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An Informational Blog on EDS and POTS

An Informational Blog on EDS and POTS. Recently, I have come across a letter (via Defying Gravity. That was written by a sufferer of POTS, Stacy Reed, and her doctor, Thomas Ahern, regarding the debilitating symptoms of Postural Orthostatic Tachycardia Syndrome. This letter would be extremely beneficial to those attending college who want their professors or their disability services office to gain a better understanding of what they suffer from. Our life. Our struggles. To Whom It May Concern:. Patients...

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An Informational Blog on EDS and POTS | edsandpots.blogspot.com Reviews
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An Informational Blog on EDS and POTS. Recently, I have come across a letter (via Defying Gravity. That was written by a sufferer of POTS, Stacy Reed, and her doctor, Thomas Ahern, regarding the debilitating symptoms of Postural Orthostatic Tachycardia Syndrome. This letter would be extremely beneficial to those attending college who want their professors or their disability services office to gain a better understanding of what they suffer from. Our life. Our struggles. To Whom It May Concern:. Patients...
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2 what is eds
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4 eds/pots correlation
5 treatment
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7 informational pots letter
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An Informational Blog on EDS and POTS | edsandpots.blogspot.com Reviews

https://edsandpots.blogspot.com

An Informational Blog on EDS and POTS. Recently, I have come across a letter (via Defying Gravity. That was written by a sufferer of POTS, Stacy Reed, and her doctor, Thomas Ahern, regarding the debilitating symptoms of Postural Orthostatic Tachycardia Syndrome. This letter would be extremely beneficial to those attending college who want their professors or their disability services office to gain a better understanding of what they suffer from. Our life. Our struggles. To Whom It May Concern:. Patients...

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edsandpots.blogspot.com edsandpots.blogspot.com
1

An Informational Blog on EDS and POTS: Informational POTS Letter

http://edsandpots.blogspot.com/2011/11/informational-pots-letter.html

An Informational Blog on EDS and POTS. Recently, I have come across a letter (via Defying Gravity. That was written by a sufferer of POTS, Stacy Reed, and her doctor, Thomas Ahern, regarding the debilitating symptoms of Postural Orthostatic Tachycardia Syndrome. This letter would be extremely beneficial to those attending college who want their professors or their disability services office to gain a better understanding of what they suffer from. Our life. Our struggles. To Whom It May Concern:. Patients...

2

An Informational Blog on EDS and POTS: November 2011

http://edsandpots.blogspot.com/2011_11_01_archive.html

An Informational Blog on EDS and POTS. Recently, I have come across a letter (via Defying Gravity. That was written by a sufferer of POTS, Stacy Reed, and her doctor, Thomas Ahern, regarding the debilitating symptoms of Postural Orthostatic Tachycardia Syndrome. This letter would be extremely beneficial to those attending college who want their professors or their disability services office to gain a better understanding of what they suffer from. Our life. Our struggles. To Whom It May Concern:. Patients...

3

An Informational Blog on EDS and POTS: EDS/POTS Correlation

http://edsandpots.blogspot.com/p/eds-pots-correlation_09.html

An Informational Blog on EDS and POTS. There are many different "causes" of POTS (some unknown). Less commonly, there is a genetic and acquired way to develop POTS. Ehlers-Danlos Syndrome is now an accepted cause of Postural Orthostatic Tachycardia Syndrome. EDS is a connective tissue disorder, which makes veins dilate excessively. When the veins are dilated(open wide), blood flow cannot be distributed effectively throughout the veins and pooling begins. Subscribe to: Posts (Atom). 9829;About the Blog.

4

An Informational Blog on EDS and POTS: September 2011

http://edsandpots.blogspot.com/2011_09_01_archive.html

An Informational Blog on EDS and POTS. Electrolytes and Enhanced Water. The most common "remedy" that many people with POTS/Dysautonomia get told is to " drink, drink, drink! But does that always help? Here are some things you might want to consider if you haven't already. Interestingly enough, many doctors fail to inform their patients that an over-consumption of "plain/tap water" can actually worsen your symptoms. When you consume excessive amounts of water (especially non-enhanced water. Electrolytes ...

5

An Informational Blog on EDS and POTS: Treatment

http://edsandpots.blogspot.com/p/treatment.html

An Informational Blog on EDS and POTS. TREATM.E.N.T. Treatment is subjective and varies with experience of every doctor *. It is unique and specific to the patient. Trial and error is often used. Every POTS patient should consume at least 3L of electrolyte enhanced fluids per day, regardless of their individual symptoms. Jobst Stockings/Support Stockings/Abdominal Binde. Increased Salt Intake/Salt Tablets. Also known as ProAmitine, is one of the most popular/most used alpha-agonists (which constricts blo...

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An Informational Blog on EDS and POTS

An Informational Blog on EDS and POTS. Recently, I have come across a letter (via Defying Gravity. That was written by a sufferer of POTS, Stacy Reed, and her doctor, Thomas Ahern, regarding the debilitating symptoms of Postural Orthostatic Tachycardia Syndrome. This letter would be extremely beneficial to those attending college who want their professors or their disability services office to gain a better understanding of what they suffer from. Our life. Our struggles. To Whom It May Concern:. Patients...

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