5 doctors and 5 years later, my medical mystery solved: I have Postural Orthostatic Tachycardia Syndrome.

I remember so clearly the first moment it happened. I was so scared and didn't know anything when I came to and woke up from passing out. I was so scared not knowing what was going on with my body.

Suddenly, all the energy drained out of me, as if all the blood had fallen to my feet and now weighed the same as lead.

The crushing fatigue and shortness of breath seemed to confirm that indeed my body was staging a revolt. Enough was enough. It was giving me no choice but to lie down.

In that moment, I went from being a vibrant person to someone struggling to do even the basics of daily life.

But I had no idea at the time how those same debilitating symptoms would haunt me for years to come.

I was sent to Vanderbilt Autonomic Dysfunction Center by my cardiologist, Dr. Chase Reynolds from Pikeville, and they did all kinds of tests on me to diagnose me with POTS Syndrome.

I now have a port put in and I have infusions at PMC, I'm not working bc if this disability and fighting everyday to hopefully win my disability but right now I have nothing and it's a struggle so any donations would be greatly appreciated from the bottom of my heart ♥️

Any prayers would be greatly appreciated. I wanna thank you to all who can help. Like I said, any little bit would be greatly appreciated and I'll be grateful and thankful.