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Published: December 13, 2007
Egg donation – my gift to the world
The perils of in-vitro fertilization
When a freshman at the University of California, San Diego, Alexandra Gammelgard said she saw a provocative advertisement in the student newspaper. "It was like 'Be an angel,'” she recalled to the Dec. 8 Los Angeles Times. "'Make money for college. A family is looking for a donor.'"
The advertisement was looking for young women to donate their eggs for in-vitro fertilization. Like many college students, Gammelgard was in need of money, and answered the ad. Through two or three agencies, she donated her eggs, getting from $5,000 to $15,000 for each donation.
What she did not know was that she was a carrier for Tay-Sachs, a neurological disease that kills its victims generally before the age of 5. She discovered the fact when a couple who had used Gammelgard’s donated eggs informed the agency she had used that their child had the disease. Gammelgard had not been tested for the disease; she was not among the population at greatest risk to be carriers.
At least four couples have used Gammelgard’s eggs, and her stored eggs may yet be used by other couples. In the U.S., there is no mechanism for informing recipients of donated eggs of congenital defects the donors might suffer from once they are discovered. Unlike with blood donations, there is no tracking system.
The couple with the Tay-Sachs child are two men, Bruce Steiger and Rick Karl of Southern California -- the latter, said the Times, “raised a conservative Catholic.” Working through Surrogate Alternatives in Chula Vista, Steiger and Karl found Gammelgard. “She was tall, athletic and blond,” said the Times. “She cited no serious family health problems. The couple picked her based mostly on a picture and questionnaire.” She had written on the questionnaire, "I feel like egg-donating is my gift to give to the world."
Karl and Steiger said Surrogate Alternatives assured them that egg donors went through a thorough health screening. Though 10% of their $250,000 in fees for the procedure went to Surrogate Alternatives, the agency did not spend the $100 to $250 it costs to screen for Tay-Sachs. Fertility doctors, however, say that to screen for every possible disorder is unnecessary and would make the process too expensive. In Gammelgard’s case, since she said she was pure Scandinavian, the fertility doctor did not see the need to test for Tay-Sachs.
Gammelgard, however, informed the Times that she had some “Irish French Catholic” lineage, and French Canadians are among the groups most susceptible to Tay-Sachs. Her eggs were mixed with Karl and Steiger’s sperm. Karl, as it turned out, was also a Tay-Sachs carrier. The resulting child, Krystie, now two, has full-blown Tay-Sachs.
According to the Times, neither Gammelgard nor the agencies that arranged the donations have attempted to contact other couples who used Gammelgard’s eggs about her being a Tay-Sachs carrier. Vicken Sahakian, the Los Angeles area doctor who performed the procedure for Karl and Steiger, told the Times, "I can't go out and tell every agency in the country to watch out for this donor. I would be totally breaking the law because I would be revealing her [Gammelgard's] private information.”
Gammelgard said she has not contacted other agencies she’s worked with -- she said she cannot remember their names. "I kind of washed my hands of it," she told the Times, "and walked away."
Posted Thursday, December 13, 2007 7:07 AM By Jack Clough
"Oh, what a tangled web we weave..." No, you don't have to do it God's way but you still reap what you sow and pay the price. Imagine all the unnecessary pain and hurt coming down the road - all because of greed, selfishness and pride. Yeah, "be an angel", an "angel of death". (jackclough.com)
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Posted Thursday, December 13, 2007 2:05 PM By Michelle K. Gross
There is no law compelling fertile couples to be tested for Tay-Sachs. Nevertheles, many people--including single people of child-bearing age--ask for screening for genetic diseases. UCSD itself has had college-age screenings in the past to let individuals know that they are carriers.
Here is the web-site for UCSD's genetic screening program, which includes Tay-Sachs, as well as screening specifically for disorders carried in the Ashkenazi (European Jewish) profile.
health.ucsd.edu/specialties/medgenet/molecgenet.htm
(Posted with permission, contact information verified 12/13/07.)
It's possible that the two carriers mentioned in this article did not have the mental model to view themselves as a couple about to have a child or as individuals who might one day conceive a child with someone who might have a similar genetic profile to themselves.
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Posted Thursday, December 13, 2007 2:49 PM By The original Frank
The "fathers" needed to fulfill a desire for their genetically "own" offspring. The "mother" needed the money. The surrogate needed the money. The doctor needed to keep his license. The agency needed to make a pile of money. Everybody tried to get their needs met, but for the child. You wouldn't have to be a Believer to see this is all wrong.
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Posted Saturday, December 15, 2007 6:59 AM By JPeterman
"What a tangled web we weave"..great way to put it Jack, Whether it's the abortion doctor with the "rewarding career in abortion" or this sad, pathetic story it's all too apparent what happens when science goes outside the law of God. These classified ads for student donors are searching ONLY for tall, athletic, blond hair, blue eyed females. I know only from my experience in this country but I imagine that the student newspapers in Scandinavian countries are filled with thee ads. All others need not apply. So, in their demonic quest for a "beautiful" offspring, this homosexual couple wound up with a child with Tay Sachs disease. Will they now be taking the child back to the donation clinic to ask for a refund? The mother certainly doesn't sound like an innocent babe in the woods. She's sold at least 4 eggs for $15k each? It's a sick world, pray the Rosary daily.
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Posted Saturday, December 15, 2007 3:58 PM By Bryan
I happen to know this wonderful family and have never met two parents more dedicated to their daughter. No, they are not looking for a refund, but instead have quit their jobs, moved to another state where she can get the best possible medical care and put their lives on hold to try and save their daughter's life and in the process formed a foundation to save the lives of other children stricken with this and other
similar terrible diseases. These parents are using this unfortunate incident to make very positive changes in the world. As a California catholic, I find it sickening that adults can actually make negative comments about a family who is devasted and dealing with a terminally ill child, I hope that is not the nature of a true Catholic. If you knew this family, you would know that this beautiful child is truly a gift from God who without speaking a word, has the ability to change all the lives she touches.
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Posted Saturday, December 15, 2007 11:32 PM By The original Frank
Bryan: Thanks for sharing a more complete story about the effect Krystie's life has on her parents. As commendable as their actions since her birth are, it seems that before the conception, their determination to have their genetically "own" offspring lead to her disease. Perhaps adoption was not an option for them? Let's ask ourselves why two men who are so dedicated to their child's welfare either weren't offered or didn't accept that option. Steiger and Karl are by no means alone in the world of anonymous genetic donations, but Krystie's example shows how serious the unforeseeable consequences can be. There's no way filling out forms at a donor agency can substitute for the time a pair of married biological parents spends together before conceiving a child. And even then, things can go tragically wrong.
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Posted Thursday, January 10, 2008 11:45 AM By Nick
This, of course, shows how complicated this all can really be. Today we are running a in-depth issue-of-the-day that really gets into issues like this of egg donating and surrogacy.
http://theissue.com/issue/8463.html is the link to todays issue.
Hope it is helpful, Cheers. Nick
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Posted Wednesday, December 31, 2008 3:39 PM By Kore
The Original Frank: In-virto fertilization didn't cause this girl's disease. A certain gene does. You're implying that Tay Sachs was the punishment that this family received for doing something that you think is wrong. Many people have been born with Tay Sachs, and they didn't do anything specifically that "lead" to the disease. Tay Sachs happens to the good and the bad. It's not a result of IVF.
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