Hi Beth and good to hear from you.  
We took the trip on blue ridge parkway a couple of years ago.  Beautiful !!
This is my favorite time of the year in Florida.  Leaves are falling and I say 
it is raining leaves.  
We usually have rain and cooler temps this time of year but you never know. 
Happy thanksgiving to you and all.  
I am still in 1 15 mg ponatinib daily. Seem to be doing good on it. 
Looking forward to Christmas.  Going to spend some time with my baby girl.  
She's 47 but she's still my baby!!!
I hope everyone is good.  Check in everyone.  
❤️😇💕🎶

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 29, 2015, at 6:31 PM, bkbarney via CMLHope <[email protected]> 
> 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]>
> To: cmlhope <[email protected]>
> 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]> 
> 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]>
> To: cmlhope <[email protected]>
> 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]> 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. 
>>> -- 
>>> -- 
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