States Hand Over the DNA of Newborns to DHS
Published on 2008-03-19 00:00:00
No doubt we can all see the benefits in testing for genetic disorders or genetic traits and tendencies that could be more adequately dealt with, in some cases actually deterring the onset of life-time illness, but that seems not to be the real thrust of these programs. It may have been initially….but not now.
As with all good things, there are always those who seek the more evil path, in essence turning what should have been a life saving tool, a preventative measure into something insidious and inhumane. This is what has happened to this national effort.
Here in Minnesota the state tests for 56 various genetic disorders and variants. At least 1/3 of these tests produce a false positive meaning that a flaw was identified that actually did not exist. Regardless, that false positive becomes part of the permanent record of the child and follows them for the rest of their lives as does any true positives. This means that the child will eventually and most likely face discrimination in employment and the ability to gain health insurance at any cost.
There are other nagging problems with this system. Although the national website http://genes-r-us.uthscsa.edu/ insists that this harvesting of DNA is a highly visible program, my own polling of parents of newborns, or the grand parents had no idea that this was being done to their children and grand children. Further, not one knew that they had the right to demand the blood and tissue samples be destroyed after 45 days per written request. Even had they known, and the samples were destroyed (you would have no way of knowing if they really were) the information gleaned from them would still be available and on file…..in perpetuity.
Also unknown to at least the new parents in Minnesota, is that once that 45 days has lapsed, the state now claims that they “own” the DNA of that child. This claimed ownership now allows the state health agency to test, tamper, alter, sell, farm out, and utilize in any way they see fit, the DNA of your newborn. It can be manipulated, spliced with other DNA, and used in ways never intended under the screening program.
Now, there are forms that have to be signed that agree to this invasion of privacy, but the problem seems to be that this is not done during pre-natal care, but rather, at the time of delivery of the infant. These forms are produced when the mother is ready to deliver and is being admitted to the hospital. That’s when these “informed consent” forms are dragged out to be signed. This is no accident. Expectant parents simply sign what is put in front of them and are told they must sign to complete admission. Nice, huh? And none of them seems to be aware that what they are signing allows this right to have those additional blood and tissue samples destroyed. No matter, the damage is done and the results of those three extra blood drops are forever recorded and along with it, a lot of genetic information about the parents.
Although this is supposed to be an opt-in program, rather than an “opt-out”, Minnesota has decided to interpret the law differently. Our legislators have decided that opting out is the way it should be…..regardless of the law. With that in mind they have gone one step further and declared that if the parent doesn’t specifically opt out….they are presumed to have “informed consent” and have opted in.
I have to give the special interests in Minnesota their dues. Federal law and the courts have upheld the concept that human DNA cannot be patented. But these fine folks, representing insurance companies, medical institutions, and big pharma have found a way around that bothersome ruling. Using a compliant legislature they have made sure a system has been put in place that allows them to indirectly access what should be the most private of all information, the most identifiable information concerning an individual and in the case of medical and pharmaceuticals, to use it in any way they see fit once the state claims ownership.
In January 2007, a lady named Twila Brase president of the Citizens Council on Healthcare, issued a written testimony to the Minnesota legislature on the unethical and hidden uses of harvested DNA by the state. The 18 page document can be located at:
http://www.oah.state.mn.us/cases/health4615/nbs-pc8.pdf
It is an eloquent treatise on the misuse of the DNA testing and the right of parents to be fully informed of what is really afoot in these programs.
Currently, we have a monumental effort under way by Sue Jeffers to petition the state to;
Oppose illegal State government ownership of the blood, DNA and genetic test results of newborn citizens in Minnesota. http://www.cchconline.org/petition/babyDNA2007.php
In July 1997, solely by an executive decision of health officials-no law-the MN Department of Health began retaining the DNA-filled blood specimens of all newborn babies. The State now claims ownership rights to the DNA of more than 670,000 children (approx.70,000 births/yr).
In July 1986, MDH began cataloging the genetic test results of all Minnesota children. Approximately 1.4 million children are in the database. Oppose the dissemination of newborn blood and DNA to genetic researchers
Oppose the Minnesota Department of Health’s refusal to fully inform parents
Calls on Governor Tim Pawlenty to direct the Minnesota Department of Health (MDH) to comply with Minnesota state privacy law, to fully inform parents of the genetic testing process and their legal rights–and to dismantle MDH’s illegal warehouse of newborn citizen DNA. (Contact Sue Jeffers directly at: S1U2E3@aol.com)
I might suggest that each of you check the national website to determine how extensive the DNA testing is in your state, especially if you have children 10 years or younger. What you find may sicken you.
The idea of the state, any state, claiming ownership of the DNA of anyone, most especially newborn babies is so repugnant to me that I cannot find the words to express how offensive this is; what an unconscionable breach of humanity this comprises. This issue is not one of party affiliation or a right vs. left drama being played out. This is the groundwork for future discrimination that will most likely surpass employment and insurance targeting but eventually could be used to decide who lives or dies, or who can reproduce.
There is however a level of humor in all the debating going on……insurance company reps along with those of the business sector assured everyone that these genetic tests will never be used to discriminate in employment or insurance coverage. Now if that didn’t make you laugh, nothing will.
But, all of us need to ask ourselves why this information would be of any use to Homeland Security? What possible reason could they have for cataloging and storing the genetic code of any newborn child?
In the end I find myself wondering where all these big religious fomenters are that railed against gay marriage, stem cell research, the right to choose for women and a host of other issues that would supposedly destroy the traditional American family. Wouldn’t losing ownership of your child’s or your own DNA be far more devastating than these issues? And yet, not one rock star preacher has spoken one word that I can find condemning this practice. Not a peep! It’s probably just a case of a lost message in all the speaking God does to them when he puts a “word of knowledge in their hearts” about the woes of society.
My advice? Find out what is happening in your own state and to what extent your state is testing and participating in this program that is so loaded with secret agendas and obviously in opposition to many state and federal laws. Maybe what is needed is a class action lawsuit brought in each state by parents who were unaware that they or their children no longer own their own DNA.