Genetic Defects :: right know genetic information forthy seven year old mimi joling found forty eight sister diagnosed breast cancer decided get genetically tested wanted more risks options available help prevent herself getting ?i thought sure would negative positive mutation totally shocked started crying really emotional ? joling remembers finding diagnosis attended two hour essays research papers fc Genetic Defects

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The Right to Know Genetic Information

     After forthy-seven year old Mimi Joling found out her forty-eight year old sister was diagnosed with breast cancer, she decided to get genetically tested. Joling wanted to know more about her risks and the options available to help prevent herself from getting cancer. ?I thought for sure that I would be negative. But then, when I found out I tested positive for the gene mutation, I was totally shocked. I started crying, and it was really emotional,? Joling remembers. After finding out her diagnosis she attended a two hour long genetic counseling session where she learned what the BRCA 1 mutation was, the possible risks, and recommendations in preventing cancer. ?After I had a few days to absorb my results I realized this was a good thing for me to know. The counseling provided me with information on all the options available, and I decided my course of action was to have my ovaries removed,? said Joling (Women?s Health Weekly 27-29).
      As with almost any new technology, the Human Genome Project has provided society with benefits and problems from its findings. It has given people the opportunity to identify whether or not they are carriers of disease causing gene patterns, like Mimi did. This enables the possible prevention if the likelihood of a certain disease is known. On the other hand, this type of information frightens people because they do not know
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