Starting Chemo in June 2005
Comments
-
Hi NoSurrender & the other wonderful ladies here ~
I, too, am a July poster, but i drop in occasionally to see what I can learn. I was wondering if anyone here has had an Oncotype DX test done on their tissue? It was also presented at the May ANSO conference and is supposed to help determine the recurrence rate by looking at the genetics of the cancer itself. I think it is specifically for patients with Stage I/II and node negative. I'm stage I, node neg, but i'm er/pr + and my cancer had a high mib rate (fast growing) so for me, my onc is using the results to see if i will need one of the taxanes after my first 4 ac's. I'd love to meet someone else who is familiar with the test.
Best wishes to you all & hugs all around!!
Wendy -
NoSurrender
Its wednesday here, we are about 12-16 hours ahead of you depending on which side of the countries.
"Fi- I have heard the expression that triple negative girls don't need taxol. Which means they are ER/PR -, Her2/nue-, and node negative."
I am all of those things
"Many docs are hitting girls with the full monty nodes or no nodes. Personally, I think it is overkill unless your cancer was so aggressive they believed they needed the extra boost Taxol can give you."
Again, that's me unfortunately aggressive (and invasive), but I now don't understand how taxol is giving any boost
IT was definitely the hormone side of it the doctors mentioned yesterday though, I remember laughing to myself about it cause it comes down to that bloody implant issue I've mentioned before as I don't have my ovaries.
I do remember very early on being told that there were "very little treatments open to me as I had one of the less common variations/combinations", perhaps its as simple as something's better than nothing, so lets give the taxol a whirl.
ps ladies, I still count my blessings every day that my skin over the lump got itchy when it did (believe it was the skin stretching too fast similar to pregnancy tummy itch if that makes sense), this trip could have been so much worse, I am lucky in so many ways, that's what keeps me smiling.
Fi -
Good Morning Ladies,
Just checking in and reading all the post. Hope all that has been at bottom of sea is swimming back up . This is the day before my next treatment of Taxotere. I think JoMac, your treatment is today and I sure hope everything goes well for you. After tomorrow I will have two more to go and then I pray, no more chemo.We keep on going down the road of our treatments and the miles sure do seem long sometime, but we are marking off those miles.
Anyone that is having treatment this week, the best to you and those of you that is off treatment this week, I hope it is a wonderful week. Maureen -
Hi Wendy-- Re: Oncotype
I've copied in a link from another board I visit-- youngsurvival.org-- an advocacy group for young women with bc. Some of the posters had an active discussion about the Oncotype assay test-- a couple of the women are research scientists, and I thought the info was helpful.
Good luck.
http://www.youngsurvival.org/?fuse=discussion.board.read&forum=24&id=6794 -
I'm freaking out! I have a lump under my arm that my onc says is a lymph node, he's not too worried and says see the surgeon in a couple of weeks if it's still there. But I'm going in to see her tomorrow to get it checked. I can't deal with more cancer, and how could it be more cancer while I'm in chemo? I'm so worried I'm making myself sick, but I know I shouldn't waste energy on worrying in advance. But how can I not? It makes it so hard to be motivated to anything productive, I'm just worried and depressed. Somebody tell me a joke!
-
Oh Brenda.... I'm so bad at jokes! Really... I can never remember them! I'm sending you lots of warm fuzzies and hugs, though! I pray that everything is ok. Please keep us posted!
-
NS and Fi - I have to have taxotere ONLY because I had very minimal node involvement. I was ER/PR+++, Her-, midline aggressiveness, clear SNB. Thought I'd only have to have A/C. But on more sensitive biopsy 2 of 4 nodes showed what my doctor called "micro-involvement". And that was enough to warrant taxotere. For whatever that's worth.
KimBe and Reeny and anyone else getting treatment tomorrow - good luck!
Candle - I'm so sorry about your bone mets.
Fi - I love your attitude!
Brenda - I'm sorry about your swollen lymph node. I'm sure your onc is right and it's nothing, but much better to have it checked out. As for a joke - I can't think of one. But how about a little self-deprecating humor?? I've started calling myself "WP", which stands for "Winking Pirate". You know those men who's torso's look like a face - their nipples are the eyes, their belly button is the mouth, they paint on a nose, etc.? Well, when I get out of the shower I see a winking pirate. I have one open, albeit droopy eye, one eye shut in a wink, a small sword slash over the open eye (my port site), and a small mouth issuing what I'm sure is an "Argh". Oh! I almost forgot. This winking pirate has lost his goatee!! -
Hi everyone this is Pam have not had anything to say but have been reading. To the Taxotere and working question...I had my third Taxotere last week. I don't have any pre-meds other than steriods and I really think I could have worked full time. Days 4-5 I am very achy and have taken a darvacet a couple of times when tylenol did not cover it. I hope you will be able to work and do fine.
I am so glad alot of you got the mouth wash I talked about I love it! (mine is swish and swollow to cover the sores in my esophogus too.)
I have two questions...I will get one more Taxotere and then start the FAC. Is it that much worse than the Taxotere? I have had no nausea or vomiting at all. What about FAC?
I have gained 20 pounds...has anyone else gained a bunch of weight? Is this normal?
Pam -
Hey Junesters,
I'll be doing AC #3 tomorrow as my WBC was good this time. Yippee.
Brenda, I'm so sorry you have to worry about this. It probably is nothing, but we worry about everything now.
I'm still having a consistent pain sort of under my ribs and back area. I saw a substitute onc yesterday as mine was on vacation. He was such a dufus. When i told him i was not having too much trouble with AC, he asked the nurse if they were diluting the chemo meds. I guess he thought this was funny. Then he looked at my bald head, and said, well, since you lost your hair, i guess we're giving you the right stuff.
I told him about my pain and he did a physical exam and then went into the corner to mumble something into his recorder. What does that mean? He never said anyting to me about it.
Pam, did you get my email? I'll be in your neck of the woods on Thursday 8/11 (tomorrow) if you wanted to do lunch.
Wishing everyone well. -
Wendy- hey girl!
I wish I could have that test! I can't because I am ER-. But you CAN GET IT if you are ER+ and STAGE 1. AND the reviews are in and they are GOOD. It seems this test is a good prognosticator. I say go for it- fight for it if you have to!
Darling Fi- I rang all the bells breaking the aggressiveness scale and my tumor was heading for the chest wall. I am ER-, Her-2/Nue- and node negative. I did not get taxol but I did my chemo three years ago. NOW they would most likely give me Taxol. Way back then (!) they only gave it to node positive women.
Taxol is a member of the taxane family of drugs. It is a chemotherapuetic agent. It is not a hormonal. If you ARE er+ you have a wonderful menu to select from. IF YOU ARE ER- then your doc would say:"very little treatments open to me as I had one of the less common variations/combinations" because they aren't working as hard as they should on ER- treatments.
Taxol is a different kind of drug. A/C works in two ways to kill cancer cells in their various stages of development and taxol works yet in a THIRD way to kill off the buggers. THAT is the boost- you are offered another weapon in your arsenal.
Pam, I gained 18 pounds with chemo. BC is one of the cancers you actually GAIN weight from. It is so not fair! BUT it is also easy to lose when you are all done.
FAC is 5-fu plus a/c... that is a strong combo but not an unmanagable one. You should do alright if you keep your stomach full at all times and drink your water and take your meds religiously.
Brenda Sweetie-
Even people with cancer can get lumps that are nothing! I know I am one of them. I had a huge lump in my breast DURING chemo that they took out. Turned out to be a 'misplaced lymph node" - I think it was a nosy lymph node that wanted to see just what in hell was going on down in my boob. It had seen a lot of action lately and the curiousity was killing it!
You could have a touch of lymphedema if it is in your affected side. Or aback up of fluids in the lymph node because they don't know which way to go any more. It could also be an infection since you have no immunity and it could be an ingrown hair!
If your doctors aren't panicking then that should be a real comfort. It is when they say "OMG! HOW LONG HAS THIS BEEN HERE!!! CALL 911!!!" that you may start to wonder if you should be worried.
Don't have any jokes but a friend has recently taught me new ways to type the things we talk about here:
If I was talking about breasts I could just write :
(o) or BIG ONES ( O ). BUT(t) it gets better:
did you know this is the international symbol for a butt?
(_!_) and a BIG one is (____!_____)?
So we have ( o ) ( o ) and (__!__)
And in case you are a pirate I guess it would be
( o ) ( ~ )????
Did I mention a MAN thought these up?
Did I have to????? -
Watson,
I had those pains from my surgery. All the nerves that got severed.
I also got arthritis from the chemo. So all that combined made me really achey.
Your onc was being Joe Cool talking into his watch like a secret service agent. Docs are really so weird aren't they? He couldn't just make a note in your chart that said- Pain in shoulder? - no he has to use his new toy.
Ignore that man behind the curtain and wait for the real onc to come back! -
NS,
I AM ignoring him. It wasn't worth my energy to ask him any questions. Just a goober all around. HE asked me if I needed any med refills. I said, well, I am running low on ambien. He told me to take benadryl, it was cheaper, then walked out the door and that was the last I saw of him!
I physically laughed when he left. If I decide to get more ambien, I'll just wait and ask my onc. However, one of my friends is a pharmacist and she's always told me to take Benadryl. (but not because it was cheaper! lol)
Thanks for the encouragement! -
Brenda...hate to see you worrying so much. It's not fun when anything new or different happens with our bodies and it's natural to panic. I really think that because the onc is so relaxed about it that it will turn out to be one of those I WORRIED FOR NOTHING deals. I hope you calm down a bit...otherwise, get some XANAX...it works wonders!
Hugs & Love,
Liz -
Hey gang,
I don't know if any of you do meditation or stress reduction techniques, I know I haven't been. So, just in case you are interested, I wanted to share an exercise I learned at a meditation class last night. I found it to be a nice relaxation. Stand with feet shoulder width apart, arms at your side. VERY SLOWLY begin to lift your arms out to the side...take as long as you like.
When your arms are straight up, hold your hands together and VERY SLOWLY bend forward as if you are diving into the water (do NOT think about the murky ocean, ladies. We've been there too many times. Think about a nice, cool, bubbly, refreshing mountain stream with the breeze gently blowing across your bald noggin...)
When you have reached as far forward as you can (like trying to touch your toes), take a deep breath and then kind of force it out. Do this 3 times, then SLOWLY come back up, still holding your hands together, to the starting position with arms over your head. When you reach the top, kind of bend back a bit and do the breaths 3 more times.
Repeat the bending/standing sequence 3 times, then VERY SLOWLY lower your arms back down to your sides. Feel aware of your body sensations at this time. Gently return yourself to what ever activity you are going to do next.
Another meditation we did was to sit with eyes closed, and then focus on the sensation of having thumbs (sounds weird, but go with it). Then focus also on having pointer fingers. After a minute, focus on the space between your pointer fingers and your thumbs. Imagine the space becoming mist or fog. Continue to focus as long as you like. It may sound funny, but it really helps you clear your mind because of what you are focusing on!
I felt so relaxed and so good after this class. It showed me how much I had been neglecting my mental health these past two months. I hope you all will try these things just once, OK??? You just might find something that helps, even for a couple of minutes. And sometimes that's enough! -
Brenda...just sent you a PM!
Liz -
LizFL - my B-day is Jan 16th.
Jenster- I will NEVER forget the winking pirate. I am headed for that look myself and thank you for giving me something to laugh at.
Nancy - I am going to try those relaxation exercises, Thanks.
Pam - Had my first of 4 treatments of FAC. Monday and tuesday weren't too bad, but today it has kicked my behind. I have nausea that reminds me of morning sickness. I haven't felt that in 24 years!!! Hopefully it won't last more than a day or two. No pain, just been sleepy all day. Good luck to you.
Take care all. -
ooookkkkk now I get it
what you are saying is that the radiotherapy doctor knows not what they are talking about when it comes to chemo drugs.
Thank you one and all for the input, I've really appreciated it.
Today I'm taking up Nancy's suggestion and heading to my favourite beach to meditate for a while, and let all my cares be picked up by the breeze and carried off into the ocean. Perhaps the mermaids will pulverise them for me with their tails?
Brenda,
post op I had a lump come up 3cms above my wound that felt way to much like the original cancer lump. My docs were so nice when they saw how much it was freaking me out and said even though they thought it was ok (I also had a hematoma) if I liked I could have an ultrasound to be sure, which I did, it was the best piece of mind, (it was an attention seeking lymph node with no irregularities other than being rather swollen) perhaps that's an option for you, the ultrasound? Hope it goes well.
Best wishes to you all
Fi -
Good luck to everyone who has had treatment this week or is due to have treatment. The "on" weeks are always rough in one way or another. Just think about how we "snowflakes" are leaving all these dead cancer cells in our wakes. Combined, we are probably killing quite a large number of them YES!!!!!!!!!
Minerva...it is hard for us Capricorns not to be able to plan everything way in advance! Drives you nuts, doesn't it!
Liz -
Once again I can't remember who posted what, but thanks for the info on taxotere. I have written down my questions for tomorrow so hopefully I will have some "pearls of wisdom" tomorrow night (I'm a Pisces but don't think I fit the saying of being wishy-washy). I admit I did not feel well at all for 9 days after my last treatment and was scared to have my blood drawn today but didn't get a phone call which I told the office initially only to call if it was bad news. Which part of chemo did you gain weight in-I have lost about 20 pounds primarily because everything tastes like burnt marshmallows and I don't eat very much at once, so I have high hopes that after tomorrow and my last AC that I can improve my appetite (know I am going to get the increase your calories lecture tomorrow). My main problem is I had gained 20 pounds the past 15 years and for me my weight was too high. I have never been so "stressed" in my life, and over small things so can relate to those of you that are worried-go with your "gut" is about all that I can say---the other thing is that when I think of NS's snowflakes it seems to relax me. Which I did try the relaxation techniques-had to keep coming back to read the instructions so will have to remedial relax there, but the second worked well!
KimB -
Being on Taxol has improved my appetite because of the steriods. I am continuing to take steriods now for the rash that developed last time.
It is strange I felt lousy the day before and of treatment but my blood counts were better than ever before. I don't even have to have a neulasta shot this time.
In the course of my itching last week I also found a lump where my lump had been. I had been avoiding that area as if it was toxic. Anyway I have had two Dr.s palpitate it now and they both agree it is regular scar tissue.
I have to get over the feeling that my breasts are loaded weapons.......
Feeling that lump again brought it all back in a rush of fear and anxiety.
I am on so many drugs now I know that my reaction was not completely my fault but somehow I have to keep feeling the breast and come to terms with them as part of my body again rather than "something other than me".
So I had Taxol number 6 yesterday. it was the best treatment I have had so far. No suprises and I slept through most of it.
I know the aches and pains will come but I feel prepared and for the first time feel like I can and will make it through the two more treatments I need to receive.
Hopefully the itching will be less this time. At least I know I will speak up sooner and more vigorously if it returns.
I keep wondering what Dana Reeves is doing and thinking about today. Does she have her hair? Has she started Chemo?
I have spend so much time obessing about my stage of BC and hearing her news made me throw my hands up in the air and say "O.k.no more!" What ever will be will be. I can't try to micro mangage the the risk factors. I know I never really thought I could but I pretended it was so. -
We're all so emotionally strung out! Fi, I am going back to the breast center today, and my guess is that they will US this lump. It is just above my axillary incision. I just want an answer. Thanks to all of you for your kind, calming words.
I ahd first Taxol on Monday, and I guess for me it's worse than AC, but I was worried more. I just didn't have much nausea with AC. But the taxol pains were quite uncomfortable last night. Just couldn't keep my legs still because of the pain and tingling. I took 4 Advil at bedtime, though, and managed to sleep half the night, then took 4 more and made it through. Today is much better. Who else has started Taxol? I haven't heard too many comments about how it's affecting everyone.
Brenda -
BRenda,
I am sure you will be getting good news today. Let us know as soon as you can.
We will be thinking of you. -
It was a seroma!!!!!! I went in and told the surgeon that the onc. thought it was a lymph node, and she felt it and said, "I think he's right. Let me talk to him and see if he wants me to take it out, or if he wants to change your treatment..." I'm thinking, oh, my god, the AC hasn't been working. She came back in and said she would put a needle in it to see if there was any fluid, and if not, she would send it off for biopsy. She stuck the needle in and she immediately looked so relieved! She said, "It's fluid, we'll send off a slide, but it'll be benign." I could tell she was really concerned, because both of them thought it was a swollen node. I am so relieved!!!!! I felt like my legs were jello, I could barely stand after she had finished. And, I was exhausted from Monday's chemo anyway. Greg went in with me, and even he said he was surprised at how relieved she looked when it was fluid. I'm gonna LIVE!
-
Hello all. Just wanted to ask if anyone has a suggestion on getting rid of the awful taste in your mouth. And I need to make a correction from my last post. I stated that I had my first FAC but I was in error it is FEC. Anyone else taken this type of chemo?
Thanks -
Oh Brenda,
HOORAY, HOORAY , HOORAY!That is the best news ever.
Enjoy your evening of not having to worry. -
Minerva, I know a lot of women get it. I asked my onc, and he says it's the standard at MD Andersen, so it's good stuff!
-
Brenda...great news!!!!!!!!!!!!!! So glad it turned out to be something minor...I think we all worried a bit in spite of telling you not to worry!
Hugs,
Liz -
Brenda - I am so happy for you. It is wonderful to have positive news.
I have been nauseated for two days and just wondered if anyone knows how long this will last. When I took the Taxol, I had it in a 12 week cycle (low dose) and didn't have the nausea.
Thanks for the input. -
Yea, Brenda!!!
-
Yippee Skippee Brenda! No more jello legs!
Minerva, are you talking about the gross metal taste? It helps me to use plastic silverware.
I had AC #3 today! Am I the only one still doing AC? lol
I don't care because I only have one more of those to go then I'll join the taxotere group.
Pam and I had a lovely lunch today before my chemo. Don't worry, we didn't talk about you guys.
Later!
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