#Awareness #Volunteer Make Medical Wigs Affordable Virtual Event Monday, February 23 – Thursday, December 31, 2026 Ask your local legislators for support of H.R. 7546 and S. 3872 to provide coverage for cranial prostheses (medical wigs) as durable medical equipment under the Medicare program. Alopecia areata is a common autoimmune skin disease which causes unpredictable, often sudden and severe hair loss, on the scalp and body. Frequently dismissed as a cosmetic condition, alopecia areata is a deeply traumatic experience, resulting in emotional and economic pain and social isolation, especially for children. It is not just hair. Many individuals living with alopecia areata utilize cranial prostheses to camouflage their hair loss, restore well-being, and support their mental health. Unfortunately, these prostheses can come with a significant out-of-pocket cost for Americans with low or fixed incomes. This is especially burdensome for children, who often require cranial prostheses for attending school. Currently, the Social Security Act determines which products are considered “durable medical equipment” for the purposes of Medicare coverage. It includes crutches, oxygen tanks, and prosthetics. However, the definition of a “prosthetic” does not specifically include cranial prostheses, which can lead to coverage challenges. Private insurance and other payers often base their coverage policies and standards on Medicare. Take action to show your support for the 7 million Americans living with alopecia areata. Click the button below to send emails to your legislators to co-sponsor H.R. 7546 and S. 3872.
#Fundraiser #Awareness Alopecia Areata Awareness Month Virtual Event Tuesday, September 1 – Wednesday, September 30, 2026 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.
#Fundraiser #Awareness 4th Annual Walk For Alopecia Saturday, September 26, 2026 | 12:00 AM, PDT 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.
#Awareness #Support Groups Charlotte, NC Alopecia Awareness Event Charlotte, North Carolina Saturday, September 26, 2026 | 9:00 AM, EDT Join us for an Alopecia Awareness Month event in Charlotte! Date/Time: Saturday September 26th from 9:00 AM to 11:30 AM Come for story time at 10am (featuring Alopecia books), games, coloring and crafts to connect with others, and come hang out and enjoy a treat at the delicious Batch Maker! Location: The Batch House 901 Berryhill Rd Charlotte, NC 28208 Please RSVP to Lindsay Walter lhwalter3@gmail.com This event is for anyone with Alopecia and their families and friends.
#Fundraiser #Awareness #Support Groups Charlotte Area Alopecia Support Group – Walk Where You Are Saturday, September 26, 2026 | 10:00 AM, EDT Join us as we come together for the Walk For Alopecia with a Walk Where You Are event in Charlotte! Link to Sign Up: I’m supporting Walk For Alopecia® Date/Time: Saturday, September 26th at 10:00 AM Location: 200 Clanton Rd., Charlotte, NC 28217 Instructions: Street parking is free. Please do not park in the U-Haul Lot. We will walk on the Rail Trail and those who are interested can join us for lunch afterwards in the area.
