Starting chemo Dec 2007
Comments
-
Hi All Sorry to have been AWOL for awhile. Taxotere just does me in for about 10 or 11 days. My MIL came for the second week (she lives in Fl.) as dh had a business trip. She is a wonderful cook and tried to cook anything I wanted but I just didn't have any appetite. She spoiled me rotten and I really hated to see her go.
This is my good week but not really, because of the work I am doing. About two years ago, some people who worked for us came into our offices after office hours, took their contracts from the files along with other confidential information on our accounts, then formed their own company in direct competition with us, although they had all signed "non-competes". We sued. There are actually two different lawsuits. The large one is still probably years away, because of expert witnesses, etc. The smaller one is almost settled. What will probably be the last mediation is set for Feb. 19, and that date was agreed on last Sept. before my dx. The problem is that is about day 6 after my next tx and I know I will feel like s#&*. The accountants will be there and it would be better if i could comprehend numbers. I see onc tomorrow and will talk to him and see if I can move tx up to this Fri. (4 days early) or postpone until 20th (which I am afraid to do). If that fails, maybe he can give me something to perk me up for 19th. Everything about this disease is a pain in the butt.So, that is how I have spent my good week, going over notes, refreshing ourselves about figures, what fun. Everytime we have to look at it, we get in a bad mood.
Other than that my life has been uneventful and that is the way we like it. We live way out in the country, 45 min. to Wal Mart, on the Tenessee River. Our house is on a dead end road, and when a car goes by everyone looks to see who it is. We lived so many years in the dog eat dog business world that we treasure each day here. We actually have a condo on the beach in Fl. and we have been once in the last year and a half. I was thinking about the condo though. I see other groups usually get together when tx is over and if all of you would like to do that, we could use our codo if you would like. We like small towns and the condo is in one of ther only small unpopulated beach towns left on the ocean in Fl. One red light, no fast food, you can throw a rock from our patio and hit the Atlantic Ocean (Flagler Beach, Fl.) Think about it, it would be a blast. i probably won't post again for a few days, legal stuff calls and I HATE it. I read every day and think of you all everyday and am proud to be associated with such a brave and determined group of warrior ladies. God Bless Joy
-
Hey all! Sorry it has taken me so long to write again. I have felt really good the past two or three days, but now I have to go back again. Tomorrow is my LAST a/c treatment. I cannot wait for it to be over. I pray the Taxol will like me better. I took my steroids tonight as I was told to do, and have my steroids for tomorrow packed and ready to go. Pray for me. I just do not feel like doing this right now.
I still have stubble growing back on my head too. I finally shaved it because I got tired of all those little strands.
The gargling seems to have done the trick as the little annoying things are gone now. My cold will not go away, though. My nose has been running for about three weeks. ICK.
I had my hubby bring home taco bell and a cheeseburger tonight as I know I wont feel like eating again for awhile and definately nothing spicy. I have noticed that spicy things seem spicer. Anyone else have that going on?
My period has not really quit, but has lightened up a lot. Unfortunately it lasts for like 12 days, but that really isn't unusual for me. I was just hoping it would stop. My legs are still hairy, too.
Well, that's about it for now. Not sure when I'll get to write again.
Kate
-
Hi All,
Just checking in after taxol #1. First of all I had no adverse reactions during infusion. It took about an hour for Benadryl and the steroids to be put in the about 3 hours for the taxol. I brought along my laptop as I was alone today and tried to watch a movie on it. I dosed off and on through the whole movie, then started waking up after it was done. (thats what happens when I watch movies at home too)
Spent the rest of the time talking to my chemo room mates (I love talking to people) topic of the day was travel, past and present. After that I drove myself home.... I don't think that was a real good idea as I was still pretty spacey from the benadryl. I'll have a driver next time.
Once I got home I collapsed onto my lazy-boy chair and went straight to sleep for a few hours. Today was payday for the guys, DH had to do a quick approximate calculation and let them know I would fine tune the deductions later. I finally woke up at about 7pm and thought it was morning, talk about chemo brain. Anyway I feel good right now, but have no recollection if I'm supposed to take any other pills this week. I'll call them in the morning. Overall day 1 is good so far, I am raising my glass of ginger-ale.
Sal, your big day is tomorrow {{{big hug}}} hope you just breeze through it.
Kate, I hope your feeling better after that throat viral infection. We also don't have Kate's dates for tx on our list at the top of the page
.
Lori, hope your feeling better. No need to suffer through bone and/or muscle pain. I think we are all fed up with drugs and pills but its only for a little while longer.
Hope everyone has a nice evening. DH has made dinner so I'm gonna grab a quick bite and maybe try to watch that silly movie again.
Big Hugs to all. I feel so thankful that I have all your thoughts and prayers.
Much Love, Suz
-
Kate & Joy, you must have posted as I was.
Kate, glad to hear your feeling better. I've had the runny nose and eyes for weeks from the a/c. Felt like a dripping faucet. I think it might have something to do with losing eyelashes and nose hairs. Good luck with your final a/c, you can do it. I hope taxol will be better on you as well.
Joy, Sorry to hear you have to deal with all this legal crap on your good days. I can relate, we are a small corporation and its just too easy for people to abuse that situation, non-competition/ non disclosure clauses or not. Its just wrong.
I hope it all goes for you with not too much stress.Also hope you get your tx dates worked out. Let us know what your new dates will be (your dates are not at the top either) know that your in my thoughts. Wishing you lots of peace and patience through all this.
Hugs and Love, Suz
-
Hi all! I'm feeling better each day so it looks like days 3-4 after tx will be the worst...but still better than the AC!
Suz, glad to hear you are good so far! Hope that continues for you!
Kate, congrats on your upcoming last AC! It feels good to have it done, doesn't it! I hope Taxol is easier for you! I would take it over AC any day!
Sally, I hope you are finding the Taxol easy today and no reactions! Let us know how it goes!
What a little group we've become.....all of us worried about Laura and afraid to voice our concerns! I do hope she is fine and hope we hear from her soon!
Joy, I love the idea of a get-together when we are done! It sounds like a nice spot you have in Florida and at home! When my grandma was alive and still lived in Kentucky (Pathfork..very small) it was the same way....when a strange car came into the holler everyone was looking to see who it was. There are alot of girls in our family (cousin's) and when we were younger and traveling with our parents the local boys would be at my grandma's before we had unloaded the suitcases! Those days were so much fun!! Sure makes me miss my grandma! What do you all think about Joy's offer?
I clarified some things regarding my insurance also and am feeling much better about the bills that are rolling in. I have reached my deductible AND out of pocket limit on the coinsurance which only needed to be met at the individual limit and NOT the family limit! Yahoo! From now on any EOB's I get will say "Patient responsibility = $0.00!! Our year runs from June 1st - May 30th so surgery and most of radiation will fall under the current benefit year at no (additional) cost to me!! Yahoo! As I posted a while back, the bills were a concern to me...Not anymore!!
Hope you are all doing well! Lori
-
Kate? You take steroids at home before and after A/C treatments? I didn't realize they did that. Good Luck today with your last A/C! I'll be keeping warm thought for you today. My last is tomorrow and so ready to be over with it also! All the best for you today!
Lori, glad you are liking this tax better than the A/C as far as we can 'like' chemo tx that is. Hope it continues to be less stressful on your mind and body and you move through it all uneventfully.Suz and others getting through it day by day, you're all in my prayers and thoughts as the days crawl by. One day we'll look back and marvel at your strenghts and belly laugh at the things that got through and that only others could laugh at with us! Shaving, or not, and all the other little things that others can't comprehend @ this horrible ride we've taken!
-
Wishiwere- Yes, they started giving me the steroids when I was so sick. It helps the nausea and gives you a good energy boost. It's a lot better with it. Last time I didn't throw up or anything. This time I'm feeling pretty good, too. Friday and Saturday will be my worst days if it goes like last time, but it's not to horrible. Good luck for you tomorrow, too! I hope it goes well. I'm both anxious and nervous to start the taxol as I've heard about the bad reaction thing. It would be just my luck.
Lori- I am so glad it's over. My cousin died yesterday morning of cancer (he's close to my age with kids around the same age as mine) so I woke up about 4 this morning and just prayed for his family. So, it was a happy-sad day for me.
Suz- glad to hear I'm not the only one with the nose problem. I still have my eyebrows and lashes, but no hair. Looks pretty funny...hehe. Not sure about the nose hairs though. They may be gone. Must be.
Suz- MY taxol dates are Feb 20, March 5, 19 and April 2 I'm 37 years old and I have stage 3 cancer. The only other thing I know is I am her2 negative, whatever that means. I know nothing about anything else really. My doc only tells me what I ask and he really doesn't want me to concentrate on stats and figures. He thinks I'll live to be older than him...hehe.
Kate
-
*doin' the funky dance* "Go Taxol! Go Taxol! Go Taxol!"
Yip, I am glad to say I sailed through today like a real skipper. Am definitely thrilled not to have that nasty sinus oogieness that I always got after the C treatment. Slept like a baby last night with the Ativan. Got Benadryl at the beginning of today's tx, which made me really loopy and tired, but I actually bounced right back. Am only feeling just a litte tired tonight, like I've had a long day-- which it was. Got there at 9:00 and didn't leave until 3:30. But so far, things are awesome. I'm starving, which is a real switch from AC. I'm gearing up for Saturday & Sunday, which I'm thinking (based on what Lori and my doc say) will be my achey days.
Wishiwere, good luck with your tx tomorrow and yippee!
Kate, congrats on your last one coming up too. Woohoo.
Also, Kate, sorry to hear about your cousin. I just had a friend pass away from cancer on Friday... left behind a wife and 2 young girls. Makes me feel kinda guilty that I'm gonna live when he's leaving behind a family. But I know one doesn't have anything to do with the other... the cancer is to blame and we all know what a horrible thing it is no matter how much or little you have to deal with it. Kate, I will add your cousin and his family to my prayers.
Lori, thanks for the Taxol updates. Sorry you have to be our pioneer, but you are definitely our hero for that and we appreciate all the news.
Suz, yippe for us to be on the Taxol team.
I think I'd be in on Joy's offer for a get together. You'll all laugh because I'm such a chatty Kathy on the forum, but I'm actually rather shy in person and can't make small talk to save myself. But to meet and celebrate with a wonderful bunch like this, I would be brave. Count me in.
Dinner is ready. Big bug to you all!
-Sal
(New Avatar is me with my Scooby Doo ballon I got when I finished AC.)
-
Well ladies, I apologize for being AWOL. I got back on the 28th and have just been so busy with work and life that I have stayed away from posting.
I had a fabulous trip - of course it was too short, but it was wonderful to see hubby and we were also able to attend the wedding of my friend's daughter that took place there. I was able to rest quite well while there, although I find that the fatigue seems to be cumulative and I got tired out very easily. I came back uneventfully but did get a bit of a sinus/headcold which took about a week to get rid of. Had fourth tx this Monday and it feels so good to be over the hump. SE's becoming somewhat routine: queasiness the first few days, yucky taste, weird appetite, leathery mouth. I find my mouth gets very dry and sometimes it seems to make no difference how much I drink. One key thing is that my chemo arm is sore. I don't have a port and I think the chemo is "cooking" my veins, so the arm hurts and feels bruised even though no bruise can be seen, and this seems to increase a bit more with each tx. My white blood cell counts have been low and my onc has prescribed CIPRO, which I don't understand so will have to phone and ask about that. They surprised me with that one when I went for chemo, not during the consult the day before, so I didn't really get an explanation of why. I suspect it is intended to aid in supporting white blood cell count but I hadn't heard of that before.
Since I've been back I've been working a lot as the project I'm on is pushing ahead towards its deadline and some things need to be tended to, so I have been very busy. Fortunately I can work lying around in bed, which is what I often do.
It is so encouraging to hear all the positive stories about shrinking/disappearing lumps, nodes, etc. Sal, I am thrilled to hear that your lump turned out not to be anything to be concerned about. Oh yes, I forgot - I went for mammo/ultrasound the day after I returned for the lump I'd found and they said everything looks normal, just lumpy breast tissue, so I am relieved also. They looked over the whole breast carefully and didn't see anything to be concerned about. Sal, the photo of your ladies at the library and the chicken is hilarious - there is nothing like humour to get us through the slogging of cancer treatment. Wishiwere - what a beautiful gesture by your little sis and her sons! Suz - ok who is that hot chick perched on the snowplow? The wig looks great!
Amy, I can definitely relate to the depression thing. We need something to look forward to, so I hope you will definitely plan for a weekend getaway or something special to reward yourself. I don't know how I could have continued without getting away to see hubby. I decided that even if it was risky, it was worth the risk, because I need to live as a person first, then as a cancer patient. I can't allow myself and my life to be defined by cancer. This has changed my perspective on a lot of things relative to this battle. We must not forget to LIVE. Because although we are all thinking positively and doing everything we can to kill the beast, unfortunately it will get some of us and I certainly don't want to ever look back and wish I had taken a trip or spent a weekend or danced, or whatever. I am going to do those things (within reason) because my life is NOW and who knows what tomorrow will bring.
Periods - mine were pretty much gone before cancer, so no change there. Hair - the remaining stubble continues to grow as some of you have reported. I razored it before I went to Cuba and it is about 4 mm long again, time to razor it again. It just looks pathetic and speckledy. Eyebrows and lashes have thinned considerably and so I am sporting false eyelashes. Generally, I feel fairly fortunate when it comes to the SE's and am mostly functional except for the first few days and the fatigue. But I was beyond crazy before, getting up at 5 and not to bed until midnight. That made no sense then, even less now, so it isn't hard to lose that habit.
It is wonderful to be back chatting with you ladies - congratulations to all of us who are over the hump, who have transitioned to the second phase of treatment. We are getting that much closer to getting our lives back. Joy, I am so sorry you are having to go through this legal slog while juggling your tx and SE's - that is really a tough challenge. Hang in there, and I hope the mediation will be speedy. Thank you for your gracious suggestion of Florida - that sounds beautiful - we should definitely consider that.
A big hug to you all, and I will not go AWOL for so long
. Sorry!
Oooh my stomach is queasy/hungry right now....I feel a deep dish pizza order coming on for dinner, lol....
It's good to be back.
Laura
-
Laura- Great to hear you are doing well. We were beginning to get a bit worried about you. Sounds like everything for you is going great!
Sal- Thanks for the prayers. I'll pray for your friend's family as well. God knows who they are. So good to hear you are doing well with the taxol. Very encouraging. I have a friend who said for her it made her very sleepy and very sore in the joints. She has arthritis, too, though.
Kate
-
Laura, so glad you are back, safe and sound, if not a little weary. Sounds like you enjoyed the much needed time away and that's what counts!
Sal, ladies, I lied today! I am so messed up with days and nights and trying to keep them all straight lately. I have my last A/C on Friday, the 8th. We were hoping dh could make it home for one tx, but alas, dosen't look that way. He's making his way through a foot of snow and it's doubtful he'll be back before I leave.
Oh well.....still will be great to be done with the red devil!
Sleep well dear friends.
{{hugs}}
-
Morning all! First let me say...
Welcome back Laura!! You had us getting worried there for a bit but I'm so glad to hear your delay in posting was just because you were living life!! So glad you had a great trip!
WishIwere, How did you do with the snow? We must have got about 10". There is no shcool anywhere around here. I'm going to head into work late after the plows have been thru (Suz, where are you?) LOL Good luck and congrats on your last AC tomorrow! Ah, the day when chemo is over, won't that be great!
Sorry to hear about friends who have passed. So hard for the young families left behind. They are in my prayers as well!
Sal, dancing with you...Go Taxol, go Taxol! Glad you got thru with flying colors. I feel great this morning..Last night I slept the best I have in about 2 months (with no drugs either!) Seems my vision is clearer also...it had gotten a little blurry and even a bit double in the mornings on the AC. That is gone now. So it seems for me days 3 & 4 after tx will be the worse dut to the body aches. I can handle that, no problem!! Love the Scooby ballon, was that your most recent? I'm glad you would be up for a get together, shy or not! I'm sure we would all have a great time! LOL, just re-read the last line of your post about the balloon! So maybe the chemo brain is still active!LOL
Amy, Thanks for keeping that top post updated. I noticed you added Kate when I was referring to it! I, for one, am still using it to keep track of everyone! I'll be thinking of you tomorrow as well.
Hope all are staying warm and taking care of themselves! Have a great day! Lori
-
Lori, so glad you doing good and sounding almost chipper this morning! Sounds like you ARE dealing much better with this new chemo tx! Great to hear!
Depending on where in the county you are, we got anywhere from 9-14 inches. I'd say, about 12 here! The blue angel that's been plowing me out after each storm came through twice yesterday and then again about 5:30 this morning! What a sweetie! I've only got a bit of one armed shoveling to do this morning before I can get out! The drifts are enormous! One out back is 4 feet I swear! Poor little bunnies have tunneled through rather than over it's so soft and light! The winds were nasty last night, blowing it into big drifts across roads, so even CMU is closed till noon! I'm in no hurry to get out in it, that's for certain!
-
Welcome back, Laura. It's SO good to "hear" your voice again.
Day after Taxol and things still looking good. I ate like a piggie last night, which is totally weird after AC. Just finished breakfast. Gotta go get ready for my full-body massage appointment... my treat after yesterday
Already making plans for the "days of pain" to come, and I'm assuming my regular 3 days of fatigue will remain the same (according to the nurse), so I'm thinking Saturday through Wednesday I'll feel in the dumps. But we'll wait and see. I'm loving things right now and that's the important thing!
Wonderin how my buddy Amy is doing. You've been on my mind often lately. When I think of going thru chemo on a weekly basis... geesh. You never get a break. At least we have a couple days here and there when we can kinda rally, but you just get beat down every week. I don't know how you do it. Super Woman. That's what you are. Super Woman.
Gotta scoot. Hugs all.
-Sal
-
Laura is back ! Hooray ! So how was Cuba? Did you get to see much of the island. I really want to get there one day, but my dh will not even think about travelling there until Fidel has passed/new regime takes over.
I also took the Cipro, day 6 after each treatment. This is an antibiotic routinely taken prophylactically by chemo patients to prevent an infection that you may/may not be exposed to in a typical day.
Sal, love the snoopy balloon, and the great news that so far your Taxol treatment has been doable. Crossing my fingers and toes for you, and the rest of our gang !
A, Sal is so right on.........you are a super hero, no doubt ! You must be one strong lady with those weekly treatments. I am saluting you A !
Menstruation update; AWOL since treatment one. Onc says may come back now that chemo is over, but no way to tell. Don't start tamoxifen til rads are over, sometime in April, so I may get it now, then lose it again. Whatever....., just as long as I don't have anymore chemo. Hair... got some gray,white,brown,black fuzz, maybe a quarter inch.My scalp has been breaking out alot too. Real attractive!
No snow here in NJ, just lots of rain, and mild temps. Can't believe how much snow you ladies in the North Country are getting. OMG!
Wishiwere, you too are one tough cookie doing this without your dh. I pray that he will be by your side soon. All you ladies are amazing, and are so inspiring with your strength. So what if we have our down days, they are going to happen, that is why we have eachother to lean on and vent !
xoxox Cindy
-
Hey, Hey, the gangs all here!
Welcome back Laura! So glad everything went well and your back into the swing of things. Gotta love that working from bed.
. Must admit you had me worried, but I'm a bit like an old mother hen trying to keep track of all the chicks.
Lori, sorry but its a 36 hr 34 min drive to Ortonville, It might take a while lol. Glad to here your still feeling fine despite all the snow.
Kate, Hope your feeling ok with your last a/c. Your over the halfway mark now and going onto the taxol train.
Wishiwere, Good luck with your last a/c Friday, Do you go on to taxol as well after this or are you done with chemo. We still don't have your dates up top yet. Its seems to be the only way I can keep track of us with chemo brain and all.
Whoo hoo Sal, welcome on the taxol train. Glad to see so far so good. I hope it stays this way. No more a/c.
Cindy, nice to see you back in such high spirits! Hair!!!!! whats that. I broke down and shaved my scruffy tufts today so I have a true cue-ball now
Amy, haven't seen you in a while, hope all is well. Wishing you lots of strength to get through your tx tomorrow {{big hug}} you can do it.
Joy, hope all is going well with your legal litigation and your not stressing over it. Your offer of the condo for a get together when we are done is very generous & kind. I think its a great idea. You can count me in.
KMK, You've been quiet for a while , hope its due to walking with the GF's and enjoying yourself.
So far so good for me. Am heading out to LGFB class. Should be interesting and hopefully fun.
Hugs to all and sorry if I missed anyone
Suz
-
Hi all--
Welcome back Laura! Well. I just hope you're happy--we were worried sick! We were all imagining you in some kind of surreal action movie--smuggling your husband into the country with lots of explosions and intrigue, bald head, IV pole dragging behind ya...well, I was imagining that...cause I'm bored... Glad to hear you're back and actually have more interesting things to think about than cancer treatment and bizarre fantasies about board members. You have such a great attitude--I think we all just missed ya!
I neglected to do my hair update: I, apparently, have a lot of hair left, according to the other ladies at my LGFB program. I think it's about 40% of what I had, but I'm still glad I shaved it, because it was falling out in chunks and creeping me out. What's left is completely grey in the front, and it is still growing. I kinda like giving myself haircuts by buzzing it. I think when I grow some color back (or have enough to dye!), and have about 1/2 an inch, I'm done with hats and wigs--I actually feel very neat and clean with my round head. I'm still shaving my legs, still have my same old sparse eyebrows and eyelashes that I've always had. Hating the wig, still wearing just hats 90% of the time.
So, welcome aboard the Taxol train, Suz, Sal and Lori (right? who else?)! Glad it's so far, so good...
Sal and Cindy, thank you so much for your words of encouragement. I'm not even going to go on about how I have the lower dose and yadda yadda--the truth is, I'm feeling very sorry for myself and feel thoroughly sick of the whole thing. And NOT encouraged by the fact that I have "only" a month left, as people keep telling me. How do people do this for like, a year, sometimes!?!
So, I'm a project person--I especially love to do stuff to my house, which we bought 3 years ago. And since November, I've been sitting in my house, staring at stuff I want to change--walls that need paint, stairs that need refinishing, furniture that needs to be moved/covered, closets that need sorting, etc etc... and I CAN'T do anything! I start projects and poop out a quarter of the way into them, leaving things looking worse than before, and driving me even more crazy!! The other day I painted a giant splotch of horrible pea-soup-colored paint on my living room wall--the one directly across from my recliner, the one I've been staring at and wanting to paint for three months--now I have to stare at THAT!!
Anyway, I have been sleeping badly, and think it's catching up to me in depression--I've even been teary all morning, which isn't really like me. I do feel like my "good" windows are getting smaller and less reliable. And I know that, as the stuff builds up in my system, I have only more of the same, or worse, to look forward to for the next month. BLAH!!!!!
My sister said "we're all very grateful to you for doing this", which is the best thing a person could say. It's doubly nice, because not only does it remind me that it's for a reason, but I sometimes feel exhausted by gratitude to other people--do any of you understand this? It's not that I'm not incredibly grateful...it's just hard to be always on the recieving end of so much generoisity for so long. I would only express this to you guys, never to my awesome friends/family.
I hear the kiddies rattling upstairs, so I'll sign off now, and get ready for treatment #5 million. Sorry to be such a downer--it's wonderfully comforting to know you're all out there.
love--Amy.
-
Taxol is still agreeing with me better than AC. I ate and ate yesterday. What a nice feeling to have an appetite.
My fingers are still sore from last week... not sure if I mentioned it but my fingertips felt like I'd gotten them squished in a door... you know how your fingernails hurt after that sort of thing? Well, it's kinda hard to tell where that pain ends and the new "pins and needles" sensation begins, but I definitely noticed the "pins and needles" sensation when I got in the shower this morning... something about the hot water hitting my fingers made them all tingly. So I'll keep an eye on that.
Other than that, Taxol has been A-Ok. *knock on wood*
Amy, you are such a hoot... laughed out loud when I read about your image of Laura, bald-headed, dragging her IV pole behind her... man, I could just picture that-- at least, me doing the dragging part-- and what a dark comedy that would make. You are too, too funny, girl.
Sorry to hear that things are gittin' ya down, though. It's a lot to handle... chemo, the side effects, this crappy winter, your house projects but no energy to finish them because of the stupid chemo, etc etc etc. But you've come so far already, buddy. You're gonna make it and we're gonna be right here beside ya cheering you on. You can cry and scream and vent all you want, but we ain't goin nowhere! You're stuck with us!!
Sending you, and anyone else who's having tx today, a great big hug. Hang in there, everyone. We're gonna get through this crap.
-Sal
-
Morning all!
Amy, First of all...{{Big Hug}}!! It is totally normal to have those self pity days! Wallow in it for a bit and it will pass and things will be better! We are going thru alot and I know exactly what you mean about being grateful for family and it being nice to be on the receiving end of some acknowledgement that what we are doing is not easy! I think our families & friends know it's hard but really have no idea unless they were in our shoes....which is why you are all so important to me!! I have not been to any support groups because you guys have always been here with kind words and support when I needed it.....while whining about bills, SE's, etc. So, thanks everyone! Amy, talk to your Dr. about the lack of sleep...that was a problem for me when on the AC and taking the steroids...you know, you feel bad as it is and then the lack of sleep makes it worse!
WishIwere....CONGRATS! Big day for you!! So happy for you and can't wait to be where you are...on my last day of chemo! You help us to see that we WILL reach the end...we just need to keep plugging along and we will get there before we know it....Well, maybe not before we know it...I think we all know exactly when our last chemo date is...Point is, it will get here! Hope it goes extra easy for you..keep telling yourself "This is it! All done!" and maybe your endorphins will keep away some SE's! You rock!!
Sal, Hope you are still doing well and that the body aches stay at a minimum this weekend. Keep us posted! I am feeling pretty darn good and (my new mantra) I'll take Taxol over AC anyday!!
Laura, Kate, KMK, Joy, Cindy, Suz and anyone else I may have missed...I hope you are all having good days and enjoy the weekend!!
-
Good morning Beautiful and Strong Ladies,
A- I know exactly how you feel.....being on the receiving end of so many wonderful and kind favors from friends and family made me very uncomfortable. Finally, I just succumbed to all, and graciously just said thank you, often while tearing up and giving big hugs. I just let it all hang out. One of my girlfriends said to me, " you are doing US a favor, by letting us feel like we are helping you". Now that I am feeling stronger each day, and am not so needy, I feel great being able to participate in life again. I even took my daughter and friends to a roller skate birthday party, and saved some of my carpool angels/girlfriends from the LOUD music, and 500 buckles and laces that I had to tie and re-tie ! But I loved feeling normal, and doing those normal mommy things. I am finally a 'giver' again, not just a 'receiver'!!!A, you will be back in control again soon, I am sure of it. Your friends and family are helping you out cause they love you, and are proud of you, and because they WANT to, not cause they HAVE to!
Sal, your little fingers, ouch! Just what you needed! SOOO glad the Taxol is taking it easy on you. "Piece of Cake" ( chocolate )!!
Loriann, no support groups needed with you SUPER supportive angels on my team. I am,however, feeling like I need to take the kids to see someone......I feel like they are dealing really well, and their teachers agree, but just to make sure, I think I will set up an appt. with the child team they have at the Cancer Center. What do I have to lose, right? I have been blowing it off, only because I did not want yet another appt. at the C.Center....will suck it up after president's weekend and book appt, just to be on the safe side.
Suz, how was the LGFB class? Did you get a boat load of new make-up? I got some great stuff that I really do use quite a bit.
WiW- Can't believe how much snow you got. After this winter with all of the BC shit, I can only imagine how SWEET this spring and summer will be for all of us. I can't wait ! Bring it on!!
To all of you ladies, I am sending warm hugs, and wishes for a terrific TGIF !! xo cindy
-
Whoa-- did someone hit me with a truck? I knew the aches and pains would hit, but I thought I had another day to enjoy first. Wham!!! Energy totally drained, aches and pains all over every inch of my body although not unbearable (if that makes any sense at all). Fingers go between tingly and achey. And a sore throat that started last night that feels like strep throat but oddly enough I'm still famished and eating like a pig in spite of the soreness. Today will definitely not rank as one of my highlight days. But still better than AC. Is my brain fried, because this makes no sense at all... this is all still better than AC.
Hubby picking up dinner. Can't wait for him to get here. I'm starved. What a weird mix of sensations. Gotta go lie back down before I fall down.
-Sal
-
Sal, you crack me up. Though I had Taxotere, they are in the same family, and I felt like my brain was fried for a week! Completely clueless, in a constant hangover, though I had not enjoyed a drop of vino!! Hang in there baby, the fog will lift! When friends would drop off dinner during my bad week, they would say, "you probably don't have an appetite......" Yeah, right, as soon as they left, I was diving in to the bounty !!!
Sending positive thoughts and well wishes to all. xo cindy
-
Sal,I know what you mean. Wow, I woke up this morning totally exhausted for no reason. Molly maid was here at 8 am and I just told them to clean whatever they could and went to lay back down. All Ive done today is sleep, eat and try to deal with constant hot flashes. Nothing at all like a/c, I don't feel really bad or anything, just ridiculously tired.
No wonder my onc warned me about weight gain during taxol. She gave me strict orders to at least keep up with my walking the dog 2 miles a day. I thought she was kidding.
Cindy, the look good feel better class was awesome, am I ever glad it was yesterday as I don't think I would have made it today. I was really surprised at the quality and quantity of products. I don't think there was a thing there that I wouldn't use. Had a lot of fun sharing stories with all the other gals there as well. I think I was farthest along treatment wise, most were on tx #1 or #2.
Hope everyone is well, time to curl up on the couch with a cup of tea.
Love and hugs
Suz
-
Sal, and Suz--sounds like you're on Taxol! I TOTALLY understand the aches/pains being not unbearable, but really unpleasant--it's hard to decide how/when to medicate, I find. I thought the sore throat was from the herceptin, but that's another one I've had all along--kinda swollen and achey feeling, like the beginning of a cold? I'd rather it was the taxol, as I'm doing the herceptin for a year!
And the appetite! So weird!!! I hate to say it, but I've gained about 9 pounds since my surgery (which took off about that much--agh!). And NOT because things taste good, or my tummy feels great, but more to settle a mild queasiness by stuffing my face...? I asked the onc about it today at treatment, and rather than telling me to walk 2 miles a day (ha! Suz! Are you doing it!? you're my hero!), she said, "look, you've got 3 months to do this, and deal with it how you can, and the rest of your life to take it off". I so deeply love her. She also gave me a scrip for more percoset and calmed me down about overuse/addiction--she was very adamant that I'm being responsible about it, and should use it if I need it. Which, tonight, thanks to steroids, I don't!
I asked the nurse: I'm getting about half of what you guys are getting for dosage each time, which apparently really cuts down on the neuropathy. Which I can just notice now, on treatment 9, if I think about it, but is very mild. My hands and feet are cold, and more sensitive to hot water, but boo hoo.
As to chemo-brain, Sal, I can't remember what I used to be like (ha ha)--I was always kinda flakey, so we're all used to it, but I have noticed it's harder to keep track of stuff if I don't write thing down. I also have a vagueness that seems to go with the fatigue--AND (great for a mom of two boys) a serious sensitivity to noise and overstimulation...
Lori--how ya doin with the Taxol--has the truck (on the train??) hit you, or are you still feelin fine? Hope it's the latter.
I've only got three more treatments! That actually sounds a lot better to me than 4. I know it will be a while after that before I feel better, but the light is beginning to show at the end of the tunnel. Also, I'm hopped up on steroids, making me absurdly perky:
see? that's me:yellow, bald and smiley. I'm really in a much better mood than I was at 5 this morning.You guys are really great.
Cindy, it's so nice to hear you're feeling better already--it's that hopping-back-into-life abliity that I'm really looking forward to. Hooray! I'm glad you're still checking in.
Speaking of which--Wishwiere--
wahooooooooooooo!! you did it!!! Congratulations!!!!! Hope you have enough oomph to celebrate in a small way, and plans to celebrate in a big way a little later.
cheers--Amy.
-
Morning all!
Sal, too funny.."did someone hit me with a truck" is almost exactly how I described it too my boss..."I feel like I've been in a car accident" was my thought! I know exactly what you mean...sore all over but still find it better than the AC. The worst of it lasted 2 days then started getting better..I hope that's how it works for you. I really did not have the foggy brain feeling like I felt on the AC...I hope that clears up for you as well!
Suz, ditto to the above. What I am finding a bit odd is that you and Sal have better appetite's than with the AC. I find my stomach still tending to be a bit flip floppy and definately not eating as much as when on the AC but I think the steroids had something to do with it too! I was sorta like Amy, picking at something all the time to settle the tummy, now I gotta think about what I want that sounds good but I'm not nauseous at all. Weird!
Amy, I wish mine was only 9 pounds...I know it was 12 and I think it went as high as 15. It's been a week and a day since Taxol #1 and I'm down 2 pounds without trying. Now if I would just start back on the treadmill I could maybe lose a bit more! Doing chemo every 2 weeks will get me done in 4 months as opposed to 6 so I'm just riding it out and will really get back on track after March 14th (my last chemo). I don't want to have to buy all new summer clothes and other clothes for Vegas. I'll have a little over 3 months between last chemo and Vegas so I'll really work at it during that time!
My DD has her big "Snowcoming" high school dance tonight. I've got a french mani to do on her fingernails, toes to paint a teal color (to match her teal dress and silver shoes), buttonierre (sp?, I know) to pick up and house to clean since her boyfriends mom is coming over for pictures.
She has 2 boys, 17 and 19. The 19 year old has never had a girlfriend, let alone went to a dance (and graduated last year) and my DD has been "dating" the 17 year old since October 2006 (when the dates consisted of him coming to our house for dinner and a movie, LOL) but this is their first dance! My DD had to assure him he would live thru it...he's all about dirtbikes and 4-wheelers and quite nervous about the dance. It's so cute!! She was trying to teach him to slow dance last night...it was sooo funny! Needless to say, his mom is very excited about the whole thing!
Thank goodness I'm feeling great this morning....we'll see how I feel this evening after all that though! DH and I thought we would try to go to dinner while DD was out so hopefully all plans remain intact!
Sal & Suz, rest as needed and I hope your aches pass soon! All the rest of you, take care! Lori
-
Ladies! #4 went great! The best this was that the room was full of all women (cept one sleeping brain recurrance man who slept a lot) All were breast cancer survivors in different stages of their treatments. On with her 3rd recrur at ages 32, 36 and now at 48, one had recon implants and another is just finishing up her herpcetin in april after one year. To talk with these ladies in person wasn't somthing I thought I'd be comfortable with, espeically since their cases were more advanced, and also be/c they were adding 4-12 Taxol on etc onto the A/C we'll all finished. I always feel like I'm so lucky and so sad when someone has it worse to even complain about my minor situation.
I think the ONLY reason I could open up with these great ladies and even (SHOW MY CUE BALL) was be/c of this forum and all the fantastic laides on here! Without you all, I'd be holded up my home and never go anywhere with any pride!
For that! THANK YOU EACH AND EVERY Beautiful woman!
Aside from that, SE's are minor this time. Did take a ABH combo last nigth and slept well. I've had minor nausea, with a bit of dizziness and vision stuff, but actually can handle that, so long as the nausea is minor!
{{{Hugs}}} to you all suffering today, worrying about getting things done that will be there tomorrow and afraid we've taken toomuch and not given enough! ALL THIS will changed ladies and we'll grow strong once again and ready to LIVE our lives as WE choose!
me
-
Oh Lori, you are giving me hope... saying that the worst of it only lasted about 2 days then started to clear. My biggest worry when the fatigue hit yesterday was "Since I used to get fatigue Monday through Wednesday, does this mean I'm out for the count for 6 days now--- Friday through Wednesday?? I can't handle that!" I sure hope I follow your example and only have the usual 2 or 3 days of crappiness.
I'm a teeny, tiny bit better today, but not gonna go anywhere. Couch potato. I must have flushed out every once of fluid I had in my body last night, between getting up every hour to go to the bathroom and sweating. I tried to tell myself that's a good thing because the chemo is getting out of my system. But I wouldn't exactly say I got a good night's sleep.
I think I'm the only one on the forum who's lost weight since starting chemo, so I'm looking forward to possibly gaining weight. I was about 135 before surgery and now I float around 120-114... depending on where in the chemo cycle I am... I weigh more chemo day than on "low wbc count" day. I hate the way my clothes hang on me, and tired of people telling me how thin I look. Bring on the fat! Plus the nurse told me my taste buds will change and things will start to taste metallic, so I figure I'll get in the food while I can.
Congrats wishiwere! So you're all done with chemo too? Wow! I can't wait to see our roster of "chemo completers" grow and grow.
Ooof. Twinge of pain. Gonna go lie back down now. Hugs ladies.
-Sal
-
Wishiwere, YOUR DONE !!!!!
Big hug and congrats sent to you. Hope you take some time out to Celebrate when you feel up to it.
I had to give myself a neupogen inj. this morning. Im sure that is going to be an interesting mix. Bone pain, muscle aches and nonstop sweating. I should start feeling real athetic soon. I just need to add a little exercise into the mix
Time to curl up.
Hugs to everyone
Suz
-
So you guys (Sal and Suz?) have begun sweating since starting the Taxol? I was sure it was the lupron/menopausal stuff...again, it sucks, but I would love to think it would stop once the taxol is done.
Sleep is a problem. Nasal symptoms/sweats! Seems minor, but it's exhausting after a while, no matter how minor the things are that wake you.
Sal, I hate to say it, but in the beginning, I seemed to have more "good days" than now--apparently the fatigue and the bone pain is cumulative, so as the stuff builds up in your system, you can expect more. I don't mean to be discouraging--my nurse warned me about it, and it was helpful for me to know that so I could plan. I don't know how it works on a bi-weekly as opposed to weekly schedule...but now, I start feeling crummy Sat. afternoon, feel a little better by Tuesday afternoon, but if I do too much, I crash pretty hard. You just have to take it easy, and baby yourself. Or better yet, make other people baby you!
Lori--so nice to hear about your daughter and her boyfriend--can't imagine that stuff is coming up for my boys in only a few years. Your daughter sounds like a great first girlfriend. And so nice that they're letting you all fuss over them. Sweet, sweet sweet.
Wishiwere--I'm so glad you feel that way about our little group--I do too. It has been so helpful to hear everyon'es experiences here, and hear about what people are able to do and how they take on the world.
Gotta go lie down again...love to all
Amy.
-
Ok, so Taxol is no longer my best buddy. The aches and pains progressed into "make me whimper" mode last night, and Tylenol doesn't do squat. Does anyone take a stronger medication for the pain? I have some pain meds leftover from surgery... think I'll call the hospital today and ask if they'll do any good. I'm guessing not, otherwise they'd probably have given me something to begin with. The onc nurse told me many times that the aches/pains and fatigue would be cumulative, as Amy mentioned, so now I'm really worried... I'm a mess right now, and I have 7 more weeks to go. I don't know if I can do this
I'm also curious how the Neulasta shot will play into all this... if I understand it correctly and the shot is what is causing the aches/pains (over-abbundance of wbc being produced), then does that mean that I won't get another big dose of aches/pains the next time I have chemo since I won't get a Neulasta shot after tx #2? But conversely, I'd probably have more fatigue since I won't get the boost of wbc. Not expecting you ladies to know the answer, just wondering out loud.
Fingers and toes a little more tingly/cold today, but I keep "squishing" them to keep the circulation flowing. Still pushing the fluids... makes me want to gag, I'm really not thirsty, but I want to flush the crap out of my system. Appetite not as strong, but I keep eating. Took a small walk yesterday, just to get some exercise and fresh air. Day dragged by so slowly.
Amy, I'm not sure if the night sweats are from the Taxol for me. I've had them off and on for the past year. But nasal problems are definitely worse because of chemo. We run our humidifier 24/7 now and that seems to have stopped my constant nose bleeds, but I still have some problems. Same with eye problems... my eye sight has diminished since chemo started, along with eye strain and watery eyes. I just hope these side effects will go away when we're done with chemo.
Gonna go lie down again and feel sorry for myself. *whimper whimper*
-Sal
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 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