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Planning
a family using donor insemination:
a letter from Olivia to would-be DI Parents about "telling"
Dear
Would-be DI Parents
Nineteen years ago my husband and I discovered that the only way
we would be able to have a child was by using
donated sperm or adopting. After nine months of quietly grieving
the child we could not have together, we decided
that donor insemination was the best way forward for us. I was lucky
enough to conceive the first time and our son
was born nine months later. It subsequently took five inseminations
to conceive our daughter.
Both
our children have known about their DI origins since they were very
little. It is now common practice to be
open with children about their origins but back in those days our
clinic was very surprised when we said we were going to tell them.
We made this decision because we couldn't imagine living with a
lie about something so important, and we have never regretted this
decision. Talking about DI to a child can feel very burdensome to
parents, but if you begin early, they accept the facts very easily.
In fact they are often more interested in who is coming to play
or what they are having for tea. The trick is to keep the language
simple and in line with their stage of development and build up
the information in small building blocks. Parents, particularly
men, worry that a child might reject them when they know that they
are not their 'real' father, but our daughter and son are very clear
that their Dad is their father, even if they don't have a genetic
connection with him.
As
teenagers now, each of our children has a different perspective
on their DI origins. The eldest, a boy, is not interested in his
donor but says that it is very important to him that he has been
told the truth. Our daughter is curious about her donor and would
like to thank him for giving her life, but despite the fact that
she will almost certainly never have this opportunity, she is adamant
that we were right to share the information with her.
Telling
children about their origins when they are young (even if you can't
give them very much information about their donor) is likely to
be in their best interests, although it can feel very difficult
for parents. It can be tempting to think that you can just have
the treatment and go home and forget about it. But ignoring or denying
the truth does not make it go away. In fact these things have a
tendency to fester and cause much more trouble later, if they are
not thought about early on.
These
are some of the reasons why 'telling' is important -
- It
is respectful of each child (young person, adult) as a unique
individual. It is their right to have this information.
- Keeping
secrets takes up energy in families which is better spent on close
family relationships
- Relationships
in families can be threatened by the secret if -
a. ANYONE else at all knows (and usually someone does)
b. The man with fertility difficulties (and/or his partner) feels
shame about this method of family creation
c. Unanswered questions or evasive answers, glances between couples
or awkward silences create an atmosphere which is felt by the
child and others.
d. The child feels 'different' in some way but having no explanation
for this, blames him or herself.
- Research
has shown that disclosure or finding out about origins in adolescence
or adulthood can be damaging to present and future relationships.
It is hard to re-establish trust when a person realises they have
been lied to for a long time.
- In
an 'information age' where DNA testing kits are available through
the Internet and many column inches and TV hours are devoted to
stories about human genetics, young people who become suspicious
about their parentage have many ways of finding out if their genetic
connections are as they have been led to believe. Those with suspicions,
and who were conceived after August 1991, will be able to check
with the Human Fertilisation and Embryology Authority's (HFEA)
register as soon as they are 18, (or 16 if they intend to marry)
to see if they were indeed conceived with the aid of donated gametes
(eggs, sperm or embryos).
The
best time to start telling
Many parents say that they feel the best time to tell a child would
be when they are old enough to grasp the idea
completely. This is very understandable. Talking to young children
about such a personal matter seems a strange idea. However, leaving
'telling' until later can lead to difficulties. For a start you
can find yourself unwittingly spinning an increasingly complicated
web of lies, both to the child and to others. This can start as
soon as your child is born. "Who does s/he look like?"
will be the question on
the lips of everyone who coos at your baby. How are you going to
answer?
Around
the age of eight children reach the stage where they begin to be
better able to understand about DI, but
by that time many people (relatives, friends, health professionals)
will inevitably have been misled or lied to.
The
upset caused by the lie can be much greater than the knowledge of
use of donated sperm. Like the offspring themselves, relatives can
be very hurt by not being trusted with the truth. Many members of
the Network who were convinced that family members would be horrified
by the knowledge of their use of donated sperm, have been surprised
and delighted at the support they received when
they plucked up the courage to tell.
Children
of eight need full explanations with time and opportunities to ask
questions in order to completely take in information about DI origins.
Many parents might feel completely comfortable doing this, but if
you have not talked about the issues for many years there is a danger
that you may not be familiar with the language - both to do with
DI and sex and reproduction - that you may need to use to help your
child understand what they are being told. This unfamiliarity or
awkwardness might give your child the message that being a DI child
is something to be ashamed of, even if you don't actually say this.
Parents who believe, for the very best of reasons, that their child
should be the first person to have information about their origins
face a similar dilemma, but with an added dimension. The child has
the burden of deciding who else should know and being the object
of curiosity when these people are told. If, on the other hand,
relatives and close friends have known from the beginning - conception
or birth - then the child grows up in an accepting atmosphere
where they are highly unlikely to be seen as unusual in any way
and can mention their origins without fear of upsetting someone.
Teenage
years are not a good time to break the news about DI beginnings.
Young people are busy finding out who they are by testing their
own and their parents limits. New information which might put in
doubt the relationship of trust in the family, is not helpful at
this time of great change. We as parents need to be strong and solid
for our young people to push against, not pulling the rug out
from under them.
Some
parents worry that teenagers are likely to throw the lack of genetic
connection back in their faces during a row ... "You can't
tell me what to do, you're not my real father anyway". I can
only say that I have never known this to happen and I think it is
because the DI families I know have made it their business to work
at good communications between parents and children and that these
children know that they can't hurt their parents this way. For an
angry teenager it's only worth using a line if it's going to cause
pain. If the family is comfortable with the truth around DI, and
it is very clear who Dad is in the household, then the so-called
insult doesn't have an impact. Odd as it may seem, starting to talk
with your child about their DI conception when they are between
three and five years old is much easier! I know of some families
where they have started talking to their babies about it - just
to get comfortable and familiar with the words. Babies of course
love to be talked to about anything!
With
very best wishes Olivia
The
Donor Conception Network was started in 1993 by a group of families
who had all chosen to be open with their children about their origins.
We wanted to help break the isolation felt by so many people using
donor assisted conception methods, and to share our experiences
of talking to our children, and to family and friends, about DI
and more recently egg donation. We have two national meetings a
year, one in London and one in the North of England, produce a Newsletter
twice yearly, have a library of books, videos, audio tapes and articles
that can be borrowed and, most importantly, we put people in touch
with each other.
Network
Membership
You can join the network as an individual or a couple. Annual subscriptions
are £15 (£5 unwaged). To join download a membership
form from the website or simply send a cheque to our PO Box
below.
The
Donor Conception Network is a registered charity, registration number
1041297
Useful
addresses
Donor Conception Network
PO Box 265
Sheffield
S3 7YX
Email: dcnetwork@appleonline.net
Website: www.dcnetwork.org
020 8245 4369
Human
Fertilisation and Embryology
Authority 30 Artillery Lane London E1 7LS 0207 377 5077
website: www.hfea.gov.uk
British Infertility Counselling Association
69 Division Street
Sheffield
S1 4GE
Information line: 01342 843880
Website: www.bica.net
There
is no charge or cover price for Planning a Family Letters and they
are copyright free - you are welcome to copy this leaflet so long
as it is not sold. But if you have found it valuable, a donation
to the Donor Conception Network, a registered charity, would be
most welcome.
Visit
www.dcnetwork.org/planfamletters where you can download free copies
and find details of costs for bulk orders of printed copies. Single
copies can be obtained free by sending an A4 SAE to:
Network
Publications PO Box 265 Sheffield S3 7YX
A
letter from Olivia to would-be DI Mums [PDF version]
Order
form - [printable word version]
[PDF
version] You will need version Acrobat Reader Version 5 to open
these documents. It is also intended to make web based versions
(HTML) available in the future.
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