I am not the sharpest knife in the drawer. (I can hear you all saying, "Thanks for that, Captain Obvious! "). When it comes to myeloma, my dullness becomes even more pronounced. Many people in my situation overheat their keyboards googling information, and wear out their doctors by asking questions. For me, that just doesn't work. Almost every time I have researched, attended a conference or read the latest newsletter from Myeloma Canada, I have found myself in the dark places of this disease. The places where you learn the incredible complexity of blood and bone marrow cancer. The places where you see the catastrophic damage both the disease and the treatments do to your body. Dark places that end in death. You might be picturing an ostrich, bearing a striking resemblance to me, with his head firmly planted in the sand. You would not be completely wrong, but I think of it more as learning things on a "need to know" basis. The confirmation came this week of an...
Brian’s diagnosis of Multiple Myeloma was in May 2018. The initial treatment was a stem cell transplant. After 30 months there was a relapse, followed by chemo, another relapse, new chemo and yet another relapse. In January 2024, the 4th treatment began. Brian currently gets weekly injections of an immunotherapy drug. Sometimes we keep the faith and sometimes we need family and friends around us to keep the faith for us. This blog is about enabling us all to be kept in the faith.