Hi Sherry.,

One thing for sure in the middle of US is "The weather will change). Today 
was a balmy 36 degrees and a wind chill that was in the mid 20's. The sun 
was shining brightly so I walked to the community mail station. The worst 
part of living in this part of the US is that when we have the Artic Blast 
is a temperature drop of 40-50 degree drop and there is no way to prepare 
for it.

Richard H. 
On Saturday, January 10, 2015 at 3:31:32 AM UTC-6, Mosey 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] 
> <javascript:>> 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] <javascript:>> 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] <javascript:> 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] 
> <javascript:>> 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] 
> <javascript:>> 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. 
>
> 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] 
> <javascript:>> 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] 
> <javascript:>> 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] 
> <javascript:>> 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] 
> <javascript:>> 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. 
>
> 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] <javascript:>> 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] <javascript:>> 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] <javascript:>>
> To: cmlhope <[email protected] <javascript:>>
> 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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