Local tuberculosis patients are getting the latest drugs but they still have to struggle with discrimination from families and even health workers.
“Our people need not feel bad about getting TB,” said Deputy President David Mabuza barely a week ago speaking at the launch of a TB prevention initiative in Durban.
A cocktail of potent drugs
But these are hollow words for the many patients facing discrimination.
“It felt like my entire family just dumped me in the hospital to die,” Nomasonto Lubisi from eMalahleni in Mpumalanga after being diagnosed with multi-drug resistant TB (MDR-TB).
Shortly after her diagnosis in December 2017, Lubisi was admitted to a provincial hospital and placed on a treatment regimen consisting of a cocktail of potent drugs.
One of these medicines was the first anti-TB drug developed in almost half a century called bedaquiline.
This makes Lubisi one of just 28 700 people on the entire planet with access to the life-saving drug.
‘My family were scared’
More than two-thirds of these patients live in South Africa, which is one of the number of reasons the country has received widespread praise for its anti-TB policies.
But Lubisi didn’t feel that fortunate: “My family were scared of getting TB from me and made me live in isolation before I went into hospital. I was in there a year and they didn’t visit me, not even once.”
Last year, the South African government became the first to introduce bedaquiline as the first-line option for treatment of patients with resistant forms of TB, which, up until that point, had entailed two years of toxic treatment that causes permanent hearing loss in up to a third of patients.
Bedaquiline is estimated to improve cure rates from 50 to around 80%. Ingrid Schoeman, a TB survivor and dietitian with the local organisation, TB Proof, said that it is not enough to introduce new drugs, as the stigma surrounding the disease prevents many of these patients from going to health facilities and testing for TB.
“Imagine how lonely it must be to be sick and fear losing your friends, your job or relationships because you got sick with TB. TB stigma causes people to avoid seeking healthcare and, without treatment, you cannot be cured,” she said.
Poor attitude of nurses
Around 160 000 people with active TB in South Africa are not on treatment and are spreading the disease in their communities. And even if patients are lucky enough to have supportive families, discrimination from healthcare workers is also rife.
Twenty-four-year-old Siphiwe Buthelezi, also from Mpumalanga is currently being treated for MDR-TB but his treatment has been threatened on more than one occasion due to fear.
“At times, if I couldn’t get my treatment when I was supposed to, I wouldn’t get it because I was afraid that the nurses will shout at me because that’s what happened before,” he said. Buthelezi has “struggled a lot to take my treatment because I do not have a strong support system on my side and then the problem caused by the poor attitudes from nurses to me as a patient”.
Currently undergoing MDR-TB treatment, the miner told Health-e News he has witnessed “people not seeking professional help for TB because of the stigma and discrimination they experience in society”.
He said: “If I didn’t get the support I have from my family I wouldn’t have been able to accept that I have MDR-TB. I probably would have died before I even got diagnosed.” – Health-e News