Starting Chemo February 2013
Comments
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Just getting caught up. Hang in there Rdrunner, sucks to get a week behind when all we want to do is get it over with! Hope you feel well soon.
Had my 4th TCH yesterday. I won't feel "over the hump" until after next week. The infusion is not the hard part, it's the week after. Thankfully I didn't have as much insomnia last night as the night of my 3rd. Hoping tonight is good too. Tossing and turning, but not wide awake for hours on end. It's impossible for me to sleep in so getting the sleep at night makes for a much better day! Hope you are all doing well, we are making progress from February to April!
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Rdrunner - hoping for the best for you..
Tangles- When I read you are a hairdresser, I totally understood why you can't go to work... I try not to be around anyone that is sick or sounds sick..
DiZZyMom - sleeping pills might be your answer - they have worked magic in my life.. a good nights sleep helps tolerate so many SE. and thank you for pointing out how far we all have come - from February to April... that made me feel better just thinking about that...
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Nancy what kind of sleeping pills are you taking? I have to start my meds Thursday for my Chemo Friday and last time I was up until 4:30am. That was after taking Lorazapam, and Ambian. I have also tried benadryl. I know I would feel better if I could get more sleep.
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Tangles - oh wow- I take ambien - it doesn't make me fall to sleep right away, but once I do I really get a restful sleep.. guess its not going to work for you..and benedryl makes me fall asleep so quickly... maybe ask your doctor for something different.
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For mouth sores my dr. recommended biotene tooth paste and mouth wash sold at any pharmacy
I'm having my 3rd treatment this Monday that means 1/2 wat through. OMG tomorrow. They cut my Neulasta in 1/2 and I didn't have the pain and shortness of breath like last time . More important didn't land in the er. I'm hoping except for no appetite that I'l be ok this time as well. Good luck to everyone
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Shasha10 halfway through YEAH! Hoping few SE and it goes quickly
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Hoping everyone heading to the bar this week has smooth sailing!
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hope all goes well for you Shasha... you mention the lack of appetite - I get that and then once my appetite sorta returns nothing tastes right... even though I can't eat near what I use to I remain the same weight.. it may change down 3 lbs then back up again.. some days I feel so bloated - is this happening to others? I guess its the steroids.. but I would have hoped with this awful chemo at least I might have lost weight
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Sasha: congrats on being halfway through. Almost there!
Iamnancy, I am on a different chemo plan then you but my tastebuds are not there either, even when I feel hungry, it is hard to eat. I have lost 6 lbs total but it does go up and down. I have tried to exercise when I can but that is not happening as much as I would like. I just try to eat what seems somewhat palatable. It is hard to find things. I am not sure how much worse the taste in my mouth will get as I go on. Ii thought it would go away for a week before next treatment but not sure that is how it will work. Good luck!
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it's official. My taste buds have crossed over to the dark side. I am not normally a fan of ketchup at all but right now it tastes so good I could just suck it out of the bottle. The really bad thing is, it's the ONLY thing that tastes good and doesn't have that bitter after taste. Milk is also my friend... my only friend. I'm not sure I can survive on ketchup and milk until the end of May.
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Heidi - makes me think creamy tomato soup might taste good to you...
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Keeping in mind everyones Chemo plan may be different my taste buds are SHOT about 3 or 4 days after treatment for about a week. Then they slowly come back and are about normal the week leading up to my treatment. Although I am hungry because of the steroids. I have not lost weight, in fact all this sitting around has made me gain a few pounds. I also think I am retaining water as my rings are tight and I have marks on my ankles where my socks are. I think I eat out of boredom sitting in the house all day. I was hoping to take a few pounds off during this ordeal but NOT! Thats Ok though I will work on it after Chemo is overwith!!!
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Tangles: yes you will! We all will get our former selves back. We have to keep thinking that. I have lost weight but I cannot do near the workouts and activity I did before this bs. My muscles are weakening and what I worked very hard for is slowly fading. It is very frustrating for sure. I hope you continue to feel better.
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Good luck today Shasha. My weight is same issue. It goes up and down, but overall I am up about 6 pounds. I can't exercise as much as I would like. And when I do have an appetite, bland starchy foods are what I crave. That plus the steroid bloat, I'm committed to the fact that I will get my old self back after chemo but not going to kill myself to try to keep it now. I got very little sleep last night and when I got home today, I had time to either go for a walk or take a nap. I chose the nap!
I hope you're all feeling well today and have a great week!
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SO gals I know this is a chemo thread but just wondered of all the sisters here with TE how are your fills going? I got what may or may not be my last fill today (460cc's) I am going to be so glad when these TE are out. I am looking at end of June. Seems like forever!! Trying to decide between the new gummy allergan 410 implants or older silicone implants. If I get the older ones I need to overfill if I get the gummy I can be about done. So what are you all getting?? Just curious....
Mary
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Tangles: I stopped at 300 cc's and have not had a fill in awhile. I have not had any problems with the TE's. I am still not sure what implants I will have. My PS and I are still deciding that. I have a couple of options, including a new one that is shaped like a tear drop and has a rough surface so it kind of sticks to you like velcro. I know a volunteer with the Am. Cancer Society who was a study for that new implant and she is very happy with it.
The surgery will not happen until at least 6 weeks after my last tx, which is May 15. The earliest will be mid to end of July. My PS won't do any surgery before six weeks clear of chemo. Good luck!
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it has almost been 2 weeks since my chemo treatment and I didn't feel too bad this weekend (other than the shortness of breath) but today I feel sickish again.. crazy.. I woke up so dry - my lips, face, feet,eyelids, arms and legs are all so dry- legs are itchy -arms flaky.. lips actually hurt ... nose bleeding, throat so sore.. I don't get this delayed reaction. Tell me, has this happened to you? this is my third treatment and I only have 1 more to go..
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Tangles... I was filled to over 800ccs in my te's. I had my exchange surgery three weeks ago and got silicon mento high profile 800cc implants. I am happy with them do far. Still settling so changing a little every day but so far so good. I go Monday for a 4 week follow up with ps. But they are so much better than the te's :-). Although I did not have much discomfort with te's.
Melissa -
Hi Nancy, I had the same thing happen. I usually feel pretty good by the end of week 2, but felt sickish and took the afternoon off and took a nap. Not sure why? I have been using Dove Visible Care softening body wash in the shower and then slathering myself with Curel Intensive Healing body lotion. I've been really happy with how it has kept my skin soft.
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Nancy: I use an anti biotic body wash then follow with a shower oil. I slather it on in the shower. Then I slather on Jergens firming natural glow lotion after I towel off. At night I use Banana Boat after sun lotion. My skin is not dry. Good luck!
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Wow Melissa- you had your TE in for a long time. Boy I am hating these things . The one side digs under my arm and they both just plain hurt. So you did not have to be overfilled? My PS told me if I choose anything but the new Gummy implants I will have to be over filled. What does high-profile mean? How long were you down after the exchange?
Ywheels- my PS said he will exchange me after 4 weeks. I'm sure I wont be 100% feeling great after 4 weeks of the last chemo, but I sure do want these out as they are not comfortable at all.
Nancy-I have lots up ups and downs. I guess that is one reason I decided it wasn't a good idea to go back to work. I went to the store with my hubby sat 2 weeks post chemo and could hardly make it through and we were just picking up a few quick things. As soon as we got out to the car I was in tears I felt so awful. I felt pretty good yesterday,17 days post chemo and thought I would walk around my block to get some fresh air and exercise. I could not make it all the way around. I was exhausted. Very frustrating from someone who used to walk 3 miles a day and go for 20 mile bike rides. I think we all have good and bad days all the way through this!!
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TAngles: You are lucky to get them out 4 weeks post chemo. My surgeon said 6 weeks, MAYBE! I will have them in from Jan 16, day of surgery until at July/August. 7-8 months! Luckily, I don't even notice mine at all. The ports on the side where the saline is injected do stick out alot though and sometimes, when I sleep I lay on them wrong and I get a twinge but nothing beyond that. I am sorry your's bother you. I think you are wise not to go back to work. It is important for you to focus on you and getting through this. It has been hard for you and you need your energy to fight back and beat this. You wil get there!
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Tangles...
Yes I had them in for a while. But I had bmx may 2012 chemo from June to nov with fills during chemo and then after chemo I still wasn't at the size I wanted so we kept filling. My ps does not fill more than 30-50ccs each time and it felt like so many fills but looking back now I am so happy she did it that way cause I had no discomfort or anything. Really never knew my te's were there. Anyway I filled until last week in jan and I was filled to over 800ccs. My ps does not really go by how many ccs u have. She goes more by size and shape and how big I want to be after exchange. She also requires at least 6 weeks after last fill to get implants which I thought was long but let me tell I after everything I love my ps!!! It took long and was a slow process but was worth it. I had an easy recover with BMX. Really had no discomfort with te's and had my exchange tuesday march 19 3 weeks ago and feel great. My surgery was 2pm I was home by 7pm. I walked into my house and my parents who were watching my kids said I did not look like I just had surgery. I did not drive til the next Monday so five days no driving but I was making my kids lunches that night after surgery out to breakfast and grocery shopping with my husband the next day. I really attribute my great surgery experiences to my ps. I took no pain meds at all after exchange. Had no drains no bandages just a steri strip on incisions. U will do fine with exchange surgery and recovery. It is so much easier than BMX! The only thing is no driving for a couple days and no lifting for 4-6 weeks.
High profile are the type of implant that has to do with more projection vs a low or moderate profile.
Any other questions let me know!
Happy to answer and help anyone out!
Melissa -
Melissa: that sounds great. I just went to 300cc's though my PS jokingly said lets do more. I was so small before, barely an A, that going bigger than a small B just didn't fit my body or my lifestyle. (I am 5'8", 133 lbs. and very active.) My te's don't bother me either. I also only did 30 cc's each time. Slow and easy was my motto. Doing it during chemo was hard enough.
I finish chemo May 15 and my PS will wait at least 6 weeks after last chemo before he does the exchange. I also plan to have my chemo port taken out at the same time. My PS said that would not be a problem. So I'm looking at hopefully the beginning of July. I am so happy to hear your exchange surgery was easy and you recovered quickly. I hope for the same and my PS is also awesome. He has taken great care of me!
Tangles: good luck!
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Have any of you on taxotere experienced neuropathy in your fingertips? It seems to just be setting in for me. I've heard of using l-glutamine but was wondering if any of you have any thoughts or other suggestions?
This morning was a nightmare :-( Tuesdays (day 5) have typically been my worst day and I sure felt like I'd been hit by a truck this morning. My daughter was being extremely difficult and I was not reacting well. Then it took me 5 minutes to get my son's socks on because my fingers wouldn't work. I was in tears, literally. Oh well, I just need to rest. 3.5 hours until my husband comes home and I will do just that.
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Ywheels you having a chemo port having taken out? I thought about having mine out during the exchange surgery but I have to do the HER2 every three weeks for a year so maybe I should just keep it. I do not like it, but getting poked every three weeks for a year doesn't sound fun either. I do not have a port on the side with my TE. I had a friend who had that a few years ago and complained about it. I asked my PS about it and he said he doesn't use those anymore, so my port for fills is right in front under the skin. You cant see it at all. He uses a magnet thing to locate it and then pops the needle in. No pain at all. I saw my sister today and she said I think you need some more fills. I need to get some other opinions as I am on the fence. For every good review I read on the gummy implants I then see a bad review. decisions decisions.........
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WEll no chemo for me again this Friday.. finishing up day 9 of fever. Still cant find anything wrong. Had a bunch of more test today. The kicker.. my o2 SAT was 84% but my chest xray they made me do immediately is clear and my lungs sound good..they have put my on TAmiflu.. shaking my head but willing to try anything at th8is point.
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Rdrunner so sorry for your delays, how are you feeling? I heard of another lady with similiar problem I dont think they ever figured out what was causing it but they were able to get rid of it. Hope it goes away soon and you can continue
I had treatment 3/4 last Wed and am suprised at how much better I feel this round. Not near the muscle aches or joint pain I had last time and a little less fatigue. But that shortness of breath and dizziness likes to stick around. One thing thats really bothering me is not being able to concentrate or prouncing words right and the struggle to find the right one. I think my brain has turned to shit and its really upsetting. The other day I was joking with my mom because I was litterally spacing out on a rock in the back yard with moss on it. You know watching moss grow
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Damn, Rdrunner I hate to hear that. I hope they get it resolved for you soon!
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Mo said something like this is usually an infection or what is called a drug fever. Infection isnt really evident yet which you would think after 9 days it would be. She said some people get fevers in response either to chemo drug or neupogen (same as neulasta but given over 8 shots).
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