Find A Youth Mentor

Hey there, I'm Molly! I'm a 25-year-old touring musician from California now living in Nashville, TN. I love music and travel all over the world performing with my band. I was diagnosed with alopecia universalis at age 3. I went through many stages of acceptance and denial with my alopecia. As a child I wore a lot of hats and transitioned into wearing wigs in high-school. My biggest fear used to be someone finding out that I wore a wig, but now I love telling people that I have alopecia because I think it's an important and amazing part of who I am. I also like to use my music as a platform to let my fans know about alopecia. As a kid, NAAF was an indispensable resource to my family and me. Each time I went to a conference I was able to come out of my shell, and see not having hair as something cool and special about myself. Having someone to talk to year round who understands what it's like to grow up with alopecia would have been so helpful to me so I'm thrilled to be a part of this youth mentor program. In my free time I like doing yoga, going to the movies, reading, writing songs, riding my bike and going to concerts. I'm here to help however I can by lending support, listening, answering questions, being a friend or just having fun together (or all of the above :))!

Hi! My name is Courtney and I’m from Odenton, MD. I’m 23 and studied International Affairs at James Madison University. I’ve had hair loss on and off since I was about 10 or so. Around my senior year of high school the patches got so bad, I decided to take the plunge and shave it all off! From that time on it’s been a lot, from losing eyelashes and wearing wigs, I’ve seen it all and would be happy to talk about my experiences. I’m also interested in all things travel, music, writing, hiking, and t.v shows. I’m excited to meet others and help in any way I can!

Hi! My name is Glenn and I grew up in a small town outside of Syracuse, New York. I’ve been a part of NAAF for four years now. I decided to stop wearing my wig after my third NAAF conference which was the beginning of my junior year in high school. I have made so many friends through NAAF and I’m truly blessed to have found such a great community of support! I have learned through Alopecia to be more confident and embrace my true self. Last year I got my eyebrows tattooed on and I wear eyeliner in place of lashes. I have a few wigs and now I only wear them on the occasion of very cold weather or just wanting to have some hair! I am currently a senior in high school and I’m applying to college for business next fall. I enjoy being outside, playing lacrosse, watching movies and traveling! I’m always up to try something new and learn more about other people! I look forward to talking with you and helping in any way I can!

Hi! My name is Andrea (Anj) and I grew up in Canton, Massachusetts. After living in Nashville, TN and Portland, ME, I moved to Newton, Massachusetts. I studied human and organizational development at Vanderbilt University and am currently working full time as a Revenue Cycle Technology Trainer. My hobbies include swimming, trivia, reading, traveling, hiking, and watching movies. Now a little more about my alopecia journey. When I was nine years old, I began to lose my hair. Within one year, all the hair on my head had fallen out and I began wearing bandanas, my signature look. A few years later, I began to lose my eyebrows and eyelashes, which miraculously grew back. I definitely understand alopecia’s unpredictability. Although I own a wig, I prefer to wear a bandana (for warmth and sun protection) or just go bald! During cold weather, I love wearing my fuzzy moose hat I acquired in Maine. Thankfully, due to the support of family and friends, I live a normal life full of relationships and adventures, and embrace my uniqueness! I truly believe alopecia has shaped who I am today and has made me a strong, self-assured individual. Due to my confidence, I have already helped others experiencing baldness from alopecia and chemotherapy. Whether someone needs advice, a shoulder to cry on, or just a friend, I am there for them! I am excited to share my experience and be there for others, since I certainly needed it when I began my alopecia journey. Together, we can conquer anything!

My name is Traci and I was born and raised in sunny California! I currently live in Los Angeles, after 5 years of living in New York, and am a journalist and writer. I started losing my hair when I was 7 years old and was diagnosed with alopecia shortly after. Growing up with alopecia was challenging because it was such a new experience for my parents and for me to navigate those conversations with my peers (as well as trying to figure out the world of wigs!), but I think it's made me a stronger person too. I've been lucky to have supportive friends and I've learned to talk about alopecia without feeling self-conscious and scared about judgement – but I also know how challenging that process is, and it's not always easy, but I know with the right support system, we can all make the world a kinder and more accepting place!

Hello! My name is Christine and I am originally from Stillwater, Minnesota and currently I am living out in Salt Lake City, UT. I attended the University of Minnesota where I studied Economics with an emphasis on Mathematics. Fresh out of college I began working for General Mills (go Cheerios!) and since then I have been relocated from MN to Utah where I absolutely love what I do. On a more somber note, I was diagnosed with alopecia areata the summer before I headed off to college (18 years old). At the time I was absolutely devastated, but as I got more comfortable with my diagnosis it became very clear to me that those who love you do not care about what you look like and that inner beauty is what truly matters. This is something that still holds true for me and has impacted my life in numerous ways. Although this disease is burdensome there always is a silver lining and hope! When I was first diagnosed, I chose to keep my alopecia a secret by covering up spots in sneaky and creative ways as well as utilizing hair extensions. I didn’t have anyone to talk to or to discuss my feelings with, looking back that was my biggest mistake. Wanting to help others with this disease and give them the outlet I so wish I had when I received the news is why I chose to reach out to NAAF and become involved in this program. I am who I am today because of this disease and it seems crazy to say but I would do it all again, it has given me strength and confidence and has instilled in me a spirit of endurance and acceptance that has led me to become the successful business woman I am today!

Hi, my name is Katy! I am from a town outside of Detroit, MI, but I am currently a student at Michigan State University studying human biology and bioethics. I aspire to go to medical school and work in pediatrics. Outside of that, I love singing, movies, reading, all things science, hiking, and spending time with my friends and family. My alopecia journey began when I was 13 years old. My first spot was on the back of my head and easily concealed… for a while. However, shortly after I had lost 75% of my hair. It grew back, only to fall out again a year later. Again, it grew back, until it fell out for a final time. With each period of growth, I was filled with hope that this time it would stay for good. The emotional toll of losing your hair is intense; mentally I struggled. During this time, I wore hats, headbands, and a hairpiece to add in some volume, but this was difficult as I very clearly stood out as “different” in the uniformed masses at my school. I also tried many different treatments, from steroid injections to topical shampoos to Anthralin. However, when my hair fell out that final time, I decided to stop treatments and instead went wig shopping for my new hair! It was daunting, and I was worried that buying new hair was “giving up”, but really it was taking back control and embracing my diagnosis instead of hiding from it. Now, I wear a wig or just go bald (though getting comfortable enough to do that took some time!). I love my alopecia. I love discussing it and educating new people on what it is. Now it is just another piece of me, like how my eyes are brown or I love to sing. However, I still remember those dark moments when hair loss was all-encompassing, and I hope to be able to provide support and a listening ear that gets it to those newly diagnosed, or those just struggling with where they are in their alopecia journey.

Hi, I’m Bill! I’m from outside Philadelphia and currently live in Los Angeles. I first noticed small patches of hair loss when I was 12 and have bounced between alopecia areata and alopecia universalis since. Over the years, I tried a number of treatment alternatives, including topical medicine and steroid injections, with little success. I turned to hairpieces and wigs for a few years, and while I think there are plenty of great benefits to these, I eventually found them to be inconvenient for me. I decided to get scalp micro pigmentation work done, and I love the results! While my journey with alopecia has had its ups and downs, I feel comfortable with and confident about my alopecia today. While the road to find acceptance wasn’t always the easiest, I truly believe that I’m a stronger and more resilient individual for it. In terms of more background on me, I graduated from Penn State with a degree in finance and spent a few years working in New York after graduation before moving to Los Angeles for a new job opportunity. In my free time, I enjoy being active and am an avid sports fan (I’m a die-hard fan of all Philadelphia sports teams). Soccer is my favorite sport and I still play and watch today! I also love music, particularly rock. I attend concerts regularly in Los Angeles and have also played guitar since I was 12. I am excited to be part of the mentorship program and have the opportunity to share my alopecia journey and to support you on your journey. I’m looking forward to meeting you!

Hey! I am Radhika Kulkarni. I am 24 years old and I’m from India. I just finished my medical education there and I am planning on coming to the US for Residency Training in Internal Medicine. I have lived in India all my life, and I was diagnosed with alopecia universalis early in childhood. Back then, especially in a country like India, no one had ever heard of it, even the countless doctors to whom we went were perplexed and tried all sorts of alchemy, none of which were successful. I had always been a bold and outgoing child, and my parents were probably the most important reason for this; for they taught me to be strong, fearless and relentless in the face of any challenge. We have been remotely associated with NAAF since 2004- my mother became a support group contact through NAAF for Indians with alopecia. Now I am trying to create a support group for people back home. We all have people at different times and in different aspects of our lives to whom we look up to for guidance and support. Through this youth mentorship program we hope to enable this during the vulnerable periods of children’s lives. I believe that your time is now, this moment is yours, believe it, seize it and purely enjoy it. I want you all to know that no matter what, everything will always be okay, if not great, and the power to ensure that lies within YOU, and I hope to help you realize that!

Hi!! My name is Samantha Myers, I’m 20 years old. I was diagnosed with alopecia when I was in 7th grade. When I got to college in the fall of 2017, my hair rapidly began falling out leaving only about 15% of my natural hair left. My biggest fear use to be people finding out about my disease so I did any and everything to hide it. About 8 months ago I finally told someone for the first time. Instead of a look of terror and shock, they gave me a look of warmth and asked me to talk about it more. Since then, I have found the more I talk about my situation the more I am able to cope with it and make light of it. I spent 6 years in fear of people knowing, only to find when I was able to be the most myself, people loved every piece about me and I was able to love every piece of me. I want to help people realize the strengths in their differences much sooner than I did! Thanks to my alopecia, I have taken a great interest in the medical field and am currently studying to be a Physician Assistant at the University of Missouri. In addition to my studies, I am on the executive board of my sorority, work at the hospital on campus as a nurse technician, and play club volleyball at the university. I’m so excited and really looking forward to getting to meet you as soon as possible and help in anyway I can!!!