In 2020 we celebrate the 30th anniversary of HealthRight International. Over the years, this organization has had many faces, but our mission has remained the same since day one: Health and human rights are inextricably linked, and we as a global society must ensure that all people can exercise this right. Since 1990, we have supported marginalized communities all over the world, and we want to share their stories with you. Below, you can explore 30 stories covering 30 years of human rights work. A new story will be added each week.
We hope you enjoy this historical exploration, may it inspire you to stand up for human rights in whichever way you can.
In 2004, an estimated 12,000 girls and women were trafficked into India from Nepal. They were coerced into forced labor and sex work, resulting in countless human rights violations. Even after they returned to Nepal, they were often unable to rejoin their families. Suffering from mental and physical trauma, potentially being HIV-positive, and facing the stigmatization from Nepali society, survivors of trafficking were unable to find employment or adequate health care. In addition, many were vulnerable to being trafficked again.
HealthRight launched an in-depth assessment in 2004 that identified gaps in service coverage and the quality of care. Through this, HealthRight was able to develop relationships with local partners and establish a field office to launch full operations. Samjhana Kachhyapathi, pictured, was a health coordinator who supported survivors of trafficking and violence. HealthRight, partnered with UNICEF, launched trainings to teach healthcare providers and community leaders how to diagnose survivors of human trafficking and prevent future abuse. When asked about trainings, Samjhana mentioned that she “began to make a network of people around me who can assist me in identifying and prosecuting abuse, as well as preventing it from happening to more children.”
In the following years, HealthRight worked to strengthen the capacity of the health sector to serve more children and provide effective services to survivors of abuse and violence.
In 2003, Romania had the highest number of tuberculosis (TB) cases in the Balkan region and the highest number of pediatric TB cases in all of Europe. Increased poverty, insufficient training for TB care, and discrimination against TB patients undermined efforts to prevent and treat the disease. In addition, certain groups, such as Roma people and prisoners, were discriminated against and labeled as undeserving of medication. Many people who could not afford to travel to health facilities to obtain medicine were labeled as “noncompliant” and were dropped from the system without a follow-up.
That year, HealthRight launched a program to address these health disparities. After collecting baseline data on TB knowledge and attitudes among marginalized populations like TB patients, Roma, prisoners, and people living in poverty, HealthRight established a partnership with a Roma NGO to strengthen the capacity and reach of education among Roma communities.
The most impactful project was a peer health educator (PHE) program which trained local Roma men and women, empowering them to address the high rate of TB within their communities. The program also aimed to reduce the stigma around TB and improve access to treatment. Carmen Andrei (pictured, in red) is a Roma woman, a mother of two, and a PHE from the village of Cracaoani in Neamt County, which contained a large Roma community.
Carmen completed her training as a PHE during the second year of the project. Having experienced harsh discrimination for her Roma background, Carmen wanted to improve the conditions in her community and advocate for equal rights. She helped many Roma obtain identity papers so that they would be eligible for health and social services. She eventually became a well-known figure in the Roma community, serving as a bridge between the community and the government. Carmen continued to advocate for the health and social needs of Roma people, including via HealthRight’s PHE program.
By the time the program ended in 2007, HealthRight had trained 40 Roma PHEs who collectively educated over 10,000 Roma people on TB symptoms, transmission and treatment and helped destigmatize the disease in their communities. Carmen later became the Executive Director of the Neamt Community Development Center.
2002: The Thai-Burmese Border
From 1962 to 2011, Myanmar, formally known as Burma, was controlled by a military government that resulted in deep internal conflict and human rights abuses, especially for ethnic minorities. What arose was a flow of over one million ethnic minority migrants to nearby Thailand. Over 50% of these migrants were not officially recognized as refugees, meaning they did not receive basic protection from poverty, disease, and violence. However, even those with work permits lacked international protection and lived in refugee-like circumstances. In the early 2000s, an estimated 100,000 Burmese worked for illegally low wages in factories near the Thai-Burma border.
These migrants were disproportionately affected by reproductive and child health problems, including high rates of vaccine-preventable infectious diseases, complicated pregnancies and septic abortions, HIV, and sexual violence. Access to health care was extremely limited for migrants, due to poverty, high mobility, and language barriers. Travel to a clinic carried a risk of arrest and deportation, sexual violence, and economic extortion at the hands of Thai immigration police. While the Thai public health system extended some prevention services to the migrant population, such as malaria control and immunization, its limited financial and human resources made it difficult to support the most vulnerable and hard-to-reach migrants.
After assessing the human rights concerns on a 19-day field mission in 2001, HealthRight began responding to the issue with local partnerships in 2002. Together with Mae Tao Clinic and the Thai Ministry of Public Health, HealthRight developed the Partnership for Migrant Health to increase access to health services for the more than one million migrants living as unrecognized refugees in Thailand. HealthRight also worked to build the capacity of local NGOs by creating an Adolescent Reproductive Health Networking Group which trained staff in needs assessment, monitoring and evaluation, and advocacy. In addition, HealthRight facilitated the implementation of the first HIV test counseling and follow-up treatment to pregnant migrant women under the Thai national program.
HealthRight and the Partnership also established Migrant Health Working Groups of Thai and migrant health providers in Tak Province to assist in the development of targeted, culturally appropriate health education, outreach and services for reproductive and child health prevention and care, including prevention of unsafe abortion and HIV/AIDS. This was HealthRight’s final project in Thailand, and closed in April 2004.
2001: Peter C. Alderman
On September 11, 2001, a series of terrorist attacks struck several parts of the US, resulting in almost 3,000 deaths. Among the lives lost was Peter C. Alderman, who was working for Bloomberg in the World Trade Center when the planes struck the towers. He was 25.
Peter grew up in Scarsdale, NY, graduated from Scarsdale High School in 1994 and from American University in 1999. He was sweet, smart, charismatic and loyal. His family and friends are always reminded of his infectious smile and positivity. “When you were around Peter, it made you a better person,” a friend recalled, ”not because of anything he said or did, but simply because his mere presence brought you joy.” Peter was able to brighten up a room instantly and make people feel like they truly mattered. It is those memories that his family and friends continue to hold dear to their hearts.
To honor Peter’s life, his parents Liz and Steve Alderman founded The Peter C. Alderman Foundation (PCAF) in 2003. His parents wanted to leave a mark that Peter had existed and that the world would be a better place because he had lived. Additionally, Peter’s childhood and college friends united as Friends of Peter Alderman (FOPA) to remember him and support the work of PCAF. “[FOPA] ensures that Peter will never be forgotten and serves as an outlet for us to tell others about what a special person and more importantly, what a special friend he was,” says Jeff Gold.
In 2018, PCAF would merge with HealthRight to form the Peter C. Alderman Program for Global Mental Health, integrating life-saving mental health interventions into HealthRight’s portfolio. To this day, Peter’s friends and family meet every year to remember him and to support the work that began 17 years ago.
In the late 1990s, Vietnam struggled with economic reform, causing a relocation of resources away from rural health care and social services. As a result, ethnic minorities and women and children in mountainous northern provinces suffered disproportionately from preventable diseases and poor maternal and reproductive health. The remote location, lack of information, and poor transportation made it difficult for these communities to access healthcare. To receive medical treatment, villagers sometimes had to walk up to four hours to reach the nearest health center. In addition, village health workers often lacked the necessary medical knowledge and equipment to provide adequate care. In 1999, only 49% of births in the region were attended by a trained midwife – the majority of births occurred at home without professional assistance.
To address this, HealthRight, in partnership with Médecins du Monde France, launched a three-year maternal and child health project in the Mai Châu District. At the time, the Mai Châu District had a population of 47,000, and more than 70% were ethnic minorities. The rates of respiratory and gastrointestinal infections were far larger than the national average and in more remote areas of the District, more than half the children under five suffered from malnutrition. The focus of the program was community-based health care access, disease prevention, and maternity and infant health.
In 2000, HealthRight opened a field office and hired local and international staff to run the project. Staff members identified ten communities for project intervention, and assessed the needs of the residents. Through this, they were able to develop services to improve the clinical skills of village health workers and recruit more women and minorities into the health system.
Among those impacted by HealthRight’s work was Vang A. Giong, a 27-year-old Hmong man. Siding with the United States during the Vietnam War increased the discrimination against the Hmong people, giving them little access to healthcare. Giong attended a three-month training course and was able to take his knowledge back to his hometown, where he taught mothers to prevent common childhood diseases, counseled pregnant women to undergo examinations, provided first aid services, and mobilized villagers to participate in national health programs for better family planning and nutrition. In this way, Giong was prepared to help his community begin to reverse the discrimination that has wreaked havoc on their lives for decades. He helped build a healthier future for the Hmong.
In total, this program improved the health and lives of approximately 16,000 women and children in rural communities in Mai Châu.
1999: South Africa
In 1999, South Africa was undergoing a healthcare crisis as simultaneous HIV/AIDS and tuberculosis (TB) epidemics spread. Approximately 4.2 million South Africans were infected with HIV – more than ten percent of the nation’s population. At the time, 40 to 50% of all patients infected with TB were thought to be co-infected with HIV in South Africa, and TB was the leading cause of death in AIDS patients. Under apartheid, South African public health services were largely reserved for white populations, so the post-apartheid government was tasked with expanding the healthcare system to serve the entire South African population, many of whom had been historically neglected. The TB and AIDS epidemic quickly exacerbated the available resources and left many people unable to receive treatment.
To respond to the strain on the health system, HealthRight partnered with the South Africa-based agency, Tuberculosis Alliance DOTS Support Association (TADSA), to help the South African National Tuberculosis Control Program provide TB treatment at the community level. HealthRight’s goal was to assist TADSA in expanding their success in facilitating training of community-based TB treatment supporters and increasing their services for TB/HIV co-infected people.
During the first seven months of 1999 alone, TADSA conducted workshops for 84 treatment facilitators, 113 trainers of treatment supporters, and 133 TB treatment supporters. Community-based health workers who were supervised by HealthRight/TADSA’s trainers treated over 2000 people in 1999.
One training participant commented “I think the course will make a difference as now I am equipped with knowledge and skills on how to conduct TB training of treatment supporters thus increasing the cure rate which is very low in our region.”
1998: Kosovo War
In early 1998, rising tensions between the Federal Republic of Yugoslavia and the Kosovo Liberation Army took a turn for the worse as the Kosovo War began. During this time, Kosovar Albanians faced extreme discrimination and many were displaced from their homes, causing them to lose their jobs and access to health services. The violence of 1998-99 intensified Kosovo’s healthcare and human rights crisis, making HealthRight’s work in the region more important than ever.
Since 1992, HealthRight has addressed critical gaps in health care – providing direct medical services to all Kosovars, regardless of ethnic background, reaching over 250,000 children with basic immunizations, and strengthening the overall health care infrastructure through training, health strategy planning, and provision of equipment and supplies.
During the armed conflict of 1998-99, HealthRight implemented three emergency relief projects in Macedonia and Kosovo that brought food and medical assistance to over 150,000 refugees and internally displaced persons. Within days of the signing of the peace accords, HealthRight returned to Kosovo and commenced a program to rebuild the maternal health care infrastructure. HealthRight also developed three long-term projects to serve the Kosovar population – the De-institutionalization of Kosovar Children Project, the Health Promotion Project, and the Tuberculosis Control Project.
Recognizing the insecurity felt by many ethnic minorities in the post-war Kosovo, HealthRight worked hard to include Serbs and Roma in its programs, and to develop programs targeting these groups. One of the most successful of these programs was a reproductive health education program directed at the Roma community, which addressed some of the needs of the most excluded ethnic group in all of Europe.
1997: Dr. Victoria Sharp
In 1997, when Dr. Victoria Sharp was appointed Director of the Center for Comprehensive Care at St. Luke’s Roosevelt Hospital in New York, she had already been with HealthRight for four years.
Vicki first contacted HealthRight when she heard about the Haitian refugee crisis in 1993, to see how she could assist the detainees, and was crucial in the organization’s push to bring these refugees to safety.
Aside from working with the HIV-positive Haitian refugees in Guantanamo Bay, Vicki’s earliest days at HealthRight were devoted to TB-affected Albanians living in Kosovo and building health systems for indigenous communities in Chiapas, Mexico. She also served on overseas assignments to Macedonia to assist refugees from Kosovo; to Russia to further investigate problems of at-risk youth; to Thailand to provide health care to Burmese refugees; and to Kenya to help establish a comprehensive HIV clinic.
Vicki became the Chair of HealthRight’s Board of Directors in 1995 and then served as President from 2002 until 2015. When she finally stepped down from the Board in 2018, after 25 years of service, she was HealthRight’s oldest and most dedicated supporter. Today, Vicki sees herself as the “historian” of HealthRight, having been a part of the organization from the very beginning. This September 2020, at the annual Health and Human Rights Awards, she will join HealthRight’s Emeritus Board in recognition of her services to the organization.
You can find a 2018 interview with Vicki Sharp here.
In the heart of the Balkans, in the southern portion of former Yugoslavia, lay one of the most underdeveloped regions in Europe. At the time, Kosovo had the fastest growing population and highest infant mortality rate in Europe. It also had one of the highest rates of infectious diseases in Europe, particularly tuberculosis (TB), with an incidence of 77 per 100,000 people (compared to 46.5 per 100,000 in New York City at the height of its epidemic in 1992). The ongoing mistrust of the official health system and worsening ethnic tensions made access to healthcare for TB difficult.
HealthRight sent its first volunteer doctors to Kosovo to vaccinate children against polio in 1992, remaining for years to undertake an extensive anti-tuberculosis program, provide essential care to mothers and infants, and promote public health education. As a prominent non-governmental organization addressing TB in Kosovo, HealthRight took a lead role in cooperation with the World Health Organization in developing a TB control strategy for Kosovo.
By 1996, HealthRight had already been working to combat TB in Kosovo, the number one health problem in the region, for two years. HealthRight worked to upgrade TB diagnostic laboratories, distributed much-needed drugs, and began providing public education on health care and recognizing and treating symptoms of TB. Additionally, HealthRight physicians provided anti-TB care that included screening and drug treatment, provided vaccinations for children, and trained clinicians on the international standards of treatment for TB.
“After two years of work in Kosovo, I see the early signs of progress, gradual improvement in health care accessibility, and movement toward a reconciliation that can bring peace and a healing of bodies and spirit to the hardened and disheartened people of this troubled region.” – Lisa Adams, MD, speaking about the work of HealthRight’s TB Vaccination Team in 1996.
Thirteen years after the breakup of the Soviet Union, Russia’s social institutions had declined to the point of collapse. As increasing numbers of families slid into unemployment and poverty, the number of children and youths seeking to escape from the accompanying cycles of neglect and abuse grew. Many of these children ended up institutionalized under the permanent custody of the state in orphanages. Far from leading them to better lives, institutionalization set these children on a destructive path. Our research showed that, of the 15,000 teenagers in Russia who were graduated from orphanages in one year, 10% later ended their lives in suicide, 20% lived on the streets, and 33% went to prison.
In 1995, HealthRight had already been operating in Russia for one year, providing critical health services to St. Petersburg’s neglected, runaway, orphaned or abandoned children and adolescents. Always engaged with the local community, we partnered with drop-in centers for street children and youth, children’s shelters, children’s hospitals, and juvenile detention centers.
Our staff of fourteen Russian pediatricians, neurologists, dentists, psychiatrists, psychologists, nurses, social workers and lawyers provided essential health care, legal, and psychosocial services for children and adolescents who lived on the streets or in shelters, and other children and youth at risk. Many of them were victims of physical and sexual abuse, most were physically or emotionally underdeveloped, and many were addicted to the street drugs: cigarettes, toxic inhalants, alcohol, and, increasingly, heroin.
HealthRight developed a sustainable system of services to strengthen families, prevent the abuse and abandonment of children, and offer at-risk children and adolescents long-term, progressive alternatives to institutionalization. We provided training for the network of providers who work with at-risk children and adolescents, supported local partners to develop new models for foster care, family care and social support, provided legal assistance, and advocated for child welfare reform with local government. This work would endure for over a decade before being handed off to local organizations to continue indefinitely.
1994: Chiapas, Mexico
In 1994, HealthRight began supporting the work of the Hospital San Carlos (HSC), in Chiapas, Mexico. Run by the Daughters of Charity of St. Vincent de Paul since 1976, the hospital was the only source of health care for an underserved populations of thousands of rural indigenous people in highland Chiapas.
Indigenous communities in Chiapas had long been marginalized, suffering disproportionately from tuberculosis and other preventable infectious diseases. Most of the patients who came to HSC did not speak Spanish – only their indigenous languages Tzeltal or Tojolabal – while doctors and nurses spoke only Spanish. This communication barrier between patients and providers added to the exclusion and inequality that indigenous patients already faced. The UN and other human rights observers have documented the harmful effect of this scenario on indigenous women all over Central America. In Mexico, for example, indigenous women have been sterilized or given Caesarean sections without explanation or consent. Mexican physicians often claimed that the women could not speak Spanish and thus the procedure could not be explained to them.
To promote the ability of indigenous patients to understand, choose, and consent to medical care, HealthRight and HSC set up an ambitious training program for a group of indigenous women to become nurse auxiliaries. This project was the first in HealthRight’s long history of strengthening local health systems, by training health workers to support their own communities.
The curriculum included physiology, basic nursing techniques, pediatric nursing, maternal and child health, and public health – as well as basic literacy, a particularly pressing need. The program involved indigenous women, ages 15 to 22, who agreed to work for the hospital in exchange for room, board, vocational training, and primary and/or junior high school-level education. At the end of their training, the women received official certificates from the Mexican government, authorizing them to work as auxiliary nurses throughout the country.
Coming from the very same families as the patients of HSC, these young nurses became an essential part of the hospital. Along with the services they provided to others, they were educated and empowered, and are now part of the improvement of their communities’ long-term prospects.
Sor Maite Galvan, the Director of HSC at the time, said, “The nurse-auxiliaries are the right hand of the hospital. In addition to the medical services, they do the translation for the indigenous patients, they know the culture, they provide the bridge between the hospital and the patients. The hospital couldn’t work without them.”
1993: The Human Rights Clinic was founded
Through HealthRight’s work with Haitian refugees who were being detained indefinitely in Guantanamo Bay (see 1992) – documenting the asylum seekers’ trauma and advocating on their behalf – the Human Rights Clinic (HRC) was born. Founded in the Bronx in 1993, the program began as a partnership with the North Central Bronx Hospital and Montefiore Medical Center’s Residency Program in Primary Care and Social Internal Medicine.
The HRC recruits, trains, and deploys a network of volunteer physicians and mental health professionals who provide forensic evaluations, translating scars and symptoms into pivotal evidence for immigrants seeking asylum and other relief in the United States.
The HRC serves immigrants who are survivors of torture and other human rights abuses. In order to be granted the right to remain in the United States, asylum seekers must prove that they have a well-founded fear of persecution if returned to their home country. Through medical and psychological evaluations, HRC volunteers document the clinical sequelae of human rights violations suffered by survivors, thus helping to ensure a fair adjudication of their claims for asylum by enhancing their capacity to present their cases fully.
These evaluations can make the difference between an asylum grant and a denial — over 90% of HRC clients are granted asylum or other relief, compared to the 35% grant rate of asylum seekers nationally. Most recently, 96 percent of HRC clients whose cases were adjudicated in 2019 were granted.
Still active today, the HRC is HealthRight’s longest-running program, continuing to provide essential services to asylum seekers. Nearly 30 years later, the program continues to work closely with Montefiore Medical Center, and numerous other partners across the New York metro area.
1992: Haitian Refugee Crisis and Guantanamo Bay
One of HealthRight’s earliest projects came out of the Haitian refugee crisis of the early 90s. Following a coup d’état in Haiti in September 1991, the new military regime began persecuting the former president’s followers and other dissenters, causing thousands to flee Haiti. By February 1992, the US Coast Guard had picked up over 14,000 refugees and detained them in Guantanamo Bay, Cuba.
Beginning in May 1992, most refugees were repatriated to Haiti, while about one third received asylum in the US. However, 270 HIV+ refugees and their family members who had been granted asylum were barred from entering the US because of their HIV status and remained in Guantanamo Bay. “These refugees lived in deplorable conditions, were subjected to violence and repression by the US military, deprived of proper medical care, and left without any legal recourse of rights,” wrote migration scholar Karma Chávez.
Jonathan Mann and several other physicians visited these refugees, conducted interviews, assessed their health, and gathered evidence about their treatment and standard of living. They used these data to lead a lawsuit in Federal Court against the refugees’ detainment, arguing that the conditions in the camps were not conducive to care and that the patients must be brought into the US.
On March 26, 1993, US District Judge Sterling Johnson Jr. ruled that the refugees would be allowed to enter the US, stating that “the government had to either provide medical treatment for those with the AIDS virus or send them where they could be treated.”
1991: Doctors of the World-USA
DoW-USA was the US branch of Médecins du monde, a humanitarian organization originally formed in 1980 by Bernard Kouchner. Jonathan Mann sought to expand upon DoW’s model to focus on linking health and human rights.
When Dr. Mann founded the organization, it had one or two paid staff and about five board members. During this time, meetings were sometimes chaotic and disorganized, but the organization worked tirelessly to foster collaboration between clinicians, public health leaders, and community organizations.
1990: Dr. Jonathan Mann founds HealthRight
“AIDS cannot be stopped in any one country unless it is stopped in all countries,” Dr. Jonathan Mann wrote in a 1987 report on the WHO Global Programme on AIDS, which he had established just ten months earlier. At the time, he did not know that he would part ways with the organization within three years to pursue independent solutions for the human rights calamities created by the AIDS pandemic.
Jonathan Mann received his undergraduate education at Harvard College, graduating in 1969, before earning his MD at Washington University School of Medicine in 1974. Following medical school, he worked as an epidemiologist in New Mexico for the US Public Health Service and the New Mexico Health Services Division.
Following a return to Harvard School of Public Health to earn his MPH degree in 1980, Mann began to apply his intellect and skills to forming international strategies for reducing and preventing the spread of AIDS. In 1984, he founded and directed Project SIDA, an AIDS research project based in Kinshasa, Democratic Republic of Congo (then Zaire), that incorporated epidemiologic, clinical, and laboratory components in a collaborative effort of Zairian, US (Centers for Disease Control), and Belgian AIDS researchers. This project, among many accomplishments, showed that HIV could be spread through heterosexual sex but not through mosquito bites.
By 1987, the fear of AIDS had led to inhuman policies across the world. 81 countries had passed laws against people with HIV or risk groups, usually homosexuals and prostitutes. In Germany, a federal judge declared it might be necessary to tattoo and quarantine people with the virus. Cuba was already quarantining AIDS patients. Some Muslim states were jailing “promiscuous” people, and Chinese officials denied the existence of homosexuals, drug users, or prostitutes in the People’s Republic. In the US, President Reagan’s secretary of education, William Bennett, fought Surgeon General C. Everett Koop’s plans for frank education about HIV prevention, favoring instead compulsory testing of all hospital patients, marriage license applicants, and immigrants. Quarantine loomed as a very real threat.
Amid this gathering storm, Jonathan Mann led public health authorities to perhaps their finest hour. Impeccably dressed in bow ties, yet with the gritty experience of running Project SIDA, Mann managed to convene more than 100 national ministers of health together in London. There, almost 150 nations signed on to a condom-based, compassionate strategy to slow the spread of AIDS. A few months later, he convinced the World Health Organization to make human rights the core of its anti-HIV strategy. These coups played a crucial role in preventing the wholesale repression of people with the virus.
Mann orchestrated this historic consensus from his new position as director of the World Health Organization’s Global Programme on AIDS. At first, recalls Daniel Tarantola, who joined the fledgling endeavor at the beginning, “the program was himself, a secretary, and one typewriter.” Two years later, Mann had rocketed the budget to almost $100 million. His m.o.: hard work, personal modesty, and an eloquence that was at once fiery and logical. “Back at a time when only a few people were screaming” for a humane and effective response, says Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, “Jonathan was an unbelievably articulate and passionate voice.” Mathilde Krim, founder of the American Foundation for AIDS Research, adds that Mann persuaded people with “the force of the argument, the morality of behaving a certain way, and the practical usefulness of being ethical and respectful of others. He convinced people.”
Mann’s message: AIDS is a global crisis, in which no person or nation is an island. More important, human rights and public health go hand in hand: “In each society, those people who before HIV/AIDS arrived were marginalized, stigmatized, and discriminated against become those at highest risk of HIV infection… The French have a simple term which says it all: HIV is now becoming a problem mainly for les exclus, the ‘excluded ones’ living at the margin of society.”
His international experiences with AIDS policy brought to his attention the link between human rights and health. He was particularly interested in the effects of health policies on human rights, the health effects of human rights violations, and the inextricable connection between promoting and protecting health and rights.
Seeing a void among the health and human rights organizations in the US, Dr. Mann founded HealthRight – then known as Doctors of the World-USA – in 1990. His aim was to create a unique organization that ran sustainable programs that promote and protect health and human rights in the US and abroad. Drawing from his experiences in the AIDS response, he promoted the idea that health and human rights are inextricably linked. Even 30 years later, this philosophy drives HealthRight’s work and projects.
Jonathan Mann worked tirelessly to improve the lives of others and never shied away from a challenge. Today, his ideals are more important than ever before.
“People say there is no use trying to change the world,” he often said, “but if we don’t try, will it change?”
Portions of this biography were first published in the New York Village Voice and quote Laurie Garrett’s book The Coming Plague.