1st Folfox w/Avastin Treatment Accomplished
My questions to all of you are: should I contact my Onc mid week to let him know what has been going on so that they can adjust the dosage on my next treatment if necessary? Does anyone have any suggestions on maybe a gentle mouthwash to help with that inflamed feeling? If you've experienced some of the same things I have, did you find your side effects lessened or increased with each treatment?
Thanks in advance for your input.
Pam
Comments
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Thanks Graci. I am going tounknown said:This comment has been removed by the Moderator
Thanks Graci. I am going to ask him about the Cal/Mag; did you get that with the day treatment or the 5-FU pump? The only ones I'm aware I'm taking are Oxi, 5-FU pump, Avastin and Leucovorin. I'll definitely do the baking soda thing. When I was growing up, if we ran out of toothpaste, my Mom always made us brush with it. I also will ask him about something for the heartburn.
Thx so much for responding!
Pam0 -
"The Mags"
HI Pam
Magnesium Sulfate worked liked a charm in managing the cold effects.
Graci has a good memory and it looks like it worked for her as well - if it does work for you, it will make your treatments so much more human and manageable. I drank cold liquids right after infusion - and Graci was able to have sundaes.
It does not work for everyone, but it is worth asking about - you'll know if it works right away.
I've heard it referred to as Cal-Mag.....my infusion center it was Magnesium Sulfate - the nurses have a nickname for it - "The Mags."
Thanks for the plug, Graci and best of luck with your treatment plan, Pam.
-Craig0 -
This comment has been removed by the ModeratorSundanceh said:"The Mags"
HI Pam
Magnesium Sulfate worked liked a charm in managing the cold effects.
Graci has a good memory and it looks like it worked for her as well - if it does work for you, it will make your treatments so much more human and manageable. I drank cold liquids right after infusion - and Graci was able to have sundaes.
It does not work for everyone, but it is worth asking about - you'll know if it works right away.
I've heard it referred to as Cal-Mag.....my infusion center it was Magnesium Sulfate - the nurses have a nickname for it - "The Mags."
Thanks for the plug, Graci and best of luck with your treatment plan, Pam.
-Craig0 -
Thanks Craig....it isSundanceh said:"The Mags"
HI Pam
Magnesium Sulfate worked liked a charm in managing the cold effects.
Graci has a good memory and it looks like it worked for her as well - if it does work for you, it will make your treatments so much more human and manageable. I drank cold liquids right after infusion - and Graci was able to have sundaes.
It does not work for everyone, but it is worth asking about - you'll know if it works right away.
I've heard it referred to as Cal-Mag.....my infusion center it was Magnesium Sulfate - the nurses have a nickname for it - "The Mags."
Thanks for the plug, Graci and best of luck with your treatment plan, Pam.
-Craig
Thanks Craig....it is definitely on my list of questions for next treatment! (I can drink really cold water but not room temperature so it's killing me on getting fluids in my body!)
Pam0 -
Your experience sounds similiar to mine
I have problems with cold in my hands and feet, and drinking cold things, except I can eat ice cream and milkshakes if I warm it up on my tongue first. But the price I pay is that my tongue won't work correctly for about 20 minutes, I sound like I had a stroke. The first 2 chemos I physically threw up, but since then, I have learned to take my zofron before I feel nauseuos, or at the very first hint of sickness, and though I still get nauseous, it is getting more tolerable, and no physical throwing up lately. The mouthwash and toothpaste that my doc recommends is called "Biotene", shop around, because the price greatly varies from store to store. Biotene also make a gum for dry mouth. My digestive tract gets really raw too, so I just try to eat things that are bland and non acidic. For me, I have only had 5 treatments, so it is hard to tell, but I think due to me paying attention and watching what I do and eat, the symptoms have slightly lessened each time. Not a huge difference, or maybe it is just my body acclimating to what is going on. Take care
Sandy0 -
Sandy, I know what you meanLove2Cats said:Your experience sounds similiar to mine
I have problems with cold in my hands and feet, and drinking cold things, except I can eat ice cream and milkshakes if I warm it up on my tongue first. But the price I pay is that my tongue won't work correctly for about 20 minutes, I sound like I had a stroke. The first 2 chemos I physically threw up, but since then, I have learned to take my zofron before I feel nauseuos, or at the very first hint of sickness, and though I still get nauseous, it is getting more tolerable, and no physical throwing up lately. The mouthwash and toothpaste that my doc recommends is called "Biotene", shop around, because the price greatly varies from store to store. Biotene also make a gum for dry mouth. My digestive tract gets really raw too, so I just try to eat things that are bland and non acidic. For me, I have only had 5 treatments, so it is hard to tell, but I think due to me paying attention and watching what I do and eat, the symptoms have slightly lessened each time. Not a huge difference, or maybe it is just my body acclimating to what is going on. Take care
Sandy
Sandy, I know what you mean about your tongue. It feels so sensitive and raw. I also can eat pudding or cheesecake even if I let it sit just a little. Not room temperature, but not freezing. I will definitely look for the Biotene. I just went in and brushed with the banking soda and it did burn a little but it feels better now. I am so glad that you think you're symptoms lessen (can you tell I'm grabbing at any positive thing I can????!!) but even if it isn't a huge difference, I'll take slight compared to what this week has been. Thanks for your input and good luck with your treatment!
Pam0
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