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In March 2007 I began participation in the Lenalidomide ( also known as Revlimid) Drug Trial as a patient at the Western General Hospital in Edinburgh. I made 5 cycles, couldn't make the 6th and then came off the trial. April 2008 and I then went on to melphalan, thalidomide and prednisolone. I'm now off that as it was of no further benefit. This blog charts this new post lenalidomide/revlimid journey.
2 comments:
I'm so glad I've discovered your blog. My husband was diagnosed with indolent MM about 5 years ago. He is mildly anaemic and has paraprotein fluctuating around 30/40 level. His white cell count is decreasing and he has lots of infections. We have been unable to glean any information from the hospital as to likely progression, and even the infections which have required hospitalisation on 2 occassions have been dismissed as irrelevant. I know every patient is different but it has been so helpful to have your account to read.
My best wishes to you and your family. I love St Ives too, went there in October- brilliant sunshine.
Hi i have just been diagnosed with MM and am scared. your blog is a ray of light i have nt started treatment yet but they are talking about thalidomide and steroids, i cant understand why there are all different treatments but am sure through time i will figure it out.
thanks for your list it shows that there is still time to do things
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