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Personal stories: by male donors
  "OPTIONS"

Having been a DCSG member and a donor for about nine years, I receive the regular newsletter and am always impressed by the amount of work people have obviously put into the group’s day to day running and activities. Of special interest are the Personal Stories telling of the necessity to be open and honest with offspring, offspring in search of donor details, and the relief of people finding an organisation to share questions, fears and experiences. It seems people were previously very much on their own.

Both families and offspring seem to very appreciative of their donor, most wondering about him, some even wanting to meet to say “Hi” and “Thanks”. The sad thing is most of the time the option is just not there. Hopefully today’s donor conception programs are collecting enough information to alleviate these problems in the future.
In this day and age, any hospitals, clinics, and donors or couples who participate in this program without providing identifying information for the resulting children are, in my opinion, putting their own needs and insecurities first. Put simply, a moral obligation exists to give donor conception offspring the option to trace their own biological origins. Sooner or later, these kids will suspect or want to know the truth about themselves, for themselves. In all honesty, who wouldn’t. Deliberately withholding information from someone, child or adult puts them at a distinct unfair advantage, and surely amounts to, using today’s buzzword, discrimination. Donor conception children, once given the information, don’t have a problem with their origins. It is we adults, that have the hangups. Prospective couples need to know what happens down the track. If the responsibility can’t be accepted, don’t go through with it. Adult offspring will be, and are, actively looking for information. It’s only natural. We should have learnt from the problems associated with adoption secrecy. As a donor, I had to consider such issues as the possibility of coping with having helped create a retarded child, or one with an all-consuming obsession with me as the biological father. I also had to come to terms with the masturbation aspect. I had no desire to hide behind anonymity and in fact left a family photo in my file at the clinic.

Being a member has enabled me to meet families and offspring and see the “other side” instead of just hospitals, nurses and doctors. I have been invited to attend seminars and even nervously speak in front of an audience. Likewise, families and offspring have been able to meet and demystify at least one donor, and to see just a normal guy, with his own family, who wanted to help.

Warren and Leonie’s family and mine (and others) have met socially on several occasions and it is all too apparent that we are all normal people. One of the things we have in common, is having accepted a “work around” to one of life’s challenges, that of infertility. Whilst I haven’t yet met any of my recipient families or children, I would be proud to have been Warren and Leonie’s donor. Anyone meeting Leonie is soon aware of a no-nonsense straightforward openness. “Dave the donor”, would just be another family friend seen socially every now and then. Inquisitive questions wouldn’t be a problem. A biological father’s true function, is to make possible a unique, self sufficient family unit which would otherwise not eventuate.

Other highlights have included meeting adult offspring and other donors:
• Bill Cordray, from the United States, where secrecy is even more of a problem.
• Geraldine, Warren and Leonie’s eldest; Lauren, Jo and Ian’s daughter; and Becky, three intelligent, articulate young women with firm confident handshakes, both actively in search of their own donor details. I wish them all the best in an unnecessarily difficult task.
• Kevin, a donor from Melbourne, who, like me, is happy to show the human side of the all too often faceless donor.

Even though I advocate openness, I am reluctant to be in the public eye in the media. I recently declined an invitation from Lingard Hospital to appear on SBS. My family is not keen and to be honest I don’t think I want that exposure. Unfortunately, media exposure is one of the most effective tools in educating the public. Thankfully there are others willing to fill that role.

Keeping in the context of honesty, my children (15 and 13) and wife have read this letter (and previous letters). Comments such as:“ did you write this” (daughter) , “ hmm, it’s good” (my wife), and “ it’s well written” (son) are the norm. They are actually pleased to think they have a half biological brother or sister somewhere. When I asked my daughter how would she feel if someone withheld crucial information from her, she replied “ Pissed off”. I think that says it all.

It will be interesting to see what options the future brings for all concerned.

Dave The Donor, February 2002

 

  Peter's story

Early 1980 whilst residing in Paddington, Sydney . I answered an ad published in a local paper. The reproductive clinic of the royal Hospital for women( Paddington) was desperate to recruit sperm donors. Being 30 years of age (at the time) and single.. I made contact and donated intermittently over a period of some 6 months. Having always harbored a strong desire to have children of my own. I felt this was one way of achieving that aim- albeit in a rather unconventional sense!

At that point in time there existed a heavy emphasis on non-identification. Obviously, this has turned out to be a very short -sighted and insensitive action. I was just a code number-supposedly never to be identified. Ironically, this has certainly been the case with me. a few years passed and out of curiosity I visited the Paddo clinic one day to met with the doctor in charge of the program. I wished to ascertain whether or not there had been any successful pregnancies on my behalf. He informed me that (at that stage) there had been three. This pleased me greatly, so I left feeling that I had achieved something worthwhile.

Years of wonderment passed and upon listening to a talk back segment on Triple J in May 1999, I became involved with the clinic yet again. I was deeply moved having listened to a 20 year old girl in her desperate quest to make contact with her donor. Feeling a sudden sense of urgency and responsibility. I was informed by the clinic that all records prior to 1983 had been destroyed( I was 1980)- just why. I never really knew. So now as I felt it was their responsibility. I requested that I be DNA tested. This was granted. so now I had to put myself out there. I also registered with the National donor conception Support Group, with whom I am in regular contact.

Obviously, I feel a deep sense of responsibility towards any offspring should they so desire to make contact. Orphaned at age 6 and a subsequent victim of severe abuse till age 16, I am well aware of the need for nurturing, understanding and adequate parenting. I never did have any children of my own, though thanks to my peers I have many in my life. In conclusion, I would encourage donors with conscience to sound out the sociological issues resulting from our actions and maybe contact the support group. We helped to create a life-let's just deal with the fact that these offspring feel the need to meet with us.- for whatever reason! What is there to be afraid of?

Peter (age 53) 6/5/2003, NSW Australia

 

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