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Posted by Lana on 4/24/2009, 8:31 pm
154.20.240.70
I have been kind of keeping my fears of a return to my bones on the QT. I have mentioned it on the main board, but until it was offical I didn't want to jinx anything.
The Good: no need for radiation treatment right now. This means I can stay in my home town.
The Bad: medication has changed from Arimidex to Aromasain and from Clodronate daily to Pamidronate monthly (IV infusion). Yea, no more having to wait after taking meds to eat.
The Ugly: there is some progression just not enough to bring out the big guns yet. This was not what I wanted to hear but much better than what I was expecting to hear. Will try the new meds and see what happens.
CT results were not ready today so will get the full report on the 4th of May. In the meantime I am rejoicing in what I have and thanking God for His faithfulness.
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