SEPTEMBER 2009 RADS
Comments
-
Betsy - I am still here. Just nothing to report. Today will be my 17th rad which will put me over the 1/2way mark (33 total). I have NO SEs at all. Just look very slightly tanned in the rad area if you look very carefully in good light. No feelings, no fatigue, NOTHING. It's just part of my daily schedule and absolutely no big deal at all so far. That's why I haven't posted.
So far so good! I'll check in after a few more and let you know if anything changes.
Good luck to all the ladies just starting. I hope it is smooth and easy for you!Amy
-
Today is #14 for me and so far, so good. The middle of my chest is a little more pink than the rest and itches a little and the rest looks tan. I am no more tired than I was before and the SE's are much better than chemo was. I am scheduled for 25 and maybe 5 boosts. I will see the doc today and I am going to ask if I will get the boosts or not.
-
Hey Ladies, finally started with rads. Seems like a piece of cake after chemo. My doc said to wait until rads are over before starting tamoxafin. I'm really glad about that and hoping by then more of the chemo SE's will be gone so I can tell what's what with the new drug in the mix.
I am beginning to be able to walk a little farther now and not feeling so weak. Going to do the walking portion of Race For The Cure this weekend in Portland. You going Betsy? I'll be there with a group of gay men on their team called the "chest-nuts".
Summer is hanging on in the Northwest so I want to make the most of it since I was too sick all summer to enjoy much. I hope the rest of you are getting your life back and that things are going well for you during rads. Mary
-
Well, it is official I start my Rad treatment on Monday. I went this morning for the CAT scan, for them to map out everything and avoid any major organs that don't need to get zapped. It wasn't bad, just laid on the table and let the machine do the work. Hopefully radiation is this easy.
Sandy, I like you am just minutes away from my treatment center. I am doing a lunchtime date with my rads. I am nice and close, so that should be perfect and if it doesn't work out I am sure I can switch times.
I also need to go shopping to get lotion and a comfortable bra.
Take care all!
Jen
-
Mary - Love the team name! LOL...I was debating about going to the RFC but don't like the idea of the crowds and frankly none of my friends do it..I didn't want to go alone. I haven't asked my dh. Maybe I'll talk to him tonight about it. Do you want to try to meet up somewhere?
Dragonfly1976- are you still going? I will pm both of you tonight.
I am so glad everyone is doing so well. I agree even with the bit of discomfort I'm feeling...it's a breeze compared to chemo.
Well today is #20...only 13 more to go. They are doing another sim tomorrow for the boosts. I am having 7 boosts.
Got to go to work. Later
Betsy
-
#12 for me today....33 total..7 boosts...just like you Betsy!. I did ask the rad onc. about the boosts. He said that they concentrated only on the high risk area...so that area gets zapped and the rest of the breast does not...he said that this would have less se's than the whole thing getting zapped.
So far, I'm feeling great doing rads....so much better than chemo...I look back at the chemo time and wonder if I could ever do it again..I just don't know! I never really had any side effects from chemo except for losing all my hair but it still was freaky! Right now I have tons of energy, only get a little tired once in a while...the staff at the rads center are awesome...and I'm eating, eating, eating...things are good!
The rad onc always asks me if I have any questions and I really don't..I have to think hard to come up with one..with chem there were a million questions...with rads there just aren't as many issues! Just show up, be zapped, and leave...and keep the area covered and moisturized...easy!!!!
-
Hi all --good to see everyone doing well!!we continue to encourage each other-- today is #r 12 for me too--I am suppposed to get 33 with 5 boosts-- will see dr. today and ask why my wbc went down and what to expect otherwise feeling about the same as everyone else--yes it is so much easier than chemo--I lthink "did I really do that" shows how we do what we have to do and get to the other side-- Hang in all --have a good rest of the week--Laura
-
I just had Rads # 17 today, and I'll put a few details for comparison (for those in the middle of their treatment like me) and for preview (for those in their first and second weeks.) My skin is doing great so far. No jinx, please. It is about 3-4 shades darker, but not bumpy, burned or itchy. I do feel a soreness on the inside, like a deep bruising without anything turning purple; and in the past day or two I have a bit of tenderness over the ribs, just if I press there. I have had about 6 days off and on where I felt tired enough to nap. I've also had about 3-4 days where I felt hyper. It's been mixed throughout. I also took vitamin B-12 some days when I knew I could not rest, and that gave me good energy for the rest of the day. I would recommend that to anyone, especially if you are trying to work through your treatments.
I really benefitted from having the 3-day Labor Day weekend extra day of recovery, so I just asked my doctor if I could have another 3-day weekend. He was fine with that. I think it will revive me and allow me to make it to the end easier. I just don't believe I have to wait til I get open blisters to get a day off. I'm seriously trying to avoid that. Let's see if I can. (Oh yeah, so far have only used some cheap Walmart aloe on my skin, 2-3 times a day.)
My total is 33 Tx, and the last 7 will be boosts. I heard that is pretty easy. My question to all of those ahead of me (or finished) is ARE THE BOOSTS THE PART THAT GIVES THE BAD SKIN-BURN?
-
I just had #11 today. So far very few side effects -- I am very pale so the "suntan" is showing but not much discomfort or pain. I'm tired sometimes -- mostly when I'm sitting or reading -- if I get up and move seems to go away -- but I cannot sleep. Thanks for the Benedryl idea -- killing 2 birds with one stone. Great idea!! I'm using Calendula Gel.
Elimar -- I also thought I would take a 3 day weekend after I was further along. My rad onc said that one day missed here and there doesn't change much -- its when you miss a 4-6 days or a week that isn't good. I travel with my job and while I did take medical leave I asked if I could make a meeting for a day if needed and he said Ok -- not a problem.
I wish I understood better why there are so many different protocols -- seems most people are getting 33 -- I'm getting 30 (25 regular and 5 boosts) I get zapped twice but others get zapped 5 times (think this may be when the nodes are also treated but not sure).
Love that everyone seems to being doing so well further into treatment -- hope I have the same experience.
-
#12 done! This goes alot faster than chemo too!
Not sure why everyone's treatments are different....Lynn..I'm sure if you asked them they would be more than happy to zap you THREE MORE TIMES! Hee Hee!
-
MTG, I am not sure of my exact number of treatments, but it's about the same as you...6 and a half weeks, and I know there's some boosts in there somewhere. I go for #3 in a little while...I feel sleepy today, but I think it's more boredom than tiredness...work is very slow and I am doing 'busy work' and catch up, which is deadly dull, LOL. I am not too far from you, I am in NJ.
-
HI everyone! I had #21 today. After #19 I just didn't seem to rebound after a little nap. I get so tired during the day. My skin is beginning to break down; especially under my arm. The doctor gave me a new cream Biafine (prescription) and I'm going to start doing Domeboro soaks which the doc also recommended. The nurse gave me some non-stick pads to place in my bra and under my arm. All the back and forth movement is making the breakdown under my arm worse and my nipple has been bleeding. I have 7 more regular Txs and then 6 boosts. The nurse said the boosts would be concentrated to the insicion area giving the rest of the breast "a break" . Can't wait. I see a light at the end of this tunnel!
Take care and stay strong.
Chris
-
I think that I will join your September group and leave the August group. I haven't had to have chemo but had two lumpectomies on the L breast for calcifications. Started Tamox on 8/24 and radiation on 8/25. 16 down, 14 to go. So far just slight redness and a little tenderness. I am just using pure aloe right after treatment and again before bed. I am glad to read that most everyone is doing pretty good so far. My treatment center is close to my work and I got the 8 am time slot so I haven't had to miss too much work. I am tired but haven't slept well since starting menopause 2 years ago so it may be that and not the rads.
-
I had treatment #5 today and all is well. I have to admit, I'm not really liking radiation. It's not bad, and I haven't had any SE's yet, but its so impersonal. And I really dislike my treatment time this week. Next week I get to go a bit later, but right now I'm dropping my kids at school and sitting in rush hour traffic trying to get to the hospital by 9:15am, which can be tricky. Next week I'll start later so after I drop off my kids, I can take my morning walk and then drive the 6 miles to treatment without the traffic!
I'm exhausted, but I'm just 2 weeks from finishing chemo and my kids just started school which means getting used to a very busy schedule. All the moms I know from my kids' school are exhausted!
It's so helpful to read about those of you ahead of me. Thanks for posting your updates, it gives me a peek into the future.
Pam
-
I asked my doc today if I would be getting the boosts and he said most likely I will because my skin is doing good so far. The only reason why he wouldn't is if my skin turns really red at the mastectomy scar. I have been using calendula lotion (homeopathic) and my doc is really impressed with it. He looked it up to make sure it is safe to use and he said there is a study about it compared to Biafine and the calendula was better.
Lmflynn...I am getting 25 and then 5 boosts, but I am getting zapped in 5 different places because of my lymph nodes.
-
I finished my rads on August the 7th. I was told that the burns (plus yeast infection under breast) would "worsen" for two weeks. Thought I would not make it through the recovery . Then ther were the flash nerve pains that at times almost took me down ...those are now fading and are referred to as "my tazer going off". My breast has gone from dark brown and red burn spots back to almost white. However my normal DDD is now a D. I am thinking maybe all those shoulder pads from the 80's may come in handy for padding and add protection from the bumps that sometime seem to add a jolt of pain.
I feel I am lucky for the early dianoses but will shoot the next person that says radiation must be a breeze next to chemicals. I have never been so tired in my life. Just when I thnk I am on my way back to normal I fall on my face again. I am giving myself two more months before I hit the panic button. I feel so alone at times and am so glad to find all these comments from gals that understand me. Thank you all for sharing.
-
ccbaby - Interesting what you posted about calendula. Today on my way home from Rads, I picked some up at Whole Foods (Weleda Calendula Ointment), I planned on trying it tonight. Your post makes me feel better. Since I'm allergic to aloe...my choices are limited. Aquaphor doesn't seem to be taking the stinging away or the redness. My breast tissue doesn't really hurt or itch, except under my arm where the stinging can get intense. But still...it's nothing to complain about at least so far. Chemo raised our thresholds for discomfort.
I'm not glad to hear others have problems sleeping but I can relate completely. I have decided to medicate (Ambien) myself through rads. After, I will just deal with the insomnia. But for now...drugs, drugs, drugs. Funny...I use to hate (actually still do) taking drugs but these days I don't hesitate to pop a pill.
Tomorrow, I am scheduled to talk with the onc about my boosts, it should be interesting.
Echosalvaje- I sent you a pm. My dh and I are going to do the walk on Sunday.
-
Hi - today I finished the 16th out of 33 rads (28 plus 5 booster). I will be thrilled that I will be over the hump by this time tomorrow. Also, I was told today that I'll have to have another SIM for the booster due to Seroma that has either shifted or shrunk or something along those lines. I'm pretty pleased that I have no real SE's other than having some of the deepest sleeps in recent memory. I suppose the only new event might be the fact that half way through the day my bra band starts feeling too tight. Is this the same problem that everyone has with the bra and what's the best fix.
-
Mersmom - I know exactly how you feel, at #22 I am wiped out. Today I felt better, but who knows what tomorrow will bring. Sorry to hear you're still going thru it. Do you work? I don't, and I rest most of the time now. But again I do have an autoimmune disease. What does your dr. say? You aren't alone. This is a great place.
-
ljh58 - As ccbaby's doctor told her, there is a study (albeit a small one) that shows that Calendula is more effective than Trolamine, which is the active ingredient in Biafine. For those interested, you can find that study at : http://jco.ascopubs.org/cgi/content/abstract/22/8/1447 or simply google: calendula trolamine, and the Phase III study should come up.
I personally have opted not to use Biafine and am using a combination of : (1) pure aloe (100% or 99% pure w/our coloring or alcohol), (2)calendula and (3) Miaderm. The aloe and calendula are relatively inexpensive, available at health food stores and, based upon what I've read here as well as the above referenced study, should be quite effective. The third one, Miaderm, is probably overkill but in addition to aloe and calendula contains a 3rd active ingredient called sodium hyaluronate. The downside is it's kindof expensive - about $23 a 4 oz tube.
sandy425 - Nice to meet you and have "company" thru this journey. I'm a former Joisey Girl myself, grew up in North Jersey and still have the majority of my family there. I'm thankful there's the ferry to and from; I cant get used to all that driving everyone on your side of the Hudson has to do. I even walk to my rad appointments.
-
Hi MTG...yes, lots of driving here...I grew up on LI where cars are king too! So I'm used to it...I always say you never know how long it will take to get somewhere in NJ, traffic ya know.
I asked the dietician at the hospital about wine, and sent her the article that was being discussed upthread...she was skeptical, and normally recommends that patients avoid alcohol during treatment. I had an experimental glass of wine last night, and have to say I didn't really enjoy it...it seemed like the effects were enhanced, and I just generally did not feel good after I drank it...so I guess I will stay away for now.
I am only 3 days into treatment, and while not exactly fatigued, I am very sleepy...hard to get out of bed in the morning.
-
Thanks MTG for finding the study about calendula. I am going to click and read about it tonight when I get back from work and rads. Like I said, it has been working (so far) for me.
-
Mersmom & Kawee - sorry fatigue has kicked your butt. But please don't be angry or frustrated that any of your sisters are "breezing" through this process. I am tickled pink for them...doing my happy dance...or those damn kick ass cartwheels. I just hope it continues for everyone because obviously things can change over night with this process. Tissue damage is real and painful. Fatigue is real and exhausting. I hope you rebound soon and know that you are not alone.
Has anyone's appetite changed recently? Up until yesterday I had a ravenous appetite, I couldn't get enough food. Today...I'm not hungry at all. I even passed up fresh peach pie last night, I MUST be sick?
ccbaby - do you know the inactive ingredients in your calendula lotion?
-
Sandy425 - Boy have I got a wine alternative for you...any anybody else thinking about doing the glass a day / reservatrol thing !!!! Although I like a good red with the ocassional steak, I rarely eat red meat and so a glass a day isn't so appealing. However, I do like my cocktails and was especially into frozen martinis and margaritas this summer. So....... take a large can of pears in heavy syrup and about an equal portion of red wine, add some ginger juice (or cook some ginger in sugar water or the pear syrup to infuse), blend and freeze. It makes a killer cocktail, or you can eat it as a tasty sorbet. Gorgeous mauve color; great taste. FYI, if it gets too frozen, microwave for a couple of seconds.
-
Betsy...I am using Boiron Calendula lotion and the inactive ingredients are Purified water, PEG 6-32 stearate (and) glycol stearate, octyldodecyl myristate, dimethicone, stearic acid, carbomer, triethanolamine, methylchloroisothiazolinone, methylisothiazolinone
Well, I am exactly half-way through my rad treatments now. I can't wait for the next 3 weeks to go by fast.
-
Betsy--my appetite is weird too-- I have been ravenous since starting rads--and have gained a couple of pounds but trying so hard not to eat everything I want--but seems like what ever I eat i am gaining weight--and i havent started on arimidex ( postmenopausal) yet so scared i will gain --surprised that your appetite has decreased--peach pie yum!!!( you can see i am in trouble) you are about a week ahead of me so I will let you know--right now I am stressed so when I get stressed i eat everything--My daughter is in arizona with 3 little ones and just broke her foot and has to have surgery--she does have a good support system but she has been here for me and now i cant be there for her to help her out--dont want to risk traveling and dont think I have the endurance to do all that she will need plus could only go during the weekend so i dont miss any rads--want to get them over with-- i have 20 more rads to go and dont think I should push it--so I am stressed--anyway let me know what happens with the appetite--hang in there!!Laura
-
Today was tx 21 for me. I'm like you ccbaby...can hardly wait for this to be over. Although, it does sound like the end might be a few weeks out from that final zap. Yesterday, my chest turned a deeper shade of red and my armpit area really started burning. Usually the burn comes and goes but not my luck today. They gave me some topical lidocaine to help. It's one of the first times it hurt holding my arm in the position over my head. I think I need to begin doing my gentle stretches again. At least I don't see any tissue damage..yet. 12 more to go...
I had an interesting visit with my doctor today. They were setting the machine up to target the boost area and I said I was not comfortable with it. The tech had showed me the color picture of where they were going to target yesterday. I said...that's not where the tumor was...why are you doing it there? They stated that's what the doctor indicated. When I said I was uncomfortable...the tech's were totally awesome and said no problem, talk with the doctor, we can do it on Monday. I spoke with the doctor he said he would review the CT scan. He said sometime's it's obvious other times it's not. After reviewing the films he added an inch to the top margin of the boost. He said there was a cloudy area and that by adding the extra area it certainly couldn't hurt. He did explain when you are laying down...the location differs from when you are sitting up. I feel so much better about it now. So...for those of you with boosts ask to see your picture. At least you will know exactly where they are aiming.
Lolly - It's natural to feel helpless regarding your daughter. Thankfully, it sounds like she has good support, but it doesn't make it any easier. Wow...with three little ones my heart goes out to you and your family.
ccbaby - thanks for the info on calendula.
-
Betsy - my appetite too has changed. Food doesn't seem to interest me lately. I even have passed up on ice cream (a personal favorite of mine). I've lost 3 pounds in two weeks. I think being so tired has a lot to do with it.
I'm using the Biafine and non-stick pads under my arm and in my bra. They've really made a difference. No more friction and that's helped a lot. Why is everyone so against the Biafine? I haven't really heard anything bad about it.
Next week I'm starting to take a couple of weeks of medical leave. I'm in a classroom and there really is no down time. The last week has been overwhelming. I am so exhausted especially after noon. My treatments are scheduled to end Oct. 5. I just finished treatment #22.
Sometimes I feel so alone too, but reading and posting here has helped. A lot of people just don't "get it" because they can't see what's wrong. It gets frustrating trying to explain that rads make you tired.
Hope everyone has a great Friday! Take care.
Chris
-
Hey Chris...we have the same ending date! I can hardly wait!
Last night as I was applying aquaphor my husband says you are swollen. Sure enough my surgery breast is about the same size again as my other breast...actually looks slightly larger. Not saying that is good, must mean it's very inflamed inside. I've heard of shrinkage from rads...mersmom referenced it...so I'm sure this is just a temporary situation. I may post that question on another board to find out when the shrinkage happens? Anyone reading this that knows, I'd love to hear from you.
One other thing I forgot to mention. Yesterday while talking with the doctor, I asked if the rads hit my GI system anywhere? Thought that might explain my appetite. He said no. But it is hitting my ribs and lung slightly. Why I didn't ask this question before...I don't know. Maybe I did and I had a chemo moment???
The one thing this entire ordeal has given me is a heightened empathy for people who say they don't feel good or are sick but they look fine. The onc's office is full of people that look that way, but you know they are dealing with mega illness's.
How is everyone doing? All those that had sims..I hope it went well this week. All those fellow radiators...hope you are having few se's.
Betsy
-
Responding to some of the BetsyBuzz issues...
Size - Had slight surgical swelling that lasted 2 whole months (in other words thru' the second week of my rads) then I got almost normal sized for a few days but then got slightly larger again when the rads inflamed the tissue slightly. So I am hoping I "shrink down"a little when rads are done, just so I have a matched set.
G.I. - Had some reflux on the first 2 days of rads. Was told it was my "nerves" over having treatment. Don't think for a minute I bought that one. Now in week four I have noticed it again, where I know I'm making some extra stomach acid. I used Maalox 2-3 times so far. I didn't even mention it to the doctor because he'll deny. He told me the rads are not hitting my esophagus. Whatever. Maybe it is the scatter, but they won't mention that. That is what has put my appetite off the last couple of days.
I'm having a 3-day weekend, at my request. My skin is good, but the soreness and tiredness make me want an extra day of recovery going into the home stretch. I'm glad I didn't have to force the issue--my doctor was just fine with that. (Take note ladies who just FEEL like having an extra day off. Just ask for one!)
Overall, I'm good; just fearing the boosts will burn me. That's not for a couple weeks, but I will tell that tale when the time comes. Have a restful weekend everyone.
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