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.
The 13 Maximize Life Campaign events happening throughout Latin America are varied, and they go from meetings that aim to raise awareness in patients and their family members, such as those taking place in Argentina, Nicaragua and Honduras, to larger scale, community involving events, like those happening in Peru and Ecuador. Patients in Chile, Peru and Mexico have perfected a stage play for children with the story of Maximo and the Big C, Ecuador will organize their customary walk through the city with all types of cancer patients and, in Colombia, children going through treatment will be treated to an afternoon of fun and games, and the message that they are not alone.
Other events include promoting the campaign in non-central cities where access to information and support is rare (Guatemala), Maximo storytelling (Costa Rica), visits to the zoo (Dominican Republic), and others.
But all these events have something in common: plenty of helpful information – both scientific and practical, volunteers giving their time and efforts in order to make the activities and success, and the message that cancer can be fought, with everyone pulling in the same direction.
Mercedes lives in Buenos Aires, Argentina where she uses her Psychology Degree to support patients throughout Latin America.
Having a strong support system can make a world of difference for people living with cancer. That includes friends, family, and the dedicated healthcare professionals who partner with The Max Foundation. For Marina from Kyrgyzstan, the medical team at the National Oncology Center are pillars of strength and support. She was diagnosed with chronic myeloid….
Cancerworld recently published an article by Ann Wagstaff titled Begging for imatinib: why do so many patients still lack access to this lifesaver? It highlights the challenges people living with CML face in accessing imatinib, a life-extending medicine that has been generic for many years. Here is our perspective on the story. We have known….
Each year, The Max Foundation chooses a colleague to receive our Excellence in Patient Advocacy Award, honoring a member of our global team who has done something especially remarkable that year. On December 17th, we were delighted to present this year’s Excellence in Patient Advocacy Award to Viji Venkatesh, Region Head for South Asia, for her tireless dedication to the patients she serves.
