On today’s episode, I’m joined by Dr. Monica Ellis-Blied, a licensed psychologist, health coach, and chair yoga instructor living in California.   In 2012, Monica was diagnosed with lupus. Over the last eight years, she has come to terms with the idea that the word “healthy” is not a one-size-fits-all term. She also reminds us that it’s OK to throw pity parties (complete with balloons and German Chocolate Cake, when the occasion calls for it).    The way she speaks about her diagnosis, her work, and her family are a true testament to her giving nature, and her willingness to face down the challenges that come with having her condition.   You’ll notice, in this episode, that Monica has a way about her that is both refreshing and inspiring. She sees her chronic illness diagnosis as a blessing, one that has helped her slow down, to find joy in the little things, and pay attention to what truly matters. I think her insights are something we all need to hear.

On today’s episode, I’m joined by Dr. Monica Ellis-Blied, a licensed psychologist, health coach, and chair yoga instructor living in California.   In 2012, Monica was diagnosed with lupus. Over the last eight years, she has come to terms with the idea that the word “healthy” is not a one-size-fits-all term. She also reminds us that it’s OK to throw pity parties (complete with balloons and German Chocolate Cake, when the occasion calls for it).    The way she speaks about her diagnosis, her work, and her family are a true testament to her giving nature, and her willingness to face down the challenges that come with having her condition.   You’ll notice, in this episode, that Monica has a way about her that is both refreshing and inspiring. She sees her chronic illness diagnosis as a blessing, one that has helped her slow down, to find joy in the little things, and pay attention to what truly matters. I think her insights are something we all need to hear.

This is Not What I Ordered: a podcast on full-hearted living with chronic illness + health challenges

59: Giving Yourself Grace with Dr. Monica Blied

Melinda Laus has always felt “different.” From her earliest memories, she struggled with asthma, allergies, and feeling like her body just worked differently than other bodies did. After working throughout childhood and adolescence to get her asthma and allergies under control, she thought she had her body somewhat “figured out.” When she experienced the tragic loss of her husband when she was 32, however, Melinda’s body went into a tailspin.   It took about 2 years after her husband’s death for her to be diagnosed with hypothyroidism and adrenal exhaustion. Since then, she’s been on a path to embracing her grief, exploring the power of rest, and accepting the ebbs and flows in her energy.   In our heartfelt conversation, Melinda and I cover grief, trauma, change, isolation, and the permission to feel deeply. Melinda shares some incredible insights with me, including how she navigated the “grief within grief” after her husband’s death and her diagnosis — from grieving family lasagna dinners to accepting that her home might look like a train wreck on any given Tuesday night.   This is a moving discussion where we talk about the gifts that come from grief, and how we can all hold joy and pain in equal measure to create a truly fulfilling life.

Melinda Laus has always felt “different.” From her earliest memories, she struggled with asthma, allergies, and feeling like her body just worked differently than other bodies did. After working throughout childhood and adolescence to get her asthma and allergies under control, she thought she had her body somewhat “figured out.” When she experienced the tragic loss of her husband when she was 32, however, Melinda’s body went into a tailspin.   It took about 2 years after her husband’s death for her to be diagnosed with hypothyroidism and adrenal exhaustion. Since then, she’s been on a path to embracing her grief, exploring the power of rest, and accepting the ebbs and flows in her energy.   In our heartfelt conversation, Melinda and I cover grief, trauma, change, isolation, and the permission to feel deeply. Melinda shares some incredible insights with me, including how she navigated the “grief within grief” after her husband’s death and her diagnosis — from grieving family lasagna dinners to accepting that her home might look like a train wreck on any given Tuesday night.   This is a moving discussion where we talk about the gifts that come from grief, and how we can all hold joy and pain in equal measure to create a truly fulfilling life.

58: Courageous Mourning with Melinda Laus

In this episode, I’m joined by Andy McLellan, a haiku poet and trainee Zen priest living in Canterbury, UK.   Nearly 25 years ago, when Andy was in the midst of obtaining his PhD, he began experiencing symptoms he assumed were associated with stress. Shortly after graduating, however, he came down with glandular fever and collapsed, never fully recovering.   Over the next 20 years, Andy would receive a diagnosis of myalgic encephalomyelitis (ME) and navigate an entirely new learning curve: how to organize his life in a way that would allow him to balance his chronic illness and start a family.    Despite knowing the signs and symptoms and understanding that he would need to slow down and take care of himself, he suffered a major crash 5 years ago which has caused him to be largely confined to his bed.   However, that doesn’t stop Andy from finding joy in the simple things: squirrels right outside his bedroom door, knitting, writing beautiful haiku poetry. It’s evident throughout our chat that Andy has not allowed his chronic illness to alter his positivity. If anything, it has buoyed it.    I felt a powerful connection to Andy, and we were both reminded just how impactful it can be to sit with people who just get it. As individuals navigating our chronic illnesses, we can connect with each other and not have to over-explain, or judge. We just take these illnesses for what they are and support one another fully.   This conversation with Andy proved a testament to resilience. He is truly an inspiration to me, and I hope to all of you.

In this episode, I’m joined by Andy McLellan, a haiku poet and trainee Zen priest living in Canterbury, UK.   Nearly 25 years ago, when Andy was in the midst of obtaining his PhD, he began experiencing symptoms he assumed were associated with stress. Shortly after graduating, however, he came down with glandular fever and collapsed, never fully recovering.   Over the next 20 years, Andy would receive a diagnosis of myalgic encephalomyelitis (ME) and navigate an entirely new learning curve: how to organize his life in a way that would allow him to balance his chronic illness and start a family.    Despite knowing the signs and symptoms and understanding that he would need to slow down and take care of himself, he suffered a major crash 5 years ago which has caused him to be largely confined to his bed.   However, that doesn’t stop Andy from finding joy in the simple things: squirrels right outside his bedroom door, knitting, writing beautiful haiku poetry. It’s evident throughout our chat that Andy has not allowed his chronic illness to alter his positivity. If anything, it has buoyed it.    I felt a powerful connection to Andy, and we were both reminded just how impactful it can be to sit with people who just get it. As individuals navigating our chronic illnesses, we can connect with each other and not have to over-explain, or judge. We just take these illnesses for what they are and support one another fully.   This conversation with Andy proved a testament to resilience. He is truly an inspiration to me, and I hope to all of you.

57: Solitude + Connection with Andy McLellan

Dealing with an invisible health challenge can be beyond frustrating. But what happens when a traditionally invisible illness becomes manifest? And how do we cope with the visual symptoms of our conditions? That’s what I’m talking to Lashana Taylor about on this episode of This is Not What I Ordered.    Diagnosed November 2018 with primary progressive multiple sclerosis, Lashana finally had an answer to her declining health. With the diagnosis came relief, but it also threw into light some of her own challenges: with how she saw herself and how she allowed others to show up for her.   During this interview, I talk to Lashana about how much she’s grown over the last year, how she’s treating her MS, and the milestones and lessons she’s gained along the way. We also get really honest about how health challenges of all shapes and sizes affect our inner and outer worlds, essentially by holding up a mirror to ourselves and others.    My favorite guidance from Lashana during our chat? Vulnerability isn’t weakness. Patience is required. And sometimes, you have to be challenged to bring out the best in yourself. I really enjoyed this heartfelt conversation with Lashana about relationships, medications and treatments, and growing as a person in ways you might never expect before a health challenge.

Dealing with an invisible health challenge can be beyond frustrating. But what happens when a traditionally invisible illness becomes manifest? And how do we cope with the visual symptoms of our conditions? That’s what I’m talking to Lashana Taylor about on this episode of This is Not What I Ordered.    Diagnosed November 2018 with primary progressive multiple sclerosis, Lashana finally had an answer to her declining health. With the diagnosis came relief, but it also threw into light some of her own challenges: with how she saw herself and how she allowed others to show up for her.   During this interview, I talk to Lashana about how much she’s grown over the last year, how she’s treating her MS, and the milestones and lessons she’s gained along the way. We also get really honest about how health challenges of all shapes and sizes affect our inner and outer worlds, essentially by holding up a mirror to ourselves and others.    My favorite guidance from Lashana during our chat? Vulnerability isn’t weakness. Patience is required. And sometimes, you have to be challenged to bring out the best in yourself. I really enjoyed this heartfelt conversation with Lashana about relationships, medications and treatments, and growing as a person in ways you might never expect before a health challenge.

56: Living With Visible Illness with Lashana Taylor

In this episode, I’m joined by Michelle Horton, a close friend and fellow therapist.   In the middle of finishing grad school and planning a wedding, Michelle went in for a routine blood test, which showed an abnormally high platelet count. After this finding, a whirlwind of tests and doctors determined that she had essential thrombocytosis and endometriosis. She was 23.    After that, Michelle had to learn how to stand in the uncertainty that her new diagnoses brought with them. Could she have a regular life? Could she have children? Ten years later, Michelle is working as a licensed therapist and is a mother to her 19-month-old son.    There have been definite struggles over the last decade, she shares, but she’s learned a thing or two along the way (some of which she shares with us in this episode). She has an inner light that her health challenges haven’t diminished and, if anything, have only made stronger. During our chat, Michelle walked me through some of the tools she’s used over the last decade to support herself and overcome the uncertainty — tools I think all of us can use.    Michelle and I connected most over the idea of “not knowing,” over the questions and challenges we both face. Despite our different conditions, our experiences have linked us together in a way that I’m excited to share with all of you. I also hope you’ll be as inspired by Michelle as I am.

In this episode, I’m joined by Michelle Horton, a close friend and fellow therapist.   In the middle of finishing grad school and planning a wedding, Michelle went in for a routine blood test, which showed an abnormally high platelet count. After this finding, a whirlwind of tests and doctors determined that she had essential thrombocytosis and endometriosis. She was 23.    After that, Michelle had to learn how to stand in the uncertainty that her new diagnoses brought with them. Could she have a regular life? Could she have children? Ten years later, Michelle is working as a licensed therapist and is a mother to her 19-month-old son.    There have been definite struggles over the last decade, she shares, but she’s learned a thing or two along the way (some of which she shares with us in this episode). She has an inner light that her health challenges haven’t diminished and, if anything, have only made stronger. During our chat, Michelle walked me through some of the tools she’s used over the last decade to support herself and overcome the uncertainty — tools I think all of us can use.    Michelle and I connected most over the idea of “not knowing,” over the questions and challenges we both face. Despite our different conditions, our experiences have linked us together in a way that I’m excited to share with all of you. I also hope you’ll be as inspired by Michelle as I am.

55: Sitting with the Unknown with Michelle Horton

On this week’s episode, I’m bringing back the Couple’s Edition of This is Not What I Ordered to share an intimate and insightful discussion with Shane and Latasha Doyle. Latasha (who you may remember from Episode 53) and her husband Shane joined me in my own living room to talk about their life together. As many of you know, Latasha is the shownotes and transcription writer for the podcast. And as you’ve found out from her previous episode, she also lives with Marfan syndrome, a connective tissue disorder. This condition affects her daily life in ways that also affect her marriage with Shane. Because of the nature of her condition, Shane and Latasha have to be open about death, illness, and what they really want from life… which isn’t always easy. I’m so thankful to have been witness to their connection, and to be able to share the conversations they have with each other. This conversation offers such beautiful insight into the relationships we all have as we live with our own health challenges, and about the hard conversations we sometimes must have with ourselves and others. I hope that you take as much away from it as I did.

On this week’s episode, I’m bringing back the Couple’s Edition of This is Not What I Ordered to share an intimate and insightful discussion with Shane and Latasha Doyle. Latasha (who you may remember from Episode 53) and her husband Shane joined me in my own living room to talk about their life together. As many of you know, Latasha is the shownotes and transcription writer for the podcast. And as you’ve found out from her previous episode, she also lives with Marfan syndrome, a connective tissue disorder. This condition affects her daily life in ways that also affect her marriage with Shane. Because of the nature of her condition, Shane and Latasha have to be open about death, illness, and what they really want from life… which isn’t always easy. I’m so thankful to have been witness to their connection, and to be able to share the conversations they have with each other. This conversation offers such beautiful insight into the relationships we all have as we live with our own health challenges, and about the hard conversations we sometimes must have with ourselves and others. I hope that you take as much away from it as I did.

54: Better Than a Cookie-Cutter Life [Couple's Edition] with Latasha + Shane Doyle

This week on This is Not What I Ordered, I am so excited to share my recent chat with a very special guest: Latasha Doyle. Latasha owns her own copy and content writing agency, but she’s also the resident show notes writer here on the NWIO Team. She has Marfan syndrome, a connective tissue disorder, and opens up about her experience living with this condition her whole life. Latasha brings her humor and her honesty to the table, and talks candidly about echocardiograms, being “out” with her condition, and how she’s learned to embrace her quirks (read: a passion for productivity tools and schedulers) to help her balance health, work, and life. This was such a fun conversation, and Latasha’s advice about interrupting social narratives really spoke to me. As a community of people living with health challenges, we internalize so much about what it means to be “healthy” or “normal,” and Latasha shared her process for working through it.  She also shared how her chosen family — her husband and her friends — are constantly showing her what it means to show up and truly love someone. I am so excited to share this interview with all of you, and for you to hear Latasha’s love for life and the deep, deep respect she holds for the condition that many people would consider a burden.

This week on This is Not What I Ordered, I am so excited to share my recent chat with a very special guest: Latasha Doyle. Latasha owns her own copy and content writing agency, but she’s also the resident show notes writer here on the NWIO Team. She has Marfan syndrome, a connective tissue disorder, and opens up about her experience living with this condition her whole life. Latasha brings her humor and her honesty to the table, and talks candidly about echocardiograms, being “out” with her condition, and how she’s learned to embrace her quirks (read: a passion for productivity tools and schedulers) to help her balance health, work, and life. This was such a fun conversation, and Latasha’s advice about interrupting social narratives really spoke to me. As a community of people living with health challenges, we internalize so much about what it means to be “healthy” or “normal,” and Latasha shared her process for working through it.  She also shared how her chosen family — her husband and her friends — are constantly showing her what it means to show up and truly love someone. I am so excited to share this interview with all of you, and for you to hear Latasha’s love for life and the deep, deep respect she holds for the condition that many people would consider a burden.

53: Building Your Grace Muscle with Latasha Doyle

In this episode, I am so excited to share my chat with Natalie Enright, an Adult Services Librarian living in San Francisco.    Natalie, who has multiple sclerosis, was first diagnosed in 2010. She attributes her early diagnosis to her husband. After seeing a decline in Natalie’s health, he encouraged her to go to the doctor without making her feel scared or overwhelmed, for which she is so thankful. Since her initial diagnosis, Natalie has not only worked to figure out how to manage and navigate her disease, but to also find the humor in the not-so-pleasant changes that come with MS.    During our talk, Natalie discussed how her attitude plays a large role in how she gets through some of the tougher times with this condition. Two of her passions, meditation and physical activity, have also helped her to stay upbeat and focused on her goals; one of which was to graduate and start her career as a librarian. Now, as a professional librarian, her excitement for her career is palpable, and I have so much admiration for her love for her work.   I was so honored to hear Natalie’s story (and humor) during our chat, and I know that so much of what she shared can benefit many in this community. I hope you’ll tune in to hear the full episode!

In this episode, I am so excited to share my chat with Natalie Enright, an Adult Services Librarian living in San Francisco.    Natalie, who has multiple sclerosis, was first diagnosed in 2010. She attributes her early diagnosis to her husband. After seeing a decline in Natalie’s health, he encouraged her to go to the doctor without making her feel scared or overwhelmed, for which she is so thankful. Since her initial diagnosis, Natalie has not only worked to figure out how to manage and navigate her disease, but to also find the humor in the not-so-pleasant changes that come with MS.    During our talk, Natalie discussed how her attitude plays a large role in how she gets through some of the tougher times with this condition. Two of her passions, meditation and physical activity, have also helped her to stay upbeat and focused on her goals; one of which was to graduate and start her career as a librarian. Now, as a professional librarian, her excitement for her career is palpable, and I have so much admiration for her love for her work.   I was so honored to hear Natalie’s story (and humor) during our chat, and I know that so much of what she shared can benefit many in this community. I hope you’ll tune in to hear the full episode!

52: You Don't Have to Apologize with Natalie Enright

This week, I’m talking to Mike Bajrami, a tech and audio agency owner living in the Los Angeles area. During our discussion, he shares his unique perspective on pain, serving others, and embracing interests. His health journey starts back in 2003, when he received a lower back injury while playing basketball.    His lumbar area injury would eventually morph into a spine disc injury, damage to multiple vertebrae, a shifted pelvis, and debilitating pain. He has also dealt with leaky gut, food allergies, skin reactions, and more, all stemming from his initial injury. But for Mike, one of the most difficult elements of this injury was the mental challenges he would face. Following his injury, Mike faced a deep depression, a “darkness,” as he put it. For three years, Mike struggled with both his injury and the effects it had on his spirit.  As happens to many of us in this community, this period brought more than pain: it also brought Mike to his true passions. Working first as a freelance audio producer and then eventually within his own tech and media agency, which he and his partners have built from the ground up, Mike has been able to create a life that finally feels fulfilling.  Mike is a beautiful example of the power that allowing ourselves time and patience to heal can have on our lives (and spirits), and I’m excited to share our chat with you!

This week, I’m talking to Mike Bajrami, a tech and audio agency owner living in the Los Angeles area. During our discussion, he shares his unique perspective on pain, serving others, and embracing interests. His health journey starts back in 2003, when he received a lower back injury while playing basketball.    His lumbar area injury would eventually morph into a spine disc injury, damage to multiple vertebrae, a shifted pelvis, and debilitating pain. He has also dealt with leaky gut, food allergies, skin reactions, and more, all stemming from his initial injury. But for Mike, one of the most difficult elements of this injury was the mental challenges he would face. Following his injury, Mike faced a deep depression, a “darkness,” as he put it. For three years, Mike struggled with both his injury and the effects it had on his spirit.  As happens to many of us in this community, this period brought more than pain: it also brought Mike to his true passions. Working first as a freelance audio producer and then eventually within his own tech and media agency, which he and his partners have built from the ground up, Mike has been able to create a life that finally feels fulfilling.  Mike is a beautiful example of the power that allowing ourselves time and patience to heal can have on our lives (and spirits), and I’m excited to share our chat with you!

51: Enjoying the Dive with Mike Bajrami

In this episode, I’m joined by Melissa Platt as she shares the story of how her challenges with hearing loss taught her to truly listen. Melissa is a clinical psychologist and therapist who specializes in helping people heal through complex trauma so they can thrive, and has been living with progressively deteriorating hearing loss since 2010. Her health journey has taken her through many different shifts over the years, including the realization that the track she was on was no longer making her happy. Melissa decided to make a change and pursue her joy, leaving her job as a researcher to open a private practice where she has more space for the reflection and introspection she was craving. As Melissa was going through these major shifts in her hearing loss journey, she started listening to the NWIO podcast and found a community and message she could really resonate with. I had the pleasure of connecting with Melissa through the Shine Your Light mastermind earlier this year, where she tapped into this community and found a place she belonged — a place where she could think creatively and be genuinely curious about her hearing loss. During our talk, Melissa shares how healing it can be to gather strength from media that you resonate with, whether that’s a podcast, guided meditations, books, or online videos. She also gives us a rundown of the polyvagal theory and how it allows her to connect with and gain inspiration from those around her. In this episode, we dive into just how complicated it can be to hold the desire to look at your health challenges in a positive light while also needing to feel the hard feelings that come with chronic illness. Melissa’s story is a study in how our health challenges can be a gift while also highlighting the relief in knowing it’s okay if we’re not ready to see our challenges in that light. In this episode, we talk about how Melissa has been working to integrate both sides of the conversation, as well as how different bodily responses can serve as indicators of resonance. By paying attention to our inner voice and the way our bodies respond, we can start accessing emotions that are harder to get to when we’re on the wrong track. She reminds us that our inner navigation system is always talking to us, and you don’t need perfect hearing to listen.

In this episode, I’m joined by Melissa Platt as she shares the story of how her challenges with hearing loss taught her to truly listen. Melissa is a clinical psychologist and therapist who specializes in helping people heal through complex trauma so they can thrive, and has been living with progressively deteriorating hearing loss since 2010. Her health journey has taken her through many different shifts over the years, including the realization that the track she was on was no longer making her happy. Melissa decided to make a change and pursue her joy, leaving her job as a researcher to open a private practice where she has more space for the reflection and introspection she was craving. As Melissa was going through these major shifts in her hearing loss journey, she started listening to the NWIO podcast and found a community and message she could really resonate with. I had the pleasure of connecting with Melissa through the Shine Your Light mastermind earlier this year, where she tapped into this community and found a place she belonged — a place where she could think creatively and be genuinely curious about her hearing loss. During our talk, Melissa shares how healing it can be to gather strength from media that you resonate with, whether that’s a podcast, guided meditations, books, or online videos. She also gives us a rundown of the polyvagal theory and how it allows her to connect with and gain inspiration from those around her. In this episode, we dive into just how complicated it can be to hold the desire to look at your health challenges in a positive light while also needing to feel the hard feelings that come with chronic illness. Melissa’s story is a study in how our health challenges can be a gift while also highlighting the relief in knowing it’s okay if we’re not ready to see our challenges in that light. In this episode, we talk about how Melissa has been working to integrate both sides of the conversation, as well as how different bodily responses can serve as indicators of resonance. By paying attention to our inner voice and the way our bodies respond, we can start accessing emotions that are harder to get to when we’re on the wrong track. She reminds us that our inner navigation system is always talking to us, and you don’t need perfect hearing to listen.

50: Hearing Loss + Listening Inward with Melissa Platt

In this episode, I’m joined by Sherry Espinosa for an insightful and full-hearted discussion about how she got more comfortable with her health challenges and started letting faith guide her journey. I met Sherry through the Shine Your Light mastermind I hosted earlier this year, where she conquered her fears and stepped back into the world to build authentic relationships with others. Over the course of her health journey, she’s undergone a major shift from searching for all of the answers to realizing that the answers were inside of her the entire time — all she had to do was stop fighting and learn to love her own heart. Living with Multiple Sclerosis and low vision, Sherry bravely opens up about the ups and downs of her winding health journey. She’s had to process multiple rare diagnoses from an early age, eventually losing most of her sight after years of medication and surgeries. During the process, she learned that by denying the pain and anger she was feeling, she was also denying a part of herself. When she realized she didn’t need to understand everything, she handed the reins over to faith and started giving herself permission to feel. Whether it’s pain, sadness, or anger, she shares a powerful message we all need to hear: Your feelings aren’t going to kill you. Sherry embodies pure love as she urges us to be gentle with ourselves and really listen to what our bodies and spirit are telling us. She is a shining example of the positive transformation that can happen when we welcome the fatigue, pain, and emotions that come with chronic illness. Our chat was a breath of fresh air and a reminder that the real healing begins when we stop being so hard on ourselves. During our chat, Sherry and I dig into our shared MS diagnosis, as well as the deep impacts her health journey has had on how she views herself. For Sherry, living with multiple health challenges has allowed her to be more authentic and shown her she has the inner strength to handle anything.

In this episode, I’m joined by Sherry Espinosa for an insightful and full-hearted discussion about how she got more comfortable with her health challenges and started letting faith guide her journey. I met Sherry through the Shine Your Light mastermind I hosted earlier this year, where she conquered her fears and stepped back into the world to build authentic relationships with others. Over the course of her health journey, she’s undergone a major shift from searching for all of the answers to realizing that the answers were inside of her the entire time — all she had to do was stop fighting and learn to love her own heart.Living with Multiple Sclerosis and low vision, Sherry bravely opens up about the ups and downs of her winding health journey. She’s had to process multiple rare diagnoses from an early age, eventually losing most of her sight after years of medication and surgeries. During the process, she learned that by denying the pain and anger she was feeling, she was also denying a part of herself. When she realized she didn’t need to understand everything, she handed the reins over to faith and started giving herself permission to feel. Whether it’s pain, sadness, or anger, she shares a powerful message we all need to hear: Your feelings aren’t going to kill you. Sherry embodies pure love as she urges us to be gentle with ourselves and really listen to what our bodies and spirit are telling us. She is a shining example of the positive transformation that can happen when we welcome the fatigue, pain, and emotions that come with chronic illness. Our chat was a breath of fresh air and a reminder that the real healing begins when we stop being so hard on ourselves. During our chat, Sherry and I dig into our shared MS diagnosis, as well as the deep impacts her health journey has had on how she views herself. For Sherry, living with multiple health challenges has allowed her to be more authentic and shown her she has the inner strength to handle anything.

49: Learning to Love My Own Heart with Sherry Espinosa

For this episode of Not What I Ordered, I’m joined by my amazing music editor and close friend, Lily Sloane. Lily is a therapist, composer, audio producer, and host of a weekly advice show with a deep passion for making the world a better place through self-healing. Learning to live with and accept her health challenges through therapy has helped her find comfort in the unknown, which she then channels into her own practice. By tearing down the notion of “perfect health”, Lily is able to help her clients -- and herself -- open the door to gratitude. Lily shows true vulnerability as she opens up about the shame and dogma attached to chronic illness, as well as how she learned to live with her illness without needing to know what it is. She also shares how therapy has taught her to accept where she is on her health journey instead of where she’d like to be -- or where anyone else expects her to be! By transforming her perspective, Lily was able to change her inner narrative, shed her need to fix everything, and learn to sit with her discomfort. Her story is a much-needed reminder that it’s okay to not have all the answers. Throughout her journey, she has learned that in order to make a change in the world around us, we must first make a change within ourselves. My open-heart discussion with Lily is full of powerful insights on making more space for acceptance and how embracing the unknown can lead to a more empowered life. I hope you enjoy our talk as much as I did!

For this episode of Not What I Ordered, I’m joined by my amazing music editor and close friend, Lily Sloane. Lily is a therapist, composer, audio producer, and host of a weekly advice show with a deep passion for making the world a better place through self-healing. Learning to live with and accept her health challenges through therapy has helped her find comfort in the unknown, which she then channels into her own practice. By tearing down the notion of “perfect health”, Lily is able to help her clients -- and herself -- open the door to gratitude.Lily shows true vulnerability as she opens up about the shame and dogma attached to chronic illness, as well as how she learned to live with her illness without needing to know what it is. She also shares how therapy has taught her to accept where she is on her health journey instead of where she’d like to be -- or where anyone else expects her to be! By transforming her perspective, Lily was able to change her inner narrative, shed her need to fix everything, and learn to sit with her discomfort. Her story is a much-needed reminder that it’s okay to not have all the answers. Throughout her journey, she has learned that in order to make a change in the world around us, we must first make a change within ourselves. My open-heart discussion with Lily is full of powerful insights on making more space for acceptance and how embracing the unknown can lead to a more empowered life. I hope you enjoy our talk as much as I did!

48: Releasing Perfectionism with Lily Sloane

In this episode of This Is Not What I Ordered, I’m joined by Sheryl Chan — a web developer, writer, and travel enthusiast living with multiple chronic illnesses. Suffering from a mild stroke at the age of 14, Sheryl was diagnosed with a rare blood clotting syndrome that set off a chain reaction of other autoimmune disorders including lupus, epilepsy, Sjögren’s syndrome, and a heart rhythm disorder. In the midst of her health challenges, Sheryl embraced her love of writing and started using blogs as a cathartic outlet. This eventually led to the creation of A Chronic Voice, where she’s able to raise awareness of silent disabilities and give other people with chronic illness a space to share their perspectives. By accepting her health challenges and freely sharing them with the world, Sheryl has taken the power away from her illness and reclaimed it as her own. She reminds us that acceptance doesn’t mean you’re giving up — it can be a powerful opportunity for transformation and inner growth. During our time together, Sheryl offers up her thoughts on why it’s so important to normalize chronic illness and gain different perspectives. She also opens up about the identity struggles that accompany chronic illness, how it taught her to respect her body, and how having a sense of wonder about the body has helped her cope.

In this episode of This Is Not What I Ordered, I’m joined by Sheryl Chan — a web developer, writer, and travel enthusiast living with multiple chronic illnesses. Suffering from a mild stroke at the age of 14, Sheryl was diagnosed with a rare blood clotting syndrome that set off a chain reaction of other autoimmune disorders including lupus, epilepsy, Sjögren’s syndrome, and a heart rhythm disorder. In the midst of her health challenges, Sheryl embraced her love of writing and started using blogs as a cathartic outlet. This eventually led to the creation of A Chronic Voice, where she’s able to raise awareness of silent disabilities and give other people with chronic illness a space to share their perspectives.By accepting her health challenges and freely sharing them with the world, Sheryl has taken the power away from her illness and reclaimed it as her own. She reminds us that acceptance doesn’t mean you’re giving up — it can be a powerful opportunity for transformation and inner growth.During our time together, Sheryl offers up her thoughts on why it’s so important to normalize chronic illness and gain different perspectives. She also opens up about the identity struggles that accompany chronic illness, how it taught her to respect her body, and how having a sense of wonder about the body has helped her cope.

47: Acceptance is Power with Sheryl Chan

In this episode, I’m joined by accomplished singer-songwriter and chronic pain survivor Stefan Alexander Weiner. Stefan lives with central sensitization syndrome, a confusing and painful condition that left him without answers and unable to perform for years. Since his diagnosis, Stefan has bravely journeyed through a multitude of doctor appointments, physical therapy, and pain rehabilitation programs to reconnect with his true love -- music. His health challenges haven’t stopped him from seeing the silver lining, though. Through his chronic illness, Stefan was able to reframe his situation, start growing his relationship with himself, and be more compassionate. As he’s moved through the trauma that his chronic illness left in its wake, he’s integrated the condition into his identity and taken ownership of it. During our insightful chat, Stefan shares how his illness has helped him be more present for the people in his life, as well as how he uses social interaction and performing to quiet the heavy questioning in his mind. He also shares how he started validating his own pain and reframed his illness to see the riches within.

In this episode, I’m joined by accomplished singer-songwriter and chronic pain survivor Stefan Alexander Weiner. Stefan lives with central sensitization syndrome, a confusing and painful condition that left him without answers and unable to perform for years. Since his diagnosis, Stefan has bravely journeyed through a multitude of doctor appointments, physical therapy, and pain rehabilitation programs to reconnect with his true love -- music. His health challenges haven’t stopped him from seeing the silver lining, though. Through his chronic illness, Stefan was able to reframe his situation, start growing his relationship with himself, and be more compassionate. As he’s moved through the trauma that his chronic illness left in its wake, he’s integrated the condition into his identity and taken ownership of it. During our insightful chat, Stefan shares how his illness has helped him be more present for the people in his life, as well as how he uses social interaction and performing to quiet the heavy questioning in his mind. He also shares how he started validating his own pain and reframed his illness to see the riches within.

46: Finding a New Way Through Pain with Stefan Weiner

On the Season Three premiere of This Is Not What I Ordered, I sit down with April Snow as she shares how her life-long health journey with eczema and high sensitivity has taught her how to live an authentic life without guilt. April is a psychotherapist and Highly Sensitive Person (HSP) who encourages others to embrace their own sensitive superpowers through mindfulness, self-reflection, and self-care strategies. Her experiences with chronic illness and sensitivity helped create the foundation for her psychotherapy practice, Expansive Heart, where she’s able to support other highly sensitive people as they learn to let go of self-doubt and prioritize themselves. April’s passion for self-advocacy and her ability to see the unique blessings of her health challenges is inspiring. During this episode, she opens up about how being highly sensitive has helped her understand her illness, the importance of self-acceptance in the healing process, and how she’s learned to create boundaries along the way.

On the Season Three premiere of This Is Not What I Ordered, I sit down with April Snow as she shares how her life-long health journey with eczema and high sensitivity has taught her how to live an authentic life without guilt. April is a psychotherapist and Highly Sensitive Person (HSP) who encourages others to embrace their own sensitive superpowers through mindfulness, self-reflection, and self-care strategies. Her experiences with chronic illness and sensitivity helped create the foundation for her psychotherapy practice, Expansive Heart, where she’s able to support other highly sensitive people as they learn to let go of self-doubt and prioritize themselves. April’s passion for self-advocacy and her ability to see the unique blessings of her health challenges is inspiring. During this episode, she opens up about how being highly sensitive has helped her understand her illness, the importance of self-acceptance in the healing process, and how she’s learned to create boundaries along the way.

45: Highly Sensitive + Thriving with April Snow

Chronic illness and other health challenges can be a real bummer--but they don't have to be the end of joy and fulfillment. It turns out we can still have epic lives, even when our bodies have plans of their own. Join San Francisco psychotherapist Lauren Selfridge for honest, humorous, and inspiring conversations with people who get what it's like to live with health challenges. Whether you're in the car, on a walk, in the waiting room, or lying in bed, we'll be here to keep you company along the way.

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This is Not What I Ordered: a podcast on full-hearted living...

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