Is There A September 2011 Chemo Group?
Comments
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Kelli - Where do you get unsweetened coconut water?
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Kimberly - I get mine at Costco. If you have an hispanic section at your grocery store, you should be able to get it there. Some of them even have little chunks of soft coconut in it. It is definitely my beverage of choice!! Oh, some healthfood stores carry it as well. I hope you can find it.
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Hi everyone, first session down and all is well. Got high as a kite on a benadryl shot so that made it easy to relax. I am biotene rinsing and hydrating and we will see how it goes:) My onc has heard of the claritin thing but says they have not been able to figure out the connection. But, he says there is no reason not to take it so go for it.
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Oh, Kim, I'm sorry to hear about your headache! I've been having minor headaches -- nothing like after treatment -- and I'm just going to go with them being stress-related at this point. I am just very curious to see what happens after treatment #2, which I think will be on the 27th.
Interesting about the Claritin -- the surgeon who did my lumpectomy recommended it without reservation, but I don't believe I've heard any mention of it from my MO or anyone at the treatment center. There seems to be this mysterious "knowledge gap" between some physicians. I can't report on its efficacy, though, as it appears I'm going to be spared the shot.
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Good evening ladies! I am glad that you had a good chemo day Cooka! That's great!
Kimberly - Thanks! I am feeling normal again. Must have just been a low day. And my voice is returning. Still not all the way back, but close enough to yell at kids on the bus today!!!
Shelley - That's so great! Almost there girl.
Still trying to build my blood cells back up. Trying to eat lots of red meat. I've got to get me some Ensure milkshakes. I'm sure that would help too.
Have to work at the convenience store tomorrow so it will be an early night tonight. The weather here is awesome! Great fall evening. I have all my windows open and the a/c is off! Yeah! Lower electric bill!
Hope you all have a wonderful day tomorrow!
HUGS!!!
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Hi everyone - well I learned today that I'm not going to start chemo until 9/30. I guess my oncologist didn't realize that I was only three weeks out from mastectomy and you have to be four weeks out to get in the clinical trial that I'm participating in. I have to admit I'm kind of glad. This way I'm going to have my treatments on Fridays instead of Mondays. My doctor gave me Ambien today because I haven't been able to sleep. Are any of you on it? Any SE's? I live by myself and don't want to wake up tomorrow to find out that I've been up and about during my sleep.
When it first came out I seem to recall hearing that people did some crazy things on this medicine. Please let me know.
I hope all of you that had treatments today are doing great.
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carla, i take ambien 10mg for sleep,no SE for me. it helps me fall asleep, i still wake up a couple times a nite to go to bathroom. after yrs of insomnia,it is a blessing for me nothing else works for me.
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Hello,
I am joining the September group, wow! I start TAC on Monday every 3 weeks x6! Seems like most of you are not on all 3. Can anyone help me understand why so varied? I realize every case is so different but I am totally confused, once again! Also, is anyone doing any homeopathic things in conjunction with chemo? thanks so much
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Hi all my wife started here first FEC chemo treatment today and she is taking nausea medication and is not taking it well. treatment finished at 1pm and by 3:30pm she threw up. I am trying to keep her drinking water sh has only taken down 1/2 glass since 5pm and has been sleeping of and on since then. is there any recommendations on how to help her though this nausea. will it subdue by morning?
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sarasowise, good luck on Monday! I start on Monday too, but I'm doing TCx4. The regimes are varied because each person's stats are so different. I was going to have to do TACx6, but when my MO saw that I was trying to avoid chemo he changed his mind.
Also, my SN was negative, but 2 axillary nodes were positive and my oncotype was 22. These stats, along with 1cm, etc. got me the TC route. Some ladies are HER+ and then there are those who do chemo before surgery and then chemo after surgery too.
I have been seeing an acupuncturist for the past 5 years. She's great for a pinched nerve, but also helped me through some emotional stuff. I've always been into more natural ways of healing. Of course with cancer, I'll deal with some less than natural stuff too :-) -
Chris - If the nausea and vomiting persist and she is not able to take fluids, I would call the oncology doctor for professional advice, even if it is the middle of the night. Somebody will be on call even if it is not her doctor.
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Hi All,
Kimberly1961, my onc also didn't know about Claritin, but told me to go ahead since it wouldn't hurt anything. I have had some bony pain, but not too bad. I guess I expected the SEs from chemo to be really incredibly bad, so I was willing to put up with the bony pain. I might try on the next round.
I am day 15 TCx4, and I have to say that the last few days I have been feeling my normal self again. Neupogen shots ended a few days ago, and since then I have been feeling pretty good. I ran out of the thrush mouthwash, and it came back, so I got more. I guess this is something that will stay with me for the duration of my treatment. Also, taste is still off. The big thing for me is that my hair started falling out in earnest yesterday morning in the shower. I am almost completely bald now. I have some nice head wraps, and a wig that I am wearing all the time now. Also, I got some "disposable hats" to sleep in, because I am losing so much hair in the night. The hat kind of catches the hair.
I went for my 2nd acupuncture treatment yesterday. I still don't know if it is helping or not. I can't tell if I'm feeling better because the chemo is wearning off, or if the acupuncture is giving me something.
Chris, my onc gave me a supply of injectable anti-nausea medication, and told me to call the home care nurse to come inject it if I was unable to keep the pills down. I think they worry more about dehydration if the nausea persists. I was really worried about nausea because I had it really bad after my mx surgery. They gave me anit-nausea pills before they started my chemo infusion, and then I was taking them for 3 days afterwards. My nausea after I stopped the pills was very low level and manageable. I was only sick once. Good luck. I hope your wife is feeling better soon!
Hugs to everybody! Have a lovely weekend :-)
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Chris, I hope your wife improved through the night. My MO gave me a script for Compazine to have on hand if I started vomiting. I am round 2, day 1, and have not vomited. For sure the dehydration is the big worry so please call doc if she has not improved. None of us should vomit. That is old school.
Suz39, you had the hair thing exactly the same time as me! Day 15 we shaved my head because watching the hair fall out was more traumatizing to me than just getting rid of it. I am wearing scarves and hats and little chemo beanies around the house. I bought a really nice wig but because I still have some stubble I am afraid the wig will itch. Plus, I sorta look more like me with a scarf than the wig and am reluctant to change my appearance so dramatically. Weird, cuz I thought I would only wear a wig when out and now am sorta proud of the scarf/hat look. Shows how much good it does to plan....reality can be so different!
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Chris, I hope your wife is feeling better this morning. Please let us know how she is doing. The study drug that I am taking twice a day is known to cause nausea so my doctor told me to just take the nausea pills proactively. This has helped me to stay ahead of the nausea instead of waiting until I start feeling the twinges. I'm sure your wife's doctor has some good advice for you.
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So my first chemo treatment went okay yesterday...just a few minor things...Number one...I really do not like my oncologist...I didn't think I liked her when I first met her either, but thought maybe I was just mad at the messenger (didn't think I would need chemo) so gave her the benefit of the doubt..until yesterday. I updated her on a change in my meds (thyroid meds, nothing to do with her but felt she should be aware..) and she got VERY snippy and said "Well OK Dr. (fill in my last name) since when do you just do that without the consult of a doctor?" So I told her that I am not an idiot and I did it with the consult of my FAMILY doctor, who prescribes in the first place.
Also, I asked for some ativan with my premeds since the steroids/nerves literally made me feel I was coming out of my skin and she said no. Well Iinsisted so I got it and even the chemo nurse said all the other dr's in the practice will give it if patient asks. Needless to say, I am switching to another dr. in the group...one that my WONDERFUL chemo nurse recommeded. Turns out I am the 3rd in a month to switch from that dr.
So, as far a s the chemo went, was pretty smooth but from the moment I got home felt like a big brick is sitting in upper stomach. Have been going to bathroom ok, and did hydrate like crazy, and took a compazine last nite and this morning. It's just a weird feeling. Also, have a weird little cough this morning..almost like when your;re waterlogged after swimming? But other than those, feeling ok...oh also weird pink flush from face to chest and arms... All in all it's ok. Glad to hear everyone else's seemed to gorelatively smoothly. Oh and the Clariton thing is all over NJ, it's even written in the recommendations from my nurse navigator and from the onc office....funny how different states are. I have my shot tomorrow morning at 8am and I plan on being on Clariton at 7!
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Well my first chemo yestderday went good, I was more scared than anything.. No problems at all.. Gosh easier I thought than many many times of Just gettting blood drawn.. or just putting in a IV for surgery.. So I guess my port was a good good thing for me.
Today, SO far, I am just super super tired. My legs ache a little, I am just kinda relaxing in m recliner drinking one water after another... Pee is getting ligher in color each time..
Hope to hear the others how yesterday went..
I go on Sept 27 for my blood work to see how I dipple.. and where they are at
I was suppose to have my expanders filled yesterday tool, but the PS held off as she wants me alittle more healed,,, So the 27 she will relook.
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Glad to hear it went well for you motheroftwins and Jersy. I felt pretty good yesterday but think I may have to take my nausea meds today...I had that coughy heavy brick feeling a bit but I felt better after I went for a walk. My dog had general anesthesia for a tooth extraction while I was getting my infusion so we are spending the day gimping around together:)
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So glad Motheroftwins, cooka and Jersey did OK yesterday. My #1 chemo on yesterday was OK also. I literally did not sleep one minute of the previous night because of the steriod so when I got home, I crashed. It was a long day putting in the port and running everything slowly-around a bit longer than 12 hours. My legs ache also and I feel very spacey with a feeling like my sinuses are filling my head. Jersey- so glad you switched oncologist, you have to go with someone you can trust and that you feel right with. Better to do it now than later. I am taking clariten tomorrow when I take the Neulasta shot. I can wait until Sun because my chemo ended so late. Hope everyone has a good night.
rjbaby69, are you feeling better?
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Findingsolace glad to hear you were finally able to get some sleep. it's weird but the steroids have no effect on me...I take them at night and go right to sleep. My onc does not have me scheduled for neulasta because my WBC count is 10...does your onc just schedule them regardless of the count?
Anyway, good to see we all made it through the first day pretty well! Take care, hope your shot goes ok.
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Welcome Sarasowise.
JerseyL and Cooka - I had the chest thing going day 3, felt like I was hit by a bus last night and this morning with flu-like, everything aches, sore throat, icky chest, headache, skin and skull aches. I was chilled sleeping in my sweats, 2 shirts and a hoodie sweatshirt. I had the hood up and still had my head hid under the covers to keep warm. I I took a leftover pain med today to get through this and am feeling considerably better and keeping mobile. All the aches are down compared to middle of the night and this morning. I did still have a little bone pain also despite the Claritin, knees, back, and skull, but not too bad. I wonder if it would be worse without the Claritin but I am not going to find out. Jersey, I am glad I have plenty of leftover pain meds from surgery. No one should have to go through such difficulty over getting a med they need to get through treatment. I am sorry to hear that your doctor gave you a hard time about the Ativan. The same kind of thing you are going through is what made me hoard my post surgical pain meds a bit, thinking I may need them later and they might not be as sympathetic to the chemo pain and discomfort.
Suz39 - Thanks for updating us about your hair situation, as you are a little further along. You are really able to wear a wig all the time? I've never worn or even tried on a wig yet, but I just didn't think they would be comfortable enough to do that. I bet you look great. Time for me to go wig shopping too I guess.
Wondering how CCJJ is doing. Hopefully she is just busy with her kids.
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It is nice to see we are all doing pretty good. I had my first round yesterday and for the most part all is okay. I have been keeping up with my kids pretty easily. My mom is taking them this afternoon so I can nap. I just took my neulasta shot. I did take clartin as well although no one in my MO office or any of the chemo nurses recommended it. I am really working to stay ahead of the nausea. I havent had any so far. They told me to take Emend and something called dexamethasone in am for the first 3 days. They also gave me two rescue nausea meds. compazine which does not make me drowsy. I took that around 2:00 even though felt fine. They also gave me Lorazepam which does cause drowsiness. Took that last night around 10:30, slept great. Plan to take again tonight whether need it or not. The chemo pharmacist told me not to be afraid to medicate right now. This is a time to take what you can. I also took a tylenol. Cooka, I believe neulasta is only for those that are getting dose dense (every other week) chemo.Then its automatic no matter what. If its every three weeks, then I believe its only if they feel your counts are in danger. I might be wrong. Chris, I am very sorry to hear of your wife's Nausea. Hope today is better. Stay strong everyone. We have started which means we are that much closer to it ending,
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FindingSolace, Cooka, JerseyL, CCJJ, and Mother of Twins: So glad that it sounds like things went mostly good with your chemo. I start in a little over a week, so I am relaxing as we speak just reading about your experiences. I hadn't read about the claritin but now that I have I will make sure I have it available ASAP. Hope every continues to do well and that things go better with the new onc Jersey.
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Hi Ladies,
Kimberly1961, I don't wear the wig all the time, in fact I can only wear it for about 30 minutes before it gives me a really bad headache. This upset me, since I spent so much on it. On Friday I went for lunch with a girlfriend. I brought my headscarf in case the headache got too bad, I would go to the washroom and change, but I found that while I was eating, the wig didn't cause a headache. Maybe because your head is constantly moving while you eat. Anyway, that was a relief, because maybe if I need to, I will chew gum or something.
For all you ladies who just had your chemo, I'm sending good vibes your way. I found the idea of chemo much scarier than the actual chemo. Day 3 through 6 were the worst for me, but as Fieryred said, something like a bad hangover. After day 6 I started feeling better every day.
One of my friends told me a really amazing story about her brother in law who was diagnosed with cancer when he was really young, 18 or something. He had many rounds of cancer, and surgeries, and she told me that he has almost no lymph nodes remaining in his body. She describes him, at 40, as being as strong as an ox. He told her to tell me to have faith in the body's amazing ability to recover and rebuild. Now that I am on the recovering side of my 1st chemo, I am really feeling this buoyed by this story. Good luck everybody :-)
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Hello all.
Glad to hear that for the most part we're all coping pretty well with everything. Day 6 today for me. The last two days weren't that great. Felt pretty crappy(still kinda do), but like everyone says it's doable. Hugs to you all!!
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ccjj - I have been taking a Lorazepam at night to help me sleep and to fight nausea. Until this diagnosis, I was one of those people who never took anything! It was very difficult for me to admit that I might need something for the anxiety. I'm getting over that slowly.
Take care everyone...
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To all that replied to my message, Thank you.
So it has now been about 36 hours since my wife's treatment of FEC. she finished on Friday at 1pm
The anti-nausea meds she was proscribed are Ondansetron 8mg, this was the med that she did not hold down yesterday at 5pm.
The next med is Prochlorazine 10mg, this med I think is causing the vomiting. I did go out and get this med in suppository form but she has not taken it.
The last med is Dexamethasone 4mg to be taken twice a day starting the day after chemo. this one seems to be OK in her system.
I also got today and she took 2 at 5pm is an over the counter pure ginger gravol. I am going to try the se
I have been pushing fluids all day today from ice chips to small freezes, and water, even warm chicken veggie broth.(no luck with that one) I would say she has taken in about 2 maybe 3 glasses of fluids today but no food that stayed down. she has been laying on the couch since 10am and mostly slept on and off all day.
Does anyone have any suggestions on something that will perk her up. I want to try to get her to drink and or eat something.
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Maybe I will reword the last part as I want to get my wife to drink more than a few sips at a time and actually eat some food( toast, crackers, what ever).
I am going to hold of the Prochlorazine and see how the night goes, maybe in the morning she will feel better. That will be day 3.
On day 4 she starts taking the Neupagen shot, for 5 days.
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Chris - I hope that your wife's doctors can find something to help with the nausea. It sounds like the FEC is a very difficult regimen.
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Chris- I hope your wife feels better and am sorry that her regimen is so difficult. Maybe the doctor could give her fluids and possibly even anti-nausea meds via IV since she is having a hard time keeping anything down. Though I wasn't vomiting, I ended up very dehydrated with low potassium and felt terrible but was able to get a fluid infusion and felt dramatically better and less fatigued almost immediately.
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Two days after chemo, My legs and hips are aching. I have no nausea yet thank goodness, I am pretty weak though. Very tired. I did start getting a head sinus pressure last night about 630pm took claritain and was gone this morning. I feel so weak I am scared to get into shower I might pass out. Not a good feeling that might happen, but I am gonna make my self today. Hope everyone else had a ok night
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