Alopecia Connection

Alopecia Connection

Join Frank and Tommy as they share their experiences with alopecia and interview other members of the alopecia community.  Connection is everything!

  1. 6d ago

    55- Ryan Gallagher: Losing My Hair, Finding My Purpose

    Episode 55 - Ryan Gallagher: Losing My Hair, Finding My Purpose "Seeing the comments of my regrowth really helped me. It's the best I've ever felt in my life, and now I want to get my PhD and work in medical research." Tommy & Frank are joined by Ryan Gallagher, who lost all of his hair to alopecia universalis around four years ago, just as he was starting his freshman year of college. Ryan's hair loss happened incredibly quickly, and the impact went far beyond his appearance. Suddenly dealing with alopecia at the beginning of college, Ryan struggled with his identity, confidence and sense of direction. He found it incredibly difficult to continue with college, eventually moving home and dropping out. What followed was a very dark period in Ryan's life. Without his hair, the identity he had built for himself felt completely different, and he struggled to see what his future looked like or what the point of it all was. Around three and a half years ago, Ryan began a clinical trial for the JAK inhibitor Rinvoq. Getting onto the medication was far from straightforward, but the treatment eventually changed his life. His hair began to regrow, and today Ryan has experienced full hair regrowth. His Crohn's disease has also been doing remarkably well. But getting his hair back wasn't the end of the story. Ryan talks about the long process of rebuilding his confidence and figuring out who he was after alopecia had completely changed his sense of identity. He also shares how he eventually found a new sense of direction through science. Now studying biology, Ryan wants to use his own experience to better understand conditions like alopecia and Crohn's, and ultimately help other people going through similar experiences. In August 2026, Ryan also joined the National Alopecia Areata Foundation (NAAF) for their “Thriving Through Transitions: Navigating Young Adulthood with Alopecia” panel, where he spoke alongside other young adults about navigating college, friendships, confidence, healthcare and becoming an advocate for your own treatment. Ryan shares some of the same experiences in this episode, but we get to go deeper into the story behind them: the isolation he experienced during his freshman year, the challenge of rebuilding his confidence, making his own treatment decisions, and how those experiences ultimately helped shape what he wants to do with his life. We talk about identity, college, mental health, autoimmune disease, JAK inhibitors, finding purpose and what it means to rebuild your life after something completely changes the way you see yourself. Ryan's story is ultimately about much more than regrowing hair. It's about losing your sense of identity, finding your way back, and turning an experience that once left you feeling completely lost into a reason to help other people. Watch Ryan's NAAF panel: Thriving Through Transitions: Navigating Young Adulthood with Alopecia National Alopecia Areata Foundation, August 19, 2026 Follow Ryan on Instagram: @ryanxaviergallagher Contact Alopecia Connection! Connection is everything! Remember to rate, review, subscribe and share! Alopecia Connection Linktree      Alopecia Connection Website *Discussions on Alopecia Connection are from the personal perspectives and experiences of its host and guests, and should be considered that.  Any personal medical decisions should only be made after consultation with one's health care provider.

  2. Sep 1

    54. William Watts! ALOPECIA AWARENESS MONTH 2026!

    Episode 54 - William Watts! ALOPECIA AWARENESS MONTH 2026! "Take off the hat. Embrace it." This September, Alopecia Connection is celebrating Alopecia Awareness Month by sharing more stories, experiences and voices from across the alopecia community. Tommy & Frank are joined by U.S. Navy veteran William Watts, who has been living with alopecia since the age of 6. William shares what it was like growing up with alopecia in the 90s, navigating adolescence, identity and an often uninformed world with very little awareness or community around the condition. We talk about his journey into the Navy, years of trying treatments without lasting success, and the shift from hiding his alopecia to fully owning it as part of who he is. William also reflects on fatherhood, self-love and the lessons he passes on to his daughter about confidence, identity and simply giving things your best shot. From feeling like the alopecia community was once left out, to seeing the surge of connection, groups and foundations today, William's story is a reminder of just how far the community has come. Follow William on Instagram: @nickxfury Contact Alopecia Connection! Connection is everything! Remember to rate, review, subscribe and share! Alopecia Connection Linktree      Alopecia Connection Website *Discussions on Alopecia Connection are from the personal perspectives and experiences of its host and guests, and should be considered that.  Any personal medical decisions should only be made after consultation with one's health care provider.

  3. Mar 22

    51. Talking JAKs, Trials, and Dermatology with Dr. Leila!

    Episode 51- Talking JAKs, Trials, and Dermatology with Dr. Leila! "Hair patients have always been a hard sync for clinicians because of the fact we don't have treatment, we don't have answers... I felt that these were a group of patients that were quite underserved and I wanted to look after those patients." Tommy & Frank are pleased to welcome Dr. Leila Asfour to Alopecia Connection!  She's the first dermatologist on the show, and is running the JAK inhibitor trial that Tommy is participating in! Dr. Asfour has studied and worked in dermatology all over the world, but has settled in London.  Her interest in dermatology and hair in particular was sparked by her experiences with her father and cancer treatment related hair loss.  She observed the impact that hair loss had on him and their family as a whole, and decided to try to make a difference for others. For more information: Alopecia Support:  Alopecia UK National Alopecia Areata Foundation (US) Trial Information: Alopecia UK Clinical Trial Research UK Clinical Research Portal US Clinical Trial Portal Contact Alopecia Connection! Connection is everything! Remember to rate, review, subscribe and share! Alopecia Connection Linktree      Alopecia Connection Website *Discussions on Alopecia Connection are from the personal perspectives and experiences of its host and guests, and should be considered that.  Any personal medical decisions should only be made after consultation with one's health care provider.

  4. 11/22/2025

    49. Thank You Paige & Kristen (Those Bald Chicks Podcast)!

    Episode 49- Thank You Paige & Kristen (Those Bald Chicks Podcast)! The Alopecia Connection guys jump on the mics for a quick episode highlighting the amazing work Paige & Kristen have done with the Those Bald Chicks podcast.  Sadly, the podcast will be leaving podcast platforms soon.   Starting in February of 2021, Those Bald Chicks spread alopecia awareness through their incredible podcast, YouTube channel, and interactive Instagram account.  Paige & Kristen interviewed so many wonderfully inspiring people with alopecia, and also produced themed episodes, as well as a special "mom" series that focused on the parents of children with alopecia.  Frank was fortunate enough to be a TBC guest back in April of 2023.   Those Bald Chicks archived episodes will be taken off podcast platforms in February 2026, so please go listen while you can! Once again, thank you Paige & Kristen for all your dedication to the alopecia community!  Alopecia Connection and others appreciate all the positive impact you've made through Those Bald Chicks! Connect with Those Bald Chicks Instagram: @thosebaldchicks YouTube: @thosebaldchicks Contact Alopecia Connection! Connection is everything! Remember to rate, review, subscribe and share! Alopecia Connection Linktree      Alopecia Connection Website *Discussions on Alopecia Connection are from the personal perspectives and experiences of its host and guests, and should be considered that.  Any personal medical decisions should only be made after consultation with one's health care provider.

  5. 09/29/2025

    48. Alopecia Awareness Month with NFL Quarterback Josh Dobbs!

    Episode 48- Alopecia Awareness Month with NFL Quarterback Josh Dobbs! "Being confident in your own skin, and understanding who you are as a person is really the only thing that matters.  It's really cool, as I said, to have the journey that I've had, to be able to go through the things I've gone through, to gain that perspective, and everyone sees that within time." Alopecia Connection is very excited to bring you a special Alopecia Awareness Month special episode with NFL quarterback Josh Dobbs!  Currently in his first season with the New England Patriots, Josh discusses his alopecia journey, supporting others with alopecia, and his experience speaking at the 2019 NAAF annual meeting.  Lastly, Frank & Tommy chat with Josh about his ASTROrdinary Dobbs Foundation, which aims to empower younger individuals through education, economic, professional, and recreational development, with an emphasis on STEM (science, technology, engineering, and mathematics) ASTROrdinary Dobbs Foundation Josh Dobbs 2019 NAAF Meeting Speech Connect with Josh! IG: @joshdobbs Twitter/X: @josh_dobbs1 TikTok: @joshdobbs Linktree: @joshuadobbs Contact Alopecia Connection! Connection is everything! Remember to rate, review, subscribe and share! Alopecia Connection Linktree      Alopecia Connection Website *Discussions on Alopecia Connection are from the personal perspectives and experiences of its host and guests, and should be considered that.  Any personal medical decisions should only be made after consultation with one's health care provider.

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Join Frank and Tommy as they share their experiences with alopecia and interview other members of the alopecia community.  Connection is everything!