So good to hear from you Millie. I though something was wrong. What did they do about the bleeding; just stop meds? Watch you stool to check for signs of bleeding. If they are dark or black, check to see what it could be. You are strong and I know you will come through this with flying colors. I had to have blood transfusions while on Tasi so keep a check on that. It can drop your counts too low. Drink Ensure if you have too to keep up your energy and nutrition. My brother-in-law had cancer and he lived for a year on Ensure so I know it works. It's hard to do when you love to eat like I do hehe. I'm good; going ot my PCD on Mon. Keep us informed and blessings, Jeanie<3 In a message dated 5/1/2013 3:57:59 P.M. Eastern Daylight Time, [email protected] writes:
Hi Jeanie....I just got home from the hospital today. Due to taking blood thinners, my levels were way off and I was bleeding internally. I was also very dehydrated and have lost over 20 lbs of weight in the past few weeks. I haven't been eating either as I was so nauseated and having pain in my stomach, etc. I was loosing so much fluid that it was scaring me. At any rate, I was due for a procedure on Tues., but when I went for testing on Monday, my doctor called and told me to go over to the emergency room at the hospital, so that's what I did and they kept me until today. They say the levels are good right now, but they did cut me down, and in some cases, did away with some of my medications. I'm now suppose to go to have the scope done on Mon. of next week, but am waiting for a call to verify that. I'm still very weak, but feeling better in every other way. I just have to work at getting stronger......and I will. They gave me vitamin K shots and also 2 units of Plasma while in the hospital, and also IV. fluid, so I'm good to go now. Just have to get stronger and I'll do that. You take care and stay healthy. I'm still doing well on Tasigna (or hope that am) I see my Onc. the end of this month. He'll run the blood work then and tell me if I'm still in remission. I'll talk to you all soon. Hope that all of my fellow CMLers are doing well. It seems like one of us is always fighting the fight somehow. I know that most of us have issues, but we are still able to fight, and that's good news. Hugs, Millie ----- Original Message ----- From: [email protected]_ (mailto:[email protected]) To: [email protected]_ (mailto:[email protected]) Sent: Wednesday, May 01, 2013 3:28 PM Subject: [CMLHope] Jim and Millie and all Thanks Jim for all your support. You there Millie? Just wondering how you are? Jeanie<3 In a message dated 4/30/2013 5:51:30 P.M. Eastern Daylight Time, [email protected]_ (mailto:[email protected]) writes: Hi Peg, I also have the cramping, I'm on Gleevec since it was approved in the USA. I was dxed 4/12,1997. I've experienced many of the known side effects. Eye bleeds, cramping in the legs(upper and lower), feet insteps, forearm, hands, I inquired abut muscle relaxers and Onc. gave me some and it didn't help. The legs and hands respond to hot water, the feet don't! My Pcr test is negative that's a plus that we are so happy for. I'm 68 and the side effects aren't bad enough for me to want to venture into the unknown with a different med. that may not even work for me or the side effects are worse than what I currently have. 18s to all my fellow warriors we must never give up research is making head way as never before who knows what they ill come up with next. some day the big "C' will stand for CURE. I pray every day for that AMEN. God Bless us all. Jim Rodeghier --- On Mon, 4/29/13, peg <[email protected]> wrote: From: peg <[email protected]> Subject: [CMLHope] TKI Spasticity To: [email protected] Date: Monday, April 29, 2013, 10:57 AM Hi all, Sorry it takes me a while to catch up these days. Just read Beth's post on spasticity and wanted to share. There are many folks having muscle related problems with all of the CML drugs. The spectrum ranges from the seriousness of myopathy to simple muscles spasms, with everything in between. Gleevec gave me myopathy. Because I was not a good candidate for Tasigna we moved directly to Sprycel back in 2010...before it was front line approved. For me Sprycel causes such severe muscle contractions that I have developed contractures in several places in my body. At first we just thought it was my arthritis causing limited range of motion, but then several months ago finally realized what had happened. I am in physical therapy now to improve my range of motion. We have also had to radically adjust the Sprycel dosing...not just for the contractures, but also the crippling fatigue, mind numbing brain fog, bone pain and Sprycel induced depression. The only time I feel really good now is on Sprycel "holidays". After many dose reductions here's where I am at...in 2011 we started dropping the daily dose....first 70mg then 50mg. We also tried 50mg every other day, then 20mg daily. All of these changes still held me at PCRU. But even at 20mg daily it was difficult to have a normal life. There was also a concern from the specialist I see who helped develop Spycel. He believes that from what he is seeing, the way Sprycel affects the CML is more related to the size of each dose, rather than the frequency, so he had a concern that 20mg a day would not hold the PCRU. Although I have heard of cases where it is. We also noted that for me a "washout" of a few days off Sprycel helped me recover from the side effects. Without that washout, the affects would load up. So this was when we started experimenting last Oct with twice weekly dosing. Unfortunately 70mg still proved to high a single dose for me, so we did a brief five months at 50mg every third day. However, the side effects from each dose are still so severe, it is like sticking my finger in a light socket, everything in my body clenches. This starts two hours after each dose and lasts for almost 24 hours. Every third day dosing was just craziness, since I couldn't plan around that well...and found myself dragging myself painfully through life every third day...hating every minute of it. We finally realized that the only way I could have any quality of life was to drop back to a twice a week dose and take those days out of my schedule...just plan on being down for the count on those two same days each week. So we are now at 50mg two days a week. I take a muscle relaxer with each dose, and again at 12 hours if I need it. This really helps with the muscle spasms. I lose two days out of my week, but the quality of the other five is much better now. We are monitoring my PCR monthly to see if the PCRU still holds. I can't recommend experimenting for everyone...it carries a risk of becoming resistant. However, the quality of my life had become so bad that the cost of saving my life was no longer worth it. Life in the absence of any quality is simply not a life. For those of you who's reactions to TKI are not as dramatic as mine, adding a muscle relaxer to each dose, even daily, might bring the muscle spasm relief you need. My drug of choice is Robaxin...but to each man his own! Warmest regards to everyone! Peg -- -- [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. 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