#BtheVoice Video Library

The B the Voice story bank is a global effort to elevate the voices of those living with hepatitis B. It’s a compliment to the #justB storytelling campaign that focuses on the U.S. Each story is unique and is told by a person living with hepatitis B. Many of the topics covered by the storytellers include stigma, discrimination, access to healthcare and more.

Michelle Liu Michelle Liu

Ibrahim’s story of living with hepatitis B in Nigeria

Ibrahim shares his personal journey of discovering he has hepatitis B after seeking medical help for his mother. Despite the shock and financial hardships he faced, including the inability to afford both food and medication, Ibrahim emphasizes the importance of perseverance. He advises others in similar situations to stay focused, follow medical advice, and continue living their lives. His story sheds light on the challenges of managing hepatitis B in difficult circumstances.

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Michelle Liu Michelle Liu

Jane’s story of living with hepatitis B in Nigeria

Jane reveals her emotional journey after being diagnosed with hepatitis B at just 20 years old during a church health screening. Shocked and confused, she faced isolation and stigma, particularly in Nigeria, where the virus is met with harsh judgment, as exemplified by her uncle’s household dismissing their maid for testing positive. Jane’s story unfolds the painful reality of contracting the virus from her mother and ultimately losing her to the same illness. Yet, through her struggles, Jane emerges as a beacon of hope, urging others to get tested and seek support. Her powerful message challenges the stigma and advocates for understanding and awareness, transforming her journey into a call for change. 

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Michelle Liu Michelle Liu

Irinam’s story of living with hepatitis B in Nigeria

When life scientist Irianm discovered he had hepatitis B, the diagnosis shook him to his core. As someone who had spent years counseling others on viral hepatitis, he never expected to find himself on the other side. His journey from shock and confusion to hope and advocacy offers a powerful reminder that hepatitis B is treatable—and that listening to those who've lived through it can be life-changing.

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Michelle Liu Michelle Liu

PB’s story of living with hepatitis B in Nigeria

PB, a medical lab scientist, discovered she had hepatitis B in July 2019 during a testing event she helped organize to encourage others to know their status. Shocked by her positive result, PB retested to confirm the diagnosis. Since then, she has been actively promoting hepatitis B awareness, encouraging others to get tested, and even supporting those who lack the resources to seek treatment. Her advocacy is fueled by the loss of a fellow church member to the disease, which has deepened her commitment to helping others.

 

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Michelle Liu Michelle Liu

TJ’s story of living with hepatitis B in Nigeria

TJ discovered he had hepatitis B during a required pre-marital examination, despite having been vaccinated years earlier. Though symptom-free, the diagnosis has had a significant impact on his life, particularly in job opportunities where he faces disqualification due to his hepatitis B status. This has led to psychological distress, as the stigma and uncertainty surrounding the virus weigh heavily on him.

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Michelle Liu Michelle Liu

John’s story of living with hepatitis B in Nigeria

John discusses the lack of awareness and support for those living with hepatitis B in his home country, Nigeria. He shares his experience of discovering his diagnosis after routine blood tests and the challenges of managing the condition, including the high cost of medication. John emphasizes the importance of living a healthy lifestyle, staying consistent with checkups, and maintaining hope, drawing inspiration from others who have lived long and healthy lives with the disease.

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Michelle Liu Michelle Liu

Yahaya’s story of living with hepatitis B in Nigeria

Yahaya's journey with hepatitis B began unexpectedly in May 2019, when he went to donate blood for his cousin. After the blood test, he noticed the doctor's concerned expression, which led to the diagnosis of hepatitis B. At the time, Yahaya knew little about the disease, understanding only that it was viral and had two types, one being a "silent killer." This diagnosis profoundly changed his life and how he interacted with others. In March 2022, before marrying, Yahaya ensured that his wife was tested and immunized against hepatitis B. He also took steps to protect his newborn nephew by advocating for early vaccination. Although he faced challenges and skepticism from his family, Yahaya emphasized the importance of acknowledging the seriousness of hepatitis B and taking preventive measures.

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Michelle Liu Michelle Liu

Francis’ story of living with hepatitis B in Nigeria

Francis was just 16 years old when a hepatitis B outbreak at his school led to his diagnosis. His mother, a medical professional, reassured him that he could still live a full life if he took the necessary precautions. However, the news deeply impacted Francis, leading to a period of emotional turmoil that affected his relationships and his aspirations. Despite his passion for cake decorating, the stigma and challenges associated with his condition made it difficult for him to pursue his dreams. Over time, Francis found the strength to move forward, deciding to live life fully and not let his condition define him. He believes that whatever challenges you face should motivate you to be a blessing to others, and he encourages others to leave the stigma behind and embrace life.

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Michelle Liu Michelle Liu

J’s story of living with hepatitis B in Nigeria

J discovered she had hepatitis B during a routine antenatal visit while pregnant. The diagnosis was a shock, especially since she had lost two in-laws to the disease. Overwhelmed with fear for her unborn child, she was reassured by medical staff that hepatitis B was not a death sentence and that her baby could be protected through vaccination. This brought her relief, and she focused on ensuring her child’s health. For four years, J has been attending regular clinic visits, monitoring her viral load, and following medical advice. She advises others with hepatitis B to remain calm, avoid harmful substances like alcohol, and maintain regular check-ups with their doctors.

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Michelle Liu Michelle Liu

Prince’s story of living with hepatitis B in Nigeria

In 2017, Prince organized a blood drive in his local community. During the screening process, he discovered he was unable to donate blood due to a diagnosis of hepatitis B. Initially, he struggled to come to terms with this news and felt lost navigating his condition. Recognizing the lack of awareness and resources in his community, Prince was inspired to take action. He founded a local organization to collaborate with the government and educate others about hepatitis B. Today, Prince works closely with the Hepatitis B Foundation, sharing his story and empowering others living with viral hepatitis.

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Guest User Guest User

Nathaniel's story of living with hepatitis B in Nigeria

Nathaniel found out he had hepatitis B shortly after losing his father to liver cancer caused by hepatitis B. He describes that many people in Northern Nigeria are unaware of hepatitis B. Nathaniel shares more about his experience with getting treatment. Nathaniel describes the challenges of accessing treatment in Nigeria can be costly. He describes that the same treatments are free for HIV and hopes that the same program can be extended to hepatitis B.

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Tyrone Robinson Tyrone Robinson

Sonia, Nigeria: #ICantWait To Vaccinate My Baby

Sonia brings a voice to the almost 300 million people living with hepatitis B in her #BtheVoice interview. She discusses how important it was for her to vaccinate her children at birth and the hurdles she faced in receiving the birth dose vaccine in Nigeria. It was costly, and unavailable in her town, so they had to travel to get the dose.  

She also discusses to issues with stigma and discrimination and admits that she has not told many people outside of the medical community. She stresses the need for understanding of the virus and states, "It does not make you less than a person." 

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Tyrone Robinson Tyrone Robinson

Ismail, Nigeria: #ICantWait for a World Without Stigma

Ismail is one of almost 300 million people with hepatitis B. He found out that he had hepatitis B when he got a required medical test. Thankfully at the time his hepatitis B was diagnosed it was found that his liver was normal and the infection was inactive.

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