The Union for International Cancer Control (UICC) has been hosting the World Cancer Congress each year since 1933. This year it was held in Malaysia – the first time in South East Asia.
Thousands of delegates from around the world convened in Kuala Lumpur, “to unite the cancer community, reduce the global cancer burden, promote greater equity and integrate cancer into the world’s health and development agenda.”
The Max Foundation was an active participant:
Side-by-side with other internationally recognized leaders, Pat Garcia-Gonzalez, CEO, shared Max’s 20-year-history in “Uncovering the Stories Behind the Leaders.”
Erin Schwartz, VP of Global Engagement, presented on the importance of including patient perspectives in “Global Equity of Cancer Care.”
Ong Mei Ching, Region Head Asia Pacific, conveyed the importance of patient-centricity in “Best Practice Patient Advocacy in Asia Pacific.”
We attended the World Cancer Congress to raise awareness for our core mission – access to cancer treatment – and how to achieve it through our patient-centered model, Max Access Solutions.
We ran an interactive booth, where attendees made video recordings of their own answers to the question: what does treatment access mean to you?
We have received overwhelming responses from key members of the UICC, counterpart organizations, cancer survivors, advocates, doctors, and healthcare providers.
At this prestigious event – empowered by more than 3,000 leaders, cancer and health experts from 139 countries, and more than 85 years of history – our own Pat Garcia-Gonzalez was honored with the CEO Award. The award was given in recognition of The Max Foundation’s leadership and drive to mobilize people and build partnerships across sectors and borders, transforming a grassroots organization into an international movement impacting the tens of thousands of lives worldwide.
Below are some of the quotes we received:
“Cancer patients in the US, in Europe, in Asia, in Nigeria are the same cancer patients. The only difference is where they live. The advocacy should get through to everyone and the treatment should be affordable to everyone.”
Mr. Runcie C. W. Chidebe, Winner of World Cancer Day Spirit Award of UICC; Executive Director of Project PINK BLUE – Health & Psychological Trust Centre, Nigeria
“I have been following The Max Foundation through the website. Max has done great works in giving support to individuals living with cancer. How do I describe Max in one word? Passionate!”
Dr. Hadi Mohamad Abu Rasheed, Head of Professional Development and Scientific Research of Qatar Cancer Society, Qatar
“The Max Foundation is extraordinary and courageous despite the difficult environment. There are not many organization that can provide such niche supports to cancer communities. I would like to explore the opportunity of collaborating with Max to bring more benefits to cancer patients in Nigera.”
Professor Sani Abubakar Malami, President and CEO of Nigerian Cancer Society, Nigeria
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.
I have learned that the pain in the heart and soul is deep and will always be there. The ‘bucket’ has a hole, and even when you dedicate every day of your life to making sure other families don’t have to live with this pain, the bucket will never be filled. I have also learned….
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.
When Ka came to Thailand for access to treatment, she had the chance to join the MaxSmiles patient group meetings. Ka started to dream about having her own meetings and soon found support from Dr. Mary Cluck, an Australian volunteer working with Cambodian CML patients. Ka stepped up and called the patients one-by-one to invite them to their first patient meeting.
