Two Books I Highly Recommend for MM Patients (or their caregivers)

Yesterday I received (and proceeded to read the whole thing), Living with Multiple Myeloma: Practical advice from a fellow cancer survivor for myeloma patients, their families, and friends. It is a very well written book by a fellow myeloma survivor and medical correspondent, Pat Killingsworth. Continue reading

New Year’s Blessings

And, Happy “Birthday” to me! Today marks two months since my transplant day. It’s hard to believe it’s been two months since I felt so miserable – it both seems like so much longer ago and also like it was just last week. Continue reading

So, It’s Been A While

Yeah, sorry for that. Been up to a lot since I last wrote. I was released from the transplant clinic on the 12th, which was the 12 day after my transplant. Yeah, I kind of rocked that. Continue reading

So Much to Be Grateful For!

Day 8, and I continue to improve. My energy is coming back well, and while I have occasional bouts of nausea and what I like to call “the trots”, they are not too bad or frequent. Continue reading

Day 6

I am doing better, although my fatigue has been worse today than it has been since this all started. My wbc’s are at their lowest right now, at less than 0.1%. That’s basically zero, in immune system speak. Continue reading

Day 0

Today was the day I got my stem cells back. It was rough, let me tell ya. I guess the stem cells are really pretty thick, and the preservative they keep them in can cause some pretty strange side effects. Continue reading

Day -2

With transplants, Day 0 is the day you receive your stem cells, and then you count up from there.

We got down here to San An around 9 last night. We didn’t go to the store, we were too tired. Today, we were at the hospital at 8am, and got “home” around 4 or so. LONG day! Continue reading