Stem Cell Transplant 12 year -new birthday!!

It was a rainy day Feb 28, 2006, when I was admitted to Sutter Memorial Hospital Bone Marrow Transplant unit. It was a small unit of only 6 rooms.  Each patient is in isolation because of having little to no immune system working. Every day, a cleaner came in and did the entire room top to bottom. The nurses were the kindest and very experienced in their field. It takes a special person to be that nurse.

I can’t exactly remember but I think I was given the Melphalan that day, and then the stem cells are given either the next day or the day after.  It’s the Melphalan that does you in as it kills everything along with the hope it’s killing the cancer cells.  Then it’s the stem cells that actually rebuild your immune system and white blood cells. But first, you go thru white blood count dropping to close to zero, plasma transfusions as your red blood count is so low, horrible diarrhea, and on and on.

12 years ago today. I’m one of the lucky ones as my SCT did work and I had 4 years of remission.

But it was singularly the worst experience of my life. Yet, I’m grateful for the medicine, my doctors and transplant specialist, nurses and of course my family. They got me through.

So Happy New birthday to me.

Simple Sunday

Our internet is out so I’m using B’s hot spot in his phone for the internet. ATT will be here this morning. After they fixed the lines that went down in the storm the wifi has not worked. This happens every 2-3 years so I guess we should have expected it.  But I was able to pay some bills and send off an email I needed to.

It is quite cold( 31 , this morning). But at least it’s sunny. Today, I’m going to the gym with my daughter who joined yesterday. What fun, now we can go together.

Flylady has 2 zones this week as Feb ends and March begins.

This also marks my 11 th birthday from my SCT. I went into the hospital Feb 28 and was released March 17. I spiked a fever and had to go back in for another night but overall it was ok. It takes a lot out of you since the drug Melphalan is basically mustard gas poison that is given to you to kill as many myeloma cells as possible. Then your own stem cells are reintroduced.  You basically have your white blood cells go to zero and red too. I needed 2 transfusions.  Finally, the stem cells start to produce healthy cells and your white blood and red blood count starts to go up.  It is very difficult and you’re basically half dead.

So as this new month begins , here’s to my elevensies birthday. 🙂

I need to go the market for some milk and ? cat food. I’m not sure what’s on the dinner menu except I have asparagus to use up so I’ll roast those in the oven. Maybe a quiche?? I need to check the freezer to see that I’ve got.