Joyce,
As for you saying "I feel like you are all family and hope you will excuse
this off-subject post. I love you all and you are in my every prayer".
What do you mean? First YOU ARE ONE OF OUR FAMILY! And There is no such
thing as an excuses for an "off-subject post" and there will never be
Hi Mitri,
So you can now see that there are good things that more and more people
with CLM can do, and your son is a living example just as Angie is.
Absolutely wonderful!
On Tue, Sep 29, 2015 at 8:39 PM, Parichart N. wrote:
> Congratulations!!!
>
> So excited to
Angie,
So I see that your finally good to go That's great!
18's,
Marty
On Tue, Sep 29, 2015 at 8:18 PM, ANGELYN ESDERS wrote:
> After 14+ years, I have been off Gleevec for 3 months.
> So far, so good... All blood counts are A-OK.
> I am starting to feel a little braver
Jim,
I am so sorry to hear this. I am wounded every time something like this
happens. If there is anything that I can do for you then please let me know.
18's,
Marty
On Fri, Sep 18, 2015 at 2:53 PM, Nadia Noles wrote:
> This is from Mr. Noles, the husband of Nadia
Dear Elizabeth and Nick, and everyone that are reading this.
I was very happy to hear that your 55 years of being married has come to
be. So far I can only claim 45 years, but we are still working on it.
You know what? I have a present for you and everyone else. Now I don't
know if you or
Dear Beth and Joyce,
Sometimes things may not go as planned but sometimes they do go as
planned. This is what life is all about. I know what the both of you are
going through, and it does take someone that has already been their and
done that, but you still live on to do what you can do.
Every
Well now.
I am beginning to see some positive progress within the CML community. This
one is doing well because things are getting better because some of you
fine people are finding their way to not being able to detect any more of
those nasty cells.
Others are also doing well because some
Hi Suzieq,
First let me congratulate you on you success about being non detectable, a
very good step in the right direction.
I already have been in touch with Skip and we talk to each other about
every couple of weeks. I have already mentioned about all of you and he is
happy for all of you. He
finestill low platelets. Life goes on.
Angie
--
*From:* Marty Gartenberg wa2...@gmail.com
*To:* cmlhope@googlegroups.com
*Sent:* Wednesday, June 17, 2015 7:29 AM
*Subject:* Re: [CMLHope] Stopping Gleevec
Hi Angie,
You are not thee only one that has
it.
Anyway, I am finestill low platelets. Life goes on.
Angie
--
*From:* Marty Gartenberg wa2...@gmail.com
*To:* cmlhope@googlegroups.com
*Sent:* Wednesday, June 17, 2015 7:29 AM
*Subject:* Re: [CMLHope] Stopping Gleevec
Hi Angie,
You are not thee
Jeanie,
I take it everyday. I used to get these horrible gout attacks. Besides
when some usually has a kidney transplant it really helps.
There are two doses one if for 100 mg the other is 300 mg. At the beginning
of a bone marrow transplant they are usually put on to 300 mg. However it
then
pain. Thanks again ❤️❤
️
My Motto: Faith and Pills
Jeanie 18,s
Dx 1/2004. CML Leukemia
Started Gleevec 2/2004
Started Tasigna 9/2009
Started Sprycel 11/2009
Started Ponatinib January 2015
Dr Balducci Moffitt Cancer Center
On Jul 29, 2015, at 2:23 PM, Marty Gartenberg wa2...@gmail.com
I am in the process of writing a book. It is on going book that is actually
my autobiography. It describes in detail what I have gone through. Part of
my book describes some of the people who have dealt with Leukemia and bone
marrow transplants.
There are more then twenty years of the stories in
Hi Jeanie.
I have been taking Cardizem also known as Dilizem Hydrochloide for my
blood pressure ever since during my Kidney transplant. It is really helping
me.
I am taking 240 mg Extended release capsule. I usually take one at about
1pm every day. let me know what happens
Good luck
18's
23, 2015, at 1:34 PM, Marty Gartenberg wa2...@gmail.com wrote:
Hi Sherri,
I feel so sorry for you to have to tolerate such a terrible taste in your
mouth, and what is even worse are those mouth sores. It is like having a
never ending battle.
Maybe I can help you with something called Biotene
Hi Suzieq,
I also haven't heard from Skip. I tried contacting him trough skype but
nothing yet.
I will keep tiring.
18's
Marty
On Fri, Jul 24, 2015 at 2:17 PM, Suzieq sheila.a.wat...@gmail.com wrote:
Was just wondering if anyone has heard from Skip in a while? I know I
haven't been very
tells me. I would much rather swallow the
pill but due to my paralyzed stomach, I can no longer do that.
So what did Cyclosporine taste like? I can't image that it was very
tasteful.
L'chaim
On Fri, Jul 17, 2015 at 2:34 PM, Marty Gartenberg wa2...@gmail.com
wrote:
Hi Sherri,
I am just
Hi Richard,
since your white counts reflect any ware from 12 to around 10, I may not be
understanding your meaning of a low white count is. That may be in the
metric system but I am not sure,
I have a white count of
RGB4.20 - 6.00 m/uL 6.00 n/ul which is considered normal. Mine is usually
low
Hi Sherri,
I am just curious I have tasted some awful things in my life, including
liquid Cyclosporine with was the absolutely worth thing I have ever tasted
in my life, but since i have never been on Gleevec can you tell me what
does it taste?
On Fri, Jul 17, 2015 at 2:32 PM, sherri swanson
Hi Choi,
Something you may be interesting in seeing.
Copy this link
http://www.medicinenet.com/gastritis/patient-comments-313.htm
It discuses a lot of the problem of different people with gastritis.
I hope it help you.
!8's, it is a symbol for life. I always use it.
Marty
On Wed, Jul 15,
Started Sprycel 11/2009
Started Ponatinib January 2015
Dr Balducci Moffitt Cancer Center
On Jul 3, 2015, at 3:19 PM, Marty Gartenberg wa2...@gmail.com wrote:
Hi, everyone,
I did have a stroke on Friday the 26 i am slowly getting better.
just affected my speech but still working through
well and I'll be
saying prayers for you. Please take good care. Hugs to you.
18s
Marcie
Sent from my iPad
On Jul 2, 2015, at 9:47 PM, Marty Gartenberg wa2...@gmail.com wrote:
Hi. Susan
unfortunately i had a stroke. getting better.
18's
Marty
On Mon, Jun 29, 2015 at 2
Hi. Susan
unfortunately i had a stroke. getting better.
18's
Marty
On Mon, Jun 29, 2015 at 2:18 PM, 'Susan Zimmerman' via CMLHope
cmlhope@googlegroups.com wrote:
Pete,
When I was at Moffitt from 2005 til 2007, I saw Dr. Javier Panilla. He is
GREAT!!!
18'S,
Susan F.
a work in your days which you would not believe, though it were told you.
Hab. 1:5
-Original Message-
From: Marty Gartenberg wa2...@gmail.com
To: cmlhope cmlhope@googlegroups.comI have
Sent: Thu, Jun 25, 2015 12:29 am
Subject: Re: [CMLHope] Humor is the spice of life. When your
, then you can put it behind you..while you are going through all
of thisjust remember how cared for, loved, and appreciated you are
...here..with us.
have a great day!! and feel good!!!
Love, 18's, and hugs, Beth
-Original Message-
From: Marty Gartenberg wa2
Tasigna 9/2009
Started Sprycel 11/2009
Started Ponatinib January 2015
Dr Balducci Moffitt Cancer Center
On Jun 19, 2015, at 8:58 PM, Marty Gartenberg wa2...@gmail.com wrote:
Thank you for praying Psalm for me. I am enclosing a copy so that
every one can read it.
Psalm 91
1 Whoever
Hi Joyce,
I see that your a night owl by getting up so early in the morning. This
tells me something. You have a lot on your mind but for good reason. When
something is running through my mind I also have difficulties sleeping and
will get up early in the morning. Sometimes I just lay in bed and
Beth, you know what Zavie would have to say don't you?
YIPPIE YAHOOY...
18,s
Marty
On Mon, Jun 22, 2015 at 10:47 AM, 'Icandoallttc' via CMLHope
cmlhope@googlegroups.com wrote:
That is really great!! [image: ❤]️[image: ❤]️
Prayers Blessings Jeanie [image: ][image: ]18,s
Dx 1/2004
Joyce, you will overcome your latest bump in the road.
I will be praying for you.
Double even triple 18's to you.
Marty
On Fri, Jun 19, 2015 at 11:54 PM, Joyce Mesnarich joy...@htc.net wrote:
Jeanie,
So happy that your new TKI is working. On July 9 my hubby and I will go
to see Dr
your talents were endless!
Jeannie, so excited for you!
18's and blessings,
Susan F. Zimmerman
-Original Message-
From: Marty Gartenberg wa2...@gmail.com
To: CMLHope CMLHope@googlegroups.com
Sent: Fri, Jun 19, 2015 12:29 am
Subject: [CMLHope] Humor is the spice of life. When your
; be utterly astounded! For I will work
a work in your days which you would not believe, though it were told you.
Hab. 1:5
-Original Message-
From: Marty Gartenberg wa2...@gmail.com
To: cmlhope cmlhope@googlegroups.com
Sent: Fri, Jun 19, 2015 4:49 pm
Subject: Re: [CMLHope] Humor
This is a little spicy but rather funny.
By now you must all know me. I have been asked many times how I can have an
operation for a kidney transplant as well as a bone marrow transplant some
26 years and still be able to spread humor. As I mentioned humor is the
spice of life and without it where
Hi Jeanie,
That is some really great news. Keep up the effort. By the way are you
PCRU? If so then for how long and is your doctor thinking about you
going off the TKI?
18's,
Marty
On Thu, Jun 18, 2015 at 4:43 PM, 'Icandoallttc' via CMLHope
cmlhope@googlegroups.com wrote:
Blood test was
Hi Angie,
You are not thee only one that has stopped your TKI and felt that way.
sometimes something that we take as far as any TKI's ends up being a crutch
for us and we always seem to worry if this or that will come back to haunt
us. It is a normal human response and we worry about it.
Angie,
Hi Skip,
With all that you have been through and still going through you are the
longest surviving CML patient that I know of. 37 years and counting, but
who is counting, you just keep on going on.
This is for you to continue on 18's dear Skip.
Marty
On Sun, Jun 14, 2015 at 9:05 AM, 'Skip
Hi Kothal,
Good question. I spoke with my doctor about this and since I have had two
episodes of the Harpies Zoster virus (Shingles) he told me to go ahead and
have the vaccine. However I am not or have ever been on any TKI's because
they were not yet available 26 years ago when I had my bone
: ][image: ]18,s
Dx 1/2004
Started Gleevec 2/2004
Started Tasigna 9/2009
Started Sprycel 11/2009
Started Ponatinib January 2015
On Jun 12, 2015, at 11:31 AM, Marty Gartenberg wa2...@gmail.com wrote:
Angie who knows what to say about this? Some doctors say no while others
say yes. Since I
Angie who knows what to say about this? Some doctors say no while others
say yes. Since I already got the shingles way before my kidney transplant
and way after my bone marrow transplant it was fine then. But now after my
kidney transplant and that I am on a lot of immune suppressive drugs,
Hi Choi,
Pleural Effusions are quite common to people that are using Sprycel
sometimes even on low doses. Since he also has the E55G mutation he or you
may want to get in touch with Dr. Brian Druker and Dr. Moshie Talpaz.
Both of these doctors are the CML experts Dr. Druker was the one that made
Hi Richard, Very good hemoglobin count! This tells me something. Your TKI
is going it's job and your kidneys are working well. It is your kidneys
that produce a hormone (can't remember the name of this hormone at the
moment) that goes to your bone marrow to help promote hemoglobin and red
blood
Dear Robert, at first I was perplexed by your question
*Is the high cost of CML care worth it? Then I read your post to the
bottom.*
*I'm sure you know no matter how much money is spent on keeping us alive is
a good investment. Twenty six years I was an experiment having a bone
marrow transplant
:
Marty, thank you so very much! I will use this help that you have given
me. I appreciate it hugely! Hugely.
Most sincerely,
Angie
--
*From:* Marty Gartenberg wa2...@gmail.com
*To:* cmlhope@googlegroups.com
*Sent:* Friday, June 5, 2015 8:47 PM
*Subject:* Re
sincerely,
Angie
--
*From:* Marty Gartenberg wa2...@gmail.com
*To:* cmlhope@googlegroups.com
*Sent:* Friday, June 5, 2015 8:47 PM
*Subject:* Re: [CMLHope] Where is everyone?
Brian J. Druker, MD
Director, OHSU Knight Cancer Institute
JELD-WEN Chair
Is everyone alright? I haven't a post from anyone in a long time.
18's
Marty
--
--
[CMLHope]
A support group of http://cmlhope.com
-
You received this message because you are subscribed to the Google Groups
CMLHope group.
To post to this
and with no platelets. They don't know WHAT
to do with me. :(
Angie in Canada
--
*From:* Marty Gartenberg wa2...@gmail.com
*To:* CMLHope@googlegroups.com
*Sent:* Friday, June 5, 2015 7:35 AM
*Subject:* [CMLHope] Where is everyone?
Is everyone alright? I
On Fri, Jun 5, 2015 at 5:54 PM, ANGELYN ESDERS esd...@rogers.com wrote:
Have you any idea how I could contact either of them? I think it could be
well worth while.
Thank you for the suggestion, Marty.
Angie
--
*From:* Marty Gartenberg wa2...@gmail.com
*To:* cmlhope
I miss my Mommy Lottie.
18's
Marty
On Fri, May 29, 2015 at 7:35 AM, 'Icandoallttc' via CMLHope
cmlhope@googlegroups.com wrote:
Hi all
I sending this to remember and honor Millie, our brave cml warrior who
lost her battle last year. She was so brave and fought pain every day of
her life.
Sherri
PCRU! EXCELENT
18's for sure.
Marty[?] You need a great big hug!
On Wed, May 27, 2015 at 3:04 PM, sherri swanson swanson.sherri...@gmail.com
wrote:
Hi Everyone!
In the mist of all the bad news I've been getting lately, I got some good
news this afternoon. My Onc called me
Ponatinib January 2015
On May 26, 2015, at 12:16 PM, Marty Gartenberg wa2...@gmail.com wrote:
Hi Jeanie,
Sorry to hear about your husband I didn't know.
Jeanie I know that you have gone through a lot of crap and there is
nothing you can do about that but put it in your past where it belongs. You
. I really don't feel like it but trying it
anyway.
Keep up the good work.
Prayers Blessings Jeanie [image: ][image: ]18,s
Dx 1/2004
Started Gleevec 2/2004
Started Tasigna 9/2009
Started Sprycel 11/2009
Started Ponatinib January 2015
On May 25, 2015, at 5:50 PM, Marty Gartenberg wa2
:19 PM, ANGELYN ESDERS esd...@rogers.com wrote:
Lovely to meet you both[image: *:) happy]
Angie
--
*From:* Marty Gartenberg wa2...@gmail.com
*To:* CMLHope@googlegroups.com
*Sent:* Monday, May 25, 2015 5:50 PM
*Subject:* [CMLHope] Picture of Marty and Shelly
Well, I have been posting here for a long time and no one knows what I or
Shelly look like. I must admit that this picture was taken several years
ago before my kidneys failed. We were on a cruise and since then I have
shed some weight.
My beautiful wife Shelly is the love of my life.
Once I'm
Hi Angie,
Please read this about the effects to not only your platelet counts but
also your red cell count. Ragavan gave you some valuable advice but you
need to find the best supplement that contains the best form of Papya leaf
extract. By the way when I had my bone marrow transplant one of my
transplant? Maybe my bone marrow transplant? Who knows but
no matter what I will still dedicate my life to try and help people if I
possibly can.
Now you know why I always end with 18's (life)
Marty
On Sun, May 24, 2015 at 8:24 AM, Marty Gartenberg wa2...@gmail.com wrote:
Hi Angie,
Please
the best to you! 18's~
Angie
--
*From:* Marty Gartenberg wa2...@gmail.com
*To:* cmlhope@googlegroups.com
*Sent:* Sunday, May 24, 2015 8:24 AM
*Subject:* Re: [CMLHope] Platelets
Hi Angie,
Please read this about the effects to not only your platelet counts
Hi Beth,
First Shelly and I would like to thank you for your birthday wishes. Now
for a couple of corrections. Yes I do try to kick azz but I don't do any
pushups on the commode, there are only two things that I use the commode
for. Up until recently it was only one thing but since my kidney
Hi Greenie,
I keep on saying that your mind is also a part of this process. You need to
learn how and when to take control of your mind. Please remember something.
When your upset or have any anxiety in your life then it effects your
endorphin levels in your brain. The less of this hormone the
all
those doc appts. I hope you get to celebrate big!
So great to hear from you, but I must get ready for vacation! Living
life to the fullest and wishing that for all of you, too!
18's and blessings on your birthday,
Susan F. Zimmerman
-Original Message-
From: Marty Gartenberg
Hi Susan and everyone else.
Well another hospital stay but I just got home yesterday. This time it was
phenomena so I was started on an iv antibiotic which I will have with me
for about two more weeks. Anyway it was my goal to celebrate my wife's
birthday which was on May 20th and mine is
Thank you greenie I just have to do what I have to do. It is only a bump in
the road but a very painful bump but I just ride it out. There are no other
choices
18's
Marty
On Sat, May 9, 2015 at 3:31 PM, Myvety2k via CMLHope
cmlhope@googlegroups.com wrote:
Marty, you are one son of a gun, I
As you already know I was discharged from the hospital yesterday with the
catheter removed. When I got home I was able to urinate but only a little
at a time. Later on in the evening I couldn't urinate at all and the pain
was getting very bad I had no other choice to go to the Bethesda west
Richard,
That's what we are all here, to share our knowledge and experiences.
Anyway, I go into the hospital again tomorrow afternoon to have my prostate
operation. If everything goes ok then this horrible catheter will finally
come out after more then ten weeks. It gave me a uti and I am on
day.
18's,
Susan F. Zimmerman
-Original Message-
From: Marty Gartenberg wa2...@gmail.com
To: cmlhope cmlhope@googlegroups.com
Sent: Tue, May 5, 2015 2:56 pm
Subject: Re: [CMLHope] My article re: CML
Well, well well Susan Zimmerman .01 Hugs,
I also notice that you use 18's
Well, well well Susan Zimmerman .01 [?] Hugs,
I also notice that you use 18's as well. Good!
18's right back at you
Marty
On Tue, May 5, 2015 at 2:17 PM, rszim0702 via CMLHope
cmlhope@googlegroups.com wrote:
Hello Vic,
I finally got tested again (bcr/abl) which showed my number as
HI Suzieq
From my understanding The first patent for Gleevec expires in July 2015.
This is the earliest predictable date that a generic version could become
available. However this will probably be something that Novartis will fight
and make some minor changes to it and maybe refilled it again.
your possession. Psalm 2:8
-Original Message-
From: Marty Gartenberg wa2...@gmail.com
To: CMLHope CMLHope@googlegroups.com
Sent: Sun, May 3, 2015 3:11 pm
Subject: [CMLHope] What is on our outsides can not compare to what is in
our insides
Hot Chocolate.
You will need power point
Hi Richard,
And speaking about the 23rd psalm.
FOOTPRINTS IN THE SAND One night I dreamed I was walking along the beach
with the Lord. Many scenes from my life flashed across the sky. In each
scene I noticed footprints in the sand. Sometimes there were two sets of
footprints. Other times there
Richard, I am glad that your feeling better
18's,
Marty
On Thu, Apr 30, 2015 at 4:48 PM, Richard H rbhuffm...@gmail.com wrote:
I spent 3 days in the hospital this week. Good news it was not
necessarily related to CML, but CML was hiding the problems. 1. I had
developed Vertigo, so we
Hi everyone,
We all go through our trials in life, some more then others but in our
lives there is so much uncertainty that we sometimes loose track of what is
really important. We are all very precious human beings and even though you
may think that the world is coming down on you we must
Hi Jeanie,
I had the same problem after my kidney transplant. My pulse was beating in
the 145 and sometimes higher. The doctor gave me Cartizem and now my heart
beats are normal but even more my blood pressure is just about perfect.
18's,
Marty
On Sat, Apr 25, 2015 at 6:24 PM, 'Icandoallttc'
Thank you greenie.
18's
Marty
On Sat, Apr 25, 2015 at 9:31 PM, Myvety2k via CMLHope
cmlhope@googlegroups.com wrote:
Marty, I'm always glad to here good news from you, it's up lifting.
greenie
In a message dated 4/25/2015 7:41:34 P.M. Eastern Daylight Time,
wa2...@gmail.com writes:
I always try to keep a positive attitude and as everyone already knows what
i have already gone through, but i don't complain because i am still here.
And if you look at yourselves and everything that your going through i want
you to remember something. First are those two numbers i always send
wrote:
Marty, I am so glad to read your upbeat email. You are a very special man
and I am thankful that you received your kidney. May God continue to bless
you and your family
Marcie
Sent from my iPad
On Apr 24, 2015, at 7:54 AM, Marty Gartenberg wa2...@gmail.com wrote:
I always try
-Original Message-
From: Marty Gartenberg wa2...@gmail.com
To: cmlhope cmlhope@googlegroups.com
Sent: Tue, Apr 21, 2015 8:50 pm
Subject: Re: [CMLHope] Marty's Post on CML2
Thank you Beth.
I am trying to do a lot of exercise to try and get back into shape. It
is working little
Thank you Beth.
I am trying to do a lot of exercise to try and get back into shape. It is
working little by little but always moving forward,
On May 7th i will have another operation on my prostate to make it be able
to pass urine. I have had a urine catheter in me for more then seven weeks
Thank you Guy. The best of health to you.
18's
Marty
On Thu, Apr 2, 2015 at 8:48 PM, gene and guy Larcher gandglarc...@gmail.com
wrote:
Dear Marty,
Hope you feel a little better each day and that you get good news from the
docs regarding your transplant.
The letter you wrote to the
Just to let everyone know, I do consider all of you as my extended family.
When someone hurts then so do we all. We are all a very tight knit group.
Please know that It has been very difficult for me to stay in touch with
all of you because this procedure has kept me in and out of the hospital
, 2015 12:01 pm
Subject: Re: [CMLHope] Re: U[PDATE FOR MARTY
Oh, Marty, it is so good to hear your voice. We understand your
situation and will continue our prayers for you. Rest and heal. God bless
and keep you.
Joyce in IL
On Mar 30, 2015, at 7:54 AM, Marty Gartenberg wrote
Hi everyone,
I did get my kidney transplant and I am trying to recover,
i am in a lot of pain but when I feel better I will let you know
18's
On Sun, Mar 29, 2015 at 8:19 PM, Myvety2k via CMLHope
cmlhope@googlegroups.com wrote:
Jeanie, let's us know as soon as you find out something. O.
Hello to everyone,
Now you all know why I do what I do. I love all of you just as my extended
family. I am so honored and grateful to be a part of your lives, your very
precious lives.
I would like to share with all of you, a letter that I wrote to my kidney
donors family. I would hopefully
I thought that everyone should know, When I arrived at dialysis this
morning I had a phone call from my transplant coordinator. She told me that
there is a kidney for me and I will have to go to the hospital late this
evening. They still need to make sure that the cross match is good. If it
isn't
.pngemoji_u1f420.pngemoji_u1f420.pngemoji_u1f420.pngemoji_u1f420.pngemoji_u1f420.pngemoji_u1f420.pngemoji_u1f420.pngemoji_u1f420.pngemoji_u1f420.pngemoji_u1f420.png.
18,s
On Feb 19, 2015, at 6:37 AM, Marty Gartenberg wa2...@gmail.com wrote:
Hi Maria,
I'm sorry to hear about your kidney problems
Hi Maria,
I'm sorry to hear about your kidney problems. If I can give you some
advice? If you are not diabetic try drinking cranberry juice. It washes out
your kidneys and keeps you hydrated.
Good luck with your BMA, I am praying that everything comes out well.
18's,
Marty
On Thu, Feb 19,
@googlegroups.com wrote:
Hi Maria--I had BMA a few weeks ago. It just confirmed my leukemia.
I'll send a highlight of mine soon. Are they going to put you to sleep?
Good luck -- you will be ok. Praying for you
Prayers Blessings Jeanie . 18,s
On Feb 19, 2015, at 6:37 AM, Marty Gartenberg wa2
Hi Suzieq,
Hopefully soon. but it will come eventually, and I thank you for the 18's
to everyone. Lately I have noticed more and more people on this site have
been also using it.
As far as the Desferal, I guess that it wasn't around when I had my bone
marrow transplant and receiving those 93
Hi Richard,
Well, your giving me more credit then I actually deserve. I lived in that
plastic bubble for seven months, and this would be my first kidney
transplant not my second. My first was the bone marrow one. All of the
blood transfusions were done for and directly after my bone marrow
Hi Richard,
Just because it didn't work (Procrit/Epogen) for you then that doesn't mean
it won't work for you now. That should be discussed with your doctor. There
are a lot of contributing factors so you can't really be sure until you
have that discussion with your doctor. Possibly you weren't
Hi Jeanie,
I hate it when a doctor tells you that something is your last hope. In my
opinion I think that you need to find yourself another more qualified
Oncologist. It just brings back some memories of my own. When I was first
diagnosed my doctor's associate came into my hospital room and right
Hi Jeanie,
Life is a complicated process.
Having hemoglobin counts under 8 is a hard rock to chew on. I know
because my usual hemoglobin counts are usually under 10 but since my
kidneys no longer produce the hormone that goes into the bone marrow to
help produce my hemoglobin my doctors give me
-it's a treasure as you are.
Prayers Blessings Jeanie 18's [image: ][image: ]
On Feb 14, 2015, at 7:38 AM, Marty Gartenberg wa2...@gmail.com wrote:
Hi Jeanie,
Life is a complicated process.
Having hemoglobin counts under 8 is a hard rock to chew on. I know
because my usual hemoglobin
Hi Shannon,
Thank you for all of your crossed joints [?] I appreciate it. I know that it
will eventually happen just as I know there WILL be a cure for CML, and
that is what I have all of my joints crossed for.
18's, and hugs [?]
Marty
On Thu, Feb 12, 2015 at 5:46 AM, Shannon L
Hi Suzieq,
Don't worry about this to much. Remember there was a different lab used and
they used a more sensitive test. I would just wait until your next ABL/PCR
test and see what happens. I have already seen this many times.
I keep on saying that there will be a cure for CML soon. It is only a
First I would like to thank each and every one of you for your prayers. As
I pray for all of you I know that you have been also praying for me.
This web site makes all of us as one caring family and it is always of help
for all of us.
I was just called by my transplant coordinator to inform me
the
good fight of faith. Every day is a victory!
18's,
Susan F. Zimmerman
-Original Message-
From: Marty Gartenberg wa2...@gmail.com
To: cmlhope cmlhope@googlegroups.com
Sent: Fri, Feb 6, 2015 5:36 pm
Subject: Re: [CMLHope] Ponatinib
Keep on going Jeanie.
18's,
Marty
Keep on going Jeanie.
18's,
Marty
On Fri, Feb 6, 2015 at 10:03 AM, 'Icandoallttc' via CMLHope
cmlhope@googlegroups.com wrote:
Good morning everyone
My blood results are in and my platelets came down a little--1050
million--WBC still at 14--still fighting.
Prayers Blessings Jeanie 18's
I got up this morning and went to the hospital to have some corrective
surgery to the fistula in my arm. This operation was a little different
from all of the others because I had to be intabated and general Anastasia
was used.
The operation lasted more then three hours, hopefully this one will
,
Beth
-Original Message-
From: Marty Gartenberg wa2...@gmail.com
To: CMLHope CMLHope@googlegroups.com
Sent: Tue, Feb 3, 2015 4:21 pm
Subject: [CMLHope] My twelfth surgery on my fistula
I got up this morning and went to the hospital to have some corrective
surgery to the fistula
Greenie,
They are called Q-Tips because all that you see from behind is like
looking at a giant Q-Tip. Sometimes you don't even see that. It is like the
car is being driven without anybody behind the wheel.
Some suddenly decide to stop right in the middle of the street for no
apparent reason .
Hi John,
Just so you know when you have CML then your uric acid will also usually be
high. That is why you are then started on Allopurinol. I have been on it
for more then 25 years and I hardly ever get anymore gout attacks.
18's,
Marty
On Sun, Feb 1, 2015 at 11:22 AM, John Barrons
Susan, I don't want to leave you out, so here it is from me to you. [?]
18's,
Marty
On Fri, Jan 30, 2015 at 11:27 PM, 'Susan Zimmerman' via CMLHope
cmlhope@googlegroups.com wrote:
Dear Jeanie,
Will surely be praying for you. Don't panic, and don't even be
anxious! Worry accomplishes
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