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 28 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.
We’ve already seen lots of activity around the world this spring: The first gastrointestinal stromal tumor patient meeting in Hyderabad, India; storytelling workshops where people facing cancer learn to share their experience with dignity and hope; and the Malaysia patient team takes their gathering public with a great picnic! See what else has been happening at The Max Foundation during the first part of 2016.
At The Max Foundation, increasing global access to treatment for people around the world living with cancer is a core element of our mission. But access to treatment is only one piece in helping all people facing cancer live with dignity and hope. Fostering care and support for patients processing the hardships of cancer is essential.
March 9th marks a somber anniversary; the day Max lost his 3 year battle with chronic myeloid leukemia (CML). For those of us who love Max, who either knew him then or who know and love him now, this will always be a day of sorrow. The words that come to mind are words such as ugly, unfair, impossible, and the feeling is one of emptiness; a whole in one’s heart. Max was a real person, a beautiful young child, whose encounter with cancer was nothing but a tragic episode.
