Women with HIV still waiting on redress after ‘forced sterilisations’

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Zandile Mkhize (32) says at age 19, she was sterilised without her consent. Picture: Sandile Duma/Spotlight
Zandile Mkhize (32) says at age 19, she was sterilised without her consent. Picture: Sandile Duma/Spotlight

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Nine months after the Commission on Gender Equality released a damning report with dozens of women living with HIV’s testimonies about forced sterilisations allegedly performed on them in public health facilities, the department of health has now moved to implement the commission’s recommendations. But it is a work in progress, Health Minister Zweli Mkhize told MPs in Parliament this week.

The commission released its final report into the matter in February this year. The investigation was started in 2017 and a draft report was sent to the department last year.

Director General in the department of health, Dr Sandile Buthelezi, acknowledged to MPs that since the commission concluded its investigation and handed the department the draft report, officials in the department “failed to present the report for discussion and comment in the department. They also neglected to make comments or raise any issues with the draft report before being made final.”

Buthelezi said the department since took action against the officials.

Spotlight’s attempts over the last month to get more information on the department’s progress on the commission’s recommendations have gone unanswered.

But after MPs raised concerns and questions about the matter, the director general and health minister on Wednesday briefed a joint meeting of Parliament’s portfolio committees on health and women, children and persons with disabilities on its progress.

Health Minister Zweli Mkhize
Health Minister Zweli Mkhize. Picture: GCIS

Buthelezi explained that after the department got the names of the 18 persons whose complaints were investigated by the commission, Mkhize wrote to all the affected hospitals’ CEOs to make available all the hospital records and patient files of the complainants.

“For those 18 complainants,” Buthelezi said, “only nine patient files were located.” The patients’ names in three of the nine files were in the hospital admission register, but the other six complainants could not be located through the hospital admission register or patient files.

Mkhize has since created a task team led by gynaecologist Professor Motshedisi Sebitloane from the University of KwaZulu-Natal.

This task team will among others interrogate the patient files, review the patients’ medical history, check if consent forms had been signed and where there are signed consent forms, they will interrogate whether it was medically reasonable and justified for those patients to be sterilised, Buthelezi said. He added that the task team will also have to identify the clinicians and healthcare workers who took part in the procedures.

Since some patient files were missing, Mkhize on November 13 asked the commission to send the complainants’ affidavits, which the task team will now study further and advise the minister.

On the face of it, it appears the task team will repeat some work already done by the commission in their investigation. The commission also studied affidavits, visited hospitals and attempted to access patient files.

But according to Mkhize, he found that investigations into this have found nothing concrete. Although there were several cases reported, the department was not privy to the affidavits, Mkhize said.

“The commission has done some investigation work with some officials in the department. There was quite a debate on whether there was adequate cooperation and so on, but when I looked at the matter afterwards, I got a sense this was a difficult investigation. Firstly the allegations, the complaints referred to many years ago for which many records are not available and lots of individuals who could have been in the service at that time, may no longer be around as they have either retired, passed away or cannot remember all the details of what happened because it happened so long ago.”

Mkhize said the goal is to find and assess concrete evidence of the allegations and then process and channel it accordingly.

“Let’s try to work on scientific proof so that we know what we are talking about,” he said.

Damning findings

The commission’s report followed a complaint by the organisation Her Rights Initiative (HRI) and the International Community of Women Living with HIV (ICW) against the national and provincial departments of health after allegations of sterilising women living with HIV without their consent.

The report, based on an investigation encompassing 14 sworn affidavits (initially there were complaints from 48 women) and visits to 15 hospitals in Gauteng and KwaZulu-Natal, described the effects of the procedure on women’s mental and physical health, as well as the negative impacts it has had on their relationships with their partners and families.

Among others, the commission found that: “The complainants’ right to dignity, bodily integrity and freedom and security over their bodies, were violated”, “the complainants were subjected to cruel, torturous or inhuman and degrading treatment, and “the medical staff breached their duty of care to the patients”.

Discrimination against people living with HIV by healthcare workers is particularly damaging.
TB/HIV Care spokesperson Alison Best

This week during the briefing, MP Lindy Wilson (DA) labelled it as “the most unholy breach of any human’s right”. “That is a decision that a person is entitled to make by themselves and the fact that anybody could even think they can sterilise somebody without consent is incomprehensible.”

Mkhize stressed to MPs that forced sterilisation is not government policy.

‘Without consent’

Two women Spotlight spoke to say they were sterilised without their consent at public sector hospitals. Both women, Zandile Mkhize and Nomkhosi*, now call for justice.

“I used to cry when I thought about this or talked about it. Now I am just angry,” says Mkhize. “I am angry at the public health system that robbed me of my womanhood, the doctor who took a decision on my body. The value of my life was denied because of my [HIV] status.”

Mkhize (32) has been living with HIV for more than 16 years. She lives with her two children in a three-roomed house in Umlazi. Currently unemployed, she advocates for the rights of women living with HIV.

She told Spotlight that she only learnt that her fallopian tubes had been tied after she gave birth to her second child in 2007. She was 19 at the time.

Zandile Mkhize
Mkhize is among dozens of women whose testimonies prompted the Commission of Gender Commission to investigate. Picture: Sandile Duma/Spotlight

Mkhize says she had a “vague” understanding of what sterilisation meant and assumed the procedure was reversible. She says she vaguely remembers the details of the consent form.

“I went for my 38-week check-up,” Mkhize recalls. “When the doctor saw in my medical records that I was in fact HIV positive and pregnant, he was furious. His tone suddenly changed, and I could feel the judgement and disgust from his expressions … He turned to me and asked me if I wanted to be sterilised, I felt compelled to agree with the procedure.”

The next day, on July 24 2007, she was due to give birth. Mkhize says as the nurses were preparing her for a natural birth, a doctor came and told them to prepare her for a C-section instead.

“Two nurses came and gave me a form to sign. I didn’t know what I was signing. All that was [on] my mind was [a] safe birth and the labour pains that had intensified and the fear of a C-section operation. Nobody explained to me at that point, what I was signing,” Mkhize says.

“I feel socially rejected. Intimate relationships become complex because you have to disclose that you are HIV positive and on top of it all, unable to have children. The operation destroys not only your womanhood, but your entire life. Some women are outcast and called names like ‘barren’ by family members and society. Their rights to obtain land in rural areas also diminish without children. The damage and the cost go beyond the operation.”

She says she often sits and thinks about the children she would have loved to have.

“The pain destroys me inside. Every time I talk about it and at night it comes back, I remember that I am incomplete, empty and half a woman. You have breasts, but who will you feed breastmilk to?” she asks.

Legal framework

Forced sterilisation refers to when an individual is sterilised without their knowledge, coerced into giving consent, or consent is obtained based on false or incomplete information.

The Constitution in section 12 (2) provides for the right to freedom and security that also include bodily integrity and extends to the right to make decisions concerning reproduction and informed consent.

Read: ‘The doctor insulted me, shouted at me’ – Women give chilling accounts of being sterilised without consent

The Sterilisation Act gives effect to these right as enshrined in the Constitution also provides for instances where consent cannot be obtained due to, among others, impaired capacity of the patient. The Act deems forced sterilisation a criminal offense. In addition, the National Health Act also promotes independent decision making and protects patients through, for example, requiring voluntary, informed and written consent before a sterilisation procedure.

The Sterilisation Act also limits the circumstances in which sterilisation may occur. It prohibits sterilisation of persons under the age of 18 and provides for consent that must be given freely and voluntarily and if the person giving it has:

  • Been given a clear explanation and adequate description of the proposed plan of the procedure; and consequences, risks and the reversible or irreversible nature of the sterilisation procedure;

  • Been given advice that the consent may be withdrawn any time before the treatment; and

  • Signed the prescribed consent form.

Another woman, *Nomkhosi, interviewed by Spotlight says the procedure ended her marriage. The 44-year-old unemployed mother of three says she was told the procedure “was [done] to save her life”. She was 31 years old by then.

“The nurses told me that cutting my tubes was to save my life. And I agreed because I also saw some other women in the ward who were told the same thing. I decided not to tell my husband because I fear the shame and judgment. He was always wanting more children and I couldn’t explain why it was not happening,” she says.

“He complained about paying lobola and getting no children in return. In the end, I accepted this defeat and moved on. I have some family support and a strong will. I now know there are many of us who went through this traumatic experience and we deserve some justice,” says Nomkhosi.

Legal and other recourse?

Director of the Women’s Legal Centre, Nasreen Solomons, says the legal recourse available to women in such cases will depend on the outcome they wish to obtain. The Women’s Legal Centre represented HRI and ICW at the time the complaint to the commission was lodged.

“Some of the options they may be presented with are a claim for damages (compensation); they may lodge a complaint directly with the hospital where the procedure took place and against the staff involved (if they have this information); they may lodge a complaint with the Health Ombud; they may lodge a complaint with the Health Professions Council of South Africa (HPCSA) and/or the South African Nursing Council; and they may continue to lodge complaints with the commission for further investigation,” Solomons explains.

We’ve submitted all the evidence and support for the investigation. Now the onus is [on] the department of health to implement the recommendations, but we are confident we will have answers in due time.
Commission on Gender Equality

But, says Solomons, according to provisions in the Prescription Act, claims for damages must be brought within three years of learning of the event that gave rise to the loss (in this case when the forced sterilisation occurred).

“Due to the fact that the 48 complainants (whose accounts formed part of the complaint to the commission) had their claims prescribe, they are unable to bring claims for damages as a result. The complaint therefore requests the intervention of the commission to provide redress in these circumstances, where women can no longer bring a claim for damages,” says Solomons.

When asked about escalating the matter to the health ombud, Minister Mkhize said: “The ombudsman will only become relevant when we have something concrete on whether there’s been a transgression. We will escalate to that level when it becomes necessary.

Commission on Gender Equality recommendations

The recommendations for the health department included scrutinising the informed consent forms provided to patients for signing in the cases to understand whether these, in its current formulation, provide for and protect the principle of informed consent. The department also had to report on the steps it intends to take to eradicate the practice of forced sterilisation and to engage with the complainants to find ways of providing redress.

Buthelezi this week told MPs the department has reviewed the consent forms and experts approved it. Translation into the official languages through the Pan South African National Language Board is already underway, he said. “One standard form will now be used across the country.”

The department is now developing a Standard Operating Procedure that all healthcare workers in public health facilities must follow for sterilisation procedures.

The commission also recommended that the department scrutinise the provisions of the Sterilisation Act and interrogate consent forms for sterilisations to check whether the provisions in the Act provide for and protect the principle of informed consent.

“A legal opinion has been obtained advising on the appropriateness of the Sterilisation Act and provisions relating to consent,” Buthelezi said. “Both the National Health and the Sterilisation Act highlight the importance of consent prior to a procedure being performed.”

Another recommendation was that the department must facilitate dialogue between it and the complainants for them to find ways of redress.

“The minister is finalising a team with an obstetrician, a psychologist, a social worker and a religious leader that will start the engagements. They will offer emotional and spiritual counselling and also ensure that they establish what further remedy is required within the ambits of the law in terms of redress process,” Buthelezi said.

According to him, the commission will then present the department’s report as part of its petition to the SA Law Reform Commission (SALRC) for amendments to the legislation to ensure consent is properly obtained, such as counselling prior to consent, the timing of consent and other compulsory information that must be provided.

The department of health is playing delay tactics and they are not taking us seriously because it has been 12 years since we have been advocating for justice to prevail.
Promise Mthembu, co-founder of Her Rights Initiative

The commission also made recommendations to both the SA Nursing Council (SANC) as the statutory body for nurses, and the Health Professions Council of SA (HPCSA) to investigate the professional conduct and behaviour of the implicated health care practitioners.

HPCSA spokesperson Priscilla Sekhonyana only responded to Spotlight’s questions saying the matter “is currently under investigation”. The SANC did not respond by time of publication.

Why implementing recommendations is important

TB/HIV Care spokesperson Alison Best explains how policies and legislation sanctioning non-consensual treatments including sterilisations violate the right to physical and mental integrity and may constitute torture and ill-treatment.

“Discrimination against people living with HIV by healthcare workers is particularly damaging. It negates the work done by thousands of other healthcare workers to make health services non-judgemental and accessible to people living with HIV so that it is easy to access the life-saving care that they need and that will help curb new HIV infections,” says Best.

“It also negates the work of healthcare workers who support HIV positive and HIV negative mothers to give birth to healthy babies, or otherwise support their sexual and reproductive health needs. For these reasons, and most importantly, because it violates the rights of people living with HIV, discrimination within the health system and by health workers against people living with HIV is unacceptable,” adds Best.

The way forward

Mandla Shabangu, provincial secretary of the nurses’ union Denosa in KZN, says the recommendations in the report relating to nurses’ conduct and ethical behaviour will need a “thorough, fair process”.

“There is no evidence that any of the nurses implicated in the report acted unethically. In cases of medical procedures, such as sterilisations, a medical doctor would have to be in charge. Nurses simply follow instructions and assist the doctors. The circumstances of the cases reported in the report will have to be thoroughly investigated because the nurses implicated might have been carrying out instructions with good intentions. We have [received no] reports from the regulator board (SANC) to further clarify if there is any evidence that nurses are involved in any misconduct. We do however condemn the alleged cases and encourage that justice be served accordingly.”

When Spotlight approached the commission for comment last week, spokesperson Javu Baloyi said the commission “is satisfied with the progress of investigation”.

“We’ve submitted all the evidence and support for the investigation. Now the onus is [on] the department of health to implement the recommendations, but we are confident we will have answers in due time.”

Despite MPs this week insisting on timeframes for the implementation process, none were given. The department, however, undertook to give updates of any significant progress to the committee.

When Spotlight put the department’s new plans to Nomkhosi, she said: “Although the progress is slow, I am hopeful that one day our voices and those that have died without justice will not have died in vain. We feel severely punished for having a disease we did not ask for.”

But not everyone is happy with the progress.

Promise Mthembu, co-founder of Her Rights Initiative, the organisation that lodged the complaints with the commission, says the recommendations and implementation have them concerned.

“The department of health is playing delay tactics and they are not taking us seriously because it has been 12 years since we have been advocating for justice to prevail. Some of our sisters have died in this struggle, but we will not stop. It’s been nine months since the report was released, yet the department has dragged their feet and taken us from pillar to post with no concrete sign of justice,” Mthembu said. “We are not happy with the response presented to Parliament. It undermines us.”

*Nomkhosi is not her real name.

*This article was produced by Spotlight – health journalism in the public interest.


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