Find A Youth Mentor

Hi my name is Morgan! I am from St. Louis, MO and I have struggled with alopecia since the age of 4. As a child, my hair began to fall out and I remember asking Santa around Christmas time very year that it would finally grow back. My Christmas wish. **laughs to self. I used some topical products for a few years but never saw any improvement. However, at that time the hair loss was noticeable but gradual which was probably the best because it would’ve freaked me out seeing it fall out drastically! I’d say I was able to live a pretty normal life. I learned at an early age hair styles to hide it and literally mastered it to the point where people never knew. For the most part, I still had a thick head of hair and that was a plus because it allowed for me to keep it a secret for years. Years! My best friends never even knew until a few years ago after asking why I was in such distress about my hair. The process of my hair loss has sped up recently and it scares me like crazy but I have decided to no longer be ashamed of it or quiet about it. It is my hope that I can educate others about it and help them realize that women are just as beautiful with or without hair!

Hey there! My name is Jessa Ponce and I’m from San Diego, California. I was diagnosed with Alopecia Areata when I was a sophomore in highschool. I lost all of my hair at 15 years old. From having a full head of hair to none, initially I felt trapped and lost, but I realized I wasn’t alone! Leading up to college my hair grew back, but ultimately my hair loss has taught me how to have compassion for myself and others. More about me, I have a lot of hobbies! I enjoy public speaking as I gave a TEDTALK in February 2022 titled “Finding Security Through Our Insecurities.” I love puzzles, in fact I can solve a Rubik’s cube in 15 seconds and have been solving them since I was ten years old. I love photography and video editing, specifically portraits and my cooking videos. I can also juggle. I look forward to meeting you and to create new experiences together! 

Hi, my name is Michael Miller. I'm a 24 year old, Dallas, Texas resident (born and raised) working in the commercial real estate industry. I attended Baylor University and received a Bachelor of Arts in Public Relations with a Business Marketing concentration and graduated in May of 2016. My hobbies include being active in my local church, traveling, water-skiing, fishing, and golfing. I've had alopecia for as long as I can remember but lost all my hair one year ago, when I turned 23. Originally seeing alopecia as something negative, I've been able to use it as a positive and see how it is truly a blessing in disguise. Even though I am new to the NAAF family, I want to help and encourage people who are going through what I've been through. I look forward to connecting!

My name is Jessica Nelson but my friends call me Jessi! I am 22 years old and live in Logan, Utah! I was diagnosed with alopecia when I was 5 years old! I have always hated wearing wigs, and prefer to keep my head uncovered! I graduated from Payson high school in 2019, and I am now a preschool teacher! I was married to my amazing husband in 2020, and we have been living in Logan ever since! I grew up at the southern edge of Utah County, with an amazing family. I love to do anything craft related, especially painting and sewing! I enjoy going to movies, reading books, and spending time with my friends and family! I also love to be outside, hiking, fishing, and swimming are some of my favorite outside activities! When I was younger I didn’t really grasp the fact that I was different than the other kids in my class. It wasn’t until I started getting bullied in second grade that I realized there was something different about me. That was the first time I struggled with my alopecia. It did not help that I didn't know anyone else with alopecia, and that's a huge part of why I wanted to become a mentor. I did not really realize until fifth or sixth grade that I didn't need to let my hair, or lack of it, define me. I am excited to get to know more people who have been through things like me, and I hope to be able to offer support to someone who needs it.

Hi! My name is Lindsey, I am 17 and a senior in high school. I am from Buffalo Grove, a suburb near Chicago. I have had Alopecia since I was 13, and by the time I was 16 I had lost all the hair on my head. This year, my once bushy eyebrows fell out as well. I was very sad and angry when I first lost my hair, but once I started being open with my friends and peers about my hair loss I felt confident and very supported. Most days I wear a wig, but I have gone to school without my wig before and it was very liberating. I am part of a clinical trial right now but have gone through other various treatments as well. I want to be there for other people with Alopecia who might be struggling, or who might feel alone. More than anything I hope to be a great friend to someone and be there to listen, to give advice, and have fun! I am very involved in school extracurriculars, where I am the vice president of my class and a freshman mentor, and I have played sports for most of my life. In my free time I love to spend time outdoors, hang out with friends, try new hobbies, and ponder life, as well as bake, eat lots of ice cream, and read!

Hi, my name is Hannah Bobo and I am from Indiana, although I was born in North Carolina (once a Tar Heel, always a Tar Heel). I enjoy playing the piano, reading and have recently gotten into photography-but I spend most of my time playing basketball. I have become really interested in pharmacy, and plan to pursue pharmacy school after I graduate high school. I was diagnosed with alopecia universalis at the age of 2. It grew back quickly, and up until the summer before I went into sixth grade I had alopecia areata. After that, I completely lost all of my hair, and have been bald since then (I am a junior in high school!). For a while, I tried topical steroids and wore bandanas because I wasn’t comfortable with being bald. After seeing other kids with alopecia and how they were able to be themselves without treatment and head coverings, I decided to stop seeking treatment and wearing bandanas. This journey has been a rollercoaster, from the self-confidence issues, the people I’ve met, countless minutes spent standing in the mirror upset that I didn’t have hair, to being able to help others with the same things I have struggled with, and the things I have been able to accomplish because of a newfound confidence in my alopecia. In the end, I wouldn’t change a thing! I’ve met some amazing people who have helped me through the journey, and I would love to pay it forward by helping others in any way that I can!

Hi! My name is Sooji and I was born and raised in Flushing, New York. I have a bachelors’ degree in Art History and currently working on an art portfolio for grad school in Art Education. In my spare time, I love to document my memories through scrapbooking. When it comes to crafting, I am always eager to learn new techniques and skills. I always found art to help me through my emotional distress when I was diagnosed with alopecia. My journey began when I was 10 years old. I had watched a tiny patch on my head get bigger, my hair line getting wider until eventually, I could not hide it anymore. Soon, my eyebrows and eyelashes were gone. I always wore a bandana and a hat to school. Within 1 year while taking steroid injections, I was grateful that my hair grew back. For 8 years, I would get bald patches that were easy to cover up. When I was 18, I was hospitalized and my body reacted to a medication that triggered all of my hair to fall out. The second time around, I did not take any medication but surprisingly, my hair grew back in three years. During those three years, it was difficult to accept my image. I decided to purchase a wig and little by little, I stopped using my wig as a safety blanket. Eventually, I only wore a bandana. In less than a year, I was able to walk out of my house with nothing on my head. That day, I felt so unbelievably empowered by my choice. Again, my hair grew back, but even today, I am facing some bald patches. Having alopecia made me a strong and confident individual. I would love to talk, listen or just have fun! 

My name is Regina, people often call me “Reg” to make it easier. I’m 17 years old and grew up in a small town on the Jersey Shore called Point Pleasant Beach (for those of you who watch MTV’s jersey shore, seaside is around 20 minutes south of my town). I have 5 older siblings, 2 dogs and 2 cats. I enjoy spending time with my friends and siblings, listening to music, and I am a big basketball fan. My favorite sports teams are all from Philadelphia! I am going into my senior year of high school and plan on applying to colleges in the fall of 2018. When I was around 6, I started to lose my hair and eventually all of it fell out. I have had no hair on my scalp since kindergarten. I never have worn a wig or decided to cover up my head because I’ve always wanted to be myself. I hope that I can incorporate my experience with Alopecia and establish reliability with other young people that have alopecia and make their days happier and easier.

Hi everyone, I’m Kayla! I grew up in North Jersey but currently am attending the University of Pittsburgh as a sophomore with a major in Communication Science Disorder. In my free time, I like to explore Pittsburgh (absolutely amazing city), go on hikes, play basketball, or really any type of sport, and am pretty much open to doing anything. I got diagnosed with alopecia summer going into my senior year of high school, when I noticed I had a missing patch on the back of my head at the hairline. As senior year went on I was doing pretty well, another spot popped up but it wasn’t terrible, until about January and alopecia did its magic and poof all my hair fell out in a matter of two weeks. Right in the middle of basketball season too, it was really hard for me to even comprehend what was going on. I was very self-conscious and embarrassed of what was going on, and I think that is because I did not think anyone would understand or even be able to relate/not know what alopecia is. I wore a wig full time, didn’t tell anybody about what was going on except for my two best friends. I tried so many different remedies to get my hair, since different things work for everybody I wanted to try them all. I felt really alone, no matter how much I talked to my therapist or best friends it didn’t help because they don’t have the experience of going through loosing your hair, so it was super difficult. I found ways to cope and learned how to become more comfortable with myself. I struggled with some mental health problems, but I was very lucky to have a really supportive parents and sisters who all helped me go through a lot. I look back on the experience and I know I am a different person today, a better person because of it. I hope to talk to someone who I can relate to and support them through a tough journey. Own alopecia, don’t let it own you!

Hi, my name’s Ashley! I live in Michigan, and I am a senior in high school. I enjoy swimming, playing the flute, baking, and math. My alopecia started when I was fourteen. There were a few bald spots at first, but eventually all my hair fell out. I tried different creams and injections from doctors, but nothing seemed to work. That was when I found so many amazing organizations that provided me with wigs. This allowed me to feel so much more confident. My biggest issue was being on the swim team. I couldn’t wear my wig in the pool, so I closed myself off from my teammates. Next swim season, I decided I was tired of hiding. I told my teammates about my hair loss, and I felt so relieved. I want to be there for others who feel like I did. I hope that people with alopecia will feel less alone.