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Posted

Well, I saw my onc yesterday and got the results of the MRI I had taken right after Christmas. Unfortunately, the spots they saw on the CT are new liver mets - the MRI confirmed this. So now I am going back on chemo, but am going to do a Phase 3 trial this time. I will be randomized to either Taxotere or Almita with or without the study drug Cetuximab (Erbitux). Anyone have experience with any of these drugs? The Cetuximab is a targeted therapy and supposed to have minimal side effects. I am wondering about the chemo drugs Taxotere and Alimita. I am not going to start treatment until 2/19, as I have a Disney trip scheduled for early February, and I would miss 2 treatments while away. So I am very happy about that, cause I don't want to be tired or nauseaus or in pain while in the happiest place on earth!!!! And I feel super right now - so I'll go off to Florida and then come back and kick some cancer butt!!!

Sharon

Posted

sharon,

Sounds like a good trial to be in. we will pray for good results. I am in Orlando now going to a Steven Ministry leaders training. I hope it warms up for you. It's a little cool for me now. I am sure it will have a great time.

Stay positive, :)

Ernie

Posted

Hi Sharon,

I am so sorry to hear about your new mets and also that you have to start that blasted chemo again. But you have a incredible attitude. With everything you have been through in your life ( and that is much too much for one person) you just keep on fighting. Your amazing, and with your attitude, you will prevail.

I am so proud of you. Good luck with your new treatments.

You are smart to wait till you come home. Have a great time in Disney World with your grandchildren. If anybody deserves a break it certainly is you!!!!!

Thinking of you girlfriend....

Maryanne :wink:

Posted

No experience with any of the drugs but wishing you great luck with them. I hope you enjoy Disneyworld..one of the really neat places in the USA as far as entertaining. Have a wonderful time and come home with your boxing gloves on.

Nina

Posted

1. I am sorry to hear about the new mets. :(:evil:

2. I am glad to hear they have a plan in place for you and I am praying and hopeful it will stop this bugger in it's tracks.

3. I am so happy to hear your going to Disney! How fun is that? YOU GO GIRL!! Have a GREAT TIME!

4. I just want you to know your in my thoughts and prayers each and every day! Keep that fighting attitude! It's half the battle, as you well know!

((((((((((SHARON))))))))))))

Posted

Hi Sharon,

I don’t have experience with any of the drugs you mentioned but I am so sorry to hear about the liver mets. Have your doctors considered a biopsy just to be sure? When all the imagining studies indicated I had liver mets, it was the biopsy that provided the definitive answer. Doing the biopsy was somewhat controversial because the other doctors thought the imaging studies were sufficient evidence. But my primary Onc argued my case before the tumor board and the surgeons and radiologists finally agreed. The surgeon had me sign a release to allow him to resect my liver because he fully expected to find cancer. So I am a pretty big proponent of getting biopsies whenever possible.

I hope you enjoy your trip to Florida. Like the rest of the East Coast we have been unusually warm this winter, so the temperatures will likely be in the mid eighties when you visit next month.

Posted

Sharon,

Sorry to hear about the new mets and that you are going back to chemo, that's just lousy. It sounds like you've got a good plan and a super attitude to take you through this.

Enjoy your Disney trip. Take the time to relax and enjoy (I know, there's not much time to relax in Disney!), then come back with both fists swinging!

Best of luck,

Tracy

Posted

I'm very sorry to hear about the liver mets but with your attitude you'll knock em' out in NO time!

Have a wonderful time in Florida.

Posted

Sharon,

Thanks for the update...sorry the news isn't better. But you have a GREAT plan in place to certainly whoop up on this thing!

And enjoy your trip...it'll be great!

Posted

Enjoy the holiday Sharon. Sorry to hear of the progression but it sounds as though you have a great plan.

All the best and I'll be thinking of you,

Sharon

Posted

So sorry to hear about the mets, Sharon. Enjoy Disney and come back ready to fight! I've had buckets of Taxotere -- starts off fine but does a number on the blood counts over time. However, it really knocked the bejezus out of my tumor, so I won't complain about it too much. Good luck with treatment; I'll be praying for great results.

Trish

Posted

My dad was on Alimta, and he did pretty well except for some fatigue. He never got nauseous though :) Best of luck to you and your fight- have a great trip too!

Posted

Hi Sharon.

First, enjoy the trip!

Then, darn, more chemo..but we have a plan.

I have been on taxotere and alimta. Both were fairly easy for me as far as side effects went, For both, I needed some extra sleep and the taxotere also seemed to cause a rash (it's always hard to be certain if it was the chemo or something else).

The alimta had no effect, maybe slight progression. The taxotere seemed to stay the same size but it was interesting that the tumor was identified as different dimensions.

Good luck.

Mary

Posted

Sharon,

I had the taxotere. Something did work for me. Could it have been the taxotere? (why not??) Many get bone pain and general malaise with it. I lost a toenail on it.

Have fun on your trip. Glad you are planned for success.

Cindi o'h

Posted

I'm sorry to hear this news...but I know you can beat this! You've been a real inspiration to my mom and I and we will keep you in our prayers. Enjoy Disneyland--I'm glad you are sticking with your travel plans...cancer can get it's butt kicked when you return. XOX Candy

  • 2 weeks later...
Posted

Sharon,

Sorry I am just now reading about the fact you are back in the fight.

Alan has not had either of those drugs so I can not

add any info there.

Praying you have great results with limited side effects.

Have a Blast at Disney world :P:P

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