August 2011 chemo, anyone w/ me?!
Comments
-
Hello ladies! I'm having my dry run today at 11:45am. Had the CT scan and was tatted up on Monday. I hate needles so that tatooing was not a pleasant experience.
The RAD staff seem confident but not an overly friendly bunch. And, they are not really flexible on the timing of appointments. The hours are 7:30am - 4pm. Had to change my work schedule to accommodate their schedule. Not fair. This too shall pass.
Will keep you posted on how the dry run goes.
Talk to you later.
Missey 29
-
Hi Everyone!
I've had 8 RADS treatments already -- only 22 more to go!! I only started last Tuesday and last Friday, they had to cancel all appointments as they were doing a machine overhall.
I think Ellen asked about the head turning -- I know for me, it's to make sure the airway is clear and out of the way. For one of my zaps, the radiation machine is very close to the left side of my face as it comes in on an angle to zap the breast. One of my tattoos is near the midline chest area and the airway has to be clear. Everyday, after I get in on that freaking hard-ass table, I have to clasp my hands over my head and hold two stationary rods and I lift my chin all the way up and turn drastically to the left.
I have zaps on the left, right and middle of the breast -- I'm being radiated also in the lymph area and clavical area. Doesn't take long at all, but too hold that positon during the simulations and films was unbearable (about an hour!).
My drive is 50mins (without traffic) and I can say it's already exhausting. I also have pangs, twinges and electric-like pain in my breast at times that lasts a few short seconds.
I'm using Keri Sensitive Skin Lotion (the center gave me this) and Aquafor. Was told to wash with Dove Senistive Skin body wash and use Deodorant without any aluminum (ie: Toms of Maine or Trader Joe's brand or something natural from Whole Foods).
I will meet with my RO every Monday after treatment, and did see him for the first time this week. I get a full BP, and Temperature Check as well as a physical to look over the breast.
I hope everyone is doing good! Can't wait for this to be all over with!
-
Chrys..Informative post. there's probably more than half of us that haven't started rads yet and need this kind of information that the official sites don't give. I'm glad to read that there is a deodorant available. I thought I was going to have to go w/o deodorant the whole time.
22 treatments left...that's good. Soon it will be your last week!
-
OK. I'm back. My dry run is over. The room is huge and warm. Had to de-robe from the waste up. Glad to be able to keep shoe and socks on. Then I had to lie down face up. Next, clasped my hands above my had and tilted my head up and to the left. It was a weird position to be in. Had the wig off and it felt great. Side note, one of the techs said she thought it was my hair (high fiving Everyone
).
There was a machine with arms that moved in from each side but they never touched me. Lights were coming from above and from the side. I have four tats. One in the middle of chest, the other below breast bone, the others are on either side of abdomen. Asked why there was a tat on my left side when the cancer was on the right. The tech said they used it to make sure I was level on the table. Has to be an easier way. Oh well.
They took plenty of films and scans. Took about 30 minutes total. I tried to sleep and distract my mind so I would not move. Sometimes I wanted to sneeze, scratch my nose, or move my head but did not move so that the process wouldn't take longer. I know it was all in my head.
They marked me up pretty good from the right side of my neck to below my breasts. Thankfully it can wash off.
Talk to you guys later!
Missey29
-
Thanks for the wig info, JMULL. What color did you get? It's so hard to tell what they'll look like from the pictures and swatches.
Wow, Missey and Chrys--I had no idea the "dry run" was that complicated! The muscles in my upper arms hurt so much from the taxotere that there's no way I could hold my arms over my head for an hour! Did you meet with an RO before you did surgery or chemo? I haven't met with one at all yet. Okay, this may sound like a stupid question but if my lumpectomy was successful (clear margins) and none of my lymph nodes were affected, what exactly are they radiating? Will they focus on the part of my breast where the tumor was?
I guessed I'd better slow down and focus on getting through my last round of chemo next week. I'm just sooooo anxious to get this over with!
-
deb, i've wondered the same thing and i'm glad you asked. i thought chemo was supposed to get rid of the rogue cancer cells that could be swimming around in our bodies. my guess is that radiation on the spot where the tumor was is just extra treatment at the previous cancer site. i'm not really sure, though.
when is your last treatment? mine is monday. YAY!!!
-
Hey Deb --
The radiaiton definately can focus on the spot where the tumor was in the event there are any 'rogue' cells in that area. While right now they are radiating my whole breast and certain fields (like lymphs), towards the end, they will do "boosts" to the actual tumor site as well as added insurance.
Here is information on Radiation from this site: http://www.breastcancer.org/treatment/radiation/
I hope ths is helpful
-
Chrys, that's how the radiation ONC explained it to me as well...whole breast with a boost to the tumour site at the end.
-
I am having my entire breast radiated.The beam comes from one side and then a shorter hit from the other. I close my eyes as soon as I assume the position, ( thus missing out on looking at the cool starry ceiling!) so I am just going by the sound of the machine. It is one of those new modulated ones so it moves a bit while beaming and can vary the intensity of its beam. I had a 2.2mm lump in my sentinel node,so I guess that is the shorter beam coming from the right side. Lumpectomies and radiation go hand in hand, and according to my RO, the number of treatments is determined by the margins. So, it is anywhere from 5-7 weeks. I am 31 treatments, even though I was told that I had good margins. What surprises me is that woman w/ mascetomies still get radiation sometimes, I think?
-
Hi Ellen --
Yes, some women who have had mastectomies can also recieve radiatio, due to certain variables:
(http://www.breastcancer.org/treatment/surgery/mastectomy/plus_radiation.jsp)
-
I'm not sure why I'm in there for so much longer than you Ellen, although the machine comes at me from 7 different angles, right to left. I watch the lights click on the computer screen across the room as each of the angles completes. I'm always excited when it hits the 4th one, 'cause then I'm halfway through. The machine does get pretty close to my face, and the angles are pretty close to my chin, so that's probably why I'm moving my head to the side.
Other than the fatigue, probably still left over from chemo, and the warm breast, I've had no other radiation s/e's so far.
Off to get the puppy today!!!!!
-
Deb - I can't remember what color I got and of course it doesn't say on anything that I have. I did get the gradient coloring - don't know if I said that before - where the roots are darker and there are hi and low lights in the coloring of the wig. I think mine had butterscotch or something in the name. I did find a different site other than wigs.com that showed the colors a little bit better. Just google the wig name and a bunch of different sites will come up to give you different views of the wig.
Thanks for all the info on rads, ladies. I need to call my RO - would have thought they would have called me by now, but oh well. I had a single mastectomy and am getting rads. My tumor wasn't that big, I had clear margins, and I only had 3 nodes. I think the reason I am having rads with the mx is that they want to throw all they can at it. Plus, since I have ILC - it's sneaky.
Hope everyone is having a great weekend.
YaYa - good luck on Monday! WOO HOO.
Robyn - enjoy the little fur ball and puppy breath!
-
Thanks, Chrys and Ellen, for the radiation info and links to websites. Somehow I feel more in control when I know the whys and hows of what's happening to me.
YaYa5--Hurrah! I'll think of you and celebrate on Monday! I'm five days behind you--my last treatment is Friday. Today is my 100th day of chemotherapy, and I am sooooo done with this! Who else on this thread has to keep going in for Herceptin infusions? I guess that's no big deal, right? No real SEs? I love the folks at my clinic, but--in truth--I'd love never to see them or their office ever again! It's getting so bad that I can't watch tv shows or commercials set in hospitals. That's all I need--one more phobia!
Our thread has really dwindled. Is everybody over on facebook? Vivie, Diana, MizMarie--are you out there and doing okay?
Peace and patience. Deb
-
JMULL--I was posting when you were. I think we have "twin" hair! I ordered the Sky gradient wig called "Butter Pecan R." Tell me it's a pretty combination of colors and not too red. Thanks for the tip about the 25% off--it actually ended last night, so I got in right under the wire. Do you wash yours? Do you have to restyle it, or does it just go back to the original style? Do you wear a cap under it? My human hair wig is nice and comfortable, but so much work! Thanks again!
-
Hi Deb,
Yes - I'm still here. Feeling much better after getting a blood transfusion and antibiotics earlier this week... The doctor doesn't think this episode will delay #5 chemo, but my platelets were below the minimum on Monday - I hope they rebound enough by next Thursday. I'll be thinking of you on Friday - isn't it amazing to finally be so close to the end of this chapter?
I had Herceptin alone when my platelets were too low to get the chemo drugs. Literally zero side effects; I could have gone to work afterwards, except it was a furlough day....
I haven't moved over to any of the Facebook groups, and don't really want to - FB is where I go when I don't want to think about BC....
-
Deb - tee hee hee - we'll have twin hair! I just went and looked at my actual wig and is says the color on the tag - Creamy Toffee is what I went with and it is very blonde, but not too blonde. Honestly, I have yet to wash it, but really need to! I have 2 wigs that I bounce back and forth between. And although the Sky is comfortable, I would rather go without, so other than for work, I don't really wear my wigs. You don't have to style it, just kind of shake it out. I don't even brush it with a brush, just use my fingers. I don't wear a cap under it and it is a little itchy, but not too bad. I hope you like it when you get it!!
Lots of ladies are on the facebook thread.
-
Hi ladies,
Not much to report, except I just took a Vicodin for my low back pain; nothing else is helping. Trying to figure out if it is from the Taxotere or the Neulasta. I keep telling myself, "this too shall pass".
I received another lovely card from one of my co-workers and in it she referred to me as a warrior. I guess I had never really thought of me in that capacity, but after this last Taxotere cycle, I am going to think of myself differently.
This dam*ed breast cancer is not for any wimps!!
And MizMarie is getting a transfusion, too! Hope you're doing ok.
Glad to read that everyone is doing ok with rads.
Have a great weekend everyone!!
-
Deb, I think you'll find the synthetic wig easy to look after. I just swish it in the sink with a little wig shampoo and then leave it to dry. I only wash it about once a month as I don't wear it very often. I have a wide-toothed comb that I use to make it look a little neater. I don't wear a cap as I found it gave me a headache. The wig lady at the Look Good Feel Better class said the purpose of the cap is to hold your hair in place so if you don't have hair, you don't need a cap.
I have my last tx on Tuesday. Yeah....I'm so ready for this to be over. I expect I'll start rads mid-December and should be done end of January.
I've joined the Facebook group but still try to check in here once every couple of days. -
Yay, Michelle! Sounds like next week is a big week for many of us. Is there a certain length of time we have to wait between the last chemo and our first rads? I want to GET IT DONE!
-
Robo - haven't flown yet, but will be in December. Let me know if you have to take it off....
Michelle - Congrats on your last tx approaching this week! So jealous of all you ladies finishing. I cannot wait to be done. 18 more days for me...
-
Deb, my doctor told me 3-6 weeks between last chemo and rads. I think they aim for 4 weeks.
-
Maryjrn -yes, the biotine worked very well --also w/the whole dry mouth thing...
Thanks everyone for all the info on rads -sounds like we're taking a trip into the universe w/all the beams etc!... I had a bmx, and I am having radiation as well --I think its b/c I had lymph node involvement --my BS sd the radiation further "sterilizes" the area where the cancer actually was
The bone pain while on taxol I think is more from the nuelasta shot from what I am hearing from everyone...I've had 3 tx's so far and the one I had w//the shot by far gave me the worst pain.
Hope everyone has a great weekend!
-
3-6 weeks to start rads after last chemo. I started at 31/2 weeks, I think. How fun to be getting a puppy Robyn! And yay! for all of you guys finishing up this week!
-
Hey Deb...I'm as okay as I can be..I'm mostly on FB now , plus the last Taxotere tx kept me quite busy with low back pain (intense) and I also spent the weekend catching up on my sleep...and to top it off , my period did a roundabout and came back after a week.November is not a good month for me , it seems.
I also got a final dx on my right arm pain - I had some temporary arterosclerosis from the red devil , plus the nurses ( incompetent ) in their haste to get me in and out they also pinched a nerve.Most pain of it is better since last week , but it's still pretty tight.I assume it'll take months for the pain to completely go away.At least I don't have to favor it as much.After this ordeal my nightmares involve needles.Nobody likes em , but now..I think I have a phobia.Ugh.
I'm about to give up and stop but my family think we've come this far , we should finish it, and they'll tell me tales of this person or that that had to battle cancer at some point ( family friends , relatives , etc ) and they 're doing good now , so I should take heart from it...BC isn't for wimps...but I'm SICK of it.I'm scared.I just want to stop and sleep and heal.January feels a lot damn farther to me than it did in August.My most hated phrase "Only two more months! only x number of tx's left! we're almost done.." I don't want to hear it , I dont want to continue, and yet...I think I reached my limit.
From what you've said girls , I'm very glad I refused to do rads.My BS tried to push them but I told them that rads is not for me.Also, with SNB clear , left side mx , and chemo...no , it's OK.I can't even imagine having to sit still and let them do that to me and suffer the burns.No.
-
Glad you're still with us, sweet Vivie! What a wild ride you've been on! I couldn't agree with you more about the most hated phrases: "just one more treatment," "just 6 more month till your hair comes back." Six more freakin' months?! That's supposed to make me feel better? I know people are just trying to help me stay positive, but I kind of feel like it trivializes what I'm going through and have yet to go through. ANYONE who has gone through chemo would judge you for saying enough is enough! Vivie, you deserve every bit of good energy and peace the universe has to give!
I''m feeling incredibly unattractive and very sorry for myself today, so, Robyn, cheer me up and tell me about your new puppy: breed? name? latest antic?
Ellen, how was the store last week?
-
(Of course, I meant anyone who's gone through chem WOULDN'T judge you, Vivie. I should proofread my postings!)
-
Ah Debin...
I always thought I wouldn't have phrases added in my 'hated' rack...bc I'm deaf , I've had a few to that specific rack already like :
"Never mind"
"I'll tell you later" - and they NEVER do.
"Oh , it's too complicated for you to understand! "
and of the same like.For that reason , when I first meet someone I'll usually be standoffish and/or rude till he/she manages to impress me with his including me.Because of that , I don't have much patience and I have few friends.Few , and much valued.
As for the BC , it is too much bc of my added disability - because that's what it is , even if I don't let it hamper me - it also puts a layer of miscommunication.For that , my doctor thinks I'm dumb and will do whatever he says due to lack of education.Ummm, no.I surprised him with knowing the possible cause of pinched nerve and of the side effects and how I said I don't like the Neulasta - they keep throwing it at me even with my WBC slightly elevated.They are rigid , understaffed and can't take any delays , but for that , I suffer all the more for it.
I'm seriously thinking not going back.It is a risk , but also , it's a mental risk too if I go back , because I feel like I'm on my last rope.I always had to fight something , and now it's on two fronts.Nobody gets it.As for the situation in Greece...it's very unstable , so I wonder what will happen on that front.
-
My puppy is definitely making me smile, 'though he seems to be bonding with my son instead of me, but that actually makes me smile, too! He's Jasper, although I seem to spend all my time saying "No Jazz, no, no...." House training is going VERY well, much better than expected! He's a golden retriever, and I love that he's still so roly-poly. When he runs, his back legs get going faster than the front, so he stumbles and trips over his own chin! He came from friends, very responsible people, and he's already crate trained, which is also awesome. He was lonely for his littermates and his mom the first night, but he went all night in his crate last night without a whimper or an "incident!"
-
(((Hugs))) to you Vivie!!!
Congratulations to all of you who are finishing up chemo!!!! Its been a long road!! I have 2 tx#s left and it seems forever!!! I just want to be DONE!!!!!
I havent been on here much I hope everyone is doing well!! Congratulations Robyn on your new puppy!!
I have a sister n law who said to me that it's going to take a good 2 years for my hair to come back. She just said it out of the blue! Who says that to someone who's going through hell!!!! She has a hard time picking up the phone to see how I'm feeling !! I am so hurt I just want to be done with her!! I am nothing but a nice person and dont deserve stupid hurtfuln comments!! Sorry just having a bad day ....:)
-
(((((((HUGS)))))) Taylor: some people are just so dam inconsiderate and dont even realize it...... You are a strong, vibrant woman, Dont let what someone says bother you. I know its easier said than done BUT You are obviously a STRONG woman, I mean your here arent you ;-) You keep your chin up and smile, you are beautiful!!!!!!!!!!!!!!!! I posted pics of me NO HAIR in the Nov 2011 thread... :-) go have a look I look..... again BIG BIG (((((((HUGS)))))))))) you are beautiful and you SHINE
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