We meet with Dr Sheehan next week just before our vacation; our “run to the south.” I am worried. We got the blood test “numbers” back today and they had, again, increased. And this is despite the chemotherapy intervention. One side of me (the rational one) wants to look at the increase as being statistically insignificant – an increase, yes, but not a big one. Then there is the cough…
We are monitoring a strange cough that Sabine has. We have discussed it with at the clinic and we are watching and seeing whether or not another chest x-ray is warranted. No temp, no tell-tale mucus signs, but a persistent cough. I am watchful for pneumonia that stalks many multiple myeloma patients.
The other side of me says, “whoa!” We’re not going anywhere until the cough gets under control. And I don’t like an increase in any of the cancer markers – even those deemed “statistically insignificant.” I hunker down. I internally shout, “Circle the wagons,” and diligently watch for any kind of trouble.
This is really the “ups and downs” of cancer. You got it. You get it under control. You watch. You wait. And then you’re back in the fight again.
Stay tuned until Wednesday when we have our scheduled appointment with Dr Sheehan.
P.S. For those of you who are number-watchers the free lambda light chains have gone from 19 in Nov., 2009 six months after the stem-cell transplant and this was still holding into last May. Then last August the numbers jumped to 42, September was 64, and 133 in November when we started the Revlimid/Dexamethasone intervention. Within 4 weeks it has reduced the numbers to 71. Now, in her second 28-day cycle of chemo the numbers have now increased to 106 (which was the lowest Sabine got in her initial Velcade chemotherapy.
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