Summer 2015 Rads
Comments
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I will join in as well. I just started rads this week. So far my only complaint is my shoulders hurting but that is being aggravated by a SE to an antibiotic. Hoping to sail through this part of treatment.
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Hi everybody! I'm going to join you here in your radiation group! I found my November chemo crew to be a great help. I just had my simulation done yesterday and will start radiation on Tuesday. I had my lumpectomy and axillary node dissection on April 17. I'm still having some trouble moving my arm and so the position for radiation was quite a stretch and quite uncomfortable. I start PT soon and hope that will help (even though I've been stretching a lot on my own already and have made great progress!)
Girls in my local support group all recommend miaderm. I bought a tube and then someone gave me an extra tube she had. It has the calendula, aloe vera, and something else that I'm blanking on (chemobrain!) and is water based. It smells nice too. It is quite expensive but I'm worth it!!! They all tell me that their skin did great until the last week or so.
Here is my issue: I have one day that I cannot do the rads because I've been working on team with the state department of education for TWO years to revise a document and we have a team meeting to finish it. And, of course, this coming Monday and a Monday in July are holidays that the office is closed. I really, really want to go to Hawaii with my husband in mid-July. That would mean I could only fit in 32 of 33 appointments. UGH. Should I buy tickets? I know from everything else in this journey that nothing ever goes as planned and there will probably be other days where the machine doesn't work or something. I will discuss with RO on Tuesday but I don't know. Can they increase the dose slightly on other days to make up for the missed day?
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My RO said that if you miss a date, they tack it into the end of treatment. They don't want to do too many of these, but they can accommodate.
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I will also be going to Radiation Summer camp but have a conference for 4 days end of June. Hope I can start after if I can't interrupt.
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ksusan, I don't want to add onto the end because that is the week of the proposed Hawaii trip. So, would they skip a week and then do one more when I got back? Or can they up the dosage earlier on for a couple of days to make up for it? I don't really know how this part works. I will talk to the RO on Tuesday
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I was told those weren't options, but your plan and RO may differ. It surprises me there aren't Saturday clinics.
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I've also heard skipping a week is a no-no. I hope you can work something out. Missing Hawaii would make me hate this mess even more.
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There might be a Weekend clinic you could go to at some point??? I remember them saying something about that if there was a Holiday or something that came up, that people on that day would just come in on a weekend... but maybe they only do that for a group of people...???
But I would think that there should be some sort of contingency for things like that, since they are just bound to happen, right? I mean, people can have some sort of emergency come up and not be able to make one of the days...
Anyway--good luck in sorting that out! I'd be ticked off about missing a trip to Hawaii, too!
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The final verdict is in. No Hawaii! RO said she absolutely would not buy tickets as it is likely I will have a few days here and there with delays, making end date later Also, she doesn't want me in sun until a month after treatment (goodbye summer!). Oh well. I'll find something else fun to do instead! And on a more "on topic" note, I had my first radiation session today. Super quick and easy. I hope they all go that well. I also lucked out because a friend who just finished radiation had an extra tube of miaderm she didn't need. so I didn't have to buy it. What type of lotions/creams are others using?
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Hi all, I would like to join this radiation summer camp as well, I'm part of the March chemo group and I have my first dose of rads tomorrow. Looks like we'll be shade seeking together this summer, sad to hear about those of you who have to miss out on swimming pools and vacations. I dont know about you but the Netflix binging is getting old and I know I'll be missing some camping adventures-my summer activity of choice- and living in Oregon there are so many beautiful camping spots! Anyway, I'm sure we can get each other through this with encouragement and venting opportunities! Viva la rads!
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welcome slothabouttown. I'm in this group but will be on the later end. I have one more chemo next week. Then a month off to prepare for rads. I'll get 33 tx so not looking forward to this at all.
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I sloth. I hear you about netflix. Was so looking forward to playing with my granddaughter age 2 in the pool .:0 (. Luckily living in Maine I am close to lakes and beaches. Just need to cover up!
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Down to 2 more rads for me. That section under my arm is getting pretty dark and sensitive. I am trying to keep my arm off of it now but maybe should have been more aware of it early on. I didn't even think of it until it hurt. I use a pillow at night to lay my arm on so it isn't against my side. The heat doesn't help it either but once rads are complete I will dust it with cornstarch. I read here on this website that is a good option. It will definitely be a shade seeking summer this year - Tamoxifen is a big reason too unfortunately.
Wendy
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Wendy, you must be so excited about finishing this week. What will you do with yourself now?!
Are the blisters on your feet all healed?
Please let these gals see a photo of your precious Bailey.
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6 down, 19 to go. And I found out I won't have any boosts. WOOHOO!! Today I felt like under my arm felt a little sunburned. Not bad, just a little touchy. Hoping it isn't a sign of things to come. Today also seemed to take forever, but it was an xray day, and I also coughed hard enough that I moved and they had to reposition me. Oops!
Here's hoping we all sail through treatment!
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Sweethope, I am totally excited to be done with TX this week!! Time to heal and get stronger. I am so lucky to have the puppy as she is good company and she gets me moving! Here's a picture from today! She is growing up fast - 3 months old now.
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Valentine99 - that's great that you won't have to do boosts! If you are noticing tenderness already under the arm, try to keep your arm from rubbing there as much as possible. I'm sure my neighbours thinks I'm quite the sight as I walk my puppy around the neighbourhood with my hand on my hip! LOL
Hear Hear to sailing through treatment for us all!
Wendy
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I met with the RO today and she said I will likely only have to do 4 weeks (3 weeks whole breast plus a week of boosts). She said they have lots of studies with 12 years of data that shows the same results as the longer course, and the most recent data shows it is maybe even a little better. I won't start until mid-June, though.
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hi all, I'm starting rads probably mid June too. I'm slated for 25 with concurrent boosts at the end of each session. Hoping to walk home the two miles after each treatment. Sims appt on June 9. I was Dx while pregnant with my second set of twins. I have four little ones now, three and under. Hoping that the fatigue isn't too bad during rads. I'm just nine days post my re-excision, and feeling pretty tired. Starting to read through the spring rads board to get some pointers.
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Monday is my start date for radiation 😓 so hopefully this is the last piece so I. can just get out of this cancer circle. No offense ladies😇 ...
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No offense taken but Last piece? Not joining the endocrine therapy party ?
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oh I forgot about that....
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we are in this together !
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thanks, yes we are. It's hard as I have felt really good since my surgery. Now back in the saddle and not knowing what I'm going to feel like with radiation.
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Gatomal, 2 sets of twins! I have one set and can't imagine 2. I was tired just from them in the beginning. I hope you have some help. I have gotten really tired already from the rads . It can hit you pretty fast.
Frefluterb, good luck as you start rads. Hopefully it will be easy for you.
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Gatomal -- wow, a second set of twins! That's a handful! congrats to you and your friends and family for being able to cope with this all!
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I'm going to start sometime in June. 7 weeks. I've been trying to put off the start a bit because I've got some friends coming into town for a visit... I already had chemo and surgery, so hopefully most all the cancer is out and the rads will take care of anything lingering... I'm also wanting to recover from the chemo and the surgery a bit more before I experience radiation... I'm feeling a lot better, but still having stomach problems.
It's nice to have a bit of a break from all the insanity that has been going on since my DX in November...!
Of course, I'm roaming about with a bunch of marks and tattoos and stickers on me from getting mapped or doing the simulation, or whatever that was...! geesh...
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Good luck to everyone starting their rads!
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How long are all of you waiting between sim and first treatment? I ask because all of this has kicked up my allergic dermatitis and I'm worried about how many days I'll need to have the stickers on.
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I had my sim about a week before my first treatment. Today, I completed treatment four. So far, no side effects or problems. They hit me from 3 angles so it takes a bit of time to get through it all (about 15-20 minutes total). From the right, from the left, from above.
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Hi everyone, I had my "sim" today and for some reason the sight of the tattoos made me cry like crazy. I didn't cry like that when I had the mastectomies, I guess I'm a little treatment weary. I finished chemo 2 1/2 wks ago and won't have actual rad tx for one more wk. Still dropping eyelashes, have about three left. eyeliner is a small amount of camouflage or distraction from my bald eyes. Some days I can't believe its me looking back at me from the mirror, other days I hold my bald head high, and have a lot of compassion for myself. This stuff isn't for sissies. good luck everyone. -
Lmoore, I had a very similar reaction. It caught me off guard since I hadn't felt much anxiety leading up to the appointment but something about the room and that machine and the techs pulling and pushing me around into position and drawing on me with sharpies that just did me in. I had my third treatment today and I'm still affected by the thought of radiation and chemo and how toxic I've become, but the daily treatment routine is settling in. Like you, I think it's just the accumulation of surgeries, treatments, appointments and side effects wearing away at my constitution. I like what you said about having compassion for yourself. It's important and also easy to forget during this mess of other emotions.
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