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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Episoder(250)

E102: Lacy from Alabama suffers from gastroparesis, pain, and POTS

E102: Lacy from Alabama suffers from gastroparesis, pain, and POTS

Lacy is a high school student who struggles to remember a time she wasn't sick. Gastroparesis is a big issue for her and she often uses a cane for stability. She's quite upbeat, though, and ready for ...

10 Des 202219min

E101: Pelvic Congestion Syndrome and POTS with Dr. Steven Smith

E101: Pelvic Congestion Syndrome and POTS with Dr. Steven Smith

Dr. Smith is a retired interventional radiologist who made a discovery in his career treating women with pelvic congestion syndrome (PCS):  His patients with comorbid POTS often said the PCS treatment...

6 Des 202251min

Christmas Poem 2022 — Why Santa donates to Standing Up to POTS

Christmas Poem 2022 — Why Santa donates to Standing Up to POTS

You can read the transcript for this poem here: https://tinyurl.com/potscastholiday22

3 Des 20224min

E100: POTS Research both Past and Future with Dr. Satish Raj

E100: POTS Research both Past and Future with Dr. Satish Raj

Dr. Raj is a world renowned POTS physician and researcher who spoke with us about three big POTS research topics: blood volume, autoimmunity, and the norepinephrine transporter. Having done much of th...

29 Nov 202251min

E99: Zoe from Utah, high school senior and aerialist

E99: Zoe from Utah, high school senior and aerialist

Zoe was diagnosed with POTS in 8th grade when she started having dizzy spells and shortness of breath. She has adjusted well, and loves to fly 30 feet above the ground doing ribbon aerial work. Great ...

22 Nov 202227min

E98: Sensory Input Shaping Autonomics in Children with Dr. Kevin Lasko

E98: Sensory Input Shaping Autonomics in Children with Dr. Kevin Lasko

What is really causing POTS? Is it a problem in the heart? The brain? The gut? Dr. Lasko believes that lower parts of the brain may not be functioning properly in many with POTS, and that correcting t...

15 Nov 202248min

E97: Mackenzie from British Columbia, Canada

E97: Mackenzie from British Columbia, Canada

Like many POTSies, Mackenzie was a teenager leading an active life when she became ill. It took her 2.5 years and a number of ludicrous diagnoses to finally arrive at POTS. At 20, she is now adjusting...

8 Nov 202230min

E96: Jackie from Vermont, working mom with great symptom management tips

E96: Jackie from Vermont, working mom with great symptom management tips

Jackie developed POTS and other chronic illnesses after surgery on her foot. She delves deeply into her interests, including ways to manage her symptoms. Her optimism is inspiring as she share things ...

5 Nov 202241min

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