When I was younger, I did not know that I had the disease. I was like every other boy, as seen by the outside, who played sports and did many other activities with my friends. Over time, with a set of many different tests, it was found that I have the disease. Afterward, my life changed from one of joy to one of grief and agony. Afterward, I was unable to continue to play the physical sports, and many of the things that I had gotten used to doing.
Why I say this is because it is a major part of my life. This disease has taken a lot from me and my family, but along with what it has taken, it has given back. It's darkest before it becomes light. With this disease, I have learned what I can do and what I can't. One wrong step, and I could go into Atypical Tachycardia. This has lead me to live my life day by day, and see what I am looking at through a different set of eyes.
For anybody who has had a major risk of dying, you will know what I am talking about. Everyone has hard times, and everyone has good times. It is what you choose to do with the times in between that makes who you are. I live my life day by day, never knowing what the next moment has in store.
That is horrible if I was told that I could not exercise vigorously I would go insane, because there goes rock climbing, running, hockey and all my other favorite sports. Is it an enlargement in both ventricles or is it just one side?
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