Held in Geneva I participated in the Communities Delegation preparation meeting as member of the delegation ahead of the 53rd global fund board meeting. The importance of meeting is significance after the pull out of US from major global entities they were funding. This brings the The Global Fund for HIV TB and Malaria programs across the globe under threat as US is one of the major funder with its commitment to match one dollar for each two dollar contribution from other donors.
Digital technology is in many ways a new frontier that is increasingly part of our everyday lives making the perspectives, experiences and lessons learned from key population communities and civil society even more crucial to ground and inform this report. As a leading expert at the global, regional and national level, Iwas invited by UNAIDS consultant Robin Montgomery to have a conversation on the topic of AI for HIV. The conversation covered a number of issues (opportunities, challenges, lessons learned, etc) where I provided the critical input to define and chart the path forward.
How do digital health innovations [and by extension, AI] figure into your organization’s/network’s current and future-oriented strategies?
What are the top 3-4 concerns/risks that you have/your organization has/your communities have expressed about integrating AI technologies into service delivery across the HIV care cascade?
What opportunities do you see for the greater integration of AI tools into HIV prevention, treatment, care and support services and programs?
What is needed to build community capacity to engage in AI for HIV interventions?
What are 2-3 key considerations that you would like UNAIDS to reflect within the incoming Global AIDS Strategy?
Are there examples of good practice digital health/AI interventions that you would recommend us to look at?
In 2024, the Youth PACT Partnership did a lot of Impactful work led by young people. In this article, we share some of the essential highlights of the year 2024.
Empowering Youth Through the UPROOT Scorecard Program
In 2024, The Youth PACT Partnership successfully implemented the UPROOT Scorecard Program in over six countries in collaboration with Youth Lead Asia Pacific YKP Network, YPlus Global, UNAIDS, and other stakeholders. This scorecard has been instrumental in assessing youth-led movements and youth engagement at the country level, empowering communities, and providing valuable insights through its comprehensive reports. Our UPROOT Scorecard strategic initiatives extended to various regions, including Nepal, Guatemala, and Madagascar. The project in India, Pakistan, and Ivory Coast since October 2020 has significantly impacted youth empowerment and advocacy.
Advocating for Human Rights and LGBTQIA+ Communities
The Youth PACT has been a vocal advocate for human rights, mainly focusing on the rights of young individuals affected by HIV, especially within the LGBTQIA+ community. Our advocacy efforts include reports, videos, and messages on our social media and website.
Participation in Global Events
Our members have actively participated in high-profile events like the 68th Session of the Commission on the Status of Women (CSW68) and the ICPD 30 Conference in Geneva. Notable contributions include Kushal Rana Singh’s participation at ICPD30 and Xu Yahan’s at CSW68. Our member Adeeba Amin has actively engaged in various advocacy events, including representing adolescent girls in the ICPD30 Global Dialogue in Dhaka, Bangladesh.
Digital Advocacy and Webinars
We’ve developed a comprehensive Digital Advocacy Manual, guiding young people in designing and implementing effective digital campaigns. Additionally, we’ve organised capacity-building webinars under ayKP Global Partnership on topics like “Network and Organizational Development” and “Monitoring and Evaluation.”
Raising Awareness of Critical Issues
The Youth PACT has been instrumental in raising awareness about criminalisation laws and their impact on the LGBTQIA+ community, with a notable focus on Ghana. We’ve consistently highlighted the importance of gender identity rights globally.
Contributions to the Global AIDS Conference 2024
Ali Raza Khan and Venicia Fernandes represented The Youth PACT at the Global AIDS Conference in Munich, Germany. During the Youth Pavilion sessions, they discussed youth-led monitoring, the impact of climate change on young people, and the HIV response.
Podcasts and Social Media Engagement
The Youth PACT has produced a series of podcasts related to the UPROOT Scorecard Program, available on our social media channels.
Addressing Emerging Health Concerns
We raised awareness about Monkeypox vaccination, especially among people living with HIV. Ali Raza Khan’s blog post “Vaccination as a Person Living with HIV” provides detailed insights on this topic.
Comprehensive Sexuality Education (CSE) Advocacy
Our advocacy campaigns have highlighted the importance of Comprehensive Sexuality Education, mainly through the CSE Asia Pacific 2024 Conference.
Highlighting Global Issues and Achievements
From championing women’s, children’s, and LGBTQIA+ rights in Sri Lanka to addressing adolescent fertility challenges in Latin America, our members have contributed valuable content to our website and social media platforms.
Celebrating World AIDS Day
We ended the year by celebrating World AIDS Day, promoting the “Right Path” for respecting and accepting LGBTQIA+ and key populations’ rights to counter HIV stigma and achieve the UN goal of 95-95-95 by 2030. For World AIDS Day, we amplified the voices of young people living with HIV, calling on global leaders to invest in youth
Personal Contributions by Ali Raza Khan
I, Ali Raza Khan, a young gay activist living with HIV from Pakistan, have made significant contributions to The PACT and AIDS 2024. My engagements included:
HIV Science & Art Exhibition: We will display work at the HIV Science as Art exhibition, highlighting community activists’ struggles.
Participation as Speaker: Speaking at the International AIDS Society’s symposium on the impact of climate emergencies on communities.
Art Installation: I collaborated with artist Khairullah Rahim on an art installation called “Pigeon in Stone Forest,” which depicts the challenges faced by community workers.
The original article written by Ali Raza Khan is available on The Youth PACT website here.
In this year’s blog series, we present the writings of Hivpoint’s Health Buddies 2024 in which they reflect on their own journey in promoting sexual health.Health Buddies spread knowledge about sexual rights and sexual health including HIV and other STIs in migrant and refugee communities. Let us present to you our wonderful Health Buddy Ali Raza Khan.
I am Ali Raza Khan, an HIV positive gay activist from Pakistan and a refugee in Finland. In Pakistan, working for gay rights and HIV awareness comes with significant risks.
As an activist and the founder of PridePakistan.org, I faced constant threats and discrimination with increasing conservative societal norms and legal challenges. It was dangerous to advocate openly for sexual and reproductive health and rights (SRHR) of gay men.
If you are an HIV positive refugee in Finland, it’s important that you have access to essential healthcare and support services. I have written down some key points to help you navigate through possible challenges you might face.
My journey from Pakistan to Finland was not easy but Hivpoint’s Health Buddy program helped me to continue working for HIV positive community members in Finland. That is why I created this little guide based on my experience for HIV positive refugees in Finland.
1. Disclosure of HIV Status to Authorities
As a refugee, you should disclose your HIV status at your first interaction with authorities even though you might feel afraid because of discrimination or stigma.
It is essential to tell about your HIV status so your treatment will continue or it will be started as soon as possible.
I have learned that when you talk about HIV status at one immigration camp, the information is not shared to other staff members. That is why you have to tell about your HIV status in each new camp.
2. Get Connected to Hivpoint and Positiiviset ry HivFinland
People living with HIV do not have to deal only with HIV but also with societal and internal stigma. Therefore, it is vital to tell the authorities and your nurse if you have psychological needs.
Hivpoint and Positiiviset both have regular activities and program for people living with HIV. There you can meet with other HIV positive individuals to discuss everyday things. I find peer support very helpful during my process.
As an HIV positive individual, I always wanted to discuss HIV related issues with other people living with HIV. Peer support has helped me dealing with internal and societal stigma.
At the street chalk event 2024 organized by Positiiviset ry, Ali draws and makes art about human rights, equality and hope.
3. Getting tested for Sexually Transmitted Infections (STIs)
Even if your HIV is undetectable, you can still get other STIs when having sex. Ask your nurse or doctor to get tested for STIs. It would be good to get tested if you’ve had unprotected sex (sex without condom or dental dam) or condom has broken.
You could get tested for STIs at Hivpoint’s free and confidential STI testing services. In addition, Pro-tukipiste offers services for those who are selling sexual services.
Apart from getting essential health and HIV services on time, you might also have some other needs. You can get help from Hivpoint and other associations.
Hivpoint is offering counselling and leisure activities for people living with HIV, and those can keep you to engage in healthy way on ground. In addition, you can participate in Positiiviset gatherings and activities for HIV positive people.
Who to contact?
You can join Pride Helsinki community’s closed refugee support groups. There you will get connected to other queer refugees in Finland and participate in queer and LGBTQI+ events.
It is crucial for your physical and mental health to continue your HIV treatment without a gap. In addition, it would be good for you to participate in association activities. It will help your mental health during the long process of your refugee hearings.
Whether you are in a big city or in distant area it is essential to contact with Hivpoint and other associations. You could do it online or face to face. If you came to Finland alone, you don’t have to be alone anymore.
Via these platforms mentioned above you can find similar people who can understand you. I recommend that you never hesitate to contact and get help from Hivpoint.
Ali visiting Hivpoint´s office at Kalasatama 2024.
Ali Raza Khan The writer is one of Hivpoint’s Health Buddies 2024
The orginal article is posted on Hivpoint.fi website, read more on their website here:
In this year’s blog series, we present the writings of Hivpoint’s Health Buddies 2024 in which they reflect on their own journey in promoting sexual health.
Health Buddies spread knowledge about sexual rights and sexual health, including HIV and other STIs, in migrant and refugee communities. Let us present to you our wonderful Health Buddy Ali Raza Khan.
My name is Ali Raza Khan, and I am an HIV-positive gay activist from Pakistan. My journey from Pakistani society to Finnish society has been one important chapter of my life.
As the founder of Pride Pakistan, I have been advocating for the health and rights of the LGBTQIA+ community, particularly gay men in Pakistan. However, due to threats to my life and discrimination based on my HIV status, I sought refuge in Finland where I am continuing my activism.
Refugees’ access to HIV, STI and SRHR services in Finland
Upon arriving in Finland, I found myself in a refugee center in a few days. There I first heard about Hivpoint, an organization dedicated to HIV awareness, advocacy, and sexual and reproductive health and rights in Finland.
One of Hivpoint’s volunteers was sharing informative pamphlets which motivated me to continue my HIV and SRHR advocacy work here in Finland. I also realized the gaps that refugees face in accessing HIV, other STI and SRHR services in Finland, particularly living away from major towns.
Health Buddy program helped me to overcome internal Discrimination and Trauma
Determined to continue my activism, I applied and got accepted to the Health Buddy program at Hivpoint. The program provided me with an opportunity to continue working openly for the rights and health of gay men.
Coming from a conservative society where I had to be cautious about everything I said and did, the Health Buddy program had a positive impact on my mental health.
It provided me an opportunity to exercise my HIV identity and gender expression openly in a new society.
The most important thing in the Health Buddy program was that I was doing activities with the support and assistance of Finnish expert colleagues that have been working for broader SRHR issues in Finland for years.
Learnings and experiences from organizing Health Buddy workshops
As a part of the Health Buddy program, I have organized more than five online and live discussions focusing on HIV, other STIs and SRHR awareness. There have been more than 50 people from diverse backgrounds participating in those sessions. This experience was very helpful for me to move ahead in my career path in a new country.
Through the Health Buddy training and interaction with participants of my sessions, I came across various perspectives of queer individuals, refugees, South Asians, students, and others regarding HIV and SRHR in Finland.
Through these workshops, I increased knowledge on safer sex, awareness of HIV and other STIs, consent, sexual rights and gender identity. In addition, I shared information about the availability of treatments and services related to STIs, PEP, PrEP, and contraceptives.
In the workshops, the participants got to know different condoms, lubricants and dental dams.
During the workshops, I realized that especially refugee community members still don’t have access to necessary basic information about HIV, other STIs, testing and treatment.
My message is to continue speaking about HIV
Despite the advancements and availability of HIV treatment, there is still stigma and discrimination towards HIV-positive individuals. It often leads to HIV-positive people not sharing their experiences or speaking about HIV with their communities.
It is crucial to continue speaking, sharing information and awareness about HIV, other STIs and LGBTQIA+ communities to end this stigma.
Ali Raza Khan The writer is one of Hivpoint’s Health Buddies 2024.
Ali Raza Khan, an HIV-positive gay activist from Pakistan, shares their journey as a Health Buddy 2024.
Exploring Financial Data as a Proxy for Monitoring Community-Led HIV Response
This discussion focuses on the use of financial data to monitor the effectiveness of community-led HIV response efforts, specifically in relation to the 30-18-60 targets. The conversation builds upon a previous discussion in March, where Deepak presented initial findings on using financing data for monitoring. This session delves deeper into the results, tracking methods, and potential avenues for using financial data as a proxy measure for the 30-18-60 targets.
Timeline and Financial Flows
Deepak begins by outlining the timeline of monitoring financial flows through community-led HIV response. He highlights key milestones, including:
2021: National assessments were pending, with no differentiation between community-based and facility-based modalities.
2022: Six pilot projects provided valuable insights into resource tracking for community-led response, leading to the development of guidelines and updates to the UNAIDS spending assessment (NASA) framework.
2024: Several countries began implementing community-led response resource tracking at a micro level.
2025 and beyond: The goal is to provide standalone resource tracking modules for communities.
Deepak then presents data on international funding channeled to communities, showing a decline from 31% in 2013 to 25% in 2023. He emphasizes the lack of data on domestic financing and the need for disaggregation by community-led organizations (CLOs) versus other civil society organizations (CSOs).
NASA Dimensions and Vectors
Deepak explains the three dimensions of the NASA framework:
Financing: Tracks funding sources, entities, schemes, and fees.
Provisioning: Tracks service providers and production factors.
Consumption: Tracks spending categories, service delivery modalities, and beneficiary populations.
He then presents data on the percentage of funding channeled through community-based and home-based service delivery modalities, highlighting a decline from 17% to 8% over the years. This data is based on 17 countries and should be interpreted with caution due to variations in reporting across regions and years.
Pilot Projects and Lessons Learned
Deepak discusses the six-country pilot project on community-led resource tracking, which aimed to:
Track community-led organizations’ own resource use.
Include non-monetary contributions, such as volunteer time and in-kind donations.
The pilots helped shape guidelines for resource tracking and highlighted the need to consider both CLOs and other CSOs in the tracking process.
NASA Implementation and Data Collection
Deepak describes the implementation of a full NASA in Pakistan, which included:
Mapping and screening of CSOs and CLOs.
Self-administered questionnaires for identified CLOs.
Virtual interviews and data collection using NASA templates.
Valuation of non-monetary contributions, such as volunteer time and donated goods.
The Pakistan NASA revealed that almost 80% of funding for community-led organizations came from international sources, with a small proportion from domestic financing. The data also showed that a significant portion of the funding was directed towards prevention services for key populations.
Future Directions and Next Steps
Deepak outlines the future direction of community-led resource tracking, including:
Expanding the use of standalone resource tracking modules for communities.
Conducting NASA assessments in more countries, with a goal of reaching 30 countries by the end of 2026.
Further disaggregating data to track funding through both CLOs and CSOs.
The discussion concludes with a focus on the importance of aligning resource tracking with costing guidelines for community-led response. Participants emphasize the need for both financial and non-financial data to advocate for increased funding and support for community-led service delivery. The group acknowledges the challenges of data collection, particularly for smaller organizations, and the need for capacity building in record-keeping.
Hello everyone, Ali Raza Khan here. As an HIV-positive gay activist and the founder of Pride Pakistan, I am dedicated to advocating for the rights and well-being of individuals living with HIV. Today, I had the privilege of meeting with key members of the UNAIDS team, including Angeli Achrekar, Deputy Executive Director for the Programme, and Christine Stegling, Deputy Executive Director for Policy, Advocacy and Knowledge. Alongside other members of the Communities Delegation to the Board of the Global Fund, we engaged in an essential discussion about the upcoming Global Fund 52nd board meeting in Malawi’s capital next week.
The Dire Consequences of Reduced HIV Funding Our discussion highlighted some alarming data from UNAIDS. A reduction in HIV funding could lead to 1.3 million deaths in 12 countries. This stark statistic underpins our grave concerns about the potential regression in our progress against the HIV epidemic. Despite significant advances, there are still 9.3 million people in need of treatment and 1.3 million new infections globally each year. The situation is particularly dire for key populations such as children, adolescent girls, young women, and other marginalized groups who continue to suffer the most.
Innovations in HIV Treatment and Prevention We also discussed the importance of embracing new, game-changing innovations in the HIV response. One such innovation is the advent of long-acting injectables for HIV prevention. These new treatments could be as close as we’ve ever been to an effective HIV vaccine, with nearly 100% efficacy in reducing new infections. However, without adequate funding and support from the Global Fund, these innovations may not reach the populations that need them most.
The Broader Impact on Health Systems Our conversation extended to the broader implications of diminished HIV funding. The HIV response has significantly strengthened health systems worldwide, from lab infrastructures to community health workers and supply chain systems. These systems, which have also been critical in responding to other health crises like Ebola, are at risk if HIV funding is cut. Integration of HIV services with TB and family planning initiatives has already shown positive outcomes, and continuing this integration is crucial.
The Critical Role of Community Systems The Global Fund’s support for community systems and human rights protection is integral to ensuring these biomedical innovations reach those in need. A shift away from HIV funding could exacerbate inequalities and make addressing human rights and gender inequalities even more challenging. Communities play a vital role in the HIV response, and their involvement is essential for maintaining progress and ensuring that no one is left behind.
Our Commitment Moving Forward The UNAIDS team reiterated their commitment to providing any data or support we need as we prepare for our board interventions. As part of the Communities Delegation, we will continue to fight for sustained HIV funding and advocate for the populations most at risk. We are at a critical juncture where the decisions made can significantly impact the future of the HIV response and the lives of millions.
This meeting reinforced the urgency of our mission. We must continue to advocate fiercely for the resources and support needed to combat HIV. I remain committed to this cause and will continue to work towards ensuring that every individual living with HIV has access to the treatment and care they deserve.
Stay tuned for more updates from the Global Fund 52nd board meeting and our ongoing efforts to secure a brighter future for all. 🌍❤️
The fight against HIV/AIDS has seen tremendous progress in recent years. However, achieving the ambitious goal of ending the AIDS epidemic by 2030 requires innovative strategies and a focus on empowering the communities most affected by the virus. This is where the UNAIDS 30-60-80 targets come into play.
What are the UNAIDS 30-60-80 Targets?
The UNAIDS 30-60-80 targets are a set of ambitious goals outlined in the Global AIDS Strategy 2021-2026. These targets aim to dramatically increase the involvement of community-led organizations in delivering critical HIV-related services and programs. Here’s a breakdown of each target:
30%: By 2025, at least 30% of HIV testing and treatment services should be delivered by community-led organizations. This includes crucial services like HIV testing, linking individuals to treatment, providing support for adherence and retention in treatment programs, and promoting treatment literacy.
60%: By 2025, a significant portion (60%) of programs that address societal enablers for HIV prevention and treatment should be delivered by community-led organizations. Societal enablers encompass broader social and structural factors that influence HIV outcomes. Examples include reducing stigma and discrimination against people living with HIV, promoting gender equality, and advocating for human rights.
80%: By 2025, a staggering 80% of HIV prevention services for populations most at risk of HIV infection, including women, should be delivered by organizations led by communities, key populations themselves (such as sex workers, people who inject drugs, and men who have sex with men), and women-led organizations. These services might include condom distribution, pre-exposure prophylaxis (PrEP), and readily available HIV testing. Why are the 30-60-80 Targets Important?
These ambitious targets are crucial for achieving several key goals in the fight against HIV/AIDS:
Empowerment: Community-led organizations are uniquely positioned to understand the specific needs and challenges faced by their communities. By increasing their role in delivering services, the targets empower these communities to take ownership of the HIV response. Improved Access: Community-based organizations often have established trust and reach within their communities. This allows them to provide services in a more culturally appropriate and accessible way, leading to potentially higher utilization by individuals who might otherwise hesitate to access traditional healthcare settings. Tailored Interventions: Community-led organizations have a deep understanding of local contexts and can design interventions that are more responsive to the specific needs of key populations and people living with HIV. Challenges and the Path Forward
Reaching the 30-60-80 targets requires addressing some challenges. Currently, there’s a lack of robust tracking systems to monitor progress towards these goals. Additionally, sustainable funding for community-led organizations is critical to ensuring their long-term effectiveness. Despite these challenges, the UNAIDS 30-60-80 targets represent a bold and necessary step towards ending the AIDS epidemic. By increasing community ownership and leadership in the fight against HIV/AIDS, these targets can help ensure that no one is left behind, and that critical services reach those who need them most.
Myself Ali Raza Khan is Committed to Accurate Information on HIV/AIDS :
On my site AliRazaKhan.com I believe in providing accurate and up-to-date information on HIV/AIDS for community and key population awarenss. I hope this article on the UNAIDS 30-60-80 targets sheds light on a crucial aspect of the global strategy towards ending the AIDS epidemic.
As an HIV-positive gay activist from Pakistan, my participation in the International AIDS Society (IAS) Regional Members’ Meeting is more than just a personal commitment. It represents the collective voice of marginalized communities striving for better healthcare and inclusivity. Being a proud member of the IAS since 2019, I have been actively engaged in its activities, ensuring that the concerns of people living with HIV, especially those from my region, are heard and addressed. Scheduled to be held virtually on 31 October 2024, the IAS Regional Members’ Meeting will gather members from Asia and the Pacific Islands. With time slots tailored for different regions (13:00 in Mumbai, 14:30 in Bangkok, 16:30 in Tokyo, and 18:30 in Sydney), this meeting aims to foster inclusive dialogue and collaboration among IAS members.
Introduction by Governing Council Members The meeting was kicked off with an introduction by the Governing Council members, setting the stage for the discussions ahead. This session highlighted the strategic direction of the IAS and provide insights into the organization’s ongoing initiatives. It’s was opportunity for members like myself to understand the broader vision and align our efforts towards common goals.
Lenacapavir: Recent Results in HIV Prevention One of the key topics on the agenda is the recent results in HIV prevention with Lenacapavir. This groundbreaking drug has shown promising results in clinical trials, offering hope for more effective prevention strategies. As someone living with HIV, the advancements in such treatments are personally significant and represent a beacon of hope for many in my community.
Availability and Accessibility of Lenacapavir in the Asia-Pacific The discussion had also focused on the availability and accessibility of Lenacapavir in the Asia-Pacific region, including aspects of voluntary licensing. Ensuring that such innovative treatments are accessible to those who need them most is crucial. This segment had delve into the challenges and opportunities in making Lenacapavir widely available, addressing regulatory, logistical, and financial hurdles. The Harm Reduction Initiative shared the GiLeads efforts mentining that Gilead will deliver LEN swiftly, sustainably and in sufficient volumes. Establishing a robust voluntary licensing program with Dr. Reddy’s Laboratories Limited, Emcure, Eva Pharma, Ferozsons Laboratories Limited, Hetero and Mylan, a subsidiary of Viatris to manufacture and supply lenacapavir to the 120 countries. Prioritizing registration in 18 countries that represent about 70% of the HIV burden and provide Gilead-supplied product at no profit to Gilead until generic manufacturers are able to fully support demand. Working on additional ways to support access in upper-middle and high-income countries to establish fast, efficient pathways to help reach people who need or want PrEP, including timely regulatory filings, engagement with partners.
Hearing from IAS Members The most anticipated part of the meeting is hearing from IAS members. This session was designed to provide a platform for members to share their experiences, challenges, and successes. As an advocate for the rights of HIV-positive individuals in Pakistan, I have contributed by sharing my insights and learning. This exchange of ideas is vital for fostering a supportive and informed community that can drive impactful change. Participating in the IAS Regional Members’ Meeting is a testament to my commitment to HIV advocacy and community leadership. Through this engagement, I aim to amplify the voices of marginalized communities and contribute to the global fight against HIV. By addressing critical issues such as treatment accessibility and sharing best practices, we can work towards a future where everyone has the opportunity to lead a healthy and dignified life.
The IAS provides a unique platform for professionals like myself to collaborate, learn, and advocate for change. Together, we can ensure that our collective efforts translate into meaningful progress for the HIV community worldwide.
By being an active participant in such discussions, I am not only representing my personal journey but also the aspirations of countless individuals facing similar challenges. Our united voice can make a difference in shaping a more inclusive and equitable healthcare landscape.
Read more on International Aids Society members website Here
Dans une récente interview avec Qlub Queer, Ali Raza Khan, un activiste gay séropositif du Pakistan, a partagé son histoire poignante de lutte pour l’égalité et la décriminalisation des personnes LGBTQ+ dans un pays où les relations homosexuelles sont criminalisées.
« Bonjour, je m’appelle Ali Raza Khan et je suis un activiste gay séropositif du Pakistan, pays qui criminalise les relations homosexuelles et les homosexuels. C’est ce qui arrive quand vous êtes séropositif et que vous entrez dans les établissements de santé. Vous êtes traité comme un criminel. Non seulement vous êtes traité comme un criminel dans les établissements de santé, mais même si vous travaillez pour la santé des hommes ayant des rapports sexuels avec des hommes ou des homosexuels, vous êtes traité comme un individu anti-étatique par les autorités sur le terrain. Beaucoup de gens ne parlent pas par peur d’être arrêtés ou détenus ou d’être torturés par les autorités. Si j’avais le pouvoir de changer les choses, je changerais la criminalisation des homosexuels au Pakistan, afin qu’ils puissent exprimer librement ce qu’ils sont. »
Le plaidoyer d’Ali Raza Khan est crucial dans un pays où le fait d’être ouvertement homosexuel peut entraîner de graves conséquences. Au Pakistan, les relations entre personnes de même sexe sont criminalisées en vertu de l’article 377 du Code pénal, qui prévoit des peines allant de deux ans à la réclusion à perpétuité. La loi, vestige de la domination coloniale britannique, est parfois appliquée, mais le plus souvent elle est utilisée pour menacer et harceler les personnes LGBTQ+ et de nombreux cas ne sont pas signalés.
La discrimination à l’encontre des personnes séropositives au Pakistan est un autre défi important. Les personnes vivant avec le VIH sont souvent confrontées à la stigmatisation et à la discrimination dans les établissements de santé, ce qui peut conduire à une réticence à rechercher un traitement et à se faire dépister. Cette discrimination s’étend au-delà des soins de santé, affectant l’emploi, la vie de famille et les interactions sociales. Le travail d’Ali Raza Khan est une lueur d’espoir pour de nombreux membres de la communauté LGBTQ+ au Pakistan. En s’exprimant et en plaidant pour le changement, il contribue à sensibiliser et à faire valoir les droits des communautés marginalisées. Ses efforts ne visent pas seulement la décriminalisation, mais aussi la création d’une société où chacun peut vivre librement et sans peur.
Regardez l’interview sur Queer Qlub instagaram : Ici ou ci-dessous
In a recent interview with Qlub Queer, Ali Raza Khan, a HIV-positive gay activist from Pakistan, shared his powerful story of fighting for equality and the decriminalization of LGBTQ+ people in a country where same-sex relationships are criminalized.
” Hi, my name is Ali Raza Khan and I am a HIV positive gay activist from Pakistan, which criminalizes same-sex intercourse, and gay people. That is what happens when you are HIV positive and getting into healthcare facilities. You are treated as a criminal. Not only are you treated as a criminal at healthcare facilities, but even if you are working for the health of men having sex with men or gay people, you are treated as an anti-state individual by the authorities on the ground. Many people don’t speak up because of the fear of getting arrested or being detained or the torture from the authorities. If I had the power to change something, I would change the criminalization of gay people in Pakistan, so they can freely express themselves to what they are “
Ali Raza Khan’s advocacy is crucial in a country where being openly gay can lead to severe consequences. In Pakistan, same-sex relationships are criminalized under Section 377 of the Penal Code, which prescribes penalties ranging from two years to life imprisonment. The law, a remnant of British colonial rule, is occasionally enforced, but more often it is used to threaten and harass LGBTQ+ individuals and many cases do not come forward.
Discrimination against HIV-positive people in Pakistan is another significant challenge. People living with HIV often face stigma and discrimination in healthcare settings, which can lead to a reluctance to seek treatment and testing. This discrimination extends beyond healthcare, affecting employment, family life, and social interactions. Ali Raza Khan’s work is a beacon of hope for many in the LGBTQ+ community in Pakistan. By speaking out and advocating for change, he is helping to raise awareness and push for the rights of marginalized communities. His efforts are not only about decriminalization but also about creating a society where everyone can live freely and without fear.
Watch the interview on Queer Qlub instagaram: Here or Below
Ali Raza Khan, a young HIV positive food expert and minorities rights activist from Pakistan, virtually participated in the Asia and the Pacific Regional Assembly Workshop during the World Food Forum 2024. The session, YA06, held on October 16, 2024 at Ethiopia Room at FAO headquarter, was an enlightening discussion on the importance of food labeling and youth engagement in food and agriculture products in the market.
The workshop delved into the critical issue of food labeling, particularly how it relates to sustainability and the Sustainable Development Goals (SDGs). In a world where young people are increasingly conscious of their health and the environment, the accuracy and transparency of food labels are paramount. Misleading labels can have significant adverse effects, making it essential for young consumers to decode these labels accurately.
During the session, various speakers highlighted the role of youth in promoting and demanding sustainable and healthy products. There was a consensus that young people must have access to products that align with their values of health and sustainability. This aligns with the broader goals of SDGs, where sustainable consumption and production patterns are crucial.
Ali Raza Khan contributed to the discussion by sharing insights on the need for universal adoption of label standards. He emphasized that a standardized approach to food labeling would ensure consistency and reliability, making it easier for consumers, especially the youth, to make informed choices. His contributions underscored the importance of transparency in labeling practices and the role it plays in fostering trust between consumers and producers.
The session also addressed the challenges posed by misleading labels. Young people are often bombarded with marketing tactics that can obscure the true nature of food products. The workshop called for stricter regulations and more education to help young consumers navigate these complexities.
This blog post aims to highlight the significant discussions and contributions from the workshop, emphasizing the need for accurate, transparent, and standardized food labeling. Ali Raza Khan’s participation in the World Food Forum 2024 reinforces his commitment to advocating for food security and climate resilience, particularly for minorities and marginalized communities.
For more updates and insights from the World Food Forum 2024, stay tuned to Ali Raza Khan’s journey as he continues to champion the cause of sustainable and healthy food for all.
Ali Raza Khan, a renowned HIV positive gay activist, will be delivering an online awareness session as part of the HIVPoint.fi Health Buddy 2024 volunteer program. This crucial event is organized in collaboration with UnitedVision.fi and aims to educate and empower individuals about HIV.
Join the session on October 17, 2024, at 14:00 (EEST) via Google Meet. (https://meet.google.com/xzv-gdko-ynv) During the session, participants will learn essential facts about HIV transmission, prevention, testing, and the available treatments in Finland that can help stop the spread of the virus. This safe space for discussion will be led by Health Buddy Ali Raza Khan, who brings a wealth of experience and dedication to the cause.
Ali Raza Khan has been a tireless advocate for the rights of men having sex with men, gay people, sex workers, and other HIV key populations both in Pakistan and globally. His dedication to raising awareness and supporting affected communities has made a significant impact worldwide.
Don’t miss this opportunity to empower yourself with knowledge. Whether you’re looking to learn for yourself or to support others, this session is for everyone!
For more details and updates, visit AliRazaKhan.com blogs sesction and follow Ali Raza Khan’s social media by supporting his continued efforts in advocating for a healthier, more informed community.
In the dynamic sphere of global health and human rights, fostering inclusive and comprehensive approaches is paramount. During the last week of October 2024, I had the distinct honor of participating in an online consultation held on 2nd October 2024, orchestrated by the Love Alliance Partnership in collaboration with STOPAIDS, WACI Health, and the Global Network of People Living with HIV (GNP+). This initiative was a cornerstone in addressing pivotal issues related to community leadership and societal enablers, especially significant for individuals like myself—an HIV-positive gay person from Pakistan.
Overview of Consultation Process The consultation, spanning from July to October 2024, comprised a series of meticulously organized meetings. These included an in-person meeting during the International AIDS Society Conference in Munich, Germany, and three online meetings. This collaborative effort was instrumental in creating a platform for linking and learning on global commitments, targets, and initiatives centered on health, rights, social accountability, and community leadership.
Core Themes Explored The consultation series honed in on three core themes:
Policies, Programs, and Investment in Community Leadership and Societal Enablers
Scaling Up Community-Led Responses and Societal Enablers
Accountability for Financial Investments
These themes were pivotal in highlighting the alignment between global targets and local policies and programs, with a key focus on the criminalization of communities impacted by HIV and LGBTIQ+ individuals.
Importance of Participation My participation in this consultation was not just a personal milestone but a significant step towards amplifying the voices of marginalized communities. As an HIV-positive gay person from Pakistan, my experiences and insights brought a unique perspective to the discussions. Pakistan, like many other countries, grapples with persistent stigma and discrimination, particularly against LGBTIQ+ communities, people who use drugs, and sex workers. Such discrimination often leads to the exclusion of these communities from essential healthcare services, thereby exacerbating health inequities.
Fostering Change Through Advocacy The insights garnered from this consultation series are set to shape a comprehensive white paper and advocacy roadmap. This roadmap aims to increase funding for community-led responses, expand civic space and freedoms, and progress towards decriminalization. It is crucial to address factors like criminalization, lack of funding, and exclusion in decision-making processes to foster an inclusive environment that upholds the rights and dignity of all individuals, irrespective of their HIV status or sexual orientation. The consultation series epitomizes a collaborative effort to dismantle barriers and champion the rights of marginalized communities. My involvement in this process underscores the importance of inclusive dialogue and advocacy in driving meaningful change. By participating, I was able to contribute to a broader narrative that seeks to transform global health policies and ensure that no one is left behind in the fight against HIV and stigma.
Participating in such pivotal discussions is not just about sharing experiences but about paving the way for a more inclusive and equitable future. Through continuous advocacy and collaboration, we can foster an environment where every individual, regardless of their background, can access the care and support they need.
Munich, Germany – At the AIDS 2024 conference, Ali Raza Khan, founder of Pride Pakistan, delivered a compelling speech on the intersection of climate change and its effects on people living with HIV, gay men, and men who have sex with men (MSM). His presentation highlighted the severe impacts of climate change on these vulnerable communities, particularly in Pakistan.
The Devastating Effects of Floods in South Punjab
In 2024, more than 100 people have died due to flood-related atrocities in Pakistan. Ali Raza Khan, hailing from South Punjab, one of the most affected regions, shared his personal experiences and the struggles faced by his community. He emphasized that the gay community members in Pakistan are significantly impacted by the changing climate, including extreme heat, heavy rainfall, and increased water pollution.
Watch The Recording Below
Ali Raza Khan founder Pride Pakistan spoke about climate and effect on people living with HIV, gays and men having sex with men during the AIDS 2024 conference in Munich.
Community Insights and Statistics
Khan presented data from studies conducted by Pride Pakistan, available on their website PridePakistan.org. He focused on the flood aspects, revealing that in the past five years, 100% of the community members surveyed reported being affected by flooding or heavy rainfall. This statistic underscores the pervasive nature of climate-related challenges in the region.
When asked about their concerns regarding climate change, 82% of the community members expressed that they believe climate change has a significant impact on their lives. Only 17% did not consider it a priority. Furthermore, 100% of the respondents acknowledged that climate change poses a threat to their health and well-being.
Beyond Climate: Additional Challenges
Khan also highlighted other pressing issues in Pakistan, such as terrorist activities and conflicts in regions like Balochistan and Khyber Pakhtunkhwa (KPK), which cover more than 70% of Pakistan’s geographical area. These areas have limited healthcare services, exacerbating the struggles faced by the communities. For instance, in Balochistan, only one community-based organization serves a vast area, and access to services is further hindered by floods and security issues.
Resilience and Adaptation
Despite these challenges, the community continues to show resilience. In Pakistan, where gay men and MSM are criminalized, community services and healthcare remain crucial. Young people are actively engaged in mitigation measures, such as plantation projects, to counter the impacts of climate change. The community is also collaborating with stakeholders to ensure inclusive efforts for those living with HIV, gay men, and MSM.
Khan concluded his speech by emphasizing the need for continued adaptation to the changing climate. He called for greater support and collaboration to address the multifaceted challenges faced by these vulnerable communities.
Ali Raza Khan’s speech at the AIDS 2024 conference serves as a powerful reminder of the urgent need to address climate change and its disproportionate impact on marginalized communities. His insights highlight the resilience and determination of these communities in the face of adversity. For more detailed information and studies, visit AliRazaKhan.com and PridePakistan.org.
Civil society has always been at the center of emergencies ensuring that their communities are able to overcome the challenges and impacts that are left behind when emergencies happen. The communities pull their resources together to address these issues and this is not an event rather a process.
HIGHLIGHTS
Whether it is floods in Pakistan, violence, unrest and natural calamities in Haiti, immigrants and refugees in Europe, UK, Columbia and Peru; the communities of people most affected come together to address the challenges head on. “Governments come and go but civil society is always there to work with communities,” shared Mary Ann Torres of ICASO who took the participants through Venezuela advocacy for Global Fund grant. As a country that did not fit what was required to get funded by the Global Fund, the civil society members organised and advocated relentlessly sharing their true lived realities and this saw the country become a recipient of the fund. “The location might be different but the experiences the same. If organisations and communities can share with each other, to learn from each other instead of reinventing the wheel, a lot can be achieved.” Shared Judy Otti of the African Advocacy Foundation. “It is important to understand emergencies last longer and have lasting impact…More resources are needed to ensure that the communities are not left on their own to figure it out.” said Mary Ann Torres
CRITICAL ASSESSMENT
Time and time again, civil society picks up the pieces of what is left of their communities after an emergency. When the rest of the world moves on to focus on the country and the next issue, they are the ones who have to figure out how to function in the new normal. For this to be possible and continue, there is need to invest continuously in these efforts.
Mpox, a viral illness similar to smallpox, has been declared a global health emergency by the World Health Organization (WHO). For people living with HIV, understanding the risks and benefits of Mpox vaccination is vital. As an HIV-positive gay activist from Pakistan, I want to share my personal experience and insights on the importance of vaccination and preventive measures.
I, Ali Raza Khan, an HIV-positive individual, have faced numerous challenges throughout my journey. My experience with HIV treatment and vaccinations has reinforced my belief in the importance of science and medical advice. Since April 2019, I’ve undergone numerous changes to my medication regimen to achieve an undetectable HIV viral load. I have seen many other HIV-positive people listening to rumours and delaying their treatments and vaccinations.
Similar rumours occurred when the COVID-19 vaccine was introduced. HIV-positive people were curious and asked many questions, including: Should we take the COVID-19 vaccine? Is it safe for us? As a health worker working in community HIV prevention programs, I was among the first to take the COVID-19 vaccine, and it was safe.
I believe in science and doctors who have saved my life over these years. I want other HIV-positive people to trust scientists and protect themselves from Mpox and other infections by vaccinating or adhering to their doctors’ prescribed treatments.”
My understanding of the risks and benefits drove my decision to vaccinate against monkeypox. I emphasise the importance of trusting medical professionals and seeking accurate information from reliable sources.
I have taken the Mpox vaccination, and from my personal experience, I can say that I didn’t experience any adverse side effects after receiving it. It was a smooth process for me.
I urge other HIV-positive individuals, as well as people from key populations, including the LGBTQ+ community, to get vaccinated against Mpox if the vaccine is available in their area. It’s a crucial step in protecting your health.
By sharing my personal experience, I encourage others to trust medical professionals and seek accurate information. Individuals can play a vital role in controlling the spread of Mpox by taking preventive measures and getting vaccinated.
For accurate and up-to-date information on monkeypox, visit the websites of your local health department, the World Health Organization (WHO), and reputable health organisations. These resources can guide vaccination, prevention, and treatment.
Monkeypox, a viral illness similar to smallpox, has been declared a global health emergency by the World Health Organization (WHO). For people living with HIV, understanding the risks and benefits of monkeypox vaccination is crucial. As an HIV-positive gay activist from Pakistan, Ali Raza Khan wants to share personal experience and insights on the importance of vaccination and preventive measures.
Ali Raza Khan, an HIV-positive individual, has faced numerous challenges throughout his journey. His experience with HIV treatment and vaccination has reinforced his belief in the importance of science and medical advice. He shares “ Since April 2019 and I have gone through a lot of medicine changes to get HIV undetectable viral load. I have seen many other HIV positive people listening to rumors delaying their treatments and vaccinations and eventually believing the science and doctors.”
He was one of the first people in his community health care workers to receive the COVID-19 vaccine when it was only allowed for health care providers, despite widespread misinformation and concerns in the community.
“Similar rumors happened in the covid-19 when the covid-19 vaccine came HIV positive people were curious with a lot of questions around having covid-19 vaccine as HIV positive individuals including Should we take the covid-19 vaccine or not? Is it safe for us or not? I was one of the first that took the covid-19 vaccine as a health worker I was working in community HIV prevention programs. I believe in science and doctors that have saved my life over these years from different infections I suffered and I wanted other HIV positive people to trust on scientists and protect themselves from monkeypox and other infections by vaccinating or adhering to their doctors prescribed treatments.”
Ali Raza Khan’s decision to get vaccinated against monkeypox was driven by his understanding of the risks and benefits. He emphasizes the importance of trusting medical professionals and seeking accurate information from reliable sources. His personal experience demonstrates that vaccination can be a powerful tool in preventing serious illnesses, even for those living with HIV.
Transmission according to WHO:
Person-to-person transmission of mpox can occur through direct contact with infectious skin or other lesions such as in the mouth or on genitals; this includes contact which is
face-to-face (talking or breathing)
skin-to-skin (touching or vaginal/anal sex)
mouth-to-mouth (kissing)
mouth-to-skin contact (oral sex or kissing the skin)
respiratory droplets or short-range aerosols from prolonged close contact
The virus then enters the body through broken skin, mucosal surfaces (e g oral, pharyngeal, ocular, genital, anorectal), or via the respiratory tract. Mpox can spread to other members of the household and to sex partners. People with multiple sexual partners are at higher risk.
Monkeypox Diagnosis according to WHO:
Identifying mpox can be difficult as other infections and conditions can look similar. It is important to distinguish mpox from chickenpox, measles, bacterial skin infections, scabies, herpes, syphilis, other sexually transmissible infections, and medication-associated allergies. Someone with mpox may also have another sexually transmissible infection such as herpes. For these reasons, testing is key for people to get treatment as early as possible and prevent further spread.
Monkeypox Vaccination for People Living with HIV
People living with HIV are generally at higher risk for monkeypox infection, especially if they have a weakened immune system. Vaccination can significantly reduce the risk of severe illness and complications. Here’s what people living with HIV should know that by having a monkeypox vaccination you are
Reducing risk of severe illness and hospitalization for yourself
Protection against potential complications
Individual contribution to public health efforts to control the spread of monkeypox in community
You might only have mild side effects, such as pain at the injection site, fever, fatigue, and headache as serious side effects are rare in monkey pox vaccination.
If you are eligible or not it can vary by country or region. Consult with your healthcare provider for specific guidance.
“ Go for the vaccination if you have some questions I would like to clear in this post. Monkeypox is declared as a global Health concern by WHO. I already have taken my first dose of monkeypox vaccine last time when I was wasting in Canada as Canada has monkeypox free vaccine for visitors as well. On the other hand in my country in Pakistan the vaccine is still not available. If it is also not available in your country you can follow preventive guidelines from WHO on monkeypox. I did not have anything wrong or any side effects after taking the monkey pox vaccine. I would also suggest other HIV positive people and people from key populations including gay community To go and get themselves vaccinated with monkeypox if they have it available in their country. ”
Preventive Measures
Even if you have been vaccinated, it’s essential to follow preventive measures to reduce your risk of monkeypox infection:
Practice safe sex: Use condoms and limit the number of sexual partners.
Avoid contact with infected individuals: Be aware of symptoms and avoid direct contact with people who have monkeypox.
Wash your hands frequently: Use soap and water or hand sanitizer.
Clean and disinfect surfaces: Regularly clean and disinfect surfaces that may be contaminated.
“It is important for us as vulnerable population of people from queer and sex work community to have basic information and guidelines around monkey pox vaccination especially for people living with HIV and also to get accurate guidance and information around Mpox from verified sources including health ministries websites and Worlf Health Organisation resources. “
Monkeypox vaccination is a crucial tool in protecting people living with HIV from serious illness. By sharing his personal experience, I encourage others to trust medical professionals and seek accurate information. By taking preventive measures and getting vaccinated, individuals can play a vital role in controlling the spread of monkeypox.
For accurate and up-to-date information on monkeypox, visit the websites of your local health department, the World Health Organization (WHO), and reputable health organizations. These resources can provide guidance on vaccination, prevention, and treatment.
Artists and scientists have worked together to create pieces of art now on display in Munich, Germany in conjunction with the International AIDS Conference. The exhibition, titled HIV Science As Art, was conceived by co-curators Jessica Whitbread and Daniel Cordner. It follows in the footsteps of their 2023 show that was on display a year ago during the IAS Conference on HIV Science in Brisbane Australia.
The art will be for sale and all proceeds will be used to support community-based HIV programs in Eastern Europe, Central Asia, and Africa. But the impact of the show extends beyond raising money for worthwhile organizations. The exhibition also challenges viewers to think more deeply about important biomedical and social issues.
One artist/scientist pair worked together to create a piece on vaccine hesitancy. Charles Ryan Long is a Chicago-based artist and long-time HIV/AIDS activist. He partnered with Dr. Heidi Larson, a professor at the London School of Hygiene and Tropical Medicine and founder of the Vaccine Confidence Project. Their piece is entitled, “The Roots of (dis)Trust.”
Khairullah Rahim, an artist based in Singapore, collaborated with Ali Raza Khan, an HIV activist in Pakistan. Their piece, “Penjaga Hutan Batu (Guardian of the Stone Jungle),” is a short video ostensibly about pigeons. But Khairullah noted that the pigeons represent so much more. These birds often are vilified as carriers of disease. Too often, he remarked, people living with HIV are similarly vilified.
Both artists remarked that the collaborations with their science partners grew very organically. Long commented that when he was speaking with Dr. Larson about her work on vaccine hesitancy, the idea came quickly. “This is about trust,” he said. “It came to me rather easily and then it was just about how to transfer that idea.”
Rahim had similar thoughts about his collaboration. The process, “was very spontaneous. We wanted to see where the experimentation would bring us. There was no very clear end product that we were interested in.”
The exhibition has been supported by the pharmaceutical company ViiV Healthcare and Münchner Aids-Hilfe, an organization supporting people living with HIV in the Munich region since 1984. Works of art are on display at Brainlab, Olof-Palme-Straß 9 in Munich through July 25, 2024. The exhibition is open to the public daily from 10:00 AM until 7:00 PM local time.
Read more on original article on Forbes website here
It was an honor to be invited by the UNICEF-led Global Partnership for Adolescents and Young Key Populations (Global ayKP Partnership) to speak at their recent event. The topic, “Connectedness & Community,” resonates deeply with the work we are doing on the ground in Pakistan for children and young people living with HIV and other vulnerable key populations, including gays, MSM (men who have sex with men), and sex workers. Here’s a summary of the insights I shared during the session.
At HIV Voices, we define ourselves as a youth-led initiative working for young people living with HIV and adolescents from key populations. Our approach leverages digital and innovative methods to reach individuals who are often difficult to engage due to their circumstances and locations in Pakistan. Our group comprises a diverse array of young people dedicated to spreading awareness about HIV, prevention methods, and addressing the unique challenges we face, including security concerns and the impact of climate change.
Engagement and Empowerment
One of our core activities involves ensuring that adolescent and young key population (ykp) voices are heard. This includes:
Mobilizing our members
Conducting capacity-building training sessions
Utilizing various platforms and methods available on the ground
Making our voices heard at national and global levels through letter and story campaigns, particularly on digital and social media platforms.
Fostering Reproductive Health and Rights
We place significant emphasis on the reproductive health and rights of adolescents and young girls. Our efforts are not just about HIV prevention but also about creating a safe space where key populations can voice their concerns and work together to tackle issues that affect their well-being.
Connectedness as a Core Theme
The theme of connectedness is at the heart of our work, especially in a conservative country like Pakistan, where key populations are criminalized, and safe spaces are scarce. We often face pressure from various security-related entities and other stakeholders, which can hinder our efforts. However, understanding and navigating these conditions is our strength. As young people and peer mentors, we know how to deal with the issues we encounter on the ground, ensuring that young people from key populations and other stakeholders remain connected and that our voices are heard.
Addressing Interconnected Issues
When working with vulnerable key populations, we sometimes overlook interconnected issues. Our programs and activities aim to bridge this gap by raising awareness and fostering collaboration among different groups. For example, we’ve facilitated exercises that help participants understand how issues affecting one key population are linked to those of another, promoting a more unified approach to addressing these challenges.
A Message of Empowerment
Allow me to share a powerful message from Aslam, a young man living with HIV and a member of our group, Young Positive People of Pakistan:
“Hello everyone, my name is Aslam, and I’m a young man living with HIV. When I was diagnosed through a community-based organization working for key populations, I felt the need for additional support and a desire to contribute to my community. Connecting with Young Positive People of Pakistan not only helped me feel supported but also empowered me in navigating HIV-related systems. Since becoming a member, I have expanded my knowledge about the global fund process in Pakistan, learned about the contributions of various stakeholders, and represented young PLHIV (people living with HIV) on national and international platforms. This involvement has enabled me to address our community’s issues effectively and advocate for our rights.”
The work we do on the ground, driven by the theme of connectedness, is vital. It’s crucial for global organizations and partnerships to continue supporting these efforts at a global level. The empowerment and collaboration of young key populations are essential to creating an inclusive and effective response to HIV. Thank you to the Global Partnership for Adolescents and Young Key Populations for providing this platform and for recognizing the importance of our collective efforts.
Munich, Germany – The AIDS 2024 conference will feature a pivotal session titled “From Ruin to Resilience: Harnessing Community Strength in the Face of Natural Disasters,” highlighting the critical intersection of climate change and public health. This scientific symposium, accredited for Continuing Medical Education (CME), will take place on July 25, 2024, from 15:00 to 16:00 local time in Room 13a for in-person participation and on Channel 6 for virtual attendees.
Spotlight on Ali Raza Khan
One of the key speakers for this session is Ali Raza Khan, an HIV-positive gay activist from Multan, Pakistan. Khan is the founder of PridePakistan.org and co-lead of TheYouthPACT.org. His work focuses on advocating for the rights and health of marginalized communities, particularly those affected by HIV and climate change.
Session Overview
Moderated by Mary Ann Torres from ICASO, the session will delve into the dire impacts of emergencies caused by pandemics, war, the climate crisis, and other catastrophic events on vulnerable and marginalized communities. The discussion will cover a range of critical issues, including:
Continuity of Care: Ensuring ongoing care for children and young people born with HIV.
Access Disruptions: Addressing interruptions in HIV prevention, testing, and treatment services.
Challenges for Migrants and Refugees: Highlighting the specific difficulties faced by these groups.
Increased Vulnerability to Co-Infections: Focusing on diseases such as diarrhoea, lung infections, and TB.
Impact of Food and Water Shortages: Examining how these shortages increase vulnerability to illness.
Inequalities in Social Protection: Discussing disparities in access to social safety nets.
Risk of Violence and Exploitation: Addressing the heightened risk of violence and exploitation in crisis situations.
Gender Inequality and Gender-Based Violence: Exploring the exacerbation of these issues during emergencies.
Forced HIV Testing of Migrants: Highlighting the ethical and health implications.
Funding Challenges: Discussing the impact of dwindling resources in the face of multiple crises.
Ali Raza Khan will share insights from his extensive work in Pakistan, where he has witnessed firsthand the devastating effects of climate change on communities living with HIV. His presentation will focus on the resilience and strength of these communities in the face of natural disasters. Khan will highlight the innovative strategies employed by community organizations to mitigate the impacts of climate change, such as plantation projects and collaborations with stakeholders to ensure inclusive efforts for those living with HIV.
Other Speakers
The session will also feature contributions from:
Juddy Otti from the Africa Advocacy Foundation, United Kingdom
Sophia Charles from Caris Foundation International, United States
These speakers will provide a global perspective on the challenges and solutions related to the health of vulnerable communities during emergencies.
Ali Raza Khan’s participation in this session underscores the importance of community-led initiatives and the need for global solidarity in addressing the multifaceted challenges posed by natural disasters and other crises. His work with Pride Pakistan and The Youth PACT exemplifies the power of resilience and the critical role of advocacy in safeguarding the health and rights of marginalized populations.