Tears in My Eyes, Hope in My Heart



Tears in my eyes tonight, hope still in my heart!

Today’s workday was a struggle … the heart was willing, the body and thinking mind not. Common sense caught up with my heart and asked passion to give it a rest. The doctor’s office called late afternoon. The doctor is placing me on medical disability through the balance of 2014. The call to my boss at the close of business was difficult for me.

Writing my formal notice about moving from intermittent to continuous leave was no easy task. The letter expressed my sincere desire to be re-selected for a job I have done for 13 years, while at the same time having to explain my need for continuous medical leave. I understand the medical necessity of disability leave through 2014, yet I still hope for a real chance at returning to work and my company sometime this summer. It’s not out of the realm of medical possibilities.

  • Keep rooting with me for these anti-Her2 drugs.
  • Keep listening for magical words – “pathological complete response.”
  • Keep hoping I’m eligible for breast conservatory procedure.
  • Keep thinking out-patient procedure.
  • Keep praying post-operative treatments are easy on me.
  • Keep positive thoughts about re-selection by my old boss.
  • Pray William and I get creditor cooperation on our financial workout plan.

William, Danene, and I travel together this coming Thursday to begin the sequence of needed tests and appointments for Cycle 3 treatments. I will return to our temporary home in Carmichael with Danene after chemo treatments. William will stay behind to finish packing the high country ranch house in Agunaga. The present plans have me stopping in for a day or two to say goodbye to our lovely home as we list it for sale.

I’m reflective tonight. We hoped-against-hope that my newish chemo regime wasn’t too powerful a personal adversary, while believing it to be the ultimate adversary for my Her2 Cancer bug. It is a worthy endeavor. There is ample reason to conclude that my personal struggles with this chemo regime means I’m kicking cancers butt. I have no way of knowing for sure for a couple more Cycles, but the tumor does feel softer and less attached to my breast bone which it pressed against. Did I write about this before? The doctor mentioned at my Cycle 2 appointment my tumors seemed to me smaller already. It’s a crude measurement, but I’ll take it.

We will do this!

Rally call:

  • Remember – pCR!
  • Remember – Remission!
  • Remember – Re-Selection!
  • Remember – I love you all!

Advertisements

4 thoughts on “Tears in My Eyes, Hope in My Heart

  1. Dawne, not a day goes by that I do not think of you, hoping the chemo is being gentle on you! I pray that you get the chemo your body needs to get ahead of the HERS? (not sure if that is what they call your type, excuse me if I am incorrect).
    I know you have been exhausted and up at all hours of the night. I am glad you decided to go out on Medical Disability. My Dr told me when I first became unable to work and my sleep schedule was screwed up to not worry about when I sleep. That’s why I am on disability and can take naps all day long…so don’t be hard on yourself about sleep, now you can sleep when you can.

    Many prayers going up, so blessing will come down!

    Let’s continue to kick cancers butt!

Leave a Reply

Please log in using one of these methods to post your comment:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s