In Vitro Fertilisation Ivf Intr PDF
In Vitro Fertilisation Ivf Intr PDF
In Vitro Fertilisation Ivf Intr PDF
Important notice: The information provided in this booklet does not replace any of the
information or advice provided by a medical practitioner and other members of your healthcare
team. If you have any further questions about IVF and ICSI, please contact your doctor.
Please note that throughout this booklet, the generic name of a medication will be stated first followed by
the brand name in brackets.
Gonal-f®, Pergoveris®, Ovidrel®, Luveris®, Cetrotide® and Crinone® are registered trade marks of Merck Serono
Puregon®, Elonva®, Pregnyl® and Orgalutran® are registered trade marks of Schering-Plough/MSD
Synarel® is a registered trade mark of Pfizer
© 2011 Merck Serono Australia Pty Ltd | ABN 72 006 900 830
Units 3-4, 25 Frenchs Forest Road East, Frenchs Forest NSW 2086 | Tel: +61 2 8977 4100 | Fax: +61 2 9975 1516
Merck Serono is a division of Merck. | ® Registered trade mark | FER-OCT-11-ANZ-26
Contents
Introduction............................................................................................................................................................................ 2
Stage 3: Fertilisation............................................................................................................................................................ 14
Surgical sperm extraction.......................................................................................................................................... 15
Using donor sperm and eggs................................................................................................................................. 15
Success rates........................................................................................................................................................................ 22
Trying again......................................................................................................................................................................... 23
Stopping treatment....................................................................................................................................................... 23
Support organisations............................................................................................................................................... 24
1
Introduction
Having trouble becoming pregnant comes as a surprise to most women and men. Many
people assume that pregnancy will follow immediately after birth control is discontinued.
In reality, up to one in six couples worldwide have difficulty conceiving in the first 12 months
of trying.1
These days, the treatment options available to help you become pregnant are relatively
simple, effective and affordable, and the success rates are very promising. Some of these
medical procedures are designed to increase the number of eggs and/or sperm, or bring
them closer together, thus improving the likelihood of pregnancy. Collectively, these medical
procedures are referred to as assisted reproductive technologies (ART) and include in vitro
fertilisation (IVF) and intra-cytoplasmic sperm injection (ICSI).
In this booklet, you will find detailed information on what is involved in the process of IVF
and ICSI, plus some methods on dealing with the stress and emotions you may feel as you
are being treated. Most of the time you will be able to cope with the pressure of the situation,
but there may be times when you need extra support, reassurance or some coping
techniques to help you manage the challenges and your stress levels. It is important that
you talk to your partner and other friends and family members about how you are feeling
throughout the IVF process. Your healthcare team, including counsellors and the support
organisations listed in the back of this booklet, will also be able to help with any concerns
or questions you may have.
2
What is in vitro fertilisation (IVF)?
In vitro fertilisation (IVF) literally means ‘fertilisation in glass’. You may have also heard
the term ‘test tube babies’ but these days the procedure involves placing an egg and sperm
together in a plastic dish to fertilise, rather than in a test tube.
IVF refers to a technique of assisted reproduction where the egg and sperm are fertilised
outside of the body to form an embryo. This embryo is then transferred to the uterus to
hopefully implant and become a pregnancy.
The first IVF baby, Louise Brown, was born in 1978 in the United Kingdom. The first Australian-
born IVF baby was born in 1980, and in 1983 for New Zealand. The technique was originally
developed to treat infertility caused by blocked or damaged fallopian tubes but is now used
to treat a wider variety of infertility problems.
IVF allows the sperm to penetrate the egg of its own accord whereas ICSI
directly inserts the sperm into the egg.
3
When are IVF and ICSI used?
IVF was originally developed for women with blocked fallopian tubes or missing tubes and
is still used to treat those conditions. It is also used when infertility cannot be explained and
with the following ovulatory or structural causes:
• problems with ovulation
• endometriosis
• fibroids
• polycystic ovary syndrome
• cervical problems.
ICSI is usually offered to couples who have had poor or no fertilisation during standard
IVF but is mainly used to overcome male infertility. It was first used in 1992 and offers an
alternative to donor sperm for those who have severe male infertility which includes:
• poor sperm morphology (abnormally shaped sperm)
• poor sperm motility (slow moving sperm)
• a low sperm count
• an obstruction which prevents sperm release (such as vasectomy)
• antisperm antibodies (antibodies produced by the man’s body, which may inhibit
sperm function).
IVF counselling
In Victoria, counselling prior to IVF treatment is a legal requirement for all couples. In other states it
is recommended but not compulsory. All IVF clinics in Australia and New Zealand offer counselling
by qualified counsellors. Their role is not to assess your suitability for infertility treatment, but to help
you deal with the stress and emotions involved in trying to achieve pregnancy.
4
The stages of IVF & ICSI
Starting IVF can be a very exciting time – it is another step closer to becoming parents.
Naturally, you will feel hopeful about a successful outcome but you also need to prepare
yourself for around two months of medications, numerous procedures and testing. Please also
bear in mind that the success rate of modern fertility treatments is high, but for the majority
of couples, multiple treatment cycles may be necessary.
The basic stages involved in the IVF procedure are detailed below. The whole process up to
the embryo transfer stage will usually take six to eight weeks.
Couples may go through a range of intense emotions. Moods can swing from hope to fear,
from joy to disappointment. Your experience and how you cope will depend on a large
number of individual factors including your own personality, your support network and
the relationship you have with your partner, how you react to the fertility medications and
the length and number of cycles of IVF you undergo.
You must give yourself time to relax and recover from each cycle of treatment and it is
recommended that you do not try to live your life just as you did before you started IVF.
You need to accept the changes it brings to energy levels and you should try to cut back
or prioritise your activities accordingly.
5
Stage 1: Ovarian stimulation
and monitoring
At the beginning of your menstrual cycle, the hypothalamus
(the part of the brain that controls many bodily functions)
releases a hormone called gonadtrophin-releasing hormone
(GnRH). GnRH in turn causes the pituitary gland to release a
hormone called follicle stimulating hormone (FSH) to prepare one
egg for release. When the egg is mature, the pituitary gland produces
another hormone called luteinising hormone (LH). This prompts the
follicle to release the one egg into the fallopian tube in the process
known as ovulation. Follicles are the fluid filled sacs in which eggs
grow to maturity.
With IVF, having a greater number of mature eggs available for fertilisation increases the
chances of pregnancy. Certain medications, are used to prevent an early release of eggs while
other medications, which are synthetic versions of FSH, are used to stimulate the ovaries
6
to develop more ovarian follicles. By having several mature eggs available for attempted
fertilisation and transfer – usually between five and 10 – it is hoped that at least one will result
in pregnancy.
These medications are taken by a self-administered injection under the skin (subcutaneous),
usually via an easy to use pen-type device. The injections are given under the skin of the
tummy or thigh. A response is generally seen after five to seven days. Injections are usually
required for about 10 days but the number of days and dose will vary depending on follicle
development.
As FSH is identical to the hormone that a woman’s body already makes naturally, side effects
relate to the typical effects a woman experiences when ovulating. These can include bloating
as the ovaries are stimulated, mood changes, tender breasts, abdominal discomfort and
backaches.
You will probably be sent home with a DVD and clear step-by-step instructions on how
to inject in the correct way. You might prefer that your partner does the injection for you
or that you do it yourself. Either way, you might feel more comfortable if you both have a
practise run in front of one of the nurses at your fertility clinic or gynaecologist’s office.
7
Taking fertility medications (cont.)
Human chorionic gonadotrophin (hCG): Given by injection one to two days after the last
dose of FSH, human chorionic gonadotrophin (hCG) causes the final maturation and release
of an egg. You will probably do this injection yourself at home at a specified time. Ovulation
should occur within 32 to 48 hours following the injection of hCG (Ovidrel®, Pregnyl®).
Luteinising hormone (LH): This medication is similar to the luteinising hormone found
naturally in humans. It is recommended for the treatment of women who have been shown
to produce very low levels of some of the hormones involved in the natural reproductive
cycle. It is used together with a gonadotrophin to bring about the development of follicles.
To minimise side effects, it may also be used to bring on the release of the eggs instead of
hCG. It includes the medications Luveris® and Pergoveris® (a mixture of FSH and LH).
8
Protocols
A ‘protocol’ is a plan or schedule of how your IVF cycle will be done. It will usually include the
medications you will be taking, instructions on how to take them, when you will need to have
ultrasounds and blood tests and the procedures you need to follow throughout the cycle. There
are a few standard protocols used and your doctor will choose the one that is right for you. The
two most common ones are:
Long down regulation: During ovulation, the release of the egg is triggered by a sudden surge
of the hormone LH at mid-cycle. During an IVF cycle, we do not want an LH surge to trigger an
early release of these eggs. A GnRH agonist is used to temporarily turn off your own LH and FSH
secretion in what is known as ‘pituitary suppression’ or ‘down regulation’. It involves the use of the
nasal spray Synarel® or a daily injection of leuprorelin acetate for at least 10 days. FSH is then given
and both drugs
GnRH Agonist
continued until the
timing of egg pick
up is determined.
Hormone
Levels
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14
Days
Antagonist treatment cycle: This is simpler and less time consuming than the long down
regulation protocol because you take a GnRH antagonist at the same time as the FSH
injections (rather than taking a GnRH agonist in the two weeks prior to the FSH injections).
With this protocol, a daily injection of either Cetrotide® or Orgalutran® is used to suppress the
LH surge; commencing 5 or 6 days after starting the FSH injections, or when the follicles have
reached a diameter of 12-15 mm (as measured by ultrasound). In both cases, daily injections
of FSH and GnRH
GnRH
antagonists are Antagonist
continued until
the timing of
Hormone
egg pick up is Levels
determined. See
diagram.
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14
Days
9
Be aware of ovarian
hyperstimulation syndrome
Ovarian hyperstimulation syndrome (OHSS) is a potentially life-threatening medical
condition, which may occur, though rarely, when your ovaries have been overly stimulated by
various fertility medications. The ovaries may increase in size and produce large amounts of fluid.
It is characterised by pain and bloating in your abdomen and if severe can cause problems with
breathing or urinating. Contact a member of your healthcare team immediately if you believe you
have any of these symptoms.
Monitoring ovulation
Throughout this first stage, your response to FSH will be carefully monitored for ovarian
hyperstimulation syndrome (OHSS) – see above – and to gain a clearer picture of what is
happening to the follicles so the right timing and dose can be determined.
Ultrasound: Your clinic (doctor, nurse or sonographer) will often use one or more ultrasound
scans to obtain an actual image of the ovaries and to regularly monitor follicle growth in the
ovary beginning on or before day eight of the cycle. As follicles mature, they grow larger.
Through ultrasound, your doctor can observe the effects of treatment on follicle growth
and size, and decide when to give hCG to assist with egg release.
Ultrasound may be performed abdominally or, more commonly, vaginally, using a slender
probe a little thicker than a tampon. The sound waves cannot be felt and the procedure is
minimally invasive and usually painless.
Blood tests: Testing the blood every few days for oestrogen levels can monitor the
response to treatment with FSH therapy. Developing follicles secrete increasing amounts of
the oestrogen hormone, in particular oestradiol (E2) – one of the main types of oestrogen.
Together with ultrasound, this can help determine the best timing for giving the hCG
injection to stimulate ovulation.
10
Stage 2: Egg (oocyte) retrieval
Egg retrieval, also known as ‘egg pick up’, is arranged just prior to expected ovulation. Egg
retrieval is usually performed 36 to 48 hours after the administration of the ovulation inducing
drugs hCG or LH. Your doctor will try to retrieve as many mature eggs as possible, although all
the eggs (oocytes) may not be used in the current IVF cycle.
Egg retrieval is done under local anaesthetic or a light general anaesthetic, most commonly
by ultrasound guided fine needle (aspiration). The mature follicles are identified using
ultrasound, and then a needle is passed through the vaginal wall into the follicle and the
fluid withdrawn from the mature follicle with gentle suction.
The fluid is immediately examined under a microscope to see if an egg has been retrieved.
The process is repeated for each mature follicle in both ovaries. All retrieved eggs are
removed from the follicular fluid and placed in an incubator.
Sometimes laparoscopy is used where a doctor uses a tube with a tiny camera on the end of it to
guide it to the ovarian follicles. An aspiration system then uses light suction to retrieve the egg
from the follicle. Laparoscopy, which requires full general anaesthesia, is usually only used when
the ovaries are inaccessible via the transvaginal approach (e.g. when large fibroids are present).
11
Number of eggs in the follicles
Not every follicle contains an egg, or some may contain post mature eggs which may not be
capable of being fertilised. So don’t be surprised if the number of eggs retrieved is less than the
number of follicles you’ve been watching develop on ultrasound. The average number of eggs
retrieved is between eight and nine and the retrieval process lasts approximately 20–30 minutes.
12
Nikki and
Steve’s journal
“I can’t believe it took us five years to try IVF. It was
the most exciting time of our lives. The drugs were
not so much fun. I got some pretty major headaches,
felt bloated and was very worn out. I don’t recall
being over emotional at that time, but Steve might tell a different story on that
one. But to tell the truth, none of it really mattered. It was like the best science
lesson we have ever had. Suddenly we knew more about how a baby is made than
we realised was involved.
Watching as they retrieved my eggs was incredible. They said I may have trouble
remembering because of the drugs, but we didn’t stop talking about it and some-
how I retained the best bits. Then the best part of all was seeing our little Billy, as a
five-day old blastocyst, before they popped him into my uterus. You don’t get that
if you conceive naturally!
I am grateful that I got over all my reservations about IVF. Parts of it are obviously
unpleasant, but no more unpleasant than the monthly let down we had for five
years before we did IVF. It doesn’t always work, but it did for us, and it was worth it.”
You can find the full story of Nikki and Steve’s journey to parenthood along with many
other personal stories at www.fertility.com
*This personal statement is the opinion of real individuals. Individual experiences will vary from person to person.
13
Stage 3: Fertilisation
About about two hours before egg pick up,
a semen sample is collected from the male
partner. Two to three days abstinence from
intercourse/masturbation is preferred prior
to the sample collection day. The sperm
sample is usually produced by masturbation
at the clinic. The sperm is processed to select
the strongest, most active sperm. This is called
‘sperm washing’. If sperm is not present in the
ejaculate, sperm collection may be attempted
surgically (see ‘surgical sperm extraction’
information next page).
If undergoing ICSI, the eggs are prepared for injection and their maturity confirmed. In what
is a delicate laboratory procedure, a single sperm is placed directly into the cytoplasm (the
centre) of the egg – hence the
name intra-cytoplasmic sperm
injection. Fertilisation can
then be identified in a similar
fashion to IVF after about
20 to 24 hours.
14
Is ICSI more successful than IVF?
Studies suggest that the success rate of fertilisation for ICSI and IVF are similar.2
The semen selected for a couple closely matches, as much as possible, the male partner’s
characteristics, e.g. eye and hair colour, height and build.
There are many factors to consider such as whether to tell friends or family about using
donor sperm and whether the child should know about their origins as they grow up.
AccessAustralia and the Donor Conception Support Group have many resources on
the issues relating to donor insemination (see contact details at the back of this booklet).
Donor oocytes
Egg donation is one treatment option for those who wish to have a child but who are unable
to use their own oocytes (eggs). The eggs may be sourced from an anonymous donor or
donated by a close friend or relative. The donor undergoes ovarian stimulation to help the
recipient. A comprehensive medical and counselling process is undertaken prior to the
initiation of such treatment cycles.
15
Stage 4: Embryo development
‘Embryo culture’ is the term used to describe the process immediately following egg pick up.
It is during the culture process that your eggs and your partner’s sperm will be combined in
order to produce a fertilised egg (known as a zygote). Your doctor will discuss how long they
will watch embryo development in the laboratory and how each embryo will be ‘graded’, e.g.
from ‘A’ to ‘F’ depending on their quality. It is common for transfer to be done between day
two (2–4 cell stage) and day five (blastocyst stage – around 100 cells) of development. This
allows assessment of embryo cleavage (the way an embryo divides) and ensures the embryo
is still developing so that only embryos capable of resulting in a pregnancy are transferred.
Some fertility specialists prefer doing blastocyst transfers because it is easier to choose a
healthy embryo for transfer at this stage. The latest statistics from the Australian Institute of
Health and Welfare show that there
is an increasing
trend towards
blastocyst transfer
over the traditional
‘3-day transfer’.3 In
2008, blastocyst
embryo transfers accounted for 38.6% of embryo transfer cycles – significantly higher than
the percentage of cycles transferring blastocysts in 2004 (17.1%).3
16
Stages of development
Zygote: A single sperm penetrates the mother’s egg cell, and the resulting cell is called
a zygote. The zygote contains all of the genetic information
(DNA) necessary to become a child. Half of the genetic
information comes from the mother’s egg and half from the
father’s sperm. The zygote spends the next few days travelling
down the fallopian tube and divides to form a ball of cells. The
term cleavage is used to describe this cell division.
Morula: When the zygote reaches 16 or more cells, it is called a morula. The morula
is no larger than the zygote, but keeps producing smaller and smaller cells through
cleavage.
Embryo: The blastocyst reaches the uterus around day five, and implants into the
uterine wall on about day six. The cells of the embryo now multiply and begin to take
on specific functions resulting in the various cell types that make up a human being
(e.g. blood cells, kidney cells, and nerve cells).
17
Cryopreservation
Although your doctor will try to fertilise all available eggs, usually only one, or occasionally two,
embryos will be transferred immediately. If there are any remaining embryos, they can be frozen
through a process known as cryopreservation. Frozen embryos are stored and most will remain
unchanged for a long period of time. About two in three embryos will survive the process of
freezing and thawing.4 An advantage of cryopreservation is that these frozen embryos can be used
in future IVF/ART cycles without having to repeat the first few steps of ovarian stimulation, egg
recovery and fertilisation.
Assisted hatching
Prior to implanting in the uterus, the embryo must emerge from its covering in a process
called hatching. In some women, the membrane seems to harden, interfering with the
hatching process.
In such cases, thinning the embryo membrane with a dilute acidic solution or laser prior
to embryo transfer may assist hatching. This procedure is performed on embryos in the
laboratory when needed. Older women or those who have not achieved pregnancy after
several IVF cycles are often helped by this treatment. Assisted hatching may also be done
in some cases following cryopreservation and embryo thawing.
18
Stage 5: Embryo transfer
Embryo transfer is not a complicated procedure – rather like a pap smear – and can be
performed without anaesthesia. Two to five days following egg pick up, the embryo is placed
in a catheter (a soft tube) and transferred to the uterus via the vagina opening. The number
of embryos transferred depends on a woman’s age, cause of infertility, pregnancy history, and
other factors.
Generally one
or occasionally
two, embryos
will be
transferred to
the uterus. It is
important to
note that the
risk of multiple
pregnancy
increases with
the number of
good quality
embryos transferred. If there are
additional embryos that are of
good quality, they may be frozen
(cryopreservation – see previous
page) for later use.
Multiple pregnancies
For those having trouble becoming pregnant, being pregnant with twins may seem the ideal
way to have an instant family. However, fertility doctors agree that the risks involved, such as
miscarriages and low birth weight, far outweigh any perceived advantages. Because of this in
Australia and New Zealand, most clinics will not transfer more than two embryos. Over the last five
years there has been a reduction in the rate of multiple birth deliveries as single embryo transfers
(SET) increased from 40.5% in 2004 to 67.8% in 2008.3
19
Stage 6: Luteal phase support
The luteal phase is the two week period between the embryo transfer and the pregnancy
test. It is usually recommended that you take it easy for a couple of days after the transfer.
After 48 hours, you can resume your normal activities – these will not affect implantation.
The corpus luteum (the follicle after the egg is released) does not produce the hormones
oestradiol and progesterone to prepare the uterus for embryo implantation as it would in a
natural cycle. This is due to the treatment prior to egg collection and the collection process itself.
In order to ensure there is adequate progesterone present, you will be prescribed progesterone
as a vaginal gel (Crinone® gel) or in the form of pessaries (inserted vaginally) to help keep the
endometrium (the lining of the uterus) in optimal condition for implantation.
After approximately 16 days, you will return to the clinic or your doctor’s for a blood test to
determine whether a pregnancy has occurred.
20
What can help?
Surviving the two week wait
After your embryo transfer, it takes around two weeks for pregnancy test results to be
accurate. This ‘two week wait’ – the time before your expected period is understandably a
time of high anxiety, worry, and frustration for women trying to conceive. Here are some
‘survival’ tips to help you get through this time:
• Try not to obsess about pregnancy symptoms – feeling pregnant does not always
mean that you are. Some of the medications can have side effects that resemble
pregnancy symptoms.
• Keep busy – this may
mean working more or planning
meaningful or fun distractions.
• Allow yourself only 15 to 30
minutes a day to think about
pregnancy, write down your
thoughts, search information
online or discuss it with your
partner or supportive friends/
family members.
• Avoid pregnancy tests – the
chance of getting a positive
result before your period is late
is very slim. The hCG injection
given to mature and release the
eggs and as a booster can also
give a false positive urine test.
21
Success rates
According to the latest figures from the Australian Institute of Health and Welfare, there were
61,929 assisted reproductive technology (ART) treatment cycles undertaken in Australia and
New Zealand in 2008.3
Of these cycles, 17.2% resulted in a live delivery (the birth of at least one liveborn baby).3
In total, 11,538 liveborn babies were born following ART treatment undertaken in 2008.3
Success rates are significantly influenced by a number of factors including:
• woman’s age
• cause of infertility
• response to medications and treatment
• sperm quality
• number of embryos transferred
• transfer and use of cryopreserved (frozen) embryos.
22
Trying again
There are a lot of reasons why your pregnancy results may come back negative. Sometimes
the embryos do not implant or they start to implant and then stop. In other cases, they could
have been damaged during the process of growth or the actual transfer. Having multiple
cycles of IVF is common and is often necessary to give yourself a good chance at success.
When you feel ready, you will need to return to your doctor to review your past treatment
and discuss your future options.
Considering these questions may help you decide whether to continue, take a break or stop
treatment altogether:
• Do I have a real chance of getting pregnant?
• Is another treatment cycle asking too much of my body?
• Am I too distressed?
• Can our relationship support more treatment?
• Can we afford further treatment cycles?
• Have I considered my other options, e.g. adoption, fostering, living without children?
AccessAustralia has a number of excellent resources on the subject of stopping treatment.
See their website at www.access.org.au
Stopping treatment
Stopping treatment is also a time of mixed emotions. Most know when it is time to stop and
seek relief from the constant procedures and disappointments. It is important to realise that
it will still take time to accept that you won’t have children from this treatment, and that
sadness and anger is normal. It may also be just as hard to realise that you may never know
why it didn’t work.
With the mixed emotions of relief and sadness there is also the realisation that the time of
being in limbo has stopped, and that it is now possible to take back control.
Some things that you may talk about at this time are:
• planning others ways to have children including adoption or fostering
• re-training for a different career.
• getting fit after all the fertility treatments.
• taking a well deserved rest or holiday.
23
Support
organisations
Australia
AccessAustralia
www.access.org.au
Ph: (02) 9737 0158;
Polycystic Ovarian Syndrome
Email: [email protected]
Association of Australia (POSAA)
AccessAustralia is a national organisation, www.posaa.asn.au
which provides numerous services and Ph: (02) 8850 9429 or (02) 8250 0222;
resources for people having difficulty Email: [email protected]
conceiving.
POSAA is a ‘self-help’ association for women
Its services include: with polycystic ovarian syndrome (PCOS)
• fact sheets, newsletters and personal and those who suspect they have it. Its
stories website includes information on upcoming
• putting you in contact by phone or workshops, support groups and fact sheets.
email with others sharing a similar
Donor Conception Support Group
infertility experience
http://www.dcsg.org.au
• a register of infertility self-help groups
Ph: (02) 9793 9335;
• listing of infertility clinics accredited by
Email: [email protected]
the Reproductive Technology
The Donor Conception Support Group of
Accreditation Committee (RTAC)
Australia is a self funding organisation run
• listing of professional infertility
by volunteers. Its members include those
counsellors across Australia
who are considering or using donor sperm,
• lobbying governments for equal access
egg or embryo, those who already have
to affordable, quality assisted conception
children conceived on donor programmes,
treatment.
adult donor offspring and donors. It offers
a newsletter, information nights, a library of
books and articles and telephone support.
24
Endometriosis Association (Qld) New Zealand
www.qendo.org.au FertilityNZ
Ph: (07) 3321 4408; Email: [email protected] www.fertilitynz.org.nz
This association provides information and Ph: 0800 333 306;
news relating to the latest research and Email: [email protected]
treatments for endometriosis. FertilityNZ is New Zealand’s national network
SANDS for those seeking support, information and
SANDS is a self-help support group news on fertility problems.
comprised of parents who have experienced It provides various services including:
the death of a baby through miscarriage, • regional support and contact groups
stillbirth, or shortly after birth. It provides • general advice and contact service
24-hour telephone support, information • comprehensive information brochures
resources, monthly support meetings, • a forum for confidential feedback on any
name-giving certificates and other support. issues or concerns
• a chatroom where you can seek on-line
Vic
support from people in similar situations.
www.sandsvic.org.au
Ph: (03) 9899 0218 (support) or Endometriosis New Zealand
(03) 9899 0217 (admin); www.nzendo.co.nz/
Email: [email protected] Ph: 0800 733 277 (free phone support line);
Email: [email protected]
Qld
Endometriosis New Zealand promotes
www.sandsqld.com
awareness of endometriosis, provides
Ph: 1800 228 655 (support) or information, education and raises funds to
(07) 3254 3422; support endometriosis related initiatives.
Email: [email protected] It includes disease information specifically
designed for teenagers, a support group
SA
network, regular seminars and workshops
www.sandssa.org
and a free phone support line.
Ph: (08) 8277 0304;
Email: [email protected] SANDS New Zealand
(quick response) or [email protected] www.sands.org.nz/home.html
(general query) Ph: (06) 868 9514;
Email: [email protected]
References
1 Assisted Conception Taskforce (ACT) Trying to have a baby. Your step-by-step guide to assisted conception. Available online:
http://www.assistedconception.net/resources/ACT_Ratgeber.pdf downloaded 27/2/11
2 US Department of Health and Human Services. 2007 Assisted Reproductive Technology Success Rates. Available online: http://www.cdc.gov/
art/ART2007/PDF/COMPLETE_2007_ART.pdf downloaded 27/2/11
3 Australian Institute of Health and Welfare (AIHW) National Perinatal Statistics Unit. Assisted Reproduction Technology in Australia and
New Zealand 2008. Available online: http://www.aihw.gov.au/publications/per/49/11525.pdf downloaded 27/2/11
4 Speroff L, Glass RH, Kase NG. Clinical Gynecologic Endocrinology and Infertility. 5th ed. Baltimore, MD: Williams & Wilkins; 1994.
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Looking for more
information?
Ask your doctor for a copy of the other booklets in
the Pathways to Parenthood informational series.