Thank you Greenie   
I need that. 
Blessings 
Jeanie

Sent from my iPhone

> On Jan 12, 2015, at 1:30 PM, Myvety2k via CMLHope <[email protected]> 
> wrote:
> 
> Hi Jeanie, hang in their,  I'm thinking good thoughts and passing them on to 
> you.
>  
> greenie
>  
> In a message dated 1/12/2015 1:08:27 P.M. Eastern Standard Time, 
> [email protected] writes:
> Thanks Susan.  
> I'm hanging in there!!!
> Blessings. 
> Jeanie🐟🐟🐟
> 
> Sent from my iPhone
> 
>> On Jan 11, 2015, at 11:17 PM, "'Susan Zimmerman' via CMLHope" 
>> <[email protected]> wrote:
>> 
>> Awwwww Marcie!
>> 
>> I am so sorry for your loss, dear one.  I know you've been being a good 
>> caregiver for several years to your dad.  You will be rewarded some day for 
>> that.  My heart hurts for you, so will surely be lifting you in prayer.  No 
>> matter what the age, the loss is huge when we are the ones left behind.  It 
>> was so kind of your rabbi to mention your CML battle.  I pray you stop 
>> having those horrible cramps, too. Traveling mercies for you all.
>> 
>> And Jeanie, also know what it's like to have a bad day from hydrea.  Many 
>> (including me) felt like they have the flu with the nausea, and I pray this 
>> will not last long at all.  A new day is coming, and I sure do hope your doc 
>> puts you on something that works! (maybe bosulif?)  Here's wishing you the 
>> best, dear one.
>> 
>> Love and 18's,
>> 
>> Susan 
>> 
>> -----Original Message-----
>> From: 'Marcie Goodman' via CMLHope <[email protected]>
>> To: cmlhope <[email protected]>
>> Sent: Sun, Jan 11, 2015 10:59 pm
>> Subject: Re: [CMLHope] Jeanie's relapse
>> 
>> Hi Jeanie,
>> 
>> So sorry you are having a tough time. I'm praying for you to have good test 
>> results and a much better week. 
>> 
>> My 94 year old father passed away on Friday, funeral was today. During 
>> evening prayers our rabbi asked that everyone pray for not only my father 
>> and our family but for our group struggling with the impact of CML. My dad 
>> hated the fact that I had this illness and knew that I had such a wonderful 
>> online support family. 
>> 
>> So lots of prayers for you and all of us headed out from Baltimore all week!
>> 
>> Much love,
>> 
>> Marcie
>> 
>> Sent from my iPhone
>> 
>>> On Jan 11, 2015, at 9:33 AM, 'Icandoallttc' via CMLHope 
>>> <[email protected]> wrote:
>>> 
>>> Hi Marty. 
>>> I feel so bad today!!!
>>> Thinks it's from the hydrea. 
>>> I will print that out and keep it close. 
>>> I love psalms also. 
>>> Keep praying. 
>>> Jeanie 18's
>>> 
>>> Sent from my iPhone
>>> 
>>>> On Jan 11, 2015, at 8:05 AM, Marty Gartenberg <[email protected]> wrote:
>>>> 
>>>> Jeanie, I know that your feeling low right now but things will work out 
>>>> for you. You must have this in your heart and I know that you do. FOCUS.
>>>> 
>>>> This was something that was given to me by one of my close friends when I 
>>>> had to live in that plastic bubble for all of those many months. I would 
>>>> read it all the time and I am now passing it on to you, and it is being 
>>>> sent to you from my heart because I remember my doubts but then again I 
>>>> also remember my strengths.
>>>> 
>>>> EXPECT THE BEST, MIND OVER MATTER. SUCCESS IS A FUNCTION OF SELF 
>>>> CONFIDENCE. TO HAVE SUCCESS AT ANYTHING YOU MUST FIRST LEARN TO BELIEVE IN 
>>>> YOURSELF. IF YOU EXPECT THE WORSE THEN THAT IS EXACTLY WHAT YOU WILL GET 
>>>> (MIND OVER MATTER) IF YOU EXPECT THE BEST THEN THAT IS WHAT YOU WILL GET.
>>>> WHAT WE HAVE TO LEARN TO DO IS TO CHANGE OUR MENTAL HABITS, OUR STATES OF 
>>>> MIND. LEARN TO EXPECT AND NOT TO DOUBT. BY DOING THIS YOU BRING EVERYTHING 
>>>> INTO THE REALM OF POSSIBILITY. WHEN YOU LEARN TO BELIEVE THEN WHAT YOU 
>>>> THOUGHT TO BE IMPOSSIBLE THEN MOVES INTO THE AREA OF POSSIBILITY.
>>>> EVERY GREAT THING EVENTUALLY BECOMES POSSIBLE FOR YOU. MY BELIEF AT THE 
>>>> BEGINNING OF A DOUBTFUL UNDERTAKING IS THE ONE THING THAT INSURES THE 
>>>> SUCCESSFUL OUTCOME...
>>>> FOCUS...
>>>> 
>>>> Yes Jeanie you just keep on focusing because you are much more powerful 
>>>> then you think.
>>>> 
>>>> Now you know why I keep on sending 18's.
>>>> 
>>>> 18's,
>>>> 
>>>> Marty
>>>> 
>>>>> On Sat, Jan 10, 2015 at 10:38 AM, 'Icandoallttc' via CMLHope 
>>>>> <[email protected]> wrote:
>>>>> Hi Marty 
>>>>> Thanks for you uplifting message. 
>>>>> I am back to square one with my counts--
>>>>> 700 thousand platelets
>>>>> 163.28 WBC
>>>>> ANC high
>>>>> Creatine high
>>>>> Potassium high
>>>>> Took me off sprycel. 
>>>>> Allipurinoll 2 pills
>>>>> Hydrea 3 twice a day
>>>>> Yes I will fight!!!
>>>>> Just so tired. 
>>>>> I think dr will put me on new drug mon.  
>>>>> Got to see if there is a mutant. 
>>>>> Prays and love to all. 
>>>>> 18's. <emoji_u1f41f.png>
>>>>> Jeanie
>>>>> 
>>>>> 
>>>>> Sent from my iPhone
>>>>> 
>>>>>> On Jan 10, 2015, at 4:31 AM, sherri swanson 
>>>>>> <[email protected]> wrote:
>>>>>> 
>>>>>> Hi Richard,
>>>>>> 
>>>>>> If it's one thing I got, It's Attitude! At least that's what my mom 
>>>>>> would tell me when I was a teenager. LOL
>>>>>> 
>>>>>> Sorry to hear about the car.  This cold weather can be brutal on a car's 
>>>>>> battery. Glad you were able to get a new and now you’re good to go.  
>>>>>> 
>>>>>> Uor wind chills have been bad too. And we have some open fields so there 
>>>>>> is nothing to block that wind.  The other morning it was so cold that 
>>>>>> the water froze in our community and none of had any water for awhile. 
>>>>>> It's a good thing I'm an early raiser and I took my shower while we had 
>>>>>> water. 
>>>>>> 
>>>>>> Currently, it is -7 with a wind chill of -25 where I live and it isn't 
>>>>>> going to be above zero until 9 am. That's cold. 
>>>>>> 
>>>>>> Stay warm Richard and think spring!
>>>>>> 
>>>>>> L'chaim,
>>>>>> 
>>>>>> Sherri
>>>>>> 
>>>>>>> On Fri, Jan 9, 2015 at 11:29 PM, Marty Gartenberg <[email protected]> 
>>>>>>> wrote:
>>>>>>> Hi Jeanie,
>>>>>>> 
>>>>>>> So many things effect your kidneys. The simple ageing factor is just 
>>>>>>> one of them. Some medicines will also contribute to kidney function 
>>>>>>> probably some of these TKI's. Mine finally gave out from all of the 
>>>>>>> chemotherapy and radiation I had more then 25 years ago.
>>>>>>> 
>>>>>>> I can make a suggestion: If you are not diabetic try drinking cranberry 
>>>>>>> juice. Not the ones that are mixed up with juices like grape juice. 
>>>>>>> Ocean Spray has pure cranberry juice so you might                want 
>>>>>>> to try it. Even if you are diabetic they also make a light cranberry 
>>>>>>> juice.
>>>>>>> 
>>>>>>> You know what? You have been through so much that this is only a bump 
>>>>>>> in the road for you, and so it is for me.
>>>>>>> 
>>>>>>> We have two choices. One, continue to fight and the other is not an 
>>>>>>> option for me or you.
>>>>>>> That is why I always end any of my posts with 18's. You just hang in 
>>>>>>> there sweetie.
>>>>>>> 
>>>>>>> Marty
>>>>>>> 
>>>>>>> On Fri, Jan 9, 2015 at 7:55 AM, ICANDOALLTTC via CMLHope 
>>>>>>> <[email protected]> wrote:
>>>>>>>> Hi Sherri,
>>>>>>>> I think the tki's contribute to kidney disease.  I                  
>>>>>>>> think that I am in the beginning of the disease and I have been on 
>>>>>>>> tki's for 11 years now.
>>>>>>>> Hang in in there; blessings
>>>>>>>> Jeanie<3
>>>>>>>>  
>>>>>>>> In a message dated 1/9/2015 3:21:09 A.M. Eastern Standard              
>>>>>>>>     Time, [email protected] writes:
>>>>>>>> Hi Marty, 
>>>>>>>> 
>>>>>>>> Thanks for the prayers and right back at ya. 
>>>>>>>> 
>>>>>>>> I've been struggling with my kidney disease for many years and didn't 
>>>>>>>> know it, and then one day voilà the doctors found that there was a 
>>>>>>>> problem and that I'd been fighting it for years hence the diagnoses of 
>>>>>>>> Chronic Kidney Disease. And the funny thing is, I'm the only one in my 
>>>>>>>> entire family that has any of these diseases. My family had its share 
>>>>>>>> of health issues from heart disease to diabetes. But never anything 
>>>>>>>> like what I have. All my doctors just shake their heads. I tell them 
>>>>>>>> that I like to keep things interesting. And what they like is that I 
>>>>>>>> have a sense of humor. And at this point, it is much better to joke 
>>>>>>>> and laugh than to worry and cry.  While I still take what I have 
>>>>>>>> seriously, I'm just happy to be here. 
>>>>>>>> 
>>>>>>>> I would be a lot happier if the weather here would warm up. For crying 
>>>>>>>> out loud                    it was -5 here yesterday and I was out in 
>>>>>>>> it. Now that is one hearty person or a very foolish one. The jury is 
>>>>>>>> still out on that one.  Today it is going to be a balmy 8.  Woohoo! A 
>>>>>>>> heat wave. And, again I'll be out in it as I have to go and get a Rx 
>>>>>>>> that I need.  
>>>>>>>> 
>>>>>>>> L'chaim,
>>>>>>>> 
>>>>>>>> Sherri  
>>>>>>>> 
>>>>>>>> On Thu, Jan 8, 2015 at 10:40 PM, Marty Gartenberg <[email protected]> 
>>>>>>>> wrote:
>>>>>>>>> Dear Sherri,
>>>>>>>>> 
>>>>>>>>> Yes, you are a fighter and it takes one to know one. I pray that 
>>>>>>>>> everything turns out well for you. 
>>>>>>>>> 
>>>>>>>>> And you are correct that all of the radiation and                     
>>>>>>>>>  chemotherapy did destroy both of my kidneys. It has been over 25 
>>>>>>>>> years that I had my BMT. It took many years for my kidneys to fail 
>>>>>>>>> and that is probably why most transplant centers will usually not use 
>>>>>>>>> total body radiation any more unless it is really needed.
>>>>>>>>> 
>>>>>>>>> 18's,
>>>>>>>>> 
>>>>>>>>> Marty
>>>>>>>>> 
>>>>>>>>> On Thu, Jan 8, 2015 at 1:31 PM, sherri swanson 
>>>>>>>>> <[email protected]> wrote:
>>>>>>>>>> Hi Marty, 
>>>>>>>>>> 
>>>>>>>>>> The doctors are trying to treat the different illnesses that are 
>>>>>>>>>> included in my condition. There are so many and they do so many 
>>>>>>>>>> different things, that I am happy just to to be here. I agree that 
>>>>>>>>>> as we get older there are some unusual things that that find us. But 
>>>>>>>>>> in the long run, we all got something. I'm a survivor. It's what I 
>>>>>>>>>> do. So when I found                        out on Monday that I have 
>>>>>>>>>> a large mass on my thyroid, I told my doctor I guess we're going to 
>>>>>>>>>> be busy this winter. At least I'm not an alarmist. <35C.png>
>>>>>>>>>> 
>>>>>>>>>> I too have trouble with my kidneys. Not to the extend that you do, 
>>>>>>>>>> I'm working to keep myself at the current level of stage III Kidney 
>>>>>>>>>> Disease. Some days, I'm good others, not so much.  Lately I've not 
>>>>>>>>>> been doing so good and I've had to go and buy new shoes as my feet 
>>>>>>>>>> have been so swollen that my current size no longer fit. I wear 
>>>>>>>>>> compression socks all the time as well. 
>>>>>>>>>> 
>>>>>>>>>> My Nephrologist ran some blood work and found that my sodium         
>>>>>>>>>>                was very low and and so was a bunch of other levels. 
>>>>>>>>>> Now, he is an alarmist. If I even look like I'm getting a cold he 
>>>>>>>>>> freaks out. I love him dearly, and I do what he says, but I can't 
>>>>>>>>>> sneeze without him making me go see my GP or                        
>>>>>>>>>> the Oncologist or whatever doctor he thinks I need to see. 
>>>>>>>>>> 
>>>>>>>>>> I've heard that when you have a BMT and have to have radiation and 
>>>>>>>>>> chemo, sometimes kidney failure is possible. How long have you been 
>>>>>>>>>> on the list for transplant? 
>>>>>>>>>> 
>>>>>>>>>> Well, I'm glad that you are here and that you are strong. You're an 
>>>>>>>>>> inspiration to all of us. Thanks for all you do Marty.
>>>>>>>>>> 
>>>>>>>>>> L'chaim
>>>>>>>>>> 
>>>>>>>>>> Sherri 
>>>>>>>>>> 
>>>>>>>>>> On Thu, Jan 8, 2015 at 10:07 AM, Marty Gartenberg <[email protected]> 
>>>>>>>>>> wrote:
>>>>>>>>>>> Hi again Sherri,
>>>>>>>>>>> 
>>>>>>>>>>> Hopefully you will be able to be treated for this condition. It 
>>>>>>>>>>> seems that as most of us get older we start suffering from some 
>>>>>>>>>>> very unusual things, but that is the price we must pay to remain 
>>>>>>>>>>> alive. We just have to do whatever we can to keep on going because 
>>>>>>>>>>> we have no other choice.
>>>>>>>>>>> 
>>>>>>>>>>> My kidneys failed four years ago and I must be on dialysis because 
>>>>>>>>>>> it is keeping me alive until I can hopefully receive a kidney 
>>>>>>>>>>> transplant.
>>>>>>>>>>> 
>>>>>>>>>>> This happened because when I received a bone marrow transplant more 
>>>>>>>>>>> then 25 years all of the radiation and chemotherapy started to 
>>>>>>>>>>> destroy my kidneys, but i'm still alive today because of it. We all 
>>>>>>>>>>> have our own battles in life and that is just the way it is.
>>>>>>>>>>> 
>>>>>>>>>>> I wish you much health and happiness in this New                    
>>>>>>>>>>>       Year.
>>>>>>>>>>> 
>>>>>>>>>>> 18's,
>>>>>>>>>>> 
>>>>>>>>>>> Marty 
>>>>>>>>>>> 
>>>>>>>>>>>> On Thu, Jan 8, 2015 at 5:19 AM, sherri swanson 
>>>>>>>>>>>> <[email protected]> wrote:
>>>>>>>>>>>> Hi Marty, 
>>>>>>>>>>>> 
>>>>>>>>>>>> Happy New Year. I hope you are well. Thanks for the research I 
>>>>>>>>>>>> enjoyed article. I could only wish it was as simple as being as 
>>>>>>>>>>>> side effect of my TKI. In my case, nothing is ever simple LOL.  
>>>>>>>>>>>> What I have is called Autonomic Neuropathy.  Basically, my 
>>>>>>>>>>>> Autonomic Nervous System has malfunctioned.  Here is a link for 
>>>>>>>>>>>> you to read if you would like to.
>>>>>>>>>>>> 
>>>>>>>>>>>> http://en.wikipedia.org/wiki/Dysautonomia
>>>>>>>>>>>>  
>>>>>>>>>>>> In a nutshell, Autonomic Neuropathy is a nerve disorder that 
>>>>>>>>>>>> affects involuntary body functions, including heart rate, blood 
>>>>>>>>>>>> pressure, perspiration and digestion.
>>>>>>>>>>>> It isn't a specific disease. Autonomic Neuropathy refers to damage 
>>>>>>>>>>>> to the autonomic nerves. This damage disrupts signals between the 
>>>>>>>>>>>> brain and portions of the autonomic nervous system, such as the 
>>>>>>>>>>>> heart, blood vessels and sweat glands. This can cause decreased or 
>>>>>>>>>>>>                            abnormal performance of one or more 
>>>>>>>>>>>> involuntary body functions.
>>>>>>>>>>>> Autonomic Neuropathy can be a complication of a number of diseases 
>>>>>>>>>>>> and conditions. And some medications can cause autonomic 
>>>>>>>>>>>> neuropathy as a side effect. Signs, symptoms and treatment of 
>>>>>>>>>>>> autonomic neuropathy vary depending on the cause, and on which 
>>>>>>>>>>>> nerves are affected. 
>>>>>>>>>>>> L'Chaim,
>>>>>>>>>>>> Sherri
>>>>>>>>>>>> 
>>>>>>>>>>>> 
>>>>>>>>>>>> 
>>>>>>>>>>>> On Wed, Jan 7, 2015 at 7:02 PM, Marty Gartenberg 
>>>>>>>>>>>> <[email protected]> wrote:
>>>>>>>>>>>>> Hi Sherri,                              
>>>>>>>>>>>>> 
>>>>>>>>>>>>> I did a little research on your no sweating problem, and it is 
>>>>>>>>>>>>> probably a side effect of your TKI treatment. 
>>>>>>>>>>>>> 
>>>>>>>>>>>>> I also ran across an article which you can read here. It does 
>>>>>>>>>>>>> mention something about the lack of sweating. It probably has 
>>>>>>>>>>>>> nothing to do with your                              problem but 
>>>>>>>>>>>>> maybe you should read it anyway.
>>>>>>>>>>>>> 
>>>>>>>>>>>>> http://en.wikipedia.org/wiki/Fabry_disease
>>>>>>>>>>>>> 
>>>>>>>>>>>>> 18's,
>>>>>>>>>>>>> 
>>>>>>>>>>>>> Marty
>>>>>>>>>>>>> 
>>>>>>>>>>>>> On Wed, Jan 7, 2015 at 5:29 AM, sherri swanson 
>>>>>>>>>>>>> <[email protected]> wrote:
>>>>>>>>>>>>>> Hello, 
>>>>>>>>>>>>>> 
>>>>>>>>>>>>>> I've had CML for 12 years and I've taken Gleevec for those 12 
>>>>>>>>>>>>>> years. I've also experienced night sweats for many years.  At 
>>>>>>>>>>>>>> first I was told that it was due to menopause because of my age 
>>>>>>>>>>>>>> at the time. Go figure. When that was no longer an option, the 
>>>>>>>>>>>>>> only thing left was the Gleevec. Since being dx'd with the CML 
>>>>>>>>>>>>>> in 2003, I've been dx'd with other chronic illnesses that are 
>>>>>>>>>>>>>> just as serious.
>>>>>>>>>>>>>> 
>>>>>>>>>>>>>> With these new illnesses came a new problem. I no longer sweat 
>>>>>>>>>>>>>> at all. So now I have the complete opposite problem. No matter 
>>>>>>>>>>>>>> how hot it is, I never sweat. I a way, it's nice because I'm 
>>>>>>>>>>>>>> always cold and I long for very hot days so I can go out side in 
>>>>>>>>>>>>>> the heat. But my oncologist has warned me to not do it for very 
>>>>>>>>>>>>>> long as I have no way to control my body temperature.  
>>>>>>>>>>>>>> Unfortunately, it works the same way with the cold. My body 
>>>>>>>>>>>>>> temperature is a constant 95 degrees.
>>>>>>>>>>>>>> 
>>>>>>>>>>>>>> So, in answer to your question, yes, the Gleevec does cause 
>>>>>>>>>>>>>> night sweats. It is one of its side effects. Unfortunately, I 
>>>>>>>>>>>>>> was not able to find a remedy for my night sweats other than 
>>>>>>>>>>>>>> going to the extreme which I do not recommend. <332.png>
>>>>>>>>>>>>>> 
>>>>>>>>>>>>>> I hope everyone has a good New Year and is healthy.  Keep my 
>>>>>>>>>>>>>> posted as to what you find out. Even                             
>>>>>>>>>>>>>>    thought I no long have this issue, I would still like to be 
>>>>>>>>>>>>>> kept in the loop.
>>>>>>>>>>>>>> 
>>>>>>>>>>>>>> L'chaim
>>>>>>>>>>>>>> 
>>>>>>>>>>>>>> Sherri
>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>> On Tue, Jan 6, 2015 at 4:19                                PM, 
>>>>>>>>>>>>>>> 'Marcie Goodman' via CMLHope <[email protected]> wrote:
>>>>>>>>>>>>>>> Hello, Susan. Gosh, we are just sweating through this it seems. 
>>>>>>>>>>>>>>> I will see what may be available naturally, as I don't want 
>>>>>>>>>>>>>>> hormones either. Sorry you are experiencing this same problem 
>>>>>>>>>>>>>>> which I hope to solve. 
>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>> Best wishes to you, Roy and your beautiful family for a blessed 
>>>>>>>>>>>>>>> New Year. 
>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>> Marcie
>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>> Sent from my iPad
>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> On Jan 5, 2015, at 10:17 PM, "'Susan Zimmerman' via CMLHope" 
>>>>>>>>>>>>>>>> <[email protected]> wrote:
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> Dear Marcie,
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> I have had night sweats for years, intensifying after my dx in 
>>>>>>>>>>>>>>>> 2005.  I have day sweats, too.  When I stand up for            
>>>>>>>>>>>>>>>>                       more than five minutes to do anything at 
>>>>>>>>>>>>>>>> all I start profusely sweating from weakness.  I think part of 
>>>>>>>>>>>>>>>> this is from the bosulif, but most is from the stroke weakness 
>>>>>>>>>>>>>>>> and need for hormones.  I will not take artificial hormones 
>>>>>>>>>>>>>>>> and have not gotten the good kind that are specially made for 
>>>>>>>>>>>>>>>> each person.  I totally sympathize with you Marcie.  You might 
>>>>>>>>>>>>>>>> want to go to a naturalist doctor about getting a test for 
>>>>>>>>>>>>>>>> hormones and then they will make a compound for you of cream 
>>>>>>>>>>>>>>>> that usually works.  Regular md's only know to prescribe the 
>>>>>>>>>>>>>>>> synthetic or horse hormones which do cause cancer.  That's my 
>>>>>>>>>>>>>>>> take on it, hope you find some relief!!!
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> Thanks for your always uplifting posts! Happy New Year to you, 
>>>>>>>>>>>>>>>> too!
>>>>>>>>>>>>>>>> Susan F. Zimmerman
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> -----Original Message-----
>>>>>>>>>>>>>>>> From: 'Marcie Goodman' via CMLHope <[email protected]>
>>>>>>>>>>>>>>>> To: cmlhope <[email protected]>
>>>>>>>>>>>>>>>> Sent: Mon, Jan 5, 2015 8:41 am
>>>>>>>>>>>>>>>> Subject: [CMLHope] Night Sweats
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> Happy New Year, dear friends. I'm wondering if any of you 
>>>>>>>>>>>>>>>> suffer with night 
>>>>>>>>>>>>>>>> sweats as a side effect of your TKI.  I do, and have, over the 
>>>>>>>>>>>>>>>> years of my 
>>>>>>>>>>>>>>>> treatment. I don't know that it is happening more frequently 
>>>>>>>>>>>>>>>> but the sweats seem 
>>>>>>>>>>>>>>>> to be more intense. Is there anything that you know of that 
>>>>>>>>>>>>>>>> will help?
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> Many thanks for always being there to offer encouragement and 
>>>>>>>>>>>>>>>> assistance. 
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> Marcie
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> Sent from my iPad
>>>>>>>>>>>>>>>> 
>>>>>>>>>>>>>>>> -- 
>>>>>>>>>>>>>>>> -- 
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>>>>>>>> 
>>>>>>>> -- 
>>>>>>>> -- 
>>>>>>>> [CMLHope]
>>>>>>>> A support group of http://cmlhope.com
>>>>>>>> -------------------------------------------------
>>>>>>>>  
>>>>>>>> You received this message because you are subscribed to the Google 
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>>>>>>>> -- 
>>>>>>>> -- 
>>>>>>>> [CMLHope]
>>>>>>>> A support group of http://cmlhope.com
>>>>>>>> -------------------------------------------------
>>>>>>>>  
>>>>>>>> You received this message because you are subscribed to the Google 
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>>>>>>> 
>>>>>>> -- 
>>>>>>> -- 
>>>>>>> [CMLHope]
>>>>>>> A support group of http://cmlhope.com
>>>>>>> -------------------------------------------------
>>>>>>>  
>>>>>>> You received this message because you are subscribed to the Google 
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>>>>>>> To post to this group, send email to [email protected]
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>>>>>>> For more options, visit this group at 
>>>>>>> http://groups.google.com/group/CMLHope
>>>>>>> --- 
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>>>>>> 
>>>>>> -- 
>>>>>> -- 
>>>>>> [CMLHope]
>>>>>> A support group of http://cmlhope.com
>>>>>> -------------------------------------------------
>>>>>>  
>>>>>> You received this message because you are subscribed to the Google 
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>>>>>> To post to this group, send email to [email protected]
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>>>>>> For more options, visit https://groups.google.com/d/optout.
>>>>> 
>>>>> -- 
>>>>> -- 
>>>>> [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 group, send email to [email protected]
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>>>>> For more options, visit https://groups.google.com/d/optout.
>>>> 
>>>> -- 
>>>> -- 
>>>> [CMLHope]
>>>> A support group of http://cmlhope.com
>>>> -------------------------------------------------
>>>>  
>>>> You received this message because you are subscribed to the Google Groups 
>>>> "CMLHope" group.
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>>>> [email protected]
>>>> For more options, visit this group at 
>>>> http://groups.google.com/group/CMLHope
>>>> --- 
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>>> -- 
>>> -- 
>>> [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 group, send email to [email protected]
>>> To unsubscribe from this group, send email to 
>>> [email protected]
>>> For more options, visit this group at http://groups.google.com/group/CMLHope
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>>> You received this message because you are subscribed to the Google Groups 
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>>> For more options, visit https://groups.google.com/d/optout.
>> 
>> -- 
>> -- 
>> [CMLHope]
>> A support group of http://cmlhope.com
>> -------------------------------------------------
>>  
>> You received this message because you are subscribed to the Google Groups 
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>> To post to this group, send email to [email protected]
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>> -- 
>> -- 
>> [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 group, send email to [email protected]
>> To unsubscribe from this group, send email to 
>> [email protected]
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>> --- 
>> You received this message because you are subscribed to the Google Groups 
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>> For more options, visit https://groups.google.com/d/optout.
> -- 
> -- 
> [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 group, send email to [email protected]
> To unsubscribe from this group, send email to 
> [email protected]
> For more options, visit this group at http://groups.google.com/group/CMLHope
> --- 
> You received this message because you are subscribed to the Google Groups 
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> email to [email protected].
> For more options, visit https://groups.google.com/d/optout.
> -- 
> -- 
> [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 group, send email to [email protected]
> To unsubscribe from this group, send email to 
> [email protected]
> For more options, visit this group at http://groups.google.com/group/CMLHope
> --- 
> You received this message because you are subscribed to the Google Groups 
> "CMLHope" group.
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-- 
-- 
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------

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