinals

Sep 21, 2018, 7:15PM EDT
The National Alopecia Areata Foundation and the Saint Louis Cardinals are teaming up to support Alopecia Areata Awareness Month in September! We’re asking for your support in this National League showdown as the Cardinals take on the San Francisco Giants! Friday, September 21, 2018 at 7:15 PM Saint Louis Cardinals vs. San Francisco Giants Left/Right Field Loge Tickets : $20.00 GIVEAWAY ALERT! Adult, Cardinals Hockey Jersey to first 30,000 fans!!! How to Order: Visit to order tickets online. Call (314) 345-9000 to speak to an attendant. Phone lines are open during...Read more

Rancho Cucamonga, CA Alopecia Areata Support Group Meeting

Sep 21, 2018, 7:00PM PDT
Support Meeting Friday, September 21, 2018 6:00 PM Location: RC Family Resource Center 9791 Arrow Route Rancho Cucamonga, CA 91730Read more

Alopecia Awareness Volleyball Match Sylvania, OH

Sep 21, 2018, 7:00PM PDT
Volleyball Match Lourdes V Siena Heights Friday, September 21, 2018 7:00pm Russell J Ebeid Rec Center 6737 Convent Blvd. Sylvania, OH 43560Read more

Le Beautique Salon, Awareness Fundraiser, Millcreek, UT

Sep 22, 2018, 12:00PM PDT
Le Beautique Salon 4700 900 E #45 Millcreek, UT 84117 September 22, 2018 12:00pm Isha Esthetics Red Rabbit Henna The Bald Stylist Chameleon Faces Bring your Friends & FamilyRead more

Team Up with the Miami Marlins

Sep 22, 2018, 7:00PM EDT
Team Up with the Miami Marlins! Tickets only $21!Read more

Team Up with the Houston Astros

Sep 22, 2018, 6:00PM CDT
Team Up with the Houston Astros on September 22!Read more

Team Up with the Los Angeles Dodgers

Sep 23, 2018, 1:00PM PDT
Team Up with the L.A. Dodgers on Sunday, September 23!!Read more

San Diego, CA Alopecia Areata Pool Party

Sep 23, 2018, 2:00PM PDT
Hello Alopecia Areata Community, I am hosting a potluck pool party for Alopecia Awareness Month. Please come to have fun in the water. I will order pizzas, and I created a sample list for what others may want to bring at the bottom of this evite It does not necessarily have to be exactly that, those were just quick ideas. Please indicate on that list what you are bringing, so that we have a balanced potluck :) Last year, we were a small group but very intimate and had a great time. My daughter Natasha is 12 with alopecia universalis, and is always open to make more...Read more