Thanks Marcie. You too!!
Jeanie🐟

Sent from my iPhone

> On Jan 8, 2015, at 1:23 PM, margood18 via CMLHope <cmlhope@googlegroups.com> 
> wrote:
> 
> Jeanie:
> 
> So sorry to hear about your issues.  Thoughts, prayers and hugs being sent 
> your way.
> 
> Marcie
> 
> 
> -----Original Message-----
> From: 'Icandoallttc' via CMLHope <cmlhope@googlegroups.com>
> To: cmlhope <cmlhope@googlegroups.com>
> Sent: Thu, Jan 8, 2015 1:21 pm
> Subject: [CMLHope] Bad need
> 
> Just got back from Moffitt.  All counts were up and uremic acid was high. 
> Dr took me off sprycel and put me on Hydrea, and other drugs.  Took another 
> blood test for mutant.  Will know next week if mutant is problem. 
> Pray for me and all in need. 
> Jeanie
> 
> Sent from my iPhone
> 
> On Jan 8, 2015, at 11:07 AM, Marty Gartenberg <wa2...@gmail.com> 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 
>>> <swanson.sherri...@gmail.com> 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 <wa2...@gmail.com> 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 
>>>>> <swanson.sherri...@gmail.com> 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 
>>>>>> <cmlhope@googlegroups.com> 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" 
>>>>>> <cmlhope@googlegroups.com> 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 <cmlhope@googlegroups.com>
>>>>>>> To: cmlhope <cmlhope@googlegroups.com>
>>>>>>> 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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