Skip to main content

Still don't know

Sorry, I told you I would know if I was in remission yesterday. Then yesterday I told you I actually wouldn't know for sure until today. And today I have to tell you that I won't know for sure until next week.

*sigh*

So here's what happened. Drs. McDermott and Patil came down and told me yet another test would be needed to determine if the cells they saw from my bone marrow biopsy are leukemia cells or Sarah cells. The test the pathologist ran was looking for a protein marker on the surface of these cells. I guess the results of this test are not conclusive enough to say for sure one way or another, and the only way to really say for sure is to look at the chromosomes. It's a FISH test, or Fluorescence In Situ Hybridization test. That's like the fanciest fish name I've ever heard. The FISH test is what they did with the first sample, which determined that we were looking at monosomy 7. The results from that first test came back on a Thursday following a Friday bone marrow biopsy. I'm told the results from this test will come back in 5 to 7 days, so that sounds about right.

I wish I had more information for you, but I don't. So instead, I'll show you this gross picture of my arm.


After they removed the picc line, I had a dressing on that hole for about a week before I finally started working on that nasty adhesive. I learned something in the process though. Most people use alcohol swabs on sticky things like this, rubbing it over the sticky to work it off. But there's something way better, at least in my opinion. My nurse today, Ewa, gave me some adhesive removal pads.


It's like goo gone I guess. Kind of oily and slippery feeling. You just hold it between the sticky thing and your skin and squeeze the fluid out as you peel the thing off. It was truly magical.

She had some more magic in her bag, too. Today for the first time I found out I can use special shower gloves that keep my picc line or IVs or whatever dry. For weeks I've had CNAs use all sorts of things to wrap up all my equipment. Aqua guard things, plastic bags cut in multiple different ways, and mounds and mounds of tape. But check out the glove sleeve on this guy!


"It's so easy I can put it on by myself!"
I can also shower in style, and smile and have big muscles, which is the most important thing.

Comments

  1. You're gonna be ripped! Hooray for the right tools for the tasks at hand.

    ReplyDelete
  2. What a relief to be able to take a worry free shower again! It's the little things......right?

    ReplyDelete

Post a Comment

Popular posts from this blog

Taking drugs is a full time job

It almost feels like I never left. After a week at UC Health, and a glorious ten days at home, I'm back at the VA for take three of chemo. I'm at the point where I feel almost recovered from the last two rounds. I can walk at a fairly normal pace, I can climb stairs without feeling (abnormally) out of breath, and my guts aren't constantly in a twist. I even had a beer with coworkers on Friday. It was really nice to see everyone, and I was pretty much my old self. So it seems a shame to put more poison in my body and fall back into the sick zone. I know in about a week I'll be feeling pretty shitty, so I don't know what kind of Halloween costume I'll be able to pull off. Any suggestions? This round of chemo is called GCLAM: three days of Mitoxantrone, and five days of Cytarabine and Cladribine. I also get shots of Filgrastim to stimulate my bone marrow to produce more white blood cells. Hopefully this will help lessen the blow of the other drugs, my cell count...

Transfusion

I didn't know I could get so excited about blood products being injected into my body. But the days of anticipation paid off and I finally got a transfusion yesterday. It was a little nerve wracking signing the waiver when they told me the odds of contracting hepatitis or HIV, but then I remembered the other odds they gave me, so I said fuck it. I got two units of red blood cells and two units of platelets. It's pretty interesting how they have all the blood components separated out. I guess blood used for transfusions like this is specially filtered and irradiated so I don't get anything, like white blood cells, that would be bad for me. fresh blood It took hours to get it all in there. It gave me a metallic taste, but after a while I felt a little more alive. I could take a deeper breath, walk outside with Brent, and eat food. Hospital food even. Though, I much preferred the strawberry banana smoothie Brent brought for me. That tasted a lot better than blood. I...

A Nearly Final Farewell from Sarah's Parents

Dear Friends - We are deeply saddened that Sarah has entered the ending chapter of her battle with this horrific cancer. The medical experts expect only days left to live. It would really lift her spirits to read about memories you've shared with her and any other comments that you would like to offer. We look forward to hearing from you very soon, and we will read all comments out loud to her. Sarah is doing her best to be her usual spirited self in spite of these difficult times. We are grateful for everyone who has been a part of her remarkable life. Sarah's Mom and Dad