Saturday, September 26, 2009

No Time Like the Present














First and foremost, a big congratulations to my precious sister and brother-in-law, Happy and Rob, who tied the knot in one of my favorite cities over the weekend. I am so thrilled for them!!!  More evidence for me that there is no time like the present to do what you want to do and go where your heart leads. Hooray for Hap! (the picture is with their two attendants, Delta and Bosco) 


And in keeping with this train of thought, this was the week that my conversations about chemo moved to the present tense. I met with my oncologist, Nancy Peacock, on Tuesday. I really like her and I think this is going to be important as we go forward with the poisoning part of my cancer treatment. I read somewhere that the treatment for breast cancer is “slash, burn, poison.”  This does not bring to mind sweetness and light does it? More like a scary harsh reality.


I am lucky to skip the burn part, I know, but I’m petrified of the effects of the poison. My answer? Carpe diem. Let’s just get it over with. So, I am. Starting next Wednesday, September 30th, I will receive Taxotere and Cytoxan four times over 12 weeks. And yes, I know what your are wondering. Yes, I will lose my hair. Not to mention all the other fun side effects. But barring infections, illness, or other unforeseen distractions, I will be finished by early December with the poison. 


I am feeling much better, now, from the surgery and am proceeding with the reconstruction phase of treatment. Without burdening you with TMI, I’m visiting my very cute plastic surgeon weekly for a bit to have my expanders gradually filled and stretched in preparation for my final surgery, hopefully in January. Wow! Although that seems like a long way away, 5 or 6 months is really just the blink of an eye in the big picture. I have already started to envision my life when my hair grows back and I am “whole” again. What will that life look like? How will I have changed? What will I have learned? I know some of this will become apparent to me as I continue on this journey.


One question I continue to ask is WHY? Why did this happen to me in the first place? If the medical community has become so good at detecting and “curing” breast cancer why can’t they figure out why 1 in 8 women will get it in their lifetime? And why is that number is growing? I believe that we will get some answers during my lifetime. Not just a cure, but a prevention. Will Susanna be able to simply get a vaccine to avoid this nightmare?  That would be amazing. 


In my recent surfing, and thanks to Facebook, I discovered ArmyofWomen.org. It is a partnership with the Dr. Susan Love Foundation and Avon to sign up a million women to help in breast cancer research. You can join the database and learn about various studies going on that you might qualify for. I love their tag line, “go beyond a cure.” At the end of the day, that’s what it’s really all about.  I encourage you to register as a volunteer, you never know who you might help in the future. 


I remain grateful to all of you who have me in your thoughts and prayers and appreciate  so much you who have reached out by mail, email, text, phone. I am humbled and overwhelmed at your generosity and thoughtfulness. 
So long for now. Talk soon!




5 comments:

  1. Barbara Keith,
    you looked great at Jamie's football game yesterday. Good Luck today on the start of your treatment. My Mom is having surgury today as well to remove a cancerous lump in her breast. Being older and post mentapausel, her course will be rather different. she has chosen a lumpectomy with radiation. No chemo for her. I am thankful for your blog and insights. keep up the good work.
    Macie

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  2. BK, thinking about you often...I pray you get through this phase with the strength I know you have. Your posts are amazingly courageous and inspiring. At the end of October, I will be walking in the ACS Making Strides Breast Cancer 5K, and now I have one more reason to do so.

    All my best...
    Jill Hershberger

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  3. Hi Barbara Keith - I'm so sorry to hear that you are having to go through this - I think anyone who reads this blog feels like they can easily put themselves in your shoes - the worry, fear, and pain... especially those of us with kids (your kids are darling, by the way!) I also wanted to tell you that you are a wonderful writer! I'll be in Nashville for the reunion and would love to catch up with you if you are feeling up to it. You are on our prayer list.

    Take care, Susan (Stimbert) Bullock

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  4. Yes, why this is so prevelant is mind boggling. Hang in there. You are surrounded by love and understanding. Kick, scream, rejoice and look into the eyes of your children. Thank you for sharing your thoughts in this blog.

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  5. Barbara Keith,
    We have met the nicest people during Mikes chemo at TO, yourself, your mom and your husband included! Who knew we had so many friends in common. I have heard your name so many times since we met.
    I hope you are doing well, as I am sure, your treatment has ended by now and know your hair is back, like your lovely photograph!
    We met w/Dr. Peacock a few weeks ago and got the great news that Mikes' liver cancer has shrunk drastically and the tumors are dying! His markers are down to 12.5. (they started at 500 if that tells you anything) Thanks be to God! We were blown away w/the news.
    However, Mike will remain on a maintenance/treatment drug, Avastin every three weeks for just 30 minutes and a CT/Pet scan every 3 months. So we will continue to meet wonderful people in the "treatment" room.
    Hope to see you at Chaps! I believe one of Mikes daughters Cassie met you in there one day.
    Best of Luck to you and your family!
    Cindy McConnell

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