The POTScast
Learn about Postural Orthostatic Tachycardia Syndrome (POTS), Mast Cell Activation Syndrome (MCAS) and more by joining us each week for a new episode. If you are living with POTS, MCAS or other chronic illnesses, you are not alone! Our goal is to raise awareness, nurture community, and empower patients with information and practical skills for living better with this chronic invisible illness. Each month, we feature episodes with top POTS physicians as well as POTS patients. Because many POTS patients are eventually diagnosed with MCAS, the first Tuesday of every month we feature a new series called Mast Cell Matters, in which top MCAS practitioners share their experiences in better treating patients. You can learn more by listening to our groundbreaking POTScast anywhere, anytime. Visit our website at www.standinguptopots.org and follow our social media accounts @standinguptopots.

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Jaksot(250)

E81: Katherine from Pennsylvania

E81: Katherine from Pennsylvania

Katherine developed POTS secondary to Lyme disease after a tick bite, causing her to complete her senior year of high school online. When at her sickest, she re-connected with the man she would marry....

20 Elo 202234min

E80: Mary Katherine Stratton from Mississippi

E80: Mary Katherine Stratton from Mississippi

Mary Katherine has developed POTS twice - first as a teen and again after COVID. Her PICC line to get intravenous fluids made lifting heavy objects impossible, especially for a cattle breeder who love...

16 Elo 202229min

E79: Employment Resources for the Chronically Ill with Chronically Capable CEO and co-Founder Hannah Olson

E79: Employment Resources for the Chronically Ill with Chronically Capable CEO and co-Founder Hannah Olson

Hannah has Lyme and POTS, and after working for others for a few years founded her own company - Chronically Capable. Featured by the Wall Street Journal and Forbes magazine, her company matches chron...

9 Elo 202233min

E78: Claire from Australia

E78: Claire from Australia

Claire developed POTS after a back injury. Work as a paramedic was triggering, and she found that she had to dig herself out of a dark hole. Volunteering for The POTS Foundation in Australia was part ...

6 Elo 202238min

E77: Abby from New York

E77: Abby from New York

Abby is a college sophomore with a love of music and crocheting. Like many, she put the pieces together to find her diagnosis. Abby is resilient despite the obstacles - finding friends who are support...

2 Elo 202230min

E76: Pediatric POTS and Related Disorders with Dr. Jeffrey Boris

E76: Pediatric POTS and Related Disorders with Dr. Jeffrey Boris

Dr. Boris is one of the top pediatric POTS docs in the world, and we were fortunate to have him share his thoughts on getting these highly achieving kids back to living their life. He covers a lot of ...

26 Heinä 202246min

E75: Madison from Illinois

E75: Madison from Illinois

Madison was a competitive rock climber before she developed Lyme disease and POTS. She couldn't walk for 7 months, but has climbed her way back to working part time in a school and practicing meditati...

19 Heinä 202239min

E74: Jolene from MN

E74: Jolene from MN

Jolene was married and enjoying an adventurous life in Florida when POTS struck. Like many, she was misdiagnosed and returned home to MN to decrease her need to fly. Now a meditation and mindfulness t...

16 Heinä 202238min

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