update
She opted for folfiri every three weeks.
We are still waiting on the biopsy results for thyroid.
It is very hard to wait and wait and wait.
I hope you all are well this holiday.
Comments
-
Tough decisions....
The good thing is that there seem to be options. I think that her decision to do Folfiri every three weeks at this point is probably a very good decision. But in order to make further decisions, you need the following questions answered:
1. Has she already had folfox? Did she respond well to it?
2. The same question goes for Xeloda/???. It would be good to know the name of the other drug.
I was never given this many options, so please let your mom know that I wish her a very Happy New Year and that things are not as bad as they may seem to her, especially having such wonderful such as yours. God bless. Monica0 -
Second Opiniontootsie1 said:Prayers
I'm sorry, dear. I know this is so hard on both of you. I'll be praying for you and our mom.
*Hugs*
Gail
I know this is so difficult for you; I wish I was as blessed as your mother is having you
to take care of her and "run interference" for her. Have you thought about getting a second
opinion from another oncologist? Also I wonder abut how much information you were given from
the docs about managing side effects........such as different things to drink if your mother
was having a hard time taking in fluids and what to do about maintaining proper level of
potassium in the body by eating certain foods like bananas? I would have to say that my
oncologist office was excellent in providing a lot of materials about managing side effects.
They can also add certain things to the chemo such as magnesium and calcium which helps.
Just tossing that out there for thought. You are in my thoughts and be sure and take care
of yourself as well; you are very important to your mother.0 -
this is our second opiniondixchi said:Second Opinion
I know this is so difficult for you; I wish I was as blessed as your mother is having you
to take care of her and "run interference" for her. Have you thought about getting a second
opinion from another oncologist? Also I wonder abut how much information you were given from
the docs about managing side effects........such as different things to drink if your mother
was having a hard time taking in fluids and what to do about maintaining proper level of
potassium in the body by eating certain foods like bananas? I would have to say that my
oncologist office was excellent in providing a lot of materials about managing side effects.
They can also add certain things to the chemo such as magnesium and calcium which helps.
Just tossing that out there for thought. You are in my thoughts and be sure and take care
of yourself as well; you are very important to your mother.
We are currently at James Cancer Center in Columbus.0 -
folfoxMonicaemilia said:Tough decisions....
The good thing is that there seem to be options. I think that her decision to do Folfiri every three weeks at this point is probably a very good decision. But in order to make further decisions, you need the following questions answered:
1. Has she already had folfox? Did she respond well to it?
2. The same question goes for Xeloda/???. It would be good to know the name of the other drug.
I was never given this many options, so please let your mom know that I wish her a very Happy New Year and that things are not as bad as they may seem to her, especially having such wonderful such as yours. God bless. Monica
She has had folfox and responded VERY well. Her CEA got as low as 8.9. After stopping Folfox and being on 5-fu avastin, CEA started to rise.
She recently had a biopsy on her thyroid which may be a met from colon cancer. If it is and they can do a thyroidectomy, well maybe that will take care of the CEA rising. SHe has no mets to her liver or lungs and virtually all of the rest of her CT results are unremarkable.
I just don't like my mom thinking that they can't do much for her now. I just want to protect her you know.0 -
Folfoxkrystiesq said:folfox
She has had folfox and responded VERY well. Her CEA got as low as 8.9. After stopping Folfox and being on 5-fu avastin, CEA started to rise.
She recently had a biopsy on her thyroid which may be a met from colon cancer. If it is and they can do a thyroidectomy, well maybe that will take care of the CEA rising. SHe has no mets to her liver or lungs and virtually all of the rest of her CT results are unremarkable.
I just don't like my mom thinking that they can't do much for her now. I just want to protect her you know.
Did your mom become resistant to Folfox, or was she taken off it due to side effects? I had to be off Folfox because of side effects, so I am now back on it (2 years after). We will see how it works. I am sorry to hear about the new primary cancer, but please don't despair. You have KathiM as a perfect example of someone who battled two cancers and won. I also agree that the dehydration/low potassium can possibly be helped with nutritional supplements and ensuring that your mom drinks a lot of fluids after chemo. I know it is not easy when you are not feeling your best, but it has to be done. I have a lot of teas, soup broths, fruit juices, etc. Anything with flavour. I hope this helps. Monica0 -
Keep hanging in there!
I have the same enzyme problem and was unable to tolerate Xeloda. Tell your mom to keep hanging in there and not give up. New things come up all the time.
Hugs!0 -
folfiriMoonDragon said:Keep hanging in there!
I have the same enzyme problem and was unable to tolerate Xeloda. Tell your mom to keep hanging in there and not give up. New things come up all the time.
Hugs!
Are you saying you have the enzyme deficiency that keeps folfiri in your system longer and makes it so you can't take normal dosage? Did you still take it at lower dosage? If so how did it work with respect to CEA level ect.? Just curious.0
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