14 Sep 2012

Share Your Story: Sally M.

Sally, Montana

Shortness of breath, insomnia, and headaches. At 34 years old I wasn't sure what was going on, but it continued to get worse. When I was finally diagnosed with pulmonary arterial hypertension, the cardiologists confirmed that I have congenital heart disease with a hole in my heart the size of a peach pit that I have had since birth. I was an athlete in school; yet the doctors told me that I was the type of kid that should have died on the basketball court. I have been on oxygen 24 hours a day, 7 days a week for two years now but physicians are still not sure what can be done to fix my heart. I've had several cardiac catheterization and echocardiograms but we still don't have the answers. You can understand why heart research is so important not only to me, but to many others. I have great support from my family and friends, but a day doesn't go by, that I'm not concerned about my future.

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For good and valuable consideration, the receipt of which is hereby acknowledged, I hereby grant to the American Heart Association (“AHA”) and its successors and anyone authorized by it the following unrestricted rights and release, all of which may be exercised without geographical, time or other limitation: In regards to the submission of stories, video or digital recordings, whether of an audio or visual nature, and photographs (collectively “Submitted Material”) for use by the AHA, I hereby release the AHA from all liability, and make the following grants and representations in connection therewith:

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