Starting Chemo Feb 2010?
Comments
-
ugh, I feel like crap STILL! I guess getting through the first 4 AC treatments with hardly a problem really spoiled me. Day 6 and I ache from head to toe...mouth is still a little raw (and the mouthwash is nasty!)...and now I'm having some intestinal issues that must somehow be related.
I'm so bored at home with hardly anything to keep my mind off of it-but so glad I don't have to work right now. I can't imagine having to do anything physically taxing. I've been struggling to keep the laundry done and kids fed.
I was looking around the forums and found one for Taxotere and permanent hair loss...wish I hadn't! Some study/report that approximately 6% of women had permanent hair loss...oh please let me be in the remaining 94%!
-
Fantastic news, faithfulc! So happy you're through with the chemo!
I'm so sorry you feel bad, burley. I get my first round of AC (with Avastin, too) on Tuesday.
-
Faithfulc, the little smiling guy with the sunglasses looks really good next to your name! Congratulations to you, Leta, Lindee, Mo, and everyone else who finished over the past couple of weeks!
I hope those feeling crappy start to feel better soon. Looking forward to the day when everyone here can say they're finished with chemo!
Cindy
-
vmarie thanks for the advice on emend, I requested it today and will ge that instead of compazine for my #5 tomorrow. It's a bit of a weight off my mind... not that I'm looking forward to treatment, but not dreading it as bad now. After tomorrow, one more to go! Yay!
-
Swiftbird-Emend is a miracle drug!! I was able to exercise, work and eat the day after my treatment! So glad to hear you are getting it!
-
Swiftbird-also, i had to call 4 different pharmacies to find one that had it in stock.
-
Congratulations faithfulc! I'm right behind you. I have my last TC on the 27th. Was suppose to be the 25th but the doc will be out of town. I hope to have recon in August, if all goes well.
Hope yall have a great day!
-
Faithfulc, you can put the little guy with the shade next to mine. I had my last round of Taxol on May 11th. The SEs of this last round have been more escalated than the previous rounds'. The Neulasta shot compounded the joint pain. I am so excited that this part of the journey is now over. Next trip - Five or more years of Femara!
Ladies, hang in there. It doesn't matter how hard it may seem now, it will all be over soon.
Hugs to all!
Marie
-
burley--hope you are feeling better now. when do you start the taxotere (?) ?..
my pain is finally letting up--think we will head to the casino tomorrow...feel the need to do something fun. it will be odd driving somewhere other than the clinic.........
anyone out there on taxol having mood swings??? the last few days i have just felt so weepy. ick. really hate feeling like something else is controlling my moods.
-
grdnslve-I started the Taxotere last Thursday. It's apparently what is making me feel like crap! I have every side effect listed-whoo hoo.
I told myself I would feel better today, and I do slightly-the bone/muscle pain is much worse at night, but right now I feel o.k. Although another mouth sore popped up, so I can't chew on one side of my mouth. I've lost 3 pounds since last Thursday from not eating very much.
I am apparently in mood swing mode because American Idol got me bawling last night...LOL
-
burley--my mistake--thought you had your last a/c & that was what was giving you problems. the ac gave me much worse side effects than the taxol is except for the pain from the neulasta..well, so far--knock wood. i am doing radiation too, and am on a 3 week cycle until i finish radiation. then will be doing 6 more treatments-weekly. ugh.. this does end, right? it is marked on the calender, but just feels like it will be going on & on & on.....
-
vmarie, thanks again on emend tip. i had heard of it before but was seeing how i'd do with the standard compazine/ativan mix, which was okay but so-far, one day out, doesn't hold a candle to emend. We'll see how next 4 days go. No problem getting it; I got to clinic pharmacy. Mayo has everyhing!
burley, sorry to here ab SEs. I'm on carbo and taxotere. I don't know which to blame for my SEs. Although I do have discoloring on my nails; I decided I'm just going to throw nail polish on them and not worry about it; I had some soreness and numbeness on fingertips and starting with some toes, but I started in on 200mg/day of B6 and 1000MG/day of glutamine and noticed a significant difference in a week. I don't even notice it now when I'm on my blackberry (the true test!) I too live in AZ so hot flashes no fun and I've noticed elevated moodiness the last week or two. I too found myself nearly bawling watching Sisterhood of Traveling Pants and definately last night during Grays Anatomy. Not usually this sensitive
Hang in there February ladies... it's coming down to the finish line. I'm counting days until my #6 -- 20 and counting! My girls are planning a celebration when I'm clear #6 in mid-June ~ dinner and SATC! Yay!
-
Congrats to all who have finished! Leta, MW943, faithfulc, ariesrottie, Leah,and anyone I've missed.... Isn't it great??!! And its so wonderful to see all those little sunglass guys next to so many names--soon we all will have a little sunglass dude!
grdnslve-I had that awful awful bone pain from my waist down after every Taxol treatment. It would hit me about 3 days later and I was in bed for like the next 3 days. It was awful, and I had rec'd Neulasta thru all 4 A/C rounds and NEVER had any bone pain. I handled the A/C better, only had nausea and vomiting the first treatment--and I took Emend for every round of chemo, so that stuff IS a wonder drug!!!
So now I am feeling OK, still with the neuropathy in my fingers and toes, and occas sharp joint aches but they seem to be decreasing. Still have the damn head cold--I can't smell a thing, or hear. But my taste is back somewhat. I am on antibiotics and have started taking Sudafed --what the hell, what's another med at this point. My sinuses feel like I'm under water, ugh. And I am constantly sniffing, I'm surprised nobody has come by and smacked me yet because its gotta be annoying to those around me.
Met with the rad onc on Monday....I start my treatments next week and I get 33 in total (5 days/week). He said that the SE's are mild compared to chemo--some fatigue, some skin irritation and redness that they will give me ointments for, and my radiated breast may become more full and firm. ( I told him no complaints there hehe, maybe I should get the other one done too). I got my markings, 3 little (permanent) tattoos, 1 on my chest that looks like a little mole or freckle (well since its kind of a blue/black color it looks like I dropped a pen down my shirt), and one on either side. Not too too noticable I guess. I had read on another discussion thread about radiation that we can't wear deodorant with aluminum (so I was checking everywhere for something that doesn't contain it --like Tom's of Maine is one) so I asked the doc about that and he looked at me like I had 3 heads, said I can wear what I want, they are going to radiate me lower, so I don't have to worry about that. Maybe its because they aren't doing any nodes. Not complaining though. I also read about not wearing a bra thru radiation and he said I can wear whatever I feel comfortable with. And I also read where some poor woman had to go have her radiation and they made her take off her head covering! Nope, I get to keep that on too....which is great since I don't see ANY hair growth...in fact, losing lashes at an alarming rate. Like all of a sudden I get this horrible pain in my eye (I wear contacts) and damn if it isnt a stray eyelash that has fallen into my eye. <sigh> Well, still haven't had to shave anywhere so I guess thats still an upside. And I am fitting into my capris and shorts from 2 summers ago woo hoo! Hoping to keep that weight off when I get to start Tamoxifen in June.
Burley...sorry you're feeling so crappy......Hope you start to feel better soon
swiftbird--I've kept my nails thru all this, even with the soreness and numbness. Its bad enough the lashes are going, I would be so upset if my nails started falling off too. Still have my acrylics on! and like you not gonna worry about it! I'm glad the vit B6 and glutamine are helping with your neuropathy at least. (don't think they are doing much for me but at least its not getting any worse).....
So many of us are almost done, hang in there!!! Take care and wishing all a SE free weekend!!!!
-
Yes, the Emend is a wonder drug! I haven't a moment's nausea since I started this crazy chemo business. Now if they can just invent a drug to protect our poor attacked intestinal systems...
I'm having my last taxotere and carboplatin on Tuesday. It's weird to both look forward to something (the end!) and dread it at the same time. My digestive system basically never recovered after round 5-- if I try to eat a normal meal, I pay for it. I'm pretty much living on Balance bars, although I just had a weak moment and had a couple of carnitas tacos for lunch. We'll see how that goes in an hour or so! But as Lindee said, at least I've lost a lot of weight.
New side effect this time-- a rash on my chest. Don't know what that's about, but luckily I had some good prescription cream (I have sensitive skin), and it's much better, although it still looks bad. And I bruise if you look at me sideways, which I guess is from the Avastin, the monoclonal antibody study drug I'm on. I keep getting that through January, so I'll be looking like a battered wife by the fall, I suspect, since I'm prone to bump into things.
-
Again, feeling slightly better than the day before...except for one damn mouth sore that's driving me crazy! I made soup for dinner last night and my daughter burned her tongue...I told her that's what my mouth feels like all the time, and she finally understood. I'll be so glad when I can actually taste food again.
Bone pain was not as bad last night, except for some shooting pains in my feet. Weird.
Kudos to you girls having to get radiation too! You're much stronger than I.
Hope everyone had a great rest of their day!
-
Had my 6th Neulasta shot today. Yeah, the last one. Today (Friday) is the beginning of a couple of slow days. In a fog. Stomach feels heavy. Bloated. But knowing that I'm done helps. Eyebrows continue to shed so the pencil is my new best friend. I think I have perhaps 10% of my brows left, or is it 5%... Oh well, doesn't make a difference if it's that much gone.
Hope everyone has a good rest tonight.
-
faithfulc and all February sisters! Congratulations to all who are finished with chemo and keeping the Feb. sisters who are still in treament (radiation or chemo or AI pills) in my daily prayers. Yahoo! It is a big effort but we are doing it with help from each other.
-
Hi Ladies,
It has been a long time since I posted, but you all have been on my mind and in my prayers.
So happy to see that so many are finished
and now you can add me to the list. I had my last chemo this past thursday. My last two chemos hit me hard, so I'm so happy that I finally had the last one, now only a few weeks and hopefully I will be feeling better.
Chemo 5 - during my steroid storm I worked in my garden and contacted poisno ivy all over my legs and arms. Yuck, it is still healing and the garden is still not done.
I now have lymphedema in my affected arm, have my first appointment with a therapist next week.
I have cyst under my affected arm that needs to be removed, will meet with the radiologist next week to see if he wants me to get it removed before or after radiation.
I believe that the cyst and the poison ivy contributed to my lymphedema - yuck.
My eyebrows and eyelashes are almost gone, I have no idea how to draw eyebrows, thankfully my wig has bangs and will hide them.
Congratulations to all my Feb sisters who are finished and almost finished, there is a light at the end of this tunnel, soon it will be blinding us with strength and health.
Hugs to all,
Grace
-
I am so impressed by the strong women on this board! Whoever coined us the weaker sex was so wrong. We rock! Even when we feel like crap we keep going, living our lives.
It's so interesting to me how different all these treatments & SE drugs are. I feel left out in the neulasta dept. since I've never had it. I had 12 taxols and have had 2 fec's. I am taking zofran for a couple of days after the iv. I talked my Dr into cutting my steroids down to 5mg! I'm so glad. I only get them iv as a premed to chemo iv, that's different too. Let's just hope all this hell is kicking this in the pants. I am so sick of the whole deal. I feel like crap today & am a little down too. Had a fever and was told to go to ER to get counts checked, fortunately I passed so they gave me a script for augmentin & are saying strep. Now my temp has been 96 for the past 3 days. Now the nausea is getting to me & the zofran constipated the heck outta me, it's always something!
Does Emend constipate ? Anyone? Maybe I will ask to change.
I have a plastics appt. this week to go over the surgical options. My onc said to ask which provides the best long term cosmetic outcome since survival is supposed to be equal.
When I look in the mirror I see some other person, I guess it's the almost non existent eyebrows, mine are blonde so you really cant see them now. I cant figure out where they went either since I never saw them go, or found them on my face etc. Same story with the lashes. Boohoo
I do still have very thin hair, which is coming out like crazy now which sucks because I only have 2 more treatments to go and I started this Feb 2. Groundhog day, how appropriate as I feel like the guy in the movie having so many treatments!
Sorry for the unload guys, I'm just at the end of my rope today. It's time to start praying for more rope.
Laura
-
I've been reading up, and am glad to hear so many have completed chemo. Sorry to hear about the LE Grace, and hope the therapist can give you some help.
My hair is actually coming back in. It's white and thin, but it's growing. I have bone pain in my hands and fingers every morning, which I guess is due to the rounds of TC. Ended up with swollen feet, too, so my PCP switched my bp med, to one with a diuretic. I'm over 1/3 done with the rads, and looking forward to having that over with. I am a pink lady now!
Sending warm wishes to all. Laura, if I had rope, I'd certainly send some your way.
-
Laura-I didn't experience any constipation with the Emend. It was truly a wonder drug! They told me I didn't have to take it for my final 4 of Taxotere, and I haven't been nauseous at all. Sorry to hear your down-but you'll be done soon! Only 2 more to go-that's terrific!
I know I only have 3 more to go, but with them spaced out 3 weeks apart, it seems like forever. My kids are just now getting out of school, and they'll be back in school before I'm done.
Feeling well enough to go to a birthday party tonight-I wish I felt good enough for a beer! I'm definitely craving one.
-
Hey ladies, just following along- we are all strong individuals and I am grateful for this place to post those highs and lows. I am on to the weekly taxol treatments. Overall they are not bad, but I was my own advocate and requested a decrease, then an increase in the weekly premeds- benadryl and some steriod. Found that some of that was totally worth the first sleepless night. Constipation and neuropathy are now SE that I can add to the list. So far the neuropathy has been short lived- a burning in my palms. Got to go to a James Taylor concert on Friday and loved it- but felt bad that I could not clap along... I do anticipate that this SE will continue to get worse according to the onc. office.
School gets out for me next week, that will make the weekly appts easier to schedule, but I worry that I will have way too much time to think being at home all day. I want to start exercising...always an end of May goal- rarely makes it past the first 2 weeks of summer. I just want to be healthy again.
I too have lost all eyebrows- mine were thin b4- I do not use a pencil- I use a flat brush and some brown powder- I think it looks less like I draw it on- maybe a bit more natural. Hair is growing back tho- encouraging. Looks like a baby's hair.
Hang tight everyone- I have 8 weeks left then will have to finish the reconstruction. Overall hoping to "be normal" sometime in Sept or Oct.
-
Hi ladies - Hope everyone has had a decent weekend. I had #3 of 4 Taxol treatments Friday. Felt ok yesterday until the bone pain started in my jawbone and around the back of my head. By dinner time, everything hurt. I made the mistake in my previous treatments by not staying ahead of the pain but this time I've been taking pain meds and I don't have the intense hip/pelvic area pain this time. Aside from being exhausted, I don't feel awful. I have been somewhat weepy the last 24 hrs and maybe I've been thinking about what an ordeal this has been and how much I've (we've) been through. It's not for the faint of heart. There is nothing nice about this disease or the treatments.
While I was at the pharmacy after my treatment, a man asked if I was being treated for bc. I said yes and he asked if I would talk to his wife. She had just had her first AC and she looked scared to death. I talked to her for a little while but how much can you cover in 10 minutes. I told her about this website and and how much infomation, support etc I've gotten from this thread alone. I will call her in a few days to check in. Poor thing, I felt so sorry for her. It sure brought back a lot of feelings.
Hang in there everyone and have a good week! Gina
-
Coming out of the fog today. I stayed away from the treadmill for 5 days and today I did one mile of walk. Feeling much better.
Hang in there, everyone!
-
Faithfulc, Grace and Maria - Congrats on finishing!!!
Burley hang in there, I be so much of what you are feeling is the Neulasta shot, that should be easier next round:)
Loosing some of my eyebrows and more lashes, hoping these are the last pieces to drop before seeing signs of growth again! Thinking I am still 3-4 weeks out before really feeling, seeing any signs of growth. Although my head has really been itching and my husband thinks that I have had growth on my head since we shaved it 17 weeks ago!!!
Next Thursday going to dinner and to see Sex and the City 2 with a group of girlfriends as a celebration that I am finished, it would have been the day for a treatment, but no more!!!! They have kept me laughing and have sent me gifts, food, flowers every week since I started. My one friend who is a nurse gave me the shot of Neulasta each week and our families would have dinner together those nights as well!
Tuesday I go to the radiologist for my markings and to schedule txs....
Hugs everyone!
Leta
-
Hi Girls......just checking in. UGH...my eyelashes are soooo falling out. Thank God for eyeliner and brow pencil. My bottom lashes are almost completely gone, and I have spaces missing on the top. I don't even want to talk about my brows. How long before they all start growing back??? I don't wear a wig, just headwraps so I can't even hide under bangs. My head is itching too, so maybe that IS the start of some hair growth, one can only hope!! Head cold is a little better, but I have lost my sense of smell. I was shopping the other day and trying to sniff Yankee Candle scents and couldn't smell a thing....went to a BBQ over the weekend and couldn't smell that either. I HOPE this is just a temporary problem from my sinus/cold/whatever I have and NOT some weird permanent SE from chemo. Has anyone else had this problem or heard of it? I can't believe how much I miss smelling things (like food, cologne, flowers, candles).....still emotionally a wreck at times too. Thank God for my Lexapro-- I cried like a baby at the finale of LOST last night, I wonder how bad I would have been without the drug lol..
Leta--good luck with the radiologist, its no big deal though, my guy is great. I am looking forward to just getting started.
I tell EVERYONE about this site, it is the best--for support, and information, and just a place to vent. I NEVER could have gotten thru this without you girls.
Good luck to all, those who have finished, those who are still undergoing chemo, and those of us starting and/or going thru radiation. Wishing all a good and SE free day!!
-
Congrats to all who have finished. What an accomplishment.
I have my last one on Friday. Like writer, I am excited for it, but also not wanting to feel the ick again. I too have been so emotional and weepy. It isn't like I am depressed, but I cry at everything. Anything really kind,sad, painful, pretty, etc. I just seem to be crying all the time. It as if my emotions are so raw and just under the surface. Me crying all the time is not something anyone is used to. So, a really different person these last few weeks.
I had an awesome weekend. My and 7 of my girlfriends went away for a girls weekend. No kids, no hubbies allowed. It was so much fun! Such a needed break. At first I was hesitant to go because I have not been sleeping very well and was worried that I may get to feeling like crap while I'm gone. But, I decided that I probably really needed a little R&R and pushed myself to go. So glad I did. So glad that I have my women friends. Felt grateful on so many levels.
Hope everyone is feeling good!
Have a great day!
V
-
lindee, it's probably the head cold that stuffed your sinus up - I hope it's gone real soon so you can smell the roses.
Sounds like quite a few more of us will be finishing up this week. We've made it this far, we can all do it! I will be gone for vacation so in the next couple of weeks update might be a bit slow.
Tomorrow morning I'm seeing my rads onc. for the first time. We'll figure something out. I know there is a separate forum thread for rads, but I've gotten so attached to this one I think I'll just come back here and post about it if you all don't mind.
Hugs!!
-
I finished my last Taxol on 5/20!!!! I am finished with chemo!!!!! I am still in a lot of pain but I am so excited. It might be my imagination but I swear I have new fuzz on my head. Thin, pointy, colorless hairs. So exciting!
I have to go for weekly bloodwork and on the 4th week I meet with the oncologist to go over my results. If all goes well then I see him for bloodwork every 3 months for 2 or 3 years.
Best of luck to everyone!
-
Hi all. I too will have my last tx this week (Thursday). I also have very few eyebrow hairs left. I look kinda funny with my left brow almost gone and my right eyelashes almost gone. The opposite eyes are thinning but can still be seen. I have to laugh when I look in the mirror. My hair is growing back slowly. It is thin, and like many others, colorless. But on the good side it seems to be getting other stubble coming in that are a little darker. Maybe it will be sugar and cinnamon like it was before I lost it.
Glad to hear so many finishing up. This journey will be over before we know it. It has been a roller coaster ride.
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