Today's guest is Lauren Lee. She is a student-athlete golfer at NCAA Divsion II, Western Washington University where she is a senior studying psychology with a minor in anthropology. She's lived with alopecia most of her life, and the journey of hair loss has shaped her resilience, confidence, and outlook on life. Balancing competitive golf and academics, Lauren has learned the importance of mental strength, self-acceptance, and finding joy in every challenge. Without sharing too much in the intro, I'll let Lauren introduce herself and share more of her story with you now. 

Thank you for sharing your time with Lauren and me today. It's important to hear the low, lows to know the way alopecia can hit each of us. It's also important to hear the ways we can transition through the lows and challenges to come out the other side. Our stories make a difference. Lauren is passionate about using hers to inspire others to embrace who they are and to raise awareness about alopecia. Looking forward, she is excited to continue to grow on and off the course, hoping to inspire others to believe in themselves and embrace the beauty of individuality.

If you would like to connect with Lauren, her Instagram link can be found here in the show notes. A quick shoutout to Abigail Tolman who helped Lauren and I connect.

https://www.instagram.com/loreuhn.lley/

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

Welcome back to the podcast.I'm so excited to start Season 7 of Alopecia Life with a guest who has a passion for making the world a better place for children impacted by skin conditions and birthmarks. She also loves building relationships and collaborating with others since she believes we are better when we lift one another up so we can all become the best versions of ourselves. Dr. Alanna Bree is a Pediatric Dermatologist, Founder and President of Made A Masterpiece, Director of Pediatric Dermatology Collaboration at Sagis Diagnostics, as well as an Advisor and Speaker for CeraVe. In addition, she enjoys teaching about pediatric dermatology and raising awareness about the impact of living with a skin condition so the world can be a more understanding, accepting, and loving place for those with visible skin differences.

I met Dr. Bree a few months ago, and was quite taken with how she spoke about patients and families, along with her dedication to creating resources to help people living with all skin conditions, including alopecia. She shares so much throughout this episode, including some of the best ways to take advantage of a dermatology appointment that you've been waiting months for. Made A Masterpiece is not only a website that provides endless free resources for all skin conditions, it's also creating a method that will revolutionize how we raise awareness with technology and interactive play. 

Thank you for sharing your time with Dr. Bree and me today. If you are looking to connect with Dr. Bree, find some of those amazing resources she shared with us today, and know more about the mission and passion behind Made A Masterpiece, those links are here in the show notes. If you are wanting to donate to the traveling museum, you can find those links here as well. 

https://www.madeamasterpiece.org/
https://www.facebook.com/madeamasterpiece
https://www.instagram.com/iwasmadeamasterpiece/

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

Welcome to this episode of Alopecia Life. It's been awhile since I've published an episode. I've been working on some big projects, and life has had a way of getting reorganized as time goes by. Thank you so much for coming back and for listening today. I'm excited to introduce Arron Johnson as our guest today. Arron shares his personal alopecia story with us from the point he was diagnosed at the age of 15. Over the last 25 years, Arron transformed from a teenager hiding behind du-rags and hats to a confident IT professional, successful entrepreneur, husband, and father. His faith-based approach to resilience has helped him through every challenge, from navigating workplace environments without head-coverings to building authentic relationships and starting a family. His book, Hairless But Fearless not only chronicles his personal transformation, but also offers practical strategies for individuals and families facing similar struggles. 

Thanks so much for sharing your time with Arron and me today. To find Arron on social media, you can find him @therealarron, and find his book at http://www.hairlessbutfearless.com/. Those links can be found here in the show notes. 

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

Welcome to this episode of Alopecia Life. We are so happy to participate in this 3rd edition of Podcasthon! For one week, more than a thousand podcasts will highlight a charity of their choice, and today, I have the pleasure of welcoming back Jeff Woytovich with the Children's Alopecia Project. 

In this episode, we talk about what's new for CAP, JAK Inhibitors, along with the ongoing conversation about community and how we continue to be supportive and focus on education. We talk about his recent outreach with a family in the UK and some of those details, and there's a full 10 minutes of discussion that had to be omitted because of the heated conversation we had around it. Both of us get fired up about this type of thing happening in this day and age. Let's welcome Jeff back to Alopecia Life. 

That wraps up this special episode as part of Podcasthon. If you enjoyed it, feel free to visit http://www.podcasthon.org/ to discover hundreds of other associations through the voices of amazing podcasters. It's a pretty cool deal to be supporting charities of our choice. As always, CAP is the number one charity I choose to fund every year because camp and gatherings for kids and their families who have been diagnosed is something that means the world to me and has such huge benefits. The link for CAP's annual giving campaign is here in the show notes, along with the Children's Alopecia Project, camp, and so much more. If you want to schedule a get-together with Jeff in your city, that link is here too. 

For those of you who are wanting an update about the family in the UK, they've received tremendous support from almost a dozen dermatologists and specialists, but at this point they are still waiting for social services to close the case. We are keeping them in our thoughts, and we hope for a swift resolution, and an opportunity for this school to receive the education around alopecia that is clearly so necessary.

https://childrensalopeciaproject.org/

https://form.jotform.com/Knjoz/cap-kid-group-get-together

https://alopeciapalooza2025.eventzilla.net/e/2138640318

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

 Welcome to this episode of Alopecia LIfe. Today's guest is Sarah Durrett. I reached out to Sarah a few weeks ago after she posted a video of herself shaving the last of her hair off after living with alopecia areata for several decades. The video is super raw, and I truly felt with her in the moment while she shared. It had a strong effect on me, and I knew for those who hadn't yet seen it and were going through something similar - it would be super helpful. 

When our hair is actively falling out, it's difficult to understand the sense of loss we are experiencing. People around us often tell us, "It's just hair." or "At least you don't have something more serious." Logically, we know this (as adults), but it doesn't mean on a scale of 1-10, it's not a 10 for us in the moment. With kids, it may be even more confusing. Our parents or other family members may be encouraging a final haircut to get rid of the wispy hair that is stubbornly sticking out of our head. It's a big deal to take this next step. When do you know it's the right time to Brave the Shave? Today, Sarah shares what led up to it, and how she is feeling now.

Thank you so much for sharing your time with Sarah and me today. Shaving is a very personal choice when living with hair loss. I never did, but looking back I wish I would have taken control instead of having that last strand of hair remain on my head until alopecia decided it would for me. Showers and bathing can be traumatizing when clumps of hair are found in the drain. I want to thank Sarah for being brave and sharing her experience with all of us. For ways to reach out to Sarah, I've posted those links in the show notes. I've also attached the video here in the comments.

For parents - If you are ready for your child to shave and they aren't - I encourage you to wait until they are. Sometimes they need to know it's an option, and other times they will refuse and that is completely up to them. It may sound harsh, but your discomfort needs to take a back seat to the wishes of your child. On the other side of this, your child may totally want to shave, and you may not feel ready. With your discomfort aside and whether they do or don't want to shave, your kiddo can experience freedom around a choice when experiencing hair loss, and that's something truly empowering.

Sarah's YT Video
https://www.facebook.com/sarah.durrett

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

Thank you so much for joining us for this episode of Alopecia Life. I've been waiting to share this episode with all of you because I knew it was important to release it at this unusual time in the US that has been so full of unrest. I'm editing this the week before our presidential election, at a time where a lot of stress and imbalance is working to right itself. Although this week has already played out and I have no idea of the outcome while editing, my wish is that today's guest, Jen Baradi, provides you with the same sense of calm and peace I felt after being with her in person and interviewing her here on the podcast. 

I met Jen a few months ago in Toronto, and I knew she would be perfect for the podcast to share all she has discovered while living with alopecia for the past 38 years. She has discovered greater well-being and support along the journey through mindfulness, yoga, and iRest® meditation practices. As an educator, Jen taught internationally for 20 years and first developed an interest in combining yoga and education while completing postgraduate research on the effects of yoga on academic achievement. After repatriating back to Toronto, she took time for wellbeing and for deepening her yoga practice. She has awakened to a path of integrating wellbeing, awareness, and education.

Whether you're here in the US, in another country, or in Canada where Jen lives, we could all use a moment of space to just breathe. 

Thank you for sharing your time with Jen and me today. To discover more for yourself, connect with her through www.jenbyogi.com. Additional ways to reach out to Jen are located here in the show notes, along with the YouTube link to the movie we spoke of, "Attack from Within."

*ADDITIONAL INFO FOR COMMUNITY TO CONNECT WITH JEN:

Discover ways to live with greater wellbeing this season with Jen:

Resources to Just Be (*for CANAAF Alopecia support group online yoga & iRest®️ Yoga Nidra Meditations)

Jenbyogi.com (*for private clients / groups / organisations / educational institutes)

Two Yogis Talking about Life Youtube (*for vodcast with new episodes inspired by iRest®️)

Doggos.ca (*for puppy & yoga playdates at Puppysphere, studio 2)

Vivayalive.com (*for recorded online yoga & iRest®️ Yoga Nidra Meditations)

Jabumind app (*for recorded iRest®️ Yoga Nidra Meditations)

Oise.utoronto.ca/wellness/past-recordings (*for hybrid & recorded online Yoga & iRest®️ Yoga Nidra Meditations)

YouTube Video - Attack from Within 

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

Thank you for joining us for this episode of Alopecia Life. Today's guest is Sharlay Sloss. Sharlay is a certified doula, teacher and author. She is dedicated to fostering positive and healthy environments where children can express themselves and fully embrace self-love. As a teacher, she has been the recipient of multiple awards including the Heart Award for her dedication and commitment to children and their families.

Sharlay lives in Virginia  with her husband, two children and dog Remy. Today, we'll be talking about her new book, Hair-Free Horace. If you're an avid listener of the podcast, you know how often I share about books as resources. The reason I love books so much is because I know how much I wanted and needed something to look at and read or hear when I was diagnosed. This continues to be a need almost 40 years later for our young readers and families who have been diagnosed with alopecia. Featuring them here on the podcast is another way to help serve the alopecia community. 

Thanks again for sharing time with Sharlay and me today. To find your copy of Hair-Free Horace or to get in touch with Sharlay, I've provided those links here in the show notes. 

Hair-Free Horace Amazon

Barnes & Noble 

https://www.hairfreehorace.com/

https://www.linkedin.com/in/sharlay-sloss-ab101912/

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

Thank you for joining us for this episode of Alopecia Life. Today's guest is Dr. Elyssa Green. Dr. Elyssa is a woman making a significant impact in the world of alopecia. After being diagnosed with alopecia in 2022, she shaved her head and embraced the beauty of baldness. Even though that sounds like an easy 2-step process, she shares the personal challenges and triumphs that led her to help others struggling with the diagnosis and all that comes with the hair loss journey. Dr. Green established Bald Bozz Beauty or B3 to advocate and bring awareness to alopecia. The mission of B3 is to provide highlights in the areas of Style, Health, and Education that impact the bald community. It's exciting to have her here today to share more. 

Thank you for sharing your time with Dr. Elyssa Green and me today. For ways to reach out, the links are here in the show notes, along with her website to find out more.

Contact:
https://www.instagram.com/baldbozzbeauty/
FBbaldbossbeauty
https://www.tiktok.com/@baldbossbeauty
https://www.linkedin.com/in/elyssagreen/
https://www.bthree.org/

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

Welcome to Season 6 of Alopecia Life. Each September, I have a back-to-school episode and find a guest to share how to make the transition easier. Historically, these are the ones that parents ask me about the most too. Our guest today is Jodie Lee. Jodie is a dedicated educator with 15 years of experience as a high school teacher. She is a passionate advocate for celebrating diversity and fostering inclusivity in schools. Jodie is the proud mother of two daughters, and her youngest, Makenna, was diagnosed with alopecia. When Jodie registered Makenna for school, she searched for a book that would highlight her daughter's bravery in confidently walking into school looking different from her classmates. Unable to find a suitable story, Jodie took matters into her own hands and wrote one herself. This endeavor was not just about her daughter's experience but also about the many challenges that students face in school environments.

In 2022, Jodie expanded her mission and founded *Different at School*, an organization dedicated to celebrating what makes each of us unique. The organization focuses on educating others about the diverse challenges students face while encouraging all students to become strong individuals of character.

Jodie is the perfect guest for this season's back-to-school episode. 

Thank you for sharing your time with Jodie and me today. You can find all of the ways to connect with Different at School here in the show notes. As always, we love seeing your questions and comments over on socials.

Instagram

Facebook 

Different At School Website

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/

Welcome to this episode of Alopecia Life. Our next guest is Ava Hanssen. I first heard about Ava when the Children's Alopecia Project reached out to say thank you for featuring them on her race car. Her racing background is super interesting, and after hearing more about who she is and what she wants to accomplish in the racing world, I thought you would all be excited to hear more about her racing, especially if you're like me and have a fairly limited bit of knowledge around the racing world. Ava started racing go karts at 4 years old, and her competitive nature now has her racing an F1600 going upwards of 130mph at the age of 14. Here's more from Ava.

Thank you for sharing your time with Ava and me.To learn more about Ava, follow her on social media, and even perhaps offer sponsorship for her racing endeavors, please check out those links here in the show notes. Her racing accomplishments are pretty impressive.Thanks again to Ava for raising awareness for the Children's Alopecia Project.

https://avahanssenracing.com/

FB: https://www.facebook.com/ava.hanssen.31

IG: https://www.instagram.com/_ava_hanssen_/

Recent News Story: CBS58 News

Support the show

Alopecia Life provides free resources for school and home education, including a growing list of alopecia books, education videos on YouTube, links to support groups within the US, UK, Canada and more. You will also find access to Head-On, Stories of Alopecia, the Alopecia 101 free course, paid Alopecia Roadmap course for parents of children living with alopecia, and personalized coaching. Together, we can make a difference. To find out more, https://www.alopecialife.com/