Re: New poll for Breathe-Support REVOTE

[Guest guest]

Since there was confusion over how to vote if none applied, Ihave

revised the poll and added " none of the others " . The one person who

had voted will need to revote.

> >

> > there's?some answers that are missing.

> >

> > If you were told absolutely nothing from your Pulmonologist

> > If you were left on your own to research and find all info you

can

> on PF

> > What if you had to diagnose & ?self treat symptoms

> >

> > ---- Original Message ----

> > From: Breathe-Support

> > To: Breathe-Support

> > Sent: Sun, 13 Jan 2008 12:47 am

> > Subject: New poll for Breathe-Support

> >

> >

> >

> >

> >

> >

> >

> > Enter your vote today! A new poll has been created for the

> > Breathe-Support group:

> >

> > What were you told by your pulmonologists to help you live with

> your disease?

> >

> > Select as many of the following as are true. You may select

> multiple answers.

> >

> > o I was told about this or another online support group by my

> doctor.

> > o I was told about PFF or CPF by my doctor.

> > o I was told places to go online for additional information by my

> doctor.

> > o I was given literature about the disease by my doctor.

> > o I was told about a local PF support group by my doctor (not

> general Lung) by my doctor.

> > o I was given information about how to live with PF by my doctor.

> >

> > To vote, please visit the following web page:

> > http://groups.yahoo.com/group/Breathe-Support/surveys?id=1979905

> >

> > Note: Please do not reply to this message. Poll votes are

> > not collected via email. To vote, you must go to the Yahoo!

Groups

> > web site listed above.

> >

> > Thanks!

> >

> >

> >

> >

> >

> >

>

______________________________________________________________________

> __

> > Meet the new AOL.ca. Free radio, music, videos, news &

> entertainment ? with a Canadian perspective.

> >

>

[Guest guest]

Thank you, all done xx> > >> > > there's?some answers that are missing.> > > > > > If you were told absolutely nothing from your Pulmonologist > > > If you were left on your own to research and find all info you > can > > on PF > > > What if you had to diagnose & ?self treat symptoms> > > > > > ---- Original Message ----> > > From: Breathe-Support > > > To: Breathe-Support > > > Sent: Sun, 13 Jan 2008 12:47 am> > > Subject: New poll for Breathe-Support> > > > > > > > > > > > > > > > > > > > > > > > Enter your vote today! A new poll has been created for the > > > Breathe-Support group:> > > > > > What were you told by your pulmonologists to help you live with > > your disease?> > > > > > Select as many of the following as are true. You may select > > multiple answers. > > > > > > o I was told about this or another online support group by my > > doctor. > > > o I was told about PFF or CPF by my doctor. > > > o I was told places to go online for additional information by my > > doctor. > > > o I was given literature about the disease by my doctor. > > > o I was told about a local PF support group by my doctor (not > > general Lung) by my doctor. > > > o I was given information about how to live with PF by my doctor. > > > > > > To vote, please visit the following web page:> > > http://groups.yahoo.com/group/Breathe-Support/surveys?id=1979905 > > > > > > Note: Please do not reply to this message. Poll votes are > > > not collected via email. To vote, you must go to the Yahoo! > Groups > > > web site listed above.> > > > > > Thanks!> > > > > > > > > > > > > > > > > > > > > ______________________________________________________________________> > __> > > Meet the new AOL.ca. Free radio, music, videos, news & > > entertainment ? with a Canadian perspective.> > >> >>