Jeanie, thanks for your respond. Have a Happy Turkey day. greenie In a message dated 11/25/2015 3:50:48 P.M. Eastern Standard Time, [email protected] writes:
Happy Thanksgiving all Greenie I have the same heart problem and high Creatine. I just had my visit with PCD and he said the skipped beat was what was causing the pounding in my right side at night. I don't notice it unless I'm trying to rest. BP was a little high. Sorry about Grace. I hope she is doing better. Turkey is defrosting and son will cook dinner tomorrow. Eat drink and be happy all ❤️😇💋🎼 My Motto: Faith and Pills Jeanie 🐟🐟18,s Dx 1/2004. CML Leukemia Started Gleevec 2/2004 Started Tasigna 9/2009 Started Sprycel 11/2009 Started Ponatinib January 2015 Dr Balducci Moffitt Cancer Center On Nov 25, 2015, at 2:30 PM, Myvety2k via CMLHope <[email protected]_ (mailto:[email protected]) > wrote: Hi Beth, Give me a call when you arrive in Fort Myers. Cell phone is (219)973-8717. Had my 4 month check up with my internist yesterday everything O. K.. Blood O. K. but my creatinine was high again 1.57. It's been between 1.2 and 1.6 going back to 1997 way before I started Gleevec in the first week in Jan. 2000. Grace had a mini stroke last month and doing O.K. which kicked my heart into over drive and my skip a beat started up. Had a stress test last week and passed that without a problem but they did put me on a 21 day monitor which is more fun then you can imagine. Other wise I'm doing just fine. You all have a nice Thanksgiving, Greenie Fort Myers, FL. Club member #48 In a message dated 11/25/2015 2:13:53 P.M. Eastern Standard Time, [email protected]_ (mailto:[email protected]) writes: thanks Richard.... And happy Thanksgiving Day to everyone tomorrow.. I hope everyone here finds themselves in a place that is peaceful and lifegiving this holiday. I wish you all a feel good kind of day in every way.... off sprycel for 2.5 weeks thus far.. initially felt a lot better..but last couple of days..autoimmune...whatever is creeping in with that deep fatigue in my muscles etc....doing detox..thanks for the advice all..I am going to take some supplements I cannot take with sprycel in the hopes of cleaning and calming my system... will keep you all posted..thinking of each and everyone here.... group hug. Beth. -----Original Message----- From: Richard H <[email protected]_ (mailto:[email protected]) > To: CMLHope <[email protected]_ (mailto:[email protected]) > Sent: Thu, Nov 19, 2015 10:47 pm Subject: Re: [CMLHope] Test Day great news that you are getting a breather from the meds. I hope your counts stay low enough you get a few MONTHS instead of weeks. We are praying for that. Richard H. On Thursday, November 19, 2015 at 7:27:26 PM UTC-6, Beth wrote: Dear Susan, Concerned to hear your news...I know you wanted to hear better..It's so hard when we hit an unexpected bump in the road....when are you coming back to see your doc? I am in town except for Dec. 12-19th...would love to meet you this time. And Greenie....will be in Fort Myers so hopefully can see you and your sweetie..and my other cml buddies who live down south...chemo brain...forgive me!. I have gone off everything...my BCR was good enough to take some time to cleanse my body...was just too sick....will go back on in a few weeks...enjoying GRAPEFRUIT!!! for a couple of weeks!. Love to all and a happy and healthy Thanksgiving to each and everyone of you... 18's and love, Beth -----Original Message----- From: 'Susan Zimmerman' via CMLHope <[email protected]_ (about:blank) > To: cmlhope <[email protected]_ (about:blank) > Sent: Fri, Oct 30, 2015 8:26 am Subject: Re: [CMLHope] Test Day Hi all, My bcr/abl results were not as great as I hoped. Last time I was .012.....almost to zero. This time I expected to be zero, but alas I am up to .348. So doc wants me to go to 300 mg bosulif, instead of 100 mg. I am compromising and will go to 200 so I don't have to stay in the bathroom all day. I was ready to get a local test next time and forego going to Chicago every 3 months. Now she wants to see me in one month after I up the dose. Ugh! So thankful I do have a wonderful doc even if I do decide myself on my dosage. She does not put me down about it, and supports me in every way. Beth, keeping my fingers crossed for you and saying a prayer. Marty, you are so loved and hope your kidney stuff is getting better. Your pics were beautiful. 18's and blessings, Susan Z -----Original Message----- From: Marty Gartenberg <[email protected]_ (about:blank) > To: cmlhope <[email protected]_ (about:blank) > Sent: Thu, Oct 29, 2015 10:11 pm Subject: Re: [CMLHope] Test Day Yes since everything has been going on I had leave my home in PA empty for nearly two years, but let me tell you something about that crisp clean air and simply beautiful colors of all of the trees that you can see for miles. An example is route 97 which separates upstate NY from PA with the Delaware river in between them. Route 97 goes from Port Jervis all the way down to past Hancock NY, and is considered the most scenic road it the United States. Right near Port Jervis there is route 97 winding like a snake on the edge of the road and is about 1,000 feet above the Delaware River. I have driven in that area and I wouldn't ever drive on it in the snow or at night. If by chance your ever there and I am in PA it is only right across the Robeling bridge which is actually a one lane wooden bridge only allowing one way of traffic then once it stops then the other way. I am wishing you well with your results. Don't forget to let everyone know. 18's, Marty On Thu, Oct 29, 2015 at 6:31 PM, bkbarney via CMLHope <[email protected]_ (about:blank) > wrote: Hi all, Just saying hi! Wanted you all to know that I am thinking of you and sending everyone a big hug and happy fall wishes... I know some of you southern folks..will enjoy your 90 degree Florida temperatures coming down...but us up north are enjoying the beauty of fall..it's cold today, but should be back up in the 60's by Sunday....Indian summer.....I just love it... did BCR on Monday..waiting for results..then will decide plan for next few months... love, hugs and 18's to all, Beth -----Original Message----- From: 'Icandoallttc' via CMLHope <[email protected]_ (about:blank) > To: cmlhope <[email protected]_ (about:blank) > Sent: Sun, Oct 11, 2015 1:07 pm Subject: Re: [CMLHope] Test Day Hi Beth I can never go off the meds either. My counts will shoot up fast. Good luck ❤️ My Motto: Faith and Pills Jeanie 🐟🐟18,s Dx 1/2004. CML Leukemia Started Gleevec 2/2004 Started Tasigna 9/2009 Started Sprycel 11/2009 Started Ponatinib January 2015 Dr Balducci Moffitt Cancer Center On Oct 11, 2015, at 1:43 AM, bkbarney via CMLHope <[email protected]_ (about:blank) > wrote: Dear Jeannie, Richard, Susan, Marty, et al...thanks very much for responding to my question. I am scared, but want to try something to help myself. We will see what Dr.Druker has to say. In the mean time, what I do know, having been off of sprycel for months at a time to deal with major surgeries several times, is that I always come out of remission, and quickly. I don't hold without the sprycel. Usually the cells are showing at very low numbers, but it means that without the agent that keeps them in check, cancer grows. I wish this were not so. And I know it's not for some lucky folks. Maybe with time, this will change for me. For now I am developing a plan..will keep you all posted. love and 18's Beth -----Original Message----- From: Marty Gartenberg <[email protected]_ (about:blank) > To: cmlhope <[email protected]_ (about:blank) > Sent: Thu, Oct 8, 2015 5:56 am Subject: Re: [CMLHope] Test Day Hi Jeannie, Beth, Richard as well as everyone on this site, I have a friend (not had a friend, and still have this friend) who had CML a little while after I had my transplant. At the time there were no TKI's but there were only two things available. One was a bone marrow transplant which was in it's infancy at the time and the other was Alpha interferon but on an early study basis which actually was a blind study. Depending on if those in this study would be receiving this Alpha Interferon or a placebo. Even before my friend I had to chose the Interferon or the placebo in this blind study. I spoke with a lot of oncologists about what to do. However there were no concise answers because on one hand there was something that was still in a blind study and who would know if that would even be given to this patient or would the BMT be the way to go? However, since there were no matching donors, but one, his brother who refused, and I could never understand that, but since there were no other choices he had no other choice but to try that blind study. Well he was lucky enough to be accepted. And I have to tell you that he really suffered some really bad side effects for years afterwards. Eventually they were unable to detect any more CML, but he still refused to go off of the Alpha Interferon and I suppose this was a crutch in his life so he still remained on it for many years. So I guess that he finally decided to go off of it. Once that happened his life took a dramatic turn. No more side effects and no more CML, and he is still alive and doing remarkably well today. As far as me, well my only choice was the BMT because of two reasons. Since my white blood counts were at the time over 486,000 and doubtful that I would survive, but basically the same thing with the BMT but at least I had my sister as a donor who just happened to be a perfect HLA match. So I tried the BMT, and it worked. But yet there is still more to this story and some of you might remember Zavie Miller and all three of us used to get together, and called ourselves The Three Musketeers. This was well after Zavie got to know Dr. Druker and he was started on STI-571 which when approved by the FDA turned into Gleevec. So after that we all turned into The Three Musketeers. All of this is ancient history but my point is that whether to go off or continue on the TKI's because you may be actually "cured" of CML but you may still hold the touch of the crutch. So you see that there are different strokes for different people. Fortunately I don't have to make the choice because I already did and believe me I really did suffer, but in the end it was worth it. Now knowing what I would do if my circumstances were different I think that I would be off these TKI's and live my life, and if something happens then you will have to deal with it, and you will. Remember a crutch is a terrible thing to have. I spend a lot of time trying to help, and your all very special people to me as I am to you. Those are my words of wisdom and please never forget what 18's stands for. It is life yours and mine! 18's Marty i On Thu, Oct 8, 2015 at 12:24 AM, Richard H <[email protected]_ (about:blank) > wrote: Just a quick glimpse about a med break. The end of March when I went to the hospital with Vertigo, The short break I had on medicine did wonders for me. Found some I shouldn't have been taking, stopped some all together. I have felt so much better that I would do it again under total control. Worried? Yes, but I realized afterwards it should have been done earlier. Richard H. On Wednesday, October 7, 2015 at 4:27:30 PM UTC-5, Beth wrote: HI Jeannie and all, ...I am due for BCR abl testing so should get it in the next two weeks, results two weeks later...so I will update when I know more...Had a consult today at the Block Center here in Illinois.People tend to love him or hate him... I really like him. He thinks all my issues are sprycel related. Thinks I should go off everything and have drug holiday to give my autoimmune system a rest....steroids briefly to try and lower cpk so I can move better without such a severe boomerang effect. Back issues are no worse. That's good news from my end....since there have been several of my fellow warriors here who have lost there remissions spontaneously after years of successful treatment with their TKI's. I am scared to go off, unless I have to ...ie. like I did for past surgeries....however, I am thinking about it...perhaps I am just too toxic, and time off would help me to rebuild and repair, and tolerate better the TKI"s when I re-uptake in the future......so I am sitting with this decision..Not sure what I am going to do...except pray, and listen to other's words of wisdom....I know if I ask Dr. Druker, he would be fine with my taking a drug holiday..but I emailed anyway......thoughts from my friends here???? Love and 18;s, Beth -----Original Message----- From: 'Icandoallttc' via CMLHope <[email protected]> To: cmlhope <[email protected]> Sent: Wed, Oct 7, 2015 12:59 pm Subject: Re: [CMLHope] Test Day Hi Beth and how are you?? Would love to have an update on all. Thanks!! ❤️❤️ My Motto: Faith and Pills Jeanie 🐟🐟18,s Dx 1/2004. CML Leukemia Started Gleevec 2/2004 Started Tasigna 9/2009 Started Sprycel 11/2009 Started Ponatinib January 2015 Dr Balducci Moffitt Cancer Center On Oct 7, 2015, at 11:35 AM, bkbarney via CMLHope <[email protected]> wrote: Dear Richard, Sounds like good news all the way around. Hope your counts continue to hold well and the November visit to the onc is a positive one! Your wife is healing well..slow and steady. Thanks for sharing the good news....Keeping you both in my thoughts and prayers. Beth -----Original Message----- From: 'Icandoallttc' via CMLHope <[email protected]> To: cmlhope <[email protected]> Sent: Wed, Oct 7, 2015 9:26 am Subject: Re: [CMLHope] Test Day Hi Richard and happy you are better. I hope your wife will be home soon. Prayers always. My Motto: Faith and Pills Jeanie 🐟🐟18,s Dx 1/2004. CML Leukemia Started Gleevec 2/2004 Started Tasigna 9/2009 Started Sprycel 11/2009 Started Ponatinib January 2015 Dr Balducci Moffitt Cancer Center On Oct 7, 2015, at 12:01 AM, Richard H <[email protected]> wrote: All is good at this house. Saw Kidney Dr. and my tests have improved the last 3 times. Took my CBC and I am keeping my Hem. is holding at 10. I hope it stays there until the end of Nov. when I visit my ONC. My wife is improving, and will see the Dr. Oct. 21st to see if she can start putting weight on the right side. Shoulder seems to be healing nicely. She has the healing knot on the shoulder and is feeding herself with her right hand and is raising the upper arm to almost shoulder height without pain. We are hoping she can come home in Nov. when she can get out of the wheel chair and up and down without help. Due to heart surgery and a pacemaker all I can due is call for help if she has a problem. 18's Richard H. -- -- [CMLHope] A support group of _http://cmlhope.com_ (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/http://groups_ (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]. 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