Hi Millie, I have been on vacation, a cruise and  staying with my baby 
daughter.  We had fun.
I too am having problems with my stomach hurting  and bloated and bad pain 
in right side under the ribs.  I knew you aren't  suppose to take those 
proton pump meds as they interfere with the digestion of  the CML drugs.  They 
tried to give that to me in the hospital and I told  them it said right on 
the Sprycel package not to take them.  You can take  tums or other types of 
antiacids 2 hours before or 2 hours after the meds but no  proton pump like 
Proselac, Zantac and others.
 
My doctor has ordered the test where they put  the tube down you throat.  
Pleas let me know how the test was done and how  it was tolerated.
I need to find a good GI doctor.
 
I take Ambian for sleep; it's the only one that  works for me; have you 
tried it.  I can't sleep without it even though I've  tried many times.  
 
Good to hear from you and Beth.
Blessings to both,
Jeanie<3 CML Warrior for almost 10  years.
Gleeved 4-5 years Quit working
Tasigna 8 months Quit working
Sprycel 4 years In remission after 3 months on  Sprycel.  Taking 50 mgs 
daily
 
 
In a message dated 4/24/2013 11:38:12 P.M. Eastern Daylight Time,  
[email protected] writes:

Hi  Beth,  I am so glad we've connected once again.  I do think of you  
often and wonder how you are doing.  I went to a GI doctor today and they  are 
doing a scope (down the throat) on Tues.  Meanwhile, I have to get a  CAT 
Scan and blood work done, etc. etc.  This is a new doctor, but he  seems nice. 
 I was seeing another one for Colonoscopies in Allentown,  which is about 
50 miles from here, and since we are getting older, it's not a  good thing to 
travel this far.  I could drive down, but my Husband is in  his 80's and 
gets confused so only drives locally now.  I didn't want to  change doctors, 
but decided that having one 20 minutes away would work better  for me.  I'm 
having such a problem with nausea, blotting, pain after  eating, etc. etc. so 
must do something to find the problem.  Wish me  luck.  It gets hard to 
deal with all of my problems at times, but I just  take them one at a time and 
try to get past it.  You will always be on my  mind, and in my prayers.  
Feel free to write anytime.  If you want  to get in touch via my e-mail 
address.  It is [email protected]_ (mailto:[email protected]) .  You can always talk 
to me 
 about anything.  It does help.  I also admire Judi.  She has a  lot of 
issues, but keeps on going.
Many  hugs,
Millie

----- Original Message ----- 
From:  [email protected]_ (mailto:[email protected])  
To: [email protected]_ (mailto:[email protected])  
Sent: Tuesday, April 23, 2013 7:47  PM
Subject: Re: [CMLHope] Skip  Duffie


Thank you so much for your post Millie.  I am sorry that you are up at 4 
a.m......and as usual, am so inspired by  your attitude. but also your 
resiliency. Judy walking the grand canyon still  inspires me, and her continued 
capacity to walk like that for this years  fundraiser. Everyone's experience 
with CML is different, but finding words,  or experiences that mirror your 
own..I find it comforting. 
 
spring will come...!!! 
 
Write soon. take care, Beth



-----Original  Message-----
From: C.M. Houtz <[email protected]>
To: cmlhope  <[email protected]>
Sent: Sat, Apr 20, 2013 3:05  am
Subject: Re: [CMLHope] Skip Duffie


 
Hi  Beth,
 
I  know  you struggle with your meds and that you have had so many side  
effects.  I'm so sorry that this new drug has caused you such  problems.  I am 
not sleeping well tonight, so decided to get up and do  some things on here 
that I've been meaning to do.  I wanted to print  out some patterns to hand 
stitch.  I haven't been feeling well, and am  seeing an Gastrointerologist 
(spelling is wrong), but at 4:00 A.M., what do  you expect :>).  When I came 
off of two months of Home Care....due  to a hip problem, I thought I'd be 
feeling better, but started with  nausea.  It's not every day, but enough 
that I am having trouble  dealing with it.  I also was in severe pain due to my 
 polymyalgia.  After years on Tasigna and dealing with constipation, I'm  
dealing with the opposite most days.  I had a sinus infection and my  doctor 
put me on an antibiotic and that got rid of it, but the stomach  problems 
have stayed with me.  I also was taking meds for acid reflux  and now, after a 
year on the stuff, Express Script has told me that it can  interfere with 
the Tasigna, so had to stop that.  My pain and  whatever has made me so weak 
that it's almost impossible for me to get up  from a chair without help.  
I'm not sure if the Arthritis has caused  this, or if it's a medication 
problem, but I can understand where you are  coming from.  I'm anxious to see 
my 
Oncologist next month and,  hopefully, I'll still be in remission.  We all 
have issues, but must  stay strong and fight it as hard as we can.  I know 
that it sounds  easy, and know that it isn't, but just remember that we're all 
here to help  one another, and you all have helped  me so much.  People look 
at  you and think...you look well, and don't realize how difficult this CML 
is  to fight.  I look in the mirror and wonder who this old lady is as my  
hair if all but gone and I no longer have eye lashes, but I try to laugh and 
 just put my wig on and go out whenever I can do it.  Lately, that  hasn't 
been to often.  The weather is getting better so one of these  days, I'm 
going to go out with my jazzy chair and enjoy the warmer  days.  I fill in the 
rest of my time with needle work.  I'm doing  a lot of embroidery right now, 
and quilting.  I have two quilt tops to  finish up and then will have 
someone get them ready for me to quilt.  I  try to fill my head with things 
that 
I love to do, and that seems to  help.  I wish there was more that I could 
say and do to help you.   I will keep you in my thoughts and prayers and hope 
that you will be in  remission soon.  Take care.......Hugs,  Millie

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