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OT-- The beast is winning


Marvel

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Many of you have been praying and sending good thoughts our way as my

wife Barbara has struggled in her fight against melanoma. The first

standard treatment wasn't working, so we stopped that. In the six weeks

she was on it, she had lesions show up on her spine, in her liver and

lungs. Her brain was clear. She was then admitted to a clinical trial,

to test a new drug. No placebos, she would be getting something that

they hoped would work.

Everyone had a surprise this week. On Wednesday, the doctor's staff

thought that Barbara was too fatigued to receive her infusion of

depsipeptide and they decided she should go ahead and have a CT scan

and MRI. The radiologist saw several lesions in the brain. There were

too many to do surgery or gamma knife and he recommended to begin whole

brain radiation. Barbara was admitted to the hospital on Wednesday

night and given a steroid to reduce the swelling in the brain tissue.

The steroid showed some improvement on Thursday afternoon and she was

released to come home. Whole brain radiation will begin on Monday

morning at Memorial Hospital in Chattanooga. Barbara should receive ten radiation

treatments over two weeks. The radiation expert at Emory, Dr. Peter

Johnstone, said the radiation is not expected to shrink the brain

lesions but to cause them to become stable and could provide long term

stability. Hair loss is expected but regrowth is possible within three

months.

Some of the new lesions are quite large, and we know at this point that

all we are going to be doing is to make her comfortable for the time

she has left. I thought I had been dealing with this pretty well. We

have received much support, from family and friends, including you

folks here on the Klipsch forum. But I guess I'm not dealing with it

very well at all. . Even though we are taking it a day at a time and

trying to enjoy what we do have, I also have to make decisions and

think about life without the love of my life, the joy of my youth.

[;-)] Thirty plus years of good times and hard times. It makes a

lot of the petty crap here seem pretty trivial.

I just wanted to vent/rant/let go a bit.

Got to go. It's a sunny day

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Bruce,

Thank you for posting the update. I am so sorry to hear things are going as they are for Barbara.

It sure make sense to me that lots of stuff would seem trivial in the light of the situation as it is and you are thinking about the things that really matter. I don't know what it really means to handle things well anyway. You put your feet on the floor and get out of bed... after that, put one foot in front of the other.... to walk and not faint... that's handling things well, I think.

This is a good place to posts rants, vents, raves... whatever... you have got alot of support and caring in this place. It's all welcome here.

If you think of it, mention to Barbara that we are keeping all of you before the Lord.

Thinking of your son, too.

Peace.

Dee

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Words are meaningless. Terrible. I hope you can find the strength to get everything out the time you have left and do the right thingd. I have a feeling you will. Don't excuse the rant, I think I speak for all that we are honored that you want to share this with us. This forum is strange in that way, it's more than exchanging facts and reviews... Keep in touch.

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Bruce,

I just don't know the words to say.[:(] Just take each day at a time and make them as wonderful as you can. Remember the good times and make some more good memories, make every day count.

I believe we are all keeping you in our prayer and I know I have shed a few tears reading your posts. Keep us updated, God bless.

Steve

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Since Barbara had been Stage I for 4 1/2 years, and had kept up with

all the research going on, the sudden leap to Stage IV melanoma was

itself a surprise. One checkup to the next, with no indication anything

was going on. Since she jumped to Stage IV in July, we knew this day

would probably come, and have just done what we could along the way. It

doesn't make it any easier, of course. The standard treatment of IL-2

only had a 16 percent chance of being effective. The clinical trial had

shown to be more effective, and someone has to try these things. We

didn't feel we should just stop trying.

The shock is wearing off a bit. She has already outlived her

statistical lifespan given what she has. Could we try other

experimental drugs? Sure, but at what cost? Emotionally and physically

draining, and all of those 'quality of life' issues start coming up.

Some of the treaments put your body through hell, and that isn't what

we want to do now.

There are, of course, all kinds of 'alternative' treatments. Helpful

friends have told us of some, but we have tried to keep current and

know what really has been effective and what has not proven to be any

help at all. Some of those treatments actually have helped some, but

they aren't 'the' cure for cancer. Melanoma is a particulary difficult

cancer to fight. It, compared to many other cancers, doesn't play by

the rules at all. Some do, so you know exactly how to fight it and have

a pretty good chance of surviving a long time.

As my wife has put it, life is a death sentence. No one gets out alive.

Some just have an easier time than others. Our faith is strong, we know

in whose hands she rests. This isn't meant to sound fatalistic. It is

not in the least. As a good friend on this forum told me, we wouldn't

always choose the road we go down, but God has us go down that road to

be the person He wants us to be when we get to the end of it.

Enough preaching. I love you guys (warts and all!). I am sure that as I

spend more time here at home, I will be able to get on here. After all,

there is only so much laundry to do and so many dishes to wash.

Bruce

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Bruce, I don't know what to say . . . .other than that: we are here, we are a family of souls united, please rant, vent and cry with us. We can (and will) all pray, but I sense you have that covered very well. Our empathetic hearts are with you and Barb, but obviously we are helpless when it comes down to the short strokes. I can't make sense out of it; I can only hope it is all revealed to us one day. We are here for you, and hopefully that gives you some reassurance that the sun will come up tomorrow and the next day, and the next . . . . . . Hold her and love her, as she loves you. God bless your family. Amen

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ditto to st. patrick - well said -

Bruce, Barbara and family, I hope and pray you find support,

love, laughter and hope in each other, with family, friends (yes -even

us) through this chapter of your lives. As for faith, it's an

open book - never-ending.

You all take care. Hamish

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