Fall Rads 2014
I've been patiently waiting for someone to start this thread. LOL. Then decided I'd go ahead and do it. :-)
I just finished chemo. My simulation is 8/26 and I will most likely start rads September 1.
If you just started rads, will be starting rads this fall or are lurking in preparation for Winter rads, jump in and introduce yourself.
Comments
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My last chemo is next Monday. Then short break and I'll be starting radiation. I think Im more nervous to start radiation than I was the chemo or BMX. Good luck with your radiation. You will be slightly ahead of me so please keep me posted. How many rounds do you have to have?
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Hi writinghelps and thanks for starting the Fall 2014 thread!
For you, and all who join you throughout the season, here's some helpful info on the main Breastcancer.org site on Radiation Therapy, includinginfo on types of radiation therapy, what to expect during the process, and how to manage side effects.Also, the Treatment Side Effects section is a great resource for tips to help manage any side effects you may experience.
You may also find it helpful to read the Summer 2014 Radiation thread, for more tips and tricks from others who've been there!
Hope this helps!
--Your Mods -
Hi Cceandme and the Moderators,
Good luck on your last chemo Cceandme.
I think I am also more nervous about rads than I was with chemo or surgery. I wonder if it's because we're tender, emotionally and physically, and so very gun shy at this point. I have no idea how many rounds I am having which is sort of unusual for me because I am usually on top of things. The RO may have told me but I didn't hear it. It may be because I am so worried. I hope the first few weeks are as uneventful as they promise. I could use the weeks to recover mentally and be ready for the discomfort toward the end.
Thanks Moderators for the links.
Peace,
Wendy
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Hello all!
I met with my RO yesterday. Will be having set up/sim tomorrow with rads to start Aug 25. As most of my rads will be in Sept decided to join this group rather than the summer group :-)
This is the second RO I had a consult with. Turns out that even though the first one I met with was part of my insurance network, his facility was not! Everyone sort of goes "what?" When they hear that, but there it is. Would have cost a small fortune to continue with him even though he came highly recommended and I personally know 3 people that had their rads with him. Plus he was part of my hospital network so he had access to all of my records.
The new RO is super nice and is actually a little closer which will be better for the daily rads. However, she is not part of the hospital network, so I will have to make sure everyone gets copies of records. Already I found out that even though she got the report of the PET scan I had before chemo, she didn't get the actual images. Picking that up today and will bring it to her office.
Looking forward to "meeting" everyone else starting this next phase of this journey that no one wants to be on! And here's hoping for minimal SE for everyone!
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Hi MakeLemonade,Welcome.
I know you from the April Chemo board. I introduced myself once but mostly lurked. I am more of a regular poster on the May chemo board.
I had a similar thing with insurance related to chemo. The facility where I got my chemo infusions done is in-network but their pharmacy was not. This made my nuelasta shot co pay around $500. I switched to mail order CVS and copay was $35! Insurance is crazy sh*t.
Anyway, glad you like your new RO. Let us know how it goes. So far you are first up. I have my sim on 8/26.
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Hi all! I had my initial Rads consult on 8/4. I have my simulation tomorrow (8/14) and my set up on 8/25. Start rads on 8/26. I will be having 25 whole breast and 5 boost. 30 treatments total over 6 weeks. Happy to be done with chemo and glad to be starting the next phase. One step closer to being done!
My RO suggesting getting a 100% cotton bra slightly larger than I would normally wear (to accommodate any swelling). Does anyone have any recommendations? The wire free bras I've been wearing post surgery and thought were cotton are actually 95% nylon and 5% spandex!
Good luck to everyone!
-Tina
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I was also wondering about bras. I will be apparently be going over suggested soaps, creams etc with the nurse AT LENGTH tomorrow or at the dry run :-) but I was given some paperwork and that suggested cotton bras. Mine also are not 100% cotton.
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Hi Wendy, and thanks for the welcome!
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Going for my second consult with RO next Friday. We will decide how much to radiate. She said sometimes they go higher than breast as well as breast but my breast surgeon thinks that's not necessary. I was on the fence about even doing rads do I'm thinking I will stick with minimum recommended. I have tissue expanders so very worried about still being able to do implants after rads. pS said depends on damage done but RO said they do a vitamin E regimen that really helps. Not sure the details yet. I know I'll have 6 weeks of Monday through Friday which seems to be pretty average.
Good luck ladies.
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Hello everyone! Hello again to my April Chemo board friends, MakeLemonade & writinghelps!I just finished chemo yesterday (Aug 13) and am meeting my RO tomorrow morning for a consultation. I am scared about rads because mostly I worry about potential heart and lung damage. I'm hoping that doesn't happen. Skin burns and fatigue should go away with time, so I'm not as worried about those. I'm also worried about cording, since I have that right now and I hear rads make it worse. Plus, I don't know if I can lift my arm high enough for the rads treatments! Will be seeing a PT for help soon. Waiting for a call back.
Cceandme: I also have TEs and am hoping after rads, my PS can make me look good.
My PS waits 6 months after rads are done to make sure all the tissue/skin has achieved "steady-state" on healing. That way, she will only need to do the exchange and tissue shaping surgery once.
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Hi MommyQ!
I have met with two RO's now ... they do say that the upper corner of the lung usually gets hit, however, we don't tend to use that part and shouldn't really notice if there is damage.
They do try to not involve the heart in any way. My BC was in my left breast so am a wee bit concerned but do trust my doctors to do the best.
I had a lumpectomy, so don't have to worry about that part. My hospital also has lymphedema physical therapists on staff and provide a free consult to discuss LE. I have gone twice since then and she was able to get almost all of my range of motion back by breaking up any remaining cording and doing a lot of stretching. I will also be going during radiation as she can then ensure the lymph is moving even though she won't be able to do a lot of massage on the part that will be radiated.
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Thought I was starting rads on the 25th, but it will be on the 27th. Then daily until done. And can you believe it, I forgot to ask how many treatments! Chemo brain ;-)
First they made a mold for me to lay down on ...will be used throughout testament. Then RO came in to put wires around the whole area to be radiated. Then had the CT scan. Apparently, she got what she needed, so didn't have to do that twice. Then the tech took off the wires and I got four pin point tattoos. They pinched, really nothing more.
Then I was free to go! Took maybe 40 minutes. Dry run and first treatment will be on Aug 27 - that one will take 1-1/2 hours but the daily treatments after that will only take 15 minutes. They need the time in between to develop the specifics of the treatment. I guess exactly where each beam goes and for how long.
Nurse told me to hydrate, hydrate, hydrate - inside and out :-). The more you hydrate, the longer it takes for the skin to dry out. Drink plenty of fluids, moisturize 3 to 4 times per day. Can not over moisturize :-)
So, now I get 2 more weeks to recover from the last chemo last week. Will be strange to not have to go anywhere for two weeks :-)
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Happy to see a fall board... had my sim today - had to make two molds...the first one wasn't right, so uncomfortable. I got seven tattoos...pinch, sting, pinch sting... could be worse I suppose. Dry run on 9/5 and then I start on 9/8. 25 treatments, no boosts.
Looking forward to this little break in between - feeling somewhat normal having finished taxol on 8/4. Need to get my stamina back up and need to LOSE some WEIGHT!~
catch up soon.
Jen
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MakeLemondade- I post the bra question on the Summer Rads thread and feedback I received was to look into BestForm front closure sport cotton bras (sold at Kmart) and Bali bras. I know Macy's sells Bali. Also, your simulation sounds exactly like how mine went.
Jenwith4kids- I also finished Taxol on 8/4 and also had my simulation today! I was hoping to start Rads after Labor Day (for a solid 4 weeks off) but RO said she could start me last week in August. I have 7 tattoos as well! Are you the one who told me they were at Morristown for treatment?
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MakeLemonade: My BC was left breast too, which is why I am worried about heart damage. I sure hope my anatomy allows them to shoot the beams away from my heart. I had looked into proton therapy, which has beams that can be controlled to stop before hitting the heart, but my insurance wouldn't cover it.
I'm glad to hear the part of our lung which will get hit doesn't do anything, LOL, so we don't have to worry about it!
I'm glad to hear that a PT can break up cording. Thanks for the run down on the setup appointment. I didn't realize there'd be a CT scan. Enjoy your two weeks away from the hospital!
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cmp, I was at Morristown for surgery and chemo but I'm doing rads at MSK in Basking Ridge. I wonder if we crossed paths today?
I could have started last week in August, but I'm having my ovaries out so i am starting 9/8.
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I had my lumpectomy July 30 and am still waiting to meet with my RO. I have to go back to my BS on Tuesday to remove stitches and they did tell me when I got my drain out that I had some margins that were not clean so I have to go back for more surgery. I assume due to this I will start Rad in Sept or late Aug. I too am worried about heart and lung zapping as mine is on the left as well. My PCP has me seeing a Pulmonologist to be on the safe side because of my Asthma and the fact that I have had Chronic Bronchitis now for the past 3 months and am having trouble getting over it.
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Jenwith4kids- We might have crossed paths! I was there (on 2nd floor) for a 10:30 appt. I'm seeing Dr. Schupak. I still don't know what time my schedule will be but maybe at some point we will be there at the same time! Have a great weekend!
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my appointment was at 9:30....also dr. schupak. Bob and Ava did my sim. I asked for first thing in the am appointments, I got 8:00 and 8:15 for most of them, starting 9/8.
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I met my RO yesterday. He was very nice and explained how everything was going to work and answered our questions. I will have 33 treatments total. I will go back week after next for the CT scan/simulation, where they'll use the wires to map out radiation areas. Then, on the dry run, they'll use permanent markers to mark reference points. He said they don't do tattoos anymore unless patients specifically request it. I'll go for the markers. Less painful and not permanent. Like MakeLemonade's ROs said, they will clip a part of the lung, but it shouldn't cause any problems. He said that now that they can map out our anatomy with the CT scans, they are better at directing radiation away from the heart and lungs. There is a very small chance of radiation causing asthma, but I think he said it was really rare, and if it happens, he can treat me with meds and it'd be temporary. And he also said that there is slight potential the heart could be affected but it's not anything that would make me die at a younger age. I guess I just have to go through with it and hope for minimal problems.
On the 25th, I go to my PT to get help on getting rid of this cording so I can be more comfortable during the radiation treatments.
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Not to sound solly but what is cording
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Starting radiation on Wednesday. Facility location stinks because it is way, way across town, but I'll deal...I'll have to! Hope it all goes well. Glad someone started this thread. Good luck to all of you!
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Hi all!
So glad to see someone started this thread. DH was just asking me today if I knew anything about how difficult rads might be for me. I have two more rounds of Taxol to go, then done with chemo! I met with my RO months ago, but don't remember too much about his plan for me. But I'm supposed to start rads in September.
I see MommyQ and MakeLemonade on here from April chemo group. Hi!
I'm looking forward to finishing chemo, but a little nervous about having to do rads. Next week I see my BS and PS before starting this next phase of treatment. I will be checking in here for info and tips from all who start before me.
Wishing you all well, lilyrose
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I went in for SIMs last week, and begin radiation this Wednesday. Because my breast cancer is now in the spine, femur, and sterum area, I will be radiated from top to femur. Only 14 days! They also made a mask for my head in case I have to have my head radiated. My oncologist expects my cancer to be everywhere. There are areas that they are ignoring. Don't get it.
At this point, it is pointless to worry about a lot; except I would like to keep my brain in tact. I had a brain mri Friday...trusting God my brain is cancer free. I have no idea what I'm going to feel like after full body rads...drinks lots of water. They said no vitamin e's, D's, or anixoitants. -
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Hello ladies, I have had 2 of my 4 TC chemos following my lumpectomy and oncotype 27. So, assuming no chemo delays, my last chemo would be Sep 18. How long did you guys have to wait between last chemo and start of radiation? I'm guessing I'd maybe start the second week of Oct?
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hi Ladies.
Thought I'd join in here as well. I finished dose dense AC-T chemo on 8/7. I head into RO for sim on the 19th with chemo start date 9/2. I expect 33 tx (28 +5 boosts). My RO's office indicated rads couldn't start until 3 weeks post last chemo.
I am nervous about rads as I'm told 50% of women then need to have additional tissue taken from back or abdomen for their final exchange surgery. I feel strong enough to get through short term skin issues but am concerned with long term cosmetic results as I start to think about moving forward.
I've heard hydration is key so I'll return to the 3 liters of water per day.
Wishing each of you lovely, strong women good health.
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Hi Everyone. I finish Taxol on Sept 5th and I guess sometime after that I start rads. Can't believe things are actually moving along. One Lump I have to go on the other side of Orlando which is about a 30 min drive with about $6 in tolls. Then it will be a long drive down I-4 to my job (another 30-40 min). I may ask for a referral closer to me.
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Thank you for the link Wendy that helped. I go to my BS Tuesday to see when my re-excision is and when I start Radiation. Hopefully it will be scheduled soon.
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Puffin, Good to see you on this thread! I didn't know whether to post here or on the Summer Rad thread, but this one is shorter. I think the timing to begin rads following chemo varies widely. My MO was thinking 3 weeks (which was quick for her), but my RO said I could start only two weeks PFC. I had the simulation set up appointment and a "test run" beforehand, and my first radiation treatment was August 7, two weeks to the day from last Taxol. The simulation appointment was much easier than I expected and the 5 pinpoint permanent tattoos were not in the least painful. I feel good about getting started on the final stage of my treatment! I see my RO after every Monday's rad. I expect to be done around September 23. So far, no problems, but then didn't expect any this early. A while ago, I had an lymphedema education session with an LE PT specialist. Baseline measurements were taken of each arm and hand. She recommends that I get fitted for an LE sleeve and glove and that I wear them whenever I fly. My first flight will be in Oct to go to Disney World with two granddaughters. I'm getting the sleeve fitting tomorrow, so I'll have it in plenty of time. I have no signs of LE so far, but it was good to know how to avoid (as much as you can) and what to look out for. I already had some nice looser nylon non-underwire bras, but before I go any further in treatment, I found some 95% cotton sports bras at Walmart at a bargain price - 2 for $10.95. Cotton is preferred as being kinder to the radiated breast.
Good luck to all of us as we begin our treatments.
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