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.

Tämä podcast on lisätty Podme-palveluun avoimen RSS-syötteen kautta eikä se ole Podmen omaa tuotantoa. Siksi podcastin jaksot saattavat sisältää mainontaa.

Jaksot(250)

E111: POTS Diary with Allison from Ohio, a nurse whose POTS got worse with concussion

E111: POTS Diary with Allison from Ohio, a nurse whose POTS got worse with concussion

Meet Allison, a long-time POTSie who gives back to the community through nursing. After a concussion, she changed specialties which is a better fit for her symptoms. Using MyChart to communicate with ...

21 Tammi 202334min

E110: Vagus Nerve Exercises with Dr. Kimberly Hindman (part 2)

E110: Vagus Nerve Exercises with Dr. Kimberly Hindman (part 2)

This episode is full of free, must try tips to increase parasympathetic tone that will offset the highly active sympathetic tone found in many POTS patients. Laughing, cool compress on the back of you...

17 Tammi 202355min

E109:  Polyvagal Theory and Trauma Release with Dr. Kimberly Hindman (part 1)

E109: Polyvagal Theory and Trauma Release with Dr. Kimberly Hindman (part 1)

Have you wondered why symptoms seem to loop over time? Why you are stuck in hypervigilance when you are safe? If so, this is the episode for you. Learn the science of the cell danger response, vagus n...

10 Tammi 20231h 3min

E108: Mel from Texas, a nurse living with POTS after a concussion

E108: Mel from Texas, a nurse living with POTS after a concussion

Mel's life changed after a concussion that led to more serious POTS symptoms. A nurse, she was struggling with symptoms when she confided in a friend who had POTS. Could it be that Mel had it too? You...

7 Tammi 202333min

E107: Benefits of compounding medications for those with sensitivities with Michelle Briest, PharmD

E107: Benefits of compounding medications for those with sensitivities with Michelle Briest, PharmD

Many in the POTS and MCAS communities react to medications. Perhaps using a compounding pharmacy that can replace inactive ingredients with alternatives that are less likely to cause a reaction is a g...

3 Tammi 202319min

E106: All Things Pediatric POTS with Dr. Jeff Boris and Dr. Jeff Moak

E106: All Things Pediatric POTS with Dr. Jeff Boris and Dr. Jeff Moak

Dr. Boris and Dr. Moak, true POTS experts, take us through their new review article Pediatric POTS: Where We Stand and discuss developmental issues for children and teens, treatment options including ...

27 Joulu 20221h 4min

E105: Karen from Missouri, a nurse and mom with POTS symptoms from a young age

E105: Karen from Missouri, a nurse and mom with POTS symptoms from a young age

Karen has had POTS symptoms for as long as she can remember, and started passing out at age 15. Unfortunately, it took many doctors and 17 years to get diagnosed. She shares her experience with POTS a...

24 Joulu 202237min

E104: Understanding myalgic encephomyelitis/chronic fatigue syndrome through research and personal experience with Dr. Leonard Jason

E104: Understanding myalgic encephomyelitis/chronic fatigue syndrome through research and personal experience with Dr. Leonard Jason

Dr. Leonard Jason, world renowned father of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) research, shares his very personal story with this illness along with what he has learned in his...

20 Joulu 202256min

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