Blood counts are down. Uric acid back to normal. 2 hydrea morning 1 nightly Off sprycel. Mutation test not back. Bma Friday morning. Ct scan next week. Wow! Tired already!!! Still not feeling well. Blessings to all!!!! 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 >>>>>>>>>>>>>>> >>>>>>>>>>>>>>> -- >>>>>>>>>>>>>>> -- >>>>>>>>>>>>>>> [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 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"CMLHope" group. >>> To unsubscribe from this group and stop receiving emails from it, send an >>> 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. >> To unsubscribe from this group and stop receiving emails from it, send an >> 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. > To unsubscribe from this group and stop receiving emails from it, send an > 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. > To unsubscribe from this group and stop receiving emails from it, send an > 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. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. For more options, visit https://groups.google.com/d/optout.

