Find A Youth Mentor

Hello! My name is Carla and I’m from southern California. I’m currently in my 3rd year at UCLA studying Psychobiology. My journey with alopecia has been a long one, to say the least. I was born with congenital triangular alopecia (CTA) and have tried every treatment possible, from steroid shots, to topical creams, to oral medications. Though the physical aspects of alopecia poses many challenges, I believe the emotional impact and struggles are even harder to navigate. Regardless of the highs and lows, I have come to accept my alopecia and work towards coping with it, rather than allowing it to hinder the quality of my life. I decided to get involved with NAAF because as a child, I never had someone in my life that could relate to me or connect with me that had similar experiences. Beyond alopecia, I love canvas painting, makeup, going to the beach, and watching Shrek 2. I can’t wait to meet and to get my know my future mentee.

Howdy! My name is Sam and I live in Oregon, but I’m originally from Washington. I have experienced all types of alopecia. I was originally diagnosed with alopecia areata when I was 8, alopecia totalis when I was 9, and universalis when I was 10. While my hair/eyebrows/eyelashes have partially grown back since then, I choose to wear wigs (the one in the photo is from Amazon if you want to match!) because I think that they are fun! I have been dancing since I was 3, and have danced competitively, collegiately, and now professionally with the Portland Winterhawks! Alopecia doesn’t stop me from doing the things I love - I use wig glue and wigs to hold my hair secure! In my free time, I love line dancing, going to concerts, reading, and crocheting. I sometimes forget that I have alopecia quite honestly, and focus on the joy in life. I cannot wait to meet you!

EHi! My name is Erin and I am a sophomore at Choate Rosemary Hall. I live in Connecticut but I’ve also lived in Korea, Hong Kong and Singapore! When I was living in Korea, I was diagnosed with Alopecia Universalis. I lost all the hair on my head and body within two weeks. By the third week I was completely bald. As a thirteen year old going through Alopecia Universalis, it was hard to adapt to my new look. I wore a wig for the first few months after being diagnosed, but as a soccer player and an athlete, it was hard for me to keep the wig on. Three months after being diagnosed with Alopecia Universalis, my hair started to grow back! Though my hair started to grow back, I was faced with the obstacle of having super short hair. I never let my Alopecia get in the way of any of my athletic contests or my hobbies. In years since, I have started to share my journey with Alopecia Universalis hoping to provide support and help others overcome any struggles. Languages spoken: English, Chinese, Korean, and Spanish.

Hi guys! My name is Natalie Wong, and I’m currently in my 2nd year at the University of Georgia. My major is Environmental Health, and I’m on the pre-med track; I hope to become a pediatric dermatologist and pursue research in Alopecia in the future! My journey with Alopecia had its ups and downs: I was diagnosed with Alopecia when I was 5 years old, and I completely lost my hair when I was 6 years old. During my freshman year of high school, I lost my eyelashes, but they grew back later (it may have been due to stress). Recently, my eyebrows have grown back too. Regardless, overtime I learned to love myself, to be more confident, and to surround myself with supportive friends. I even was able to convince my classmates to vote for me for “Best Hair” for my senior superlative (I still can’t believe I won). I love wearing colorful, floral headbands to highlight the fact that I DON’T have hair. It’s sort of my signature style :D. I can’t wait to meet with my mentee and share my experience with Alopecia! Apart from that, I’m into film photography, traveling, watching movies/shows, makeup, cooking, collecting vinyls, and listening to music. My favorite genres are kpop, rnb, and jazz, but I honestly love all so give me recs! These are a few of my interests, but I’m open to try out new things!

Hello! My name is Camden Kantaparn. I am 16 years old and live in Northern Virginia, 30 minutes outside of Washington, DC. I was diagnosed with alopecia areata when I was about 19 months old and lost all of the hair on my head and eyebrows by the time I was 3. Growing up, being a good student and athlete helped to build my self-confidence. I played travel soccer for 7 years and am currently running track for my high school team. In addition to running, I enjoy reading, traveling (I’ve been to Thailand, Cuba, Iceland, Croatia, Portugal, and Peru just to name a few!) and playing video games. Looking forward to connecting!

Hello! My name is Maia Campbell and I'm from Indiana. I recently graduated from Ball State University where I studied pre-med biology and chemistry, and I am currently applying to physician assistant master’s programs! I currently work as a pediatric vision therapist and love my job. Most of my free time is spent reading, playing tennis and golf, or doing creative activities like scrapbooking and crocheting. I’m also a huge IndyCar fan and was an Indianapolis 500 Festival Princess last year. I was diagnosed with alopecia areata at age 2 and tried every treatment under the sun, then eventually decided to lean into being different and have fun with wigs, hats, and headbands! I began wearing wigs in high school and eventually lost all my hair in college. I’m currently in a clinical drug trial for alopecia and have seen amazing results so far! Though there were times I struggled to cope with bullying, self-esteem, and mental health struggles, I’ve always found such great encouragement and resources from people in the alopecia and NAAF communities. Alopecia awareness and education has always been important to me, and I’ve found the most comfort in having a “teaching” mindset when someone asks me about alopecia. Whether it be holding a fundraiser for NAAF, doing an immunology project on alopecia, or being open about it on social media, there is so much power in education. I am very excited to become a youth mentor and look forward to meeting more people in this community!

Hi everyone! My name is Niki, and I am currently a medical student living in New York City. I was suddenly diagnosed with alopecia a couple of years ago, which caused patchy hair loss in my scalp and eyebrows. Since then, I have tried various treatments in an effort to manage my condition; however, I continue to experience cycles of hair loss and growth. Despite the ups and downs, I have learned to embrace my alopecia and see it as a part of who I am. While the physical effects of alopecia can be difficult, the emotional impact can be just as challenging. I decided to get involved with NAAF because I understand the importance of finding support and compassion from individuals who have undergone similar experiences. I am eager to share my story and offer encouragement and guidance to those affected by alopecia to help them feel less alone in their journey.

Hi! I'm Margaret McGraw, a 25 year old working for a fintech company and living in New York City! I've had Alopecia since I was a little kid and wore a wig until this past year. I ran the New York City Marathon in 2022 to raise awareness for Alopecia Areata, and during that process, I stopped wearing my wig all together. I'm an active person who enjoys running, hiking, playing tennis and walking around/exploring! I'm a huge Francophile, and speak French fluently. I love to cook, watch new tv shows, hang out with friends, and read new books! 

Hi! My name is Serena Kas-Mikha and I am 20 years old. I live in Michigan and I’m a social work student. I enjoy spending time with my family and friends, listening to music, and going to the gym. I developed Alopecia Areata when I was 9 years old. I lost my eyelashes, eyebrows, and developed bald spots around my head. I would get about 6-7 patches at a time. In 2020, I lost almost all my hair and it happened suddenly. I was devastated and I allowed what I was going through to take over my life and alter the way I felt about myself. It took a toll on my mental health, but I was lucky enough to have supportive people in my life who helped me through it. It’s been a journey filled with ups and downs but it’s one I’m so grateful for. As my hair eventually began to grow back, my experiences have become a part of who I am. Alopecia has taught me self-love and that my worth was never defined by the number of hairs on my head. In the midst of your struggle, it can feel like you’re alone, but I promise you’ll get to the other side of what you’re going through. Lean on the people closest to you, they want to help, you don’t have to face anything by yourself. As a mentor, I hope I can help someone feel less alone, loved, and supported throughout their journey.