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What is the history of Dysautonomia / POTS?

When was Dysautonomia / POTS discovered? What is the story of this discovery? Was it coincidence or not?

History of Dysautonomia / POTS
4 answers
It has been around for years, no one has found a cure yet which sucks.

Posted Aug 17, 2017 by Miranda 2150
Dysautonomia or autonomic dysfunction is a condition in which the autonomic nervous system (ANS) does not work properly. This may affect the functioning of the heart, bladder, intestines, sweat glands, pupils, and blood vessels, although it has many causes, not all of which classify as neuropathic.[1] A number of diseases can feature dysautonomia, such as Parkinson's disease, multiple system atrophy, autonomic failure, postural orthostatic tachycardia syndrome, and autonomic neuropathy.

The diagnosis is achieved through functional testing of the autonomic nervous system, focusing on the organ system affected. Investigations may be performed to identify underlying disease processes that may have led to the development of symptoms or autonomic neuropathy. Symptomatic treatment is available for many symptoms associated with dysautonomia, and some disease processes can be treated directly.[2]

https://en.wikipedia.org/wiki/Dysautonomia

Posted Sep 28, 2017 by Lbond94 4100
Translated from spanish Improve translation
Before he was known as the heart of a soldier, because they realized during the war that the soldiers were fainting to be a lot of time standing and motionless, he has been given the name of neurasthenia circulatory dystonia neurovegetative, Dysautonomia which is a generic term to call various failures of the autonomic nervous system and currently intolerance Ortostatica chronic and among them is the POTS, vasovagal syncope or neurocardiogenico and intolerance Ortostatica without tachycardia.

Posted Jun 2, 2017 by Aurora Saez 3201
Translated from spanish Improve translation
I was discovered by the cardiologist after I started to have fainting spells frequent 20 years

Posted Sep 10, 2017 by Annie 2050

History of Dysautonomia / POTS

Dysautonomia / POTS life expectancy

What is the life expectancy of someone with Dysautonomia / POTS?

11 answers
Celebrities with Dysautonomia / POTS

Celebrities with Dysautonomia / POTS

3 answers
Is Dysautonomia / POTS hereditary?

Is Dysautonomia / POTS hereditary?

8 answers
Is Dysautonomia / POTS contagious?

Is Dysautonomia / POTS contagious?

9 answers
ICD9 and ICD10 codes of Dysautonomia / POTS

ICD10 code of Dysautonomia / POTS and ICD9 code

7 answers
Natural treatment of Dysautonomia / POTS

Is there any natural treatment for Dysautonomia / POTS?

6 answers
Living with Dysautonomia / POTS

Living with Dysautonomia / POTS. How to live with Dysautonomia / POTS?

11 answers
Dysautonomia / POTS diet

Dysautonomia / POTS diet. Is there a diet which improves the quality of lif...

13 answers

World map of Dysautonomia / POTS

Find people with Dysautonomia / POTS through the map. Connect with them and share experiences. Join the Dysautonomia / POTS community.

Stories of Dysautonomia / POTS

DYSAUTONOMIA / POTS STORIES
Dysautonomia / POTS stories
Hola soy Aurora tengo 39 años, algunos conocen mis artículos pero nunca he escrito mi vida. Pues a los 17 años me diagnosticaron epilepsia, mi vida cambio, tuve que dejar la escuela por un año mientras encontraban el mejor tratamiento y así fue....
Dysautonomia / POTS stories
While I still worked as a ballet dancer and later a ballet teacher (stopped performing at age 35) my dysautonomia symptoms were easily managed, but durubf times when I did not dance they were much more pronounced.  At 32 I had a heart attack due to ...
Dysautonomia / POTS stories
I've had Hypotension attacks since age 11.  I am now 69 and was just diagnosed for Primary Autonomic Failure.  I know that my diagnosis is really a term that includes Parkinsons (PD), Multiple Systems Atrophy (MSA), and Pure Autonomic Failure (PAF)...
Dysautonomia / POTS stories
I was diagnosed with IST in 2012, was taking calcium blockers to try to control it and I just had to keep increasing them as they kept turning up inaffective. January 2015 I got very sick after taking a vacation. Recovered from that (virus) but never...
Dysautonomia / POTS stories
It's a year this October that i've been ill. Was diagnosed just this past May. Struggling with doctors and medications. Hoping to get better.

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Dysautonomia / POTS forum

DYSAUTONOMIA / POTS FORUM
Dysautonomia / POTS forum
How many of you have received the Gardasil Vaccine (HPV Vaccine) that now have Dysautonomia? 
Dysautonomia / POTS forum
Anyone gets POTS after talking synthrpid or being induced with pitocin?
Dysautonomia / POTS forum
I have renal damage. Hypotension may have caused it. Anyone else?
Dysautonomia / POTS forum
  Hola! Somos Disautonomía Chile La misión de Disautonomía Chile es contribuir a la sociedad mejorando la calidad de vida de las personas diagnosticadas, en busca de diagnóstico, cuidadores y familias de personas con Trastornos del Si...
Dysautonomia / POTS forum
  Hola! Somos Disautonomía Chile La misión de Disautonomía Chile es contribuir a la sociedad mejorando la calidad de vida de las personas diagnosticadas, en busca de diagnóstico, cuidadores y familias de personas con Trastornos del Si...

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