Starting Chemo in JAN 2007
Comments
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Caya, I am blown away at how well this Effexor is working for me. Like you, I NEVER in a bazillion years saw myself on an anti-depressant. EVER. Did I mention ever?
I began it about the beginning of Oct. and I saw a marked difference at about 4 weeks later. I began feeling better rather quickly, but really took note of it the last two weeks. It is amazing. It's like a serotonin transplant. Plus, losing 5+ lbs. has been nice. It's the only antidep. I've heard of where weight loss is a side effect vs. gain. Can't say enough good about it. I am going to become a spokesperson for Effexor and Emend, my chemo antinausea drug. (Funny, I never barfed but I STILL cannot eat at Chipotle after eating there on chemo day #1.)
Caya, thank God you mentioned having a MUGA this week. I totally forgot I have an echo. today. Speaking of which, what is the diff. btw. a MUGA and an echocardiogram I wonder...
I also only remembered my Herceptin infusion last Thurs. a day or two before. I don't think it's chemo brain. I think it's that I'm starting to get on w/my life a bit and I'm forgetting about the medical stuff more so... it's so much easier to put this behind you when you have some hair. I didn't realize how much of an impact that had until now that I have some hair again. I didn't really mind the whole scarf thing... not that I liked it, but it was just the cost of doing business. But, I feel a lot better now that there is no visible sign of cancer.
Nancy, try not to stress about the pap. I had my first abnormal one in my early 20's, had a colposcopy... they have been normal now for years. You can have abnormal ones for a while and then they revert to normal. I did not hear about tamoxiFUN causing yet that too (abnormal paps).
Cindy, will be waiting to hear from you...and hoping for an easy wake up w/no nausea from anesthesia. I've become somewhat of an anesthesia phobe.
Melia, sounds like a good deal at your job. I'd try to relax, accept any/all help and just get through the three years. You'll be home free after that. And boy do we know how fast a year can go! Glad your trip is over and was successful.
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Caya, I should mention that I started on one Effexor a day for two weeks and the dr. then upped it to two...total is like 75 mgs. Anyway, the first two days I took two pills I felt like a meth head I (not that I know what that feels like, but...
I was FLYING. So I went back to one pill. I considered pill splitting and taking 1 1/2 but that's such a PIA. I eventually just sucked it up and took two and within a couple of days the flying feeling stopped. Now I just have a lot more energy than I had pre-Effexor, which is a nice thing. No afternoon slumps, naps.
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Cindy, we are all thinking of you and surrounding you with strength and love.
Melia
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Keeping Cindy firmly in my heart today. You will be fine girl (or else).
HUGE HUGS from Edison
{{{Cindy}}}
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Cindy, we're with you today, you will be fine!
Joni, those are great pictures...you have tons of hair!
Melia, I'm glad you stood up for yourself about those business trips. I can totally relate, they are grueling. I remember the days when it was really cool to go on a business trip...wow, I get to go to new places and they pay. Now, I'd just rather be home.
I still haven't downloaded the pics from my vacation yet, but will. I'm trying to get my XMAS shopping done and am about 1/2 done. My mom is still living with us, so it's just been a challenge around the house lately. She/we did put an offer in on a mobile home...just need it to pass inspection and Mom's moving out in a couple weeks. woo hoo! I love my mom, but it's really hard living with her. I'm sure she feels the same. She'll only be 15 minutes away (she used to live 45 minutes away), so she'll be close by and be able to help after my surgery. We'll also get to see each other more often.
I bought myself an iphone the other day...it's really cool!
gotta get to work, have a great day!
love and hugs,
Lynn
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Hi Everyone,
Cindy all thoughts and prayers are with you and that surgery. What wonderful co-workers you have, too, to do that for you. Can't wait to hear back from you.
Melia, you have a great boss. I didn't remember that they bonused you the pay. I'd stick with them too if I were you, especially for just 3 more years.
Nancy, yes do check out the Pap but keep in mind the statistics are on your side. I did say I still have neuropathy, in my feet every time I stand up I totter like an old lady. I wonder if it will ever go away.
Caya, use whatever you need to make it! If Effexor does the trick, then Effexor it should be. And no guilt, we gotta do what we gotta do. On those flu shots, I was just reading an AP article this morning that most flu shots contain mercury...one shot has four times the daily "safe" level for an average person. The manufacturer uses it as a preservative in large, multipaks of vaccine. But it is possible to get a mercury-free one, although harder to find.
Speaking of Effexor I could have used a shot of that last night, should have known DS2 would not get back from his NY weekend without incident. Outstanding parking tickets caught up with him and his car is now booted in the airport parking lot. He is still there...I'm hoping I don't have to drive to Chicago today on a rescue mission. Caya, may I say OY?
On the up side, it's another beautiful fall day here and I'm hoping to clean out my window boxes and maybe put lights outside. Yesterday I raked the branches and leaves that had fallen on the upstairs deck and pitched them over the rail onto a tarp; that was a pretty good task to accomplish and tells me I'm making progress. Now you're all inspiring me to do some baking too. Here's to returning energy! - Skye -
Skye dear - You may say OY!!
xoxo Caya
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Cindy,
Thinking of you today, and wishing you all the Best.
Warm hugs...Joni
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Skye, that Grendel is just so adorable I can not take it! What a cute little face! His mom is absolutely beautiful…she has such a wonderful expression on her face in that photo (love the ears). 8 boobs….NO THANKS!!!!! Sheesh. Parking tickets caught up with DS, eh? Owen and I saw a car with a boot on it in a parking lot the other day and he had a very hard time wrapping his brain around what it was for and why anyone would let something like that be put on their car unless they had a key. Maybe it is a male thing. We have been having plumbing issues as well…my washer has gone berserk and has flooded the basement 4 times in the last two days. I have to watch it carefully when it fills to make sure it does not run over because the pressure switch is not working. I ordered the part last night…hope it gets here soon because a washing machine is NOT optional in a family of 5!
Lynn glad you are home, and great to hear that you had a fun time….I am sure you will post some pics of your trips to paradise…..I hear you on being sick of Drs…I have had a nice break from them, but I just looked at my calendar and I have an appointment each Monday for the next 4 weeks or so….Flu shot, Dentist, mammogram, MRI. BLECH!!!! I also found out that since I have implants, I always have to go for diagnostic mammograms….so I guess I get to camp out there (they said to expect to be there about 3 hours or so). On the plus side, no waiting for results since I will be seeing the radiologist personally I am sure.
Tina I hate it when a restaurant gets a good review like that and the food is awful. Makes me sick, and makes me question the objectivity of the papers.
Melia, good for you on seeing the need to delegate! I agree with what the others have said, you should definitely stick it out the last three years (clearly you have skills, and they want you!) but there is no need to torment yourself.
Happy birthday Mary! Sounds like you had a nice time as well.
Jan I hope your munchkin is feeling better. Nothing is more miserable than a sick three year old….except maybe the three year old’s mom!
Joni you look awesome! That looks like a great trip.
Caya hang in there!
OK, I think I am up to date now with old posts…..
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ACKKKKKKKK!!! I have homework from a class I'm taking and I cannot think. This chemo brain is really getting to me. I thought I was fine, but now that I'm in the thick of things at work, it is really apparent that my brain is fried. I have no idea what to do. I have figured out ways to remember things like where I park my car at the grocery store, but when I have to use once familiar terminology, I am at a loss. This class is killing me and all it involves is doing lesson plans for English language learners. I do this all the time, but to actually write it down it beyond me.
I wonder how long this will last? The terrible initial fog during chemo is long gone, but this other sh-t is for the birds. I really hate not being able to *think* and use words I used to use with ease. I also find that I am really easily distracted. Anyone else? I will have to talk to my onc about this on our next visit, but I fear there's not much to be done about it.
Thanks for listening. And now back to the books. What was I thinking?
XXOO Amera
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Oh Amera I hear you and I sympathize for sure. I am in very much the same boat. I often find myself questioning my teaching skills, and at times I have been afraid to face my English Comp class for fear of analyzing something wrong or explaining something improperly. My lexicon is hopelessly scrambled and very, very slow I can not concentrate for as long as I used to be able to, and multitasking is waaaaaay beyond me. When I am required to do things that the "old me" would have done without a thought I find myself getting anxious and sometimes lashing out. It is very frustrating. Sigh. I do not know when the chemobrain will end, or if it will. In the meantime I carry a notepad now, and leave a trail of reminder notes everywhere I go.
{{{Amera}}}
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Oh Amera and Rebecca - I hear ya. I find myself grasping for the dumbest everyday words sometimes - and I am so easily distracted now. I always have the best of intentions to do many tasks throughout the day, but I can't seem to handle it like I did before BC... hopefully this will all clear up eventually, I mean we're all mostly just 6 -8 months done with chemo.
Lynn, I hope it all works out soon with your mom moving not too far away - sounds like the best of both worlds, she'll be close, but not too close.
Is it just me or did the site undergo another transformation today - the blue background is gone (which I hated) - but the main list of the different subjects is missing the lines/borders to separate each subject, making it seem rather messy and crowded. Also it seems you can't go back and read the previous posts from previous pages, you can only read the page you're on. I hope they fix this, here we go again with "if it ain't broke, don't fix it."
xo caya
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I wonder if part of the chemobrain thing is an underlying current of still being distracted/obsessed/worried about the whole BC thing. Even though it's not at the forefront of our minds as much as it was before, it's still always there and I'm sure that's competing for "brain space" with the stuff we are trying to concentrate on.
I haven't had to take any classes in a long time but I do notice that when I do things that require concentration, i.e. I did the DH's resume yesterday, I try to avoid it like the plague. I just don't have the level of concentration I used to back when I was working. Of course, then, I had only myself to worry about too. If it were now, I'd be working and multi tasking in my brain about the bazillion things I'd have to do after work for the kids, etc. I def. recall that while on chemo I'd have to re-read paragraphs several times before they'd sink in. I've always been a rather "quick" person too...(if I do say so myself
... meaning that I could read/process/respond very fast...sometimes too much so, I'm sure.
Had my echo. yesterday and of course, they give you zero indication of how it went. Not worried, but I'm sure this is a contributor to the mild undercurrent of anxiety that courses through me each day.
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Speaking of processing things quickly, my mother is starting to concern me. She is 65 and for at least the last year, I'll tell her things and literally within seconds she'll ask me about exactly what I just told her. It gets me pissed as I feel like I'm wasting my time explaining things (like tx. stuff) and she's either not paying attention or whatever. She does it to my father too. I swear, sometimes it feels like it's on purpose, to aggravate us. It seems to really be picking up, though, the last few months, which is beginning to concern me that it isn't a passive aggressive form of torture.
But she can be totally focused when she wants to be... so I just don't know. It is very frustrating though, I've gotta say. (Maybe she's just sick of hearing from me as we talk several times a day!)
Lynn, it was great having my mother here too, last year, for my surgery. She did it all around here, from cooking to laundry to taxi'ing the kids around. She offered to come up for my surgery next week but I feel it's not necessary as the DH is home. I'll prob. shoot myself later.
Anyway, as great as it is to have them around, I could only take it in small doses. "Nearby" is good. In the same house is tough.
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I agree Tina, I think that at least part of it is a result of distraction, worry, and and perhaps a touch of depression (at least in my case). I do not, however, think that this is enough to explain the changes in my thinking and the decrease in quickness I have experienced. I truly think that the chemo damages the brain, causing these rather subtle defecits. There does seem to be some research emerging that supports this notion...this after Drs scoffed at us for YEARS about chemobrain. Survivals stats are now very high, so the population exists to study such things....I am sure we will be vindicated in the end! Chemo-fog sisters UNITE!
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Wooohoooo... got a 60 on my echocardiogram which is basically where I started out before I began A/C and then later, Herceptin. So I feel good that that's in order before my surgery. Also, I spoke to the NP today and they will do my next herceptin "in house" while I'm in the hospital so I don't have to tie up my entire Thurs. before. Ever the multi-tasker. And, she said on Dec. 20 we can discuss switching to an AI...which she says takes care of any residual estrogen, i.e. the stuff from the adrenal glands. Sounds good to me. However, some dr's want you to do two full years of tamo. so we'll see what he say's.
I started getting nervous at what feels like elective surgery again today but I then remembered my high oncotype score...I have to keep recalling that...which is reason in itself to do this.
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Hey Ladies,
Caya, thanks for the OY! I ended up having to drive to Illinois, though not downtown Chicago thank goodness, yesterday with a chunk of cash that needs to be repaid to me now. DS had a worse time than that, spending many hours trudging back and forth on train, bus and foot and dealing with the downtown city government. I think he has learned his lesson on parking tickets. I'll say it again, OY!
Rebecca, 8 boobs would be SO over the top, wouldn't it? Poor little Lhasa mommie. And she is a very pretty dog. Grendel's genetics should be good.
Amera, Rebecca, Tina, everyone I hear you on the chemo brain and I agree it is probably damage from those chemicals and will probably take a long time to heal. All those delicate synapses and neurons, still suffering the shock of being bathed in Red Devil every 2 weeks. I have felt it in my writing, grasping for words that should be there, and sometimes on the radio shows when I completely lose my train of thought mid-sentence and have to ask the host to clue me in. In my case, I know a little of it is due to age, too, and I did have the preexisting condition of fibromyalgia which has its own "fibro-fog." So I guess I'm mentally screwed three ways. :-)
Tina congrats on the great echo score. We Herc gals must pay attention to our tickers. I do take COQ10 daily to help with that. My neighbor who has been on Herc for 4 years and is in total remission from Stage 4 was going to have to be taken off the Herc due to imminent heart failure. Someone told her to take the COQ10 and her scores rose enough to stay on it. She's the one that got me taking it, with my oncologist's permission (200 mg daily).
I'm basking in the glow of having finished my editor queries 2 days early, but they are like zombies in grade B flicks, they just keep coming back and get uglier every time. - Skye -
Hi all,
I just read through all the posts- very good reading. Everyone seems to be keeping busy.
Happy Belated birthday,
Rebecca and Mary.
Caya,
Your Shabbat dinner sounded delicious. Sounds like our Passover dinner.
Skye,
Is the ibuprofen working? Are you feeling better? I am going to try some CoQ10. My Muga score went from a 62 to a 55. My onc doesn't think there is a need for concern. It could just be a give and take difference in the tests. I think that is has something to do with my surgery. I had the test two weeks after my surgery and my heart rate was higher after the surgery. I am no doc, but I am guessing my heart was a little stressed after the long 12 hour surgery. Hopefully next time my score will be better. Your puppy is so cute.
Cindy,
My thoughts are with you. Looking forward to hearing from you when you arrive home.
Sharon,
How did your genetic counseling go today?
Tina,
That is great you will have the herceptin treatment while you are in the hospital."Multitasking" is the way to go.
I had my hair colored yesterday. My hairdresser also evened out some loose ends and now my hair flows a little better. It is still very short, but I feel much better now that it is colored. She used a semi permanent because she wants to see if I like the color. The color will fade in around 4-5 weeks, and I can change colors easily if I am not happy. Even though she did not put in highlights, it looks like she did. My salt and pepper is now blond and light brown. I like it!!! I am later than most of you, but now I finally feel comfortable enough to go topless. Finally!! Only problem, now my head is cold. Are any of you cold on top now that winter is here?
I have my herceptin tomorrow. It is weird, but I associate the chemo room with food. I always had lunch during my chemo, and now I feel the need to bring some tea and a snack with me. I actually look forward to eating when I am there. Weird or what? I think it is just comforting.
Have a good night.
Viddie -
Viddie I'm glad I checked back in before hitting the hay so I could see your message. The hair color sounds lovely. My head is only cold when I go outside so I'm back to winter hats. And I do the same thing for Herceptin! I bring special teabags, something munchy and a piece of chocolate, my reward. I do feel comforted by having a snack, and am always there so long I need it.
As for the ibuprofen, I can't say it seems to be working at all, it's just as sore and I actually don't feel real great. However I still have to go through Sunday to do the 10 days so maybe it will improve yet, thanks for asking. - Skye -
Evening, very quiet here, DH still at work and the kids are working too. I went to the Dr. today about the meds. I felt stupid but I brought all my meds with me. Lo and behold he took one look at my Effexor bottle and said umm I wanted you on Effexor XR this is a low dose generic. I should be on 75 mgs and my bottle said 1 tab every night before bed. @ 25 mgs! So he got me the right Effexor and by Thanksgiving I should be on the 75 mgs. The two "effexors" don't even look the same. I hope I soon get it together. He wants me to see someone too, that I can talk too. I got the weirdess thing in the mail today from my breast surgeons office telling me my appt in Dec. has been cancelled. Why? there was no explanation. I plan to call tomorrow, but I just thought that was strange.
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Hey, ladies....I'm home!
Honest to God, I've had the best experience - surgically speaking of course. The anesthesiologist changed some of the meds they've used on me before, the surgeon held the morphine this time and used Dilaudid for pain control and I took my last Emend pill at bedtime the night before surgery.
It all worked! I didn't have one rumble in my stomach, no vomiting . It was great. I was up walking the halls about 7 hours after surgery was completed yesterday. This morning my daughters and I had played two games of Scrabble before lunch.
I didn't get home until after 5. The doctor didn't make rounds until after 2 and it took the nurse another two hours to prepare the discharge orders and being me a 'going away' pain pill.
I had decorated my breast with the butterfly tattoos and then had my daughter write on the breast: "uh-huh, it's gotta be this one". I understand the operating room staff took a moment to admire it all.
The initial report from the SNB is 'all clear'! Woohoo. I'll get the pathology report on the breast tissue next week at my follow-up appointment.
I have two drains in and already the area where the tubes emerge seems to be tender. The doctor told me specifically not to do any stretching or exercising on the left side until after she sees me. I'm just to let myself heal and then I can work on regaining full range of motion.
I'm amazed. I'm just not used to feeling this good after surgery. I'm thankful and so appreciative of the blessings in this experience.
I'm ready to sit in my recliner for awhile.
Have a good evening, everyone!
Cindy
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Cindy I am so glad to hear that you are doing so well! Keep it up, and it will all just be a nasty memory before you know it!
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Cindy, so glad to hear your good report and that you had a good experience! That makes all the difference. You have been in my thoughts the past couple of days for sure. Take it easy now and don't overdo it. I'm sure you'll do well.
I've been reading, but haven't had time to post for a few days. Life is so much more complicated when work enters into the picture! It is going well, however - feels good to be back at work and working with people again, and better for me to be thinking of others instead of myself. But it is tiring, and I'm glad I'm not obligated to be working full time just yet.
Remember how I was changing oncologists, to the M. D.Anderson lady oncologist? Well, I had an appointment tomorrow with my old oncologist, that I had never cancelled. He called me personally the other day, because my disability insurance company had called him (instead of the other one - they just didn't get that right) and he wanted to be sure we were on the same page and that he was telling them what I wanted him to tell them. He was so nice about it. So, long story short, I couldn't tell him I wasn't going to use him any more. So I'm going to keep my appointment, and deal with this later on down the road. He really is a nice guy. I think my boss is going to leave me part time through December, so I need his cooperation.
I'll try to post more tomorrow. I love you all, and am reading and keeping up, just haven't had time to post. I'll do better, promise.
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Oh, Cindy, sooooooooooooo glad you got through that SNB so well. I can say now that when I read you were having it I about fell off my chair. I am scarred for life by those three letters. Never thought about asking for Emend for the evening b4 surgery. Good idea...
Skye, haven't heard of that drug. Is it a vitamin? If my scores fall at all, I may take. I have so damn many pills now, I think I'd be sick if I had to pop even one more. However....that drug may prevent damage down the road from the Herceptin. Am I right in that damage can occur long after we use it? Viddie, my score was once at 58 or something. I may have began at 62 or 65, I'm not sure, I'll have to look. But... it went back up from the 50's, so that can happen. I wonder if the test is subjective to who is interpreting it. Also, are MUGA and echos the same thing?
NANCY! So glad you brought in the pill bottles. That was so smart! You will be wowed at the difference when you get the correct Effexor dose. They tried to start me on the XR (extended release) version but I asked for the regular as there is a generic. (I hate $40 copays when I could be paying $10.) Be prepared for that rush the first few days you take the two pills....it will subside and when it does, boy, do you feel better. I can tell just by my posts... I wasn't really posting at all for weeks. I didn't even have the motivation to "talk" to anyone because I was so blah. Clearly, that's over. Ha-ha!
Mel, awkward sitch with the old dr. calling. I hate stuff like that. Esp. when they are nice guys. I hope you can stay part time thru Dec. too. Holidays are busy enough.
Viddie, good to hear from you. I know you've been busy reacclimating to your real home. I find unpacking from a weekend daunting...never mind a summer. Congrats on the hair color! I really think that gives you a new lease on life.
Skye, I'm confused. I thought your son's vehicle got the boot in NYC, not Chicago. And speaking of Chicago, did anyone see that police chief on the Today Show w/Matt Laurer yesterday? The one who is suspected of killing his 23 year old wife? He is unreal... he is trying way too hard to portray an innocent man...acting as calm as could be... but he doesn't see that he's acting WAY too calm. Matt called him out on that. You could tell Matt thought he was so full of it. I can tell this is going to dominate the media now. I am interested in the case now (my obsession...Court TV, Forensic Files, true crime stories). I bet the police chief is glad OJ got indicted so that will take up a lot of the airwaves. Personally, I think the latest OJ case is bull but I hope he gets his this time, regardless of how foolish the whole situation is.
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Hi All,
Cindy, so glad you are doing well and had a good experience, or as good as that gets, I guess. Viddie, nice to hear from you. Are you back at work too? Mel, I am sure the readjustment is difficult, but I think what kept me from completely falling apart was being at work where other folks didn't know. Of course, my job is a desk job, completely diff from nursing, which is so much more physical. But I still get really tired, was in bed asleep last night at 8.
I agree with everyone about the brain damage. My memory is weak, I find myself searching for words, and I am not as good at concentrating as I used to be. I still love to read, but it has to be a very compelling book. I lose interest otherwise within a few pages. I used to give a book 100 pp to prove itself, and now I am bored in maybe six or eight if it doesn't grab me. And I can't seem to knit. I mean, I can, but I don't want to. I used to knit a lot while I chatted with my husband or watched tv. And I have something I must finish for my daughter for xmas. I feel stunned a good deal of the time, have to plow through that to get to any intelligence. Does that make sense?
Nancy, good for you for being your own advocate. That is exactly what you should do. I know you will feel better soon.
Caya, have you started the effexor, or when will you? I hope it helps you too.
Skye, congrats on meeting your deadline early, and good luck with your son. We never stop parenting, I guess.
Ok, off to work. I hope everyone has a sweet day.
Melia
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Hi all, just a quick check-in from San Antonio. Weather is warm. Conference is going well so far, although I just got in yesterday afternoon. Skipping the first session this am for a quick work-out, then I'll be ready for a full day of networking.
Cindy - I am so glad that you had a positive experience and that you are home recovering. Definitely take it easy until you get those drains out. Get lots of rest - even if you feel OK your body needs its energy to heal.
Hope everyone has a good week.
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Hey ladies,
First, Cindy, great relief on the positive surgery experience and the all-clear. I hope that OR staff truly appreciated your fine sense of humor, and it sounds like they did. Many good recuperation wishes!
Nancy, smart girl to take the bottle in. YEAH that you will now get the right stuff!
Tina, COQ10 is a type of vitamin, you can get it at any vitamin shelf. Not cheap but worth it. I also take milk thistle, mainly for the liver (before I started it I had cysts I could feel every time I bent over, now I don't!) but it also is protective for the heart. My first MUGA score was 75 and they didn't tell me the second one, just said it was "good" but I will find out next week.
Jan I'm glad things are going well for you at the conference. Heck, if you can climb rocks you can do anything!
Melia, I know what you mean about getting thru feeling stunned to get to the intelligence. That is a good way of describing it.
Oh and Tina, DS flew to NY but left his car in an O'Hare parking lot, where cops evidently patrol and check license plates for overdue tickets. Grrr, I'm still striving to stay calm.
Mel, I probably would have done the same as you and stayed with the old onc after that.
Today is my one-year anniversary of the nightmare mammo. I celebrated by staying in my pj's and watching Robin Roberts get her head shaved on the morning news show. She looked lovely bald. - Skye -
Cindy,
Glad to hear you are doing well. Make sure you look after yourself, and pamper yourself a bit, especially til you get the drains out. Loved what you did before surgery.
Jan, hope you are having fun in San Antonio.
Viddie, so are you all moved back home? Good to hear from you.
I'm off to Spokane for a 4 day shopping trip with my sister, her friend Bojalais, myself and my friend Anita. Should be fun....hope the Canadian dollar stays high.
We're staying in Coeur d'lene, and going to drive in to both Spokane and Post Falls (shopping outlet)
Leaving on the weekend, should be back next Tues. Dan will be home looking after Thor & RC.Big hugs to all...Joni
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Cindy, so glad to hear you are doing well! Was the emend leftover from your chemo?
Just checking in quick, I've been sick the past couple days. Came down with a fever Tuesday night and still have it. Also was up half the night last night in the bathroom. This is kicking my A**!
I have to drive into Boston tonight because I have my pre-op appt. w/ PS and preop testing at the hospital. Not looking forward to the 2 hour drive at all. I might leave later on this evening hoping I'm feeling better.
Joni, you world traveler you, have a great time shopping!
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Tina, what should I expect? My Dr. did mention that I would have some "sensations" the first few days and to ride it through, not sure what he meant or what to expect but ... Today dispite taking advil every 4 hours I have what I consider a "cytoxin headache" ( remember those?) that was the worse headache I ever had and I get migraines. But I am worried because one of our techs has the "genuine" flu and he was in turning in paperwk.I hope t hat is not why my head hurts, Egad if I get it.....!!!
I am going to take a little nap though, see if I can sleep it off. Bye for now, OOOH OOOH Cindy almost forgot.....GET WELL SOON!! So glad that is over with, Now we must get Tina taken care of, is anyone else going in for surgery?
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- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team