YAHOOO!!! YIPPEEE!!!
Number 770 in the Zero Club
Zavie

-----Original Message-----
From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED]
Sent: December 8, 2004 8:53 PM
To: [EMAIL PROTECTED]
Subject: Re: Re: [CML] Marque(long)




> I read these posts and do sometimes respond to them. It is so scary when
you hear of someone dying and do feel as is you somehow personally know
them. I am at zero and am considered in remission. I was dxed in March and
just got the good news. But I have to admit I can NOT shake the feeling the
medicine will quit working in only a matter of time. I dont know why but it
is sometimes a daily thought which I hate. I try to live day by day, but I
always wonder when.... I am so sorry for the loss and I am sure all were
better for the knowing. j
> From: Adrienne Davis <[EMAIL PROTECTED]>
> Date: 2004/11/30 Tue AM 08:16:47 EST
> To: [EMAIL PROTECTED]
> Subject: Re: [CML] Marque(long)
> 
> Thank you for this post.
>  
> Adrienne
> 
> rgebauer2001 <[EMAIL PROTECTED]> wrote:
> 
> I have rarely posted to the group, but I am a constant visitor, and 
> usually find a very inspirational story when I do.
> 
> For those old timers on the list,  I am the author of "My 10 Favorite 
> Things About Interferon" posted a few years ago.
> 
> Every now and then we are all saddened by news such as Marque's 
> passing. I thought it would be appropriate to share my story as a 
> counterpoint to this loss, and to help renew the faith for those who 
> let a little doubt creep into their thoughts when we lose a member of 
> the group.
> 
> I recently celebrated my six year anniversary since diagnosis. I was 
> diagnosed when I went to an eye specialist complaining of blurry 
> vision. This was two days after I had a complete physical for 
> insurance purposes, and all my tests were normal, including blood 
> counts. Needless to say, I was shocked to find out I had CML after 
> receiving a "clean bill of health". Obviously, I caught my disease 
> very early on, in fact you could speculate that I was diagnosed a day 
> after my symtoms manifested. By the way, the blurry vision 
> dissapeared immediately after I was diagnosed. A sign perhaps? In any 
> event, I threw myself totally into researching the disease and into 
> looking for treatment. Eventually, I went on the Interferon/Ara C 
> regimin, which did absolutely nothing except make me miserable(see 10 
> favorite things about Interferon). During this fun time I stumbled 
> upon Dr. Drucker's trial, and sent him an email. He responded within 
> an hour, and three weeks later I was in the trial. I am in one of the 
> very first groups. Anyway, in six months I was in total remission(or 
> barely detectible, if you prefer) measured every conceivable way. I 
> go to Portland every six months and have a BMB once a year. Blood 
> tests every six weeks.
> 
> During these trips, and tests are the only times I think about my 
> medical challenge. I know I am blessed, and totally believe that in 
> my case, the "challenge" came into my life because I had to make some 
> serious changes in my life. I now give CML very little time, and I 
> feel terrific, but, I 
> constantly work on the things I did that let the disease become part 
> of my reality in the first place. That's a whole other story.
> 
> Marques passing is a tragic loss, but it is not harbinger of anything 
> for the rest of us. It is instead a reminder that life is ever 
> precious, and 
> should be treasured, above all else, for everyone on or off our list.
> 
> Keep the faith, and Happy Holidays to everyone.
> 
> Sorry for the length of this post.
> 
> Rob
> dx 11/13/98
> STI/Gleevec 400mg per day
> 
> 
> 
> 
> 
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