Sunday, April 21, 2013

Rethinking the Battle Plan

Bortezomib is not living up to its fierce and aggressive sounding name.  I began low dose Velcade (Bortezomib) treatments in January, receiving injections every other week.  During that time my lambda light chain numbers kept going up, the kappa/lambda ratio kept going down and  the Beta 2 Micro-globulin serum continued to trend up.  

                                 01/3/13    01/31/13    03/06/13    04/10/13
Kappa Light Chain          7.83         8.25           6.09           6.71  
Lambda Light Chain      51.37        62.64          83.81       100.86
Kappa/Lambda Ratio      0.15          0.13           0.07           0.07

                                  07/05/12   10/26/12   01/31/13   04/10/13
Beta 2 Micro-globulin      2.60          2.81          3.03          3.97

The kappa light chain is staying well within the normal range of 3.3 - 19.4 mg/L.  However, the lambda light chain has moved out of the  normal range of 5.7 - 26.3 mg/L.  It crossed that threshold back in October and just keeps  moving up.  The ratio between the kappa and lambda light chains is below the normal range of 0.26-1.65 and that is not a good thing. The rise in the Beta 2 Micro-globulin is an indicator that low dose Velcade treatments are not working.  The normal range for this component is <OR=2.51 mg/L.

These latest numbers have made it necessary to begin a more aggressive treatment plan.  Beginning on April 23, I will be having Velcade injections twice a week for two weeks in a row and then have one week off. After six weeks of this regimen, we will assess where I am and if we are not making progress in reversing this upward trend,  my doctor will probably add other drugs from the multiple myeloma arsenal.  

I spent about 18 months in remission after my stem cell transplant and even though I knew the myeloma would come back some day, it seemed like that day would be a long way off.   It felt good to be living an almost normal life and I could easily tell myself that the myeloma probably wasn't coming back in the next week or the next month, so I would think, "I don't have to worry about that right now."  I felt like Scarlett O'Hara......"I'll think about it tomorrow."   Multiple myeloma returned sooner than I had hoped or imagined.

Now, I am back thinking about it a lot.  I won't say I dwell on it because I don't, but it has wormed its way back to a more prominent place in my consciousness.  It is always there ready to worry me if I let it.  Some days are harder than others to keep it at bay.  It is difficult to be back in the battle against this disease and I am having a bit of a hard time accepting it.  I know I will overcome that and be able to gather the strength of mind and body to wage this war successfully.  I'm just not quite there yet.

I would like to end on a more uplifting note and share a picture I took last week in the beautiful Skagit Valley of western Washington.   Each spring Skagit Valley hosts a Tulip Festival and tens of thousands of visitors from all over  make the trek to see the acres and acres of glorious tulips.  I am fortunate that this spectacle is just about a 30 minute drive from my home.
Skagit Valley Tulips
 

9 comments:

  1. Carole Leigh - I am sorry to read that the lower dose treatment was not enough to ward down those numbers. Praying that this new regimen will do better for you and no more aggressiveness is needed.

    You always have my prayers and faith for the best.

    I am so happy to see the tulips in your photo. I had hoped to get up there this year but that was not to be and so you bring me joy to view the blooms "here".

    Much Love and continuing prayers -
    Lynn

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    1. Thank you Lynn. You are always in my prayers too!
      Love,
      Carole Leigh

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  2. Carole Leigh,

    I'll keep you in good thoughts.
    Thank you for sharing the picture of the beautiful tulips.
    Cheryl

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  3. Thank you, Cheryl.
    Love,
    Carole Leigh

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  4. dear carole leigh,

    well, darn it all! very sorry to learn the big battle bomb fizzled. but take heart - at least your medical team is on top of it, and not letting you go on and on, being very pro-active about changing up the strategy.

    i hope that your proclivity towards moving in closely to the things that bring you comfort helps assuage the big, bad what-ifs. i am so glad you got to see those gorgeous tulips,and i hope that spring time will be a soothing tonic for you.

    please know i am keeping all my best hope and thoughts for you close to my heart, "believing" that better days are ahead.

    love, XOXO

    karen, TC

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    1. Karen,
      I can't thank you enough for your continued support and encouraging words.

      It has been hard to get my head back into the game. I so enjoyed being in remission and not having to be battling this disease. I am finally getting adjusted to this new phase.

      Love,
      Carole Leigh

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    2. Hi Karen,
      You can email me at caroleleighi@gmail.com
      Love,
      Carole Leigh

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  5. I'm not far away, across the water, sending you healing Reiki energy and holding you in the Highest Light of Healing and Energy for the new weapons of mass destruction to do their work on those marauding MM cells, and this IS for the highest and best good of all concerned, so be it and so it is!

    It is, I am sure, like living with the sword of Damocles hanging over your head when the numbers go up and up, but take heart... there are a number of people living for a long time with high numbers - are you taking curcumin too? Huge hugs from the OP, SB

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    1. Sandy,
      I am receiving your Reiki energy. Thank you! My dentist just recently recommended Reiki to me and spoke very highly of the results she has seen. Her sister is a practitioner (I had her in the fourth grade!) and her father, who was my dentist before her, passed away last year from multiple myeloma.

      Thank you for encouragement from across the water...
      Love,
      Carole Leigh

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