---inspite of having glevic regularly my dad is having constant temp 
from last 10 days ,temp controling medicines are not very effected. 
do any ony one of u have ever  experienced any such thing





 >




 > 
> > In [email protected], "Richard" <[EMAIL PROTECTED]> wrote:
> > > Thank you for making it clear that you are refering to Glevic 
> when 
> > > you speak of chemo, that really had me concerned!
> > > 
> > > I am sure you have good doctors there who are genuinely 
concerned 
> > > about your father's health. The first six to twelve months I 
was 
> > on 
> > > Glevic my blood counts changed dramatically, they still change 
> but 
> > > not quite so much. This is normal! The really important test 
is 
> > the 
> > > bone marrow. If no CML shows up there that is great news.
> > > 
> > > I am not certain what "symptoms" you mean? Blood test results 
or 
> > side 
> > > effects of the Glevic or CML?
> > > 
> > > I had a lot of skin problems and problems with my finger nails 
> and 
> > > toe nails. I have anemia and I do fatigue easily. As far as my 
> > life 
> > > style is concerned I work three days a week at a stress free 
job 
> > and 
> > > I exercise daily by playing about one hour of golf or taking 
long 
> > > walks. I also do some weight training and a 20 minute home 
work-
> > out. 
> > > I take vitamin supliments under the supervision of my onc.
> > > 
> > > I hope this helps and I hope you father's condition improves!
> > > 
> > > 
> > > --- In [email protected], "amiablelook439" 
> <[EMAIL PROTECTED]> 
> > > wrote:
> > > > --- Sir by chemo i mean taking glevic, and as far as 
specialist 
> > are 
> > > > concerned we have consult to the best doctors over here but 
we 
> r 
> > > not 
> > > > satisfied,his reports r not much stable sometimes no cml is 
> > > reported 
> > > > in his bone marrow but u can say once in 5 times of his 
reports 
> > he 
> > > > get the symptoms again which is almarming for us.  any ways 
u 
> > tell 
> > > > me what kind diet doctors suggest u to preferably take and 
tell 
> > me 
> > > > something about ur life style now adays...
> > > > 
> > > > 
> > > > 
> > > > 
> > > > 
> > > > 
> > > > 
> > > > 
> > > > 
> > > > 
> > > > 
> > > > In [email protected], "Richard" <[EMAIL PROTECTED]> 
wrote:
> > > > > --- In [email protected], "amiablelook439" 
> > > <[EMAIL PROTECTED]> 
> > > > > wrote:
> > > > > > .
> > > > > > my dad is suffering from cml.he was diagnosed in 2003. . 
he 
> > is 
> > > > > > having chemotherapy having glevic.but u know as glevic 
is 
> > just 
> > > > for 
> > > > > > prolonging the disease its not a proper cure so ups and 
> > downs 
> > > in 
> > > > > his 
> > > > > > condition are found to be there.he can be said in early 
> > phase 
> > > of 
> > > > > > this disease. can any body who is already having 
treatment 
> > > guide 
> > > > me 
> > > > > > what measures i should take for making his health stable 
> > like 
> > > > for 
> > > > > > example any clue about the diet preferable for cml 
patients 
> > etc.
> > > > > > also if u can suggest me any authentic doctor whom i can 
> > > contact 
> > > > > > through net... 
> > > > > > (Mr Rob reply for u is there as well)
> > > > > > 
> > > > > > 
> > > > > 
> > > > > 
> > > > > Hello, my name is Richard and I've been on Gleevec since 
> 2003. 
> > I 
> > > > am a 
> > > > > 61 year old man. Last September the doctors reported that 
> they 
> > > > could 
> > > > > no longer find any CML in my bone marrow.
> > > > > 
> > > > > I am not a doctor but I have never heard of anyone 
receiving 
> > both 
> > > > > chemotherapy and Gleevec. Gleevec is now the main therapy 
for 
> > > CML. 
> > > > > Unless your father has some other type of cancer I do not 
> > > > understand 
> > > > > why he would also be getting chemo?
> > > > > 
> > > > > Gleevec is not for just prolonging the disease! No one 
knows 
> > if 
> > > it 
> > > > > will produce a cure in the long term. It may well prove 
that 
> > most 
> > > > > people can stay on Gleevec indefinately or until something 
> > better 
> > > > > comes along. I do not know what your access to medical 
care 
> > is, 
> > > if 
> > > > > you can you should get your father to a CML specialist! 
Only 
> a 
> > > > > specialist will have access to the latest information 
about 
> > this 
> > > > > disease and the best treatments! Much new information has 
> been 
> > > > > learned in the two years your father has had this disease, 
> his 
> > > > doctor 
> > > > > needs to be informed about all of this.
> > > > > 
> > > > > Richard Troxel




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