I developed SVT during my second pregnancy, and I had no idea WHAT it was let alone HOW to treat it. I only knew of my family history, and at age 31, I became a regular visitor at the cardiologist. I had stress tests, leak tests, EKGs, MRIs, CAT scans, Ultrasounds, you name it, I did it. Unfortuantely, to date, there are no findings of any defects, so for now, I can do only what I can control. I wanted to know everything I could do to "control" my heart palpitations without going on a lifetime of medications. Therefore, I learned my personal triggers (caffeine, too much alcohol, eating too much, etc). After making some changes, my symptoms lessened. After my Dad's passing, I decided that I needed to do EVERYTHING I could do to be healthy. It has been a process, and it has taken me 4 years to get to where I am with my diet and exercise are today. As of today, I only have minor palpitations, if any at all, so I will continue to do my part.
I can't change the fact that it is hereditary, but I can change how I live each one of my days. If that means I can't eat some things or I have to exercise a little harder, then I will do my best. I mean, after all, that is what I can control, right?
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I love you Daddy....
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