Unusually cold in FL.  
Get out your sweaters. 
Blessings
Jeanie🐠

Sent from my iPhone

> On Nov 18, 2014, at 3:09 PM, "'Susan Zimmerman' via CMLHope" 
> <[email protected]> wrote:
> 
> Greenie, we're traveling to Florida to Treasure Island, arriving Saturday the 
> 22nd.  Only be there 4 days, then going to New Orleans for T-giving..  Keep 
> that warmth going for us for just four days.....please!  It's 17 degrees here 
> right now.  Just FYI
> 
> Susan
> 
> 
> -----Original Message-----
> From: Myvety2k via CMLHope <[email protected]>
> To: cmlhope <[email protected]>
> Sent: Tue, Nov 18, 2014 11:06 am
> Subject: Re: [CMLHope] Great NEWS
> 
> I'm getting out all of my ice fishing clothing, long john's, etc, it's 60 
> deg. here in Fort Myers, FL.  But then my daughter is visiting friends at the 
> Wisconsin Dells and they live in Hawaii.  It's 12 deg. their.  It's going to 
> get back up in the low 80's by Thursday here. They warm everyone.
>  
> greenie
>  
> In a message dated 11/18/2014 10:23:10 A.M. Eastern Standard Time, 
> [email protected] writes:
> Great day I Florida. Glad everyone is good. 
> Happy dance to all. 
> Jeanie 
> 
> Sent from my iPhone
> 
> On 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]
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