Greenie,

I recommend Moffitt also. You know I go to Dr. Altman becuz I'm up here in 
Indiana. But my old doc was Pinilla that Jeanie recommended. They will help u 
get your medicine. A lot less expensive to go there!!!

Blessings,

Susan F. Zimmerman

On Sunday, August 6, 2017 Myvety2k via CMLHope <cmlhope@googlegroups.com> wrote:

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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