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Episode 26: T. Sydney Bergeron Mikus

T. Sydney Bergeron Mikus is an award-winning writer, artist, designer, model, and activist based in NYC. They live with TBD (tick borne disease), including Lyme, Bartonella, and ehrlichia, as well as POTS (postural orthostatic tachycardia syndrome). They create work driven by healing advocacy, art, and narrative as tools for change, and self-care as disruption. They…

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Episode 25: P. Brendon Lundberg

With a vision to build the safest, most consistently effective and non-invasive solution to the epidemic of chronic pain, Brendon Lundberg (a chronic pain survivor himself) co-founded Radiant Pain Relief Centres in Oregon. The centres use an FDA-approved and Mayo Clinic-tested treatment for chronic pain called Scrambler Therapy, which targets the brain’s response to pain…

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Episode 24: Noah Gardner

Noah Gardner is a scientist based in Massachusetts. He was diagnosed with type 1 (juvenile) diabetes in 1995, at the age of 12. While this autoimmune condition is genetic, his diagnosis came completely out of the blue to both him and his family. A little background on T1 diabetes: in an autoimmune reaction, the immune…

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Episode 23: Em & Kate

Em & Kate are the sisters behind the wellness blog Two Being Healthy. Both live with lupus, postural orthostatic tachycardia syndrome (POTS), Ehlers-Danlos syndrome (EDS), mast cell activation disorder (MCAD), and cytochrome mutations (which have affected their ability to metabolize certain drugs). Having spent much of their adult lives living with and navigating the symptoms…

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Episode 22: Ilene

In an effort to preserve this guest’s privacy, we are using an alias in this episode – an Uninvisible first! Ilene is an award-winning 6th-grade elementary school teacher. She is also a survivor of rape, “endometrial symptoms” (aka, undiagnosed endometriosis – chronic pain that was only compounded by her sexual assault), and hypothyroidism. She joins…

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Episode 21: Jameisha Prescod

Jameisha Prescod is a London-based activist who lives with lupus, Raynaud’s, and femoroacetabular impingement (FAI); she is also waiting on possible diagnoses of endometriosis and celiac disease. She is the founder of You Look Okay To Me, an online platform for pain and chronic illness that is chock-full of content about invisible illness, disability, and…

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Episode 20: Alison Yates

Alison Yates is a multi-hyphenate creative living in Los Angeles. A comedienne and actor, producer, writer, photographer, social media manager, website designer, and skincare consultant (phew!), she performs sketch and comedy regularly with Second City and the Groundlings, and has a production company called The People Zoo. She’s been featured on several TV shows, including…

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Episode 19: Sascha Alexander UPDATE!

Join us for another joyous installment with the incomparable Sascha Alexander. Remember that time she thought she had toxic mold, in addition to interstitial cystitis, candida, and Hashimoto’s disease? Well, guess what? That toxic mold ain’t so moldy…it’s Lyme! Lauren sits down with Sascha to find out how she was ultimately diagnosed, and how she’s…

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Episode 18: Dominique Viel

Dominique Viel is the founder of InvisiYouth Charity, a 501(c)3 nonprofit organization that helps teens and young adults around the world with varied chronic conditions and disabilities discover empowering lifestyle programs to live full lives while battling illness. A natural progression of speaking engagements she began as a teen in research hospital treatment centers, she…

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Episode 17: Calliope Tsoukalas

In our 17thepisode, Lauren brings back a familiar guest: Calliope Tsoukalas, a nutrition and wellness coach based in Los Angeles, CA. Calliope is on the show again not only to go more in-depth about her practice, but also to share her experiences living with one of the most nebulous of invisible illness diagnoses: IBS. Key…

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