CMLInfo
Hello,
I am trying to gain some insight into the types of information patients and/or loved ones struggling with Chronic Myelogenous Leukemia may be looking for when they are initially diagnosed and where they turn to for information. Specifically, how did you initially find out you (or your loved one) had CML? Did your physician adequately explain the condition to you and what to expect, as far as treatment? Did you turn to any support groups, the internet, etc. for additional information? What type of information do you feel may be lacking for CML patients and their loved ones?
If you wouldn't mind, I would greatly appreciate any information you could share about your experience. Feel free to share your experience within the boards, or if you prefer to keep your experience anonymous, I have put a survey online for your to share your experience(s).
http://rosetta.checkboxonline.com/Survey.aspx?s=9b2829cf05174ed697f54cb826ed9519
Thank you.
I am trying to gain some insight into the types of information patients and/or loved ones struggling with Chronic Myelogenous Leukemia may be looking for when they are initially diagnosed and where they turn to for information. Specifically, how did you initially find out you (or your loved one) had CML? Did your physician adequately explain the condition to you and what to expect, as far as treatment? Did you turn to any support groups, the internet, etc. for additional information? What type of information do you feel may be lacking for CML patients and their loved ones?
If you wouldn't mind, I would greatly appreciate any information you could share about your experience. Feel free to share your experience within the boards, or if you prefer to keep your experience anonymous, I have put a survey online for your to share your experience(s).
http://rosetta.checkboxonline.com/Survey.aspx?s=9b2829cf05174ed697f54cb826ed9519
Thank you.