Hi Dave,

I am in Montreal Quebec.  I have heard of your doctor, he is a top 
doc in Atlantic Canada.

I am organizing a meeting for CML patients here in the Montreal are 
for January 28th (it's a Saturday) just in case you are interested in 
trying to join us, we will be about 50 CML patients.

Let me know if you want more details.

Cheers,
Cheryl-Anne

--- In CML@yahoogroups.com, "da06761" <[EMAIL PROTECTED]> wrote:
>
> Thank you for your reply!
> 
> I am from Fredericton, New Brunswick. My Dr. is Dr. Cubon in 
> Halifax, NS.
> 
> I did not ask that question, but I will. They did mention the 3 log 
> reducion, but I was under the impression that if I was put on 800mg 
> I would stay at that dosage until the 12mths was up.
> 
> Dave 
> 
> 
> --- In CML@yahoogroups.com, "cher111376" <[EMAIL PROTECTED]> 
> wrote:
> >
> > Hi Dave,
> > 
> > I am glad that you have been helped by these posts.
> > 
> > I am aware of the trial you are speaking about as we have this 
> trial 
> > going on here in Montreal, Qc, Canada - where are you located.  
My 
> > Doctor here in Montreal is the P.I. for this trial.
> > 
> > I know of a couple of patients who have participated in this 
trial 
> > and overall the higher dose has helped to improve the molecular 
> > response.  Additionally, for the most part the increased dose did 
> not 
> > significantly increase side effects either.
> > 
> > What isn't clear to me at the moment, and this is mostly because 
I 
> am 
> > PCRU and would therefore not qualify for this trial, so I didn't 
> ask 
> > this question before, is that once you achieve a 3 log reduct or 
> > better how long will you need to remain on the increased dose?  
> Have 
> > you asked this question?
> > 
> > Thanks for posting, it is always interesting to hear from 
> people "out 
> > there".
> > 
> > Cheers,
> > Cheryl-Anne
> > 
> > --- In CML@yahoogroups.com, "da06761" <[EMAIL PROTECTED]> wrote:
> > >
> > > Hi,
> > > 
> > > My name is David, I have been a silent member for 4 years now 
> and 
> > to 
> > > start I want to thank everyone for their posts. They have 
helped 
> me 
> > > in a large way.
> > > 
> > > My history is as follows:
> > > 
> > > Name: Dave Blackier
> > > dx age: 28
> > > dx: Dec 17th, 2001
> > > Gleevec: Since January 2002
> > > Current Dose: 400mg
> > > 
> > > I started Gleevec at 600mg which caused my white blood cell 
> count 
> > to 
> > > drop. I was reduced to 300mg and gradually increase until I 
> reached 
> > > 600mg again. Once at 600mg I quickly achieved CCR followed by 
> MMR. 
> > I 
> > > was dropped to 400mg and have been there for 1.5 years now. 
> > > 
> > > 
> > > I have been asked to take part in a Novartis clinical trial 
> where 
> > > they will evaluating the effects of increasing the Gleevec 
> dosage 
> > to 
> > > 800mg on individuals that are currently having a molecular 
> response 
> > > at 400mg. The purpose of the trial is to understand whether 
> > > increasing Gleevec dosage has a positive effect on people who 
> have 
> > > had little luck at 400mg. I want to help, but where I have been 
> > > extremely sensitive to Gleevec past and I'm afraid of the side 
> > > effects of 800mg. I discussed this with my Doctor and he 
> approved 
> > of 
> > > my participation. Where my Doctor is the principal 
> investigator,  I 
> > > would welcome everyone's feedback or opinions!
> > > 
> > > Sorry for the length of the post.
> > > 
> > > 
> > > Cheers!
> > > Dave
> > >
> >
>






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