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Anyone here familiar with dysautonomia?

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I know someone who has been diagnosed with this. If you have had any firsthand experience with dysautonomia (POTS, NCS, etc.) -- yourself or an immediate family member-- would you please tell me about your situation? I am trying to understand this condition and how it affects a person's quality of life.

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I started with dysautonomia a year ago April. It was debilitating for me. There are degrees of this and it can present in various ways so I'm not sure my experience is going to be helpful to understanding others but I'm happy to answer questions for you. Feel free to pm me.

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