THANK YOU SUSAN, YOU ARE A VERY KIND PERSON.

18'S

MARTY

On Tue, Nov 18, 2014 at 9:04 AM, 'Susan Zimmerman' via CMLHope <
[email protected]> wrote:

> Thanks Marty and everyone for your kind words.  I'm also gaining back
> energy daily.
>
>  Hey there, as a wrestler that Marty claims for me, I'm wrestling for all
> of YOU to steadily move forward in your own healings or remissions, which
> means I am praying for you to our precious heavenly Father, who knows your
> hearts.  Marty, we expect news soon of a kidney transplant happening for
> you!!!  Meanwhile all of our wishes are for you to feel well and have no
> problems with dialysis and energy.
>
>  Love and 18's,
>
> Susan F. Zimmerman
>
>
> -----Original Message-----
> From: Marty Gartenberg <[email protected]>
> To: cmlhope <[email protected]>
> Sent: Mon, Nov 17, 2014 10:38 pm
> Subject: Re: [CMLHope] Great NEWS
>
>  Susan,
>
>  Are you sure that in your former life you weren't a boxer or wrestler?
> You beat the crap out of CML! Good for you! We are all doing the "happy
> dance" for you.
>
>  So now you really know the meaning of 18's.
>
>  Marty
>
> On Fri, Nov 14, 2014 at 12:18 AM, 'Susan Zimmerman' via CMLHope <
> [email protected]> wrote:
>
>> Hello All,
>>
>>  Great e-mail to the new "Sue", Marty!!!  You are adorable and I love
>> you.  Welcome Sue from one to another....I have GREAT NEWS:
>> You guessed it, I am MMR!!!!!  My numbers are .04% after 8 months on
>> lowest dose of bosulif.  YAY, doing the happy dance for all He has done for
>> me.  I went 7 yrs and 2 mos. without any medication after being on gleevec
>> 400 mg. for 2 yrs and 3 mos....had a brain hemmorhage, then another, so
>> stopped gleevec for 7 yrs.  Tried every other one and had some adverse
>> bleeding effect that kept me from taking it.  In 2010 had a major stroke,
>> but doing fine now.  Their only reasoning is I have cavernous malformations
>> in my brain.  Do you think this is any indication of the fact that I pride
>> myself on being a little wacko???    Wanted to share how my numbers have
>> plummeted:
>>
>>  March 2014 - 23.5 Int'l. Scale BCR/ABL
>> April 2014 -    9.0 Int'l Scale WITHOUT any meds
>> May 2014 -     5.85 on bosulif 100 mg for only 30 days
>> June 2014 -    3.7, 60 days on bosulif
>> Oct. 2014 -    .11%
>> Nov. 2014    .04%, achieved MMR - hooray!!!
>>
>> Please continue praying that I have no bleeding side effects from 100
>> mg.  They keep encouraging me to take 200 mg, but I say why rock the boat
>> when this is working just fine?  I am a rare bird, so don't try to copy
>> what I do, anyone.....(about meds)
>>
>>  Y'all are always in my prayers.  I thank God for being able to know you
>> and have the privilege of calling all of you my friends.  Greenie and I met
>> a few months ago, and it was wonderful!  Try to enjoy every day as if it
>> were your last, because we never know when He'll call us home!  Just lost
>> two good friends, and know they are in a better place.
>>
>>  Love and 18's,
>> Susan F. Zimmerman
>>
>>
>> -----Original Message-----
>> From: Richard H <[email protected]>
>> To: cmlhope <[email protected]>
>> Sent: Thu, Nov 13, 2014 11:45 pm
>> Subject: Re: [CMLHope] newly diagnosed
>>
>>  Safe Travels my Friend.
>>
>>  Richard H.
>>
>> On Wednesday, November 12, 2014 11:16:26 PM UTC-6, wa2yyx wrote:
>>
>>> Hi Marcie,
>>>
>>>  We are all captains of our own ships because we steer our own ships in
>>> a positive direction. Do you remember me saying that Leukemia is not only a
>>> disease of one's body but their mind as well. It is how you handle yourself
>>> that makes a big difference. If someone goes around with a terrible
>>> attitude then that is what they will get. If someone goes around with a
>>> good attitude then that is what they will have.
>>>
>>>  Anyway, I have an appointment at Tampa Hospital for an annual exam for
>>> a kidney transplant. It's just that I have to be current with everything
>>> just in case it happens.
>>>
>>>  The hospital is more then four hours away so I have to get some sleep
>>> now.
>>>
>>>  18's,
>>>
>>>  Marty
>>>
>>> On Wed, Nov 12, 2014 at 8:53 PM, 'Marcie Goodman' via CMLHope <
>>> [email protected]> wrote:
>>>
>>>>  Marty,
>>>>
>>>>  What a lovely email to Sue. We are traveling together and I feel like
>>>> you are the Captain of our ship!
>>>>
>>>>  Thinking about you and keeping you in my prayers
>>>>
>>>>  Love and 18s,
>>>>
>>>>  Marcie
>>>>
>>>> Sent from my iPhone
>>>>
>>>> On Nov 12, 2014, at 8:34 PM, Marty Gartenberg <[email protected]> wrote:
>>>>
>>>>   Oh yes Sue, family. Well you know what they say? You can pick your
>>>> friends but your family is here to stay good or bad. No matter what you
>>>> can't change them.
>>>>
>>>>  As my father used to say, "never argue with a moron, fool, idiot or
>>>> liar or someone that won't listen to what you have to say because no matter
>>>> what you try to tell them they will never change.
>>>>
>>>>  But your focus shouldn't be on them but people that are willing to
>>>> help you. That is what this site is all about as you can see.
>>>>
>>>>  When you travel on your journey all of us will be traveling along
>>>> with you. I really mean that, and you will see that your not alone but with
>>>> some very nice people that will be supporting you along.
>>>>
>>>>  18's,
>>>>
>>>>  Marty
>>>>
>>>> On Wed, Nov 12, 2014 at 4:25 PM, smgedit <[email protected]> wrote:
>>>>
>>>>>  Hi,
>>>>> First off, I love your terminology! (I'm a writer and editor by
>>>>> trade). Secondly, thanks for your support. I'm limiting who knows and who
>>>>> doesn't know what is going on for now but unfortunately one of the 
>>>>> ignorant
>>>>> statements was by a family member. Oh well. I'm happy to have found this
>>>>> site and to be meeting nice people like you on it.    Sue
>>>>>
>>>>>  Hi Sue,
>>>>>>
>>>>>>  I read your post and just wanted to make some comments. Personally
>>>>>> I think that your hanging around with some people that I would classify 
>>>>>> as
>>>>>> Anal Orifices. And I only say that to be polite. Or even more possible 
>>>>>> they
>>>>>> suffer from Rectal Cranial Inversion (their head is up their Azz.
>>>>>>
>>>>>>  I have to tell you that if one of them had CML or any other type of
>>>>>> cancer then they would certainly have a different attitude.
>>>>>>
>>>>>>  I hate to say this but sometimes you should keep some things to
>>>>>> yourself because of people like that. The less they know about you then 
>>>>>> the
>>>>>> better it will be for you.
>>>>>>
>>>>>>  Anyway, now that is off my chest let me go into something more
>>>>>> important. First, you have come to right place. All of those that are 
>>>>>> here
>>>>>> are very compassionate and really care about each other. They have 
>>>>>> already
>>>>>> gone through this and will be very happy to help you out with any 
>>>>>> questions
>>>>>> and anything else they can and will help you with this.
>>>>>>
>>>>>>  CML is not what it used to be because it is not a "death sentence"
>>>>>>  anymore. There have been so many improvements in it's treatment, not 
>>>>>> like
>>>>>> in my day. I don't know what you may know about me but I am here to help
>>>>>> you out in any way that I can.
>>>>>>
>>>>>>  If you have read any of my posts you will see what I mean. Remember
>>>>>> any time that you would like to post anything please feel free to do so. 
>>>>>> I
>>>>>> would like to welcome you to this site.
>>>>>>
>>>>>>  Sue, whenever I end any of my posts I end it with two numbers 18
>>>>>> which is the symbol for life.
>>>>>>
>>>>>>  18's to you Sue.
>>>>>>
>>>>>>  Marty
>>>>>>
>>>>>> On Wed, Nov 12, 2014 at 10:23 AM, smgedit <[email protected]> wrote:
>>>>>>
>>>>>>>  I was diagnosed with CML a little over a month ago and had a bone
>>>>>>> marrow biopsy and started taking Gleevec last week.  I'm trying to 
>>>>>>> learn as
>>>>>>> much as I can about CML and my oncologist is great about giving detailed
>>>>>>> explanations and answering questions. But I was wondering if anyone else
>>>>>>> ever got what I consider a strange reaction from others about my news. 
>>>>>>> In
>>>>>>> the past week, I've had people say the following things to me which 
>>>>>>> upset
>>>>>>> me a lot.
>>>>>>>
>>>>>>>  "So what's the big deal? So you have to take a pill...I have to
>>>>>>> take this antibiotic for my tooth infection this week too."
>>>>>>>
>>>>>>>  "There is so a cure for leukemia. Plenty of people are cancer
>>>>>>> free. You don't know what you are talking about."
>>>>>>> (This after explaining about the drugs and "response," vs.
>>>>>>> "remission." etc.)
>>>>>>>
>>>>>>>  "Well I hope you have a speedy recovery. Good luck."
>>>>>>>
>>>>>>>  I know I can't put my energy into dealing with this right now but
>>>>>>> it is weighing on my mind anyway. It made me happy to find this group
>>>>>>> online where I know people can at least "get" it and where some of you 
>>>>>>> have
>>>>>>> been living with CML for quite a while.
>>>>>>>
>>>>>>>  Anyway, that's my first post. Nice to meet you.
>>>>>>>
>>>>>>>  Sue
>>>>>>>  --
>>>>>>> --
>>>>>>> [CMLHope]
>>>>>>> A support group of http://cmlhope.com
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>>>
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