I have recovered from POTS and would like to connect with researchers to help others. Please help

I'm not a researcher but I think I might have pots. Any help is welcome.

I will share my story with you.  I began having  strange symptoms after some type of illness. I first began feeling dizzy, short of breath and fatigued. As months went by, I developed heart palpitations, tachycardia while in an upright position, more shortness of breath, orthostatic hypotension, severe dizziness, along with multiple GI symptoms.  Mild exercise, length strengthening, a change of diet, and dietary supplements helped me to recover. It felt like my immune system was on steroids, things that I had never had a reaction to, all the sudden I had sensitivities to, and etc. I pretty much replaced dairy with almond/soy, did not consume any foods that contained MSG, due to triggering headaches, and ate more fresh fruits and vegetables, along with increasing my water intake. My immune and nervous system were in overdrive, so I reduced stimulus, like loud music, large crowds, and made sure I received plenty of adequate sleep. My exercise routine was walking shirt distances, and after a few months I was able to ride my bike a short distance which helped with my legs and reduced my POTS symptoms. I also saw a cardiologist to keep a check on my blood pressure and heart rate. Hope this helps. It gets better with time. Individuals recover differently.