As of now, I'm on 10 MG Revlimid and 25 mg Prednisone. For those of you in the know, 10 mg is still a therapeutic does of Revlimid and Dr. V admits that he is being somewhat aggressive with my treatment. He did agree to reduce it from 15 MG when I complained of some digestion issues. The Prednisone is a welcome alternative to the more commonly used steroid, Dexamethasone. It is much easier to take as it does not have the wired/tired extremes associated with Dex. It also doesn't make me into a raging manic (which Dex does) and it doesn't seem to affect my appetite. Aside from the digestion problems, which have not dissipated with the lowered dose, the only real side effects I am aware of are occasional cramps in my hands and feet. But they are infrequent and mostly tolerable. All in all, I'm very pleased with my state of affairs.
This week, the Wall St. Journal printed a very well written article on Myeloma. Accompanying the article is a video with most of the same info that I just stumbled across from 2013. I'm providing links to both here.
In the video, Dr. Brian Durie, whom you may recall was the 'tie breaker" when I was trying to decide on whether or not to have a stem cell transplant, says two interesting things:
- 1) Average life expectancy is now up to 7 years (from diagnosis, I presume) . As for me, I was diagnosed in July 2006, so I'm approaching 10 years.
- 2) He expressed optimism that a "cure" is actually achievable. The "C" word is being bandied about now by the two research based foundations that focus on the disease, and by some of those who treat the disease, most notably the ones currently or formerly associated with the UAMS Myeloma Institute who promote a Total Therapy program which I describe as a "kitchen sink" approach intended to wipe out the disease in their patients.
My transplant was on February 7, 2012, so my 4th birthday is coming up in less than a month. I feel good and extremely grateful to be where I am