You really crack me up that you posted this for everyone to see. Like
I told you this does not embarass me, and no I wasn't having a bad day
I was actually having an awesome day. I don't know how you don't
think that the first e-mail you sent me was agressive??? All I was
doing why trying to
Here we go again!!!
Date: Fri, 2 Jul 2010 07:15:08 -0700
Subject: [CMLHope] Re: I wrote to Sheila offline to spare her embarrassment
From: dsh...@midwaynet.net
To: cmlhope@googlegroups.com
You really crack me up that you posted this for
Oh also, My cholesterol went way down on Gleevec.
In a message dated 6/25/2010 9:43:30 A.M. Pacific Daylight Time,
sheila.a.wat...@gmail.com writes:
I've not been getting anything either, Greenie. Like Martin says, you
probably just need to give it a good cleaning to get rid of some
Hi John Have any of these drugs been okd yet?
Jeanie3
In a message dated 6/30/2010 1:06:42 A.M. Pacific Daylight Time,
fanruif...@gmail.com writes:
Hi there
I am a sophomore in china. I diagnosed with CML on Feb 18th,2010.
And i started to take Gleevic since Feb 21st.
Fortunately now
HHT SITE _http://www.nature.com/leu/journal/v11/n5/abs/2400608a.html_
(http://www.nature.com/leu/journal/v11/n5/abs/2400608a.html)
In a message dated 6/30/2010 7:41:25 A.M. Pacific Daylight Time,
ted...@aol.com writes:
John...what is HHT...I googled it and got lots of hits...but none
Found this online about Dr Talpaz
Moshe Talpaz, M.D.
Associate Director of Translational Research and
Alexander J. Trotman Professor of Leukemia researchMoshe Talpaz, M.D.,
Associate Chief, Division of Hematology/Oncology, is a leading clinical
investigator in hematologic malignancies.
This group is a wonderful griyo and I have been on it since the beginning
way back when it was a yahoo list.
Sometimes arguments like this happen, but it doesn't in anyway diminish
what this group accomplishes. It has helped me in more ways than I could
say. For you to say this list is a
There are 4 million CML patients in China.
And I believe we can beat CML in future !
Come on!!!
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To post
Really, Ted, 4 million? That seems like such an unreasonable number
to me, since I was told in the beginning when diagnosed back the last
of January, '04 that this was a 'rare' form of Leukemia. And, the
information given to me back then was that there were only around 5000
to 6000 cases of
Jeanie:
I have no idea about the foodsI do remember that after my surgery,
I still had some problems and the doctor sort of made me avoid fried
foods and spicy foods for about six weekssort of like they use to
put people on a bland type diet who had ulcers.but that was it.
Mom told me
Thanks!
In a message dated 7/2/2010 11:28:21 A.M. Eastern Daylight Time,
icandoall...@aol.com writes:
HHT SITE _http://www.nature.com/leu/journal/v11/n5/abs/2400608a.html_
(http://www.nature.com/leu/journal/v11/n5/abs/2400608a.html)
In a message dated 6/30/2010 7:41:25 A.M. Pacific
WOW, what a milestone. That gives us other folks some hope. Greenie
Good luck to you.
In a message dated 7/2/2010 1:37:56 P.M. Central Daylight Time,
skipd_2...@yahoo.com writes:
Hello to the group,
Jeanie I agree with you, if we have a difference of opinion then, we
should take it
I feel so sorry about all these... My friends, please, remember that the
purpose of this group is to help each other - let´s focus on this purpose.
On Fri, Jul 2, 2010 at 3:45 PM, myvet...@aol.com wrote:
WOW, what a milestone. That gives us other folks some hope. Greenie
Good luck to
Just to voice my opinionI agree with you Ricardo. We are here to help and
support one another. Please remember this as we're all in the same boat and we
need each other. Millie
- Original Message -
From: Ricardo Gadelha
To: cmlhope@googlegroups.com
Sent: Friday, July
Hello back to you
I have had cancer since 1993 and survived breast cancer, and now am fighting
CML.So far Tasigna is working for me as Gleevec stopped a while ago. I
feel luck as I've had this for 12 years now, and when diagnosed was only given
5We are all fighting for the same
Skip, very well said! So, your at 33++ years out. EXCELLENT!!!
I am 21+ years post bone marrow transplant.
They are working on CML from all angles and I know they will find a cure for
this disease.
May GOD bless each and every one of you brave people.
Marty
On Fri, Jul 2, 2010 at 2:37 PM,
http://sites.google.com/site/u5jT1VnzhZRj/mtetsuhz
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