Murder in Illinois

Michelle Shapiro had built a career helping others get healthy when she was hit with a debilitating health crisis. Doctors were unable to identify the cause of her symptoms - no matter how hard Michelle pushed for answers. So unwell that she could barely function - Michelle made it her mission to get to the bottom of what was going on only to find that the condition she was experiencing is still being understood by the medical community. We want to hear from you! Share your own medical mystery or tell us about the episode you connected with the most at [email protected] or drop us a voice note at https://www.speakpipe.com/Symptomatic. DISCLAIMER: By submitting your voice note using the link provided, you acknowledge that we have permission to potentially include that audio in future content. * * * * * * ****** SPOILER ALERT BELOW ****** You can follow Michelle on social media @michelleshapirord and on her website michelleshapirord.com. You can take the Highly Sensitive Body quiz here: https://michelleshapirord.com/hsb-quiz Dr. Tania Dempsey can be found on instagram @drtaniadempseymd and online at drtaniadempsey.com. Her podcast is called Mast Cell Matters.See omnystudio.com/listener for privacy information.

What began as intermittent rashes that popped up years apart turned into excruciating, long term flare ups with no reprieve for Kristen Willard. Unable to sleep, shower, or even put on pants - Kristen’s quality of life plummeted. With no common trigger to explain the debilitating flares, she was forced to endure for months on end without relief. After decades and at the end of her rope, Kristen seeks answers one last time. We want to hear from you! Share your own medical mystery or tell us about the episode you connected with the most at [email protected] or drop us a voice note at https://www.speakpipe.com/Symptomatic . DISCLAIMER: By submitting your voice note using the link provided, you acknowledge that we have permission to potentially include that audio in future content. * * * * * * ****** SPOILER ALERT BELOW ****** You can learn more about Chronic Spontaneous Urticaria at chronic-urticaria.org and you can find the Global Allergy & Airways Patient Platform at gaapp.org.See omnystudio.com/listener for privacy information.

Rockstar Casey McPherson and his family were shocked to the core when his daughter Rose was diagnosed with a rare genetic mutation that has no known treatment. Faced with the possibility of losing his daughter, the front man of the Flying Colours dropped everything to devote his life to trying to find a cure before time runs out. We want to hear from you! Share your own medical mystery or tell us about the episode you connected with the most at [email protected] or drop us a voice note at https://www.speakpipe.com/Symptomatic. DISCLAIMER: By submitting your voice note using the link provided, you acknowledge that we have permission to potentially include that audio in future content. * * * * * * ****** SPOILER ALERT BELOW ****** You can learn more about AlphaRose at https://www.alpharose.com/, To Cure A Rose Foundation at www.tocurearose.org and TCAR RareLabs at https://www.tcarrarelabs.org/. You can follow Casey @casey.mcpherson on instagram. See omnystudio.com/listener for privacy information.

For as long as Cienna Ditri can remember, she has had random bouts of “heavy legs”and loss of vision. As she got older - that sensation grew into episodes in which she could not move altogether. Cienna was passing out multiple times a day and frequently losing vision. After a slew of misdiagnoses - she was unsure she would ever understand the cause…until one doctor found the needle in the haystack. We want to hear from you! Share your own medical mystery or tell us about the episode you connected with the most at [email protected] or drop us a voice note at https://www.speakpipe.com/Symptomatic. DISCLAIMER: By submitting your voice note using the link provided, you acknowledge that we have permission to potentially include that audio in future content. * * * * * * ****** SPOILER ALERT BELOW ****** You can learn more about Periodic Paralysis at periodicparalysis.orgYou can follow Cienna at @chronicallyperservering on instagram, tiktok, facebook, and youtube. You can find Cienna’s substack “In Rare Form” at chronicallypersevering.substack.comSee omnystudio.com/listener for privacy information.

Ian Stedman suffered 32 years with full body rashes, debilitating headaches, joint pain and hearing loss without a clear diagnosis. His Mother Barb had gone over 60 years with the same symptoms. After hundreds of doctors visits and decades of frustration - they had resigned to believe there were no answers. That is until Ian’s daughter, Lia was born covered in that all-too-recognizable rash. Ian re-ignited his search for answers in an effort to save his family. We want to hear from you! Share your own medical mystery or tell us about the episode you connected with the most at [email protected] or drop us a voice note at https://www.speakpipe.com/Symptomatic. DISCLAIMER: By submitting your voice note using the link provided, you acknowledge that we have permission to potentially include that audio in future content. * * * * * * ****** SPOILER ALERT BELOW ****** You can learn more about the Canadian Autoinflammatory Network at www.autoinflammatory.ca SickKids CA can be found online at www.sickkids.caSee omnystudio.com/listener for privacy information.