March 2010 Chemo Start
Comments
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Heather - I'm sorry about your neuropathy! I only had a little neuropathy around #3 and it went away. Is it in your hands or your feet or both? I had it mostly in my feet. By my calculations you made it through 3/4 of the entire course so you've actually done really well. Even though you didn't make it totally through chemo you still have rads and tamox in your future, right? So there are a few treatments left in your arsenal. ;-)
Angi - Yeah! It's great to be done! Congrats!
Well, I've got almost as much hair as Ana does in her avatar. I can't believe we actually finished chemo on the same day. I'm so far behind in hair growth. I'm still bald on the very top but eyelashes are finally growing back. They are too little to put any mascara on but they are growing!! Woohoo!
Charley
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I second that Charley - Heather - you got through 100% of AC - and most of the taxol/abraxane - Hugs ((Heather)) , it's been a long road already hey? From what I gather, our oncologists err on the side of caution (within the realms of evidence) - and you've had plenty of ass kicking chemo already.
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Dear Charley & hereandnow;
Thank you for your words of encouragement. I have an appointment on Monday to see if there are other options like lessening the dose so I'll keep you posted. My neuropathy is primarily in both feet and is pretty constant. I have some in my hands that seems to fad in and out. I guess I figure that since all has gone so well up to this point that I should be able to sail through the remainder of chemo.
Charley, my hair is growing but is also extremely sparse on top, male pattern baldness is my current look!
Heather
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hmh23 I have pretty severe neuropathy and my onc wouldn't even hear of me not finishing all my taxols. I can't feel my toes, the ball of my feet, my fingertips or my back (very strange feeling btw), I am happy to say I made it through all 12 of my treatments on Wednesday...I will let you know how long it takes for the feeling to come back. Good luck!! Angi
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Dear Angi;
I spoke at length to my onc and we have decided to forge on with my last 4 treatments. He has already moved me onto Abraxane which is from the Taxane family and used for Stage 4 cancer. It has less side effects. I'll deal with the neuropathy. Congrats on finishing all 12 treatments.
Heather
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- Angi - CONGRATS!!!! It is a great feeling. Now you can have a chance to let your body get rid of the toxin. Be patient - it takes awhile (my fingers are still tingly and it has been 6 weeks)
Heather - Sending positive vibes your way. You will get through this and soon you will be able to put it behind you.I'm half way through rads and feeling pretty good - no skin effect, slight fatigue. My feet and ankles have really taken a beating - damn edema just won't go away. I feel like an old lady (OK, so I AM an old lady, but I never really felt that way).Hugs to all. Marilyn -
Heather - my best thoughts are with you - gutsy chick you are. I'll be sending you good abraxane vibes each week til it's done.
and Marilyn - last week I did an afternoon where I stood up still for about 6 hours - I had pitting edema of my ankles - freaky hey? But mine goes away when I put my feet up, and until this has settled, I'm wearing my elasticised stockings for any long periods of standing/sitting, have you tried stockings?
Also, for any fellow tamoxi babes - the flashes have been driving me caarraazzyy. jumper on, jumper off, doona on, doona off - ssscccrrreeaaammmm. Last night I took 2 panadeine (acetominophen/codeine) and an ativan - and I slept through without waking once in a sweat. I will experiment tonight with plain acetominophen but will be delighted if I've discovered a cure for night flashes. fingers crossed.
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Lisa - The hot flashes are more bothersome at night for me too. I hate waking up hot and then a few minutes later I'm freezing to death!! I read somewhere that it is a good sign that you body is metabolizing the tamox and it is working. <sigh> So SEs are good.
Here's to some good sleep tonight!
Hugs, Charley
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The day I've been waiting for is finally here!! I'm leaving now for my LAST chemo!! I'm so excited. Strange...this is the first time I've been happy to go to chemo. I made my nurses a beautiful cake and will have my husband pass a piece out to all the patients and nurses (I'll be hooked up so I can't do it) and we are going to celebrate and have a party! Hopefully I will see all those people again under different circumstances.
Lisa: I take the same medication at night and haven't awaken to a hot flash yet. It has been months. I only take the pills at night so I still have a hot flash or two during the day but at least I sleep the whole night through. My oncology doctor told me to do it. I was afraid I would get addicted and he said no. He wants me to sleep and he said he knows what he's doing. So, I trust him.
Okay girls! I'm off!
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Hello Ladies -
I haven't written lately but I have been reading all your posts. Yeshua4me -CONGRATS - Charley - you hang in there -
I had my final test - Eco - and everything is fine - still have the water retention but at least now they know there are no blot clots and my heart is fine so it's onto T - I've been reading about your hot flashes and I also have them although I call them power surges - and the worst are at night. I notice during the day if I get stressed I have a surge otherwise I'm okay. I have been taking much better care of myself and have lost the 12 lbs I gained during chemo and intend on going to reach my goal of 50 lbs. more. Want to look and feel good for the cruise in May.
Sending warm wishes and hugs to you all - and as always you are in my prayers. - Stacey
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I did it! Chemo is over!! I am so happy! I danced with my husband after chemo was over. The nurses put on some music and it was wonderful. I said good-bye to them all and wished them well and hoped that we wouldn't meet again under these same circumstances. I had made a cake for the celebration for the nurses, patients, doctors, and volunteers. I got to pass it out and say a special goodbye to each person. I made a HUGE cake and only had 3 pieces left. Probably fed at least 30 people. It was a great day. So all I have to do is wait for the chemo to kick in, ride out a few SE's for a couple days, and then BAM! All done. I actually made it!!!
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HIP HIP HOORAY - ANOTHER MARCH GAL DONE!!!!!
HereandNow - I have tried the stockings, but I should wear them more regularly - after all they are sooooo attractive - NOT! I'm finding the humidity is a major factor. August in DC, there is no getting around that.
Tamoxi question - I started going through menopause prior to diagnosis and had been having hot flashes / night sweats before this. Onc is still debating whether I go on Tamoxfin or Aramix??? - will I go through a whole new round of flashes/sweats??? Anyone out there postmenopausal on HT?
Let's all join Yeshua4Me and go out and DANCE AND EAT CAKE!!!
Marilyn
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Congrats Yes! It feels great doesn't it??
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hip hip hooray Yeshua4me -
we spit in your eye, cancer, and stomp on your toes, and punch you in the kidneys, and chemo, you can take a flying leap too!
phew- hold me back.
hope your side effects are few, and your celebrations many,
Lisa
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congrats Yeshua4me - it's so good to be done!
Marilyn - I was in peri-meno prior to treatment, had had two periods in 6 months - one last June and another this past December. I actually bought a pregnancy test in September - holy cr*p PG at 50? Thankfully it was negative and I got a Christmas blessing lol. I haven't had a period since then. Anyway, onc put me on tamoxifen not arimidex. And hoo-boy am I having the night sweats! Lisa, I may try your acetaminophen trick, thanks.
Although it's greatly improved, I also still have some ankle edema. It's worse at the end of the day, or if I don't hydrate enough. Walking is good - except I could not do it those awful hot humid days last week - but deliberate deep breathing while walking really seems to help. I believe it helps stimulate the lymphatic system, another reason I signed up for a yoga class, to learn deep breathing.
Take care everyone! {{hugs}}
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Marilyn and Yeshua4me;
Thx for the good vibes!!! I completed #9 today....3 more to go. The neuropathy has lessened so I'm forging ahead. Sorry you are experiencing problems with edema. Sending good vibes your way on this one.
Yeshua4me; CONGRATS on finishing up. Another favorite quote from "HOPE...", "There comes a time when every cancer survivor must simply step out the door and do it....and for us, the 'it' is to live." I think you'll be shutting that door and running!!!!
While wondering around the Cornell campus yesterday after getting our daughter settled into her apartment, my husband came up with a great idea.....Where is Wanda (my wig)!!! I only wish that we had thought about it before going to Toronto, Hamilton, NYC. It would have been a comical photo diary of Wanda in different places.
I have to say that the cyber-friendships found on this site have provided me with the support, laughter and strength to go on. THANK YOU!!
Heather
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Hi Ladies,
WOW! So many strides have been made!
Angi and Yes: congratulations on finishing chemo!
Marilyn: Half way through rads. Way to go.
Heather: So Sorry to hear of your trouble. Glad your neuropathy has lessened and you are able to continue on. Only 3 more to go!! The end is in clear sight. I love the idea of the photo diary of "Wanda". That would have fun to look back on and to see how strong you were through this whole ordeal.
Charley: Thanks for the input on the TE. I wanted to be bigger than i was, but not too big. And it is very difficult to tell since I only have one foob. I have the same size as you and decided last week's fill to be my last. (I could have one more) I am very glad I did, as I was in sooooo much pain after the fill. If I was going for one more that would have put an end to it anyway. I don't think my body could handle any more. And of course my liver has been acting up again and I was extremely limited on taking any pain meds. So I suffered!!! Of course, I will have to do it again on the other side after rads. But I'm not going to think about that now.
Lisa: I love your rant against cancer. You go girl!
Stacey: Congrats on the weight loss! Keep up the good work.
Well, I was unable to have chemo the last 3 weeks due to my liver enzymes. Needless to say I was very frustrated with the whole situation. I have an appt to see a liver Dr. at Jefferson for a second opinion on the 27th. I am so far behind the original schedule. I still have 9 more chemo to go! Of course I am at the beach this week and am able to go tomorrow. But by next week, my numbers will be back up over the limit. Is anyone else still doing chemo?
I also have hot flashes but I'm not on the tamox.. Does anyone notice a flash after you finish eating? Charley, I too whip the sheets off, flip my pillow as I can't stand it hot when I'm flashing, start to doze, wake up again because I'm freezing. My husband said I was huffing and puffing during a flash, which was waking him up, so I am careful not to let any verbal annoyances slip out.
Keep celebrating everyone!!! You are always in my prayers, Michelle
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Kayne - I'm sorry you missed some treatments. It must be very frustrating.
On a much lighter note, I had to laugh at your description of sleeping - my husband tries to be supportive, but at least 2-3 times a week I wake up to find he's flown the coop and gone downstairs. He gets a better night sleep curled up on the living room floor, than he does in our comfy bed, sleeping next to his huffing/puffing wife. Given my potential for insomnia, hubby is forbidden from nudging me in the middle night to get me to turn over or to stop snoring OR snorting.
I can also relate to the sweating / freezing /sweating dance I do every night - and I'm not even taking the damn drug yet!!!
RADS - 21 down / 14 to go.
xoxoxo
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hi guys, hope everyone has had a reasonable week - kayne I'm sorry to hear about your liver enzymes, that must be very frustrating. I hope the liver specialist can give you some answers, and you can get this bloody thing over with soon.
I was getting flashes before I got on the tamoxitrain - they just got worse especially at night. So for the last several days I've had a couple of acetominophen and an ativan - and have slept all the way through. I haven't wanted to stop that combo because the sleep has been so nice. I feel like I've got 5 months worth to catch up on.
Hugs to everyone - have a good week-end, Lisa
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Hello, Marchers! I had my last chemo treatment today, AND had my PICC line removed (did not feel it!). I will not be on any meds (triple negative), so I am both relieved and feeling "set adrift". I'll see the onc next week, and then will be monitored every three months to start, and then less frequently. No scan at this point. I'm happy to join the post-chemo crowd, and send best wishes to those still in the chairs/receiving RADS.
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Congrats Marigunn! I take it a picc line is a little different than a port? The site where my port was removed is still a little sore ... 4 weeks post op. Got the ok to start exercising again on Thursday. RFC only 4 weeks away! Hopefully exercise will help with some of these sleep problems ...
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Yes, a PICC line (Peripherally Inserted Central Catheter) is inserted in the upper arm, into a vein that goes near the heart, and then the chemotherapy meds are hooked up to a nozzle-type cap that's outside the arm, thus avoiding the needle stick and blown veins. I understand nurses like the port better. Good luck with the sleep problems. I did not have much trouble sleeping until last night -- no sleep at all! Glad you're also near the end of all the problems!
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congratulations marigunn, I hope you're not having too many SE's from the last one. It must be nice to finally have a shower without the PICC line. enjoy.
And Charley, I hope your port site settles soon. How's the hair coming along - mine is pretty short all over, thicker on top, and so gray.It's not quite long enough to colour yet.
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congratulations marigunn, another March sister done!
In addition to the 8-week yoga class through work I mentioned before, I also signed up for a 90-minute Yoga Heals workshop through Breast Cancer Recovery. It sounds so intriguing and is partially funded through Komen Madison, so I feel good knowing that some of the money I helped raise, is going to help survivors. Here's a link if anyone's interested:
http://www.bcrecovery.org/pages/Yoga-Heals.php
I went on-line and bought a travel yoga mat and carrying strap. Feeling better already, but maybe it's the after-effects of retail therapy! LOL {{hugs}}
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Congratulations marigunn! Way to go!! I hope you are feeling well.
My hair is short all over, with more on top as well. I'm not really liking the look right now. I hope it improves. Still sporting bandannas except when I'm home. I spent the week at the Jersey Shore with my children and my sisters. It was alot of fun and very relaxing. My DH was not able to join us as he had deadlines to deal with.
I was able to have chemo on Wed.!! Wooo Hooo! 4 down and 8 to go. Hoping for good blood results on Monday so I get the green light for this week. I am getting concerned with too much time between treatments. Always something to worry about! I go on Friday to the liver spec.
We formed a team for the SG Komen Walk for the Cure on October 3rd. Our team name is "Nu Nockers". I have never participated before, looking forward to it. Now we are working on designing our shirts and fund-raising.
badger: I have just signed up for my first Pilate's class. It is given by our Breast cancer resource center and is only for women currently diagnosed or in treatment. It starts in Sept.
Did anyone have joint pain while on Taxol? My hips are very achy. I am slow to move, feel like an old lady.
Wishing everyone a good week! One week left and the kids go back to school. I'm not looking forward to that. Michelle
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great you were ble to get that next chemo Michelle - fingers crossed for Monday. I had really achy legs on taxotere - I had to take panadeine forte to sleep at night - 30mg codeine in those. It's all settled now although, I still feel a little old lady creaky when I get up and start walking around. I've been working quite alot more and really want to look into yoga and pilates - thats a good idea.
hugs to all my March sisters,
Lisa
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YEAH Marigunn - Congrats. It is indeed great to be done with Chemo.
I'm still plugging along with rads - 23 down / 12 to go!! I know this is TMI - but I"m just letting in all hang out - my boob is slathered and airing out. So far it is just pink, but starting to get a little raw.
I had lunch with a friend who has been on Tamoxifin for 3 years. I know this doesn't sound hopeful at this stage in the game, but she said the first year is the hardest, but by now she has very few SEs - some leg cramps here and there, but nothing major. She also said it took her about 11 months after treatment, but one day she woke up and felt no trace of any of the brutality we've just been through. As we each get stronger day after day, we need to remember that one day this will be behind us and we will continue on with our lives.
Warm hugs to all. Marilyn
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AUGGGGHHHHHH!!! That's all I can say. I was unable to get chemo today, due to my damn liver. My ALT went from 96 to 224, with 40 being the high end of the range. I feel like I am on the verge of panic attacks due to postponing the chemo. I am glad to be going on Friday to a specialist. Hopefully he can shed some light. Then I think I need to speak with my onco and devise a plan. I mentally cannot keep going this way. Every Monday I go for blood test, call five times on Tuesday for the results, then answer the damn phone from family members wanting to know if I am going for chemo. Oh and answer 20 texts on Tuesday from people asking if I got my results yet!! I am sure I'm dis-placing my anger, but everyone asking really annoys me!! And they don't want me taking any meds. Something needs to give, fix my liver or give me meds to calm me down!!
So, OK, the nurse just called and said my Onc. is going to reduce the Taxol by 20% the next time I am able to have treatment. Well, I guess it's somewhat of a plan.
Lisa: thanks for the input on the joint aches and for crossing your fingers for me. My aches have subsided somewhat, so that's one positive note.
Sorry to rant but I feel better!! Hugs and smiles to everyone, Michelle
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Hugs and prayers for all.
When looking at the board today, it hit me how far we have all come since joining. March chemo start date and here we all are six months later. I don't know about you, but back in March, August/September seemed to be an eternity away!
I did something yesterday that just thrilled me - I got a haircut!!!! It was just a trim of the nape and a trim to tidy up around the ears. My hair is still super short, but getting a haircut made me feel so normal. It was great!!! And I feel like this short short do now has a little style....it doesn't really, but I feel that way.
Does anyone who had a lumpectomy have a lump at the site? My radiologist and onc have assured me that it is a hematoma, but it still worries me a bit. I also am have twinges of pain in the breast. Just wondering is anyone else is experiencing this.
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kayne I'm glad you're seeing a liver specialist. My ALT went up after the first chemo and stayed up the whole time, but only around 55 or so. Chemo certainly can cause some damage to lliver cells, but also the liver has a very cool way of repairing itself once the insult is removed. Has your oncologist sat down with you and had a good talk about your concerns - you have a right to the communication you need.
they also need to advise you on your other medications - for example you should avoid acetominophen with elevated enzymes like that.
Lilly - i didn't have lumpectomy so don't have any personal advice- but I'm sure one of us who has will pipe up soon. I think too that breast pain after radiation is fairly common.
I'm very jealous of your haircut.
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