practice and tried to run through it. Once me and my family realized that this wasnt any easy fix
we decided to call the doctors.
Over the course of the next few weeks, I had several doctors appointments.They did an
ultrasound of my heart, just to make sure nothing was structurally wrong with it. Next they did a
stress test. I lasted 8 minutes. I didnt even get to the running part of the test yet. They called for
one more test, a tilt table test. With this, you're strapped to a table with iv fluids in your arm, just
incase you pass out. You start out lying down and then they bring you up to an upright position.
They do this to see your heart rate or something, Im not really sure. I never passed out but, I
failed the test. Because of me failing, they were able to figure out whats wrong with me. The
doctors told me and my family that I had Postural Orthostatic Tachycardia Syndrome or POTS
for short. The doctors used really big words when they explained it but basically, my heart and
brain dont talk. Weve never heard of this before and now I have it. To treat it you take
Fludrocortisone. Im not really sure what this does but, it helps me. Within a few days, I was
back to normal. I returned to soccer and I went 5 months healthy. Everything went fine until
September 20th.
September 20th was a Sunday night. I was playing a soccer game. I played the whole first half
and everything was going well. Then with about 10 minutes left in the game, it hit me. A rush of
dizziness came over me. I tried to stand still but it wouldnt pass. I raised my hand for my coach
to take me out but, he wouldnt do it. He said that I had to stay in the game. So what did I do? I
just sat down. If he wasnt going to listen to me, then I would make him listen. Hes lucky a
teammate of mine saw me sitting down and kicked the ball out otherwise, they might have
scored. When I went over to the bench, I told him what was wrong. Needless to say, he wasnt
happy about it. I knew right there that I had a relapse.
That week I didnt go to school at all. We went to our primary care doctor and she said that she
didnt know what was happening. The next week is when things started to get really bad. I
started to get really bad headaches. They were so bad in fact that we had to go to the
emergency room. There we learned that I had high blood pressure. So when you have high
blood pressure in the emergency room, they keep the blood pressure cuff on your arm and
every 10 to 15 minutes, it takes your blood pressure. And when it's high, it does a horrible
beeping sound. So, it beeped the whole time. I went to the emergency room 3 more times
before we saw a neurologist.
I thought the neurologist would be just me talking to them about what's happening and then get
some medications. I was 50% right. After we talked for a while and they told me all the new
medications that I was going to be on, they told me that I was going to get nerve blockers. Little
did I know, it was 4 needles shoved into certain trigger points on my head. They didnt hurt to
me but, Ive learned that I have a high pain tolerance. Within a month or so with the nerve
blockers and all the new medications, I was back to school. On December 1st, I went back to
school.
I made it through the whole month of December with no issues. I even went to Mexico without
one issue. Shocker, I had another relapse. This time it was January 4th. I again, went to the
neurologists and got nerve injections. This time I got 14. Ya, that was fun. Those didnt work this
time around. Since that didnt work, they went bigger. I now got to get drugs pumped into me.
Its called a DHE infusion. You get 4 different types of drugs pumped into you to try and help get
rid of your headache. Zofran, compazine, benadryl, and DHE. I did this for 2 days until
something bad happened to me. Tuesday night I had an allergic reaction to the drug compazine.
I dont know how to describe but it looked like a cerebral palsy. I had this for about 3 hours. This
put so much stress on my body that the DHE didnt work. We then found out that my body
doesnt like that many medications in it at once so I can only talk one at a time and that's my
POTS medicine. So now I have to try alternative methods. Im now doing acupuncture every
week for six weeks and massages.
Ive been doing this for 3 weeks now. I go to school part time. But if Im being honest, it doesn't
seem to be helping all that much. So I basically just do what Im told and hope for the best.