Starting Chemo, November 2013 Group

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  • ellischestnutgirl
    ellischestnutgirl Member Posts: 28
    edited December 2013


    Port placement went well with minimal discomfort. It is way up in my chest. First chemo on Monday.


    Gayle

  • VirginiaNJ
    VirginiaNJ Member Posts: 634
    edited December 2013


    yay for you Amazon :)

  • wrenn
    wrenn Member Posts: 2,707
    edited December 2013


    amazon you sound like someone who just found freedom. So happy for you. :)

  • jab
    jab Member Posts: 220
    edited December 2013


    Hi all,


    I started my first Chemo on Nov 28 so I guess that makes me part of the Nov group. I am on the FEC-D regime (Fec now D later) like some of the other Canadian ladies and have certainly found it interesting. The one thing that is a constant is nausea. Even with the full arsenault of anti nausea drugs I was not able to keep my stomach settled for the first two days and now still find solid food very difficult. The nurses in Oncology have been amazing and making sure I am hydrated with IV's and I am trying new meds (the non oral type) but if anyone has any ideas I'd be very interested.


    With regards to Christmas this year - I will be very happy to see it come and go. It's hard to be cheery with your head in the toilet!

  • audra67
    audra67 Member Posts: 521
    edited December 2013


    Yay Amazon !! I loved your thankful list and so glad you are home! Hospitals are HORRID!

  • lisa137
    lisa137 Member Posts: 569
    edited December 2013


    @jab everyone keeps telling me that if my anti-nausea meds don't work I should try marijuana for that. So far I haven't needed to consider it, but if it was a choice between that and barfing, you can probably guess which I'd choose. Hint: I *HATE* being nauseous.

  • SpecialK
    SpecialK Member Posts: 16,486
    edited December 2013

    If you have intractable nausea that is not eliminated, or reduced enough, by oral meds, ask your oncs about the Sancuso patch -

    http://www.sancuso.com/patient/index.php

  • lisa137
    lisa137 Member Posts: 569
    edited December 2013


    More on my HGTV obsession: I'm watching one of those episodes where the young couple is looking for a house to buy, and they are just APPALLED by all the wild and crazy wallpaper choices in this house, and the weird colors, and the tile, and pretty much everything... and this occurred to me: Wouldn't it be AWFUL to be sitting around watching one of those episodes and realize that it was your own old house that was being shown and your own ...eclectic...design decisions that were being ridiculed? I gave myself the giggles thinking about it.


    My temp is still hovering at a less-than-interesting 99.5, but my husband came home with a GRAND case of the sneezes and sniffles. Yikes.

  • jab
    jab Member Posts: 220
    edited December 2013


    Thanks Lisa137 - I also hate barfing and I am raw from it. I have Emend, Ativan and Prochlorazine, and a quick desolve Zolfran lined up for the next round of Chemo. I'm opting for gravol supp in the interm to keep the damage to my stomach to a minimum (already puking blood). I may pass on the Zolfran as I too had a monstor headache which I am sure was the Zolfran. If this doesn't work, marijuana might be next. - Do I get it from my dr???

  • lisa137
    lisa137 Member Posts: 569
    edited December 2013


    I guess that depends on whether you live in a place where medical marijuana is legal or not. It's certainly not *here*, so if I have to go that route, I'll have to go to a more direct source, as it were.


    BTW, does your doctor know you are puking blood?

  • Bec65
    Bec65 Member Posts: 312
    edited December 2013


    Welcome home, Amazonwarrior! Enjoy your own bed tonight and all the other comforts!

  • jab
    jab Member Posts: 220
    edited December 2013


    Lisa137, my onc knows about the blood. I guess its not that uncommon. Anyway, nobody said this was going to be easy... Keep that husband at bay tonight, and watch that temp! Take good care.


    JAB

  • Bec65
    Bec65 Member Posts: 312
    edited December 2013


    Lisa, was that the episode with the girl with the purple hair? I was watching that one today too! I have to say, even with her purple hair and weird random "pops" of color they chose, they seemed among the most down to earth couples I've seen on one of these shows in a long time. And, re medical marijuana, my daughter is quite willing to bring me home some "yummy chocolate" from college!

  • lorreymom
    lorreymom Member Posts: 149
    edited December 2013


    jab - I go for acupuncture the day before my chemo. My acupuncturist picks points to control nausea & boost my immune system. Maybe it worked for me as I had only a bit of nausea & no vomiting. I also have a small pharmacy of anti-nausea meds. And I would not gp without either acupuncture or meds...so can't say which works for me, likely both. Just a thought to help you with your next dose??? I wish you all the best. Hope you are feeling better soon.


    Oh...I also chewed on candied ginger & ginger snaps & drank ginger tea. Also suppose to help.

  • lisa137
    lisa137 Member Posts: 569
    edited December 2013


    @Bec Yes! It was indeed the purple hair girl. And I agree, I liked the couple a lot, but man, they were really hatin' on some wallpaper, lol. Not that I could really disagree with them.

  • lisa137
    lisa137 Member Posts: 569
    edited December 2013


    re: ginger snaps and ginger tea.... I got lucky in that my mom made a (quite gingery) pumpkin pie for Thanksgiving and sent the entire thing home with me. A slice of that with some cool whip was an INSTANT queasiness-killer. Kind of magical.

  • lisa137
    lisa137 Member Posts: 569
    edited December 2013


    @jab okay, just checking. :) Keeping the husband at bay hasn't turned out to be a challenge: He took a child-sized dose of children's benadryl, went loopy and hilarious on facebook for about 30 minutes, and passed out cold on the couch.


    I love that man.

  • Lissy2304
    Lissy2304 Member Posts: 60
    edited December 2013


    AUDRA67 - I don't know...I just do it. Got infusion Wednesday and going back to work tomorrow. I just hope I get a few "no-shows".


    AMAZON- Welcome back!


    Today was a good day! Got compliments on my hair (hehehe wig) I wasn't about to tell....


    81degrees F in Texas today, JUST GORGEOUS!

  • Lissy2304
    Lissy2304 Member Posts: 60
    edited December 2013


    Anyone lost their eyelashes or eyebrows?

  • inks
    inks Member Posts: 746
    edited December 2013


    Lssy2304 - my lashes are thinning, nothing noticeable with the eyebrows, but I am doing AC, one week out from my second treatment.


    Sending prayers and minimal side effects to everyone getting their treatment this week!

  • Palameda
    Palameda Member Posts: 259
    edited December 2013


    Going in for tx2 today. Woke up at 4 am...I'm not nervous at all, and that's faster a sleeping pill. I've been fighting a cold, it's really mild so I don't think it'll be a problem. Lots of anxiety about doing this again. I didn't find it that much fun the first time, so I don't see the point in doing it again. My husband has a terrible cold, and is depressed about doing this again too. Ugh. He's been a marvelous support, which has been a pleasant surprise. Previously when I've been sick he's been impatient with me, since he's hardly ever sick, but this time he seems to get it, and has had to take on much more work since I can't do so much stuff.


    For those of you who have continued to work: I am awed. Truly warrior women. You need tattoos and face paint to show the world your bravery and strength.


    Amazon, welcome home! I had only one day, you had what, a week? Freedom!


    Ok, Bec and Lisa, Smrlvr you keep me smiling! HGTV I've never watched it. What i cant stand the commercials the SPCA is running now about abused and starving animals. Way too upsetting for me to handle! They should be banned. I'm probably their target audience, but I have to mute those depressing commercials. What I have been watching is streaming Dexter episodes. Yeah, yeah, it's about a mass murderer and all, but it's not stressful or in your face violent, I find them funny and amusing. My brain is obviously much more twisted than everyone else's! I LIKE my granite counters: easy to clean, can put burning pots on it, but they're boringly ubiquitous.


    I am utilizing "alternative medicine" to help with my symptoms. It's legal here in California, you get an rx from a doctor who just does that, not your regular doctor. There are lovely stores with all sorts of nice edibles. It helps with nausea, stress and sleeping. My therapist points out that it's less addictive than Ativan, which I've got tons of. Has anyone noticed how when you get the big C, it's like you hit the jackpot on a slot machine? Drugs just pour out at us, even those that usually you have to fight the doctors for. It's overwhelming. Somehow they're not worried about us getting addicted/habituated during this period. Unless we're stage IV, we're going to have to go back to real life soon, so it's interesting. It's like this diagnosis scares the medical community too.


    My eyebrows are thinning. They need cosmetic help now. I've been wearing wigs because my hair looks like a 60 year-old man with a bad combover. Quirky, I've got a halo wig. I thought it looked good before I lost my hair, since then I haven't been able to make it look good.


    Lorrymom, my muscle aches/cramps continued through my second week. I'm going in this morning to see my MO, we'll see if that was taxotere or neulasta. It doesn't really matter which is was, it was painful! I got Baclin which is a muscle relaxer from the md when I was at the hospital, which I used with the pain pills the MO gave me.


    Shout out to Paulette...hope you're getting on with tx2 effects. We need your bubbling posts.

  • QuirkyGirl
    QuirkyGirl Member Posts: 383
    edited December 2013


    Good luck today, Pat! The day my chemo was postponed my sister insisted I watch Orange is the New Black. Dark humor and I'm hooked and saving the rest for chemo days. Was thinking the same about Paulette.

  • audra67
    audra67 Member Posts: 521
    edited December 2013


    Patalameda Paulette! Happy #2 day, mine is tomorrow. Praying for minimal to NO side effects for you both! Keep us posted!

  • Palameda
    Palameda Member Posts: 259
    edited December 2013


    Oh yes, Orange is the New Black! I watched it all when I was laid up with my original infection. Funny, dark and engrossing. I also like the analogy that we're spending time in prison for the duration, we've been sentenced to a particularly tough unit where they shave our heads, mark our bodies, insert under our skin "ports" that are clearly actually tracking devices. We receive physical and mental torture, and the only bright spot are the friendships we make with our fellow inmates.

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited December 2013

    Wishing for very easy times in the BGC and minimal side effects for everyone this week!!!  Keep breathing.... it just means one more down and you are closer to being finished.  I know it's hard to get yourself mentally prepared.  Remember that your time in chemoland is like running a marathon.... you know that the rest stops are there along the way and you know that the running between each rest stop gets a little harder and harder...... you get a break during those weeks in between each chemo to take a regroup and recover.  You just have to keep pushing forward and get to the other side.  I am waiting for each of you, ready to ring that bell at the finish of chemo and to do the happy dance......  HUGS!!!!

  • lisa137
    lisa137 Member Posts: 569
    edited December 2013


    My temp seems to be back to pretty much normal today, and my husband is less sniffly and sneezy, so that's good.


    In the category of things I'd only say HERE or to my husband, even though I haven't been constipated at all through this first round of chemo, nevertheless, a little while ago I went to the bathroom and Pooped a Mighty Poop (was concerned for the welfare of my toilet,) immediately FELT my temperature drop to normal, so checked it and sure enough, it was a textbook 98.6. I went and asked my husband (who is working at home today) if I looked skinnier to him than I had 15 minutes earlier and he appraised me and agreed that yes, I did look somewhat skinnier. :)


    I would feel a LOT better in the mornings if I would duct tape my mouth shut before I go to sleep, or something. I apparently cannot sleep with a closed mouth---especially if my partial dentures aren't actually in my mouth--so I'm waking up EVERY morning with an open mouth, dry sore tongue, and sore throat. The magic mouthwash and a bowl of oatmeal fixes all that right up, but damn I'm tired of waking up that way, especially since I'm sleeping SO GOOD when I get woken up by the painful tongue.


    Pat, you've convinced me to check out Dexter. My challenge is always finding things that husband and I can watch TOGETHER, because we love watching stuff together but our tastes in what to watch are so radically different that it really IS a challenge. Right now though we ARE working our way through the entirety of Grey's Anatomy (funny that THAT show doesn't bother me, isn't it?) but when we are done with it---or if we lose interest in it along the way, we'll need some new stuff to watch.


    Actually, I'm open to suggestions for other things we might both like, so I'll tell y'all that in the past, we were both addicted to CSI (the original version, with the original cast,) and were both VERY addicted to House. He's not much into sitcoms, but he did love Everybody Loves Raymond (although the REASON he loved the show is because the Raymond character is SO MUCH like himself.... so yes, basically I live with Raymond.) We also both like Deadliest Catch a lot---though it's started to wear thin over the past season or so, but that's pretty much the only reality show I like....well unless you count the HGTV stuff and Antiques Roadshow.


    re: HGTV and the fact that my husband is at home today: He came in here a few minutes ago just as I was waking up from a nap, and said "Hey did you hear that one of your "fix 'em up" guys got killed in an accident?! I was *immediately* wide awake and the first words out of my mouth were "OMG It wasn't Jonathan was it?" as I reached wildly for my computer trackball so I could find out. And there, friends and neighbors, is the REAL reason for my HGTV addiction. Jonathan from Property Brothers. As it turns out, it was Bill Beckwith from Curb Appeal...and I feel a little like someone I know has passed away, but seriously, if it had been *Jonathan* I'd have been in deepest mourning for days, most likely. My husband was like "Which one is Jonathan," and I said "The good looking one," and husband says "But they're IDENTICAL TWINS," and I said "they aren't THAT identical...and Jonathan knows how to DO stuff....." My husband found this pretty amusing...I guess he's not threatened because he knows that that's part of why I married HIM: He knows how to DO STUFF, too. :)


    Ditto on not being able to watch the pitiful animal commercials. I can't even listen to Sarah Mclachlan sing *happy* songs anymore (does she even HAVE any happy songs?) I'd save them ALL if I could, but we're up to our necks already with the two dogs and, presently, a YARD FULL of kittens that we have to figure out what to do with because a local stray decided to have kittens on our front porch right around the same day I was diagnosed with ILC. And we don't have a single animal that we acquired by deciding we wanted a new pet and going out and picking one out. They are ALL rescues to one degree or another. But I still wish I could save them ALL. :/


    Has anyone else found that chemo slows down time? All my life it has seemed like time has been speeding up, but the week and a half since my first chemo seems like it's been MONTHS long. I'm actually kind of enjoying that effect!


    My second AC will be on Monday. For those who've are ahead of me on the AC trail, what should I expect? Is the second round pretty much like the first? Worse? Much worse?


    My scalp is starting to feel a little sore ...actually it's my hair that's sore...here and there. Is this just because I'm napping too much, or a sign that my hair is getting ready for its Great Exodus? I still haven't buzzed it, or gone shopping for hats/scarves; I guess I should get on the ball with that.


    Anyone else get the hiccups REALLY EASILY? Anyone else HATE GETTING HICCUPS as much as I do? Argh!


    I feel so *normal* today. I can even TYPE correctly for the most part! My husband asked me how to spell something a little while ago and I didn't have to hesitate to spell it correctly for him. I'm not an idiot today! Woohoo!


    Hopefully that will stick until chemo day on Monday; my house could use some attention. Okay, a lot of attention.


    I hope everyone has a GOOD day. Hugs to all. :)

  • lorreymom
    lorreymom Member Posts: 149
    edited December 2013


    Pat - Good luck today! You can do it again. As my MIL always says "this too shall pass!" I tell myself that everytime I discover a new side effect.


    Lisa - glad you are feeling better.


    I have the Look Good Feel Better workshop tonight. Looking forward to it.


    Also had my in-home fitting for mastectomy bras & prosthesis this morning. Good news: 1 prothesis & 2 bras are 100% covered by our insurance with my surgeon's prescription. There are some pretty bras too. And my super nice fitter will have them here before Christmas. Woot!


    I am having a good morning. A little leg pains still, but tolerable. I won a Tassimo brewer from Kraft Canada & it arrived today. Hope my good luck continues. I sure need a bit of happiness now. Hubby has left today for a 3 day business trip. I am nervous about being without him, but I have lots of support from family & friends, so should be okay for 3 days.

  • smrlvr
    smrlvr Member Posts: 422
    edited December 2013


    Amazon- glad you are home!


    Lisa, did AC#2 Monday of this week. They slowed down the cytoxin drip and the headache wasn't as bad tins week. They also thought the headache could have been from the zofran so my mo changed me to Ativan which seems to work better and helps me sleep. This round seems to be going better than last. I am only 2 days out though. We will see if I get fatigued later this week. My hair has started to come out in small clumps. I don't know how long it will take at this point for it to come out enough to get me to shave it.MO said he has seen it take as long as a month.


    When I am not nauseus I switch from HGtV to the cooking channel. Since this ordeal began my husband has hooked me on two netflix series, the first is Weeds. The first few seasons were entertaining, but them they got ridiculous. My husband also likes Sons of Anarchy which I didn't think I would like because of the violence. But they really develop the characters and I am enjoying it.


    Someone on another thread suggested an eyebrow kit from sephora. I ordered that in anticipation of losing my eyebrows.


    Have a great week, ladies!

  • Amazonwarrior
    Amazonwarrior Member Posts: 485
    edited December 2013


    Thanks to everyone who welcomed me back!Smile


    Today is my day 20 after my first CT. My hair is shedding like crazy. I even vacuumed it a couple of times, since I don't like the hair to be all over the place. I have a lot a hair to shed though. Even my hairdresser commented on it last time I got my hair cut.


    Thank goodness, my wig arrived yesteday. I tried it on and it doesn't look bad at all. It came through mail from TLCdirect. It's a cute pixie style in a chestnut colour .


    My next CT was postponed by 1 week due to my infection and a hospital stay. I need the time to recover before I get 'punched and hit' again.


    My infection site is swollen, tight and tender, but keep taking those antibiotics to hopefully resolve that issue.


    The port site is a bit tender as well, however my overall energy level is higher today than before.


    As far as TV goes, I totally blocked out news. I find things there quite depressing. The only station that I can watch is Oasis HD. Yes, nature shows to calm my nerves.


    Audra & Pat: If you don't mind me asking you: Why did they place your port in your neck? They put mine in the upper left arm on the outside. In fact, I actually requested that location after I pondered on the idea for a bit. They told me that if the vain is good, then it doesn't matter to them where they place it.

    Pat: How did you chemo go today?

  • lisa137
    lisa137 Member Posts: 569
    edited December 2013


    @Pat oh yeah meant to comment on what you said about drugs, too. You're right: at this point I have a "reserve supply" of both hydrocodone and percoset, neither of which I've used in weeks if not more than a month since I have no pain anymore, plus the ativan and klonipin.


    I'm not too concerned about that aspect of it at this point though; I rarely touch the ativan, and I do believe that the klonipin is beneficial enough to me that it outweighs any risk of addiction. It's kind of been my miracle drug, and so far at least I don't seem to be building a tolerance to it or needing any additional, so I suspect it may be my companion for a while even after I'm done dealing with the most immediate fallout from the cancer diagnosis. Or then again, maybe not; I've skipped my second daily dose a few times recently just because I never felt the first dose "wear off," and therefore never needed the second one. My PCP said that might happen; that once I could put my anxiety aside and use my full capacities to learn to deal with cancer and the aftermath of that diagnosis, that I might find I needed the drug less. I think the key for me was that he put me on a low dose---just enough to keep me from being a complete wreck, but not enough so that I was artificially happy, if that makes sense. So it's not as if I "crash" when it wears off.


    But yeah, I think that health care providers who deal with cancer patients are very much aware that keeping our mental and emotional states as "up" as possible goes a long way towards getting us through this very very difficult time, and that the benefits do outweigh the risks, in our cases. Since I started the klonipin, a little over a month ago, I guess, other than a few weepy moments here and there, I have not had a single episode of feeling hopeless or terrified or panicked, or any of the other awful things I was feeling before, and that's GOT to be helpful for dealing with chemo and healing, right?


    And, what can a person do? I mean, I could skip that drug and be as depressed and anxious as I was before it was prescribed, and therefore utterly miserable through all this, or I can take the drug, and possibly have to deal with being weaned off it slowly later. Easy choice, for me, honestly. If..."alternative medicine" was legal here I might be quicker to go that route, but I'm not sure how well that would work for me , since back in my younger days I did some of that recreationaly, and it actually *caused* me to have anxiety. No clue if that would still be the case---may find out though if I get bad nausea problems as chemo moves along.... I have several sources queued up and ready to help me out if I need it,, though I won't get all the tasty edible choices you do, unfortunately.

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