first chemo done
Comments
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I don't think we're looking to "blame", ourselves or something else; rather we're looking to understand our circumstances or even better, to glean some wisdom from this experience. And, for those of us with daughters, to pass along that wisdom.
I agree that this experience is one that will weave the tapestry of our lives. Trust me, I never thought I'd be on this journey. For gosh sake, I got my Teaching Certificate less then one year ago, I never even got to get a full time teaching position! But, for whatever reason, some "greater entity" has uprooted me in the midst of my plans and detoured me towards their plan. I accept that (even if, as is often the case with detours, I don't know where I'll end up). This is who we are now...and like you said Jill, we look toward the future stronger, wiser and with more peace.
Jill, one more thing I can agree with you about, I, too did some crazy-ass things to myself during my teens and early twenties, God, don't you miss the '80's?
Janet
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Hi Janet !
Nice to hear from you !
Let me clarify something on my point. Actually, I have seen a lot of what I call the "blame game" with this disease. Just last week I had a woman tell me that it was "inevitable" that she get this because of the things she had done. I am not kidding. My chin was on the floor. I have also seen women who have done the HRT thing just beat themselves up over doing HRT. True, supplementing with estrogen COULD spur on a ER positive tumor, but who is to say it did. Certainly not with all women, but there are a lot out there that seem to have a need to fixate why they got this disease on something (for clarification, I have never seen you do this). I guess that is fine if it makes them feel better, but for me personally, I think this is wasted energy because it is question that cannot be answered - and at times it creates added anxiety and guilt unnecessarily. That was the point I was trying to illustrate.
That said, I am impressed with your attitude - I like your detour analogy. That is exactly what it is... a detour. Who knows where it will take us - but let's look forward as opposed to backward, eh?
As for the 80s... I hear you sister ! Care to divulge ?
Jill
P.S. What did you do before you got your teaching certification ?
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Hi Jill,
Oh I did my share of searching, even asked my mother if she was given DES while pregnant with me (doesn't the "mother" always get blamed?
) I thought, perhaps, I didn't wash my fruits/veggies enough, etc. However, if the experts don't know what brings this about, I figure I certainly can't figure it out. The past is past, I need to enjoy today!
Before teaching I was a Paralegal in the New Jersey Attorney's Office. - Yeah, I know, quite a career change! But when you think about it - working with Lawyers or 6-year olds - it's not that different - a lot of hand holding and breaking up fights!!! However, teaching is a much better "fit" for my personality.
Well I am off to enjoy today. I want to take a walk and go Kayaking before going to a picnic. Tomorrow I have my first chemo so I'm not too sure when I'll be able to enjoy being really active again. May you all have a wonderful day with your loved ones.
Janet
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Hi, Jill and Janet. I'm not playing the "blame game" so much as I look for answers to most things, it helps me make sense of what is going on. I truly believe there are some things we don't have answers for, and it's better not to dwell on what is in the past - I am definitely a look to the future person - I look forward to bigger and better things for myself, and see this disease as a huge speedbump in my life that I will have to learn how to drive up and over and away from. The logical part of me just likes to know the whys and hows of things to help sort out what I am supposed to do in the future. Especially if there was something I could do now to prevent it from coming back or help prevent the other breast from developing it. Maybe there is nothing I can do, and it is fate, but part of me refuses to think that only fate is at play here.
The biggest thing I have learned from dealing with this unexpected and life changing disease is that I do need to take time for myself, spend precious time with my family and hold them even closer than before. I have learned that I am beautiful with or without hair, though some days I have a hard time believing that, and that my true friends love me and are there for me through thick and thin, as I will be for them. I am also proving to myself that I am stronger than I ever thought, and while I am regaining my physical strength back day by day, my belief in God, myself and my family is renewed and strengthened. And, that I will win. No matter the cause or the whys or what-ifs, and believe me, more than you think have spent time dwelling on this, and unfortunately, some will do nothing but dwell, but that is not me.
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I do sort of miss the eighties... Not the clothing, but I really miss the excitement from the music. I remember being so excited to get my first Cure record, and trying to tape Depeche Mode and Heaven 17 off the New Wave show on the local college radio station, and heavy black eyeliner and putting safety pins in my ears... Crashing frat parties with my friend Jacque... whoo, okay, should quit now before Memory Lane becomes Trash Alley...
The psychology of cancer is really fascinating. I know a woman who's been clear for 6 years now, which would thrill most of us. However, she's not moved on, and there's always a new explanation for her cancer, whether it be plastics, milk, hormones, chemicals, pollution... I'm a bit of an environmental nutwing myself, so I'm not unsympathetic to any of this, and certainly believe that we've changed our environment and we're dependent on a massively complicated food system in ways that are probably not great for any of us. I loved Mark Bittman's book "Food Matters" on this point...
Anyway, six years out from her last chemo, this individual's life is still organized around keeping her personal environment as pure as possible, to point that her entire life remains consumed by cancer. After reading Jill's post, I began to wonder if this individual does in some sense blame herself for getting cancer, and if her life now isn't anything more than a fierce atonement for her dissolute past (which probably involved beer, eating the occasional hamburger and a handful of Brach's candies now and then). It's an oddly obsessive and joyless way of living.
Fortunately most of us aren't so singleminded. Chelev is right; it's all about balance. There's a fine line between identifying risk factors and minimizing those, and becoming obsessed with controlling our lives and world so that this never happens again. I'll do my best to prevent it from coming back; but I also plan to shelve this project at some point in the not-too-distant future.
I'm a bit of a Buddhist, and my beliefs about all of this boil down to one simple thing: we are temporary beings. None of us are exempt from disease or suffering. Cancer brings that home in a very powerful way and most of us, I think, find that to be an oddly joyful gift.
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Good evening, Ladies !
I hope everyone had a wonderful Memorial Day. I just finished cleaning the kitchen after a big old cook out. I used oak planks, so I reek of smoke. I forsee a shower in my not so distant future.
Anyway, if you haven't figured it out, I put that topic out there to be a bit provocative. You ladies did not disappoint (as usual). But, I really did mean the things I said.
Laura - VERY well put. I agree with you. Your story of the lady 6 years out was very interesting - and a little sad. You know, maybe it is a death wish or something, but I figure if I let this thing control me the rest of my life, it wins. Of course, I won't do anything overtly stupid, but nor will I adopt a "puritan" lifestyle. Perhaps I am a little Buddhist myself.
Sadly, I know some ladies that have convinced themselves that they brought cancer upon themselves and/or live in dire fear of the future to the point their lifestyles are highly restricted. I tend to be a very emphathetic type person. So, it breaks my heart. It is a bit like adding insult to injury. But, alas, they are grown women and have a right to live as they choose.. just as I do.
As for the 80s... well.. it is a good thing we did not know each other then because I am sure that one or both of us would not likely be around now to talk about it !
Janet - I will be thinking about you tomorrow. Remember, the anticipation is often worse than the event itself. Watch over doing it after chemo, because it is possible you will still be on the steroid buzz for a day or so afterwards. OK to let others take care of you.
Oh, and BTW, I asked about what you did prior to teaching because my husband is also a little later in life converted teacher. He got his teaching certification after a different career in business and sales. If you can't tell, I have great respect for those that realize teaching is their calling and dedicate themselves to education. It takes a special person to do this type of work.
I gotta go now. Take care everyone.
Jill
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I really don't care what caused it, I just want it over with..........I do wonder, and was inquisitive about chelev taking the estratest too...but not to the point of extremes. For all I know, nothing could have caused it, just one of those things. I guess in the long run, none of us will ever know, just another turn in the corner of life.
At any rate, go for my first radiation appt today, guess will be measured and all of that. I've had a month where no one has poked, stuck or pushed on me, have enjoyed it alot, guess that's over with! LOL......but after radiation, all i have left is the armidex and I am thrilled!!!!!!!
Hugs and prayers
Deb
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Hi Ladies....
Should of....could of...would of....and that is LIFE in a nutshell....
Deb...good luck with the Rads appointment. How is your underarm area doing? Still need draining? Hope you are done with that by now.
As for me...I had number 8 today...and only 25 more to go... 1/4 of the way done...YIPPEEEE...
My DH and I had a great time wiht our friends in SF...we walked all over the city...went shopping at Neimans,...Nordies...and Macys...and didn't buy a thing...Also we all had dinner at Scoma's on the wharf...good food...I had the famous Crab Louie...YUM...and I could really taste it....They said that I didn't miss anything on the cruise and that they were on the cruise from hell...I guess they missed several ports because of the PIG FLU...which is all a big nothing...and most of the passengers were pissed and wanted their money back...so they gave them all 25% off their next cruise...kind of glad we didn't go afterall...but we would have had fun with our friends...
Today I took a long walk with Roxy and we had a great time...got some sweat going on...and she enjoyed it so much we plan on walking every day to get stronger.
Hugs...ladies....
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Hello All,
Well, as expected the first chemo treatment went well. I got home a little bit ago and feel pretty well. I told my daughters that the onc. nurse said to stay hydrated and suck ice, so I guess that means that chemo days are now Water Ice days! I do expect some yucky side effects, I only hope they are minimal.
Cruise: It was so good to hear the word "port" used in the context of cruising and not "chemo-ing"
. Glad to hear you had a good weekend. Isn't it amazing what doing "normal" things can do for the soul?
I try to check back later or tomorrow. Take care and thanks for all of the good wishes and thoughts.
Janet
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Hi Janet. I'm glad your first chemo went well and hope it stays that way. Rest when you feel the need and take care of you.
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Hi Janet !
One down ! I hope you continue to stay well. I was thinking about you today. While chemo is no fun, at least you got this first one out of the way. That, in of itself, is a milestone. Do you get the Neulasta shot tomorrow ?
Take care now and write when you feel up to it.
Cindy - Hello. Sounds like a wonderful week end. You know my feeling on Scoma's. Now I am jealous. Also sounds like you did not miss much on that cruise. So, let's hear it for saving your money. I am sure you got a big old cruise planned for when you are done, don't you ?
I am beat tonight. So, going to sign off. Got herceptin tomorrow for the first time in seven weeks, but at least I can start again. Will catch you ladies later.
Jill
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Hi Ladies...
Janet...so good to hear everything went well....be careful...if you get the Nuelasta shot...it may hit you afterwards...just rest and DRINK LOTS OF FLUIDS...to flush it out of your system. Eat protein too...it will help...trust me...
Jill...so good to hear that hercepting is back on...and you are on your way with that again. Yes...Scomas was awesome as you could imagine. We watched the Princess ship sail away to Alaska...that is where it was going...after it dropped off our friends. You are right...we are planning a Western Europe cruise....next year if it all works out with work...LOL
Going back outside to enjoy the pool....later ladies....
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Hi all,
Janet - Glad to hear you did well with your first chemo - it is a good feeling to know you are on your way.
Cruise - Sounds like you have a great group of friends - we all know how important those support systems are!
Jill - Did you see Oprah Winfrey on Monday? She had Christina Applegate on along with an entire audience of breast cancer survivors, Susan G. Koman's sister and some oncologists - the thrust of the program was prevention, especially in regards to enviornmental factors. I thought of you and the discussion here about finding out the reason we got breast cancer. What I realized listening to this program was that science is a long way from figuring this out, and if a bunch of brilliant minds can't come up with sure fire prevention, how could I possibly figure it out. We just have to keep supporting each other and the research that will hopefully save our children from going through this.
Deb - good luck with rads appointment
I am reluctantly going for my 3rd A/C on Thursday, a week late - I say reluctantly because this time last week I was in the hospital with high fevers and viral pneumonitis. Onc checked me today, says lungs are clear. I told him I was nervous about getting another treatment so soon, and he said "I understand, but I'm not nervous - you'll be fine. You just had bad luck". He doesn't want me to fall too far behind on treatment, so we go! You can believe that if I get a tickle in my throat, that phone of his will be ringing!
Hope everyone has a good week
Geri
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inthemoment...good luck on Thursday...you will be fine...sounds like your doc knows best.
The Oprah show you were referring to aired last October...after watching the show and getting advice from a co worker...the next day I went to my GP and that is when she sent me to my surgeon and my BC was discovered. The only thing they didn't bring up on the show was that if you notice anything unusual about your bodies to not ignore it and get it checked out...such as a nipple not looking like the other one...I wish they would have covered that so that other women who have unknown BC will get it checked out. I was thinking of writing to Oprah...but never did. I am glad that she supports women's health and she has such a huge audience.
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Janet... CONGRATULATIONS! One down and five to go. I'll be joining you in a couple of weeks. I get my port on the 9th, chemo class on the 5th. I'm going scarf and makeup shopping this weekend - gonna go to Bare Minerals and get some nice stuff to make me look purty...
Jill - will be thinking of you today as you get that Herceptin tx, girlfriend!
Cruise - I haven't been to Scoma's, but when I'm in the Bay area (my sister is a high school principal in San Leandro, just south of Oakland), we go to Scott's in Jack London Square. MMMMMM - steamed clams and mussels with sourdough bread and a bottle of Pinot Grigio, heaven...
Geri - I'm crossing my fingers that you sail through this next treatment. I hope your oncologist is right and this one is a piece of cake.
Hugs to all,
Laura
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Good Afternoon Ladies...
Jill...I am anxious to hear how it went for you today...
Kaidog...if you like Scotts...you would love love love...Scoma's...
Geri...I am crossing my fingers for you...tomorrow...good luck!
Janet...how are you doing today????
Hugs...to all you beautiful ladies....going out in the backyard and enjoy a good book and the heat...its going to be 95+ today....eek...
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Hello all !
Done now with hercepin # 6. Only 12 more (i.e 36 more weeks) to go. I just had to look at the calendar. Assuming no more delays, that puts me done sometime around the first week in February 2010. Port out maybe a month or so later. Sigh.... I guess one treatment at a time.
While herceptin is much easier than regular chemo, I still feel like I get hit by a truck the day I get it - largely due to the Benedryl I think. Today was no exception. I slept it off all afternoon.
Today's was especially potent. We had something really weird happen today. When I arrived at the treatment center, the power was off. They only have a back up generator for the really important stuff like the refrigerator they put some meds in. Anyway, they first thing they said to me was that they were not sure they would be able to give the treatment. I though.. oh, no... yet another delay. Well, anyway I told them I still wanted to see my doc because I had an appointment before scheduled treatment anyway. So.. they get all the vitals, poke my finger, using the old fashioned manual equipment. Then, take me back to a room. My doc shows up with a flashlight. I am not kidding. Pitch black in that office and she and I talking in the dark with a flashlight. Weird. About halfway through the visit... the lights go back on ! Yea !
Anyway, due to the power outage, they were WAY behind. Took me forever to get back to the treatment center, and when I did, it was packed because of all these backed up people. I was nervous since my port had not been accessed for 7 weeks. But, lo and behold, it worked just great. Doc decided to get the full chem panel this time because I have been a little fatigued and sore (no results yet, but my counts are good). So, they took blood and then hooked me up to saline. Like to have taken forever for the herceptin to be hung. Well, this nurse started dripping it real slowly (supposed to take about 90 minutes), but damn... seemed like it was going soooo slow. I think she realized it, and at one point said "I am going to speed you up". She did that, and that is when I felt like I got hit by a truck. Could not even keep my eyes open. Next thing I remember, she is waking me up and telling me I was done. Came home and slept for like three hours this afternoon. Still a little groggy, but much better now. But, I was at that center for for about 4 and a half hours today - just for herceptin.
We also had some funny dynamics in the treatment center today. I went way in the back where it was nice and quiet. There were people in there, but everyone doing quiet activities. TV was off. There are two TVs and the one in the front was on, which is why I went in the back. I listen to my Ipod. Anyway, a little later this grumpy lady comes to the back, and complains that the TV is not on. To which, this other grumpy lady says she does not want the TV on. I thought we were going to have a cancer/chemo cat fight right there in the treatment center. The lady who wants the TV on wins out, (much to the dismay of the rest of us). The other grumpy lady stuffs tissues in her ears. I turn up my Ipod. And I STILL managed to fall asleep in the midst of all this. Helps when you feel you get hit by a truck.
Also, doc and I talked a while about my heart being "abnormally" normal. I read the report the cardiologist sent. He did call it "equivocol" and said my EKG was slightly "abnormal", but given the pictures from the ultrasound taken during the stress test, he cleared me for treatment. That was good enough for me. Doc also mentioned that the "puffiness" from all this stuff done to me on my right side (i.e. surgery and radiation) was "changing" and that likely it would get "harder" over time - like a rubber ball (lovely). She said that all this soreness I am feeling on the right side around my rib cage was typical and that it could take months or even years to go away. She was just a wealth of good news today.
But, I have to admit, I do like my doc. She is cautious but thorough, listens to me, takes time with me and explains things well. So, can't ask for much more. We have come to an easy truce on tamoxifen - we just don't bring it up any more. I think she knows what I am going to say, which is I don't want to take it. She treated me as if I were ER/PR neg (which I essentially am). I just don't see the benefit of taking tamoxifen for my situation given the benefit/risk ratio. I think she thinks I have a point on this.
Well.. I did not expect this post to get so long, so I will start a different one to check on you ladies.
Jill
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Back again....
Sorry for the long post. I type really fast and have a hyper brain - dangerous combination.
Geri - First, I am wishing you the best tomorrow. Now... let's stay out of the hospital this time, eh ? In all seriousness, you call if ANYTHING feels weird to you. I will be thinking about you. You are getting there.
As for my philosophical diatribe.. well, I struck a nerve with that one, didn't I ? Believe me, I am all for prevention of this disease and anything that can help our daughters and sisters avoid this. I think they are making progress every day. However, the scientist in me knows there are soooo many variables to be considered. There just isn't an easy answer to point to and I doubt there ever will be. In my case, I am convinced my situation has a genetic component - even though I am BRCA negative. I just think the gene mutation in my case has not yet been discovered. But, in the vein of not obsessing about what I can't control, I choose to look forward. My daughter, however, knows that unless things change dramatically over the next several years (and they might), she will need to be concerned about early detection as her best course of action. But, I am glad Oprah is working on the awareness. Quite the lady !
Deb - Best of luck with rads. Much easier than chemo or surgery, but I am finding the "effects" (while not earth shattering), last longer. I am nearly three month out and am still sore on my right side. Like I said in the above post, doc says this is normal. Also, still got one tan boob. Oh well.
Janet - I hope you are doing OK today - well, relatively speaking. Pipe in with a sentence or two when you feel up to it so we know you are OK.
Laura - Hey Lady ! I will answer your PM shortly. You do know how to bait me to get a million things going in my head at once. But, what fun. I enjoy that after my day of getting hit by a truck. A little like "brain gymnastics".
Cindy - You are VOLUNTARILY going outside in 95 degree heat ? You are a sicker woman than I thought.
Take care ladies. Hope to hear from you soon.
Jill
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Hi All,
I just wanted to let you know that I am feeling very well. I know it's only day one (or was treatment day #1) and most SE will happen on day 2 or 3, so I'll wait to see what happens then. I did go today for the Neulasta shot, so I'l also wait for the bone pain.
Oh, daughter just reminded me that I have to take her to soccer, will try to get back to you all later tonight....I have some questions (of course.
Janet
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Janet, I LOVE HEARING THAT YOU FEEL GREAT! You're inspiring my attitude! I'm in the waiting-for-chemo-to-start lull....so keep us posted, okay? And do me a favor - if you feel rotten, lie to me.
Jill, just sent you a note on email... WOW, sounds like a bizarre and exhausting day. I hope your ribcage doesn't permanently resemble a rock-hard kickball.
Laura
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Janet....good to hear all is well so far. Keep us updated...it will help Kaidog too...
Jill...herceptin..has not been easy for you. My gosh of all people to have the power go out. You know sleeping through it...was a good thing.
I went outside for about 5 minutes...and came in the house and sat under the ceiling fan...it was a scorcher today...
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Geri ... Good luck with the chemo today. Try to be positive that's half the battle.
You will be in my prayers today.
kathy
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Geez another thing that causes cancer
------------Please do not turn on A/C immediately as soon as you enter the car. Open the windows after you enter your car and turn ON the air-conditioning after a couple of minutes.
Here's why:
According to a research, the car dashboard, sofa, air freshener emit Benzene, a Cancer causing toxin (carcinogen - take time to observe the smell of heated plastic in your car).
In addition to causing cancer, Benzene poisons your bones, causes anemia and reduces white blood cells. Prolonged exposure will cause Leukemia, increasing the risk of cancer. May also cause miscarriage.
Acceptable Benzene level indoors is 50 mg per sq. ft..
A car parked indoors with windows closed will contain 400-800 mg of Benzene. If parked outdoors under the sun at a temperature above 60 degrees F, the Benzene level goes up to 2000-4000 mg, 40 times the acceptable level... people who get into the car, keeping windows closed will inevitably inhale, in quick succession excessive amounts of the toxin.
Benzene is a toxin that affects your kidney and liver. What's worse, it is extremely difficult for your body to expel this toxic stuff.
So please open the windows and door of your car - give time for the interior to air out -dispel the deadly stuff - before you enter. -
Hi ladies, well i started to post a new post that i had my first chemo tuesday and it hit me that i already did that wow! wasnt expecting chemo brain so soon lol! its been 2 days, and other than my port still being sore, (it was done on the same day) and then i had the nulesta shot yesterday,some bone pain already last night, not much, but today iam feeling it some more, pretty much tolerating it, i hope i breeze right thru this, i think i mentioned onc said if you put the shot in slow it wont hurt, but being the big baby that iam about shots i was so scared, she talked me into doing it in the stomach, the thought of that made me want to pass out, but i did it, she asked did you feel it? I said its done?? she says yes, i was like, I love you so much lol! So ladies tell your onc nurses to go slow and i promise the stomach didnt hurt at all.
Debfrom ohio- nice name! ha! where did you get the bear logo? I love it!! And thnaks for the tip on the benzo in the airconditioning, there is so much stuff that keeps coming out, who knows what tstarts any cancer, but i will take every precaution that i have to, to stay healthier! thanks! I will keep you all posted on progress,
angel hugs- debbie
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Hi Everyone,
Day 2 and still doing pretty well. I'm tired, very tired, but not nauseous. (Thank God!) I did get the Neulasta shot yesterday - is bone pain a definite SE or just a potential SE of the shot? I've been doing a lot of saltines and water so I think that has helped with the queasiness.
DEB 6122: Hope you're doing well. Seems like we're on the same schedule.
DEBFROMOHIO: Thanks for the info.
KAIDOG: I'm happy to give you encouragement. So far it really hasn't been too bad. Didn't sleep too well last night even with two benedryl. That could even account for today's fatigue.
JILL: Your power outage story was amusing. The Chemo Cat fight must have been a charming scene. (I have to admit, I find that I'm getting upset with things a little easier than usual today
)
Cruise; Thanks for all of the good advice. So, how many days do I have to keep pumping down water? Seems a shame to wash away all of those expensive drugs.
I want to thank everyone for their care and concern. I know most of you are past this part that I am just embarking on and the fact that you can enlighten me is a comfort. I must say that I go on a couple of other threads, but there isn't a thread out there where the women are as kind, caring and smart as you. I am blessed to have found this supportive network. Thanks.
Janet
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Well, I have completed tx #3 of 4 A/C today - 75% done and then on to Taxol/Herceptin. The onc nurse was very attentive today when I told her how nervous I was because of the pneumonitis last week. She hung out near me the whole infusion time, and checked my oxygen saturation level, just because I asker her to - the level waas back to almost normal which made me feel much better. I am off to nap, as I didn't sleep too well last night because of the anxiety. Will try to check in later.
Thanks Kathy and all the others who offered encouragement, prayers, good thoughts etc. It helps so much to have people (no, make that friends) who truly understand all that we're going through physically, spiritually and mentally.
Geri
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Good Afternoon Ladies...
I had number 10 Rad this morning which means I tomorrow I will be a third of the way done....only 23 more to go...No burning on the boob yet...so that is good. I heard that another patient in the room next to me this morning just started to get some blistering and she is 5 1/2 weeks into the radiation...hopefully I will slide right through it all.
Janet...You need to continue to drink lots of water...and you will feel like you are floating sometimes...but it will help with the side effects and get that stuff through your system...think of it like a cold...the more you drink the bad stuff gets out and flushes through your body.
Geri...glad it went well for you today...keeping our fingers crossed and prayers going for you...
Debbie...sounds like you are doing well...I had no bone pain with Nuelasta...just a slight fever afterwards. You will get tired and fatigued...that we couldn't avoid.
Deb...thanks for sharing the auto air...I had heard that before..but I thought the law had changed for the car manufactures and what they put in the air conditioners.
Okay...still warm here in CA...so I am heading out to the pool to cool off...Take care ladies...
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Janet, unfortunately, the bone pain is usually a regular se of the Neulasta shot. Try some Claritan (either brand name or store brand) - it seemed to help me and some of the other women. Other things you can try is a nice warm soak in the tub - I did that as well with epsom salts and it felt wonderful.
You will need to push your fluids until you are no longer feeling chemo foggy - it really does help get the stuff out of your system. Believe me, you aren't flushing good money down the toilet, by the time it gets to your bowl, it has already attacked everything in it's path!
Good luck with your treatments!
Geri - glad you are doing better - here's to staying out of the hospital!!
Jill - did you do your gastrointestinal study yet or is the pain better?
Had #12 of rads today - so far so good, minimal se's - just a little swelling and tenderness under my arm, and some rib pain, which is normal. Nothing like what I went through on chemo, so there's hope I can take this treatment all the way through - they are watching me like a hawk for severe or odd se's, because of my history. The folliculitis on my scalp is almost gone as well - follow up with the derm next week to make sure it's history.
Hope everyone is doing okay.
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That blew me away when I read that about the car because just like everyone else, I get in and turn the A/C on...can't help it....now I roll my window down! NOT taking any chances..........
That bear thing..mmm...can't remember where I got it, probably off of myspace...........LOL...
Hugs
Deb
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Evening, Ladies !
Man... lots to respond to here. But, as I read through the threads it occurred to me that this group is really making some progress. Everyone just motoring right on through those treatments. We'll get through this stuff together, eh ?
Janet - Hey Lady ! Glad to see you doing so well. The Neulasta shot.. that is a tricky one. I find (as with most everything else), that it treats everyone a little different. I hope you are one of the lucky ones and breeze through. I was not so lucky with that thing - hated it almost as much as the chemo. I would get these pulsating pains around my lower back that would extend out to my sides. That said, I took a tip from some of the ladies on the board and tried a regimen of Aleve and Claritin (like Chelev mentioned). Started it the day before and took it two days after. It really seemed to help a lot. I still got some pain with subsequent shots, but it seemed diminished.
As for your diminished "patience" - you are going to think this is strange, but looking back on my chemo experience now, emotional upheaval was one of my largest side effects. I also found myself getting easily upset and very depressed at times. It was like I did not have control of my emotions sometimes. So... while I don't want to make this a self fulfilling prophecy, emotional reactions are somewhat normal. Damn steroid practically made me snap people's heads off. And even if it wasn't the drugs causing the emotional upheaval.. hey... with all the junk they put in our bodies... we have a right to be just a little pissy !
Geri - Glad to hear things were relatively uneventful for you. Get some rest now and take care of yourself. We look forward to you sailing through this one ! (hope, hope, hope)
Debbie - Hi ! They gave my Neulasta shot in the back of my arm and gave me the choice of "fast or slow". I never got the choice of the stomach (and not sure I would have taken it that way... too chicken!). But, I also found "slow" worked a whole lot better. You know that thing is like $2000 or something like that ? Unreal. One little shot. But, I am glad it worked for you. Take care and let us know how it is going for you.
chelev - I see the GI doc tomorrow. A day after the herceptin treatment and chest heaviness is back... so... it appears related. Will check out the GI angle tomorrow. But, at least I know the ticker is OK ! Thanks for asking.
OK, ladies - I am off to answer some more correspondence. You all have a great night.
Jill
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