anyone starting chemo in Nov 2005
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Lat56 - good to hear from you. I am 4 weeks post chemo and so far have not had any other tests done besides the mammogram and breast ultrasound. I do have an appt with the Onc later this month and I think he said he would order a PET scan but I'm not sure. I'm trying to take this journey one step at a time.
OK ladies - I could not look at peach fuzz anymore, it had become very messy and uneven so I buzzed it! Maybe now the real hair will come out. Anyone else thinking of buzzing their fuzz?
Good night ladies, hope everyone is doing well tonight. -
LOL, buzz the fuzz. That's a new one. I still have the fuzz, doesn't bother me yet. I still wear the wig when I'm out most of the time.
Only , this past week end, I did wear just a white ball cap. I need to take a picture like that. Not to bad, wish I had eye lashes and brows
Will the fuzz fall out Odalys?
How long after chemo is over? I'm almost a month out.
(Where did the time go?)
I know I'm glad that chapter is behind me. Rads starts next week. YEAH!!!!!!
Well I need to get back to the laundry, never thought I would be so happy to be doing house work. I'm looking for things to do
Not even a dirty dish left. It is just to cool to work in the yard today. May just catch up on my scrap booking.
Hope all are doing well this week , and moving along with treatment.
(((HUGS)))
ML -
MaryLou - I read in another thread that the fuzz starts to fall out a month after the last chemo. I don't know if this is true for everyone but mine was certainly falling. Yesterday I found fuzz in my coffee...yuk!!! The last taxotere took whatever hair I had left and most of the eyelashes and eyebrows too.
Great to hear you are trying to find things to do. I too have experienced a new burst of energy and have been very productive lately both at home and at work. No more chemo fog!!!! -
I am nearing the end of chemo fog!! Last taxol + herceptin today!!! So one more hyper Wednesday, one more boohoo cranky Thursday, one more tired Fri and Sat,, and by Sunday I should be almost there and Mondays I feel great. Mostly I can't wait to have an energetic week, not have a nosebleed and taste my food again. Oh, and not have to take stool softeners anymore.
I don't know if I have fuzz, it is more downy. Like a baby's first hair coming in. Some gray up top. I tried using a colored mousse (comes out in 8-10 washes), but the color didn't take. Regardless, I can go hatless now if I wanted. But too cold and rainy. I hope the fuzz doesn't fall out.
My schedule:
4/11 thyroid u/s (fingers crossed)
Easter week- vacation in San Diego- turn me loose!!
4/24 week- ovaries and gall bladder surgery
4/30 start Arimidex
June- first Pet scan, whole body crossed
August- reconstruction (flap surgery) Stage 1
Oct/Nov- reconstruction Stage 2
New years present- nipple tatoos
I am so glad we November ladies are all finishing up chemo. Everyone done or close by the end of the month?
Fuzzy coffee- goes with all the other things you learn here, but your docs would never tell you.
Have a wonderful week everyone. I love to see posts in this thread. Hope all those side effects are easying up on you girls.
Take care and Happy Spring,
Margerie -
Margerie- Hope you are doing okay on your "boohoo, cranky" Thursday. The emotional roller coaster we endure throughout treatments. Hang in there!! Rest up & take care!
I'm exactly 3 weeks out from last chemo treatment and my fuzzy head has gotten fuzzier!! AND...I had to shave my legs today - first time in months! My eye lashes have started to grow back (hurray!) and my fuzzy eyebrows are quite comical looking!!
I have decided not to have reconstruction surgery. I had a small margin - close to the chest wall- so I am concerned about "covering it up". Has anyone else had this fear? (Even before my surgery, I said that I did not want the reconstruction done.)
Thanks to all for being supportive & inspirational with your strength & humor!
Hugs & prayers for all-
LAT56 -
Margerie - Yeah...you are done with chemo. One more sister conquers evil chemo. Congratulations! Downy??? Ah...Easter week vacation sounds wonderful. Have a great time and hang loose!
Lat56 I know what you mean about the eyebrows looking comical. A couple weeks ago son noticed my eyebrows and said Mommy, your eyebrows look like they caught on fire!
Take care ladies. -
Just a tip I 'm going to use when I get some eyebrows. Take a toothbrush and a little Vaseline and comb them. They have to be trained again.
Brush straight up, and then run the toothbrush over the top and then down to shape, this can later be done with a little hair gel too.
I really don't have anything to share tonight. I know I'm in a lot of pain. I see my Onc tomorrow morning. Sure hope he has some answers. My legs and feet hurt so bad. Did to much yesterday I guess.
I feel down today
I have stayed in bed most of today and felt sorry for myself. Only my legs think they have been standing all day. I just don't understand this at all. Can all of this pain be from the Nueropathy????? It just sucks the life out of me.
I'm sick of this journey, and really wanted to feel better by now. I have been post chemo for 4 weeks. Thought I had been through the worst.
Hope you all are feeling okay. Bless you all.
Sorry I'm in a foul mood -
Hi ladies, I just wanted to check in-I know I haven't been around for a few days. Just know I have thought about you all way more than I have paid attention to the stuff we were doing! TAXES! Ick. My hubby wanted us to file an extension. I said NO WAY!
Anyway, I am still praying that I finish treatment in the end of this month. I won't believe I am done until they unhook me from the chemo drip and say the magic words, "You're Done!"
Anyone do anything special for their chemo nurses? I got them pencils that say CANCER SUCKS, because I wear my shirt to every treatment and blood draw and they all just love that. I wanted to do something else for them, too. They have been great.
I am heavily medicated now so I have to go to bed....I just wanted to let you all know I haven't forgotten you! I still have to catch up on all these posts, but that will be another night.
Love and prayers, Debbie -
I won't say goodbye to my chemo nurses till next January. I get my last Taxol/Herceptin next Monday but then go in once a week for the Herceptin alone (for 42 weeks!), so I guess I won't be celebrating the end of chemo like the rest of you. Sigh.
This time my Decadron high seems to be extending beyond the normal two nights. Dare I take an Ativan again tonight? I have only ever taken it two nights in a row. I'm so wound up....
Oh, Mary Lou, are you taking the vitamin B complex, the B6 and the L-Glutamine? I'm so sorry to hear you are in such pain a full month after the end of your chemo! I hope your oncologist gives you something helpful.
I look like a boy with a good quarter inch of pretty healthy looking hair on my head. Not fuzz. It's too short to be curly, but it is swirly, so I know I'm getting my curls back. I wouldn't mind straight.... It looks blondish, actually a little lighter than before I shaved it. I rub it all day long. What will I do when it's too long to rub? I love how it feels dishevelled when I first take off my fleece cap.
I have down on my face, though. Very very pale, but down all the same. Weird. Nothing anywhere else. I never had much to speak of on my legs. My eyebrows, which have always been pretty pitiful, have stayed with me through chemo. They're still as sparse as ever, but they're a little presence all the same. And I still have a few eyelashes. Funny how I have learned to like my face more through this experience. I don't feel like I absolutely need to darken my eyebrows or eyelashes anymore. I used to feel naked without a wee bit of mascara, but now I'm quite okay just with my three or four very blonde lashes. I guess my perspective has changed.
Has this past year been the strangest experience or what? I had my "bad" mammogram on May 5th last year. I'm reliving those days and everything that led up to the diagnosis. I hope I only put myself through this re-enactment once. It's not necessarily a good thing to do, but I feel I have to take myself through everything step by step.
Silly me.
Enough of this, I will take that Ativan.
I send hugs to all my sisters and hope we all find beauty and hope in the renewal around us.
Anna -
Anna, I will take a Ativan anytime I need it. I even took one the other day for the Neuropathy. I had forgotten my pain meds. It did relax me.
Today was my month check up. I told him about the pain. He gave me another pain med, ( Lortab 5/Tylenol 500 and said to take 900mg of Neurontin 3X's a day.
I sure hope this works better. I have been taking the B-6.
I will be taking Tamoxifen for 5 years after the rads is over. I wonder how soon I can have "NEW BOOBs" after rads. I forgot to ask That's okay, I have to have my port flushed in 2 weeks I'll find out then.
I have to see my surgeon the day before the rads starts. The Onc wants to follow up a lump. It is high on my chest. I felt it getting bigger. No way scar tissue grows that fast. Hope it is nothing.
I won't get myself all worked up till I know for sure. I'm one of those people that just takes one day at a time. Never get to shook up over anything for long.
Just hope I get to stay away from chemo -
Debbie, good to see you. Yes, I'm going to take the nurses a cake when I go for the flushing of my port. That will be in two weeks.
Their kindness has been just wonderful. It is the least I can do. -
Mary Lou,
I am so sorry to hear of your battle with neuropathy. I wonder if the low dose weekly taxol kept me out of that vicious cycle. I feel very lucky to have had none and wish you didn't have to suffer. What a PIA and I hope it gets better really soon.
FYI I am having plastic sx consults (flap procedure) and the docs say wait 4-6 months after rads for reconstructive surgery. -
Thanks Margerie. Wow, 4 to 6 hmmmmmm, I thought I would get to start before that. Oh well. I need to find out what that lump is first. I really dread having to worry about that again. Lumps are a PIA.
I just want to get on with my life. -
Debbie, have you heard where it is? I would think it made it to the west coast by now.
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Hello all. I sent a message earlier (or tried to) but I don't think it took. Anyway, I found a lot more messages from you than when I originally logged in. Weird but wonderful.
I have a vision of all of our heads looking like Easter chicks. Anna, sounds like you have the most. I'm waiting for rads when I am not traveling and have 7 weeks for it to go crazy. I have about 4 long eyelashes and others--I'm not sure if they are new or old. Anna, I love what you said about learning to love your face. I too have really connected with my 2000 parts and feel very tender about my scars and dings.
Hope you all have a wonderful weekend.
Nancy -
I feel for you and the neuropathy. I'm 7 1/2 weeks out from dose dense A/C and Taxol. The pain wakes me at night and I have to lay down at work. This week my oncologist gave me lyrica for the pain and numbness. I think it may be starting to work. My right ring finger and pinky are getting feeling back and I have slept for 2 nights. Good luck.
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Mary Lou, I am sorry you are in so much pain. I hope the new meds will help. When are you going to know answers regarding the lump they are following?
Debbie, good to see you. I've been pretty sparce myself. I haven't seen the package yet. Anxiously waiting.
Margerie, I am so happy to see you have finished chemo treatment. Yahoo!!! I won't be joining the rest of my sisters finishing up chemo this month. That makes me very sad, but with mets who knows how long before dr's figure out what chemo is working and controlling the mets.
Being on the Xeloda, my hair is sort of coming back on my head. (nowhere else) It is coming in some grey and then I have dark patches all over. It is weird. My son (9 years old)asked me when is my hair going to come back to the old way I don't want to see you bald anymore. Oh that made me so sad. I asked him if he wanted me to wear my wig and he said no I just want your old hair back.
Kim -
Hi ladies, I am still way behind on all the posts, and I am totally not going to be able to catch up on them tonight. I had treatment on Thursday, and the fatigue has really set in.
Anyway, Mary Lou-what is the latest on the lump?!?!? Man, this is a sucky disease. Let us know as soon as you can-I worry about you guys like you are my real-life sisters.
I love what you guys are saying about loving your 2000 body parts, etc. It is so true that we need to embrace our new selves. I still cringe when I look in the mirror, but am growing tired of that. I am trying to find happiness when I look at myself, like I should be estatic that I lost all the baby weight I gained when pregnant (just not under pleasant circumstances). I am wearing clothes I haven't worn since our honeymoon! Not that is was that long ago, our anniversary is on April 13th (married 3 whole years!). I know most of you have been married way longer, and I applaud that!
Anyway, I am going to take my drugs and drift off to a pleasant slumber.
By the way, I haven't heard anything about the ribbon exchange....anyone? anyone? I am anxiously awaiting it!
Love and prayers, Debbie -
It's all up and down, isn't it? My husband is off visiting his daughter for the weekend and working through some issues with her; it's nice to have some quiet time to regroup. I go in on Monday for Taxol/Herceptin #12 of 12, after that it's the weekly Herceptin alone. The nurses tell me it will take 30 or so minutes each time and that I won't get any pre-meds after Monday. It's weird, I'm scared of this change in routine. It was getting so I knew what to expect, now everything will change.
These days I am trying to learn not to worry about every little dull pain or twinge I feel. After all, I had twinges and pains before breast cancer, right? I didn't think the worst then, why do I imagine horrors now? I've been having dull pains on my right side, where I think my appendix might be, or maybe an ovary. I'll bring it to the oncologist's attention, then let go.
I still absolutely love my dishevelled crewcut, I can't keep my hands off my head!
To all my sisters, I hope you have a peaceful Sunday full of love, calm, healing and no pain.
Anna -
Girls, I will see the surgeon about the lump this Tuesday. I'll be sure and let you all know. I'm nervous, didn't sleep well last night. I'm taking an Ativan tonight for sure.
Liz, that was so sweet that your son wants your hair back. And My prayers are with you all this week.
Debbie, hope you feel better and find our exchange.
Anna, enjoy your "ME" time. It is priceless.
Nancy, hope you are doing okay. -
Hi Ladies -
I haven't posted recently, but have been keeping up with all your posts and keeping you all in my thoughts and prayers!
I've just signed up for the Boston Breast Cancer 3-Day to be held in August! I finished 8 dose dense chemos on 3/22 and will start radiation this month.
Thought if anyone else is signed up for a 3-day somewhere, we might be able to offer moral support, training tips/encouragement, fundraising tips, etc.
Chins up!
Lana -
Hi ladies, hope everyone is pain free and feeling well tonight.
Just want to let you know I started RADS today (1 down and 29 more to go) and it is so much easier than chemo. I was very nervous before the treatment but it turned out to be similiar to having a scan taken. There is no pain, no needles, no pre-meds, no nausea, no Decadron high, and best of all no chemo fog! Thank God!
You are all in my thoughts and prayers. Please hang in there and take care of yourself.
Love and hugs... -
Mary Lou, LOVE the website! Very cool idea!
I feel pretty decent tonight....I plan on going out tomorrow and getting Daniel's Easter stuff tomorrow. We didn't do anything for him last year (too young!), but I think Mommy (Easter Bunny) will be going a little nutso this year.
Love and prayers, Debbie -
Hi Deb,
I was looking for you because I hadn't seen you post for a few days.. and noticed some concern about the Ribbon Exchange. Glad to hear you are feeling a bit better.
I seem to remember, a couple of weeks back that someone HAD received it, but was leaving on vacation. I can't recall who it was, but she did mention that she probably wouldn't have time to get it back out until she got back.
I'll let you know if it comes this way as soon as it arrives. (West coast)
Meanwhile, take care of yourself, and enjoy Easter with your son. They are soooooo much fun when they are little, then they grow up!!!! Dang it!!
Love and prayers for you,
Carol -
Hi Carol and everyone else,
I just saw a post on the original invitation I posted, and yes, Peggie went to Florida and said her son did not send it out for her like she wanted. She felt badly, and said it is on it's way. YAY!!
Ugh...I'm joining the neuropathy club....feeling it in my toes, bottom of right foot, and right index finger.
Time for bed! Love and prayers, Debbie -
Well girls, I went to the surgeon yesterday to have the lump checked. He is doing a lumpectomy tomorrow morning 6:30.
I have to tell you I'm a nervous wreck. I have a strong faith. And I know it is all in Gods hands.
But I also have gut feelings that I'm usually very good at, and this just feels bad. What do I do, I really don't know what to do if its cancer again.
I didn't get to start my rads , so now I feel like I'm back to step one.
I'm so down, and just want to lay around and feel sorry for myself, but feel if it is cancer, I should make the best of today.
And it is a full moon, wow, I feel like I'm on a roller coaster of emotions. -
Oh Mary
I am so sorry
you have to go through this
Hoping and praying for B9
results for you
xoxo
Patti -
Mary Lou, if you had a beeper on you that beeped every time I think of you right now it would drive you absolutely crazy. I am praying and praying and won't stop till you tell me everything is just fine. That's what I am praying for. Stay positive and picture yourself healthy and strong.
Love, Anna -
Mary Lou,
So sorry to hear you have to go thru this. Not fair!! Well, none of this is to any of us
I am routing for b9 and that you get your groove back soon. My little friend Justine is in the mail heading your way.
Take care and big hug,
Margerie -
And I just got the results of my thyroid ultrasound. Trouble. Swollen nodules, some cacifications. Consult for possible biopsy with an ENT on April 26th. It could be benign disease or not. Fun!
BTW, when getting my rads records for my reconstruction consult I read the CT scan taken for rads set up. They saw some calcifications in thyroid and they had recommended f/u. Rad onc might have rememebered on his own, but I am so glad I saw it and asked for f/u.
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