South Africa: Immigrants report extortion for access to life-saving medication at Gauteng clinics

Immigrants say they are being charged for ARVs, chronic medication and baby immunisations at some Gauteng clinics

  • Immigrants say clinic staff at Spartan, Jeppe and Yeoville clinics in Gauteng are extorting money from them by charging them for antiretrovirals (ARVs), other chronic medicines and baby immunisations.
  • The going rate for a three-month supply of ARVs appears to be R300.
  • The National Department of Health says it is unaware of this but condemns it and requests that anyone with evidence contact the department or law enforcement.

Last week, the Gauteng High Court ordered the government and police to take firm action against “xenophobic vigilantes” blocking immigrants from accessing health services at clinics. This came after months of reportsthat vigilantes were screening out immigrants at Johannesburg clinics. In November, the high court interdicted Operation Dudula from demanding to see IDs of members of the public.

We have subsequently heard from immigrants that clinic and security staff, sometimes in cahoots with Operation Dudula members, are extorting money from them in return for access to state health services.

At some clinics, immigrants are admitted but then never served, or they are told that there is no stock of the medicines they require. The desperate patients are then open to extortion. This takes the form of clandestinely selling them ARVs and chronic medicines.

GroundUp went to various clinics in Gauteng and was told of extortion at all the hotspots where Operation Dudula has been blocking immigrants from healthcare.

Spartan clinic

We received a tip-off that some staff at Spartan clinic are secretly sharing their WhatsApp numbers with immigrants desperate to access healthcare. The staff then offer ARVs, other chronic medicine, baby immunisations, prenatal care for pregnant mothers, and other services for various fees. Those who agree to pay are admitted to the clinic by special appointment.

To protect our sources, we will not be naming patients.

Q, a patient at Spartan since 2019, would collect her ARVs from Spartan clinic every three months. But since October, because she is an immigrant, she has been chased away at the gate.

A fellow immigrant then gave her the WhatsApp number of a nurse, who told her she could get her ARVs if she paid.

“I was desperate and feeling sick from spending weeks without my medications,” says Q.

She made an appointment and was ushered in by the nurse. It surprised her that the same security guards and Operation Dudula members who had previously chased her away, did not stop her this time.

Inside, she paid R200 for a month’s supply of ARVs. She was told it would cost her much more at a private pharmacy.

“The money I earn as a food vendor is very little. My life is now in danger because I need to take my ARVs to survive,” says Q.

K, also an immigrant, shared screenshots of a conversation she had with a staff member at the clinic. ARVs are quoted at R200 for one month and R300 for three months supply. Diabetes medication was offered for R200.

GroundUp also received this price list after we messaged the clinic staff member.

“As immigrants we feel vulnerable, because clinic staff and Operation Dudula members are now taking advantage of our desperate need for chronic medication to make money. They should be stopped,” said K, who has been struggling to collect her ARVs for months.

Jeppe Clinic

When we visited Jeppe clinic last week there was a long queue. It included a few immigrants who had returned after being chased away previously.

P, an immigrant, said she had managed to get inside on Monday and Tuesday last week for the first time since August, but she left empty-handed, with the staff not willing to serve her.

P then bought ARVs for R300 from a woman who has connections with the clinic staff.

This woman, M, says she is helping fellow immigrants who are struggling to get their medication from clinics. We met her with bottles of ARVs in her backpack. She was delivering them to her “clients” in one of Johannesburg’s “dark buildings”.

M has chronic high blood pressure. Previously, she was also chased away from Jeppe clinic by members of Operation Dudula. Then a staff member gave her WhatsApp number and asked her to find other immigrants who need chronic medication.

M says she buys ARVs, PreP pills, diabetes and blood pressure medication from the clinic. The staff member gives her R50 kickback on every R300.

Yeoville clinic

At Yeoville clinic, immigrants told us Operation Dudula and clinic staff now allow them entry if they have valid permits and asylum documents. Meanwhile undocumented immigrants are turned away. Security guards confirmed this to GroundUp.

Z, who sells airtime on the street, has a Malawian passport that has expired. She says she was chased away from the clinic. She said her Zimbabwean neighbour paid R150 to a staff member to have her baby immunised at the clinic. We did not speak to the neighbour.

Ethel Musonza, from an organisation called Zimbabwe Isolated Women in South Africa, said a number of immigrants had contacted them, claiming chronic medication has to be bought from clinic staff at Jeppe, Yeoville and Rosettenville clinics.

“Many people have defaulted on their HIV and AIDS treatment, and some people who were on PreP can no longer access it,” Musonza said. She called for urgent intervention from law enforcement and the Department of Health.

“For us to act, we need information,” says governmentThe Gauteng health department did not respond to our requests for comment.

But spokesperson for the national health department, Foster Mohale, said the department is not aware of any extortion.

“If this is true, it is unlawful, and we condemn it with the strongest terms it deserves,” said Mohale.

“We request anyone with evidence to share it with the department or law enforcement agencies so they can swiftly investigate.”

He said none of the clinics we visited had reported a shortage of any medications.

“⁠The department treats these allegations seriously, but for us to act, we need information,” he said.

South Africa: Asylum seeker in Durban denied medication due to anti-migrant clinic blockades

Anti-migrant groups force asylum seeker with HIV and TB off medication

Ali Burundi,a 58-year-old living in Durban, is facing a life-threatening struggle. Living with both TB and HIV, he’s received his medication consistently from Gateway Clinic at Addington Hospital since 2019.

But for the past two months, he has been unable to access treatment due to blockades by a group known as March-and-March, a collective that describes itself as a “citizen-led movement tackling illegal immigration’s impact on SA”.

“I’ve always been able to go to the clinic and get my medicine. Now, since Dudula started, there’s no more medicine. Every time I go to the clinic, they fight me, and I run away,” says Burundi, referring to Operation Dudula – another anti-migrant group that has also been denying international migrants access to government health facilities.

Originally from Burundi, Ali has lived in South Africa for 20 years as an asylum seeker.  He works as a barber, cutting hair for a living, which means he interacts closely with many people every day.

“It’s harder for me to work because I’m afraid I could infect someone with TB, but I have to work to eat,” he says. “It’s even harder when you are a foreigner in South Africa. I have legal papers, and I was granted asylum, yet I am still being denied access to my medication. That puts me and everyone around me at risk.”

Sharing ARVS

Seeing his desperate situation, one neighbour took pity on Burundi and decided to share her HIV medication with him.

“It broke my heart to hear him cry because he couldn’t get his treatment, as we know how important the medication is,” says the 69-year-old woman who asked not to be named. She explains that she had received a three-month supply of antiretroviral drugs.

“I lost one of my children to HIV years ago, so it brought back painful memories, which is why I cannot let him suffer like that. I pray the government can resolve this soon.”

 

Mexico: Lack of national ID number leaves HIV positive migrants without medication

Migrants with HIV are left without treatment for not having CURP, AC denounces in Tijuana

Baltazar Lujano, a member of Al Otro Lado, urged health authorities to exercise greater discretion.

Foreign migrants are left without access to antiretroviral drugs because they do not have a CURP (Unique Population Registry Code), said Bridget Baltazar Lujano, coordinator of the programme for the LGBTIQ+ community at the organisation Al Otro Lado.
The activist reported that there are cases of people living with HIV who arrive in the city without medication and spend days or weeks without treatment because of this requirement.

There are people who have been living with HIV for years and arrive here without medication, and regaining access to this drug is a real challenge, she said.

Baltazar Lujano urged health authorities to be more flexible, as they do not authorise the delivery of these drugs if people do not have regular immigration status that allows them to have a CURP.

‘Being without medication for a day, two days, three days can have an impact. It is not a medicine that can be obtained in a pharmacy, only the State Secretariat has access to it,’ she said.

He stressed that this problem has worsened since the implementation of IMSS Bienestar, as the digital requirements have excluded people in a context of mobility who have not been able to establish themselves regularly in the entity because the process can take months.

‘There is a very serious violation of people’s rights to access healthcare. They are asking for documents that people do not have and are not looking for a solution,’ he said.

The coordinator of the programme for the LGBTIQ+ community at Al Otro Lado pointed out that migrants from Colombia, Venezuela, Honduras, Nicaragua, Guatemala, El Salvador and Russia are currently arriving in the city.

He mentioned that another problem facing the LGBTIQ+ migrant community is the severe difficulty in finding safe and adequate places to live, as the lack of specialised shelters and discrimination increase their vulnerability.

This problem has always existed, but now it is more complex because people are staying here, he concluded.


Baltazar Lujano, integrante de Al Otro Lado, urgió qué debe haber más criterio por parte de las autoridades sanitarias.

Migrantes extranjeros se quedan sin acceso a medicamentos antirretrovirales por no contar con CURP, expuso la coordinadora del programa para la comunidad LGBTIQ+ de la organización Al Otro Lado, Bridget Baltazar Lujano.

La activista acusó que hay casos de personas viviendo con VIH que llegan sin medicamento a la ciudad y pasan días o semanas sin tratamiento por la falta de este requisito.

Hay personas que llegan viviendo con VIH por años y llegan aquí sin medicamento, y volver a acceder a este fármaco es todo un retoexpresó.

Baltazar Lujano, urgió qué debe haber más criterio por parte de las autoridades sanitarias, que no autorizan la entrega de estos medicamentos si no cuentan con un estatus migratorio regular que les permita tener el CURP.

“Estar sin medicamento un día, dos días, tres días puede afectar. No es un medicamento que se pueda conseguir en una farmacia, solo la Secretaría del Estado tiene acceso”, comentó.

Recalcó que este problema se agravó tras la implementación de IMSS Bienestar, ya que los requisitos digitales han excluido a las personas en contexto de movilidad que no han logrado establecerse regularmente en la entidad debido a que el proceso puede tomar meses.

“Hay una falta muy grande a los derechos de las personas de poder acceder a la salud. Están pidiendo documentos que las personas no tienen y no están buscando una solución”, manifestó.

La coordinadora del programa para la comunidad LGBTIQ+ de Al Otro Lado, precisó que actualmente a la ciudad están llegando migrantes provenientes de Colombia, Venezuela, Honduras, Nicaragua, Guatemala, El Salvador y Rusia.

Mencionó que otro problema que enfrenta la comunidad LGBTIQ+ migrante, son severas dificultades para encontrar espacios seguros y adecuados donde vivir, ya que la falta de albergues especializados y la discriminación elevan la vulnerabilidad.

“Esta problemática siempre ha existido, pero ahora es más compleja porque las personas se están quedando aquí” concluyó.

Russia: 21 foreigners deported due to their HIV status in the Ryazan region

Translated with Google translate. Scroll down for original article in Russian

In the Ryazan region, the number of HIV carriers, which was sexually transmitted, has increased. The statistics were shared by the head of Rospotrebnadzor for the Ryazan region Larisa Sarayeva in an interview with GTRK “Oka”.

As of October 1, a total of 6,317 HIV carriers have been registered in the region. According to Larisa Saraeva, about 200 new cases or 20 new cases per 100,000 population are recorded every year. 90% of carriers receive therapy with antiretroviral drugs.

68% of all HIV cases are observed in the demographic range from 20 to 39 years. Indicators are above average in Pronsky, Zakharovsky, Skopinsky, Miloslavsky, Mikhailovsky and Starozhilovsky districts and Ryazan.

In addition, Rospotrebnadzor deported 21 foreigners in 2025 in connection with HIV detected in them.


В Рязанской области депортировали 21 иностранца из-за ВИЧ

В Рязанской области выросло число носителей ВИЧ, который был передан половым путём. Статистикой поделилась глава Роспотребнадзора по Рязанской области Лариса Сараева в интервью ГТРК «Ока».

По данным на 1 октября, всего в регионе зарегистрировано 6317 носителей ВИЧ. По словам Ларисы Сараевой, каждый год фиксируют около 200 новых случаев или 20 новых случаев на 100 тысяч населения. 90% носителей получают терапию антиретровирусными препаратами.

68% всех случаев ВИЧ наблюдается в демографическом диапазоне от 20 до 39 лет. Показатели выше средних в Пронский, Захаровский, Скопинский, Милославский, Михайловский и Старожиловский районы и Рязани.

Кроме того, Роспотребнадзор в 2025 году депортировал 21 иностранца в связи с выявленным у них ВИЧ.

Peru: Ombudsman urges national authorities to guarantee full health access for all people living with HIV

Translated with Google Translate – For original article in Spanish, please scroll down

Ombudsman urges the Peruvian State to guarantee access to health services for people living with HIV in Peru

  • On World AIDS Day, the importance of health education is recalled to prevent the disease, ensure timely diagnosis and access to antiretroviral treatments (ARTs); and to avoid any form of discrimination and stigma.

In commemorating World AIDS Day, the Ombudsman’s Office highlights the importance of the Peruvian State ensuring adequate health care to more than one hundred thousand citizens who would currently live with the HIV virus in our country, with a human rights approach that guarantees access to antiretroviral drugs and eliminates any form of stigma or discrimination; as well, to ensure the implementation of public health policies at all levels of government.

According to global figures, it is estimated that as of February of this year the number of HIV infections in Peru was around 110,000 people, which includes highly vulnerable populations such as sex workers, population deprived of liberty, indigenous people and migrants, among others, who face greater obstacles to access timely and quality health services.

Faced with this, the Ombudsman’s Office urges national authorities, such as the Ministry of Health and EsSalud, as well as regional health directorates or managements, to guarantee the continuous supply of antiretroviral treatments and diagnostic tests. As part of the requirements for health organizations, it is also requested to implement effective mechanisms aimed at avoiding any form of discrimination in health services, as well as ensuring the timely affiliation to Comprehensive Health Insurance (SIS) of all people who require it, without unjustified barriers.

It should be noted that the development of each of these actions must be based on a human rights approach that recognizes that all people, without distinction, have the right to access to timely, quality and discrimination-free health services. In this sense, the Ombudsman’s Office develops permanent supervisory actions that aim to identify barriers, delays and shortages of antiretrovirals, as well as to monitor that there are no discriminatory practices in health services and promote immediate corrections in the face of any violation of rights.

These actions, however, must be articulated with other sectors such as the Ministry of Education and educational management units at the national level to develop constant educational activities as a preventive measure to reduce the transmission of the virus among the population.

The Ombudsman’s Office reaffirms its commitment to the protection of the right to health and equality of all people living with HIV in Peru, we renew our vigilant work so that each policy or health service contributes to a more humane, equitable and respectful national response of the dignity of people. The protection of people living with HIV cannot depend on the situation, but on sustained public policies, strengthened health leadership and affirmative actions aimed at the most exposed populations.


Defensoría del Pueblo exhorta al Estado peruano a garantizar acceso a servicios de salud a las personas que viven con VIH en el Perú

  • En el Día Mundial de la Lucha contra el SIDA, se recuerda la importancia de la educación en salud para prevenir la enfermedad, garantizar el diagnóstico oportuno y el acceso a tratamientos antirretrovirales (TAR); asimismo, evitar cualquier forma de discriminación y estigma.

Al conmemorarse el Día Mundial de la Lucha contra el SIDA, la Defensoría del Pueblo destaca la importancia de que el Estado Peruano asegure una atención en salud adecuada a más de cien mil ciudadanos que vivirían actualmente con el virus del VIH en nuestro país, con un enfoque de derechos humanos que garantice el acceso a medicamentos antiretrovirales y se elimine cualquier forma de estigma o discriminación; así también, que asegure la implementación de las políticas públicas sanitarias en todos los niveles de gobierno.

De acuerdo a cifras globales, se estima que a febrero de este año la cifra de contagios por VIH en el Perú era de alrededor de 110 000 personas, que comprende a poblaciones altamente vulnerables como trabajadores sexuales, población privada de la libertad, personas indígenas y migrantes, entre otros, quienes enfrentan mayores obstáculos para acceder a servicios de salud oportunos y de calidad.

Frente a ello, la Defensoría del Pueblo exhorta a las autoridades nacionales, como el Ministerio de Salud y EsSalud, así como a las direcciones o gerencias regionales de salud, a garantizar el abastecimiento continuo de tratamientos antirretrovirales y pruebas de diagnóstico. Como parte de los requerimientos a los organismos de salud, se pide también implementar mecanismos efectivos dirigidos a evitar cualquier forma de discriminación en los servicios de salud, así como asegurar la afiliación oportuna al Seguro Integral de Salud (SIS) de todas las personas que lo requieran, sin barreras injustificadas.

Cabe precisar que el desarrollo de cada una de estas acciones debe sustentarse en un enfoque de derechos humanos que reconozca que todas las personas, sin distinción, tienen derecho a acceder a servicios de salud oportunos, de calidad y libres de discriminación. En ese sentido, la Defensoría del Pueblo desarrolla acciones de supervisión permanentes que tienen como objetivo identificar barreras, retrasos y desabastecimiento de antirretrovirales, así como vigilar que no existan prácticas discriminatorias en servicios de salud y promover correcciones inmediatas ante cualquier vulneración de derechos.

Estas acciones, sin embargo, deben ser articuladas con otros sectores como el Ministerio de Educación y las unidades de gestión educativas a nivel nacional para desarrollar actividades educativas constantes como medida preventiva para disminuir los transmisión del virus entre la población.

La Defensoría del Pueblo reafirma su compromiso con la protección del derecho a la salud y la igualdad de todas las personas que viven con VIH en el Perú, renovamos nuestra labor vigilante para que cada política o servicio sanitario contribuya a una respuesta nacional más humana, equitativa y respetuosa de la dignidad de las personas. La protección de las personas que viven con VIH no puede depender de la coyuntura, sino de políticas públicas sostenidas, rectoría sanitaria fortalecida y acciones afirmativas dirigidas a las poblaciones más expuestas.

Colombia: Constitutional Court affirms right to continuous HIV care for vulnerable migrants

Translated with Google translate – Scroll down for original article in Spanish

Court demands comprehensive and barrier-free care for migrants on the street with HIV

2025 Ruling T-415 requires the elimination of barriers and guaranteeing health care for homeless migrants with HIV and comorbidities.

The Constitutional Court ordered to guarantee comprehensive, continuous and unadministrative care to homeless migrants who face HIV, associated diseases, mental health and drug dependence. In Judgment T-415 of 2025, the Third Review Chamber concluded that responsible authorities violated fundamental rights by not managing in a timely manner the services ordered by specialists for a Venezuelan citizen in a situation of extreme vulnerability. The ruling establishes a reinforced standard of protection and details immediate obligations for the competent entities.

Constitutional Court sets a reinforced standard of health protection

The sentence originates from the guardianship presented by “Manuela” in favor of Josué, a homeless Venezuelan migrant diagnosed with HIV, tuberculosis, hepatitis C, seborrheic dermatitis, severe mental health effects and drug addiction problems.

The Third Review Chamber, composed of Magistrate Lina Marcela Escobar Martínez (rapporteur), and Magistrates Vladimir Fernández Andrade and Jorge Enrique Ibáñez Najar, determined that the entities involved violated the patient’s rights to life, equality, human dignity, health and social security.

The ruling recalls that article 100 of the Constitution guarantees foreign people the same civil rights as Colombian citizens, while article 4 establishes their duty to comply with the Constitution and the laws. In the face of extreme vulnerability scenarios, state attention must be guided by the principles of human rights, intersectional approach, pro persona, solidarity and human dignity.

Diagnosis and therapeutic continuity: essential pillars of the right to health

The Court reiterated that the right to diagnosis is an integral part of the fundamental right to health. For this right to be guaranteed, three essential components must be met:

  1. Adequate identification of the patient’s condition,
  2. Evaluation and follow-up by the specialist,
  3. Prescription and continuity of treatment.

In the case analyzed, the lack of timely authorizations prevented the continuity of specialized services ordered by treating doctors, which deepened the vulnerability of the patient. The corporation recalled that opportunity and continuity are mandatory principles of the health service, and that administrative barriers cannot be interposed when the life or integrity of the patient is compromised.

Mental health and drug dependence: non-negotiable components of care

The Court pointed out that mental health is an integral part of the fundamental right to health, so Josué had the right to access the psychiatric and toxicology care ordered by his attending physician.

Likewise, he specified that people in a street situation, due to low therapeutic adherence and the complexity of their needs, must receive a’rmative actions that facilitate access to rehabilitation treatments, with or without hospitalization, according to the medical order.

These a’rmative actions as indicated in the legal glossary included in the bulletin – exist to level the conditions of those who have faced historical barriers that prevent them from exercising their rights on equal terms.

Institutional shortcomings: violation of rights due to lack of timely management

The Third Chamber concluded that the entities responsible for the case were unaware of the condition of subject of special constitutional protection of the patient by not managing in a timely manner all the services ordered by the specialists.

The Court stressed that Joshua’s situation represented exceptional and borderline circumstances, requiring an intersectional approach and a comprehensive understanding based on the pro-person, solidarity and human dignity principles.

Denying or delaying services prescribed by dealing professionals, the corporation said, contradicts the constitutional jurisprudence that protects people with multiple conditions of vulnerability.

Orders and measures of immediate compliance

Judgment T-415 of 2025 establishes precise orders to ensure the patient’s effective access to services:

1. Entities responsible for social care

The Court ordered a new classification interview, ensuring that the patient is not excluded from the “street dweller” category, a condition that determines reinforced protection measures and guarantees access to differentiated care routes.

2. Territorial health authorities

The ruling instructed the competent entity to immediately and comprehensively authorize all the services ordered by the specialists regarding their diagnoses related to mental health and drug dependence.
This includes evaluations, therapeutic interventions, prescriptions and follow-ups defined by the treating clinical team.

All these procedures must be carried out without administrative barriers, in accordance with the principles of opportunity and continuity that govern the fundamental right to health.

New obligations for health authorities after Judgment T-415

The ruling of the Constitutional Court, sets guidelines that must be observed by the entities in charge of caring for people in extreme vulnerability:

  • Express recognition of homeless migrants as a population of special constitutional protection.
  • Effective guarantee of the right to diagnosis, specialized assessment and continuity of treatment.
  • Elimination of administrative barriers that prevent the attention ordered by specialists.
  • Application of affirmative actions to facilitate therapeutic adherence and access to comprehensive treatment in mental health and drug dependence.
  • Institutional responses articulated between social and health sectors to avoid interruptions in care.

This precedent reinforces the State’s responsibilities regarding the protection of people with multiple vulnerabilities, especially when they are at risk of life and require urgent intervention.


Corte exige atención integral y sin barreras para migrantes en calle con VIH

Fallo T-415 de 2025 obliga a eliminar barreras y garantizar atención en salud para migrantes habitantes de calle con VIH y comorbilidades.

La Corte Constitucional ordenó garantizar atención integral, continua y sin barreras administrativas a personas migrantes en habitanza de calle que enfrentan VIH, enfermedades asociadas, afectaciones en su salud mental y farmacodependencia. En la Sentencia T-415 de 2025, la Sala Tercera de Revisión concluyó que autoridades responsables vulneraron derechos fundamentales al no gestionar de manera oportuna los servicios ordenados por especialistas para un ciudadano venezolano en situación de extrema vulnerabilidad. El fallo fija un estándar reforzado de protección y detalla obligaciones inmediatas para las entidades competentes.

Corte Constitucional fija un estándar reforzado de protección sanitaria

La sentencia se origina en la tutela presentada por “Manuela” en favor de Josué, un migrante venezolano habitante de calle diagnosticado con VIH, tuberculosis, hepatitis C, dermatitis seborreica, afectaciones severas en su salud mental y problemas de farmacodependencia.

La Sala Tercera de Revisión, integrada por la magistrada Lina Marcela Escobar Martínez (ponente), y los magistrados Vladimir Fernández Andrade y Jorge Enrique Ibáñez Najar, determinó que las entidades involucradas vulneraron los derechos a la vida, igualdad, dignidad humana, salud y seguridad social del paciente.

El fallo recuerda que el artículo 100 de la Constitución garantiza a las personas extranjeras los mismos derechos civiles que a los ciudadanos colombianos, mientras que el artículo 4 establece su deber de acatar la Constitución y las leyes. Ante escenarios de vulnerabilidad extrema, la atención estatal debe guiarse por los principios de derechos humanos, enfoque interseccional, pro persona, solidaridad y dignidad humana.

Diagnóstico y continuidad terapéutica: pilares esenciales del derecho a la salud

La Corte reiteró que el derecho al diagnóstico es parte integral del derecho fundamental a la salud. Para que este derecho sea garantizado, deben cumplirse tres componentes esenciales:

1. Identificación adecuada de la condición del paciente,

2. Valoración y seguimiento por parte del especialista,

3. Prescripción y continuidad del tratamiento.

En el caso analizado, la falta de autorizaciones oportunas impidió la continuidad de servicios especializados ordenados por médicos tratantes, lo que profundizó la vulnerabilidad del paciente. La corporación recordó que la oportunidad y la continuidad son principios obligatorios del servicio de salud, y que las barreras administrativas no pueden interponerse cuando está comprometida la vida o la integridad del paciente.

Salud mental y farmacodependencia: componentes innegociables de la atención

La Corte señaló que la salud mental es una parte integrante del derecho fundamental a la salud, por lo que Josué tenía derecho a acceder a las atenciones por psiquiatría y toxicología ordenadas por su médico tratante.

Así mismo, precisó que las personas en situación de calle, debido a la baja adherencia terapéutica y a la complejidad de sus necesidades, deben recibir acciones afirmativas que faciliten el acceso a tratamientos de rehabilitación, con o sin internado, según la orden médica.

Estas acciones afirmativas según lo indicado en el glosario jurídico incluido en el boletín— existen para nivelar condiciones de quienes han enfrentado barreras históricas que les impiden ejercer sus derechos en igualdad de condiciones.

Falencias institucionales: vulneración de derechos por falta de gestión oportuna

La Sala Tercera concluyó que las entidades responsables del caso desconocieron la condición de sujeto de especial protección constitucional del paciente al no gestionar de manera oportuna la totalidad de los servicios ordenados por los especialistas.

La Corte destacó que la situación de Josué representaba circunstancias excepcionales y límite, exigiendo un enfoque interseccional y una comprensión integral basada en los principios propersona, solidaridad y dignidad humana.

Negar o retrasar servicios prescritos por profesionales tratantes, indicó la corporación, contradice la jurisprudencia constitucional que protege a personas con múltiples condiciones de vulnerabilidad.

Órdenes y medidas de cumplimiento inmediato

La Sentencia T-415 de 2025 establece órdenes precisas para garantizar el acceso efectivo del paciente a los servicios:

1. Entidades responsables de atención social

La Corte ordenó realizar una nueva entrevista de clasificación, asegurando que el paciente no sea excluido de la categoría “habitante de calle”, condición que determina medidas de protección reforzada y garantiza el acceso a rutas de atención diferenciadas.

2. Autoridades territoriales de salud

El fallo instruyó a la entidad competente a autorizar de manera inmediata e integral todos los servicios ordenados por los especialistas respecto de sus diagnósticos relacionados con salud mental y farmacodependencia.
Esto incluye valoraciones, intervenciones terapéuticas, prescripciones y seguimientos definidos por el equipo clínico tratante.

Todas estas gestiones deben adelantarse sin barreras administrativas, conforme a los principios de oportunidad y continuidad que rigen el derecho fundamental a la salud.

Nuevas obligaciones para autoridades de salud tras la Sentencia T-415

El pronunciamiento de la Corte Constitucional, fija lineamientos que deberán observar las entidades encargadas de atender a personas en extrema vulnerabilidad:

  • Reconocimiento expreso de los migrantes habitantes de calle como población de especial protección constitucional.
  • Garantía efectiva del derecho al diagnóstico, valoración especializada y continuidad del tratamiento.
  • Eliminación de barreras administrativas que impidan la atención ordenada por especialistas.
  • Aplicación de acciones afirmativas para facilitar adherencia terapéutica y acceso a tratamiento integral en salud mental y farmacodependencia.
  • Respuestas institucionales articuladas entre sectores sociales y sanitarios para evitar interrupciones en la atención.

Este precedente refuerza las responsabilidades del Estado respecto a la protección de personas con múltiples vulnerabilidades, especialmente cuando se encuentran en riesgo vital y requieren intervenciones urgentes.

 

 

Ireland: HIV stigma persists despite progress as stories of migrant women reveal gaps

‘It hits us harder’: immigrant woman shares stigma of living with HIV

HIV Ireland’s Glow Red Campaign aims to raise awareness of the disease and tackle misconceptions
‘With all the racism going on, we are just afraid to come out,” says Marina, one of five HIV activists from migrant communities who feature in HIV Ireland’s Glow Red Campaign. All are masked to protect their identities.
“Because of stigma and discrimination, and as a woman in a foreign country, you don’t want to be seen as a woman living with HIV,” she says.
“I think, because of all the things happening here in Ireland, the far right being against migrants — and definitely we stand out because of our skin — they would attack us.”
The campaign, Glow Red – Let’s Get to Zero HIV Stigma, features advocate Rebecca Tallon De Havilland alongside HIV activists and migrant women, some living with HIV, others not, to show how stigma persists in Ireland.
“This year’s accompanying banner message on the photo is ‘HIV doesn’t discriminate. Neither should we. Unmask stigma’,” says Stephen O’Hare, director of HIV Ireland. He said the new campaign highlights that HIV stigma is a barrier for women as well as men. “It hits women harder, and particularly women of colour who can face intersectional barriers and discrimination such as HIV stigma, misogyny, sexism and racism.”
There were 989 cases diagnosed in Ireland in 2024; 74% were among people born outside Ireland, with 23% born in Ireland and 3% unknown. A new report from the Health Protection Surveillance Centre said: “Since 2022, there has been a steady increase in rates among women while rates among men have remained stable.”
Professor Fiona Lyons, national clinical lead at the HSE Sexual Health Programme, said research has found late diagnosis is often related to fear of diagnosis and stigma.
“Being diagnosed late means a person may have had HIV for some time before they are diagnosed, and it has already started to damage their immune system,” she said.
Marina (not her real name), who arrived in Ireland from Malawi nearly two decades ago to study, was diagnosed in 2018 when she was in the late stages of the disease. In the last five years, she has experienced a change in attitudes in Ireland and repeated racism, mostly while travelling on public transport.
​She now finds herself adjusting her behaviour to avoid confrontation. “Before five years ago, we were comfortable, we were OK. I have a partner, he’s Irish, and I felt at home. But nowadays, when we walk, we’re watching, you know, who’s coming behind. What if they just beat you up for no reason? On the Luas or the train, we might even give up our seats to people just because you don’t want anyone to say something to you,” she says.
She explains that her late-stage diagnosis came after months of worsening symptoms and missed chances.
“When I was diagnosed in 2018, I was just finishing my course of four years, and the last month was very hard, because I didn’t know I was living with HIV.”
The night before her last exam she realised something was seriously wrong. “I read the whole night, but in the morning, everything was gone.”
Despite volunteering at a sexual health service, GOSHH, she was blindsided by her diagnosis.
“I was sitting at the reception every day, ushering people to come in and test. And I never did, not even once, think about testing,” she adds.
“Not everyone knows how they got HIV. I don’t know how I got it.”
When she finally went to her GP reporting exhaustion, flu-like symptoms and her inability to retain information, blood tests were done, but not for HIV.
Instead, an abnormally high platelet count prompted an oncology referral to rule out cancer. Eight months later, with no clear diagnosis and her platelet levels now normal, she sat in front of a Sudanese doctor who was preparing to discharge her from the service.
She protested that she wasn’t fine. “I feel like I’ve got the flu all the time, I’m always tired nowadays, also I feel like my neck is carrying a mountain,” she explained to the doctor.
Listening intently, the doctor asked whether anyone had ever checked her CD4 count — a key HIV marker. Looking back, Marina believes that the doctor recognised the signs instantly.
Two weeks later, she was told she was HIV-positive. Today, she says her medical treatment has completely reversed those debilitating symptoms. “All of a sudden, everything changed, and I started becoming OK.”
Mr O’Hare explains that 50pc of first-time diagnoses in 2023 were among the heterosexual population, a shift from the traditional perception that HIV primarily affects gay men.
“The total number of people living with HIV, pre-pandemic in Ireland, was estimated to be about 8,000, but since the pandemic, and since the change in demographics, including inward migration and the war in Ukraine, you’re probably seeing in excess of 10,000 people now in Ireland with HIV.”
He is calling for Ireland to follow the UK in rolling out opt-out HIV testing in emergency departments.
“They’ve had great success in identifying cases that were unknown. Ireland could follow suit,” he adds.​

South Africa: Court declares anti-migrant actions against health and education access illegal

Anti-migrant group ordered to stop blocking foreigners from South African healthcare

A South African court has ordered an anti-migrant group to stop blocking foreign nationals from accessing public health facilities and schools, saying such actions are illegal.

Operation Dudula has been picketing hospitals and clinics in Gauteng and KwaZulu-Natal provinces, checking identity cards and stopping anyone who is not South African from entering. This has since extended to schools.

But the high court in Johannesburg has ordered the group to stop “intimidating, harassing [or] interfering with access” to these facilities, following a case brought by rights groups.

South Africa is home to about 2.4 million migrants, just less than 4% of the population, according to official figures.

Most come from neighbouring countries such as Lesotho, Zimbabwe and Mozambique, which have a history of providing migrant labour to their wealthy neighbour.

Xenophobia has long been an issue in South Africa, which has been accompanied by occasional outbursts of deadly violence, and anti-migrant sentiment has become a key political talking-point.

Judge Leicester Adams, handing down judgment on Tuesday, also barred Operation Dudula from making statements that can be construed as hate speech, “unlawfully evicting foreign nationals from their homes… [or] from their trading stalls” and instigating others to do so.

“Dudula” means to remove something by force in the Zulu language.

He also barred law enforcement from conducting “warrant-less searches” in foreigners’ private spaces and said they must have “reasonable suspicion” that a person was in the country unlawfully before asking them to identify themselves.

South African police came under scrutiny after human rights organisations accused them of failing to act against Operation Dudula or protect the public from their unlawful conduct.

Several Operation Dudula members were arrested for blocking the entrances of public health facilities in August. They were later released with a warning.

The organisation says it is disappointed by the ruling and intends to appeal against it, according to South African online publication News24.

Kopanang Africa Against Xenophobia, one of the organisations that took the case to court, said the “judgment provides critical protection for those targeted by xenophobic attacks”.

“In a country founded on the rejection of apartheid, we cannot allow ourselves to be subjected to the xenophobic hate promoted by Operation Dudula,” the human rights organisation said in a statement.

Kopanang said there would be proactive monitoring at schools and clinics to ensure compliance with the order and that it would hold the police accountable for enforcing it.

“Should the police fail in their duty to enforce the order… we are prepared to report their inaction to formal oversight bodies,” the organisation told the BBC.

South Africa’s Health Minister Dr Aaron Motsoaledi said the ruling “was to be expected” as it echoed the government’s stance that no-one should be denied access to healthcare, irrespective of their legal status.

Dr Motsoaledi met Operation Dudula leaders in August, at the height of their protests at health facilities, and criticised their methods.

“I told them [at the time] that whatever concerns they have, some of which might be legitimate by the way, they are [using] the wrong method,” he told local broadcaster 702 on Tuesday.

One of the demands the group had for the minister when they met was that anyone without documentation be turned away at healthcare facilities but Dr Motsoaledi said this would be difficult as 11% of South Africans do not have national ID cards.

The minister also criticised South Africa’s neighbours for not doing more to help reduce the pressure on the country’s overburdened healthcare system, suggesting this was being worsened by the influx of migrants.

“It is South Africa which is suffering, not them. In fact, many of them are relieved,” he said.

European studies reveal systemic gaps in HIV care for migrants

EACS 2025: Are Europe’s migrants acquiring HIV after arrival?

More than 60% of HIV diagnoses among migrants in Switzerland occur after arrival, with some groups waiting up to 6 years before detection; findings that expose significant gaps in the country’s prevention and screening strategies.

A new analysis of the Swiss HIV Cohort Study shows that among 1713 migrants diagnosed between 2010 and 2024, 62.1% were diagnosed post-migration. This challenges the longstanding assumption that most infections occur before arrival from high-prevalence regions and aligns with another recent analysis estimating that about 30% of migrants acquire HIV after migration, underscoring ongoing risk in host countries despite prevention programs.

Presenting the 15‑year analysis at the European AIDS Clinical Society (EACS) 2025 Annual Meeting, PhD researcher Jessy J. Duran Ramirez of University Hospital Zurich, Zurich, reported that migrants now account for 49% of new HIV diagnoses in Switzerland — a share that has risen steadily even as rates in other European populations stabilize or decline.

“Despite the overall decrease and stagnation in new HIV diagnoses, migrants remain disproportionately affected,” Duran Ramirez said.

Delayed Diagnosis Patterns Emerge

Among the study’s key findings were notable diagnostic delays across migrant populations. Compared with 5 years for men who have sex with men (MSM) and just 2 years for female heterosexuals, male heterosexuals from migrant populations wait a median of 6 years from immigration to HIV diagnosis.

Key Statistics from 3490 participants (2010-2024):

  • 1777 Swiss nationals; 1713 migrants
  • 62.1% of migrant diagnoses occurred post-migration
  • Median age at diagnosis: 38 years (migrants) vs 44 years (Swiss nationals)
  • CD4 count at diagnosis: 339 cells/µL (migrants) vs 404 cells/µL (Swiss nationals)

Migrants from Asia experienced the longest delays overall, with a median of 12 years from immigration to diagnosis.

These delays resulted in significantly lower CD4 counts at diagnosis compared with Swiss nationals, indicating more advanced disease progression.

The demographic profile of post-migration diagnoses also differed markedly from that of Swiss nationals. Women accounted for 27% of migrant diagnoses vs only 11% among Swiss nationals, while MSM represented 43% of migrant cases compared with 63% of Swiss cases.

Cultural and Structural Barriers

Jürgen Rockstroh, MD, head of the HIV outpatient clinic at the University of Bonn, Bonn, Germany, identified multiple obstacles preventing effective screening among migrant populations across Europe.

“People who are migrating to Europe, or are refugees, have difficulties in accessing the healthcare system because there are language barriers, there are insurance and cost coverage barriers,” he said. “The question is, how can you reach these populations?”

He pointed to successful European models like Malta’s mobile health units, which embed HIV testing within general healthcare services, and Athens’ targeted health centers designed specifically for migrants and refugees, where peers guide others from their community to access care.

“African women, for example, are not going to go to a more gay-dominated testing space. They just don’t feel comfortable there. I think we need more targeted, market-specific checkpoints,” he explained.

Promising Innovative Approaches

The PARTAGE project in France demonstrates one effective strategy for reaching migrant men, a traditionally difficult population to engage in healthcare. By offering health checkups to expectant fathers during their partner’s pregnancy, the program achieved HIV screening rates of 95%-96% across all groups.

PARTAGE Project Results (1347 expectant fathers):

  • 63% held immigrant status; 8% without health coverage
  • HIV screening achieved in 95%-96% across all groups
  • Medical diagnoses: 18% (all participants), 22% (immigrants), and 41% (immigrants without coverage)
  • Healthcare referrals: 17% (all), 20% (immigrants), and 41% (immigrants without coverage)
  • Social support referrals: 11% (all), 17% (immigrants), and 72% (immigrants without coverage)
  • Vaccination updates: 44% (all), 52% (immigrants), and 73% (immigrants without coverage)

Pauline Penot, MD, from Centre Hospitalier André Grégoire, Montreuil, France, who led the PARTAGE study, found the intervention particularly effective among disadvantaged migrants, leading to (any) medical diagnoses and healthcare referrals in 41% of participants without health coverage.

“This is the first structured health intervention to address adult men’s health by using the symbolic event of expecting a child,” Pinot said. “It showed greater attendance, and more effects were observed among disadvantaged migrants.”

Pinot noted that migrants often arrive in Europe healthier than native populations, but their health deteriorates faster, especially among those from poorer regions. She suggested that scaling the PARTAGE model across France and other European countries could help reduce social and gender health inequalities.

Policy Implications

The Swiss data underscores an urgent need for culturally sensitive, accessible screening programs that can identify HIV infections earlier in migrant populations across Europe. With roughly one third of post-migration diagnoses occurring within the first year of arrival — a period of particular vulnerability — the window for intervention remains narrow but critical.

For Duran Ramirez, the next phase of research will focus on determining whether these post-migration diagnoses represent infections acquired after arrival or pre-existing infections that went undetected.

“Understanding the timing of HIV acquisition and diagnosis in migrant populations is essential to designing prevention strategies that reach them earlier,” she said.

The findings suggest that current European prevention infrastructure, while effective for established populations, requires significant adaptation to address the complex healthcare needs of its increasingly diverse migrant communities.

Duran Ramirez reported receiving research grants or fellowships to her institution from Gilead Sciences Switzerland Sàrl and ViiV Healthcare that were unrelated to this work. Rockstroh reported receiving honoraria for educational talks for ViiV Healthcare, Merck, and Gilead Sciences. Penot reported having no relevant financial relationships.

Russia: From March 2026, migrants will be required to undergo screening for hepatitis

New medical requirements are being established in Russia for foreign citizens planning to engage in labor activity. The Ministry of Health of Russia announced that starting from March 1, 2026, migrants will be required to undergo screening for acute hepatitis, as well as chronic viral hepatitis types B and C.

According to the newspaper Vedomosti, this requirement will apply to all foreign citizens entering the territory of Russia for employment, as well as to stateless persons, asylum seekers, and those applying for temporary refuge in the country.

The draft amendments to the procedure for conducting medical examinations have already been posted on the federal portal of regulatory legal acts. The explanatory note states that these changes are necessary “to improve the organizational foundations and the procedure for conducting medical examinations.”

According to the new regulation, every migrant who wishes to obtain a work permit, temporary residence permit, or permanent residence permit in Russia will have to provide a medical certificate. This rule is based on the law governing the legal status of foreign citizens in the Russian Federation.

At present, migrants are mainly tested for the presence of narcotic substances and diseases that pose a danger to others, including HIV, tuberculosis, syphilis, and leprosy. The new requirements provide for broader health monitoring.

According to officials, these measures are aimed not only at protecting public health but also at expanding opportunities for early detection and treatment of illnesses among migrants. In addition, they are intended to ensure medical safety in the labor market and to create a healthier environment.

Given that migration processes in Russia have become more active in recent years and the number of labor migrants continues to grow, the new procedure is viewed not only as a preventive measure but also as part of state policy focused on strengthening public health.

Thus, starting from 2026, every person arriving in Russia in search of work will be required to provide detailed medical information — through this, the state aims to make the labor environment more controlled and safer.