I Blame POTs

As time goes on the more I notice weird symptoms. I am thinking some may be side effects from all the prescriptions I am taking. For example, I will get these patches of pin and needle pain in random spots on my body that will last awhile. The last one I had was on my right shoulder and it was awful. It is difficult to get things done when you are in constant pain. That pain in my shoulder lasted for about a month. Then in a few more months, I will probably have another patch but it will probably be somewhere else.

I will also get some numbness and tingling all over sometimes. Which then leads to some weakness in my body and then that leads to pain. And all of this just seems like it would be something neurological. I saw a neuro doc over a year ago and he told me to try to work on "getting better" and see if the other symptoms would get better. I didn't completely understand that. But I things got worse and I made an appointment with him a few weeks ago. He wanted to do some more tests, I got an EMG and a few MRIs of my spine and brain. And nothing. 

I feel relief and confusion. 

What the hell is going on with me?

I blame POTs. That is ultimately my conclusion. POTs is still so misunderstood and we don't know everything there is to know about POTs. If it isn't that then it is probably the meds. Which I have to take because of POTs. So, I went through so much testing for no answers.