Radha Bai Chandra is a 62-year-old widow, a mother, and the longest-surviving beneficiary of Max’s programs in Fiji. Although her search for treatment was long and challenging, the second life she now has from that search is worth it. In 2005, Radha Bai noted a change in her energy levels. She was usually an active person. She started to need longer naps and couldn’t complete everyday chores. At this time, she lost a lot of weight. Her husband and 11-year-old daughter also noticed she was more tired than usual. A neighbor helped her to be seen in the hospital, and after many tests, she was told she had a ‘Blood Disorder.’ Somehow she managed to travel to Auckland, New Zealand, where she was diagnosed with Chronic Myeloid Leukemia. Unfortunately, her treatment plans were too expensive, and she returned to Fiji with only a few months’ supply of medication.
In 2006 Radha Bai faced a dwindling supply of medication and no health insurance. During this time, she lost her husband to a sudden illness. Without warning, Radha Bai was a new widow and a single mother with Leukemia. She made the tough decision to send her daughter to live with her brother in New Zealand.
Her Doctor in New Zealand did not give up and found a Max contact. After communication back and forth with paperwork, tests, and prayers, she was approved to get treatment through Max. In her own words: “The Max Foundation gave me the gift of a second life” Radha Bai is looking forward to traveling in October 2022 to attend her daughter’s wedding in New Zealand.
Radha Bai complies with her treatment requirement; she is punctual at the clinics and responsive to her doctor’s instructions. Besides her occupation helping with domestic duties, she is a powerful advocate of good health to her friends, relatives, and community. Her advice to patients who live with CML: “Live a healthy lifestyle, obey your doctors, ensure your medication is stored well, and be compliant!”
For the 16 years living with Leukemia, Radha Bai’s message to all of us at The Max Foundation: “VINAKA VAKALEVU (Thank you) for saving me and the second life you have given me through the free medication.“
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.
Dr. Jayasree Iyer, Executive Director of the Access to Medicine Foundation (ATMF), sits down with The Max Foundation and answers seven questions about the Access to Medicine Index, emerging trends in treatment access, and the role of collaborative access initiatives in treating chronic diseases.
When he was initially diagnosed with chronic myeloid leukemia, Prashant’s first concerns weren’t whether he would be able to afford treatment, it was about how much time he had left…years? Months? Would he be able to complete his degree? Would he be able to care for his father?
But his doctor reassured him. Treatment was available, and before he could worry about the cost of it, Prashant was connected with The Max Foundation and worked on getting enrolled in the access program we administer.
Un Paso Max, meaning “Un Paso Mas” (One More Step) is a fitting name for a group led by cancer survivors who are willing to take an extra step to help others. Un Paso Max is the name of the CML and GIST patient association in the Dominican Republic. One can trace the origins of this group to a small meeting in 2008. It only took a bit of encouragement and support on the part of The Max Foundation to unlock the passion of a handful of courageous survivors in Santo Domingo, and the seed of a patient association was planted.
