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Mountains

 

Bob and I went to the mountains and had lunch in an old hotel there. We had

green beans, potatoes, fried chicken, rolls and pecan pie. The sky was clear

and the weather was almost balmy for February. After lunch, he stayed in the

hotel lounge while I wandered in and out of some gift shops. We were gone six

hours. We had not been to the mountains in over two years. He was leary about

being able to drive that far since his neuropathy has affected his legs, but it

was okay.

 

At home, he hit the bed and I went to the computer. Next Tuesday he is due back

at the oncologist's for his monthly Aridia and to see what the doctor recommends

that he do next. I keep hoping that he is in at least a semi-remission.

 

I picked a fight with him this morning because he waited until then to gas up

the car and get money from the ATM. This is a familar fight with us. He is a

"wait till the last minute" and I am an early starter. Cancer changes nothing

much...not really. We are the same people we married long ago. Love is bigger

than our fights and fears. Our getting along one hundred per cent of the time

is as possible as his cancer being cured. Why do I say that? Because there is

little romance in spirituality but rather shocks and hard knocks over a long

period of time. Mr. G. was right. Everything has to be paid for; nothing is

given.

 

I look back on the last year and realize how every month had its particular

tortures for us. High-dose chemo, blood transfusions, months of the new drug

and then one week on the drug that led to his having seizures. Zowie. Where do

we go from here? It is either resuming the drug which gave him neuropathy or

once again considering a stem cell transplant. I think that would kill me. In

the meantime, I write and write and write. In the last analysis, we do what we

do and never quite know why. Hitting the send button, for me, is like the

analyst saying that the fifty-minute hour is up. Thanks for listening.

 

Vicki Woodyard

http://www.bobwoodyard.com

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I look back on the last year and realize how every month had its

particular tortures for us. High-dose chemo, blood transfusions,

months of the new drug and then one week on the drug that led to his

having seizures. Zowie. Where do we go from here? It is either

resuming the drug which gave him neuropathy or once again considering

a stem cell transplant. I think that would kill me. In the

meantime, I write and write and write. In the last analysis, we do

what we do and never quite know why. Hitting the send button, for

me, is like the analyst saying that the fifty-minute hour is up.

Thanks for listening.Vicki Woodyard

 

Dear Vicki:

 

I had started to write this to you once before but stopped myself. But now, you ask...

 

Where do we go from here? It is either resuming the drug which gave

him neuropathy or once again considering a stem cell transplant. I

think that would kill me.

 

Reading your posts on the treatment takes me back to when my life was

controlled by fertility treatments.

My goal was to achieve life, while yours is to defeat death. Still

the emotional roller coster

associated with this process is much the same. When Bob is getting

chemo, I cringe. A few weeks ago when

you wrote to say that you were in between treatments, I sighed a sigh

of relief. I was glad to know that

you told him to hush, and that he told you that you snored. (and to hush :-)

 

When people would suggest to me that I stop the treatments and adopt, I bristled at the thought.

Failure, that would be failure. Then as God continued, unrelenting,

to give and then take away,

I finally took the time to stop and honestly examine why I had to be the one who produced the child.

Once I got past the need to "perform" as a woman, I reached the stage where I could affirm that

what I wanted was a child. If what I really wanted was a child, then why did I have to define

how that child came to me? It was then that I began to explore

adoption. Although I continued IVF,

inside me the pressure was off because I had crossed a certain

threshold in what I wanted rather than how I wanted it.

 

I look back sometimes on the three years I spent in treatment and laugh, knowing that it was all

an ongoing lesson. At the time, though, I was miserable, cried all of

the time, and thought of nothing

else, literally. There were no normal moments, because all of the

hormones made me, well, crazy!!!

I will not judge myself for what I did then as I know everything was and is exactly as it should be.

I do not judge you either. Still, I ask you to consider whether Bob

and you should go back into treatment

at all right now.

 

What is your goal, really? To defeat death, or to delay it? You can

make the choice to spend the time left,

whether it be 10 months or 10 years, as it comes, free of the

agonizing treatments that seem to provide

more misery than comfort. It seems that Bob is sick most of the time

from the treatments anyway. Maybe you

want to consider continuing that break for a little longer and see

what happens. You and Bob deserve it.

 

Love,

 

Joyce

 

PS I am told I snore too. I myself have never heard it :-)

But, a few years back a woman who shared a room with me at a seminar

declared that I snored like a "steamroller." I think I have stopped since then ;-)

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, "Lady Joyce" <shaantih@c...> wrote:

>

>

>

Dear Joyce,

 

Thank you for your thoughtful post. There are some differences in our

situations, you will admit. Bob has made all his own decisons regarding chemo;

multiple myeloma demands active chemo when it is out of remission. I love him

and will do whatever I can to support him....altho I have told him that a stem

cell transplant would not be something I could get through. He may even decide

to do it wihout my getting involved. Who knows? Life is like nothing I have

ever known....

 

Love, Vicki

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Dear Vicki:

 

Yes, there are many differences in our situations. I knew that even

as I wrote it to you. I just wanted to give you a longer break.

I know you know that I meant it mostly for that reason.

I know nothing about the requirements of cancer treatmentSo, keep writing and I will keep listening.

 

Love,

 

Joyce

 

 

 

 

Dear Joyce,Thank you for your thoughtful post. There are some

differences in our situations, you will admit. Bob has made all his

own decisons regarding chemo; multiple myeloma demands active chemo

when it is out of remission. I love him and will do whatever I can

to support him....altho I have told him that a stem cell transplant

would not be something I could get through. He may even decide to do

it wihout my getting involved. Who knows? Life is like nothing I

have ever known....Love,

Vicki/join

"Love itself

is the actual form of God."Sri RamanaIn "Letters from Sri

Ramanasramam" by Suri Nagamma

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