November 2011 Rads
Comments
-
Hi Missey - I only have three to go, also. It would have been only two, but after driving an hour to my center and waiting for 3 hours to see if they could repair the machine, the tech apologized and sent us all home without treatments. Oh well - I will try again tommorow! (Yes, that darn itching - I actually pulled off the road yesterday and applied Aquafor - the itching was unbearable and if I rub the itchy area, it hurts! Good thing a policeman did not stop to see if I was okay - I had my grandsons stuffed Yoda in the passenger seat and my granddaughters huge teddy bear strapped ibn the carseat in back. They send them to watch over me. The policeman would have really thought I was losing it.)
-
MrsMot - so sorry about your throat problems. I know what you mean about rads - in many ways it is not as bad, but it is in others - especially emotionally - hard to explain, but regretfully, we all know what I am trying to say.
-
I was finding rads pretty easy until this week...it seems every day is like a bad sunburn - am so pink/red on the side toward the underarm. Nipple is getting leathery and tender. The original skin damage is getting really dry and peely. I can't scratch - it hurts now. I have steroid cream that really works.
I am extremely tired. I do not know if it is from the holidays and doing way too much; or if it is the combo of the 2 hours in the car and the cumulative draining effects of treatment. I have 3 more before boosts. I wonder if the boosts will cause trauma. I have a lot of red sensitive area in the crease underneath. My underarm and SNB incision is still good. My surgical area is being treated from the right side of L breast and that is where the most damage is already. The burned area is very distinct now, and there is a line where there is no damage. It burns most of the time and I feel like I have chills.
While I'm venting.....I have a friend who has been cleaning my house - she really needs the money and I need the help -- well, yesterday she brought a helper who had a seething cold and bad cought....I cannot believe how many times people have been totally inconsiderate of the fact that I should NOT be getting sick during rads. Nobody cares! So am not sure if my tiredness and chills is the rad burn or a respiratory thing brewing.
I want to keep doing the fun things I've planned (trip to DC over the 3 day break) but am soooo extra tired.
Rads or life or both? -
Anandagram-So sorry you had to wait for so long for nothing. I do love the image of the teddy bear and Yoda in the car with you. I agree it would have been quite a sight for a police officer. Prayers that tomorrow will be better.
MrsMott-Hang in there. For me it seemed to go much more quickly after I hit the half way mark.
Joan811-How awful that people aren't keeping your health into consideration. I guess it's easy to forget what is happening to you. The side affects aren't as visible as the chemo ones.
Natters-How are you doing with the whole "You're done, let's all celebrate!" phase? Every time someone talks about celebrating after my last one tomorrow, I say yay of course...but in reality I don't feel like celebrating at all. I keep thinking and worrying about what the future will hold.
-
Nans - I know what you mean about the worrying. Once treatment ends, I guess I'll feel a bit insecure about whether the BC is really gone. We have all seen so much in the waiting rooms and we know what others are going through. I will have to consciously practice positive thinking and living after this.
-
I finally started to wear a bra on Christmas Eve! It feels great! All of my skin issues are completely healed. I had an an appointment with my MO yesterday to get my prescription for Tamoxifen. I thought it was at 9:30 but it was a 9:00. I was there at 9:20 and they refused to see me. I thought I was a little early! Now I don't see him until the end of January. That upsets me because my insurance is changing and now I have to pay him for the entire visit. The receptionist was very nasty. The sad part about it is I'm NEVER late for an appointment. Plus, I took the day off for this one. I would have thought they would have been a little more forgiving.........
-
Nans, I am VERY relieved to be done with treatment but my partner and I broke up this week (we were together 4.5 years and I thought we would be together forever). So I haven't felt very happy or celebratory. on the other hand, I've been too sad and pre-occupied with the details of my "divorce" to worry about a recurrence. I won't see my RO until Feb 3rd and my MO until Feb 9th - but I have an appt with a lawyer this month
but at least Jan is Dr-free.
On a more positive note, my skin is healing nicely and the hot flashes from the Tamox seem to have completely disappeared. I'm glad because taking Tamox feels like just a little extra insurance.
Nat -
Hello all, I have been lurking in the shadows and encouraging you all in my thoughts. For those of you who are close to the end...hang in there.
Joan 811 - Toward the very end, I tired very easily. If you feel up to your trip, I say go for it, but be aware that you will get tired easily (one trip through the grocery store about did me in). Take your time and allow yourself multiple resting spots. Usually after about a half hour or so of resting, I was able to get up and go again for a while. Just listen to your body and don't over do!
rnforbabies - Isn't it totally unfair that a doctor can keep you waiting for hours in the waiting room to see them, but if you are late just a few minutes, they refuse to see you!. What makes them think that OUR time is less valuable than theirs. I would make sure that I told the doctor what happened! Perhaps they are not aware that the front office turned you away. At least they could have asked if you could be worked in...after all those appointments usually last only about 10 minutes max! Even if they do have the policy of not seeing you if you are late, I would definately give the doctor a piece of my mind!!!
Natters - I am so sorry! The stress both of you have been under must have finally been too much. It sounded like things weren't going to well in your previous posts, but that doesn't make the break up any easier. Now that your treatment is ending there should be some joy in your life...now this! This dam_ disease takes so much from us that it isn't fair that it also attacks our relationships. I will especially be thinking of you. Here is a hug {{{{{{{{{{{{{{{{HUG< HUG< HUG}}}}}}}}}}}}}}} It is a big strong one because you definately need it!
If you ladies want some irony...after all the treatments, side effects, burning, etc was over, I now have a lump in the exact same spot in my breast again. The RO said that it is just swelling and tissue reaction from the radiation and may never go away. She told me that, when she first started, they used to hurry patients into a mammagram right away to check it out but it was always just tissue reaction at the bed of the tumor site. Every morning, I feel that lump and wonder..... Will be asking my MO in January when I have my appointment though...hope I get the same assurance from her. This just never seems to end! The book I read, After Breast Cancer, said that whenever you feel something that doesn't seem right, wait two weeks to see if it changes before you react. So I will wait until Friday the 13th (that is when my MO appointment is) and try not to think the worst!
-
kdajay - thank you for the hugs. At least my friends are rallying around me and trying to keep me busy during this difficult time. And at least I am slowly starting to exercise again, so that will hopefully help my mood. And I might even get a full night's sleep one of these days soon
That sucks about your lump, though. I am the kind of person that easily builds scar tissue so I'm assuming I'm going to have a certain about of radiation fibrosis and I won't even bother examining my breasts. I'm just going to let the RO do it early Feb, because he's pretty senior and after all these years examining radiated breasts, I am confident he'll be able to tell the difference between fibrosis and a concerning new lump. Plus, I'm seeing my MO the following week so I'l get that backup opinion. When in January do you see your MO? I hate that we are going to be scared about things like this now the rest of our lives.
I have a friend getting a biopsy tomorrow, too
Nat
-
Natters- So sorry to hear about your partner and you separating. I'm glad you have friends to support you now. Your right about keeping busy. That can make all the difference.
Kdajay-Prayers that your lump is nothing. I wonder if any of us will every relax about our health again. Probably not, and perhaps best that we don't
I had my last radiation appointment today. My husband called after it was over to tell me congratulations and see how I wanted to celebrate. I told him I didn't feel like I did when chemo ended. I wanted nothing more than to celebrate that ending. Now I just feel tired. I keep thinking that I now am not doing anythng active to fight this. I guess I have to start considering my exercise routine and good eating habits as my fight. That seems hard to do...maybe if I have a doctor call me to set up the exercise time I feel like it is.
-
Last week's machine break down, led to me just giving up. I cancelled the next day's appt; and then on Tuesday, I called and told them that I quit. I was taking it one day at a time; but they seemed to be taking days from me due to the holidays. Plus, I've been extra tired and I'm tired of the 20 minute drive (I know many of you drive further. I don't know how you do it?). I'm supposed to go in tomorrow to talk to the doctor about it all. I dunno? I'm just tired!
-
Toomanycocktails, Its rough. We all have had too many shocks and turmoil with this diagnosis but I really encourage you to stick it out and finish radiation. Yes you will be tired, yes you will probably burn some, but you really need to consider that it is killing those bad cells and looking at what you have posted as your diagnosis you need every tool in the arsenal to fight this battle. I will be here for you as will everyone else on this forum. We all need to stick together.
-
Toomanycocktails - I completely understand about quitting. But you can't. You need to kill any cell that could be in you. I am stage 3a with a 7mm size tumor that had already become invasive. Chemo was rough but this is a different torment. I so want to quit. I cried today in treatment cos I hurt and I don't want to do this anymore. I am tired of being sick and tired. But I can't quit. We both have to continue and get through this. Go see your doctor and talk about this with him/her.
Natters - So sorry to hear about your breakup. Not fun. Hang in there. You have been through so much already. Sending hugs your way.
I have broken out in a red rash and am all red. All this has happened with the last few treatments. Everything was ok before. My RO gave me a steroid topical oinment to use. Fatigue has hit me now too. I just want this done. But I don't want to go through this ever again so I will buck up and continue. Thank God tomorrow is Friday.
-
Natters - I am so, so sorry to hear about your breakup. I knew things had been rough but I was hoping the counseling would get you both through these hard times. I hope the healing begins soon.
-
Too Many Cocktails, I am so sorry to hear of the continued disruptive rads experience and the discouragement you must be feeling. It's been a tough journey for you. I hope you will come to some agreement with your doctor to finish the treatments. We need to throw everything we can at the beast. (((HUGS))) for you...you are not alone.
Nat, As if BC isn't enough, you have to endure more loss with your break up. When things get so bad here, I usually stop talking about it and try to write down everything I remember and what I'm feeling so I can get it out of my head. I know that looking ahead to spring and getting back to exercise and competition will be good for you. But I am sorry for your pain. We are here for you, friend. -
Nans, Congrats on having your last treatment. You must feel so spent after the emotion and physical drain of chemo and rads. Your celebration may be just to catch up on sleep or things you've missed....
As annoying and disruptive the daily appointments are, we do feel like we are blasting the BC out of this world. So when we finish, it may be a a time of new worries for us.
Today I had #23/25 regular tx. They told me when I arrived I'd have my planning session today for the boosts (5). I was unprepared and had left my iPod in the car....but I had music on my phone and they were really supportive. I had to lie on my back, but it won't be bad for 5 tx.
I felt very emotional about getting to the end of this. I know I will cry on the last day...
Celebrating is not what I'll be doing since I have to have a cardiac catheterization as soon as rads are done. I hope I do not need surgery; my skin is in no shape.
m4babies, It is hard to believe they couldn't squeeze you in. My cancer center has put me in numerous times for a quick check whenever needed. If I'm close to my arrival time for rads, they will take the person after me if she's already there. There is a need for flexibility and you deserve better. I admire your patience waiting another month.
kdajay, I am glad you mentioned the lumpiness after rads. I wouldn't have known what to think.
I am so grateful for all of you here and your help, comforting words, and personal courage.
Joan -
Natters – Sorry about the break up! I hope you will heal inside as well, soon. Good that you have friends who keep you busy!
TooManyCocktails – I think it's irresponsible of the radiation center to not keep their machines running. Maybe you could tell the doctor that you fully understand your need for radiation, and that you need them to provide it on a regular basis. You can't just spend your days driving there for nothing. No wonder you want to quit. It does look like you need the treatment, but perhaps you could go to another radiation center? I hope you will find a good solution, anyway.
The hospital I went to closed down for service now and then, but they planned it and told us a week in advance. They have several machines and I never ever had to leave without treatment. Well, you can't go to Stockholm for treatment ... but it does upset me that your radiation center don't keep their machines running for patients who need them.
-
To those who want to give up... I remember my last week of rads when I put my hand over my head for treatment and the skin felt like it was tearing. I cried right there on the treatment table...those silent, painful tears that we all have spent because we just can't hold them in anymore. The techs thought it was because I was in pain but really it was because I was really tired, just didn't want to hurt anymore, and wanted to quit more than anything (after all, I never was really sure if it was helping anyway!). My RO came in to look at my burns and broken skin and she put a hand on each of my sholders and looked me straight in the eye with a very serious expression and said, "Don't stop now. Give us just those few extra percentage points to beat this." This was from a woman who on a good day seemed to be pretty much of a cuckoo!
So this is me, with my hands on your shoulders, looking you in the eye and saying "Don't stop now. You have fought this long and so hard. I know you want to give up, to stop being tired, to stop hurting, to stop giving this disease ALL it will take. You are strong enough to do this after all look how far you have come already. Just give us those few extra percentage points to beat this thing!"
-
I am done!! Finished yesterday after taking a break because of skin problems. I would almost rather do chemo then do this again. it went so well at first then like hitting a brick wall. Mind numbing fatigue-I even fell asleep at the dinner table at my Moms. they finished eating and cleaned up around me while I snored. My sis said she would have woke me if it looked like I was going to do a header into the mashed potatoes!!
<Y chest looks like someon put an iron on it an dleft it til the whole thing melted. Big scabs and oozing places. I thought I would have no problems because i have very thick tough skin. They told me it will get worse for a few days then start to turn around. Becasue all but 5 of my treatments used the bolus it was way more damaging to the skin-or so they tell me. I made them continue when they wanted me to stop but it finally got to the point where we couldn't do it. I see the rads guy next Tues then wont see him again for 6 months.
Good to read so many are finishing and looking forward to less doc stuff in 2012. I will continue my every 3 week Herceptin but not much of anything else.
-
lilylady - So glad you are done! If it is any consolation, the healing happens pretty quickly after they stop the rads. In another couple of weeks you will be doing the happy dance again.
Oh, and thanks for the image of you sleeping at the dinner table while they cleared the dishes! Guess my falling asleep in the recliner every night during the news doesn't seem so bad now. I have slept more in odder places since this all began but never at the dinner table. Wish they had thought to get a picture for your avatar! that would have perked everyone up! (did I just say that out loud?)
-
Yippee! I'm done. So glad the RADS are all done and I can get back to my normal life. On to the next thing. Pray that we all continue to make positive strides for years to come. I'm taking Jan. 2012 off from all dr. visits so I can focus on something else for a change.
-
Well ladies, I went in to see the RO. I told him my concerns (I have other health issues and is it safe to continue the radiation without damaging or causing something else basically). He listened and he deferred me back to the MO. He did not push the radiation tx's on me. I guess, he wants to be safe and to know that all is well too. I'll be seeing the MO early in January.
Thanks for all your kind replies. It's nice to know that someone cares.
-
Congratulations, lily and Missey!!!you made it!!!
cocktails, I'm glad you're getting a break until you see your MO. Try o enjoy the holiday weekend.
Nat -
missey29 - so glad you made it! It wasn't easy for you, was it?! Just be a little patient about getting on with your normal life. The burning will continue for a bit before the healing commences in earnest. But it will happen. Party on!
-
Happy New Year to all of us!! We so deserve a healthy, happy 2012 and many more happy new years ahead. Let's drink a glass of bubbly to rejoice.
-
Lily lady, you have been through so much; you have had long healing issues and had to wait a long time for these treatments. I know exactly what you mean about the wall....I hit it a few times a week now. I am active and mostly pain-free and still I suddenly crash and cannot move. I doze off and try to let others drive when possible.
I hope and pray that your long journey will result in gentle healing and a new start for the coming year. You deserve it.
Same to all -- BC is brutal and it affects us all.
Love and hugs ((((Sisters))))
Joan -
Hello--I am responding to our friend who was charged for an appointment and not seen either, because she thought her appointment was 10 minutes after she arrived, not 20 minutes earlier, making her late. I suggest that you write a letter to your physician (if you cannot speak with him or her) requesting that he or she review the decision (and the way you were treated). I am shocked at the way you were treated and I am so sorry. It's hard enough going through this...have a happy and healthy new year.
-
Happy New Year everyone! I for one am glad that 2011 is over. A wretched year for me.
Congrats Lilylady and Missy! You are done. I am jealous. Hope you are healing!
Eleven left for me. These past 3 days off from rads have been so healing for me. I feel better when I don't have a treatment. But tomorrow is back at it.
Missy - how is the hair growth? My hair is growing in...I look like a man right now with my very short short hair. But my scalp is covered (with very gray hair). The 13th I am getting it colored! Can't wait! I have to wear big earrings so I look like a girl!
-
Hello again friends--Tomorrow is #22--6 to go. I've felt good for the last 4 days (no rads and I've been getting more sleep). I'm determined to finish my graduate work--I will have to push through it. Research and writing through March (Master's thesis) then Comprehensive Exam and defending my thesis in April. I miss my job but I would not be able to complete my Master's otherwise. Do you find that you need a lot of sleep--I do--a minimum of 8 hours--I usually try for 10-11. Best to all of you and thank you for your support.
-
#23 for me tomorrow, just 3 more full treatments then 5 boosts to my scar line. The area of my skin that is being zapped for my mammary nodes is just raw. Everything else has held up pretty well so far.
Oh how I wish I could sleep for ten hours! I'm lucky to get six or seven. Fortunately, so far, I've not noticed any unusual fatigue.
2011 was indeed wretched!
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