The CEO's of these companies and their higher ups are making  Big Bucks 
while we pay the bill.   Such a shame.
 
greenie
 
 
In a message dated 10/6/2014 3:47:15 P.M. Eastern Daylight Time,  
[email protected] writes:

Hi Greenie:  


I watched 60 Minutes and was appalled that the US cost is 3 times higher  
for Gleevec than in Canada, Europe and Australia.  I have insurance but  in a 
couple of years I'll be going to medicare and I'm not certain how that  
will work out for me.  Hopefully there will be generic Gleevec by that  point.


Hope you and Grace are well and that all of our friends on this site are  
enjoying some good health, too.


Marcie


-----Original  Message-----
From: Myvety2k via CMLHope  <[email protected]>
To: cmlhope  <[email protected]>
Sent: Mon, Oct 6, 2014 7:33 am
Subject:  Re: [CMLHope] Digest for [email protected] - 1 update in 1 
 topic


 
Hi Gang,  did any of you folks watch 60 min. last  night.  It was about the 
cost of cancer drugs and Gleevec was on the list  of high cost.  Some 
people can't afford to pay the co-pay so their not  getting the drug. Some 
people 
are taking haft the amount that their suppose to  take to same on cost.  
It's all about money.  In my mind you can't  tell me they don't have a cure 
for CML they would loose so much money plus all  of the research, etc.   
Novartis has made billions of dollars since  the begining in May of 2001.  I 
would say they have received their return  of investment spent on research by 
now.  I hope all is well with  everyone out their.
 
Greenie
 
 
In a message dated 10/5/2014 6:44:32 P.M. Eastern Daylight Time, 
[email protected]_ (mailto:[email protected])  writes:

Hi Marcie,  


We all seem to have our own afflictions so it isn't only me but every  one 
of us that needs prayers for a healthy new year no matter what religion  we 
may be.


I so much appreciate your prayers for me to find myself transplanted  with 
a kidney soon. Hopefully...


18's,


Marty


On Sat, Oct 4, 2014 at 9:00 PM, 'Marcie Goodman' via  CMLHope 
<[email protected]_ (mailto:[email protected]) >  wrote:


Hi Marty,


How are you since your last surgery?  Here's hoping that the New  Year will 
bring abundant blessings to all, but especially to you, dear  Marty, for a 
transplant to come your way very shortly. 


Marcie

Sent from my iPad

On Oct 4, 2014, at 8:10 PM, Marty Gartenberg <[email protected]_ 
(mailto:[email protected]) >  wrote:




Hi Maria,  


We are still around so you don't have to worry. 


Today is my New Year and I prayed for everyone to have a happy and  healthy 
New Year. May any afflictions that anyone has become healed, and  by the 
grace of GOD that will happen. I know in my heart that there is a  cure coming 
for CML.


18,s


Marty


On Sat, Oct 4, 2014 at 2:02 PM, Maria Cashion  <[email protected]_ 
(mailto:[email protected]) >  wrote:

Hi everyone!!!!  
I hope that all is well with everyone of you!!!!! Haven't noticed  any 
activity in a while and that worries me!!!!


Maria


On Sun, Sep 28, 2014 at 6:18 AM, <[email protected]_ 
(mailto:[email protected]) >  wrote:


    [email protected]_ 
(https://groups.google.com/forum/?utm_source=digest&utm_medium=email/#!forum/cmlhope/topics)
   _Google Groups_ 
(https://groups.google.com/forum/?utm_source=digest&utm_medium=email/#!overview)
    
(https://groups.google.com/forum/?utm_source=digest&utm_medium=email/#!overvie
w)  
 
Topic  digest 
_View all topics_ 
(https://groups.google.com/forum/?utm_source=digest&utm_medium=email/#!forum/cmlhope/topics)
  
 
    *   jeanies blood  results and Marty - 1  Update 

_jeanies blood results and Marty _ 
(http://groups.google.com/group/cmlhope/t/9c8e85c9ec5718c8?utm_source=digest&utm_medium=email)
 
Susan Zimmerman <[email protected]_ (mailto:[email protected]) >: Sep  27 
11:38PM -0400 

This is so helpful, if I can  figure it out, lol....


Always wondered  what ANC  was......


Susan




-----Original  Message-----
From: 'Skip Duffie' via CMLHope <[email protected]_ 
(mailto:[email protected]) >
To:  cmlhope <[email protected]_ (mailto:[email protected]) >
Sent:  Sat, Sep 27, 2014 4:44 pm
Subject: Re: [CMLHope] jeanies  blood results and  Marty








http://www.mdcalc.com/absolute-neutrophil-count-anc/
Hi  Jeanie and all. Just reading your report, as it seem different  to our 
reports here in NS... I will try to explain ANC as best  as I can. First if 
you look to the right of my actual counts,  you will see what the count 
should be. next you will not find  ANC, this count is a combination of white 
cells and  neutrophils, These counts do not appear on the copy of your  
results. To find this count (ask your nurse or lab tech) see  mine from this 
Fri. 
the formula is ANC = through the years  
I found a way not exact but just take %of neutrophils and  multiply by 
white count,what this indicates is how immune  compromised your are. In fact I 
think its the most important  count you can get. Neutrophils indicated how 
your system is  retaining bug fighting capabilities and they call it ANC I  
still figure mine out twice week. If I have all the  information like % bands 
and Segments as in the formula above  will use it. but most times I just use 
my method. I hope I did  not confuse you but if your neutrophils are up 
(see my report)  that's good but if low avoid crowded spaces ( I miss church)  












On  Friday, September 26, 2014 10:03 PM, Marty Gartenberg 
<[email protected]_ (mailto:[email protected]) >  wrote:





Hi  Jeanie,


Pain especially severe pain is  the worst thing that someone could ever go 
through. I have  been through a lot of severe pain in my life. Having my 
spleen  surgically removed was really bad but then I had some very  severe gout 
attacks, but even worse was two bouts with the  shingles. However the 
absolutly worst pain in my life were the  terrible mouth sores when I went 
through my bone marrow  transplant. It hurt so badly that I was put on a 
morphine 
drip  that I was able to control with a button. The only thing that  it did 
was to make me hullicinate and throw up. It got so bad  that I removed the 
morphine tube and went on with the pain. I  just decided to put my mind in a 
different place. The  transplant nurse gowned up and came into my bubble and 
held my  hand in her gloved hand and whispered through her mask three  
words into my ear. I always remembered those three words to  this day. She said 
"It's only temporary" and even though I  suffered greatly I would say those 
words over and over again.  They helped me deal with the pain, but it still 
hurt and I  wouldn't let my mind soak it  in.


18's,


Marty



On  Fri, Sep 26, 2014 at 9:50 AM, ICANDOALLTTC via CMLHope 
<[email protected]_ (mailto:[email protected]) >  wrote:


Hi Marty and so glad you are  home; I pray that everything goes well. 
As we walk through  this life, it seems pain is very much a part of it. I 
try to  cope, and I remember Millie telling me that she would cope  with the 
pain as well as she could. My sister has knee pain  and I would tell Millie 
that she woke up each morning in pain;  so I told her we could all join 
together in a prayer in the  morning as we all woke up with pain.

Coping with pain  is hard because you don't know what is safe to take for 
the  pain. As Sprycel is already a blood thinner, and most pain  pills are 
blood thinners, you have to be careful that you  don't get your blood too 
thin. I believe Millie had that  problem, and she finally got a machine that 
would tell her how  thin her blood was. However, as my platelets are high, I  
probably don't need to worry about the blood being too thin.  Those with low 
platelets would have to watch it  carefully.

I was taking Tramadol for pain and it helped  some. I learned recently that 
it has been put on controlled  drug list. My doctor never told me this drug 
could be  addictive, so I took it at least once a day. Now I find out  that 
it is addictive, and that you can't just go off of it.  You have to cut 
down gradually as it affects the brain. If  anyone is on this drug, google it 
and it will tell you all  about it.

I had my visit at Moffit yesterday; it was  good news. My platelets are 
back in the normal range but still  higher than I would like at 362k/ul. WBC 
were 7.75 k/ul and a  little higher than I would like. My onc however was 
happy with  them and said I could come back in 3 months. I told him about  my 
jaw pain, and he said to have the dentist x-ray my jaw, so  I will have that 
done soon; if the jaw is ok then the onc  might want to do other test. The 
pain in my jaw is much  better, but not all the way well.

ANC was high; anyone  know anything about this?
Thanks  Blessings,
Jeanie<3

Here is a copy of my blood  results for those that are  interested:







In  a message dated 9/23/2014 7:54:08 P.M. Eastern Daylight Time,  
[email protected]_ (mailto:[email protected])   writes:
Hi Jeannie and everyone else.

I had my  surgery today and just got back home. Hopefully  everything
went well but I won't know for sure until I get  my dialysis tomorrow.

I am still a bit woozy and  starting to have more pain right now so I
will continue  this some other time.

Jeannie, I just want to say  how badly I feel that you have such pain.
I hope that it  gets better very soon.

You see that this CML site  is something that makes all of us really
care for and about  each other. We are actually just like a big loving
family.  Sometimes people that haven't experienced what we go  through
really have no idea of what we do go  through.

18's to each and every one of us. Today  starts the Jewish New Year and
as such we are all hopefully  written into the book of life. No matter
who you may be no  matter what your religious beliefs are I truly wish
all of  you a healthy life.

I would personally like to  thank everyone for all of their good
thoughts and prayers  that you are saying for me and to everyone  else.

18's

Marty

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