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Mri

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NedClocker

Member
Joined
Sep 12, 2001
MRI

My wife goes again tomorrow to MD Anderson for another mri of the brain and spine. Got to be there at 7:30 for the first one. Doctor appointment at 1:30. I'm sure you'll all wish us well.
 
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Thanks, muddocktor. God has brought us this far. All prayers are welcomed and appreciated.
 
hello nedclocker. i wish you guys good luck on the mri...but i'm wondering, if you don't minde me asking, what your wife has? my mother has alzheimer's and that is the biggest reason that i am folding. she has had to get a few mri's over the past year when they were trying to decide what it was that she had. now that they've finally narrowed it down to alzheimer's, it sucks but you've just got to go on with life, you know? well best of luck, and fold on.

jeff
 
Good Luck Ned. Needless to say the thoughts and prayers of everyone here are with you.
 
NedClocker said:
My wife goes again tomorrow to MD Anderson for another mri of the brain and spine. Got to be there at 7:30 for the first one. Doctor appointment at 1:30. I'm sure you'll all wish us well.

This is the reason we fold . . . . Wish your wife the best for me.

Karl
 
Thanks, guys. This has got to be one of the best groups of people there is.

ok. Good news, or, at least, not really bad news. The tumors only grew a little, maybe 5%, so the chemo is keeping it slowed down.

Here's what's wrong. I know some already know. I'll just copy it from a PM I sent to someone who inquired, so I don't have to type it all again. It's a little long, but it started 4 years ago.

Breast cancer that has spread to the protective lining of the brain and spinal cord. Leptomeningeal disease, Leptomeningeal Carcinomatosis, Leptomeningeal metastases of Breast Cancer. All mean the same thing. You've heard of bacterial or viral meningitis? You could call this cancer meningitis, I guess. It's in the meninges, the protective lining of the brain and spinal cord. Terminal diagnosis. And, it has paralized her from the bottom of the ribs on down.

Late July, 2000, we were told she had 6 to 8 weeks without treatment, maybe 3 or 4 months if there was a treatment that would help her. Might be able to extend her life, but there is no cure.

Well, 20 months later, she's doing pretty well. MRI yesterday showed about a 5% growth in tumor size.

The tumors had completely disappeared from the mri, but they took her off of her chemo because it gave her diahrea. (She was in the hospital 1.5 weeks for diahrea. That's serious diahrea.)

4 weeks off of the chemo, and you could see the tumors in the mri again. Came back pretty quickly. . So, doctor put her back on the chemo, dose reduced to 90%. Tumors grew a little. Up dose to 95%. Tumors grew a little. Now he's uped dose to 100%. Hopefully this will knock them out again.

The 2 drugs that have worked for her, Herceptin at first, and now Xeloda, were both approved for use in 1998. They are both "Smart" drugs, attacking primarily cancer cells and leaving normal tissue alone.

No way to tell this story in short form. It's a long story. I forget what I've told who. Considered creating a web site to detail it all but figured she wouldn't live that long. Might as well go ahead and do it. Looks like she'll be with us a while longer.

Oh, yeah. I'm 41. She's 39. We have a 4 year old son. She discovered the lump after she stopped breast feeding. She was 35 then; I was 37.
 
damn man, i've so sorry to hear of your wife's ailment. there's not much that i can say that hasn't probably already been said to you. i don't know how life threatening my mom's alzheimer's is, but regardless it is something that hits home hard and i'd rather not deal with. well you know that we're here for you and we can support each other. hope everything turns out for the best.

jeff
 
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