Starting Chemo in JAN 2007
Comments
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Mary, so glad to hear you got the rad issue resolved. Our son is in law school, and I keep telling him how much I am looking forward to having someone to write threatening letters on legal stationary! Way to hang in there!
I am feeling really punk tonight, the swelling is worse, and I didn't sleep last night. I think I am going to lie down and feel sorry for myself. I am interested in everyone's postings about stress and am going to write more about that, but right now I need to go feel very sorry for myself. Fortunately, Steve will be home soon and I can dump on him. Lucky guy that he is.
Sweet dreams,
Melia -
Skye - glad you are taking extra time for your book outline, and good luck on Monday with your rads. Also glad you got the "pee" situation cleared up!
Lynn- glad your headache is better, thanks for your experience with Tamox.
Rebecca - I probably have around 50 - 60 pairs of shoes and boots at one given time - When we built our house 6 years ago I had the custom closet guy build me special pull out shelves in my closet that can hold 8 pair of shoes at a time - and I have four shelves on each side of the closet - so that means up to 64 pair at one time! I have to wear the new patterns each season (it's a dirty job, but someone has to do it)...
Jan - hope your DD is feeling better, strep is the pits, sure hope you don't catch it. Have fun tomorrow at the DogsWalk for Cancer. I am hopeful now that my night sweats will diminish once I start the Tamoxifen, and that my sleep will also be better.
Joni - I am THRILLED for you. Your treatment plan sound very thorough, and you onc. sounds amazing.
Mary - ah the powers of the legal letterhead! Glad you will finally start your rads on Tuesday. Good luck
Mel - glad you are recuperating well. I hear you on the DH and the lack of interest - I think they just can't cope.
Tina - glad your son got his problem all worked out - this always happens with kids,doesn't it - we drop everything to run to their aid, and then BAM - it's over.
So I have some gorgeous pix of DD's prom, but I can't figure out how to download them to the site - it says you need a website to do it, and I don't have one. DD tried to do it, says she can't. Any suggestions gals?
thanks
caya -
Tina, congrats on going out without hair - seems like everybody's doing it now! Although if you look anything like you do in your picture, you're more than ready. That was a full crop of hair! Glad your son got his problem with the neighbor straightened out - maybe he learned something, do you think? Poor little guy - jumped in the deep end and didn't even know it. You enjoy that vacation - you've more than earned it.
Tami, have fun at the Relay. Somebody else said they were doing that this weekend, I think. You'd think I'd remember who but it has left me already. Nancy did it already I think. I just missed the second one in Houston that I know of - surely there is a way to find this out in advance around here. Thanks to you, and Amera and Caya, for letting me know my particular guy isn't the ony one who is avoiding a little bit. We just had a long talk about it, where he said that he wasn't consciously avoiding anything, and I said I understood that, but that if he was unconsciously avoiding I wanted him to bring it up to conscious level where we could talk about it, and if he didn't want to participate in certain things, he probably wouldn't have to. I just don't like expecting and then not getting my expectations met. I can always modify the expectations. Anyway, the end result was, we removed my dressing, cleaned the drain sites, wrapped me back up in an ace wrap, put my camisole on, and I feel much better. Tomorrow we'll do a better job, but it went pretty well for his maiden voyage. And for my part, I tried not to micromanage every little thing.
I have a drain pocket in my camisole, but with three great big drains crammed in there it is really a funny look! Sort of takes the "camisole" out of camisole. Sure is nice and soft though.
Caya, go to photobucket.com, or one of those photo-sharing sites. It's easy as can be to sign up and create an online album, then you just link to that website. It's surprisingly easy. -
Cindy,
Good luck tomorrow. So you are permanently topless? You go girl!!!!
Caya,
I am also being honored in our local Relay for life. Unfortunately it is on the day of my infusion, so I will not be attending. I would have liked to though. My oncologist had not mentioned tomaxofin yet. I just assumed it would be after the herceptin. I will ask her when I see her again. I am so jealous of all your shoes. LOL
Tina, Skye, Nancy- has your oncs mentioned tamoxifen or arimidex yet? Am I missing anyone on herceptin?
Mel
I am so glad you are home and feeling better. DHs can be blind sometimes. You have to tell them exactly just what you want them to do.
Last night after my taxol tx, I slept until 8:00, and when I woke I asked him if he would make dinner. He made hot dogs and beans for himself. I do not like hot dogs. He thought he was doing me a favor so I would not have to cook for him. He forgot about me. Lol. When I asked where is my supper, he asked me if I wanted blintzes. I love blinzes- they are like crepes. I buy them frozen and fry them- yumm- in a pinch. I got up and put them in a fry pan, assuming he would watch them. I went on the computer and in a few minutes smelled something burning. MY BLINZES!!! I called him and told him I thought he was making my dinner. He then said that I should have asked him to watch them. DUH!!!!! They can be thick sometimes. The moral is they need step by step directions and orders.
Have you worn your transitional gown yet? I am thinking of getting one. Is it comfortable or would a regular robe be just as good? I am glad you worked things out with your DH.
Rebecca,
That is so frustrating. They should be calling or writing your doctor who ordered the test, not you. Bureaucracy: AAAAARRRRGGGGHHH is right!
Jan,
Have fun at your DogsWalk for cancer tomorrow.
Oh Joni,
Congratulations!! I am so happy for you. That is such great news! Now you can really enjoy your Mediterranean cruise on October.
Volunteering sounds like fun. It gets you out of the house and also doing something you will enjoy. What a good idea.
I cannot believe how up you have sounded despite how you frightened you must have been. I am so glad you got such great news.
Mary,
Good for you for straightening the radiology department out. It certainly got their attention, especially if the doc called you.
Melia,
I am sorry your swelling is not better. Have you tried elevating your feet with a pillow? When I walk, my fingers swell up, but I havent noticed my feet giving me a problem yet.
Tina,
You too topless!! Good for you! Kids can drive you crazy sometimes. It was actually good that they ironed thinks out before you came home. You didnt have to get involved, and things worked out. Perfect ending. If all their problems could work out that way .. -
My day!!!
I called the chemo department and spoke with the nurse who was helping the new nurse and explained that I was a little concerned about the herceptin dosage. I told her that I usually get a half hour dose and I got an hour dose. I told her it was okay with me if she just slowed the time,but I was concerned that she perhaps gave me a double dose. The nurse was not happy with my accusation and coldly told me that the pharmacist checks it, and then two other nurses checked it before she gave it to me. She didnt even acknowledge that there could have been a mistake and didnt tell me she would check to make sure. I think she was just concerned that I had the nerve to double check their work. I insulted her. Oh well. She probably did check after I got off the phone.
My sister called at 4:00 today to tell me that she just heard on the news that two nurses and one employee at the Cape Cod Cancer Center have whooping cough. Great!!!! They said that anyone receiving chemotherapy between May 17 and June 5 should come down to the hospital to receive an antibiotic to prevent getting whooping cough. I called the cancer center and they put me through to the infectious disease center. They told me that they just closed and I will have to wait until Monday to receive my medicine. Great!!!
As I was hanging up, my friend called me and told me that that was outrageous and I should call back and demand that they have someone there give me my antibiotic today. I called back and told them that with my low wbc, it would not be very good for me to wait until Monday. That might be too late and I did not want to find out. They were accommodating and my dh and I drove down there and got our azithromycin z-pacs.
Apparently it was on the radio and news all day, but I did not have either one on today. It is all over the news tonight. They said that they were calling all the cancer patients. I did not receive a phone call yet. Tonight one of the oncologists was on the tv saying that cancer patients were not at any bigger risk for getting whooping cough than the general public. What a crap if sh-t. If our wbc are low from receiving chemotherapy, how can we not be at more risk of infection? I think he didnt want to scare anyone, but really! I think they should be open all weekend to hand out antibiotics to cancer patients. I also think they are making a mistake by making little of it. I am glad I listened to my friend and made them wait for me to get my antibiotics.
I am glad today is over and now I can relax.
Viddie -
Viddie, glad you questioned the nurse. God, you'd think she'd be apologetic or offer an explanation for your fears...we are all WELL AWARE that the "numbers" are checked by two nurses, etc., but mistakes still happen. And this isn't baby aspirin!
Too much on the whooping cough. My daughters little K friend who always comes over to play, came while I was on chemo and told me her brother had "pertussis". I knew exactly what that was and had to laugh at her big term..her mom is a doctor. But I was thinking jeez, I hope she didn't catch that...
Thanks for the support on my son. Yes, Mel, he DID dive right into the deep end. Last night when he got home and we talked he told me that the mom (my friend) was pretty irate at him, saying "WHAT ARE YOU SAYING, MY KIDS A LIAAAAAARRRRRRRR?????". This "liar" accusation seems to really strike a chord in her because a neighbor girl last year called her son a liar over some totally stupid kid thing and her dander went straight up and she lit into the girl, 3rd grade. The girls mom would not speak to my friend for the better part of the last year, despite repeated apologies by my friend. My son's aware of that too. I told him to use this as a lesson, that you have to tread very lightly before saying ANYTHING that can even resemble an accusation.
Speaking of accusations, my SIL is trying to draw me into family drama again. Won't bore you w/all the details, but when Caya was talking yesterday, Caya and Cindy, I believe, about can stress bring this on... which theoretically, they say it can't... I have to wonder. I was under TREMENDOUS stress w/teh "IL" crew for the last four years. No more. Part of my new plan: will not deal w/those that drag me down. -
Mel, my DH was amazingly great after my surgery.....changed dressings, etc. I was floored, as he is so not into medical stuff. He really stepped up to the plate. However, do not feel bad if this isn't the case in your house... they all have their "things". Mine wasn't physically present after the first couple of days in the hospital because my mother was here...he was off the hook. And he travels all the time, etc., so I am running a one man show out here in OH most of the time...
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Rebecca - glad you got that insurance co. straightened out. They must have a billing code for "wasting client's time"! It seems to be a bit of a game - deny first and see if it works - some may not complain.
Joni - what excellent news. You are healthy now. You have certainly not been a drag, you've coped with this admirably.
I too have wondered about the cancer/stress connection. I don't mean the having a demanding job/hectic life kind of stress, but the gut-wrenching problems kind of stress. My son had a spinal cord injury 7 years ago and uses a wheel chair. He was 21 at the time, and I have had a hard time accepting this for my child. It was a very stressful time and it took a good 3 years for him to get settled. Then last March my Mother commited suicide after 2 years of depression. Looking back, after my son's accident I was in quite a state for awhile - put on weight, especially around my middle, and I'm sure my cortisol levels were sky-high. 2 1/2 years ago I decided enough, and lost weight, started eating right and exercising. My dr. says cancer was there 8-10 years before diagnosis. Who knows? But I definitely want to learn to handle stress - emotional stress - better. I can't bleed for everybody anymore.
DH and I went to the Relay for Life yesterday. We helped set up during the day, and went to the "Survivors Banquet" in the evening, then I walked the survivor's lap. Met some wonderful people. They treated us like heros - I don't think of myself as a hero, that's for sure! It was very emotional. A woman and her two daughters spoke after the dinner about the dad's death from multiple myeloma. One daughter said - "I don't remember if my Dad's tools were in order, or if the car was clean - I remember the time he spent with me." I'm sure there was not a dry eye in the place. If cancer can teach us that, it's a lesson worth learning. -
Joni and Mary thanks for sharing the good news. What a relief.
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Good Morning all,
Feeling a bit better today. I think I was tired yesterday, physically and emotionally, and the swelling worried me; it got so bad so fast. But I elevated my feet and it is definately better today. My doc called about 6:30 last night, surprised me as his nurse had called earlier. He said the swelling worries him as it is a side effect of taxotere, not taxol. Now that seems odd. I read that it was a side effect, and Mel had it .... also another lady I know. Anyway, he said to keep my feet elevated as much as I can, and if it doesn't improve by Monday or if it gets worse, he wants to run heart tests and get me on a diuretic. Since it is definately better, I am not worried. I really fell apart with my husband though, and he was very sympathetic. I think it is just now hitting me that the breast is gone forever, and that I won't have a full head of hair til TG or so. It just all felt like so much. My husband suggested we just have a quiet weekend at home, not try to do much, and see how I feel Monday.
When I read about everyone's stress, I do realize that I have had it easy. A son in a wheelchair and losing a mother to suicide is so sad. But I think there is something to the idea that stress can trigger this. Who knows, we can never prove it. Somehow I need to just accept that it happened, that it could have been worse, that I am lucky in so many ways, and I need to shake this mood!
Melia -
Mel, I agree on the caregiver issue. My DH just does not know what is needed. He doesn't actually see the "need." It is hard to ask for help or confront what is actually going on inside. He too did not show up when I needed to change my dressings for the first time. I only had one side so I was able to do it myself. Yes, keep doing the exercises even if they feel easy. It's easy to stiffen up. The drains were the pits. Did they tell you that when one went down you can get that one out? I didn't know that and kept the two in longer than I needed to. Of course when I had one out, the other one picked up more, but that is what my dr wanted. Sometimes they don't communicate that well.
Melia, sorry to hear about your swelling. The heat surely has something to do with it too.
Jan, hope no one else at your house gets strep!
Skey, good luck on rads, you are one day ahead of me.
Viddie, I'm glad you called the onc even though they yelled at you. You're right, they probably doublechecked everything after your call. That whooping cough stuff is scary.
Dar - glad to hear from you. You really have had stress with your son's injury and your mother's death. They say what doesn't kill us makes us stronger, but it surely is a test.
Viddie, what is a transitional gown?
Tina, I too am tired of my wig but not ready to retire it for good yet.
Those on Tamox, have you heard anything about weight gain associated with it? I'd just like to know before I gain the weight...what to blame.
My SIL goes to the onc on Monday to discuss whether to have a lumpectomy with radiation or a mastectomy. Keep her in your thoughts. -
MELIA! This is so odd - my onc told me EXACTLY THE SAME THING when my swelling started up!! It's a side effect of taxotere, not taxol. Therefore, he pretty much ignored it the first few weeks. Same thing with my tearing problem - can't be the taxol, that's a side effect of taxotere! I got very upset after a while - after all, I wasn't making those things up. Finally, after I had a crying fit in the chemo room one day and the chemo nurses told him about it, he began to think outside the box a little bit. My symptoms still mystified him, because he said all along I acted like I was on Taxotere...but he finally accepted that I was different and started addressing my issues. And, he apologized, sincerely.
I think that cancer treatment is overall very rigid and governed by formulas and statistics. They all learn a certain set of rules, and work from those. And, sometimes you have to slap them upside the head to get them to think outside what they "know" to be true. I suspect it's an occupational hazard.
Anyway, I think it's very interesting that we even had the same WORDS said to us, exactly, when we presented with the same atypical complaints. -
LOL, Dar on code: wasting clients time. Good one!
Mary, I'm down 8 lbs. or so since finishing Taxol despite beginning Tamoxifen. I read in Breast Cancer for Dummies that a placebo study on Tamoxifen showed it doesn't cause weight gain. So there's some good news.
Oh, Dar, just read about your son and mom. I'm sorry that you've had to go through that. Very difficult stuff. Boy, some of us really do get far more than our share..
OK...I'm off to shower for my flight and to try to make this "hair" presentable... need to remember to pack my security blanket (wig) just in case. It even feels so gross now, around my neck. I feel like I have an animal on my head. I think I'm really over the wig thing. -
Mel, I think they are taught the same "words" in medical school. Do you recall me recently telling Lynn that my dr., VERBATIM, told me to start my Tamoxifen "in a few weeks"? Just like Lynn's. I swear, it's in Bedside 101... let patient feel like they have some control over their life.
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Jan, I'm thinking your kids must be out of school by now, in NC. I figured they picked up strep at school, though. It went around my kids school the very last week. I thought we were far past that season. Knock on wood, my kids didn't get it this year. For the first time, they had flu shots. Jaclyn ended up w/perfect attendance. I didn't even realize it. (Only because I didn't take her out to go on vacation because I couldn't...I needed to be here the entire time since last Sept. for tx.)
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YEA, JONI!!!!!!!!!!!!!
What wonderful news for you and your family. Start packing your bags, woman!
Hope this is a great weekend, celebrating the news, absorbing the relief. Turn on the radio to an oldies station, grab your husband and dance up a storm.
Cindy -
Viddie, I think the transitional gown is worth buying. It really is designed specifically to meet the needs of diep patients and the like. Very well made, comfortable, and the pockets on the inside are in exactly the right place. It's short sleeved, and snaps up the front and on the sleeves, so you can get into it no matter how mobile you are. It's a good weight for summer, also. You could use it in place of a robe, also, so it could do double duty. It isn't the most flattering thing I've ever worn, but it's hard to look sleek and sexy with three big old drains hanging off of you. But I think it's worth the money. And if you get one, take it to the hospital with you - it might make things a lot easier. I wished I had taken mine .
I'm sorry that you were met with such defensiveness by the chemo nurse. I hope she did check - or maybe she is one who doesn't believe she is capable of mistakes. She at least owed you the courtesy to check to relieve your anxiety about it. I'd be tempted to go over her head. You shouldn't be treated like you were attacking her personally. So what if there's not much chance of an error...you were worried, she should have reassured you.
Glad you got the whooping cough matter taken care of. That's wild. I think there was an outbreak of that here recently also. Hmmmm. -
Viddie, the next step would be to discuss this with your physician when you have your next appointment. They rely on the staff to handle everything and if they hear that the interaction was less than concerned/appropriate someone else probably will hear about it.
Remember, you are the consumer - not just the patient. I'd talk about the infusion concerns, the attitude of the nurse you spoke with on call-back and then the concerns related to how the whooping cough problem was handled. Or almost NOT handled by the center.
I have a concern about the infectious disease office closing. If they can't handle this somewhat 'minor' problem, there's no confidence that they'll handle a more extensive problem that affects more of the population. (I mean no inference that the concern over the whooping cough should be minor, just relatively minor in terms of number of affected persons.) As a member of the medical community, it concerns me.
Have a relaxing weekend, Viddie.
Cindy -
Well, God works in mysterious ways!!!!
There are no words or smilies to express my appreciation in order for you all to comprehend how greatful I really am!!!
I am so in shock!! I just don't know what to say. I was blown away the other day, but on Friday, out of the blue, BAM!!!
How am I ever to thank you all? You have no idea how much this has helped me out. The last thing I need is to be homeless during treatment.
I was going to write a long letter but I don't want to get into whinning about my situation and/or problems, I just don't know how I can ever thank you all enough.
You all know who you are. You will all recieve a personal thank you through the mail. I wish I could do more. If you guys ever need ANYTHING you let me know!!!!!!
I am going to take a nap now. My boob has an open sore under the fold and is killing me!! I am exausted!
I Love You Guys...I am your true friend FOREVER!!!
RobbinJaye -
Mary Several people have told me that they gained weight on tamoxifen. Id forgotten about that until you mentioned it. Ive intentionally gained a few pounds to get up to my pre-bc weight so that I wont be too skinny for diep. I actually liked the during-chemo weight better.
Tppj yes, my oldest (shes 6) just finished school last week, but the youngest is in daycare. Strep had been going around the 6 year-olds classroom since February but my obsessive hand washing seemed to help avoid it. I guess I slacked off a bit after my counts went back up. Now they both have step (the oldest one started a temp tonight). Hopefully theyll keep it to themselves. Back to the obsessive hand washing. I wont slack off again.
Viddie next time you go in mention it to your onc nurse (not in the chemo room) or your onc and see if you can get a less defensive reaction. I think its worth following up on for your own peace of mind. (LOL I just saw that Cindy said something similar great minds think alike .. and fools seldom differ).
RobbinJaye open sore? OUCH!!!! I hope that gets better soon.
Here's a pic of my DD and one of our dogs at the DogsWalk for Cancer this morning: -
Hey Robbin, we love you back. I feel like we are all BFF's here.
Viddie, that is just too much about the whooping cough. Seems like time and time again we all have to stand up for ourselves just to get minimum, common sense care. I'm so glad you and dh got your meds for it.
Tina I am admiring your toplessness. I'm hoping maybe in a month I can do it. And Mary, so glad you got things settled.
Mel I do think the cluelessness of most dh's is testosterone-related, a guy thing. Mine USED to be that way until he had cancer first, and was dependent upon me to do all sorts of things for him. It changed him a lot, and I know he wouldn't have been nearly so attentive or helpful if not for that...because I remember how he was both times I came home from C-sections!
Tina I'm glad the fracas with your son and teammate got settled. Sounds like a very unpleasant experience for all of you. Kids do keep life from being boring. :-)
Here is a pic I took this afternoon of a baby woodchuck that's been hanging out on our deck and my flower garden. It may have lost its mom, or may be sick, hard to tell. I'm also going to try to change my avatar to the new wig too.
And thanks to all the other crooked pee'ers for fessing up to the problem. It DOES help to know I'm not the only one. On the pubic hairs, I was reading a book about post cancer life the other night and there were a few paragraphs on that. It said they might grow in to be "more luxuriant" than they were. That cracked me and the dh up. Who really wants luxuriant pubic hair? Anyway, hope everyone gets the smile from it that I did. -
Jan your post popped in just as I was sending mine. Beautiful dog pic! And do watch that strep, maybe lots of extra hand-washing all around? - skye
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Joni- that is FABULOUS news! I am so glad your scans were so good (particularly the rib) and that your onc was so optimistic. You are SO not a downer, we want to hear all about it good and bad.
Mary- congrats on going topless. Who cares about the looks! I am pretty much planning to start ditching the scarf as soon as I do not have visible scalp (still got some time on that one). Great that you finally got those Rads going that Dr should be completely ashamed of himself and his staff for doing that to you.
Yikers Tina and I thought that drama was limited to daughers. That will probably be the last time he will say something like that without checking it out first sounds like it blew up in his face. Glad is worked out well. From the pic that you sent me you CLEARLY have enough hair to do away with the wig! Let it blow in the wind ladies!!Quote:
Part of my new plan: will not deal w/those that drag me down.
Tina sounds like a plan to me! We will never know if stress did this to us, but I think that one thing that we can all walk away from this experience with is the ability to stop and realize that most of that CRAP really doesnt matter, and it is worthwhile to edit it out so that we can enjoy the days that we have been given.
Mel, glad that you are feeling well. My DH was actually very good with the medical stuff, and for about 90% of my time on chemo he shouldered everything and took care of the kids and house etc. Towards the end he got a bit fed up and I did more than I should have I think but overall he was awesome. He is getting a break now since I am back up to speed, but in Aug when I go back for my implant surgery he is going to have to start doing some things again as I think I will have restrictions on my activity (lifting and carrying mostly) that will keep me from doing things like laundry (machine is in basement) or vacuuming. He will cope I am sure. I was glad to hear that YOUR DH came around as he did. I think basically they all mean well but might not really know what to do with themselves at times.Quote:
Rebecca - glad you got that insurance co. straightened out. They must have a billing code for "wasting client's time"!
Dar do you have the CPT code for that? I think I want to submit a claim.
OMG Skye luxuriant pubic hair? Is that for real? ROFLMAO
Hope everyone is having a good Saturday! -
Hi all,
Fellow Herceptinans,
Any of you on tamoxofen or arimidex yet? If not, have your oncs mentioned when they will start you? I will be on one of them, but she has not told me when I will start. I assumed it would be after I finish my herceptin, but I do not know.
Fellow taxolians,
On day 3 (Saturday) I start to feel yucky. On Friday I feel great and I have enormous energy. I can do anything: clean the house, food shopping, exercise, mow the lawn (but I don't-lol), take long walks, and I am very up. On Saturday & Sunday, I crash and feel very yucky all day. I know it is the decadron. Besides getting bloated on those days, my biggest conplaint is my mood. I am very very sad. I sometimes cry for no reason on these days. Not a happy camper at all. My question is did or do you all have that reaction, being sad enough to cry for no reason? Those feelings go away by Monday. I am an emotional see-saw on the weekends. I hate that decadron!!!! I do not think the ativan will make me feel any better- it is for anxiety. Any suggestions besides to grin and bear it? I know it is temporary and I tell myself that. Oh well, just whining. Thanks for listening.
Viddie -
Hi Everyone
Well, Day 2 post Herceptin wasn't so great - felt a bit nauseous, really tired and had a headache - but I was okay today. I took 2 percosets last night and the headache went away, didn't sleep all that great, but hopefully tonight will be better.
Viddie - my onc. is starting me on Tamoxifen on July 10 - exactly 2 months after my last chemo (Taxotere), and just after my 2nd Herceptin. The plan right now is to stay on Tamox. for about 2 years, then switch to one of the A.I.s - however if I take out my ovaries I will go right to an A.I. I hear you about being moody and sad - try an ativan, it may help. I think it is partly just due to the fact that you are also mentally exhausted from the chemo, not just physically. Try some chamomile tea with honey, and maybe watch an old movie musical or a light romantic comedy.
Dar - sorry about your son in a wheelchair - how's he doing now? And dealing with your mother's suicide must have been very stressful.
Skye - the woodchuck is cute. Cuter I think than the pubic hair will be - OY!!!!
Not much doing here today. I mixed up some choc. chip cookie dough, which I put in the fridge overnight and will bake tomorrow. Read the newspapers for what seems like the first time in months and -got the approval from the onc. to have a manicure and pedicure post chemo - so I had them today - this was really nice.
Tina - have a nice trip.
Hope everyone else is having a nice relaxing weekend.
caya -
Skye - your avatar just changed to your new wig when I posted - it looks great. I think I am going out tomorrow to buy a shorter one - as I know it will be months before I will have enough real hair to wear out in public.
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Fellow taxolians? Sounds like an alien race! Feels like one too, doesn't it, Viddie? I had my taxol on Wednesday, and by Friday night, continuing through Sunday night, I was pretty much totally miserable. Exhausted, aching everywhere, no energy, bad attitude, etc. I don't remember actually crying or being that sad, but I do remember feeling like I had no coping skills at all, for anything. And, I take an antidepressant, too - maybe if it weren't for that, I'd have been sad and crying too, because I must admit it does do wonders to keep me in a positive frame of mind. We all react to this stuff slightly differently, but I was pretty consistently in a WORSE place over the weekend than at any other point during the week. It also seemed to get a bit worse every week. Oh, and I didn't feel exactly full of energy while the Decadron was in my system, either. I just felt wired, tense, and headachey. Restless, but never got anything done. For what it's worth, that's my experience.
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Skye, I love your new avatar! You look great - and even more like Leslie. Thanks for sharing the wonderful pic of the baby woodchuck - I hope he's ok. The photo really brightened my day. And yes, Caya, he IS much cuter than the you-know-what will be. You crack me up.
I want to share something - you guys may or may not think it's as cool as I do, but it really, really made me happy. After my surgery, I had lots of phone calls, cards, four bunches of lovely flowers, all kinds of good things from the wonderful people in my life. Even the gift of a song! But by far the best thing was what my mother and sister did for me - they adopted me a baby elephant!! I don't know if any of you saw the tv piece on the elephant orphan's project in Kenya, where they raise up the baby elephants (who age the same rate as humans) paired with keepers who stay with them 24/7 until they are old enough to be transitioned back into the wild. It was the most wonderful story. Anyway, you can adopt the orphan of your choice, and they send you pictures, and keeper's notes about how your baby is doing and behaving, and all kinds of info. I have a little girl elephant named Lempaute, who was born in October, 2006, so she's still a baby. She was found wandering all alone in an area where there were no elephants, so evidently was unable to keep up with her herd during a stampede. I've been smiling ever since I learned about this. Guess it takes a family member to know what quirky little thing will make you happy, huh? If anyone wants to check this stuff out, go to http://www.sheldrickwildlifetrust.org/index.asp - you can even see my little girlie. -
"Any of you on tamoxofen or arimidex yet?"
Hi Viddie,
Tae will see Dr. on Wed to get started on arimidex. also get the appt for a pet scan. At her support group meeting several women had bad experiences with arimidex, but a nurse at her surgeons office just finished her 5 year program and had no problems with that drug. we'll have to wait and see how it affects Tae.
Hi everyone,
we are getting our life back to normal or as close to normal as it will probably ever be. Tae's hair is growing back in. it is long enough to pinch a little in the back. still very easy to get tired, but enough energy to take an interest in her flowers. if only we could get some decent rain. last weekend was a full house, my sister and mother, our son and family (twin 3 yr olds), and our daughter and her family (just back from overseas). they just left today for an air base in florida and now the noisiest thing in the house is the ceiling fan. it was a great visit especially after the last five months of chemo.
take care all,
Terry 4 Tae. -
Yes Mel, I remember being very irritable when the Decadron was wearing off about Sunday Afternoon, I had tx on Fridays, then I would feel horrible until Tuesday, Weird how you could practically set the clock by how you were going to feel. I went to a grad party this evening, I drank 2 beers! That's the first alcohol I had since well forever... There were 5 people there that had some sort of cancer including me that was obvious. 4 of us in scarves. So for once I was someplace where I wasn't alone. What I didn't understand is why they all had their eyelashes and brows and I don't! I can deal with my bald head I just really hate not having a normal face. OMG, I wore my puff ball boobs and I ended up in the restroom stuffing them into my purse. I will never ever wear those lousy things again. They creep up and just drove me crazy! Then I lost a button on my blouse and my port would show through. Fortunately, I got a jacket from my SIL's cousin, then I felt better and was able to enjoy the party. Well, getting sleepy, I'll see ya all tomorrow.
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