This episode I apologize have taken a long time coming. This is a continuation of my summer last year, but also an inner struggle of losing what I felt was my independence and the woman I have become. This episode is very dear to me and speaks on sensitive topics, so please listen with an open mind. I share my experience to assist others in knowing they are not alone and help if I can.
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11:33
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11:33
Myths & Questions About POTS
On this episode we will go over myths and questions that I myself have been asked or seen from others who have this disorder. Below are the websites I visited for my information, if you would like to visit them. They are: National Library of Medicine, John Hopkins Medicine, SJOGREN'S ADVOCATE,
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8:31
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8:31
Ablation or No Ablation
In this episode, I touch more on my medical leave and a new procedure that is introduced from my cardiologist.
There is also a poll, feel free to answer and leave any questions or comments.
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7:32
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7:32
"I'm not lying"
On this episode, I share my experience with the heart monitor, as well as a new challenge I face at the end.
Side note, please be patient if my posts are late. With the weather change into summer, my POTS has been flaring up and I been in and out of the hospital.
Thank you again for your support and listening to my story.
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8:11
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8:11
"Changes"
This will be part 2 of my ER visit in the previous episode. I will discuss medication changes and what each one does, as well as research I did after my diagnosis.
Hi, my name is Shannon. And I have POTS (Postural Orthostatic Tachycardia Syndrome). Join me as I raise awareness of this chronic condition. From explaining what it is, the symptoms, the myths/beliefs, my own personal journey, and much more. After all, there is power in knowledge, and who knows, someone you know may have POTS and be unaware.