Nick's Myeloma Blog

I created this blog so that I, and others, can track the progress of my Multiple Myeloma and my efforts to combat it. I am blessed to have my family and many good friends to help me defeat this and if you are reading this, you are likely included in that group. Thanks for your support -- with it, I will beat this. So for your edification and perhaps even amusement, read on!

Tuesday, December 17, 2013

Hmm...partial answers from Dr. FVR from UAMS

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So I was on this panel today with Dr. Van Rhee, who did an admirable job of explaining the total therapy philosophy. I told him I was a fe...
3 comments:
Friday, December 13, 2013

Myeloma panel with Dr. van Rhee of UAMS next Monday

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Next Monday I am participating as a patient panelist on another Cure Talk call, hosted by the wonderful Priya Menon and the Cure Talk organi...
1 comment:
Wednesday, December 11, 2013

No longer suffering from chemo brain

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I went to a neurological oncologist to get a "new baseline" for my cognitive abilities.  I wanted to make sure that I had survived...
Thursday, November 28, 2013

Enough already! Or, be thankful and hugs your kids.

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So here I am, busy not dying from cancer, when I almost died from an auto accident. Near as I can tell (because I couldn't see anythin...
3 comments:
Tuesday, November 26, 2013

Past and future Myeloma panels

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Hello folks. I had the opportunity to participate in another Myeloma Panel hosted by Cure Talk and the wonderful Priya Menon.  Last week...
1 comment:
Tuesday, November 19, 2013

More research on the new protein

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As I suspected, Mayo was not willing to let me have a phone conversation about this particular topic.  So rather than contemplate flying to ...
Monday, November 18, 2013

New energy to get to the bottom of this new M protein

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Howdy folks. So I got my monthly tests back last week and saw that "faint monoclonal lambda light chain" present under IFE.  Sti...
2 comments:
Thursday, November 14, 2013

Well, well, well...five years passes.

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Yesterday was the five year anniversary of my diagnosis. I had had my bloodwork come back and the doctor had said that "everything is...
4 comments:
Thursday, November 7, 2013

Five years ago today, my first detailed blood test for Myeloma

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I remember going to the hematologist, who had told me that I could have MGUS or Myeloma but that it was very unlikely that somebody my age w...
Tuesday, October 29, 2013

Five years...the first of several posts on the topic

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I'm sitting at my desk right now.  It's a sunny October day in southern California and the sun in streaming in.  The desk is a pipe ...
Monday, October 21, 2013

Interesting publication on benefits of transplant

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I rarely re-post other articles -- there are other blogs for that sort of thing.  But this one struck me as important. There has been cons...
2 comments:
Wednesday, October 9, 2013

The Strep That Wouldn't Die, and other stories. Or other story. Or question, really.

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So after being symptom free for a few days I woke up yesterday with a painful sore throat again.  Took a Vicodin immediately, and a Tamiflu...
5 comments:
Wednesday, October 2, 2013

How a simple cold turns into hell with a compromised immune system

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Hello friends. So there's been a little bug going around.  Seems some people have a sore throat which then turns into a cold in some p...
5 comments:
Thursday, September 19, 2013

An idiot's guide to cytogenetic abnormalities.

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This will be a curious post in some ways, because it will provide partial answers and half-truths.  Not in the sense that I'm keeping an...
Wednesday, September 18, 2013

An update, with help from a fellow patient

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I have had the good fortune to connect with two fellow MM sufferers on a couple of different topics recently and would like to acknowledge b...
2 comments:
Monday, September 16, 2013

From the Doctor's mouth...

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Every time I think I don't need to worry, I find more to worry about. In the wake of last week's little goof-up with the remission...
Wednesday, September 11, 2013

Talk about false alarms! What a day I had yesterday...

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Regular readers will know I encourage patients to learn as much as they can about their disease and their treatment.  This is, generally, a ...
3 comments:
Monday, September 9, 2013

Ruminations on last weeks' tests

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I try not to overthink all this stuff, really, but it's a fine line between wanting to know everything I can about my condition and the ...
2 comments:
Saturday, September 7, 2013

An update: the good, the bad, and the ugly...

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Clint Eastwood: * My MRD test (the most sensitive marrow test they have) tested more than twice as many cells as last time, owing to a bet...
7 comments:
Wednesday, September 4, 2013

Concern allayed

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I had the pleasure of having dinner (and wine!!!) with BB, his lovely wife, his irrepressible chief of staff BJ and a colleague of theirs wh...
1 comment:
Tuesday, September 3, 2013

An unnerving update from Arkansas

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I have been in Little Rock for about 16 hours, and already managed to get my pizza fix in from the always-delicious Dam Goode Pies. Sadly,...
1 comment:
Wednesday, July 24, 2013

When does a negative test not feel so negative?

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When instead of saying "the original protein cannot be detected", as most of my tests from Arkansas have said, it comes back ...
6 comments:
Tuesday, July 23, 2013

Curetalk panel with Dr. Kumar from Mayo Clinic...any questions?

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Hello folks. I've participated in a number of panels over the last year with various Myeloma specialists.  Thursday of this week at 7P...
1 comment:
Friday, July 19, 2013

Only a false alarm. Immunofixation negative!

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So I saw my Dr. GD out here on Tuesday, and explained to him I was uneasy about the immunifixation test.  He didn't seem to get the grav...
Monday, July 8, 2013

Incomplete feedback from a couple of doctors on my labs

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So in the wake of my alarming little reappearance of the word "monoclonal" on my labs the other day, I did a little inquiring. B...
Thursday, July 4, 2013

Another false alarm?

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The Iron Law of Oligarchy. I remember literally nothing else about a class I took in comparative political structures of developing nation...
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Nick
Los Angeles, CA
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