Chemo May 2011
Comments
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Marybe, a doorbell- exactly! A big doorbell!
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Cyborg - did you wear something between your head and the wig? I'm thinking it would be scratchy if not.
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Ah, I have a beautiful view of the spaceneedle and a peek a boo view of water. The night lights are gorgeous! Up late because a bit nausous, just took some ativan, so I should be sleepy agin soon, Hard to sleep in the hospital without my doggies and hubby. Started the ac drip about 8pm, so I won;r br out of here until after 8 pm Saturday. I was hoping for an earlier start. as I was in the hospital by 12!. I am shedding, I would almost say profusely, hair soesn't really look thinner yet, but it will! I leave a trail on all pillows. The clippers are coming out soon, as I do not tolerate the shedding very well and would rather just get it over with.
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Well the hair has decided to depart at day 19 post FEC and luckily it was a sunny, windy day - I sat in the sun and had a great scratching session- bliss without the clean up as my long suffering strands decorated the garden lol. I start my fast tomorrow in preparation for chemo no# 2 on Tuesday. That will be hard as I have been enjoying my food now my sense of taste and smell is back to normal. Funny but I think that chemo has cured my Samters syndrome. I rarely have a functioning sense of smell or taste as I have chronic inflammation of upper airways, asthma and react badly to aspirin or NSAIDs.
I have been working with only a couple of days off. I took a month off after the BMX and that was vital to recovering enough to tackle chemo.
I hope everyone is having a restful weekend and not feeling too blah! -
Well the hair has decided to depart at day 19 post FEC and luckily it was a sunny, windy day - I sat in the sun and had a great scratching session- bliss without the clean up as my long suffering strands decorated the garden lol. I start my fast tomorrow in preparation for chemo no# 2 on Tuesday. That will be hard as I have been enjoying my food now my sense of taste and smell is back to normal. Funny but I think that chemo has cured my Samters syndrome. I rarely have a functioning sense of smell or taste as I have chronic inflammation of upper airways, asthma and react badly to aspirin or NSAIDs.
I have been working with only a couple of days off. I took a month off after the BMX and that was vital to recovering enough to tackle chemo.
I hope everyone is having a restful weekend and not feeling too blah! -
Robyn - I see you fast before chemo. Tell me more about that, please. I have my first treatment Monday, and have been contemplating whether fasting would help.
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Robyn_S I too am post FEC but still have my hair it's day 13 I hope that it will stay till day 19 like you.
Have been feeling way better too. My mom had breast cancer 16 yrs ago and she has asthma and she didn't have an asthma attack in 5 years, she thinks the chemo cured her for those years. I already got a turban and a hat but still need to get more stuff and a wig soon. Hugs and kisses to all, hoping everyone one has a good weekend.
Thanks Cyborg, you're our inspiration in this folder.
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Yes I would like to hear about fasting as well. Chemo for me Tuesday. Still feels like a bad dream!
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bkj66: Your place sounds like my place...6 dogs, mostly rescues that appeared one day, down to only 2 cats due to old age and no recent appearances, and, yes, chickens, one lonely old pygmy goat whose lifetime companion just died last week, cockatiels and a cockatoo with beak-and-feather disease (also a rescue)...who am I missing? Oh, yeah, down to one very old pigeon, who has someone avoided the hawks that think I had pigeons just for their hunting pleasure. And in my high school classroom are my snake, walkingsticks, toad, tarantula, turtle, and geckkos...DH does the plants, I do the animals. Mostly, I've been able to do it still, except for a few rough days here and there. We'll see how the poison affects me as I hit TCH#3 this Friday...oh, and I did have human children...just added them to the menagerie, is all. They grew up just fine.
Hugs to all of us with the coming week's adventures in the poison chair! -
Sunshinyday: My onc center is a doc who's also a hematologist, and the chemo room is not big enough to hold the 4 lazy boys plus paraphernalia it has. Rural, plus. When I mentioned ice for nails, I got a shrug from the nurse, incredulity from the onc nurse, and 'whatever' from the doc - I like the guy, mind you - so I bring my flexible ice pack in a baggy and my DH pins it to my toes, and I hold my fingernails on a small icepack...heck with them, I'm the one's gonna suffer, so I'm willing to try what the big centers seem to take for granted and provide for their clients.
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Lifelover; dark green is the nail color I chose and a gray opaque color as well.
Bought a couple of baseball hats today. One bright pink and one lime green. Happy. Most comfy in baseball hats hoop ear rings and pretty lipstick. Née Cee I have a soft cap that I wear with the seems outside and it really helps. I purchased it from the wig place at UCLA. Very comfy. Wore it for quite a few hours yesterday. -
Just finished Doppelgangster - Stephanie Plum- type humor in a vampire world, and Blood Challenge, part of Eileen Wilks series, FBI agent and werewolves. Fun, escapist, the bad guys aren't human or cancer.
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re: insurance and Neulasta. My Blue Shield will only pay for Neulasta, not Neiupogen, and only once my counts dropped sufficiently. Then they okayed a shot after each TCH, so every 3rd week - my onc said once my counts drop like that, it'll happen each time.
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Hi, Katarina! Where in the Bay are you? I'm a couple hundred miles up the 101, but a son lives in Emeryville and a daughter attends Mills. And summer's finally arrived!
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Fasting sounds interesting --- are u just fasting with water or juice?
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bkj66: I've been standing in the yard watering, and had a Cooper's Hawk swoop in and latch on to a barred rock chicken - these are big chickens! Couldn't get off with it, but sure did give it a try...We've lost dozens of free-flying pigeons to the hawks, and I'm sure a number of our cats have disappeared over the years to bobcat, box, coyote, puma, bear, feral cats...it makes for a curious mix of enjoying country living right along with the price of protecting our domestics. I'd keep my chickens cooped for a few months until the coyote lose interest, which they will.
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The fasting is for 62 hours pre and 24 hours post chemo. There is a thread in this forum about this but basically there is research by Dr Valter Longo of USC which in a series of case reports found that chemo SEs are lessened by fasting. The theory is that during fasting low glucose levels trigger a protective mode in healthy cells like hibernation, while cancer cells do not listen to these signals and continue to do their thing. The effect during chemo means that healthy cells are much less affected by the chemo drugs while the cancer cells are still targeted effectively. The result is less damage which we feel as reduced SEs, to healthy cells.
I have discussed this with my MO last week and she was happy for me to try this. There are a number of clinical trials- one at the Mayo clinic is due to finish next 2012 which will be too late for our treatments, but I have read the research and would qualify for inclusion based on BMI and general health. I have contacted windlass who has done treatments with and without the fasting nag reported dramatic differences. Again, would not do this without my MOs knowledge and approval.
The fasting bit is easy- no calories for 62 hours pre and 24 hours post infusion. Keep up fluids! - black tea. Water, diet soda, black coffee. The mayo clinic trial is doing 4 interventional arms with 24 hours fast pre chemo tx; 48 pre; 48 pre/24 post and control no fast.
If you search for ' Nutra / Valter Longo' you will find his company web site which has his research papers conveniently available in PDF.
My motivation as I am missing my breakfast is simply to keep as healthy as possible both during and after chemo- the knowledge that the drugs will affect the heart muscle and leave an increased risk of leukemia is motivation enough to do something to protect the healthy cells that have to carry me to an old age!!
I have had one treatment without fasting so it will be interesting to contrast with fasting intervention!
Another windy day here in Oz so the rest of the hair is in the garden! Hats n scarves from now on!
Time to cook Sunday dinner for the crew- chicken and potato bake.
Happy Sunday everyone! -
I just updated a picture to my profile. This is the picture for the day after I had the port put in (May 17, 2011). Day before I had my lung biopsy. Me with the long hair. It is short now.
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Nice picture 38 years old, I bet your hair looks cute short too!
WOw Jackifp, your house does sound like mine! Yeah< i used to get very upset when I lost a chicken to a predator, but now am coming to terms to how that is the food chain. I will still do all I can to protect all, and yeah, for now, the chickens must stay in their run during the day and the coop at night. Neighbor even spotted a couple of bear cubs, I thought we had been seeing bear scat around...
Well, looks like I have 2 more hours in the hospital.
Robin, the fasting sounds very interesting, but 62 hours before chemo? I don't know if I could make it, I get shaky and weird just without eating for 12-24 hours. I wonder if it would do any good just to eat really light?
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That seems like a long tine to fast so the chances are that it will protect the heart? That is very interesting.
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Cyborg- The theory behind fasting is to give a push for the natural protective mechanisms that healthy cells possess and cancer cells don't due to the oncogenes being jammed in the on position. The body has to be stressed to switch to famine mode which is induced by low blood glucose levels. This initiates the protective pathways.
BKJ66- The mayo clinic trial also looks at shorter periods (24 hours) of fasting but I would not count on a light diet producing the protective effect. the 62 hours pre/24 post comes from Dr Longos research and what he has advised Windlass who has communicated with him.
I have been lucky in that my appetite is somewhat diminished and being not too enthused looking ahead to the next week after feeling so good for the last 10 days! Only 5 more to go!!!! -
So I will start after 8or so this evening and try through Monday unless my onc says no. Are u taking steroids too? I start tomorrow with the steroids.
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Cyborg- I am doing FEC and get steroids via infusion and dexmethasone tablets for 2 days after. You would need to discuss with your MO if you have medication that needs to be taken with food
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Hello
I have been reading the blogs for awhile now and finally decided to write. I do not havecancer but my mother does. She is my best friend and I have been by her side through it all. This is the hardest thing I have ever endured and I can only imagine how it must feel for you all. My mother has been on several chemos and just got her scans and they were not good. Her breast cancer mets has spread to bones,lungs and now liver. It scares us to know that the liver is involed. She has been fighting for 4 years with the reoccurance. Originally diagnosed 20 years ago and had a lumpectomy, chemo and radiation. thought she was good till 4 years ago.
Doc says it will never go away but we will do what we can to slow it down and maintain a quality of life. She just finished the new drug Halavan but didnt work for her. We are so disappointed.
She is suppose to try the drug Doxil and he said the side effects will be harder than Halavan. She is at the point now where the SE have been difficult to handle now. So the thought of it getting worse is hard to take. I know she has been thinking about not doing chemo anymore but then she changes her mind. Going back and forth this past week. Its very hard to accept this especially when your only 64 yrs old. Wasnt the plan for after retirement.
I keep telling her to join the blog or group so she has a way to get it all out and vent and question others feeling the same way. But she says no and wants to be private. I feel she has so much to say but she holds it in to protect me.
If anyone has any info or encouraging stories about this chemo Doxil, please let me know. I will keep trying to get her to join or at least read this. I love her so much and will be here for her always .
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viacheryl, I am so sorry to hear about your mother....her story is a lot like mine and I have mets in exactly the same places she does, liver, bones and lung and was lst diagnosed in 1990. I am doing havalen now and am sorry it did not work for her. Later today, I will send you a PM....do you know how to do that? Hang in there, both of you. Marybe
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viacheryl
There is another thread that is stage IV met. I was reading there about survivers of 20+ years. several 13+.
I am waiting on results from my lung biopsy. When they did the PET scan they found spots in Lung liver rt leg and left leg. I was only diag March 2011. So I am not quite sure how she feels about having BC then being in remission. I went from finding a lump on my own then the lumpepame (sorry about spelling) to waiting on test results to find out if it has met.
Talking and reading here does help some, to know you are not the only one.
Take care
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Thank you 38 yearold I will check out the other thread you spoke of, good luck with your tests. Keep me posted.
Marybe Im not sure about how to get a PM, what do I need to do ?
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I don't think I will be trying the fasting as I have already lost enough weight and am concerned that I won't be getting enough nutrition as I constantly have to remind myself to eat as it is.
I still have another week before my next treatment. Good luck to all of you starting at it again next week!
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My port lump looks like I've got a bottle cap stuck under there...
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At the top of the page there is a black line, beneath the red/wine or whatever that color is....it will say Favorite Topics, Home, Acitve Topics and the very last box says Private Messages . If you have a private message there will be a little Number in parentheses and you click on that box and your PM will come up. I still intend on writing to you, but right now am just waiting for my husband to see if he can fix the sweeper belt so I can vacuum before doing the rug shampooer again.
I myself, would worry about the fasting just because I would think that if you have nothing in there the chemo might hit you that much harder and if you would get sick, what is going to be in there to throw up....dry heaves are no fun. But I have never had nausea so maybe that is not the SE you are trying to avoid.....but isn't that an awfully long time to go without food? My onco is always asking how's your appetite?, not that I ever have any problem in that respect, but he wants to make sure I am eating and always wants his patients to eat so they keep their strength up.
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