Meet Ashika! She’s been with The Max Foundation for almost 14 years, working as a program officer in India. Learn more about why she started with Max, what she enjoys about her job, and a special memory she had with a patient.
When did you start with The Max Foundation, and why were you interested in working here?
I started with The Max Foundation in September 2011. I was drawn to the organization because of its mission to help cancer patients access life-saving medications and to create spaces where they can connect, share their experiences, and support one another. That purpose deeply resonated with me, and I felt a strong desire to be part of something so impactful and meaningful.
What do you enjoy most about your job?
What I enjoy most about my job is the opportunity to connect with people from diverse backgrounds and help build a strong, supportive community. It’s incredibly inspiring to see how these connections can ease the sense of isolation and empower patients in their journey.
What is a special memory you have with patients?
One special memory that stands out is from a Patient Support Group meeting, where a patient I had only interacted with over the phone came up to me with a smile and said how happy she was to finally meet the voice that had always listened and supported her. She thanked me for being there through her cancer journey. That simple, heartfelt moment reminded me how powerful and meaningful human connection can be, even over a phone call.
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.
Cancer impacts entire families, not just the person receiving the diagnosis. Salsabila was 16 when she found out her father had marginal zone lymphoma. She’s the eldest of three siblings, living with her family in Malaysia. Navigating her father Mr. Azmi’s symptoms and treatment was difficult for them. Despite these challenges, Salsabila continued to study….
Each year on October 19th, Max’s Day, we honor Maximiliano “Max” Rivarola and his legacy of lifesaving support for cancer survivors through the work of The Max Foundation. This year, on Max’s Day at The Max Foundation’s 20th Anniversary Celebration, I wrote a letter to Max, reflecting on what his legacy has meant for patients,….
In Latin America, the Maximize Life Campaign has become something like a tradition – a time when each patient organization creates an event or activity of their choice and powers it up for a campaign that takes on a life of its own!
13 patient groups from 11 Latin American countries joined this year’s movement, bringing together patients and caregivers with the purpose of telling the community that cancer is an issue, that ignoring it is not going to make it go away, and that the best approach is to learn about it in order to know what to do about it. From governments to the general public, everybody can get involved in figuring out how to treat cancer patients as members of society and not as a burden.
