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.
All content for POTS: The Chronicles Of The Unknown is the property of Shannon House and is served directly from their servers
with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
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.
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.
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,
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.
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.
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.
In this episode, I explain more symptoms, as well as more life changing events that accompanied it. During my journey at this time, I finally found myself on a path that someone knew what was going on with me. You can imagine the relief I felt, yet only ended in more questions for the unknown.
In this episode, I start off with a brief explanation of what POTS is and its symptoms. This is the beginning of understanding the unknown, which is POTS. I myself when I was diagnosed, I was so confused and lost when I first heard this. Before I can get into my journey and what I have been going through, a clear definition needs to be introduced. I hope this helped, and I look forward to sharing my journey with you all.
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.
