Last visit to my haemo in September I wasn’t able to get any results. It seems Medicare are tightening their belt and decided that they will only pay for the leukaemia marker test every three months. I’d seen a different doctor the time before and he’d ordered the test a month early, so it wasn’t processed.
End result: my September consultation was a bit of a waste of time for all concerned, although it was good to have a chat with my haemo and find out what’s happening in the world of CML.
The following week I dutifully trotted off to pathology to have the test redone and settled back for a month’s wait for the result.
Yesterday afternoon the result finally came in and it was FANTASTIC news. It seems after dawdling along for a while the drugs have well and truly kicked in and my leukaemia levels are now very, very low. It’s still there – that’s the nature of this drug treatment. The CML rarely goes away completely, but when things are working as they should, the disease is controlled at a very low level. Which I’ve finally reached after about 3 1/2 years.
So I’m a happy little vegemite. Probably lucky for my doctor that I wasn’t in his office when I got the news or I might have jumped up and planted one on him.
Now to decide how to celebrate …
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Congratulations, That is the best news ever
Thanks Emma. I’m pretty excited!