🌟 Canadian CML Patients — We Need Your Voice! 🇨🇦
CML patients around the world are standing up and sharing their voices in our global Quality of Life Survey —
but where is Canada? – THE WORLD NEEDS MORE CANADA 🇨🇦
We’ve heard from the USA 🇺🇸, Australia 🇦🇺, France 🇫🇷, the UK 🇬🇧 — now it’s our turn to show the world that Canadian CML patients are strong, proud, and ready to lead the future of patient-centered care! 💪
🔹 This survey takes only 10–15 minutes.
🔹 It will directly help create a new care pathway — built by patients, for patients.
🔹 It’s your experience that will push Canadian healthcare to improve side effect management, TFR support, and outcomes that actually matter to us.
Several Provinces in Canada have reviewed VBHC with their Health Ministers, and they all agree – VBHC is the way to improve patient outcomes and manage escalating healthcare costs.
🌎 Don’t let Canada fall behind. Let’s show the world what patient leadership looks like!
✅ Click here and answer today: https://forms.office.com/r/rQKqU7cSW4
Every voice matters.
Your story matters.
Together, we change the future. 🇨🇦
#CMLCanada #PatientVoice #CMLStrong #CanadianCMLChallenge #ValueBasedHealthcare
Your voice matters in shaping the future of CML treatment. Thank you for your participation.
In collaboration with the TFR Group on Facebook, we are conducting a survey to gather essential insights from Chronic Myeloid Leukemia (CML) patients who are currently in Treatment-Free Remission (TFR) or have previously attempted TFR.
This survey aims to collect valuable data on patient needs, experiences, and treatment outcomes, helping us better understand the impact of TFR on the CML community.
🔹 Who Can Participate?
📌 Why Your Input Matters:
By participating, you will help shape future advocacy efforts, treatment strategies, and patient support initiatives. The findings will be compiled and shared with the community once a sufficient number of responses have been collected.
📩 How to Participate:
Follow the link below to complete the survey and ensure your voice is heard.
If you have any questions or require further information, please do not hesitate to reach out info@cmlsociety.org. Your participation is greatly appreciated and will contribute to ongoing efforts to improve care and outcomes for all CML patients.
