jm's Adventure with Multiple Myeloma: 2nd ASCT Transplant Day

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Showing posts with label 2nd ASCT Transplant Day. Show all posts
Showing posts with label 2nd ASCT Transplant Day. Show all posts

Friday, May 18, 2012

2nd Autologous Stem Cell Transplant for Relapse - May 18 2012

After I relapsed on 27 February 2012, I was prepped with chemotherapy and received my 2nd Autologous Stem Cell Transplant today, May 18 2012. I will attempt to outline the steps for you here.

First, gather the "fun squad" for smiles and laughs. My bestest sister, Jani and Faye Hummel (both were with me during my 1st Autologous Stem Cell Transplant 13 September 2011 too).

Add 2 RNs and the Stem Cell Technician and the party is almost ready to commence. Me, RN Sarah, RN Emily, and Stem Cell Technician Cassie.
I was especially happy to see Stem Cell Technician Cassie because she was the technician that collected my stem cells for frozen storage last August 2011.
Lots of number checking and double checking to make sure the stem cells were mine and the batch that Dr. Myint had selected for the 2nd autologous stem cell transplant.
Cassie prepares the warm water bath (about body temperature) to thaw the frozen stem cells in.
Cassie gets my stem cells out of the liquid nitrogen container with a temperature of minus 190 F.
My stem cells in a flat little package.

Cassie puts my frozen stem cells into the warm water bath.
Through experience, Cassie knows exactly when the stem cells are thawed and ready for administration.
Then RN Sarah and RN Emily hang the stem cells to run by gravity into my PICC line. They do not use a pump to administer stem cells because it can damage the cells. So getting my stem cell transplant is a lot like a blood transfusion except the stem cells are thicker and require saline flushing to keep them running through my little PICC line.
My stem cells entering my PICC line.
Since the stems cells run by gravity, I had to lie flat to allow them to run more affectively.
Faye Hummel made sure I had my Judy Richter Jolly Rancher candy to suck on to offset the taste and smell of the stem cell preservative, DMSO, which smells a lot like burnt cream corn! I can tell you watermelon and cherry flavors go pretty well with cream corn, but candy apple is AWFUL!!!
Constant flushing to get the stem cells moving in. I felt nothing during the stem cell transfusion. I was pre-medicated with hydrocortisone IV and NOT Benadryl this time. It was soooooo much better, as I was alert and able to party along with everyone in the room.
The empty stem cell bag double checked again.
My transplant doctor, Han Myint, MD, arrived at the end of my 2nd autologous stem cell transplant. I will have to wait 10 to 14 days for the stem cells to engraft in my bone marrow. Hopefully, this transplant will get me into remission again.
But, remember, stem cell transplantation in multiple myeloma is just a treatment and NOT a cure. I will have to go on maintenance chemotherapy after engraftment....yet to be determined.

Thanks everyone! Me, Dr. Myint, RN Sarah, RN Emily and Technician Cassie.
And don't forget my support team and photographers extraordinaire, Jani and Faye!!!

2nd ASCT - Day 0 - May 18 2012

My 2nd autologous stem cell transplant went well today. Here is my transplant team after my stem cells ran in. Me, Han Myint MD, RN Sarah, RN Emily, Stem Cell Technician Cassie. Lots more photos to follow tomorrow showing all the steps!
Advanced Care Partner Emily.
Kemmer waiting in Greeley for me. Thanks Lisa Mathews for the photo.


Thursday, May 3, 2012

Lab Results - May 3 2012

Had a lot of labs drawn today in preparation for the 2nd autologous stem cell transplant if my bone marrow biopsy results are satisfactory for the transplant.

My white blood cell count is 4.3 (norms 4-11.1) which is absolutely NORMAL for the first time ever. My hemoglobin remains low at 9.4 (norm 12.1-16.3) and my platelets are low, but good for me at 111 (norms 150-400) which means I continue on full dose Fragmin injections (15,000 units) daily.



My immunoglobulin G is good at 406 (remember, this is the blood test that the norms don't really apply to me) since my cancer is reflected by HIGH values of immunoglobulin G.
My LDH is fine at 162.
They ran a bone marrow transplant panel and I'm non- reactive to all of the viruses they test for except CMV. However, they tell me almost everyone  is positive to CMV Virus.