I commit to listening to patient and caregiver experiences and helping others from what I learn.

I commit to developing meaningful patient programming with our clients.

I commit to creating a culture where my team is encouraged to share patient experiences and participate in patient community activities.

I have been running our online platform for German-speaking leukemia patients for more than 14 years, and have helped to found and grow the CML Advocates Network for more than 10 years. I am supporting CML patients on a daily basis. This keeps me close to the real need of real patients, over and above being a cancer survivor myself now for 16 years...

I am committed to facilitate patient engagement in R&D by increasing the "system readiness" in patient organisations, academic groups and pharma to involve patient experts in a meaningful way.

I am involved in a number of educational activities and networks that work on patient information and patient empowerment, including EUPATI, PFMD, EURORDIS, Leukaemie-Online, CML Advocates Network, Acute Leukemia Advocates Network, WECAN and many more.

As the caregiver and advocate of one, I'll make sure our patient experience is relayed in the most articulated and constructive way since the margin for progress is massive

I will ask the next 5 patients I'm going to meet in the context of my profession as a manager patient affairs for a pharmaceutical company, what my company can do to improve her/his live most.

As a manager patient affairs, I will connect all German AZ teams of specific therapeutic areas with patients, to gain a better understanding of the patient perspective and patient needs, to develop better support materials and programs for patients and medical staff.

As a manager patient affairs, I will connect all German AZ teams of specific therapeutic areas with patients, to gain a better understanding of the patient perspective and patient needs, to develop better support materials and programs for patients and medical staff.

As a manager patient affairs, I will always response to any patient request within 10 working days.

As a Patient Centricity Excellence Director in the pharma industry, I will co-create with patients when building capability and training programs on how to best work with patients.

I will make sure i communicate the end results of the protocol simulation

I will listen to patient feedback on stigma associated with Acromegaly

All patients need to be included in RWE studies: real representativeness

As the head of Global Publications team, I will work with my team and stakeholders to identify how best we can ensure every publication has a meaningful and relevance to patients.

As a design strategist, I will co-create experiences, products, and strategies with patients. I will live up to the motto "nothing for me, without me".

As a medical writer, I will work to develop materials to support patient engagement strategies by pharmaceutical companies, involving patient review and co-creation of content wherever possible

I will partner with patients to ensure they shape their medicines and patient services of tomorrow, by ensuring myself and my team always include patient(s) input when developing solutions/services.

I will find someone who can act as a patient mentor and advise if what we think is a good idea actually addresses a need.

As Chair of the Patient and Public Involvement group at my local health trust, I will ask at least 1 patient representative 1 question at each meeting

I will work closely with PFMD patients and patient organisations members of PFMD, those of today and new ones, to understand what are the barriers they face

I will find a patient and spend time with them in the next 6 months to learn about how I can take their needs into consideration more in my role when I arrange meetings that involve patients.