News and Stories


‘Let’s Grow Together’: Voices for PEN-Plus Team Expands

‘Let’s Grow Together’: Voices for PEN-Plus Team Expands

Two sickle cell warriors from Kenya and two type 1 diabetes warriors, one from Uganda and the other from Zambia, recently joined the Network’s Voices for PEN-Plus advocacy program. “Your story makes a difference, your story has impact,” veteran Voices advocate Moses Echodu said in welcoming the newcomers. “And, importantly, your story is what will keep someone else hopeful.”

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Transforming Pain into Power: Mentors Encourage Young Warriors to Become Advocates
Mike Lawrence Mike Lawrence

Transforming Pain into Power: Mentors Encourage Young Warriors to Become Advocates

Emmanuel Kisembo and Lwimba Kasongo—who live with type 1 diabetes and sickle cell disease, respectively—are tireless advocates for awareness and education about their conditions. They are members of the NCDI Poverty Network’s Voices for PEN-Plus program and were co-captains last summer at an integrated PEN-Plus camp in Zambia, where they mentored nearly 60 youth with noncommunicable diseases. In this article, they share their lived experience and reflections on mentorship, advocacy, and the power of integration in fostering peer support.

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Celebrating the Network’s First Five Years
Paula Byron Paula Byron

Celebrating the Network’s First Five Years

Five years. Twenty-nine countries. Over a hundred PEN-Plus clinics. More than 14,000 patients. Together, the many collaborators that compose the NCDI Poverty Network deliver hope and healthcare to children, adolescents, and young adults navigating the dual challenges of poverty and severe, chronic noncommunicable diseases. And this is just the beginning.

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Health Leaders Commit to Accelerating PEN-Plus in Africa

Health Leaders Commit to Accelerating PEN-Plus in Africa

At the second International Conference for PEN-Plus in Africa, recently held in Abuja, health leaders, policymakers, and development partners across Africa renewed their commitment to an accelerated implementation of the PEN-Plus to significantly expand access to care for people living with severe noncommunicable diseases.

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‘Community Is Crucial’
Paula Byron Paula Byron

‘Community Is Crucial’

In recognition of World Diabetes Day, educator and advocate Edith Mukantwari shares her personal story of living with type 1 diabetes in Uganda, the lessons she’s learned, and the importance of a supportive community.

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Building for the Future
Paula Byron Paula Byron

Building for the Future

The PEN-Plus clinic in eastern Uganda began as a gathering under a tree and has blossomed into a standalone structure with consultation and treatment rooms, a training center, and a pharmacy.

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From Words to Action
National Commissions Paula Byron National Commissions Paula Byron

From Words to Action

The first International Conference on PEN-Plus in Africa provided a platform for health experts, policymakers, civil society organization representatives, donors, people living with noncommunicable diseases, and community advocates to expedite political and financial backing for PEN-Plus.

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PEN-Plus in Action Introduces a Global Partnership to Fight Severe, Chronic NCDs
Guest User Guest User

PEN-Plus in Action Introduces a Global Partnership to Fight Severe, Chronic NCDs

More than 60 representatives of leading global health policy, technical, advocacy, and financing institutions and people living with NCDs gathered at UNICEF House in New York on September 15, 2022, to introduce the PEN-Plus Partnership, a major international initiative to address the global burden of severe NCDs and injuries that cause more than 500,000 avoidable deaths every year among children and young adults living in extreme poverty.

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Overcoming Stigma to Become an Advocate for Kids with Cancer in Uganda and Beyond
Allison Westervelt Allison Westervelt

Overcoming Stigma to Become an Advocate for Kids with Cancer in Uganda and Beyond

“I fought cancer and won, and now I’m fighting the stigma that people with NCDs are doomed to die, because everyone deserves access to affordable NCD treatment,” says Moses Echodu. “I hope others who have lived with cancer and other NCDs will feel empowered to share their stories to break down stigma and demand access to treatment for all.“

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