Eithne01,
The treatment of chronic myeloid leukemia (CML) has changed significantly since the late 1990s, with the development and subsequent approval by the Food and Drug Administration of imatinib (in 2001), the first of a class of medications called tyrosine kinase inhibitors, which target the specific abnormality that causes CML.
Before that time, patients were treated with other therapy, including interferon and bone marrow transplant, and had very poor outcomes.
My doctor told to come for additional test in two weeks. Now my WBC is 1.3 and absolute neutrophils count is 0.04. I was told to stay home on antibiotics. How long it may take for my counts to clime back to safe range. And of course, I'm off gleevec right now. Does it seem that dose of 400mlg is too high for me.
I have been diagnosed with CML since Novmber of 2007. I am still a little confused about some things. and i guess when my WBC's got back to 4.5 I was excited and thought I was all good- In the clear huh... Well in less than a month my WBC's dropped back down to 1.8 and they say that I am good as long as I don't go past 1.5. Ok fine. I don't go back for another month and I already feel like **** and have had pneumonia 2x in the past month.
t know how warfarin is affecting your life style. I have been on warfarin for years and had no concerns about running and bike riding, and using power wood working tools. All of these activities puts one at an increased risk of a cut and bleeding, but I simply take the risk. On the other hand, I don't sky dive, or pick fights ....
My 24 year cousin is my best friend and was just diagnosed with CML and her doctors are very optimistic, but she has so many qiestions she is scared to ask. They are going to put her on the "Miracle Pill" will she lose her hair? Will is hurt her chances of have children? As optimistic as the doctors are, is there any chance that this is a fatal condition?
We are scared should we be?
ginger and glucosamine sulfate will affect coumadin (warfarin) I'm on warfarin and can't take ginger or glucosamine and a host of other supplements.
Seven months ago I had a pulmonary embolism and I am told this may have been the second one.I am taking 7 mg of warfarin a day and my INR is 2.5.I had a liver transplant 10 months ago,and was told my vascular system was not great.Given my overall situation I am concerned about heart attacks and strokes.Do you think I should be taking 75mg of aspirin a day as well as the warfarin?Thanks.
She has been on warfarin and monitors it regularly. She also has past history endometriosis and has always had heavy periods and problems with her periods. She also has uterine fibroids that have been giving her problems, even more so since the warfarin. Between the uterine fibroids and the warfarin, her menses are extremely heavy. She is on iron because she tends to be anemic around her period. Her periods are so heavy that she can go through 4-6 large pads an hour, sometimes more.
I believe it could be a FATAL mistake if you stopped taking the warfarin. Mechanical valves will clot without warfarin and this could cause a heart attack, stroke or heart failure and could cause you to have to have another open heart surgery. PLEASE ,PLEASE talk to your doctor about any changes in the warfarin.
A drastic change in diet can alter INR also, but in my own personal experience, it has usually been other meds that caused me to need to change my warfarin dosage and not my diet. An INR that is consistently out of range is dangerous. Don't worry about maintaining the same dose of warfarin. Worry about maintaining an INR that is consistently within range. Whatever dose of warfarin you have to take to stay in range is okay.
Sometimes aspirin is used in place of the Plavix, and the patient will be on aspirin and warfarin. That type of combo regimen is used when the doctor doesn't think that one drug alone is enough to do the job, and one drug obviously wasn't enough in your case. It seems that your Plavix and warfarin regimen is working, so I'll join you in giving thanks for that.
I have been on Coumadin for 18 years due to Lupus Anticoagulant (Antiphospholipid Syndrome) and several DVTs. In 2005 had MI with occlusion of the LAD artery and had drug stent inserted and I am still on plavix. My doc has debated when to take me off the Plavix safely....what are the recent studies about this dilemma? thanks so much!
I was put on Warfarin immediately and have been on it ever since. Six weeks after starting the Warfarin, I had another TEE and the clots were 90% gone. They tried for seven and a half hours to do the ablation, but were not successful unfortunately. I will be on the Warfarin forever, but that is fine because you can’t eat leafy green veggies when you are on it and I despise green veggies so now I have the best excuse not to eat them.
Given that yesterday he said to not take the warfarin he was changing me from the genertic warfarin and putting me on the brand name of the med coumadin. Said some folks do not tolerate warfarin well but do well on coumadin and i am to start the coumadin today. I would be lying if i didn't say i am a bit gunshy at this point. This med has made me absolutely miserable and today is my 43rd bday...
In three months on Warfarin, I thinned over the top and front of my hair (I am a female aged 70) and also my nails went chalky, plus I couldn't sleep well and felt very off colour. The blood tests which were weekly due to an unstable INR became an ordeal when it took two or three attempts. I took Warfarin (for AFib) for about three and a half months and then refused to take it any longer, saying that I would take my chances on aspirin only.
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