Case Law[2022] ZAGPPHC 712South Africa
Ex parte MCM and Another (28084/22) [2022] ZAGPPHC 712 (26 September 2022)
High Court of South Africa (Gauteng Division, Pretoria)
26 September 2022
Judgment
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# South Africa: North Gauteng High Court, Pretoria
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## Ex parte MCM and Another (28084/22) [2022] ZAGPPHC 712 (26 September 2022)
Ex parte MCM and Another (28084/22) [2022] ZAGPPHC 712 (26 September 2022)
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sino date 26 September 2022
IN
THE HIGH COURT OF SOUTH AFRICA
GAUTENG
DIVISION, PRETORIA
CASE
NO: 28084/22
REPORTABLE:
YES/NO
OF
INTEREST TO OTHER JUDGES: YES
REVISED:
NO
26
September 2022
In
the
Ex Parte
application of
MCM
First
applicant
and
D
Second
applicant
Professor
D
Thaldar
amicus
criae
JUDGMENT
Van
der Schyff J
Introduction
[1]
The first applicant, MCM, and the second
applicant, D, are both South African citizens, married and residing
in Gauteng. They intend
to have children of their own but require the
assistance of a surrogate mother due to MCM suffering from a
permanent and irreversible
uterus condition. They have, however, not
yet identified a suitable surrogate mother. To preserve MCM's current
health and fertility,
the applicants would like to proceed with
artificial fertilisation at this stage. Although they intend to
utilise MCM and D's gametes,
they will use the gametes of an
anonymous egg donor should MCM not be able to produce sufficient
gametes.
The
applicants’ submissions
[2]
The applicants explained that the
gametes (oocytes) of either the first applicant or the anonymous
donor would then be combined
with the gametes of the second applicant
in a laboratory by
in vitro
fertilisation (IVF) process. The embryo(s) will be cryopreserved and
only transferred to the uterus of a surrogate mother after
the court
confirms a surrogacy motherhood agreement.
[3]
The applicants surmised that they would
not be able to proceed with oocyte retrieval and the fertilisation of
the retrieved oocytes
without first obtaining the court's approval
due to the restricted wording of the provisions of Chapter 19 of the
Children's Act
38 of 2005 (the CA). Section 303(1) of the CA provides
as follows:
'No
person may artificially fertilise a woman in the execution of a
surrogate motherhood agreement or render assistance in such
artificial fertilisation, unless that artificial fertilisation is
authorised by a court in terms of the provisions of this Act.'
[4]
Section 296 of the CA also speaks to the
'artificial fertilisation' of a surrogate mother, and the section
provides as follows:
'(1)
No artificial fertilisation of the surrogate mother may take place –
(a)
before the surrogate motherhood
agreement is confirmed by the court;
(b)
after the lapse of 18 months from the
date of the confirmation of the agreement in question by the court
[5]
The term 'artificial fertilisation' is
defined as follows in the CA:
'"
artificial fertilisation" means: the introduction, by means of
other than natural means, of a male gamete into the
internal
reproductive organs of a female person for the purpose of human
production, including-
(a)
the bringing together of a male and
female gamete outside the human body with a view to placing the
product of a union of such gametes
in the womb of a female person; or
(b)
the placing of the product of a union of
male and female gametes which have been brought together outside the
human body, in the
womb of a female person'.
[6]
The applicants explain that the broad
definition of artificial fertilisation is an all-inclusive definition
that includes and touches
on three separate processes, namely:
i.
Egg retrieval to enable the
fertilisation of the oocytes that are removed from the ovaries of a
woman, outside the body;
ii.Intracytoplasmic
sperm injection, which brings about the fertilisation of an ovum with
male sperm outside the women's body; and
iii.Embryo
transfer into the uterus or fallopian tube of the recipient.
[7]
The applicants expressed the view that
it is an unintended consequence of the broad definition of the term
artificial fertilisation
used in conjunction with the term ‘rendering
of assistance in such artificial fertilisation' that prohibits any of
the three
aforementioned processes in the absence of a court order
authorising same, where the treatment is undergone in the context of
a
couple who wants to use surrogacy as their reproductive avenue.
[8]
The applicants thus approached the court
for an order directing the doctors concerned to perform
in
vitro
fertilisation, including
oocyte (egg) retrieval, intracytoplasmic sperm injection, and
cryopreservation of the blastocysts (embryos)
created by such IVF
procedures. They aver that s 303(1) is open for a broad
interpretation in that both the phrases' artificial
fertilisation'
and 'render assistance in such artificial fertilisation' can be
interpreted to necessitate the authorisation of
the procedures where
the procedures will be executed with the view of approaching the
court at a later stage to approve a surrogacy
motherhood agreement.
The
amicus curia’
s submissions
[9]
Subsequent to the issue of the
ex
parte
application, Professor Donrich
Thaldar applied to be, and was, admitted as
amicus
curiae
. In his initial
correspondence, before the application to be admitted as
amicus
curiae was filed, Professor Thaldar
expressed the view that:
‘
The
novel practice of ‘breaking up’ surrogacy applications by
first launching an
ex parte
‘pre-surrogacy’
application regarding the creating of embryos with ART, followed by a
full surrogacy application, is
unnecessary and costly – this
practice only serves to increase the legal costs of surrogacy
applications for members of the
public.
We
intend to submit that this novel practice is unnecessary, as the law
on this issue is clear and unambiguous. Nothing in our law
prohibits
the creation of embryos through ART – provided that it is done
in accordance with the relevant regulations in terms
of the National
Health Act.’
[10]
Professor Thaldar formulated the legal
question underpinning this application as follows:
'Is
the act of creating embryos through
in vitro
fertilisation
(IVF) for reproductive purposes by health care professionals on
instruction of persons who intend to use surrogacy
as their
reproductive avenue, but who have not yet obtained a court order that
confirms their surrogate motherhood agreement –
(i)
lawful,
(ii)
only lawful if confirmed by the court in
terms of Chapter 19 of the
Children's Act, or
(iii)
unlawful?'
[11]
Professor Thaldar analysed the
definition of the term artificial fertilisation as used in the CA,
and submits that it can have three
distinct meanings. The meaning of
the term that is intended in a particular provision, he then submits,
is determined by the context
within which the terms are used in any
specific section of the CA. He further submits that the prohibition
in
s 296(1)
and
303
(1) of the CA relates to performing embryo
transfer or intra-cervical or intra-uterine insemination on a woman
in the execution
of a surrogate motherhood agreement, but not to the
'bringing together of a male and female gamete outside the human body
with
a view to place the product of a union of such gametes in the
womb of a female person'. This interpretation is based on the
construction
of both
sections 296
and
303
which refer respectively to
'artificial fertilisation of the surrogate mother' and 'artificial
fertilisation of a women'
[12]
Professor Thaldar submits that an
application in terms of Chapter 19 of the CA to authorise IVF is not
legally competent. He opines
that Chapter 19 creates a specific
sui
generis
type of
ex
parte
application, namely an
application to confirm a surrogate motherhood agreement. In his view
a party may, however, seek declaratory
relief in respect of an aspect
of surrogacy, and ultimately proposes that the court grants a
declaratory order declaring that the
applicants have the right to
have embryos created through IVF with the intention that said embryos
will eventually be transferred
to a surrogate mother still to be
identified.
[13]
Professor
Thaldar drew the court’s attention to the judgment by
KeightleyJ in
Ex
parte: MS and Others
[1]
and to
Regulation 10(2)(a)
of the Regulations relating to the
Artificial Fertilisation of Persons in his heads of argument. The
relevance of the latter is
discussed below.
[14]
Keightley J remarked in
Ex
parte: MS and Others
that a
surrogate motherhood agreement must, 'ideally', be confirmed 'before
there is any prospect of conception.' She pointed out
that
s
295(b)(ii)
of the CA requires that the court must be satisfied that
the commissioning parents are in all respects suitable to accept the
'parenthood
of the child that
is to
be conceived
'.
(My
emphasis.)
The
amicus
critisised the court’s approach in
MS
,
on this aspect.
[15]
Reference
must be made to the expert evidence of Ms. Els-Smit presented by the
amicus
curiae
on
affidavit. Ms. Els-Smit has over 15 years clinical experience as an
embryologist. Ms. Els-Smit points out that it is not uncommon
for
commissioning parents in a surrogate motherhood agreement
confirmation application to already have cryopreserved embryos. This
is because the commissioning parent typically first, unsuccessfully,
attempts to fall pregnant herself through IVF and embryo
transfer,
before being diagnosed as being unable to carry a pregnancy to term.
In such cases, surplus embryos often remain from
the commissioning
parents’ fertility treatment. A reported judgment on a
surrogate motherhood agreement confirmation application
where this
was the case is
Ex
Parte Kaf 2.
[2]
In her expert opinion commissioning parents may have objectively good
reasons to wish to create embryos in anticipation of a surrogacy
arrangement.
[16]
The
amicus
curiae
and the applicants jointly
provided the court with a draft order that provides for a declaration
of rights, in the following terms:
‘
Declaring
that the applicants have the RIGHT to have embryos created through
in
vitro
fertilisation (IVF) with the intention that said embryos
will eventually be transferred to a surrogate mother still to be
identified,
provided that:
The
applicants comply with the relevant provisions of the Regulations
relating to the Artificial Fertilisation of Persons; and
If
and when a surrogate mother is identified by the applicants, embryo
transfer to the said surrogate mother may only transpire
once a court
of competent jurisdiction has confirmed the applicant’s
surrogate motherhood agreement with said surrogate mother.’
Discussion
[17]
It
cannot be gain-said that the science in the field of assisted
reproduction is ever advancing. As stated in the South African
Law
Reform Commission’s Issue Paper 32, Project 140,
[3]
assisted reproduction is used to treat infertility and entails the
use of fertility medications and medical techniques to bring
about
the conception and birth of a child. It is stated in the Summary of
the Issue Paper that:
‘
Children
are conceived using donor gametes in techniques such as
in vitro
fertilization, mitochondrial replacement theraphy and genetic
surrogacy. Assisted reproduction in South Africa is regulated by
the
National Health Act 61 of 2002 and the Regulations Relating to
Artificial Fertlilisation of Persons, 2012 as well as the Children’s
Act 38 of 2005 and the regulations thereto.’
[18]
Khampepe
J in a minority judgment in
AB
v Minister of Social Development
[4]
stated
that we are fortunate to live in an era where the effects of
infertility can be ameliorated to a large extent trough assistive
reproductive technologies.
[19]
Assisted reproduction should, however,
be facilitated within the existing statutorily prescribed legal
framework. In the context
of parties opting for surrogacy, this legal
framework is composed of the applicable principles of both the
National Health Act
61 of 2002 and its concomitant regulations, and
the Children’s Act 38 of 2005 with its associated regulations.
The interaction
between these two statutes is highlighted in the
application before me.
[20]
If the initial relief sought by the
applicants,
id est
an order authorising the doctors concerned to perform
in
vitro
fertilisation and
cryopreservation of the blastocysts created by the
in
vitro
fertilisation process, is
considered, the context within the relief is sought is important. The
applicants inform the court that
they intend to utilise the
assistance of a surrogate mother because they are unable to have
children of their own due to the first
applicants’ irreversible
and permanent medical condition.
[21]
The
Children’s Act regulates surrogacy as a mechanism of assisted
reproduction. In order to ensure that there is legal certainty
in the
relationship between the parties involved before the prospective
child is a reality, and to ensure that the rights and obligations
pertaining to the prospective child and the child's legal and
parental status are settled, the legislature requires the
confirmation
of the surrogacy motherhood agreement before a woman
(the surrogate) may be artificially fertilised in the execution of
such an
agreement.
[5]
In the
context of surrogate motherhood, the artificial fertilisation of the
surrogate mother can only be authorised by the court
confirming the
surrogate motherhood agreement after the court has satisfied itself
that the requirements for the confirmation of
such agreement as
prescribed in Chapter 19 of the Children’s Act are met.
[22]
The
second Act that contributes to the legal framework regulating
artificial fertilisation, and specifically
in
vitro
fertilisation and the cryopreservation of blastocysts or embryos, is
the National Health Act, and specifically the Regulations
Relating to
the Artificial Fertilisation of Persons (the Regulations).
[6]
[23]
In the case of gestational surrogacy,
artificial fertilisation entails the ‘bringing together of a
male and female gamete
outside the human body with a view to placing
the product of a union of such gametes in the womb of a female
person’. This
procedure is referred to as
in
vitro
fertilisation (IVF).
[24]
For the purpose of this application,
regulation 10(2)(a) is of specific importance. The regulation
provides as follows:
‘
10. Control
over artificial fertilisation, embryo transfer, storage and
destroying of zygotes and embryos.
(1) No
gamete—
(
a
)
that has not been imported, removed or withdrawn
in terms of the provisions of the Act or these regulations;
(
b
)
from a gamete donor of whom the results of the
tests, analysis or examination referred to in regulation
7 (
e
) to (
g
), as the case may be, are
not available yet; or
(
c
)
from the gamete donor younger than 18 years of age except in the case
of a medical indication, may be
used for artificial fertilisation.
(2) (
a
) A
competent person shall not effect
in vitro fertilisation except
for embryo transfer, to a specific recipient
and then only by the
union of gametes removed or withdrawn from the bodies of—
(i)
such recipient and an individual male gamete donor; or
(ii)
an individual male and an individual female gamete donor;
(
b
) an
embryo, referred to in paragraph (
a
) shall be stored
in a frozen/cryopreserved state in a prescribed institution;
(
c
) a
competent person shall destroy an embryo, which she or he has in
storage as soon as the recipient for whom that embryo
has been
effected conceives or as soon as it is decided not to go ahead with
the embryo transfer into that recipient, unless—
(i)
the competent person decides, and with the informed consent of the
recipient,
to store such embryo for a further period for the purpose
of a subsequent embryo transfer to that recipient; or
(ii)
the recipient consents in writing that the competent person—
(
aa
)
may, with the informed consent of such recipient, use such embryo for
transfer to another specific recipient;
or
(
bb
)
may, with the informed consent of such recipient; use the embryo for
a purpose, other than embryo transfer,
which purpose shall be stated
in that consent;
(
d
)
a competent person shall destroy an embryo that has been unclaimed by
the recipient for a period of 10
years.’
[25]
The prohibition in regulation 10(2)(a)
that a competent person shall not effect
in
vitro fertilisation except for embryo transfer to a specific
recipient,
gives rise to the
question whether the court can authorise the
in
vitro
fertilisation in the absence
of an identified surrogate recipient. The answer to this question
depends on the interpretation of
the phrase ‘specific
recipient’.
[26]
The
amicus
proposes that the phrase ‘specific recipient’ is
susceptibe to a narrow and broad interpretation. According to the
narrow interpretation, the recipient must be exactly named as
precondition for IVF. This would exclude the possibility of creating
embryos prior to confirmation of a surrogate motherhood agreement.
According to the broad interpretation, the recipient must either
be
named, or capable of being named, as precondition for IVF. Since
there are commissioning parents involved who can, at an appropriate
stage in future, name their surrogate mother, this interpretation
would, according to the
amicus,
allow the possibility of creating embryos prior to confirmation of a
surrogate motherhood agreement.
[27]
To interpret regulation 10(2)(a) the
meaning ascribed to the following terms need to be considered: (i)
‘in vitro fertilisation’
is the process of spontaneous
fertilisation of an ovum with a male sperm outside the body in an
authorised institution; (ii) ‘embryo
transfer’ means the
placing of the embryo into the uterus or fallopian tube of the
recipient; (iii) ‘recipient’
means a female person in
whose reproductive organs a male gamete or gametes are to be
introduced by other than natural means’;
or in whose
uterus/womb or fallopian tubes a zygote or embryo is to be placed for
the purpose of human reproduction;(iv) ‘Surrogate’
means
a voluntary recipient of an embryo who will carry such embryo to
birth for contractual parents.
[28]
Professor
Thaldar, the
amicus
before this court, published an article in 2020, titled ‘The
in
Vitro
Embryo and the Law: The Ownership Issue and a Response to
Robinson’.
[7]
In his
opinion, the term ‘recipient’ as defined in regulation 1,
refers to the intended gestational mother, and not
necessarily the
intended legal mother or the genetic mother. He proposed that
regulation 10(2)(a) means the following:
‘
A
competent person (in this context, an embryologist) may create an in
vitro embryo only if the following conditions are met: (a)
the in
vitro embryo is intended for reproduction in general (and not for
scientific research, for instance); (b) there is a specific
recipient
for the in vitro embryo; and (c) the in vitro embryo will be created
from gametes (not from a denucleated egg and the
nucleus of a skin
cell, or from an induced pluripotent stem cell, for instance).
Condition (b) is relevant to our present purposes.
Clearly an in
vitro embryo may be created only if there is a specific woman who
intends to become pregnant with such an embryo.’
(My
emphasis)
He,
however, had a change of heart, and now submits that after careful
consideration, he is of the view that the phrase ‘specific
recipient’ must be broadely interpreted to include a recipient
‘capable of being named’.
[29]
I do not agree with the proposition that
the phrase ‘specific rescipient’ as it is used in
regulation 10(2)(a) is subject
to the broad interpretation proposed
by the
amicus
.
The context within which the phrase is used, militates against any
interpretation other than that the recipient of the embryo
must be
identified before in vitro fertilisation may be effected. Reference
is made in regulation 10(2)(c) to ‘the recipient
for whom that
embryo has been effected’; and in regulation 10(2)(c)(aa) and
(bb) to ‘the informed consent of such recipient’.
In
addition, regulation 18 deals with the ownership of zygotes and
embryos, and regulation 18(2) provides that after artificial
fertilisation the ownership of a zygote or embryo is vested in the
recipient. The recipient thus needs to be identifiable from
the
moment that the embryo comes into being. In this context, the term
‘specific recipient’ requires a narrow interpretation,
and the broader interpretation contended for is not supported in the
Regulation’s language. It cannot be interpreted as proposed
by
the
amicus
in
this application, to refer to a person ‘capable of being
identified.’
[30]
The interaction between the National
Health Act and the Children’s Act, as far as assisted
reproduction by way of gestational
surrogacy is concerned where no
embryos were created in the period before it became apparent that the
woman concerned would not
be able to carry a fetus to full term
pregnancy, is that a surrogate motherhood agreement needs first be
confirmed by the court,
before
in
vitro
fertilisation can commence.
Once the surrogate motherhood agreement is confirmed, the surrogate
mother is identified and she will
be included within the definition
of recipient and more importantly, within the phrase ‘specific
recipient’ as it appears
in regulation 10(2)(a).
[31]
I
accept that the science regarding
in
vitro
fertilisation and embryo transfer developes swiftly, and that
situations can arise that are not catered for in the existing legal
framework. However, this court cannot, in an
ex
parte
application, authorise a competent person as defined in the National
Health Act, who is not a party to the proceedings before the
court,
in the absence of the Minister on whose authority the Regulations
were published, to contravene the Regulations promulgated
in
terms of the Act.
[8]
The court
can also not after being approached on an
ex
parte
basis, grant a declaration of rights that may have a far-reaching
effect, or consider the constitutional validity of the existing
legal
framework.
[32]
Despite Ms. Els-Smit’s expert
opinion that good reason exits for applicants to want to cryopreserve
embryos rather than individual
male and female gametes, the current
legislative framework does not provide that option to applicants who
are bound to choose gestational
surrogacy as their method of assisted
reproduction before a specific recipient of the embryos is
identified. If the applicants
want to challenge the wording, or
constitutional validity of regulation 10(2)(a) they will have to join
the Minister of Health
to such proceedings.
[33]
The relief sought by the applicants thus
falls outside the ambit of the Children’s Act since it has no
bearing on the execution
of a confirmed surrogate motherhood
agreement. The Regulations Relating to the Artificial Fertilisation
of Persons, as it currently
stand, prohibit
in
vitro
fertilisation
except for embryo transfer to a specific recipient. In the absence of
a constitutional challenge to the
Regulations with interested and
affected parties joined to the proceedings, the application stands to
be dismissed.
ORDER
In
the result, the following order is granted:
1.
The application is dismissed.
E
van der Schyff
Judge
of the High Court
Delivered:
This judgment is handed down electronically by uploading it to the
electronic file of this matter on CaseLines.
As a courtesy gesture,
it will be sent to the parties/their legal representatives by email.
For
the applicants: Adv.
R Randall
Instructed
by:
AMA
Law
Amicus
curiae
:
Professor
D Thaldar
Date
of the hearing:
9 September
2022
Date
of judgment: 26
September 2022
[1]
Ex
Parte MS and Others
(48856/2010)
[2014] ZAGPPHC 457 (2 December 2013).
[2]
Ex
Parte Kaf 2
2019
(2) SA 510 (GJ)
[3]
‘
The
right to know one’s own biological origins’, Issue paper
32, Project 140.
[4]
2017
(3) SA 570
(CC) at para [3].
[5]
Ex
Parte MS
(48856/2010)
[2014] ZAGPPHC 457 (2 December 2013).
[6]
GNR. 175 of 2 March 2012
Government
Gazette No.
35099.
[7]
PER / PELJ 2020 (23).
[8]
See
Schierhout
v Minister of Justice
1926 AD 99
at 109, and
Ex
Parte WP (Unreported case) Case No:3167/2019, Western Cape High
Court (24 June 2019) at para [36].
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