Spring 2014 Rads
Comments
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Hi everyone! Thank you all so much for the congrats on finishing my tx! You all will get there, I promise
My skin is slowly getting less itchy and peeling. Nipple is almost all peeled over and that was the worst. Now slight peeling under my arm and under my boob. They told me not to shave or use deodorant for another week, but we have had 80* weather this weekend, so I put deodorant on the top part on my armpit. You can see the definitive line of red, so I figured half of a non-smelly armpit is better than nothing.
I am still battling the fatigue and my lyme dr wouldn't clear me to go back to work. I can consider it in 3 weeks if I am feeling better. My blood work, WBC's especially are really "off" and she wants me on some good supps to bring that back up. I also asked her about Vit D, since I have read that it can help inflammation. She said that there is a big controversy that Vit D can actually *cause* inflammation. Something about the ratio of D-D3 and you need a specific blood test to see where that is at. Since Lyme and cancer are connected to inflammation, she is running that test on me. If I find anything else out, I will let you all know.
Sweet puppy! I am going through puppy-cravings like some women go through baby cravings.
Red- That sounds like a meal my Italian-Am. mom would cook too.
Lisa -- good luck balancing work and rads. Its hard to do (at least for me!) but you have to put your health first.
Hope everyone has a very happy day!
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Hi All,
Just checking in. I have 4 more boosts to go and my skin is holding up amazingly well. On Friday morning, I woke up with a stomach ache. It turned into a small bowel obstruction. I have had them before (I have a lot of adhesions from a prior abdominal surgery). I could tell I needed to be hospitalized, so I went to rads first and asked them if they could take me early. They took me right in. Then I went to ER, next door. They admitted me in a heartbeat. They are amazingly fast with cancer patients with complications. They put in an NG tube which I HATE but needed desparately. The obstruction finally started to resolve itself Saturday night and by Sunday afternoon, I was home again. It will be another week or so before all the tenderness is gone from the obstruction.
Funny thing, I didn't even think about my skin all weekend. I was in so much pain from the NG tube and the obstruction. I didn't put any lotion on or anything and my skin is fine! My boosts cover my nipple, but I'm hoping it won't be too sore. By Thursday, I'll be done. Almost 9 months from the time I started treatment until the time it's done. It's been a long road.
Hugs,
Kay
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Good for you Phebe! I am half way through rads. Like you I have Herceptin... to go til last week in Nov.
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intothewoods- I agree that sounds early for redness----could you be reacting to your crème? Ask a nurse to look at it when you go for treatment. I started getting red blotches on my 3rd WEEK. Make sure you are covering the entire area generously---clear up to your clavicle if you are not being treated ABOVE the clavicle. Someone else said that we break out where we have had prior sun damage. that would be consistent for me. the area of my red bumps is where the sun would always get me first., although now it is spreading over to my underarm area, where it was never sun exposed!
Phebe---good for you. You are closer to the end than me! How is your skin holding up? are you doing boosts?
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Happy Mon
Phebe & VintageGirl- like you I am on Herceptin every three weeks. I have a question: do you start counting the year from when you started full chemo, or from when you started just the Herceptin? I never thought to ask.
I have 7 full tx's and 5 boosts left. I am very red, but not too much pain-I think because I have very little feeling there since the surgery. It looks like I should be screaming with pain, but I haven't even needed an Advil yet. Now that I've actually said that, I am sure I will be in agony shortly.
I am surprised at my family's reaction to the radiation. When I show them how red it is, or when I come home complaining that I was on the table for 40 minutes and my arms are hurting (which I don't do very often), their response is universal- "yeah,Mom, but it will be over soon." I know it will be over soon- that doesn't mean my feelings and discomfort are any less real. They were great thru the chemo and surgery, I don't know if they've had enough of me being sick or what. I am so glad to have all of you to listen.
Anne
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Anne
I started A&C end of Sept, for 2 months. Taxol & Herceptin started right before Thanksgiving so my year of Herceptin will be up end of Nov. Port can finally be out in Dec if all goes according to plan!
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Our radiation machine broke! Today's appointment is cancelled! That means another day is added in my treatment. I really don't want that!
16 + 5 boost remaining out of 30 rad tx.
Skin is okay, so far so good!
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Just finished 23 of 33. Bit itchy so RO recommened hydrocortisone 1%. Seems to help a bit.I'm using the pure aloe several times a day and lots of cornstarch too.
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I am on #29 today. 2 more boosts. Will be done on Wed. I feel like my breast is starting to heal. Less redness, less itching, less heat, less soreness and nipple sensitivity! WHOO-HOO. Will see RO on Wed and I hope he has good news so I can go see my MO for my HT.
Hang in there ladies, the end is in sight.
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Simple-hope you are feeling better today! I have 7 more rads to do then finished! No boosts for me as I had a mastectomy. I saw PS today to see how my skin was holding up, he was very impressed how well my skin looked and how soft it was. He gave the ok to schedule reconstruction about 6 weeks after I finish rads but I will wait and enjoy my summer. I will try and schedule middle of August. Good luck with rads and happy to see so many of you have finished!
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Thanks, Redheaded1 I just returned from tx and saw an RO at the center . He said it was a little early for redness and also mentioned hydrocortisone for itching. I told him I was using the 100% aloe 3 x a day and he said maybe it was too much. I am a bit of "if a little is good more is better" kind of person and have been heaping it all over. He said we can have reactions from whatever we are using so I might switch to calendula cream if easing up on the aloe doesn't help. My red area was also consistent with where I have sun damage but I was glad to hear RO say that how we react to the sun has no connection to how we will react to the rad. Seems counter-intuitive.
Puppy cravings! I get them every time I see a chihuahua- puppy or not. I am obsessed with chihuahuas. My little guy now is a chihuahua-whippet mix.
Nice to hear the encouraging words from those farther along.
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intothewood get some Epson salts and use just on that area twice a day w warm water. Take washcloth dip and lay on area. Helps to calm and heal also real aloe plant gel. Good luck hope it works for you.
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keep the faith you are almost there!!! I am doing great saw the onc today. He said enjoy your summer see you in three months and we will run blood work and mammo. Glad to get the break. Feeling good getting energy back. No peeling just sunburn feel healing each day. Yey! No blood work because it wouldn't be accurate due to rads.
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I am in the home stretch... tomorrow I start 1/5 boosts! I will be glad to be done with this leg of the journey.
Keep on Kickin A$$!
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flagirl I'll try the epsom salts. thanks for the suggestion. Good to hear you are getting energy back and let us know how your visits with Pip go!
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hi everyone: I start counting herceptin even when it's mixed with taxotere so I'll be done December 15. Next treatment May 20th. Three more radiation then I'm done. I did 22/25 no boosts. Skin is very red but not peeling. I notice something very funny. I used to have a bit of hair growing on my face before, today I notice I have a little bit of hair on my face lol and very tiny black hair sticking out from my head lol like a brush cut
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Travel Mom---I will be glad to be done too--- I have 6 more (no boosts) so if everything stays on track, I am done next Tuesday. Dreading the Arimidex.
FlaGirl-how long after you stopped rads before your energy returned? Did you get any warnings about sun exposure, etc. Does the Arimidex cause any issues for you? I would like to be in your shoes.
Phebe- you mean you have less hair on your face than you did? That would be good for me, ever since my surgical menopause I been thinking I needed to wax my face.....LOL.
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Anne- hope you are feeling a little better today! I sometimes feel like I can't or really shouldn't complain. One of my sisters went through multiple surgeries and chemo as a young widow with three young kids, my other sister really did well with one surgery and radiation, and my husband's mother battled breast cancer twice and passed away at 43. And I am going to complain? I consider myself very lucky but that doesn't mean my skin feels any less sore or my body doesn't feel a little fatigued keeping up with all we do in every day. I am grateful and I know others have so much more to deal with but I can not wait to be done. So I am also thankful to have the support of the group. I am sure your family appreciates what a strong lady you are. It is frustrating for families, too. I just had 24 of 25 whole breast and will start 8 boosts Thursday and my husband keeps saying almost done. If he could take my last 9 treatments he would but I doubt my RO would go for that!intothewoods- all our doctors seem to say different things but mine said areas where skin sun damaged may react differently to radiation. Not so much how you react to sun=reaction to radiation. I have had several treatments at dermatologist for precancerous areas and my upper chest-where skin exposed by bathing suit-reacted similarly to radiation. Good news radiation will knock out most areas that may have needed superficial treatment later.That area is less bothersome now more redness in armpit and areas not exposed to sun so it did clear up but was itchy early on. Wishing you well!
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Down to the wire and the RO office calls to tell me machine is down due to last nights T-storms! UGH!
Only 2 TX's left! I am grateful that she called before I left the house and wasted my time and gas for nothing, though!
flagirl, good for you!
have2laugh, I know what you mean; I too am grateful that I have not had to endure as much as many others, but will still be glad to get to the other side. You're exactly right; being grateful does not diminish the SE's, pain and anguish that we feel as we go through our own battle. But we understand and you can always come here to "complain"!
It looks like a few of us will be done this week! Let's PAR-TAY!
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Have4laugh and other girls,
when a woman is in labor, it is painful and even if millions of women from ages had gone thru' this pain, it is still her pain, unbearable, and difficult. it is not less due to the fact that other women had gone thru' and going thru'. So, vent and speak your mind.
I have similar situation at home. Some family members lost interest in how am I doing each day. Just giving hug, asking simple question can be helpful, feels better, but it's routine for them. While I was talking to my friend, I just mention that I feel guilty now when I complain. And he gave me above analogy. And it is true! Isn't it?
Sometimes, I get spasm and can't stand it. And it is painful. So, I am going to say it is painful without caring about anybody's reaction.
So, vent here. Hang in there, be strong!
This too shall pass......
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hi gals, just jumping in since I too will be starting Rads in the next week or so. Read through the earlier post and seems like a lot of you are all done or nearly done, wonderful for you all. Hope you are all healing.
I see a few of my Dec sisters here also. I had my initial consult back in Dec and really forgot most of what he said. I go for RO visit,CT and simulation on Thursday. Was told to expect to be there a little over 2 hours. Dry run the next week and not sure when the actual start will be. It will be 3 weeks PF'ingC on the 22 th. Would be nice to start before Mem Day and get a 3 day weekend.
Really not sure what to expect. I did well through chemo and hope theRT goes as smoothly. Not much choice for me getting it. Good to get all the tips you have shared.
Barbara
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keepthefaith- good for you almost done! Sorry the machine is down-I am sure you just want to get to the end of treatment. I missed one day to something similar so I finish on a Monday instead of Friday if all stays on schedule. I told my tech today I started off jokingly referring to radiation as "going to the rotisserie" but now it's not so funny! They are so nice where I go I can't say enough good things. I will miss the staff when done but not the process or the time out of each day.Hope you have some plans to celebrate this weekend!
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Redheaded1 Hang in there you are almost done! I am still a little pink and kinda raw on the underside fold area. No peeling tho just slight itching. I have been pretty busy today the energy level is back, and I'm loving it. The fatigue kicked my butt the first weekend after finishing, but the Monday after that (yesterday), my energy level started to pick up. The Armidex isn't too bad for me had some flashes and night sweats in the beginning but it has lessened somewhat. I take it in the evening because it made me sleepy in the beginning so I take at 630 pm. No sun in the beginning especially on the breast. I was told to get a UV protected shirt to wear if I am going to be out for any length of time in the direct sun. Going to celebrate this weekend so I am holding off the diet til Monday. NO, really I gained ten lbs but lost a lot of muscle. Gotta get back on the bike... I have more projects to do than I have energy for but all in good time. You can have 1-2 glasses of wine or beers while on Armidex but no liquor. My boobs have shrunk so I guess it's working to suppress the estrogen levels. Good luck, you will be done before you know it and back to a new normal life. YIPEE hugs
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Hi everyone ,
Welcome Barbara. I am down to single digits! 4 more reg, then 5 boosts. The machine better not break down- I have my final boost at 8am, Wed, May 28th, then I am on a plane home that afternoon at 1:10 to be a GS's graduation from preschool that night.
I went to my PCP this morning about pain in upper left arm. She sent me for X-rays. After all the signing in, etc, and waiting about a half hour, they told me Dr forgot to specify which shoulder, and she was closed for lunch, so I would have to come back after 2. This was about 12:30. I am at least a30 min drive, so couldn't see the sense in coming home for 45 min. I ended up going to 2 banks, a health food store (for pure aloe , which my RO says not to use until I am finished with tx) then sat in the parking lot for 40 min. reading. Had rads, then had to go back to hospital for X-rays. I am exhausted.
Hope you all have a great night
Anne
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Anneb1149 so sorry you had to go through all that. It gets pretty exhausting towards the end so anything "extra" seems difficult at this point. The boosts are easy so don't sweat that part. You are almost there and then you will have a great time with your family. Just pace yourself, I was really fatigued that wkend following last one and gave into it. I recovered by Monday and today is even better. ENJOY your trip!
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Thanks Flagirl.
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Anneb1149 I hope you get some good rest tonight. The preschool graduation will be awesome! Guaranteed. We have a "kinderbration' at my school and I was just reminded about last year and one of my favorite kids. Each child was telling the audience what they wanted to be when they grow up and this particular student said he wanted to be a dog. I think he is brilliant now- dogs are really good at living in the moment. And they take lots of naps!
have2laugh, thanks for sharing your experience and the upside (besides the obvious) to radiation. I agree- can be both grateful and miserable. Not mutually exclusive.
Welcome, Barbara. I'm just 7/27 and I hope i can be of help to you as these great ladies have been for me.
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Today was #15 of 31. Tomorrow I will have crossed the half way mark. Itching and burning started on #13. Today it is really bad. Worries me that it is so bad now and I have 3 more weeks to go. How bad will it look then? Tomorrow I begin infusions for the HER2+. My cancer is DCIS with three 1mm each micro invasive spots. Too big for the DCIS HER2+ study with Herceptin, yet too small for chemo + Herceptin routine. I'll be doing 4 infusions 3 weeks apart.
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welcome motherofone: I do have been taking herceptin every three weeks. Good luck in your recovery. Hope you get better on your radiation area. I have two more treatments and I'm done
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Flagirl, thanks for the words of encouragement and a glimpse into the post rad experience!
Have to laugh----love the rotisserie---I call it the microwave.
Anneb- UGH- Doctors Offices----I don't suppose you could have some early lymphedema could you? I worked in my garden (surgery on left) and weeded, putting my left arm down to support me while I used my right hand. Later my neck hurt then the whole arm, and I had some numbness when I went for rads on Monday. I tried to see our Breast Navigator to see if she would measure my arm for me, but she was out. Now it seems better, but I still wake up with it sore every morning. Let us know what you find out. The whole Lymphedema lecture just gave me the willies. I need to MULCH but we have had so much rain, I will have to weed again.....I will be really upset if the C wreaks my favorite hobby. This garden gal is not a candidate for condo living or outsourcing the yard work.
Motherofone---what has your RO suggested to help with itching/burning? Many of us were told Benadryl, Hydrocortisone, or pure Aloe. My RO says only 2x a day for them. I also took a Benadryl tablet one night when the itching was really bad. I slept like a baby....You might try a different moisturizer too, if they will let you. The Calendula crème is nice and I hear good things about Miaderm. I tried to avoid Aquaphor, but over a long weekend, I did use it on whole area and I thought it improved things. I apply mine 3X a day----after treatment, at bedtime and then again early a.m. (I go to rads at 1pm, nothing closer than 4 hours ) I am a fair redhead who burns blisters peels, freckles and then starts all over in the sun. they say Rads isn't like the sun, but its our closest comparison---Hope things get better for you. I pray for this group when I get my treatment-so today I wil have your name in my heart at 1pm. Healing for all and thanks given for how you have each helped me. Love you all!OH- ps. I got my tattoo yesterday---didn't hurt at all. Wish they had just done them during Simulation like I thought. I still have two stickers on.
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