Chemo in June 2015
Comments
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Congrats to everyone finishing chemo. I finished that stage last Thursday. Those of you still in it, my words of advice are to take treatment one step/stage at a time, you will get through this.
I've got herceptin for a year, hoping the side effects go away. I'm really achy right now. Then radiation.
Happy to hear all your stories. It helps to feel the togetherness. Thank you warriors!
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thank you for the encouragement Espanola!!
i have a question. does our hair only fall out once ? or does it fall out again with each new chemo, i didnt lose my eye hair with FEC , and it was 45 days into docetaxol when they did drop. will docetaxol bald me again? or is it constantly falling and its so fuzzy and whispy i dont notice it??
Hugs to All !!
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DayLily- Did your hair start to grow back? If so Taxotere will likely cause it to fall out again. I had 4 rounds of cytoxan and taxotere and lost the hair on my head by Day 18. I always had some fuzz but no new growth. I'm 7 weeks post final chemo now and am seeing good growth on my head. The eyebrows started to go about 3 weeks ago (a month after I finished chemo)and are almost gone now. I still have eyelashes, but a few are missing and who knows, I may still lose those. I was told that it is common for the brows and lashes to be the last to go.
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Thank you they callme commodorable. .your hair growth pattern seems similar to mine but your lashes held out a lot longer. so chemo only affects hairs that is growing around the time of the infusion, ok thats good, i seem to recall being skin bald at the time of my first docetaxol, my head hair is growing quite fast this week, 3 almost 4 weeks out of last tax dose. all my eyelashes and eye brows are gone. so i will cross my fingers that the new growth stays
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Hello all! Finished last chemo round 10/6 and still having SEs. I've seen where others here are "achy"....I'm taking Hydros to avoid as much pain as possible because mine has been really tough! Lots of "pain" - even with the Hydros, lots of lower ab pain - not as much nasea as in the beginning - more like very painful gas/constapation. But my big question is about what I would call "muscle pain" ... I know that bone pain is common - I'm not sure I can tell the difference between bone pain and muscle pain. But I want it to STOP now. Enough is enough. I get these frequent "jabbing" pains - sort of like being shocked by electricity - sudden sharp pains that bring me to my knees! It could be in my bones - or my muscles - I can't tell. But even with the Hydro pain killers - the pain is there. I know if I can get through the next week or so I should be on my way! Rads next!
Anybody else having these sharp, stabbing pains? When do they finally stop?
Thanks! Prayers to all & many Blessings!
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December- Congrats on your last Chemo! Hoping the pain goes away soon! Bone pain for neulasta hit me about 4-5 days later, but Claritan and Aleve helped. So does an Epsom salt bath.
My last chemo is next tues, oct 20th. SE dujour has my face breaking out with red ugly bumps. Lots of them😳 have had a few thruout tx, but this looks awful. Will call MO tomorrow, but has anyone else had this??? AND my breast still hurts!! Haven't had surgery yet, just biopsies in May. Maybe it's killing the nasties in there??
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Catfurr - I've heard of some people getting the red bumps - but I don't know what the solution is. That's the one thing I got real lucky about - my skin looks better than it ever has. And as far as the biopsy - I thought it hurt like H*&^!!! I know they said it wasn't supposed to hurt - but I thought I would jump though the ceiling! I'm sorry you are still having pain from the procedure. Pain sucks.
Come on Oct 20th! I know you are more than ready to end this part of your life. I'm still having SEs, but I just keep reminding myself that I don't have to go back for more. That is a GREAT comfort.
It was suggested to me today that my body aches might be a SE of the hormone blocker that I started right before chemo - I guess I'll know in a few weeks since body aches are not supposed to be a part of Rads (starting that mid Nov.) If the body aches are a SE of the hormone blocker - don't know what I'll do. Can't be on pain killers forever!
I wish I had some helpful advise - but I don't. Just encouragement and prayers. And since you are coming upon your last treatment, maybe the red bumps will go away on their own. Well, we can only hope.
Please keep us all posted because someone else probably has the red bump SE, too. Or someone who comes into chemo a year from now. I know I've read most every post here - especially during the early dx time - looking for any info I could find. I appriciate some of the older posts - very helpful.
Also, keep us posted about your chemo SEs. I'll try to keep my SEs posted to let people know how long they can expect SEs to linger, well, at least in my case.
Prayers and Blessings!
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Catfurr, if the MO doesn't have any suggestions, go to the dermatologist. They deal with this kind of stuff all the time. Sometimes skin reactions can be dealt with by antibiotics, either internally or topically. I have found that my "normal" doctors know how to deal with quite a bit of stuff. Like I got stung by a bee during chemo (eek!) and the MO sent me to my primary care doctor for an antibiotic and a steroid cream just in case of cellulitis.
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December--the bumps are a little better today. Just add it to the SE list and move on😄 Maybe your MO could switch your blocker to something that might be easier on you?
Italychick--thanks for the suggestion! Will certainly do that if it gets worse!
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Hi Ladies,
Congrats to all of you who have finished chemo. I wish you all speedy healing and a return to normal energy levels soon.
I'm more than one month PFC (post final chemo) now and almost halfway done with my radiation. My eyebrows are still thinning and no sign of new eyelashes or nose hairs yet, but I have peachfuzz! It's very short (maybe not even 1/8 inch and very light coloured so there's no way it would show up on a photo, but I'm happy it's growing. Radiation has been good so far. I'm having 16 treatments and 4000 centiGray (40 Grays) total and as of today have had 7. My skin looks and feels normal. I have no pink even. I've been exercising lots and still staying really well hydrated. I'm also tracking my protein and fruit/veggie intake. So far, so good. I slacked off on putting lotion on my feet for a while and they're peeling a bit. I'm not sure if it's a left-over of the hand foot syndrome or if I have fungus that came back or never really cleared up, but I'm back to moisturizing them regularly again and they seem to be doing better. I would say me energy level is very good; pretty much back to normal. I'll post photos of hair growth as soon as I can take a photo that you can see hair on.
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Hey Kickin?? How you feeling?? A little more than 3 weeks out. Been thinking of you! xo
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PFC, post final chemo eh? I have another word I might insert but wolud NEVER say it!
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Last chemo was 9/18 - I have fine baby soft hairs growing in (my little sproutlets)! I can see both coarser dark patches and these white hairs. Still have eyebrows and sparse lashes, although the brows seem to get thinner every day. I have a touch of neuropathy and chemo brain...
Surgery for the double mastectomy is 11/16, then 6 weeks of radiation. Oncologist switched me to every 3 weeks for herceptin (thanks to your postings on the subject, I raised the subject and he agreed that I could do that!)
Thank you all for being so wonderful - it was a comfort to know that I was not going thru this alone.
Best Wishes Always,
Alex
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Last chemo was 8/20. Hair is coming back, but doesn't show well in photos. We dressed up as Lurch and Uncle Fester for Halloween! Laughter is the best medicine!
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Last chemo 10/06 - Rads next week. Chemo is do-able. Hang in there! Hair on head feels like I haven't shaved my legs in two weeks. Gained 15 lbs on chemo! Now hoping to loose it. You can live off icecream!
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Hello girls .. Do you have living with vision problems after chemotherapy .. Ophthalmologist said there is no problem in my eyes.
But I can not identify a fad .. You also have something like that ..
hug and kiss
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Last Chemo was October 20th and my MRI showed "no residual abnormalities" YAY!! Lumpectomy tomorrow with SNB, ready to get it over with! Both girls get a slight reduction and a lift! PS said not enough to change cup size, but they will be higher and perky! Rads start dec 15th, don't know yet how many but I'm assuming 30. So far, I haven't been impressed with this weight loss program, but that's ok. I'm just great full that I've only vomited once in 4 months
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OMG Theycallme what a GREAT Halloween costume!!!! I agree, laughter is the best medicine!!! Thanks for the laugh! BTW< I was laughing when I saw the original Lurch and Uncle Fester and then when I scrolled down it was a guffaw!
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I feel Great! have had 2 sx lumpectomy and then re excision to get better margins. 2nd surgery was successful! (10/28) Saw the oncologist on Friday at 5 Never will I have another Friday afternoon appointment RUINED my weekend! Although the surgeon told me no more Chemo just some radiation the oncologist is suggesting 12 rounds of Taxol because there was trace amounts of cancer in one lymph node....SO PISSED! Of course Ill do what ever I need to but really!~ UGh! I am going for a second opinion just because that will make me feel better about doing more. I initially did 4 rounds of neoadjuvant AC chemo...YUCK! Oh well whatever it takes! Hugs
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Hello all! It's been a few months, but just checking in at the end of chemo. Last is tomorrow, I keep trying to talk myself out of it due to mild neuropathy and diarrhea, but going to get my bloodwork done anyway...taxol has been easier in some ways and harder in others. Theycallme I LOVE YOUR COSTUME!!! Thank you for posting. That was one of my costume ideas as well, since I'm rocking that same look (yes December you can live on ice cream -and donuts, I've gained 30 lbs!!) but I confess vanity and the chance to wear a wig without pity looks got the better of me so I was a princess instead (lol) my BMX surgery is scheduled for 12/14. Happy Thanksgiving everyone! Keep smiling/crying or doing WHATEVER makes you feel good! Xoxo
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Hey ladies its been awhile but I had to share that my pathology report came back after mastectomy and no signs of cancer left
Complete response to treatment. Since I have IBC I have to do radiation once I recover but I am happy all the crappy Chemo side effects and pain were worth it !! Sending you all happy and healthy healing vibes, Stay Strong ladies ! Keep posting because I know we all like reading the updates.
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Hey Ladies! It has been a year since we all started chemo. Since this board has been quiet, I hope that means that everyone's life has moved on and that your focus is on something besides cancer. I've grown accustomed to my new gray look!
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Steph you look great! I'm hoping that you're right, everyone's moved on from this roller coaster. I have as much as I can, still a little haunted by it all. Trying very much to grow my hair back, I look a bit like a mop. So far my cancer is not coming back, so I don't mind the bad hairdo so much. Take care my friend!
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Yesterday, I graduated to yearly mammograms!! As you all well know, this journey is difficult and terrifying, but we got thru it! Still have some lung issues caused by radiation but hoping it will eventually resolve too. Hugs to all my sisters💕
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