Find A Youth Mentor

Hello! My name is Harrison Goldberg, I was born and currently live in the New York Metropolitan Area. I was diagnosed with Alopecia Areata Universalis when I was 6 years old. I lost all of the hair on my head within three weeks - and the rest of it within three months. In the beginning, it was very hard for me to make friends and I was made fun of in school for being “different” than everyone else. That same year, I attended my first NAAF conference in Houston, Texas. Ever since then, my journey through Alopecia hasn’t been exactly smooth. But what I can say, is that Alopecia has gifted me with great advice, greater memories, and most of all life-long friendships. Currently, I am a junior in High School and I plan on applying to colleges next fall. I love to talk about anything whether it be sports, T.V, news, or just anything in general. In the beginning I, like any other person, struggled greatly through Alopecia. However, if there’s one thing I’ve learned from having Alopecia is to constantly persevere - the storm always comes to pass! It’s always been a dream of mine to help out kids who went through the same struggle I went through nearly ten years ago; to see those thoughts come to reality is more than a dream come true. I would be more than happy to share my experiences regarding Alopecia or just talk in general. Thank you for your time!

Hi, my name is Ali Cavanaugh and I am no stranger to autoimmune disorders. At the age of 13 months old I was diagnosed with diabetes, at the age of 6 I was diagnosed with Hashimoto's Thyroiditis, at the age of 8 I was diagnosed with autoimmune hives, at the age of 13 I was diagnosed with Vitiligo, and finally at the age of 25 I was diagnosed with Alopecia. I wont lie, being diagnosed with Alopecia was probably one of the hardest things to hear…and I have heard a lot of things. To know that there is nothing that I can do to keep my hair from falling out was devastating. But, instead of crumbling into pieces I picked myself up and embraced being bald. I grabbed a pair of razors and shaved what remained off. I found a great wig place in my area, Wigs R You, and have so many different wigs that I can be a different person every day of the week. When I get tired of wigs or head scarfs I just take it all off and enjoy the freedom. Alopecia has not hindered my life in any way…I won’t let it. I still play sports, go to work, ride horses, got married, and so much more. I would love to use my experience dealing with Alopecia Universalis to help you accept who you are and discover that you are more than just hair.

Hi! I’m Aubri! I’m 27 years old from Spokane Washington! I love to create! My favorite things to create range from fun videos, art, photography, cooking to more! I also love playing games of all kinds- board games, card games and video games. I’m a huge Nintendo fan! Learning languages is a passion of mine and watching foreign movies. Best believe I will never turn down a karaoke party. I love all types of music, including main stream, indie, Latin and K-pop. I studied piano for nine years and sang in choir for 7! I have twin toddlers and we love going on adventures. I was first diagnosed with alopecia when I was 6 years old, and lost all of my hair in 1st grade. I don't wear wigs or hats. I just go bald and embrace my shiny head wherever I go!

Hey, I'm Ezra. I'm a high school senior in Houston, Texas. I enjoy playing musical instruments (guitar, saxophone, and piano), soccer, watching football (Fly Eagles Fly), and playing video games. I was diagnosed with Alopecia Universalis at 11 years old, and lost all the hair on my head, eyebrows, and arms/legs in the weeks after my diagnosis. As a mentor, I hope to spend quality time with mentees and impart any tips or advice I've learned throughout my Alopecia journey while having some fun!

Hello, I’m Ben Israel and I am from the suburbs of Detroit. I lost my hair when I was 7 years old and have been pretty much bald ever since. I have a passion for all sports, especially ice hockey. I played NCAA D1 Ice Hockey for 4 years at Colorado College. I am also very interested in business and investing. Having alopecia was difficult at times, especially during middle school and high school, but it has made me so much stronger. I am extremely excited to meet people who have alopecia as well and help them realize the strength that they can gain from it too. I would love the opportunity to share my experiences with alopecia as well as support children and families through theirs.

Hello! My name is Grace Duhs. I am 17 years old. I live in sunny San Diego California. My mom discovered my Alopecia Areata when she was routinely brushing my hair and found a bald spot the size of a quarter. I started just losing my hair until I was completely bald. I now have Alopecia Universalis but I'm still living a positive life! My favorite hobby is acting in my school plays for the past six years! I was recently in the play Lion King and I was the comedic character Timon! I also love baking, doing track and field, soccer, and hanging out with my friends. I have 2 fluffy dogs named Toby and Hana and they are the best dogs. I want to help support kids who have Alopecia and be a friend to anyone who needs it. I want to help them gain confidence and show them they are made beautifully inside and out. My favorite quote from my Alopecia experience is, “Why fit in when you are born to stand out.”

Hello! My name is Mary Wills. I was diagnosed with patchy alopecia in 1994 and universalis in 2011. I am currently a mental health therapist and licensed social worker. I completed my undergraduate degree at the University of Mount Union, graduate degree at Case Western Reserve University, and studied abroad in northern India. I have experience in diverse social work settings, treating the psychological needs of patients with chronic health conditions. I'm currently married and I've traveled to all fifty states. I enjoy sewing, crafts and spending time with my cats. I'm excited to meet a mentee to provide emotional support through his or her alopecia journey. 

Hi I’m Nell! I’ve been living with Alopecia almost my entire life and have experienced alopecia areata, totalis, and currently have universalis. I have gone through an incredible and intense journey with my alopecia and have ultimately come out of it a stronger and wiser person. I got involved with NAAF two years ago when I went to my first conference and decided to stop wearing my wigs. The conference empowered me so much that I immediately got involved with the organization, with the aim to give back to the amazing community that changed my life. I am 18 years old and going to Sarah Lawrence College next year. I’m hoping to study something in the humanities and creative writing realm, but am undecided. When it comes to hobbies, I like to do anything artistic! I’m a spoken word poet/rapper, ultimate frisbee player, a Buddhist, and am extremely involved with my alopecian community. I am the co-creator of this mentorship program and am dedicated to helping younger kids and parents struggling with alopecia. I do a lot of work for NAAF and have a personal goal of making alopecia more mainstream to help find funding for a cure. Currently I have a lot of experience with younger children through tons of babysitting and meeting and hanging out with younger kids with alopecia. When it comes to personal traits, I pride myself on my fearlessness and my passion (I can thank my alopecia for making me unafraid and strong). I also rock the bald look and am at a point where I accept and love my alopecia

I am an undergraduate student at the University of Washington double majoring in Public Health and Spanish and minoring in Diversity. I am passionate about minority health and hope to use my degree to help marginalized communities. I have had Alopecia since I was 10, went through a million and one treatments to grow it back, but lost it all when I was 12. For two years I wore a wig, but it inhibited from being the outgoing and charismatic Chiara that I was meant to be, so when I was 14, I decided to stop wearing one and have not put one on since! I am all about embracing the bald look, but I usually wear headbands, which have become my staple. When I am not at school or work, I am traveling. All my money goes towards exploring the world! I am Eurasian (Italian/Chinese), so most of my family does not live in the United States, which gives me an even better reason to travel and visit them. I love talking about Alopecia, Diversity and Inclusion, Makeup, Body Positivity, Feminism, Travel, and everything else in between! I did not know a single person who had Alopecia when I was originally diagnosed, so I want to be that support system for someone else who now stands in the shoes that I once did.

Hi! My name is Leah Krut and I am 17 years old. I live in Boca Raton, Florida, and I am a junior in high school. I would consider myself a fun and social person. I enjoy participating in activities such as dance and art. I also love to hang out with my family and friends and try new things.  I developed alopecia areata when I was 11 years old, which caused some patches of my hair to fall out. I never knew when it would flare up, and it caused me anxiety. I also did not know anyone else struggling with this, making me feel insecure. This was a difficult experience for me, but I was fortunate enough to have my hair grow back out eventually. However, it did take a toll on my mental health, and I was grateful to have a supportive group of friends and family around me. With this, I’d love to be able to be a friend to someone else with alopecia. I understand all of the confusion and emotions that come along with alopecia and would love to be able to make someone's life even just a little bit easier on this journey. Despite this challenging experience, I have learned to embrace my differences and have become more confident in who I am. I am excited to see what the future holds and am excited to be able to help others in this journey.