My week off of being a human pin cushion ends tomorrow; though the needle sticks in the arm really hasn't bothered me; back to the clinic for a blood test tomorrow. I was reviewing my blood tests from cycle 2 and so far the WBC has climbed every time I had my blood tested in cycle 2, so I do have some high expectations for tomorrow's blood test. I expect my platelets to be down since two of the medications I am on reduce platelet production. I believe there will be 4 vials of blood drawn tomorrow, 4 different tests.
- CBC
- INR - Blood thinner
- Chem - Kidney, Liver...functions
- Free Light Chain - Checks the lamba and kappa light chains, the original test was really out of whack, hoping for better numbers.
Anyone every complain about peeing in a cup? Try a 24 hour urine test, when you pee in a jug for 24 hours, and the jug has to be kept cold. Not only do I get to go to the refrigerator for a drink, but to expel the drink also. I get to start this test tomorrow. I did one of these a few months back, which led to my diagnosis. The test showed high monoclonal protiens, the test that starts tomorrow will show how well the first two cycles of treatments are going.
Well it was a pretty good weekend despite the weather. Down to just one medication this week, just the steroid.
Sunday, April 17, 2011
Wednesday, April 13, 2011
April 2011 - Induction - Cycle 2 - Day 17
Nice day today, the weather was good and was able to get out for a walk. The last couple days have been pretty good. Though Jane is suffering from a toothache and will have a root canal done tomorrow (Thursday), she is having a tougher time than me right now. She is in a lot of pain and on antibiotics, which gave her the chills in the middle of the night last night.
Had a call today from the Patient Coordinator from the Hospital that will be doing the Stem Cell Transplant (SCT), and have some updated information. I will complete Cycle 4 of my treatments in the Middle of June. The Patient Coordinator states the SCT usually occurs 6-8 weeks after the last treatment cycle. So, here is a tentative schedule on how things will occur. After cycle 4 is complete, it will be test time. Another bone marrow aspiration, heart test, lung test, blood tests, skeletal survery...and any other tests the insurance company requires. All of these tests can be done at the local hospital. Then around the beginning of July I will meet with the involved parties at the hospital. At this time the hospital will also submit all the necessary paperwork to the insurance company for approval. This sets the SCT process to start around the middle to end of July.
Below is some additional information from the Patient Coordinator:
- While in the hospital I will get to walk the halls 4 times a day
- Most people are only in the hospital two and half weeks
- Only one day / dose of high chemo, possibly as out patient then check into the hospital the next day to start the proces.
- I can bring my computer and the hospital has wireless Internet access.
I have had a lot of offers of blood donations in my name (thanks for all the offers), so I brought this up with the patient coordinator, and only platelets can be directed to a patient. Platelets only have a 5 day shelf life and would have to be donated directly at the hospital. There is some type of virus check against the platelets and if the donator has had a virus that I have not, then they can't be used (I think I understood this right).
Had a call today from the Patient Coordinator from the Hospital that will be doing the Stem Cell Transplant (SCT), and have some updated information. I will complete Cycle 4 of my treatments in the Middle of June. The Patient Coordinator states the SCT usually occurs 6-8 weeks after the last treatment cycle. So, here is a tentative schedule on how things will occur. After cycle 4 is complete, it will be test time. Another bone marrow aspiration, heart test, lung test, blood tests, skeletal survery...and any other tests the insurance company requires. All of these tests can be done at the local hospital. Then around the beginning of July I will meet with the involved parties at the hospital. At this time the hospital will also submit all the necessary paperwork to the insurance company for approval. This sets the SCT process to start around the middle to end of July.
Below is some additional information from the Patient Coordinator:
- While in the hospital I will get to walk the halls 4 times a day
- Most people are only in the hospital two and half weeks
- Only one day / dose of high chemo, possibly as out patient then check into the hospital the next day to start the proces.
- I can bring my computer and the hospital has wireless Internet access.
I have had a lot of offers of blood donations in my name (thanks for all the offers), so I brought this up with the patient coordinator, and only platelets can be directed to a patient. Platelets only have a 5 day shelf life and would have to be donated directly at the hospital. There is some type of virus check against the platelets and if the donator has had a virus that I have not, then they can't be used (I think I understood this right).
Sunday, April 10, 2011
April 2011 - Nice Weekend
Starting to recovery from my down days of last week. The good weather helps with this and being able to be outside. Looking forward to hopefully two good weeks before Cycle 3. No scheduled doctors appointments or blood tests this week, first week I have had off in about 6 weeks I think.
A rash has started on my arms, not sure if this is caused by the medications or the heat (unseasonably warm this weekend) or something else...the rash seems to come and go.
A rash has started on my arms, not sure if this is caused by the medications or the heat (unseasonably warm this weekend) or something else...the rash seems to come and go.
Thursday, April 7, 2011
April 2011 - Induction - Cycle 2 - Day 11
Back to the clinic today for my last injection in cycle 2. CBC counts so far are holding strong for this cycle.
WBC - 3.2 - Up a little from Monday
Grans - 1.9 - Down a little from Monday
Platelets - 102 - Down from Momday but expected.
I had a lot more energy during cycle 2 treatments, though both the doctor and nurses told me I would probably have less energy. Energy levels were pretty good up until yesterday and today, though I think the steroids might be partially the cause for energy loss.
Now my body gets two weeks to rest and rebuild before cycle 3 begins. As each cycle completes I am one step closer to the stem cell transplant; which the more I read about the less I look forward to it.
WBC - 3.2 - Up a little from Monday
Grans - 1.9 - Down a little from Monday
Platelets - 102 - Down from Momday but expected.
I had a lot more energy during cycle 2 treatments, though both the doctor and nurses told me I would probably have less energy. Energy levels were pretty good up until yesterday and today, though I think the steroids might be partially the cause for energy loss.
Now my body gets two weeks to rest and rebuild before cycle 3 begins. As each cycle completes I am one step closer to the stem cell transplant; which the more I read about the less I look forward to it.
Monday, April 4, 2011
April 2011 - Induction - Cycle 2 - Day 8
The weather her yesterday was nice and spring like, got out for a walk yesterday and today. Not 100% sure the walks are having a positive impact on my treatments, but at this point in time I am going to say they are helping my counts. I also switched to drinking a liter of Smartwater a day, which is plain water enhanced with electrolytes. I started this last week and maybe that has an impact on my counts also? I spend a lot of time on the Internet searching and reading and if I find something that seems simple to try, that might help, I run it past the nurses or doctor and try it out. Sometimes I think the nurses and doctors think I am crazy, but nobody cares more about me than me. Spending time on the internet can be a very scary, sometimes it can play be a roller coaster on ones emotions, I am surprised Jane has not taken my computer away yet.
Back at the clinic today for another treatment and now what I wrote above might make more sense. My CBC test came back pretty good, I was concerned because at this point in cycle 1 my counts really took a dive.
WBC: 2.8 - up from last Thursday
Grans: 2.4 - Wow - best since 2009
Hemoglobin: 12.3- Wow - Best since 2009
Platelets: 120 - Down but expected, the drugs destroy and prevent platelet production. Just hoping the platelets stay above 50 when I am rechecked on Thursday. When the platelets drop below 50 is when extra precautions are required.
My counts might explain my increased energy level today. I actually had good energy today and was not tired at all, though Wednesdays and Thursdays are usually my down days, that is when I am crashing from the steroid. Though Cycle 1 Week 2 I was taking power naps during lunch and before dinner.
Last night I experienced a new side effect, the bottom of my feet swelled up and had an itchy rash from my ankle to the bottom of my foot. I elevated my feet and everything returned to normal. Asked the nurse about this today and she stated it could be a side affect of the drug Revlimid that I am taking and it was nothing to worry about since it cleared up quickly.
Taking the Zantac has also helped my steroid enduced hoasreness, I don't think I sound hoarse at all, though Jane tells me I sound a little hoarse.
Hope you are still awake after reading my wordy entry.
My quote for the day:
"It doesn't matter what you've heard
Impossible is not a word
Its just a reason for someone not to try".
This is a lyric from a group by. The name Kutless, song title - What Faith Can Do. It is a very inspirational song, click the link to listen: Kutless - What Faith Can Do. I never let my girls use the word impossible, because I myself never think anything is impossible.
Back at the clinic today for another treatment and now what I wrote above might make more sense. My CBC test came back pretty good, I was concerned because at this point in cycle 1 my counts really took a dive.
WBC: 2.8 - up from last Thursday
Grans: 2.4 - Wow - best since 2009
Hemoglobin: 12.3- Wow - Best since 2009
Platelets: 120 - Down but expected, the drugs destroy and prevent platelet production. Just hoping the platelets stay above 50 when I am rechecked on Thursday. When the platelets drop below 50 is when extra precautions are required.
My counts might explain my increased energy level today. I actually had good energy today and was not tired at all, though Wednesdays and Thursdays are usually my down days, that is when I am crashing from the steroid. Though Cycle 1 Week 2 I was taking power naps during lunch and before dinner.
Last night I experienced a new side effect, the bottom of my feet swelled up and had an itchy rash from my ankle to the bottom of my foot. I elevated my feet and everything returned to normal. Asked the nurse about this today and she stated it could be a side affect of the drug Revlimid that I am taking and it was nothing to worry about since it cleared up quickly.
Taking the Zantac has also helped my steroid enduced hoasreness, I don't think I sound hoarse at all, though Jane tells me I sound a little hoarse.
Hope you are still awake after reading my wordy entry.
My quote for the day:
"It doesn't matter what you've heard
Impossible is not a word
Its just a reason for someone not to try".
This is a lyric from a group by. The name Kutless, song title - What Faith Can Do. It is a very inspirational song, click the link to listen: Kutless - What Faith Can Do. I never let my girls use the word impossible, because I myself never think anything is impossible.
Thursday, March 31, 2011
March 2011 - Induction - Cycle 2 - Day 4
Back to the clinic today for the second treatment in cycle 2. Mondays treatment had a little impact on my CBC numbers, but nothing too bad. WBC actually went up to 2.6 (Grans down to 1.5), platelets down to 163 (still in the normal range, though I expect the platelets will continue to drop through next week due to the treatments). If the grans number goes below 1.0, then I have to be extra careful about what I eat (no fresh fruit, everything must be thoroughly cooked...).
Monday and Tuesday were pretty good days, feeling the affects of the medications yesterday and today; feeling a little tired; but not too bad. Actually got a walk in on Monday and Tuesday, trying to decide if I have the energy for a walk tonight.
Taking Zantac in the morning of Mon, Tue and Wed really helped the heart burn / acid reflux from the steroids.
Monday and Tuesday were pretty good days, feeling the affects of the medications yesterday and today; feeling a little tired; but not too bad. Actually got a walk in on Monday and Tuesday, trying to decide if I have the energy for a walk tonight.
Taking Zantac in the morning of Mon, Tue and Wed really helped the heart burn / acid reflux from the steroids.
Monday, March 28, 2011
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