Jeanie, I'm so sorry for your loss. You will always have them in your heart. I lost my parent a long time ago but I miss them as if it were yesterday. When I read your message, I looked at their photo and asked them to take good care of your dad.
L'chaim, Sherri On Mon, Jan 12, 2015 at 1:14 PM, 'Icandoallttc' via CMLHope < cmlhope@googlegroups.com> wrote: > Thank you Greenie > I need that. > Blessings > Jeanie > > Sent from my iPhone > > On Jan 12, 2015, at 1:30 PM, Myvety2k via CMLHope < > cmlhope@googlegroups.com> 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, > cmlhope@googlegroups.com writes: > > Thanks Susan. > I'm hanging in there!!! > Blessings. > Jeanie[image: 🐟][image: 🐟][image: 🐟] > > Sent from my iPhone > > On Jan 11, 2015, at 11:17 PM, "'Susan Zimmerman' via CMLHope" < > cmlhope@googlegroups.com> 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 <cmlhope@googlegroups.com> > To: cmlhope <cmlhope@googlegroups.com> > 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 < > cmlhope@googlegroups.com> 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 <wa2...@gmail.com> 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 < > cmlhope@googlegroups.com> 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 <swanson.sherri...@gmail.com> >> 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 <wa2...@gmail.com> >> 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 < >>> cmlhope@googlegroups.com> 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, >>>> swanson.sherri...@gmail.com 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 <wa2...@gmail.com> >>>> 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 < >>>>> swanson.sherri...@gmail.com> 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 <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 >>>>>>>>>>> >>>>>>>>>>> -- >>>>>>>>>>> -- >>>>>>>>>>> [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 CMLHope@googlegroups.com >>>>>>>>>>> To unsubscribe from this group, send email to >>>>>>>>>>> cmlhope-unsubscr...@googlegroups.com >>>>>>>>>>> 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 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are subscribed to the Google Groups >> "CMLHope" group. >> To unsubscribe from this group and stop receiving emails from it, send an >> email to cmlhope+unsubscr...@googlegroups.com. >> 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 CMLHope@googlegroups.com > To unsubscribe from this group, send email to > cmlhope-unsubscr...@googlegroups.com > 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 cmlhope+unsubscr...@googlegroups.com. > 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 CMLHope@googlegroups.com > To unsubscribe from this group, send email to > cmlhope-unsubscr...@googlegroups.com > 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 cmlhope+unsubscr...@googlegroups.com. > 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 CMLHope@googlegroups.com > To unsubscribe from this group, send email to > cmlhope-unsubscr...@googlegroups.com > 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 cmlhope+unsubscr...@googlegroups.com. > 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 CMLHope@googlegroups.com > To unsubscribe from this group, send email to > cmlhope-unsubscr...@googlegroups.com > 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 cmlhope+unsubscr...@googlegroups.com. > 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 CMLHope@googlegroups.com > To unsubscribe from this group, send email to > cmlhope-unsubscr...@googlegroups.com > 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 cmlhope+unsubscr...@googlegroups.com. > 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 CMLHope@googlegroups.com > To unsubscribe from this group, send email to > cmlhope-unsubscr...@googlegroups.com > 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 cmlhope+unsubscr...@googlegroups.com. > 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 CMLHope@googlegroups.com > To unsubscribe from this group, send email to > cmlhope-unsubscr...@googlegroups.com > 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 cmlhope+unsubscr...@googlegroups.com. > 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 CMLHope@googlegroups.com To unsubscribe from this group, send email to cmlhope-unsubscr...@googlegroups.com 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 cmlhope+unsubscr...@googlegroups.com. For more options, visit https://groups.google.com/d/optout.
