First Folfox treatment
Comments
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Congratulations!
Just anted to second the suggestion to keep a diary. It really helped me (bad memory). I kept track of the food I ate, (what worked, what didn't), my mood, sleep patterns, etc. It helped me to remember what worked during each two week cycle.
Best, Vita
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ALKALINE WaterColoncancerblows said:Ana,
I'm a big water drinkAna,
I'm a big water drink anyway so have been chugging that down. Don't want to get dehydrated. I ended up buying a Brita water bottle and have been filling it with lukewarm tap water so that's helping a lot.
Hey! This is to all of you, I'm still trying to learn my way around the site, but I just wanted to chime in on the water topic....You all probably already know (I didn't, as I don't know A LOT of things, still learning) that "Alkaline Water" is suppose to be the best thing to drink. I had never even heard of it, but I've been reading "The PH Miracle" by Robert O. Young, & it talks about how important having the right PH amount in the water you drink is. It recommends having a PH of 9.5. I found some jugs of water at Kroger, it's called "Hydrate" (how appropriate ),it has a high PH of 9+, it says it hydrates 6 times faster, says it's "Alkaline Ionized Water", it acts as an effective antioxidant, reduces acid buildup in the body, & increases the body's alkalinity. A friend of mine told me about the PH Miracle book & it really is amazing. I'm not gonna try to push it on anyone, obviously you can use your own judgement, but "I" feel that it's something worth looking into. Anyway, I just wanted to share the thing about the water. Hope this helps. Kris
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New to Site
Hi all, I am new to the site so if I am not following etiquette please let me know. I was diagnosed March 1 2012, rectal. Lymph node involvement. 7 week pre surgery chemo/radiation. Big, bad surgery in July. Petscan showed lymph nodes were clear at the time so they only took out part of them...petscan wrong 100% removed were still involved when the path came back so they assume what was left was also still involved. The surgeon found pelvic wall involvement as well that had grown while I was having the first round of chemo/rad. So not a very good prognosis. Started chemo again in August, 12 treatments, down to one left. Handled pretty well (some tiredness, some narly pain for a few days each time) until the last month, neuropathy exploded, hands and feet, much more tired, much more pain etc. Ready to be done!!! Last treatment scheduled the 26th through the 28th of this month. CT March 11th, results the 15th...wish me luck! My infusions are 200 miles away, my surgeon 400 miles away, so done a bit of traveling in the last year. Husband is also dealing with stage 4 prostate cancer diagnosed at 55. The same age that I was diagnosed... Bummer. Looking for people that have had radical APR, permanent colostomy that nothing fits, very sunken and retracted, as well as herniated.
I remain positive!!! and confident!!!
Laura
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Any idea how to find it ingizzyluv said:ALKALINE Water
Hey! This is to all of you, I'm still trying to learn my way around the site, but I just wanted to chime in on the water topic....You all probably already know (I didn't, as I don't know A LOT of things, still learning) that "Alkaline Water" is suppose to be the best thing to drink. I had never even heard of it, but I've been reading "The PH Miracle" by Robert O. Young, & it talks about how important having the right PH amount in the water you drink is. It recommends having a PH of 9.5. I found some jugs of water at Kroger, it's called "Hydrate" (how appropriate ),it has a high PH of 9+, it says it hydrates 6 times faster, says it's "Alkaline Ionized Water", it acts as an effective antioxidant, reduces acid buildup in the body, & increases the body's alkalinity. A friend of mine told me about the PH Miracle book & it really is amazing. I'm not gonna try to push it on anyone, obviously you can use your own judgement, but "I" feel that it's something worth looking into. Anyway, I just wanted to share the thing about the water. Hope this helps. Kris
Any idea how to find it in Maine?
Judy
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Cyn
I'm glad it's going we'll for you. I was one of the lucky ones too, just the cold and jaw pain, and oh, in case you get them sometimes a twitching of an eye, or cramping of hands or legs, not a painful cramping, but they would sometimes draw in (my hands) and my legs would not quite behave right but it does go away after a few minutes.
may the force remain strong in you, LOL.
Winter Marie
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No, sorry....wawaju04976 said:Any idea how to find it in
Any idea how to find it in Maine?
Judy
No, I don't....I just happened to run across it at the grocery store. I'd say they sell it at the health food stores though. You can also buy PH Drops to add to your water to make it have the right amount of PH. I've only seen those online, but again I bet the health food stores sell them. I'm gonna be checking around here to see if I can find the drops, because the gallon of water I bought was almost $4.00. (can't afford that!) Good luck & please let me know if you find it! Kris
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To: Laura (swordranch)swordranch said:New to Site
Hi all, I am new to the site so if I am not following etiquette please let me know. I was diagnosed March 1 2012, rectal. Lymph node involvement. 7 week pre surgery chemo/radiation. Big, bad surgery in July. Petscan showed lymph nodes were clear at the time so they only took out part of them...petscan wrong 100% removed were still involved when the path came back so they assume what was left was also still involved. The surgeon found pelvic wall involvement as well that had grown while I was having the first round of chemo/rad. So not a very good prognosis. Started chemo again in August, 12 treatments, down to one left. Handled pretty well (some tiredness, some narly pain for a few days each time) until the last month, neuropathy exploded, hands and feet, much more tired, much more pain etc. Ready to be done!!! Last treatment scheduled the 26th through the 28th of this month. CT March 11th, results the 15th...wish me luck! My infusions are 200 miles away, my surgeon 400 miles away, so done a bit of traveling in the last year. Husband is also dealing with stage 4 prostate cancer diagnosed at 55. The same age that I was diagnosed... Bummer. Looking for people that have had radical APR, permanent colostomy that nothing fits, very sunken and retracted, as well as herniated.
I remain positive!!! and confident!!!
Laura
I see that you have specific questions about APR and colostomy.
Please don't hesitate to start a new topic so that you get answers to your questions. There are very experienced people here that can help. Just put in your topic line something to draw their attention to, like "questions on APR and colostomy".
Not everyone here has those, so you want to catch the attention of those who do, so that they can jump in and help you.
You are very far away from your doctors so you will benefit from an internet forum like this.0 -
Double blowswordranch said:New to Site
Hi all, I am new to the site so if I am not following etiquette please let me know. I was diagnosed March 1 2012, rectal. Lymph node involvement. 7 week pre surgery chemo/radiation. Big, bad surgery in July. Petscan showed lymph nodes were clear at the time so they only took out part of them...petscan wrong 100% removed were still involved when the path came back so they assume what was left was also still involved. The surgeon found pelvic wall involvement as well that had grown while I was having the first round of chemo/rad. So not a very good prognosis. Started chemo again in August, 12 treatments, down to one left. Handled pretty well (some tiredness, some narly pain for a few days each time) until the last month, neuropathy exploded, hands and feet, much more tired, much more pain etc. Ready to be done!!! Last treatment scheduled the 26th through the 28th of this month. CT March 11th, results the 15th...wish me luck! My infusions are 200 miles away, my surgeon 400 miles away, so done a bit of traveling in the last year. Husband is also dealing with stage 4 prostate cancer diagnosed at 55. The same age that I was diagnosed... Bummer. Looking for people that have had radical APR, permanent colostomy that nothing fits, very sunken and retracted, as well as herniated.
I remain positive!!! and confident!!!
Laura
I am so sorry to hear that both you and your husband are suffereing this journey. That has to be so hard.
"Ready to be done" Oh, I hear you, but i'm only on treatment #3.
I also have to travel 300 miles round trip. All of my Doctor's are in the big city. I'm so glad that I am on a two week schedule (until the raditation).
Good luck.
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