Jeanie thank you I wait and see what happens if things don't  work out for 
me I will go their.
 
greenie
 
 
In a message dated 8/6/2017 5:56:57 P.M. Eastern Daylight Time,  
cmlhope@googlegroups.com writes:

Hey Greenie,
I would like to suggest Moffitt cancer center here  in Tampa. They will do 
everything to help you to get your meds. It's where I  go and they have 
saved my life twice.  They accept Medicare and medicate  assignment.  If you 
need help with copayment a there is a cancer  copayment company called PSI. 
They paid my copayment for several years. You  just need to start making calls 
and get the ball rolling.  However I pray  they keep sending the meds. You 
and I have been fighting this for  years. 
I go to dr Balducci head of senior oncology center  in Moffitt but the head 
of leukemia is dr Pinnalla. Check spelling. It's  great/ you go in an hour 
ahead of Drs meeting for bloodwork right at hospital  and by the time you 
meet your dr your blood work is done for him.  Every  three months they do a 
PCR.  They have vallet parking. 
Praying for you. 
Jeanie❤️❤️❤️❤️

My Motto:  
Faith and Pills
With Love
🐠18's
Dx 1/2004 CML Leukemia
Started Gleevec 2/2004
Started Tasigna 9/2009
Started Sprycel 11/2009
Started Ponatinib 1/2015
Doctor Balducci Moffitt Cancer Center 


On Aug 5, 2017, at 6:25 PM, Myvety2k via CMLHope <cmlhope@googlegroups.com> 
 wrote:



 
Hi Rien,   I started a study the first week in  Jan. 2000 at Northwestern 
Hosp. in Chicago at 400 mg each day before it was  approve my the FDA. They 
changed it later to 300 mg because of the Gleevec  rash.  I got sick in 2009 
and stopped Gleevec for 26 days because of  sinus infection and the Doctor 
at home put me on an antibiotic which made me  sick so I stopped for those 26 
days.
 
     Then I started up again and had  my blood work done at Northwestern 
and started on a trip out west.  My  Cancer Doctor called me while driving and 
said," David your blood work  showed that their are cancer cells back in 
your blood".  I told him  remember I quit for 26 days and he replied that's 
right I forgot, did you  start Gleevec again I told him yes and he said " well 
if it worked before it  will work again and hung up and I never heard from 
again.  I later  received a letter from him that he moved on to a different 
Hosp. in New  York, NY. and that was the end of that.
 
So, June 7th of this year I flew in from South Fort Myers.  FL. to Chicago 
to get my blood work see my new Doctor pick up my drugs and  be on my way 
home.  But instead I was told their no longer a study and  you won't be 
getting the drug any longer.  That took my breath  away.  Before I left they 
then 
told me that they changed their mind and  would give me the drug and 7 month 
supply and would sent the rest later  because they were short on Gleevec..
 
Last week I received a call telling me that for me to  receive the drug 
that I would have to fly in every 3 months, that's not  going to happen with 
the cost of flights, car rental, etc., not with my  income at 78 years old.  
They called me last week and they are suppose  to have a meeting and let me 
know. 
 
When I started this study their were 8 of us out of 200  people nation way 
and that I would receive the drug STI571 for as long and I  could tolerated 
it or stay alive.  Well that changed.  I am  waiting for a phone call and 
I'm afraid it's not going to be good  news,  So, my question is should I take 
a chance and stop the drug and  get blood work in 3 months and see was 
happens with my blood count? I am a  basket case waiting to see what happens.
 
If you have some answers please let met know.
 
Thank you,
 
David (greenie) Greenberg
South Fort Myers, Florida
 
 
 
 
In a message dated 8/5/2017 5:26:55 P.M. Eastern Daylight Time, 
rien16...@gmail.com writes:

 
Hello!


I stopped  taking Gleevec after 13 years. I had my checkups every month, 
but only in  the first year. In the second year every two months and from now 
on every  three months for the rest of my life.
It seems  that everybody reacts in a different way. I myself had more 
bonecramps  after having stopped than while taking Gleevec; but after the first 
year  it gradually went better and now I have these cramps only a few times 
per  year during the night. The swallen eyelids completely disappeared and  
unfortunately, my face became a lot thinner. Another side-effect: my hair  
was not grey anymore after havinig stopped, it is still dark, which was  not 
the case before. After all I am glad that I took the decision, the  problems 
of the first year will disappear, so I strongly advise you to do  like I did.
Feel free  to contact me for further information.
Greetings  from the Netherlands - and let's be grateful that Gleevec 
exisits!!


Rien


2017-08-05 19:18 GMT+02:00 Vivi <vkrei...@gmail.com>:

After seventeen years on Gleevec, and considered "in  remission," my 
oncologist asked me if I would like to stop taking  Gleevec.  
At first glance, this sounded spectacular but then she said:
"you'll have to come in once a month to be tested."
After deep thought (about twenty seconds), I said, "Talk to me  about this 
again in ten years."
Has anyone else stopped taking Gleevec after years of being "in  
remission?"  If so, how's it going?
What has changed in your life?  Have any of the obvious  physical 
side-effects (leg cramps, blood in the whites of your eyes,  swollen eyelids,
abdominal fat) retreated or been reversed?
I'd appreciate any information other CMLers might have.
Best to all.   

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-- 

 
Dr. Marinus Jonkers 
Ravenhoflaan 5 
NL- 4706 WD  Roosendaal 
Tel. +31 165 8  22128 
117 Bd de la 1ère Armée,  no. 21 
F – 83330 Le  Beausset 
Tél. +33 494 06 01  87 
email: rien16...@gmail.com 



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