As per the first notice sent out on March 3, 2008: The survey is located on the CML Society website: www.cmlsociety.org
The icon for the survey is located on the upper left side of the main page. Cheers, Cheryl-Anne On Mar 17, 8:47 pm, "[EMAIL PROTECTED]" <[EMAIL PROTECTED]> wrote: > Hello All, > > Since the launch of the CML Society Patient Speak out Survey, we've > had many requests to open the survey up to fellow CML patients around > the world. > > We are pleased to announce that the survey is now open to fellow CML > patients everywhere. > > As you can imagine this lends an exciting dynamic to the survey. We > will be able to review, compare and contrast feed-back from CML > patients categorized by their country of residence. However, please > not that the survey is still completely anonymous. > > The survey takes a maximum of ten minutes but will provide important > and insightful information back to our treating physicians. > > Please make time to stop by and fill out the survey, if you haven't > done so already. > > Let's see which country will post the most responses - The race is > on... > > Looking forward to sharing the data with you. > > Cheers, > Cheryl-Anne, Stewart, Margo, Shalyn, Cam and Coralee --~--~---------~--~----~------------~-------~--~----~ [CMLHope] A support group of http://cmlhope.com ------------------------------------------------- You received this message because you are subscribed to the Google Groups "CMLHope" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [EMAIL PROTECTED] For more options, visit this group at http://groups.google.com/group/CMLHope -~----------~----~----~----~------~----~------~--~---
