Richard,
Thanks for posting this,  I was thinking of doing the same.
I was surprised to find out on the last newsletter that they only 
have 24 people enrolled currently, thought they would get more.

For those that are considering it, its real easy no meds or anything.
They send a survey every 6 months and a kit to have blood drawn and 
send to them.  The blood draw is done by your dr during your regular 
appt.  They now also are allowed to provide some of the test results 
back to your dr.

I think the more we can get involved the better as the more data 
they can collect the more they should be able to learn.

Sharon


--- In [EMAIL PROTECTED], rrockef1 <[EMAIL PROTECTED]> wrote:
> Dear Friends,
> 
> I've been meaning to send the following to you for ages, but have 
been
> delayed because of because I became so time-consumingly (and 
unexpectedly)
> involved in presidential electoral politics.  Respecting this 
group's
> non-political ground rules I won't say on whose side, though those 
of you
> who know me can probably guess - and I'm happy to tell others off-
list if
> you email me.  I've been in Wisconsin for much of the past two 
weeks.
> 
> But back to my point: though the Harvard CML Study has been 
working to
> recruit volunteers for some time, they still need help.   It's 
described
> clearly below, so I won't repeat any of it - but will say that 
getting as
> many of us as possible involved will result in information that 
will benefit
> all of us here, as well as other sufferers from this disease who 
are not so
> fortunate as to be part of this (usually, except when we're 
fighting)
> wonderful family.  Please join the study if you're can.
> 
> Love,
> Richard R
> __________________
> 
> Harvard Chronic Myeloid Leukemia
> 
> (CML) Study
> 
>  
> A study for people with CML
>  
> Toll Free:
> 1-866-HAVE-CML
> (1-866-428-3265)
>  
> What is the Harvard CML Study?
>  
> The Harvard CML Study is for people across the United States who 
have
> chronic myeloid leukemia (CML). The goal of the study is to learn 
more about
> people in the United States with CML, and how their disease is 
being
> treated. 
> 
>  Your participation in this study will help us learn important 
things about
> people with CML, such as:
>  
> � How are treatment decisions made?
> � What kinds of things are associated with good or poor responses 
to
> treatment?
> � What are the long-term effects of treatment?
> � What health, emotional, insurance, and work issues are important 
to people
> with CML?
>  
> Researchers on the study will learn about people with CML by 
analyzing
> survey information and blood samples.
>  
> Who can join?
>  
> You are eligible to join if you:
>  
> �  have been diagnosed with CML in the last one year
> �  are age 18 or older
>  
>  
> 
> What will I be asked to do if I join the Harvard CML Study?
> 
>  
> 
> If you would like to take part in the study, we would ask you to:
> 
>  
> 
> � Complete a survey every six months. Each survey would be mailed 
to your
> home and would take between 20 and 30 minutes to complete.  The 
surveys will
> contain questions about your diagnosis of CML, your treatment, 
your quality
> of life, your symptoms and general health, and your experiences as 
a CML
> patient. 
> 
> � Donate blood samples every six months. Specimen kit used for 
drawing blood
> will also be sent to your home and 35-50 cc�s (about 7-10 
teaspoons) of
> blood will be collected when your blood is being drawn for routine 
care. You
> may choose to allow us to provide your doctor with any standard 
test results
> performed on your blood samples that your doctor could have 
ordered.  To
> receive the results, you would need to contact your physician.
> 
> � Sign a release of medical information form. This will allow us 
to request
> copies of medical records that relate to your CML diagnosis and 
treatment.
> 
>  
> 
> How do I find out more?
>  
> If you are interested in joining the study or would like more 
information,
> please call our toll-free number 1-866-HAVE-CML (1-866-428-3265) 
or email
> [EMAIL PROTECTED]








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