Hello everyone!
Tonight I will be participating on a talk show on ESPN2. The topic of our talk is the use of "genetic testing" in athletes. While we all know this is a very personal matter it has been subjected to mass misinfomation in the media and it is my hopes that tonight we will be able to clear some of this up.
In short this is what I am planning on talking about:
1. We should all call our congress person and demand passage of HR 1227 the Genetic nondiscrimination act - currently pending in Congress and has already passed though the Senate.
2. I hope to clearly explain the differences between genetic "screening" and the use of genetic testing in someone with suspected disease.
3. I will be explaining that this information should be kept private and not appear in the newspapers without the consent of the patient.
4. The athlete has every right to decline testing.
5. Teams have the right to use all cliniclly available tools to ensure the players health. Players must agree to all testing or the test can not be done.
6. If the NBA or other team wanted to screen all player to see if they carried a known gene for HCM - The HCMA would strongly oppose such actions. Presents of a gene mutation does not mean you have clinical HCM, thus should not be used to evaluate the health of the player.
I will post later and let you know how it all goes!
Take care,
Lisa
Tonight I will be participating on a talk show on ESPN2. The topic of our talk is the use of "genetic testing" in athletes. While we all know this is a very personal matter it has been subjected to mass misinfomation in the media and it is my hopes that tonight we will be able to clear some of this up.
In short this is what I am planning on talking about:
1. We should all call our congress person and demand passage of HR 1227 the Genetic nondiscrimination act - currently pending in Congress and has already passed though the Senate.
2. I hope to clearly explain the differences between genetic "screening" and the use of genetic testing in someone with suspected disease.
3. I will be explaining that this information should be kept private and not appear in the newspapers without the consent of the patient.
4. The athlete has every right to decline testing.
5. Teams have the right to use all cliniclly available tools to ensure the players health. Players must agree to all testing or the test can not be done.
6. If the NBA or other team wanted to screen all player to see if they carried a known gene for HCM - The HCMA would strongly oppose such actions. Presents of a gene mutation does not mean you have clinical HCM, thus should not be used to evaluate the health of the player.
I will post later and let you know how it all goes!
Take care,
Lisa
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