Starting Chemo April 2009
Comments
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Yay! Betsy got her drugs! I'm thankful for that! And my job and my DH and kids and spring and all of you on here..oh..and that Kansas and Georgetown got beat in the b-ball tournament and will help my Buckeyes immensely....can I say that????
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Hi all, hope you are all enjoying the wonderful Spring air!
Amy - I too have hot flushes at night, but have never heard of the nightie - please let us know if it works.
Geri - So sorry about your setback, I know that you wanted the surgery over with, but it is def better finding this out, before you undergo major surgery. Hang in there, always here for you!
Titan - I remember the anniversary of my surgery, I had a terrible day, I felt like I was reliving it. Now, I too say that it was the easy part compared to chemo. I am glad that you are feeling better now.
Betsy - I hope that you start to feel better soon! Hang in there! Thinking about you!
Alaina - what can I say? You are a true inspiration! You need to write a book so that when I feel down, I can just pick it up and realize all the good things in my life - thank you!
Hugs to everyone! Judy x
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Just passing through quickly today : )
Geri - how are you doing?
Hugs to all, Judy x
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Good news...I saw the cardiologist today, and he will clear me for my surgery next Wednesday 3/31. He started me on new medication to lower my blood pressure and said while there are changes to the electrical conduction of my heart, it is not from chemo or Herceptin, and is most likely age and stress related, with all that's happened in this past year. Of course, i burst into happy tears - I never thought I'd be so glad to hear I can have surgery! Now, I just have to get through this next 9 days, have the surgery and be done with another part of this.
Thank you all soooo much for your care and concern Very few people, including my dd, knew about the heart issue because I didn't want to worry anyone, so you, my sisters, were who I turned to, and as always, you were there for me, as I will be there for you.
Geri
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GERI: HOW WONDERFUL. Congratulations about good news. Bring on the surgery!
It really is SO bizarre how we look forward to things one would think we would shy away from. The day before my last chemo, there was a possible problem with my port and as they were testing it to make sure it was ok (which it was), I was crying and begging "I just have to have my chemo tomorrow. Please...can you just do it through a vein if the port doesn't work? Please???" And the whole thing was so ironic that here I was begging for chemo. Same as you being so glad to have the surgery next week.
Truly - what a long strange trip its been. (Old rock/roll reference - who knows where it's from?
)
Again - so happy for you!Amy
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Yay Geri! Go for that surgery! That is certainly relief...just age and stress...and that is a good thing? Guess so...I'm happy for you! Let's us know what is going on
And here are comforting thoughts right back to you!It is weird Amy isn't it that we would do anything to not be delayed in our treatments..our main goal was/is to get this freaking stuff over with and go on.
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Thank you Amy and Titan - yes, we certainly do get a slightly (?) weird spin on things, having been through so much. In my head, I am finishing Herceptin (therefore all my infusion treatments are done) on June 29th. I've had this date marked on my calendar since before Christmas - even a delay of one week could send me into an uncontrollable rage! I will be done June 29th, and the onc better not be standing within reach if that date changes!....But - it won't change...it won',t won't, won't.
Treatment #38 of 52 is tomorrow. I will be going out for a celebratory martini when I reach single digits (April 27th - 9 infusions will be left), and I'll virtually invite all of you, so put your orders in now
Drinks on me (alcoholic or not, doesn't matter so long as you join me!
Geri
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Hey Geri...it's great to hear that you are pushing forward to the finish line. Getting that surgery out of the way, then wrapping up the Herceptin....the end is in sight. Yippee..
Now don't laugh at me...but I've never had a martini...I will use your celebration to try something new. I will work on getting my dh to fix one for me and toast to you.
I scheduled four physical therapy sessions with a lymphedema specialist today. I still don't have the results from my biopsy but I don't start PT until April 5th so I think it will be ok by then. My last scheduled PT will be April 26th. So I too will be celebrating...so I will toast to me too!
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Geri - such good news! I am so pleased that you are able to have the surgery. I also remember, my husband practically dragging me to chemo every 2 weeks and then when they did the blood count, I was hoping above all that it would be ok to have the infusion that day! It is all such a strange shift in priorities and having everyone here who actually understands some of this madness is incredibly important for us! That way, we know we are not actually going crazy : ) Good luck Geri, we will be thinking of you so much over the coming week. I love Martinis, so looking forward to that!
Betsy - it is good to hear that you are also looking forward.
Helen - how are you doing?
Hugs to all for a good day,
Judy xxx
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I haven't had a martini either! But I'm thinking it is time to try one! or two? April 27th? Sounds good!
I think now you can get fruit ones...I remember going to cocktail hour many years ago with this lady I worked with..I swear she was 80 years old then but she couldn't have been..and she always got a martini...I think it had vermouth in it and olives and it smelled horrible...but she looked so cool drinking it plus her very long cigarettes...(remember this was probalby 30 years ago)...anyway, she just died not to long ago...I think she was like 95.
Bring the martinis on!
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Judy, Geri and Betsy:
I'm so glad you're all OK by now (and good luck with the surgery, Geri)! {{{{{hugs}}}}}
Alaina -- I'm glad you're enjoying life, even though I don't believe in celebrating cancerversaries.
Amy and Titan -- I can't afford $50 nightclothes but yeah, wouldn't it be nice to have something to wear that negated the sweat of hot flashes!! Ewwww, I am so sick to death of the hot flashes. I fhought going off the Tamoxifen would have stopped them, but noooo......I get 'em both day and night, STILL. >:-P GRRRRR!
This hasn't been a good week for me though. I got taken off the Tamoxifen because of a blood clot, well, every day starting last Tuesday I've had to go get Lovenox injections! Yes, every single day, including over the weekend. Tomorrow is the last one (er, well, hopefully: I originally thought YESTERDAY's would be the last but my oncologist changed the order to add shots for today and tomorrow, plus an extra blood test on Friday). Weekdays I get the shots at the cancer center -- which was closed over the weekend so I had to get the Sat and Sun shots at the hospital.
THEY HURT WORSE THAN NEULASTA! Neulasta shots only hurt me WHILE they were being administered, but once the nurse finished giving me the Neulasta shot, I was fine right away. Well this Lovenox crap hurts MORE than Neulasta when I get it (in the STOMACH -- I tried one Neulasta shot in the stomach, hurt like hell so I said "in the arm" for the rest of them: still hurt but not AS bad as in the stomach). I don't have the option to get the Lovenox shots in the arm -- believe me I asked! -- they say I can ONLY get them in the stomach, and on top of it hurting while I get it, it hurts for half an hour AFTER! I never thought I'd "miss" Neulasta shots, but here it is -- I'd rather get Neulasta shots than this f***ing Lovenox crap!
Here's a scary thought -- what horror is next in this stupid cancer "journey" which will make me look back with nostalgia on Lovenox injections? :::::shudder:::::
~Lena.
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Lena - I hope that you are doing ok today!
Hope everyone is doing well. Take care and hugs to all,
Judy x
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Thank you all for the good wishes - one week from tonight and the surgery will be over. Just keep sending hugs, pryers, thoughts....anything that you think will help!
Lena - sorry that you are having a rough time with the Lovenox. I had to give my daughter those injections many years ago, and I recall her sreeching at me when I gave them, so I know they are not pleasant.
Judy, you always ask us how we are doing....how are you?
Geri
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What in the heck is a Lovenox shot????
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Lena, sorry you are going through more problems.....(((hugs)))) .. hope you feel better soon and don't have to have any more of those nasty shots.
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OMG - nostalgia for neulasta shots...wheew...Lovenox (LOVE NOT)must be bad. I didn't recall the shots hurting that much, it was the bone pain afterward that I remember vividly. I am sorry to hear you are having to deal with all this crap Lena. Sending you a big hug.
Still no biopsy results. I'm thinking no news is good news.
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Betsy - I remember the horrible aches after the Neulasta shots. You know sometimes even now, I get "phantom" bone pain in my jaw bone. Yuck!
Lena - I hope you are ok and not suffering too much!
Geri - thanks for asking, I am generally doing ok. I have been trying to wean myself off prilosec this week and so far I have been ok. My hair is growing in curly and I cannot manage it at all. I keep on complaining, but then remember, it is better than the alternative. I am also very tired a lot, but I just try to push past that. I am feeling lucky, that even with all my little ailments, I am here and adjusting to the "new me". Now I just have to decide if I want to have reconstruction, but I am not in a hurry at the moment to have any more surgery.
Hugs to everyone, take care, Judy xxx
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Hey Judy...good to hear about YOU....yes..those wonderful (?) neulasta shots...honestly..and I know I continue to whine about those but I really, really hated those things...I tolerated everything else pretty well...but those shots..I just hated them..when the nurse was shooting me she would say..are you OK...and I would say...I'm fine except for these freaking things...if I had to do it over I would decline them...they MADE me have them and I was too chicken to say no...well..here I go again about those things and it has been 8 months since I had one!
Anyway...can you believe that we have almost come full circle here....we all started posting about chemo at this time..I waited awhile to post..but I was was "creeping" as my kids would say until I actually signed up....
Betsy..no news may be good news but actually hearing good news is better...you shouldn't have to wait this long..that is torture....
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Hi all
Betsy - do you have your results yet? Are you ok?
Titan - thanks! I know, I started my chemo on April 21st, I can hardly believe that it is almost a year! What I find so amazing is that I can still relive the whole chapter as if it was yesterday! I wonder if that will fade in time.
How is everyone doing today? Geri, are you getting ready for the big day? Helen, how are you holding up at the moment? Lena, how are you doing?
Dawn - we miss you! How are you doing?
Hope everyone has a good weekend!
(((((HUGS))))) to all of you wonderful ladies! Judy xxx
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Hi everyone,
Five more days until surgery - I can't say I'm looking forward to it, just looking forward to getting through it! I have seen the Primary, oncologist, breast surgeon, plastic surgeon, cardiologist and pulmonologist in the last 6 days, had pulmonary function test, echocardiogram, electrocardiogram, mammogram and ultrasound - exhausting to go over all the surgeries, treatments, medications etc etc - but everyone has cleared me, so it's a go. This time next week I should be home and whining about the drains - oh how I hated the drains
Funny - I had my first (and last) mamogram and ultrasound on the non-cancer breast this week, just to see if there would be any suprises when they do the elective mastectomy. Got a letter in the mail from the radiologist with the "goode news" that my mammo and ultrasound were clear, but to be vigilant with self-exam, as not everything is found on these tests - no joke! That is why the boob is coming off...because you congratulated my right boob on being clean last year, but oops...surgery found this pesky grade 3 cancer, and away we went. I know, I am being a bit bi**chy right now, but that's what nerves does to me!
Come on, Lena, I need a good story from you - you can always make me smile with your irreverent outlook on everything. Judy, Titan, Betsy, Helen, Amy - and anyone else I've forgottent to mention, just ignore my crankiness for the next few days - I know you all understand that it's the anxiety of being back in "that place" from a year ago - just the thought of my chest being bandaged the same way is giving me bouts of nausea...oh well, I'll get through it, with all of your help for sure!
Geri
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Geri, you are entitled to be cranky, especially here where we all understand. I'm thinking of you and hoping for surgery to be as easy as possible for you. Please let us know how you are doing.
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Hi all...no official results from my biopsy yet but the unofficial dr assistant reading is that I have RIF - radiation induced fibrosis... & some other tissue damage - collateral damage from RADS...she could not pronounce it but the good thing is that a "bacterial infection" is ruled out. So thank God..no more antibiotics that reek havoc with the rest of my body.
Geri- I can totally relate on being cranky. It's ok...be bitc*y...you are entitled. It's been a hell'va year. It's hard to believe it's been a year since this all started. My first chemo was April 14th. I had to look it up since my mind is still fried from all the drugs. Ya...I'm still using that as an excuse, I'm milking it for all it's worth.
Judy - I'm ok..but not normal. Of course my family would probably say I was never normal!
I'm glad to hear you are at least attempting to see how your digestive system is working naturally. I hope and pray...it is healing on it's own. I know how painful it is. I'm keeping my fingers crossed that you will be drug free soon.
Lena - I hope your LOVENox is now out of the picture and Pack Rat is back in. Thinking of you.
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Geri..good luck with your surgery....you will be fine! We will be here to listen to your whining about the drains...!
Tell me about being back in that place! I went with my DD for an appt...she had a lump in her throat..which is kinda freaking me out a little...they are also testing her for hypothryroidism...I think i spelled that right..but I swear that my BP was up just sitting there waiting for her...The magazine I was reading was 2 years old and I read an article about how if you had treatments for BC you should have your heart checked periodically...of course we already KNOW that...but then I was thinking..my heart hasn't been checked since b-4 chemo...I'm thinking that it needs to be checked..just to be sure....there is some heart issues on my dad's side so it may be the thing to do,
Hey Lena...how is that Pack Rat..and how are you doing...Geri is right..we need a story,,,,,
Betsy, glad to hear that your biopsy came out..well ..OK...the rad fibrosis (spelled wrong I'm sure)..is not fun but you will deal with as well as you have dealt with everything else.
What the h is normal anyway...I think that we are all way beyond that! I was maybe a little beyond normal before...now I know that I'm way out there!
My boss had me in tears this week..had my evaluation...he said that I had had a tough year (yes) and that several people came up to him commenting on the fact that I still made it to work every day and did my job....My DH and I had talked about me going on a leave of abscence but I really didn't want to do that..I wanted things to be as normal as possible while I went through chemo...funny thing..but do you guys really remember the time during chemo? I feel now that I was in a constant fog and cannot believe that I actually was able to do my job...
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and Helen..what has been going with you..got some hair coming in? I hope so...How long is it? I think the biggest part of our healing is looking like a "normal" person not a freaking cancer patient.....I still look at people with short hair and wonder...is that hair their choice or because they had chemo...I still wonder if I look like a cancer patient but I don't know...I think my hair is about 3 inches long but it was curly.frizzy before and now with our spring weather it is even curlier...I thought it may come in straight! But not..it is the same as it was before,
I'm chatty today aren't I?
Dawn...where in the heck are you? Let us know what you are up too?
We still haven't planned our get together...it sure would be nice to see all of you..what can we do,,..I'm free this summer....my DD is getting married in a year and a half so I will be plenty busy then....hopefully I will still be doing well by then...but I guess you never know,
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Hi all, just passing through quickly this evening.
Geri - we are all thinking of you and you can be as cranky as you like, we will listen as much as you need or want us to : ) Good luck for this week!
Titan, I really enjoyed your posting, I like to hear you chatting away. I am in awe of anyone who managed to work through chemo, I was completely useless for most of the time and so depressed that I almost disappeared into myself. I never thought that I would ever pull myself out of it. I am still extremely frustrated by my family members who think that every thing is back to normal when it just isn't for me. I am so tired and find that I struggle through the day sometimes. Anyway, enough whining for one day.
Betsy - hope that you start to feel better soon. So far, so good without the prilosec!
Sending you all hugs and have a good evening, Judy xxx
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Judy...that is just it..when I was going through all this junk I was so very quiet...at work, before, I used to get in trouble for being loud and talking too much..then when I went through this junk I was so very, very quiet...I hated that..quiet is just NOT ME...I can usually talk about everything and anything and drive people nuts..my mom is the same way...these kinda of chatty people can be somewhat annoying though! Anyway, I feel that my employer likes me being talkative and loud again...I think that maybe they missed it..anyway, don't think I will get in trouble for it again...
About the chemo..I absolutely hated it...but I'm the type that has to be busy, busy all the time...I freak if I have time on my hands without something to...I will start cleaning out drawers or something....
Hugs right back at you Judy...you have had too much to deal with with your stomach problems......hopefully things will clear up soon for you..having heartburn is such a miserable thing...
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Hi Judy and Titan,
I too love your chattiness, Titan, and like Judy, I can't imagine working and going through chemo at the same time. I went back to work part time when I finished the Adriamycin, Cytoxin and Taxol - I'm still on the Herceptin, but I manage about 3-4 days/week to work, and like Judy, I'm really exhausted a lot of the time. Well, I'll be out again for at least 4 weeks with the surgery on Wednesday, so a forced work-rest.
Thanks for the ok to whine - I'll try not to take advantage of it
. Can't believe tomorrow is Monday already - oh well, this time next week I'll be in recuperating mode!
Where's my story, Lena - come on, we need you!
Glad your stomach is behaving more Judy - I too remember that nasty heartburn...and you've been dealing with it for so long - you deserve a break (come to think of it, we all deserve a break!)
Geri
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Titan - if you ever have extra time/energy, you can come over and clean out my drawers! Plenty here to do!
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I love passing through and reading the day's news! Geri, thinking about you for Wed!
Helen, how are you doing?
Dawn, we miss you!!!
Hugs to all and take good care!
Judy xxx
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Thanks Judy - 48 hours from now I'll be post-op!
Geri
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