April 2015 Chemo Crew... Starting in April? Please join us!
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I'm so happy for all of you that are finishing up! I don't mean to be a Debbie downer here but I'm feeling depressed I seem to be having more issues than I would like I do feel lucky I know it can be worse but I have to recieve taxotere over 3 hours instead of 1 and recieve 20mg of steroids and 75 mg of Benadryl just to get it into me because of reactions I'm her 2 positive which has come such a long way I'm so thankful for herceptin and perjeta but a lady sitting next to me at chemo was her2 pos back a 2 time 3 years later and then another lady next her was stage 4. I'm 30 it's not fair I feel like this is going to come back and then Of course I read some studies done saying if you had a baby 5 years or less after being diagnosed with breast cancer your chances for it to spread are 3 times more likely why I feel like everything is against me..When all this was happening at my chemo session my dr is MIA where was she why should they be consultingwith the PA on what to do I don't even see my dr anymore my appts are with PA and she couldn't answer several of my questions I am going to call and demand to see my dr next appoinent sorry for the rant I'm doped up on tons of steroids
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good morning ladies I hope everyone is feeling well decent at least. Today is date night for the hubby and I. Going to try my wig today out in public to:) I'm just wondering how many of you has less yucky feeling with their taxol treatments? My MO told me most people do better on it- but I want to actually hear some ladies stories myself. Does the fatigue usually build up over time? And about the nails- do they get worse over time? Is that usually the drug that causes eyebrow and eyelash loss? If so can some ladies recommend some awesome eyebrow products? Is it sad that I'm more worried about my eyebrows than my hair?! I just worked so hard to get these brows looking awesome and now I'm going to lose them?! Anyway I hope everyone has an awesome day with minimal SE
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Stephmoen....HUGS and MORE HUGS. I feel so so much for you and that is a lot of shit to put up with. now you get that MO to respond to you; they work for you and not the other way around and they get paid a lot. We are here to help you knock this cancer out of town and it is possible!!! But your feelings are completely normal and valid. And you have been through a lot. 💞
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alliecat - hang in there. I know how hard this is and especially when you are dealing with other pressures.
Addie - beauty with that wig and without!
Ksusan - heh, heh! Love your partners response!!
Arlene - survivor you are! We have made it this far and there ain't stopping any of us bald chicks now!
littleblue - you are spirited with humour! Way to go despite all the chemo SE and pain
I am coming to accept that this will be a new normal, one where I cannot let my guard down as I move forward in treatment. I am always in awe of the people who are in stage IV and fighting cancer off. I have met so many that turned a 4 month prognosis into over 15 years of life! We got this and by the time we plow through this stage, newer treatments and technologies will make our lives longer and cancer free. The clinical trials I have been researching are promising
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Haapy Friday heading to chemo #3 of 6. Will be halfway!!! Anyone else headed to the chemo spa today?
Addie: great eyebrow pencil called It! Sold at Ulta cosmetics store and online. It is a bit pricey at $24. Love it! I happened to get in my look better cancer society makeup bag. If any of you have programs like Look Better, Feel Better sponsored by the national cancer society by you GO! Grab a friend and get your goodie bag, tips for eyebrows, lashes, how to wear wigs, caps, and more. Well worth it!
Stephmoen: that treatment from your MO and PA just awful. Make a complaint to an administrator. Stand up for yourself we are with you. You have patient rights it is a federal bill of rights. Get a copy and make a complaint. Or change your treatment center if you can't get resolution.
Happy weekend and you are all in my prayers.
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Hi Cyto_Destructo, welcome to BC.org, and welcome to this wonderful group! We're sure these ladies here will help you deal with everything that comes along with your treatment. Keep posting, and let us know how you're doing.
Hugs,
The Mods
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Cytodestructo, welcome. It sounds like maybe you are on AC and then Taxol. Many others here are on that regimen too.
Arlene, Congrats on finishing!
Stephmoen, If you cannot get in to see your MO, see if there is another there (is it a group) who you can see. You need answers and you deserve answers.
Addie, Enjoy your date night. I am on Taxol now. No more "yuk" feeling that AC brought. I am exhausted...more than before, but that may be because I have not slept well for a couple nights, or it may be the cumulative fatigue...maybe a bit of both. I have a little bone pain today, but not bad enough that I've even taken Tylenol yet. I am also on day 4. Days 3 and 4 are usually worst on this, so if this is the worst for this round, it is not bad at all. Days 1 and 2 I noticed nothing at all.
Littleblue, I was my wig in cold water with wig shampoo about every week or every 2...depending on how mu I've worn it. I was warned not to overwash it. As far as scalp care, I just use regular soap or a tiny bit of regular shampoo. When it annoys me and breaks out, I use some type of exfoliant...probably not recommended, but I hate the breakouts and it helps.
ksusan, great response by your partner!
Allicat, Karen, and sheshe, glad to see you back. I hope you all start feeling better.
Stacy Mc, Welcome to Taxol. I hope all goes well for you on it.
AJ, Congrats on finishing AC!
Andrea, Your wig looks nice!
Swissm, I haven't heard of anyone on kadcycla. Is it similar to herceptin?
Rockerwife, I hope the extra shot does the trick.
Vanmama, glad you could get your treatment in.
gkodad, ask about dose dense versus weekly...the MO should be able to go over pros and cons of each with you. usually it is just personal preference of the doc. Mine did not give me a choice.
Has anyone else had blood in their urine? My MO did a urinalysis a couple weeks back and it was clear except for the blood, but I can still tell there is some blood there. It looks like day 2 or 3 after AC because of color, but it is blood and not "A". I know it's from the Cytoxan which can cause bladder irritation...just hoping it goes away soon. I will ask MO at next appointment how long it usually lasts. It's not enough to be worrisome; I just want it to stop.
All is fine here; I just wish I had more energy. I am exhausted and need my mojo back by 0700 tomorrow morning!
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Hi, I second Renee's recommendation for the Look Good, Feel Better program. I don't think I ever posted a review of mine. I was able to find one at a local hospital - not the one where I am getting treated - for after work, it started at 5:30 PM. There were only 3 people, I think they expected more. One woman was on rads already, but she still didn't have much hair. The other one had been through 2 treatments and was with her daughter - they were so cute. She had ovarian cancer.
Anyway, I got a Clinique eyebrow pencil, it's called "instant lift". The color is perfect for me - I have very pale brows anyway, and I hardly ever wear pencil because they all look too dark to me, but I've been wearing this because I figure I'll get people used to seeing some eyebrow color so that when I have to paint them on it won't be so weird.
The program was good, we did our makeup first, and you get free make up from moisturizer to lipstick, and then we practiced scarf tieing and tried on all sorts of headwear. The presenters were awesome.
I have to say, though, that the these other two ladies were the first women that I've seen with wigs that I knew were wigs and didn't think they looked that great. The woman who was doing rads - she had her wig for a while now, and the wig presenter said it probably needed to be trimmed and styled and that she would to it. They were both longer styles. The ovarian cancer lady, her wig was new, but it came down to her shoulders, and something just looked fake. I thought of all of you - how fortunate we are - because you all are rocking the wigs - even Andrea's hot pink wig!
Lynne
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My sons class is participating in a relay for life at school today notice the left corner ❤️ Made my day a little brighter
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Stephmoen, sorry about your reaction, but I'm glad that they could continue with your Taxotere Big hugs, you are so allowed to feel down, this situation is highly stressful, and our threshold for reactions is lowered by that stress. Please come here to vent ANYTIME. Your son's poster brought tears to my eyes.
Lisa, did final shot help raise neutrophils?
Swissm2002 – how are you doing after AC#3? I had my worst day 3 and 4 after my 3rd treatment, but I think a lot of how I feel is attributed to the Neupogen shot, which you don't have. Wishing you no/lo SE
Jen – lol about them turning us into trees. I want to be a redwood! I am checking with my bald co-worker on tips, he is very cool and knows that I'm going through chemo, so I know he'll be real with me. I still have all-over fuzz, and I have been using Dove sensitive skin body wash to wash it in the shower. Wig probably needs it first wash this weekend – they told me every 14 days of wearing.
Sheila, so sorry to hear that #3 was so horrible. Mine was bad also, but no puking!
Andrea, I also developed mouth sores, really tongue sores – they are along the left side of my tongue, and it is just miserable. Now after #3, same thing – on Wednesday it started coming back, and by now, it makes eating and talking very painful. Last time, I bought some benzocaine mouth sore relief, and it does help for a while. I did everything to prevent. I started taking Lysine when they appeared last time, and I swear that helped, but I did reduce the dose once the sores were gone, I probably should have stayed with taking 3-4k mg.
AJ and Tina, good luck with your next phase of treatment!
Lorraine, I keep wanting to say bummer about your anal fissure, but then I crack myself up about the unintended pun. Sorry. No Laughing Matter. I'll probably get one now – but I'll have your good tips!
Karen, good luck at the SPA today, AC#4 – Yay! Sounds like a lot of us had our butt kicked with #3. You and I are on very close schedules because my #4 is on Monday. Then on to Taxol DD for me.
Laura! Good to see you check in, let us know how you are doing after round 3. Hopefully those shots will help. I have to look in my "knowing your blood counts" book to see what ANC is, I'm drawing a blank.
Stacy, how are you today? I hope still no SE from the Taxol. Did you have any reactions?
Allison, I was wondering where you had been, I thought you had mentioned that your children were visiting, so I figured they were keeping you busy. Don't let DH (and, in this case, it doesn't stand for "dear husband") bully you. I love the idea that you will be able to help other women who are going through this alone! That's an awesome way to look at it. Oh, and I'm not feeling like I'm doing so great with working and small (well, is 9 small?) children. I am scraping by.
Ksusan, LOL at your partner's comments.
Cyto, welcome. We love late to the party , brings a new infusion (and usually some much needed alcohol). Sorry you have to be here, and that sucks about blood clot.
Arlene, thanks for your post and picture, it's very inspiring. And, right back atcha.
Renee, good luck at #3 – Karen is also going to SPA today.
Heather, I know I saw a post from you, but now I can't find it. I was glad to see you check in. We are on similar schedule, I'm just one day ahead of you. I should see MO on Monday for the first time since I started. I'm guessing that this is so we can discuss Taxol schedule/what to expect, etc.
To everyone else, even if you haven't checked in in a while, I'm thinking of you and sending positive energy.
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Steph, the poster brought tears to my eyes too. My daughter made me a Mother's Day card, and on it, among other things, it says:
Marvelous
Outstanding
Mom, who rocks and never stops fighting.
I look at it every time I need motivation.
Lynn, ANC is absolute neutrophil counts. How have you been feeling, by the way? I also got a brow pencil from LGFB program (in 2013). I am still using it.
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I'm signed up for Look Good Feel Better on July 6th, I'm very excited to go:)
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I am feeling pretty good today, 12 days out, except for the tongue sores. It really sucks, because other than that and the fatigue, I would feel almost normal. I ended up squeezing my toe yesterday, and I had a lot of fluid come out, and now that actually feels better.
I worked at work from Tuesday - Thursday, and today I am WFH. I have to go to neurologist to have botox for my eye twitch - something that I was treating before bc. I am also busy getting my daughter's dress ready for her 8th grade semi formal.
I am dreading next week. I know I shouldn't be paying interest on money I haven't borrowed, but I felt so shitty on day 3 and 4 after #3, that I just don't want to do this again.
I'm also trying to decide if I should go on a full-time leave of absence from work. I've been taking sick time, but just applied for a partial LOA that allows me to be paid up to 8 hours a week for time off due to illness. I could go out on full-time leave and get paid at 100% for 60 days. I feel ok and like I can do my job on week #2, but then I don't have any energy for anything else. I get dinner made, and some laundry done, and that's it.
At work, I had 2 of my project re-assigned, so I'm only at 50% capacity. This week my manager mentioned giving me another assignment, and it doesn't sound too taxing either, but I'm torn - should I even take on something new? What if I feel or decide I want to take a full leave? Should I just do that now so that I don't get into a place where I have to transition even more. I'm so conflicted. I know that I could push through - I'm sure I could do whatever was required at 80% time, but it will take a toll on my family life and responsibilities.
I think I will have an answer after next week - once I meet with MO to discuss Taxol, and also how I feel after #4 will give me the information I need to decide, and hopefully I won't have gone too far down a path at work. I'd love to hear your thoughts and opinions.
Lynne
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I am pretty sure the shot is working because I've been having awful back pain since last night. When I did the four shots days 1-4 post chemo, I had no pain from the shot. Just SE from chemo. Wonder why I feel the single shot and nothing from the four in a row?I won't know how high of ANC until June 9. Last tc June 10. Appt on June 2 with RO.
Ksusan- love the comeback . That is classic !
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Lorraine! Love the looks - rocking both!
Ok, here's what my buddy Don (bald Armenian - so funny because his beard still grows like crazy, so he's totally bald on top, but has all this facial stubble), he's definitely a metro:
1. Buzz using clipper at 0, don't shave - that creates breakouts and requires more maintenance.
2. Moisturize morning and night after washing - he uses a 30 SPF moisturizer that he gets from the place he gets his facials (told you - metro :-)
3. Make sure that clipper blade is oiled weekly.
That's it.
Lynne
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Started chemotherapy April Fool's Day.... kinda funny.... would like to join this forum please.
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EmbraceHappy, welcome! Are you doing dose dense? If so, you have probably finished AC...yahoo!
Lynne, Hard decision. I like working part time because when I am home too much, all I seem to think about is cancer. Work gives me a good distraction and mental break. Working 80% may be too much. I don't remember if you are doing weekly taxol or dose dense. So far, I feel fine on the weekly, but I am definitely more tired days 3 and 4. I will let you know if that energy picks back up the other days. That being said,. I was so exhausted this morning I did not think I'd get in a run or a walk, but I just got back from an easy 5.5 miles...walked half ran half, alternating miles, and I feel better now than before I left. Maybe I just needed to get my blood moving.
Rockerwife, Is the single shot Neulasta instead of Neupogen? Neulasta is higher dose and time release so it can cause quite a bit of pain...or maybe it's just all of the build up of he toxic crud. I hope teh pain eases.
Positive spirit, you have quiet a bit of hair left! Hopefully the rest will fill in soon. Your scarf is very pretty.
Addie, Enjoy the program in July. The big bag of free make up...way better brands than I'd ever bought...was great!
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Welcome, EmbraceHappy and Cytodestructo! It sux that you have to be here, but we are awesome, no doubt about it. Very glad you found us!
Lynne- First of all, thank God for your Metro Bald guy! Yes, you can be a redwood. Tower of beauty and strength. I read that the Yew tree that give us taxol is sacred to the Celts and many NW Coast Native tribes as a powerful healing plant. How did they know?? Kind of interesting.
I never thought to oil the clipper blades, but that sounds like a really good idea. Maybe disinfect them as well. I wonder what kind of moisturizer is the best? I'm thinking unscented something with a bit of tea tree oil mixed in? Feels gross to have a wig on all the time at work LOL, but whatever.
Good to know to wash the wig ever 14 days. I have been doing it once a week. I got wig wash, but don't like the smell. Wonder if Dr. Bronners soap would work the same? I feel like its mostly the cap part that needs to be washed. Its funny, because in real life at work, i'm such a dirt ball LOL. Not much point in shampooing if you are camping for 14 days at a time or working out 2x a day and hiking in between. Now, though, I'm the biggest germophobe!
Positive Spirit, you truly live up to your screen name, and you look beautiful! Is you hair already growing back?
Steph, BIG HUGS, girl! What kind of tree do you want to be? I'm scared too. Its a shit sammich. We have to remember, though, that we are NOT numbers or statistics. When you read stats of survival for this, remember that A., the odds are in our favor of beating this by a large percentage, and B., death rates are just that. death rates. from everything, not just cancer, within the first 5 years or whatever. So yeah, a certain percentage who are being tracked die from cancer, but another percentage dies of something else, like getting hit by that damn bus that everyone says is coming for us. Also, clearly reoccurance is not a death sentence. Witness our fearless leader, KBeee. Its an annoyance. Now all this doesn't make it ok, but after enough Ativan, it does help me sleep at night. Sorry to go all Pollyanna on you, just wanted to share some thoughts that help me sleep, like I said.
KBEEEEE, I can't freakin believe you are doing a half marathon tomorrow. I know I said I'd do it with you, but It may take me a few days to complete LOL. Still pulling for ya! You are an inspiration! So, do you actually heal muscle tears from exercise faster on Taxol than on AC? Just curious if i could start ramping up a bit after being a lazy chemoslug since the 16th...just felt so crappy with this 4th one, wah wah wah. I have 30 miles of road to survey sometime this summer....last summer, it would have taken me two days. Now????
Rpayton, Good luck at the spa today! Another one bites the dust!
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KBeee! I forgot that was tomorrow! Oh my gosh, good luck!!!
My MO said partial reason for us being tired is having less red blood cells to move oxygen around - so exercise actually can help more than rest in that case, as it gets those cells moving and delivering oxygen more quickly! (not that we don't need those naps!)
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feeling pretty good today after first taxol. Def feel the nail pain and tingling fingers... Feet are still hurting ( I feel like exercise would be great but my feet and toe nails are so painful). Didn't have any other reactions as of yet. Keeping my sore fingers crossed:
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Lynne, and anyone else trying to balance work, I have always worked full time, type A driven personality. Even thru pregnancy complications at age 29 I worked as much as possible. I think there is a balance we have to find and that is different for everyone. I have made a decision to give up my position that I love dearly but is too toxic of an environment. HR has agreed and sided with moving me (I believe my standing up for myself with proof convinced them that I was in a hostile, discrimination situation) I hope to be taking a position that is flexible, full time, and in a completely different entity real soon. Feeling excited and nervous about it as not what I had planned during treatment. But why haven't I learned by now not to plan, right?! LOL
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If this helps with anxiety: Side effects or lack of SEs is not an indicator of whether treatment is working.
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Ac done! That last dose kicked my butt for 11 days before i felt better. I had a headache for days after i quit taking the anti nausea meds. I cant imagine that red devil more than 4 times that's for sure. Anyway i start weekly taxol Monday. I've been trying to catch up on here with who had already started it and how it was going. I'm nervous. Here is a picture of my youngest loving on me. She loves mamas bald chemo head.
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KBeee: you go make that marathon and push on for all of us! Way to go! I'm not a runner myself but I totally get the satisfactory feeling from my long walks. The 5k I did a few weeks ago was spirit lifting. Hoping to get breaks in the rain and do this weekend. Well in my mind that is the plan, depends how hard #3 hits me with the steroid crash. ;-)
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Welcome to the community EmbraceHappy! We are glad that you reached out. Keep us posted on how things go for you. Stay connected. The Mods
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Hi All
I have been using sick time and FMLA since my MX in late february. I was lucky to have accumulated over 100 sick days. I am going back to work in 2 weeks...then summer break, I currently work has a Certified School Nurse in a very urban area, with 3 and 4 year olds at various PeKs and Child Care Centers, for the past 11 years. I spent 20 years as an ER RN, (I continued to work part-time in the ER as well as after school centers until 3 years ago), and 10 years as a NYC EMS Paramedic in Bed-Stuy, Flatbush, Coney Island and East NY, Brooklyn, NY, right after college. I am going out of my mind at home, but at my age (57), my MO thought it easier to stay healthy if I didn't go to work. My kids are from all over the world, and their disease and vaccine status is often sketchy. I feel for all of you with young children, (my 4 boys/men are 19 to 28 yrs old, #1 lives with his girlfriend, and # 4 is a US Marine-OORAH!), and jobs that you cannot take off from. This is a tough enough battle without the added stressors--ugh.
I completed my TC Chemo yesterday and after these SEs subside (usually by Day 12), I will get my Genetic Test results and make definite plans for my recon sx, scheduled for July 7. I am feeling emotional knowing chemo is finished. Praying there are no cells left. My path report from surgery showed close, <1mm margins, in my anterior left MX, so my BS and PS will be scraping around in there before I get my left implant. I am a good nurse, lousy patient...lol. I lost 2
1/2 pints of blood with a clogged drain 3 days post mx...so I am hoping no more excitement with this implant and right redux/lift. Ugh...who invented boobs, anyway?
I am always thinking os all of you...hoping your SEs can GO AWAY... and wishing your chemo can move forward quickly and BEAT THE SHIT OUTA THOSE ROTTEN CELLS!
Love and Hugs to all...be on the mend...better and stronger everyday!
Love, arlene
Hers' a pic of me and my ONCO RN, Anne...She did a Great job keeping me port and allergic reaction free...and made me laugh!
I don't know why these pics end up all over the place?
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thanks for the uplifting posts everyone
littleblueflowers you always crack me up! Kbee thank you for the advise I am going to ask my oncologist about abraxane I looked it up. I am receiving my neulesta shot and fluids today and my chemo nurse said to me I think you need to talk to your dr about stopping taxotere you scared me yesterday and I'm afraid your reactions will get worse ugh not what I want to hear now I have to wait almost 3 weeks to talk to my oncologist about what to do next
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Go KBee!! We'll all be thinking of you tomorrow for sure!
Well after feeling like crap all week, it seems as if the cloud has lifted today. Took the dog for a walk in the nearby park. Reached out to a friend and we're going to see a movie tonight!
And I'm cleaning my tiny apartment today after not being able to get up off the sofa for more than half hour at a time earlier in the week. I made an empowering playlist on spotify with mainly women singers of favorite dance songs....
So picture a bald, overweight woman cleaning up her tiny solo apartment and stopping to dance every few minutes. Here's the link. It starts with Kelly Clarkson's Stronger and ends with Ms. Helen Reddy's I AM WOMAN! Yes, I'm showing my age, but I hope y'all enjoy it:
https://open.spotify.com/user/1262817855/playlist/19gE2Km83fuw7ndXuNkmP7
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going for an event at kids school
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