The Maximize Life Campaign is a chance for people facing cancer to raise their voice and fight stigma about cancer. This year, we asked our regional teams to share stories of patients and caregivers that have inspired their work. We kick things off with Latin America.
Antonia was three years old when she was diagnosed with Chronic Myeloid Leukemia, and four years old when she attended her first Maximize Life Campaign event in Nicaragua, organized by the local patient group Fundación Alas de Vida in October 2014. The event consisted of a patient meeting, the biggest meeting the organization hosts each year, where patients and caregivers from all over the country gathered to support each other and share their stories and experiences regarding their diagnosis. Little did they know at that time that one of the strongest supporters present in the meeting would be Antonia, with her young age and her love for life.
Her mother, Fernanda, was the one who initially volunteered to provide her testimony – she talked about how this diagnosis impacted the family in a way they had never expected and how, despite everything, Antonia herself was the one who became the driving force of her parents.
Fernanda’s testimony inspired everyone present, but what was most surprising was the testimony that followed – Antonia’s: “Hello, my name is Antonia, and I am happy to be here!”
After getting to know her, every member of Alas de Vida adopted Antonia as their own example to follow. She became The Princess, the little warrior who spreads optimism in the group.
Last year, Antonia was diagnosed with malignant cells in her brain and she received radiotherapy. So far, her prognosis is good, and she was able to attend the 2015 Maximize Life event together with her friends in the patient organization, where she had her photo taken with everyone.
Currently, Antonia is travelling to Mexico to receive treatment. On behalf of The Max Foundation, we wish for her to recover like we know she will, and to continue showing the world that Maximo can be a Princess, too.
The Max Foundation is a leading global health nonprofit organization dedicated to accelerating health equity. For 27 years, Max has pioneered practical, scalable, high-quality solutions to bring life-extending treatments and patient-centered health care to more than 100,000 people living with cancer and critical illness in low- and middle-income countries. Max believes in a world where all people can access high-impact medicines, where geography is not destiny, and where everyone can strive for health with dignity and with hope.
October is my favorite month of the year. It marks a changing of the seasons in both the southern and northern hemispheres that brings a sense of reflection and excitement. As such, there could not be a more appropriate month to celebrate theMaximize Life Global Cancer Awareness Campaign, an initiative that encourages people impacted by cancer to reflect on their experiences, celebrate their resiliency, and share their stories with the world.
As part of our 20th Anniversary Celebration on October 19th, The Max Foundation was honored to have Princess Dina, President-elect of the Union of International Cancer Control, reflect on our global efforts over the last two decades. We share her letter here with gratitude and humility. “Lack of access to treatment” is a five-word sentence that is….
Thousands of patients are diagnosed with chronic myeloid leukaemia (CML) annually around the world. CML, like any other cancer, does not discriminate. It affects people from all regions and walks of life. However, unlike many other cancers, CML has an amazing story due to advancements made in its treatment in the last decade. It was only 15 years ago that a patient newly diagnosed with CML would have a prognosis of survival of less than 5 years with the treatments available at the time.
