14

How do I know if I have Dysautonomia / POTS?

What signs or symptoms may make you suspect you may have Dysautonomia / POTS. People who have experience in Dysautonomia / POTS offer advice of what things may make you suspicious and which doctor you should go to to receive treatment

Do I have Dysautonomia / POTS?

How to Determine if You Have Dysautonomia / POTS


Dysautonomia refers to a group of conditions that affect the autonomic nervous system, which controls various bodily functions. One specific type of dysautonomia is Postural Orthostatic Tachycardia Syndrome (POTS). POTS is characterized by an abnormal increase in heart rate upon standing up, leading to symptoms such as dizziness, lightheadedness, and fainting. If you suspect you may have dysautonomia or POTS, here are some steps to help you determine if you have the condition:



1. Recognize the Symptoms


The first step is to familiarize yourself with the common symptoms associated with dysautonomia and POTS. These may include:



  • Orthostatic Intolerance: Feeling lightheaded, dizzy, or faint upon standing up

  • Tachycardia: Rapid heart rate, often exceeding 100 beats per minute

  • Exercise Intolerance: Inability to tolerate physical exertion, leading to fatigue and weakness

  • Brain Fog: Difficulty concentrating, memory problems, and cognitive impairment

  • Headaches: Frequent headaches or migraines

  • Gastrointestinal Issues: Nausea, bloating, constipation, or diarrhea

  • Temperature Regulation Problems: Sensitivity to heat or cold



2. Consult with a Healthcare Professional


If you experience several of these symptoms, it is important to consult with a healthcare professional, preferably one who specializes in autonomic disorders. They will evaluate your medical history, conduct a physical examination, and may order specific tests to determine the underlying cause of your symptoms.



3. Undergo Diagnostic Tests


There are several tests that can help diagnose dysautonomia or POTS:



  • Tilt Table Test: This test involves lying on a table that is then tilted to simulate standing up. It monitors your heart rate and blood pressure changes in different positions.

  • Autonomic Function Tests: These tests assess how your autonomic nervous system responds to various stimuli, such as changes in temperature or breathing patterns.

  • Electrocardiogram (ECG): An ECG records the electrical activity of your heart and can help identify any abnormalities.

  • Blood Tests: Blood tests may be conducted to rule out other potential causes of your symptoms.



4. Keep a Symptom Diary


Keeping a detailed diary of your symptoms can be helpful in identifying patterns or triggers. Note down the date, time, and severity of each symptom, as well as any activities or factors that may have preceded them. This information can assist your healthcare professional in making an accurate diagnosis.



5. Consider Lifestyle Changes


While awaiting a diagnosis or in conjunction with treatment, certain lifestyle modifications can help manage dysautonomia or POTS symptoms:



  • Hydration: Staying well-hydrated can help regulate blood volume and improve symptoms.

  • Diet: A balanced diet rich in nutrients can support overall health and potentially alleviate symptoms.

  • Exercise: Engaging in a tailored exercise program, under the guidance of a healthcare professional, can improve cardiovascular fitness and reduce symptoms.

  • Medications: In some cases, medications may be prescribed to manage specific symptoms or regulate heart rate.

  • Compression Garments: Wearing compression stockings or abdominal binders can help improve blood flow and reduce symptoms.

  • Stress Management: Learning stress-reduction techniques, such as deep breathing exercises or meditation, can help manage symptoms triggered by stress.



Remember, only a qualified healthcare professional can provide an accurate diagnosis of dysautonomia or POTS. It is essential to seek medical advice and follow their recommendations for proper evaluation and treatment.


Diseasemaps
7 answers
You should go to a cardiologist or a neurologist. They're your best bet to get a diagnosis of POTS/dysautonomia

Posted Aug 17, 2017 by Chelsea 2335
There's no true way of knowing without going to the doctors but if you think you have it and even the slightest way then you would know by symptoms like foggy brain, passing out unexpectedly after you stand sit or lay down, extreme fatigue.

Posted Aug 17, 2017 by Miranda 2150
The signs/symptoms I showed were feeling faint, dizziness, blood pooling in my hands and feet... among other signs.

Posted Sep 28, 2017 by Lbond94 4100
Translated from spanish Improve translation
Fainting, dizziness, constant fatigue, much sleep, no insomnia, constant anxiety, memory problem, stomach problems, feeling too cold or too hot, your thyroid studies comes out negative or not better with treatment. Tachycardia when standing,

Posted Jun 3, 2017 by Aurora Saez 3201
Translated from spanish Improve translation
If you have fainting or dizzy spells... if you increase while standing still, if it gives you tachycardia, if you feel you tides when you stand. I think you should go to a specialist in dysautonomia, but a cardiologist and I recommend support of a good psychiatrist if you are very symptomatic.

Posted Jul 7, 2017 by Ana 2050
Translated from spanish Improve translation
when you have a lot of tiredness or fainting spells frequent

Posted Sep 10, 2017 by Annie 2050

Do I have 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
Natural treatment of Dysautonomia / POTS

Is there any natural treatment for Dysautonomia / POTS?

6 answers
ICD9 and ICD10 codes of Dysautonomia / POTS

ICD10 code of Dysautonomia / POTS and ICD9 code

7 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.

Tell your story and help others

Tell my story

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...

Ask a question and get answers from other users.

Ask a question

Find your symptoms soulmates

From now on you can add your symptoms in diseasemaps and find your symptoms soulmates. Symptoms soulmates are people with similar symptoms to you.

Symptoms soulmates

Add your symptoms and discover your soulmates map

Soulmates map