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Severance Magazine
Tag:

donor conceived

    ArticlesDonor ConceptionNPEs/MPEs

    Q&A with Daniel Groll

    by bkjax April 11, 2022

    Conceiving People: Genetic Knowledge and the Ethics of Sperm and Egg Donation, by Daniel Groll, is a fascinating exploration of attitudes about whether donor offspring are entitled to knowledge of their donors, but the issues and questions it raises are pertinent to adoptees and NPEs/MPEs as well. Comprehensive and academic in approach, it may be challenging to readers not well-versed in philosophical discourse, but it’s key reading for anyone with a stake in the debate over access to genetic knowledge. And although Groll ultimately stands against anonymity in donor conception, some NPEs and MPEs may take exception to some of the arguments that led him there. Therefore, we asked him to address some of those arguments, and he readily agreed.

    Severance was the target of a critical article last year in a publication called Real Life that accused it of numerous transgressions, including promoting bionormativity. It insisted that the magazine’s content poses genetic family as measured by DNA as “the norm against which all forms of family should be judged.” It further states that if we view the genetic family as something from which one can be severed, non-genetic family “will inevitably be understood as secondary, extraneous, and even pathological.” Additionally, it charges that those of us looking for genetic information are indicating that “biogenetic kinship is the most true, essential, and valid form of family” and that such a belief places queer families in “legally precarious positions but undermines the larger value of ‘love makes a family’ for all families.” The argument rejects the idea that there can be a desire to know one’s genetic history that is apolitical. Clearly, I don’t believe Severance makes any such assertions, and based on having heard hundreds of stories and experiences, it’s obvious that most of us grew up with non-genetic families. I, for example, was raised by a man who was not my father. He was my family. I didn’t wish to have another father, but I did wish to know who my biological father was. I didn’t imagine my biological family would be a better family, or a more real family. I simply wished, as I believe most people who lack this information do, to know from whom I got my genes. My question is, how does simply wanting that information valorize traditional families or diminish nontraditional families?

    Before I answer this, I just want to explain my connection to the issue of donor conception since people inevitably wonder about it. I am a known donor to close friends who have two children. The children know both who and what I am in relation to them. Our families are in regular contact. From the get-go, everyone agreed there would be no secrets and that we all need to be open to how their children understand their experience and let that guide us. Maybe the fact that I’m a donor will cause some of your readers to stop reading, but I hope not.

    On to your question! One thing I want to make clear is that I think people who create children with donated gametes should not use an anonymous donor. So I am totally with you: I don’t think that wanting genetic knowledge—as I call it—necessarily or always or even usually valorizes traditional families or diminishes nontraditional families. One thing I try to do in my book is to make exactly this case. There are really good reasons for taking people’s desire for genetic knowledge seriously without committing ourselves to the view (which I don’t subscribe to) that biological parents are normally the best parents or that the traditional family form—of a man and woman and children that are genetically related to both parents—is somehow the best kind of family.

    Having said that, I think it’s worth taking seriously the idea that an interest in genetic knowledge is not apolitical, if that means that it floats free from, or exists independently of, the contingent cultural norms, practices. and institutions that shape our desires. I want to be really clear: this isn’t a point about the desire for genetic knowledge in particular. Rather, I don’t think we should see any desire as obviously apolitical. Even what we might think of as our most basic desires—for sustenance or for social connection—take the particular forms they do as a result of the culture they are embedded in. We might put it this way: all of our desires are filtered through, or suffused with, the culture (the norms, the values, the practices) they are located in.

    As a result, I think it is always worthwhile to ask two questions about our wants, desires. and interests: 1. “In what ways have they been shaped by our cultural milieu?” and 2. “Is that shaping a good or a bad thing?” In the book, I talk about certain gendered desires – like, for example, a boy’s desire to not cry in front of his friends—as examples of desires that are a) clearly shaped by our cultural milieu and b) a bad thing.

    Now, I don’t think the desire for genetic knowledge is like that. I’ve already said that I think we should take people’s desire for genetic knowledge seriously and that doing so leads to the conclusion that people shouldn’t use anonymous donors. But I think it’s undeniable that we live in a culture that highly valorizes genetic connectedness and often tells simplistic, reductive stories about family resemblance, genetic ties, the significance of “blood” etc. I think it’s worthwhile for everyone—not just donor conceived people or others who lack genetic knowledge—to interrogate their commitments about the significance of genetic ties in light of the culture we’re in. We should all ask, “Why do I, or do people in general, care about this so much?” and “Is it a good thing or a bad thing?” I try to give an account in the book about why many people care about genetic knowledge in a way that shows how it can be a source of meaning. But I also try to show that, oftentimes, people’s reasons for being attached to genetic knowledge are shaped by forces that do unjustifiably valorize the biogenetic conception of the family.

    Why can’t I uphold the rights of people who wish to create nontraditional families and still want my genetic information? Why is it an either/or? Why is it not acceptable to honor and uphold nontraditional families and at the same time say that genetic knowledge also matters?

    I think it is acceptable! Indeed, that’s the position I try to carve out in the book: we shouldn’t see the interest in genetic knowledge as ineluctably bound up with biogenetic normativity. One can do exactly what you say: honor and uphold nontraditional families and at the same time say that genetic knowledge matters.

    A problem emerges, however, when people put an emphasis on the significance of genetic knowledge—and genetic ties— that automatically downgrades the status of non-traditional families to “second best.” I’ve seen this attitude on display in a number of contexts. Sometimes the idea is that someone who isn’t raised by their genetic parents is (usually, though not always) worse off for it. Sometimes the idea is that a life without genetic knowledge is necessarily and seriously deficient. Sometimes the idea is that contributing gametes for the purposes of procreation without the intention of raising the resulting child is, by itself, morally unacceptable (equivalent, perhaps, to abandoning one’s child). I take all of those ideas to downgrade—if not outright reject—non-traditional family forms. So to the extent people’s attachment to genetic knowledge goes through those ideas, then I think there is a tension between caring about genetic knowledge and honoring non-traditional family forms. But again, I have no objections whatsoever to your way of thinking about things.

    It seems that the objection to wanting genetic knowledge asserted by some individuals creating nontraditional families has to do with the fear that their children will be somehow less connected or see their parents as somehow less than traditional parents when I believe there’s no research or even anecdotal experience to suggest that is true. Is that right?

    I think you’re right. Certainly, parents who do not want their donor conceived children to know that they are donor conceived sometimes cite as the reason that they’re worried the child will be less connected to their non-genetic parent. One thing seems clear: when people find out later in life they are donor conceived, that very often does cause a rupture. But the issue there seems to be mostly about secrecy and deception, and not about the fact of genetic non-relatedness itself. As far as I know, there is no evidence that people who are donor conceived and have never been led to believe otherwise are generally less connected to their non-genetic parent. Part of the issue here, though, is that we would need a better of understanding of what “less connected” even means. One thing I would definitely want to reject is that “being connected” is a zero-sum game so that if a donor conceived person forms a connection to their donor they are thereby less connected to their social parents.

    It’s important to note here that it’s only some families that can realistically keep their donor conceived child in the dark, namely heteronormative families that can “pass” as “traditional” families (i.e. families where children are genetically related to both parents). I think doing so is, generally speaking, deceptive and wrong. I think oftentimes a parent’s worry that their child will not connect to them in the same way if they (the child) know they are donor conceived reflects the parent’s own preconceptions about the significance of genetic ties as well as, sometimes, shame about not being able to conceive (particularly for men).

    At some point in Conceiving People you say that people can be influenced or educated to believe that genetic history is not as significant as some would have us believe. There seems to be no evidence to assert that genetic information is unimportant. On what basis can that claim be made?

    This is a great question. One thing to say up front: clearly genetic information can be super important for medical reasons. I do not want to deny that! Nor do I want to suggest that we should try to “educate” people to believe otherwise. But the medical reasons for wanting genetic knowledge are not—for many donor conceived people—the whole story: if it were possible to get the relevant medical information without knowing who your genetic parents are, many donor conceived people would still want to know who their genetic parents are. So, when I suggest that maybe we can move people toward caring less about genetic knowledge, I don’t mean that people should care less about the medical reasons for wanting genetic knowledge. I mean, rather, that perhaps people can be moved to care less about genetic knowledge for the reasons that go beyond the medical reasons.

    What do I mean when I say that perhaps people can be “moved” in this way? To answer this question, let me lay out one key idea I argue for: while genetic knowledge can provide a rich source of meaning in answering the question “Who am I?”, I don’t think it is either the only source or a necessary source. I think there are ways of telling a rich and truly complete story about who you are as a person that doesn’t put a lot of emphasis on genetic lineage. Now combine that thought with one I discussed above, namely that we live in a society that puts a lot of emphasis (in my view, undue emphasis) on the significance of genetic ties. These two thoughts together suggest one way that we might move people—everyone!—to care less about genetic knowledge, namely by working to make society less bionormative overall, where that means we try to change our cultural schema so that lacking genetic knowledge isn’t necessarily seen as having this massive void in one’s life. That’s a tall order (as are all calls to effect change at a societal level). I don’t have anything particularly insightful to say about how to go about doing that.

    At the individual level, one thing I say in the book is that people have a choice about how to construct their identities, about what parts of their life to treat as important and which to treat as comparatively unimportant. In retrospect, I would have not put things in terms of “choice” because I don’t think it’s really possible to just make up your mind to either care or not care about something. What I was trying to convey is that I don’t think there is a fact of the matter about who we, as individuals, are. There’s not a single answer to the question “Who am I?” out there, waiting to be discovered. Rather, there are many different rich, full answers to that question and not all of the answers require having genetic knowledge. So, it’s not about “educating” people, but rather creating a culture, a climate, where there is less pressure—from all avenues of life —to pursue what I call the “genetic route” to answering the question, “Who am I?”

    Crucially, I think one of the ironies here is that insisting that genetic knowledge doesn’t matter at all or withholding information from people is not the way to create that climate. Quite the opposite: I think practices of secrecy and anonymity function to heighten the perceived significance of genetic ties. I think honesty and an openness to what the philosopher Alice MacLachlan calls the “abundant family”—a notion of family that extends beyond the typical notion parents and children—are more likely, over time, to put genetic knowledge in its proper place as a source of identity determination, but not an absolutely necessary source.

    What about truth? How can wanting to know truth be dismissed as somehow unethical or immoral? How can truth be immoral? Couldn’t it reasonably be argued that trying to deprive someone of their birthright—of information most other humans have—is deceptive and unethical or immoral?

    Let me tackle the second question first! I think it is indeed deceptive and, generally speaking, unethical to not tell a donor conceived person that they are donor conceived. What about not giving people access to genetic knowledge by, for example, using an anonymous donor? The central argument of the book is that that too is, in general, unethical (I wouldn’t call it deceptive, though, unless it’s paired with non-disclosure).

    I’ve almost answered your second question, but not quite, because you put things in terms of people having a “birthright” to genetic knowledge and I didn’t use that term in my answer. I don’t use the language of “birthright” for two reasons. First, just as a philosophical matter, I’m not entirely sure what I think about natural rights in general, so my thinking just doesn’t tend to run in the direction of explanations that appeal to natural rights. But even if it did, I think it’s well worth asking what makes something a right in the first place. In other words, I’m not satisfied with saying, “Well, it is my right to have this information and there’s nothing more to be said.” I think rights call for explanations, so even if I did want to put things in terms of rights, I would still want to go on to do all the stuff I do to explain what gives rise to the right.

    Your first question—about whether truth, or wanting the truth, can ever be immoral—is super interesting. I don’t think truth, as such, is either moral or immoral. It’s just the truth! Facts are neither moral nor immoral. But I think that wanting the truth can be immoral. Suppose I want to know some embarrassing fact about you so that I can blackmail you. My wanting the truth, in that case, would be immoral.

    Now, wanting genetic knowledge is not at all like that. I’m just giving a case where it seems pretty clear that wanting the truth can be immoral. My point is just that if someone wants to defend the right to genetic knowledge, it’s probably not best to make that case by claiming that it is never wrong to want the truth. We need to know why people want the truth…and that returns us to some of what we discussed about interrogating the source of the desire for genetic knowledge.

    Who benefits and how do they benefit by wanting to discourage the gaining of this information?

    This is a great question, and it’s not one I take up in the book, at least not in detail. I think there are four broad communities that benefit from practices of anonymity. The first community is heteronormative parents who want to pass as a “traditional” family and don’t want anyone—least of all their child—to know that they have a donor conceived child. I think this interest is often born out of a sense of shame about being unable to conceive, combined with the kinds of worries you mentioned above (e.g. that a child who knows they are not genetically related to one of their parents will, as a result, love them less).

    The second community is non-heteronormative families—gay and lesbian couples for example—whose status as parents has been, and to some extent still is, legally and socially tenuous. Living with the prospect that the donor might swoop in and claim parental rights—and that the law might side with the donor —is profoundly unsettling. A friend of mine describes it as living with a feeling of “terror,” and recent developments in the legal landscape in the United States—like the recently “Don’t Say Gay” law passed in Florida, the legal attacks across the country on reproductive rights, and the legal attacks in some states on trans people—show that that feeling is not remotely unfounded. I think those of us that have not lived with the prospect of having your family torn asunder—or your whole identity targeted—by the law can have trouble understanding the force of this concern. It’s understandable—to put it mildly—why, in that context, people might care that the donor is anonymous.

    The third community, of course, is the fertility industry which has a massive interest in ensuring a supply of donors and avoiding limits on how many offspring can be conceived with the gametes of one donor.

    The fourth are prospective donors who donate to make money and also to help people who cannot conceive, but do not want any involvement at all with their genetic offspring.

    How much should we care about these interests? Let me start with the fertility industry. I am not an expert on the fertility industry (and, I’ll add, I have absolutely nothing to do with it), but I have little-to-no sympathy with their set of concerns. The same goes for prospective donors who want to be anonymous—I argue in the book if you’re going to donate, you shouldn’t be an anonymous donor. I can understand, of course, why a donor would want to be anonymous. But I argue that those interests really don’t count for much at all.

    I am, however, sensitive to the interests and concerns of the first two groups I mentioned. Crucially, I don’t think such concerns win the day. In the book, I consider why prospective parents may prefer to use an anonymous donor and—while I understand where those preferences come from—I find them wanting when compared to a donor conceived person’s interest in having genetic knowledge.

    I’ll also add that I think I think the best way to address the legitimate concerns of the first two communities is not by upholding practices of anonymity—which, as we all know, are increasingly impossible to uphold in the world of 23andMe etc.—but rather to transform the cultural norms and beliefs about the nature of families so that, for example, infertility is not a source of shame, the bionormative family is not seen as the “gold standard” (to borrow a phrase from Charlotte Witt) of family forms, and the law provides protections for non-traditional family forms.

    You stop short in your book of weighing in on the right to know. Could you look at this and comment not as a philosopher but as a person with curiosity. Reverence for ancestors has been communicated since the beginning of time. Genealogy is the world’s leading hobby. People have always and will continue to want to know where they come from. If the vast majority of people in the world, now and apparently in all time and all cultures, were able to know who their parents are and that knowledge mattered to them, is it reasonable to think it isn’t a problem for those of us who are deprived of that information? Perhaps reduce it to an absurd point. Say, bread isn’t necessary for life, but if 95% of the people in the world want bread and are allowed to have it and you can’t have bread, wouldn’t you be upset, and might you not wonder why you are not entitled to have bread, even if it weren’t vital to your life? Why are all the philosophical arguments you construct necessary if, as the studies you cite suggest, the majority of donor conceived people feel that genetic information matters? Why is their lived experience not enough to demonstrate that, for whatever reason, they feel impoverished by not having the same genetic information others have?

    I want to reject the dichotomy between looking at things as a philosopher and looking at them as a person with curiosity! For me, philosophy is all about being curious and trying to get to the heart of things. To be sure, I don’t think it is the only or the best way to be curious or to get at the heart of things: music, poetry, art, fiction, creative non-fiction, not to mention all the other academic fields of study, are also conduits for curiosity and thinking things through. Philosophy is just one way. But it’s a way that speaks to me. There’s not “Philosophy me” and “Here’s what I really think me.” It’s all just me!

    So, when I consider your fantastic questions as a person with curiosity, I unavoidably take up a philosophical perspective. And when I do, it seems to me that it’s not enough to note that lots of people want something in order to conclude that they should have it or are entitled to it. Now: it’s definitely relevant. Indeed, my whole argument against anonymity is centered on the fact that the majority of donor conceived people want genetic knowledge. But—at the risk of sounding like a broken record—I think all desires, all wants, are candidates for critical scrutiny. We should scrutinize the forces that generate the wants, desires, interests, and aims that people have. Sometimes we’ll see that the forces are benign or even positive. Other times we’ll discover that they’re not positive. And still other times, we’ll discover that it’s a mix.

    The point is just that we shouldn’t treat people’s desires, interests, or aims as beyond scrutiny and as the thing that settles the matter of what people should have or be entitled to. We need an account of what is behind the interests, desires, etc. I try to provide such an account when it comes to the desire for genetic knowledge—among the population at large, not just among donor conceived people. And I try to show that even if certain problematic cultural forces are in play, the desire for genetic knowledge is nonetheless worthwhile and should be respected. Anyway: that’s why I spill so much ink on this topic.

    Daniel Groll is an associate professor in the philosophy Department at Carleton College in Northfield, MN and an affiliate faculty member at the Center for Bioethics at the University of Minnesota. He writes on a variety of issues in ethics and is currently spending time thinking about the nature and significance of family resemblance. When he’s not doing philosophy, he’s probably making music for kids with Louis & Dan and the Invisible Band. Get a 30% discount on Conceiving People with the code AAFLYG. Find him on Twitter @dang_pigeon.

    April 11, 2022 0 comments
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  • ArticlesDonor Conception

    Q&A With Peter Boni

    by bkjax March 28, 2022
    March 28, 2022

    In 1995, when Peter J. Boni’s mother experienced a stroke after open heart surgery, the walls she’d built to hold back a secret for nearly half a century crumbled. In rehab, she began to tell visitors what she never told him—that his father wasn’t his father, that he’d been donor conceived. And so began a quest to learn the truth of his origins and the nature of the societal forces that led to the circumstances of his birth—the subject of his new book, Uprooted: Family Trauma, Unknown Origins and the Secretive History of Artificial Insemination. Roughly halfway through his narrative Boni says, “Never doubt my resolve.” But his dogged determination is evident from the first page. Early on, it’s clear that after serving as a US Army Special Operations Team Leader in Vietnam, he was the go-to guy in his business sphere, where he was a successful high-tech CEO/entrepreneur/venture capitalist and more—and he tore into his personal mystery with the same can-do attitude—a tenacity that fueled him through the 22 years it took to solve the puzzle of his parentage. Uprooted is comprised of four parts that add up to exceptional storytelling. It’s compelling memoir of a troubled childhood with an unwell father, a determination to succeed, and the challenges of grappling with the emotional fallout of his family’s secrets. It’s also an exhaustive and insightful account of the history of assisted reproductive technology; a cogent indictment of the flaws of the largely unregulated, multi-billion-dollar industry; and a rallying cry for advocacy with a prescription for change. Boni’s scope is ambitious and he succeeds on every level. Donor conceived people will see themselves reflected in his moving testimony about the consequences and repercussions of the inconvenient truth of donor conception. Many will feel seen and heard as he describes genealogical bewilderment and the roiling emotions aroused by the revelation of family secrets, the shattering of comfortable notions of identity, and the lack of knowledge about his genetic information. It’s a must-read not only for donor conceived people but also for donors and recipient parents as well as fertility practitioners, lawmakers, behavioral health providers, and anyone contemplating creating a family through assisted reproduction. While the actors in a deeply flawed industry who are motivated solely by profit aren’t likely to be swayed by Boni’s arguments or embrace his suggested reforms, Uprooted may fuel a wildfire of advocacy that has the potential to give rise to meaningful legislation, transparency and accountability, and a true cultural shift.

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  • ArticlesDonor Conception

    When the Truth Finally Comes Out

    by bkjax October 22, 2021
    October 22, 2021

    As a professional coach* working with donor conceived adults, parents, and donors, I’ve observed a common issue among many donor conceived clients seeking support: feelings of anger or disappointment that their parents kept the truth of their conception secret from them for so many years. Because there may be disruption in the relationship between these adults and their parents, one or both parties seek coaching to help them work out their differences and adjust to the newly challenging reality. My donor conceived clients of all ages typically discover the truth of their conception either from their parents or from having taken a DNA test. Less commonly, they find out from a person other than a parent. Donor conceived people are often confused as to why their parents didn’t think such information was vital enough to share with them much earlier on. Indeed, many donor conceived people feel that knowing the identity of both biological parents is a basic human right for multiple reasons (psychological, cultural, and medical); they therefore feel violated and betrayed by their own parents for denying them this right to their complete family heritage—information that most others take for granted. Donor conceived people sometimes point out their parents’ hypocrisy in having chosen gamete donation over adoption for the purpose of establishing a biological connection to at least one parent and later complaining when their adult child shows interest in the typically anonymous biological parent. Should biological relatedness only matter to parents but not to children? The parents may say things like, “It shouldn’t matter. Love is all you need, and you received that.” Yes, but we also need to make sense of our traits and know where we came from so we can form healthy adult identities, not to mention our need for an accurate family medical history. Equally hypocritical, some parents enjoy doing genealogical work on their own family trees but criticize their adult donor conceived children for also valuing and investigating their true and complete heritage. Parents’ explanations for their failure to disclose the manner of their children’s conception are often confusing. For example, they may say, “We couldn’t find the right time,” or “We thought it would be better for you not to know.” They may state that they didn’t want to layer on additional challenges when their children were going through difficult life events, such as going to college, or when there was trauma, loss, or divorce in the family. These justifications may or may not be excuses to avoid the difficult “telling conversation.” Sometimes, donor conceived people recognize their parents’ good intentions, but the problematic secret, which they consider a major lie, may overshadow those good intentions. Many feel there were numerous opportunities over the years for their parents to tell the truth. There are several psychological reasons why parents may keep such secrets. Recipients of donor sperm may experience denial, as some may have lied to themselves for years by believing that the donor sperm didn’t “take,” while theirs (or their partners’) did. (Egg donation doesn’t afford the same opportunity for denial, since in vitro fertilization is necessary.) And in the past, fertility professionals encouraged such denial by mixing the sperm of two men—donor and intended father—or by telling heterosexual couples to have sex the night of the artificial insemination. Even today, most fertility professionals aren’t well informed about secrecy’s negative effects on donor conceived people and their family lives, being only concerned with running their businesses and achieving results.

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  • AdvocacyArticlesNPEs

    Advocacy: Misattributed Parentage Experiences

    by bkjax June 28, 2021
    June 28, 2021

    The advent of over-the-counter DNA testing has unlocked the closet where many family secrets were kept. While many learn one (or both) of the parents who raised them are not their genetic parent from a DNA test, sometimes people find out in other ways. A mother with a 104-degree temperature might let it slip that she had a son as a teenager. A family friend may tell someone mourning his dad, possibly at his funeral, that the suffered from infertility and had used a sperm donor. And sometimes having a child of their own prompts individuals to search for their biological family because they grew up with a vague idea of who their fathers were. Regardless of how one learns about misattributed parentage, the process of coping with such an experience is daunting and life-changing. Right to Know is a non-profit founded on the principle that it’s a fundamental human right to know one’s genetic identity. We believe in inclusivity and embrace anyone who facing misattributed parentage. To that end we use the term misattributed parentage experience (MPE) to describe the phenomenon of coping with the fact that you did not grow up knowing your genetic parent. It’s a term used by mental health professionals for decades. We believe the word experience best describes the long-term effects we all have, as opposed to “event,” which is a one-time occurrence. The ramifications of an MPE last a lifetime to some degree.

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  • ArticlesDonor Conception

    The Emotional Life of Donor Conceived People

    by bkjax April 23, 2021
    April 23, 2021

    It’s not news to donor conceived individuals that they have feelings about the manner in which they were conceived—feelings that may never occur to, or be acknowledged by, others. According to a new study published in the Harvard Medical School Journal of Bioethics and discussed in a recent article in Psychology Today, not do individuals experience significant distress upon learning they were donor conceived, they think about the means of their conception often. The authors of the new study reviewed existing literature and recognized a dearth of research concerning how donor conceived people feel about learning of their status, about the ethics of assisted reproduction, how their sense of identity is affected, how they’ve coped, and more. Rennie Burke, Yvette Ollada Lavery, Gali Katznelson, Joshua North, and J. Wesley Boyd developed a survey with questions about these issues and Dani Shapiro, author of the Inheritance: A Memoir of Genealogy, Paternity, and Love about her own discovery donor conception discovery, to help them recruit respondents. The response rate was 96.6, with 143 demographically diverse respondents, most from the United States, and the majority of whom were conceived through anonymous sperm donation. Among the findings: 86.5% believed they were entitled to non-identifying information about their donors 84.6 experienced a “shift in their ‘sense of self’” after learning they were donor conceived 48.5% sought psychological support 74.8% wished they knew more about their ethnicity 63.6% want to know more about their biological parent’s identity Highlights of the researchers conclusions are that increased attention to counseling is important, anonymous donation should be discouraged, and donor medical history should be provided to offspring, and the full potential implications of DNA testing should be considered before individuals proceed. J. Wesley Boyd, MD, PhD, took time to discuss the research.

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  • Donor ConceptionEssays, Fiction, Poetry

    My Father the Filmmaker

    by bkjax February 3, 2021
    February 3, 2021

    Whenever I tell this story, there’s always the same reaction: “I don’t know what to say.” And who am I to blame them? How could they? I wouldn’t either. Sometimes, I still don’t. I’ve always known. From my earliest waking memories, I knew I was special; I knew that he was special too. Because he was a donor, and I was a donor child, in our unusualness I had a bond with this mystery man. But I didn’t know who he was, and he didn’t know I existed. When you’re a donor child with a single mother by choice, something can happen. There’s a certain void. An abyss. Not a crater, because that would imply something was once there. You feel empty. You feel lonely. You didn’t have a choice. In this situation, everybody but you had a choice. Let’s backtrack. It’s April 2018, and I’m lying on my stomach, stretched out on the stone-cold floor of St. Luke’s Episcopal Church, on a retreat. Only three months until my 18th birthday. We were told to take some time to write and meditate. I’d been meaning to write this letter. Now I finally have time to do it. “Dear Dad.” No, that’s not right. Wait, yes it is! “I love you!” “Please love me!” “Please…want me.” Want me, goddammit. I never sent the letter. My 18th birthday arrived. Finally. I reached out to California Cryobank. The deal is that you get three tries to reach out; if the donor never responds, you aren’t allowed to facilitate contact ever again. And the donor has a right to his anonymity. Anonymous until 18. But he still has a right to turn you down when you turn 18. Such a bright age, 18. Shiny, almost. Full of promise and potential. Hope for the future.

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  • AdoptionArticlesDNA SurprisesNPEsSearch & Reunion

    New Support Group for the Emotional Side of DNA Discoveries

    by bkjax January 26, 2021
    January 26, 2021

    Recognizing the challenges facing individuals who experience DNA surprises, Adoption Network Cleveland (ANC) has launched the DNA Discoveries Peer Support Group, a virtual peer support program focused on the emotional impacts of the journey and  It kicks off with a special panel on February 2 facilitated by ANC’s search specialist Traci Onders that will feature an individual who’s discovered misattributed parentage, a donor-conceived person, and adoptees who have found birth family. Onders spoke with us about the program and the personal journey that led her to working with ANC. How did you come to Adoption Network Cleveland and how did you become interested in this work? I started as program coordinator for adult adoptees and birthparents in 2016. I’d begun volunteering at Adoption Network Cleveland (ANC) prior to that because its mission was personally important to me. Adoption Network Cleveland advocated for adoptee access to records in Ohio for more than 25 years, and finally in 2013 Ohio passed legislation that opened up original birth certificates to adult adoptees. It’s hard to imagine this would have happened without the steadfast determination of ANC, and as an adoptee, I wanted to give back to the organization that made it possible for me to request and receive my original birth certificate. ANC is a nonprofit organization and has a reputation for advocacy rooted in understanding, support, and education—a meaningful mission to me. I was born to a woman who was sent to a home for unwed mothers to hide the shame of pregnancy from the small town in which her family lived. There was no counseling available for the grief of relinquishing a child, and she was told to go on with her life and forget about it. These homes no longer exist; we know now how awful and hurtful this practice, rooted in shame, is. My birthfather died a year later in a tragic accident. He was also an adoptee, raised as a son by his maternal grandparents. I will never know if he knew who his father was, but thanks to DNA, I do. I first searched for my birthmother more than 20 years ago after my children were born. Pregnancy and childbirth made me want to know more about the woman who carried me and gave me a deep understanding that she made decisions that had to be extremely difficult and painful in a way that I had not previously appreciated. I had complicated pregnancies and no medical history for myself or my children. As a mother, I felt compelled to know and understand more about both my history and my beginning. At that time, I discovered that the agency that handled my adoption, Ohio Children’s Society, had destroyed its records. I had no information at all to work with, and my search hit a brick wall. It was important to me that I connect with my birthmother in a way that was respectful. I didn’t know if she had told anyone she’d relinquished me, and I was concerned that if I hired a private investigator, the PI might use tactics that I wasn’t comfortable with or make a possible secret known to others, and that this somehow might hurt my birthmother or her family. Until I could request my original birth certificate in 2015, I didn’t have many options. In 2015, adoptees were finally able to access their original birth certificates in Ohio, and when I did this, it named my birthmother. I also discovered that I have a maternal half-sister. My birthmother and I reunited very shortly after that. I was finally able to learn her story and to gain a more complete and ongoing medical history. Knowing these things and my relationship with her have been blessings in my life that for many years I did not imagine would be possible. A few months later I met the extended family, and their warm welcome touched my heart.

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  • Short Takes

    Genetic Genealogy with DNAngels

    by bkjax January 21, 2021
    January 21, 2021

    Direct-to-consumer DNA testing via Ancestry, 23andMe, and other companies has rapidly replaced the arduous tasks of hands-on library research, grave searching, and contacting strangers for the purposes of finding long-lost relatives—a tremendous advance since just a decade ago, when locating biological family or records to validate family lineage was a near impossible feat. While these tests—which rely on saliva samples—are simple, quick, and affordable, interpreting the results is often a confusing and time-intensive process. An International Case In November 2019, I took on a special challenge that illustrated the tenacity needed to solve cases. The case involved a search for records from Panama and Columbia to help determine the client’s origins. Bob called on DNAngels to help him find his mother’s biological father. Ann, his mother, was born in New York in 1961 and raised by an Italian-American mother and stepfather. Her mother refused to tell her who her biological father was and took his name to the grave. Ann thought that was it—that she’d never know her paternal family—and gave up on the thought of trying to find him. Bob, wanting to help his mother in any way possible, ordered Ancestry DNA tests for her, himself, his sister, and a few other relatives. Once he received the kits, he mailed them back immediately in hopes of finding the man Ann had spent decades wondering about and answering her questions. Was he tall? Was he a nice man? Where was he raised? What were his parents like? What did he look like? Bob found the results that came in a few weeks later both exciting and confusing. Ann’s ethnicity report had significant amounts of Spanish, Panamanian, and Columbian heritage. This gave them their first clue about where her biological father could be from. For Bob, looking at the numbers and trying to figure what it all meant was like trying to read a foreign language. He needed help.

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  • AdoptionArticlesDonor ConceptionNPEs

    New Webinar Series from Right to Know

    by bkjax October 5, 2020
    October 5, 2020

    Don’ t miss the latest in a series of webinars from Right to Know (RTK), a nonprofit organization that advocates for the rights of MPEs (misattributed parentage experiences), including NPEs (not parent expected). On Sunday, October 18, from 4pm-5:30 EST, the webinar will address mental health issues experienced by MPEs. Moderated by DrPh candidate Sebastiana Gianci, the panel will include Jodi Klugman-Rabb, LMFT, therapist, cohost of the podcast Sex, Lies & The Truth, and creator of the innovative training program Parental Identity Discovery; Cotey Bowman, LPC Associate, creator of the NPE Counseling Collective, and Lynne Weiner Spencer, RN, MA,LP, a therapist specializing in donor conception, adoption, and the experiences of NPEs and MPEs. Among the topics to be explored are trauma, identity, grief, ambiguous loss, anxiety, and rejection. In November, the series’ presenter will be Libby Copeland, award-winning author of The Lost Family: How DNA Testing is Upending Who We Are. (Look for our Q & A with the author here.) And in December, RTK’s webinar features the DNA Geek Leah Larkin, an adoptee and genetic genealogist. If you’d like to attend the upcoming webinar, request the Zoom link at RSVP2RightToKnow.us, and check out RTK’s event page to stay in the loop about upcoming presentations. If you missed the last webinar, “Understanding the Medical Ramifications in Your DNA Test,” you can watch the recording. Right to Know, created by Kara Rubinstein Deyerin, Gregory Loy, and Alesia Cohen Weiss, aims to educate the public and professionals about “the complex intersection of genetic information, identity, and family dynamics.” It works, as well, to change laws with respect to related issues, including fertility fraud. Find it on Facebook and on Twitter and Instagram @righttoknowus.

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  • Short TakesShort Takes: People, News & Research

    The Coalition for Genetic Truth

    by bkjax September 2, 2020
    September 2, 2020

    It was a movement waiting to happen. It only needed a catalyst. Enter Dr. Laura Schlessinger, an unapologetic bully and “infotainment” therapist masquerading as a helping professional. Host of the Dr. Laura Program heard daily on Sirius XM, Schlessinger bills herself as a “talk radio and podcast host offering no-nonsense advice infused with a strong sense of ethics, accountability and personal responsibility.” A Los Angeles marriage and family therapist, she’s no stranger to controversy, for example, when it became known that in the early days of her a television program, her staff posed as guests or when, two decades ago, she declared that homosexuality was “a biological error” and made racist comments that temporarily derailed her radio career. Now, with audience of eight million, her Sirius XM audience doesn’t shy away from the sensationalism that ratchets up the ratings. Recently, she directed her venom at NPEs (not parent expected.) On July 7, a segment of “The Call of the Day”—“My Mom Never Told Me the Truth”—was subtitled, “Torri’s uncertain she can continue to have a relationship with her mom after discovering her dad is not her biological father.” The caller, Torri, sought Schlessinger’s help, stating that she wasn’t sure how to continue on in her relationship with her mother after learning, only recently, that her dad wasn’t her biological father. Schlessinger asked Torri if the man who raised her was nice, and when Torri said he was, Schlessinger launched into an assumption-filled toxic diatribe. She berated Torri, asking “What in the hell is wrong with you?” When Torri tried to explain she was upset by her mother’s lying, Schlessinger responded by saying, “So what? So what? Who gives a shit?”

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  • BooksShort Takes

    Everything You Ever Wanted to Know About DNA Testing

    by bkjax February 28, 2020
    February 28, 2020

    Just over a decade ago, when autosomal DNA tests first hit the marketplace, offering consumers a new tool for advancing genealogical research and a way to discover genetic cousins, few imagined how popular these tests would become. In this short span, more than 26 million Americans have traded a hundred bucks and a spit or swab sample of DNA for a backward glimpse into their ancestry. The majority of testers get precisely what they pay for—a pie chart indicating their ancestral heritage and a list of DNA cousin matches. They learn from whence and from whom they came—information that makes them feel better connected to their forbears and more knowledgeable about themselves in some essential way. Countless others, however, get much more than they bargain for and—sometimes—more than they can handle. For these consumers, DNA testing leads to a genetic disconnect from their families and the erasure of an entire swath of their self-knowledge. They discover that they’re genetically unrelated to one or more of their parents. Even more shocking than the existence of these genetic disconnects is their sheer numbers. Although no one knows exactly how many testers have discovered misattributed parentage—and estimates within general population are likely overstated—headline after headline and the swelling ranks of secret Facebook groups devoted to supporting those disenfranchised from their families suggests the numbers are significant.

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  • AdoptionArticlesDonor ConceptionLate Discovery AdopteesNPEs

    Healing Retreats

    by bkjax December 5, 2019
    December 5, 2019

    Facebook groups and virtual support groups can be lifesavers, but nothing beats face-to-face time with people who know how you feel and have been where you’ve been. That’s why Erin Cosentino and Cindy McQuay have begun organizing retreats for adoptees, late discovery adoptees, donor conceived people, and NPEs (not parent expected) at which participants can get to know each other and share their experiences in a relaxed setting while learning from experts about the issues that challenge them. It’s not therapy, but it may be equally healing, and undoubtedly more fun. Since the day that Cosentino, 44, discovered at 42 that her father was not the man who raised her, her mantra has been “Nothing has changed, yet everything has changed.” McQuay, 56, has known her entire life she had been adopted. Both married with children and busy schedules, each devotes considerable time to advocating for people with concerns related to genetic identity and helping searchers look for biological family. And each runs a private Facebook group, Cosentino’s NPE Only: After the Discovery, and McQuay’s Adoptees Only: Found/Reunion The Next Chapter. Among her advocacy efforts, McQuay, who describes herself as a jack of all trades, helps adoptees locate the forms necessary to obtain original birth certificates (OBCs). A strong voice for adoptee rights, she strives to enlighten non-adoptees about the often unrecognized harsh realities of adoption, helping them understand that “not all adoptions are rainbows and unicorns.” Countering the dominant narrative, she’s quick to point out that adoptees “were not chosen, we were just next in line.”

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  • BooksShort Takes

    Lost and Found: Dani Shapiro’s “Inheritance”

    by bkjax June 19, 2019
    June 19, 2019

    Author Dani Shapiro has explored family secrets from every angle in an exceptional decades-long writing career that until now yielded five novels and four memoirs. Revisiting those works, it’s tempting to believe everything she’s experienced and written has been prelude to her 10th book, the bestselling “Inheritance: A Memoir of Genealogy, Paternity, and Love.” In an earlier memoir, for example, “Still Writing: The Perils and Pleasures of a Creative Life,” she describes herself in childhood as having been strangely aware unknowns were waiting to be discovered.

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  • AdoptionArticlesNPEsPsychology & Therapy

    Ambiguous Loss: When What You Don’t Know Hurts . . . Forever

    by bkjax June 19, 2019
    June 19, 2019
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    1 FacebookTwitter
  • AdoptionArticlesGenetics & HeredityNPEs

    No Family Medical History? How DNA Testing Might Help

    by bkjax June 19, 2019
    June 19, 2019
    Read more
    1 FacebookTwitter
  • Speak OutYour Video Stories

    Your Video Stories: Cassandra Adams

    by bkjax May 30, 2019
    May 30, 2019
    Read more
    1 FacebookTwitter

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What’s New on Severance

  • There Was a Secret
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  • We Three

After a DNA Surprise: 10 Things No One Wants to Hear

https://www.righttoknow.us

Call Right To Know’s resource hotline to talk with another MPE be paired with a mentor, get resources, or just talk.

Original Birth Certificates to California Born Adoptees

https://www.youtube.com/watch?v=erHylYLHqXg&t=4s

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Recommended Reading

The Lost Family: How DNA is Upending Who We Are, by Libby Copeland. Check our News & Reviews section for a review of this excellent book about the impact on the culture of direct-to-consumer DNA testing.

What Happens When Parents Wait to Tell a Child He’s Adopted

“A new study suggests that learning about one’s adoption after a certain age could lead to lower life satisfaction in the future.”

Janine Vance Searches for the Truth About Korean Adoptees

“Imagine for a minute that you don’t know who your mother is. Now imagine that you are that mother, and you don’t know what became of your daughter.”

Who’s Your Daddy? The Twisty History of Paternity Testing

“Salon talks to author Nara B. Milanich about why in the politics of paternity and science, context is everything.”

What Separation from Parents Does to Children: ‘The Effect is Catastrophic”

“This is what happens inside children when they are forcibly separated from their parents.”

Truth: A Love Story

“A scientist discovers his own family’s secret.”

Dear Therapist: The Child My Daughter Put Up for Adoption is Now Rejecting Her

“She thought that her daughter would want to meet her one day. Twenty-five years later, that’s not true.”

I’m Adopted and Pro-Choice. Stop Using My Story for the Anti-Abortion Agenda. Stephanie Drenka’s essay for the Huffington Post looks at the way adoptees have made unwilling participants in conversations about abortion.

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@2019 - Severance Magazine

Severance Magazine
  • About
    • About Severance
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    • Psychology & Therapy & Coaching
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Severance Magazine
  • About
    • About Severance
    • From the Editor
    • Submission Guidelines: How to Contribute
    • Contact Us
  • Articles
    • abandonment
    • Adoption
    • Advocacy
    • DNA & Genetic Genealogy
    • DNA Surprises
    • Donor Conception
    • Family Secrets
    • Genetics & Heredity
    • Interviews & Profiles
    • Late Discovery Adoptees
    • Psychology & Therapy
    • NPEs/MPEs
    • Search & Reunion
  • Essays & Fiction
    • abandonment
    • Adoption
    • DNA surprises
    • Donor Conception
    • NPEs/MPEs
    • Late Discovery Adoptees
    • Search & Reunion
    • Secrets & Lies
  • Short Takes
    • Short Takes: Books
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    • Short Takes: People, News & Research
    • Short Takes: Podcasts & Radio
  • Self Care & Coping
    • Coping Strategies
    • Self-Care
  • Speak Out
    • Micro-Memoirs
    • Your Video Stories
  • Resources
    • Start Here
    • Abandonment
    • Adoption
    • DNA & Genetic Genealogy
    • Donor Conception
    • Genetics & Heredity
    • Late-Discovery Adoptees
    • NPEs (Not parent expected) & MPEs (Misattributed parentage experience)
    • Psychology & Therapy & Coaching
    • Search & Reunion
    • Secrets & Lies
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@2019 - Severance Magazine