December 2010 Rads
I thought since I would be starting rads tomorrow 12/1/2010 that I would start a new group. I have had many delays and thought for sure I would have started in November, but here I am. Hopefully there will be others to join in this group and share experiences. I have learned alot from the November 2010 group of ladies.
I will be receiving 34 total rad treatments (28 reg and 6 boost)
Comments
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ebann,
I am sorry to hear that you are going through radiation a second time. I hope that the side effects will not be severe and they can control or shrink your bone mets.
Sherryc.
It is nice to hear that many people do well with TE and radiation. I look forward to getting to know everyone on this thread.
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Hey Michelekb, I have TEs and went through 25 rads treatments -- finished early October -- and really didn't have any issues. I was really nervous about the whole thing too because even though there is A LOT if breast cancer in my area, neither my PS nor my Rads Onc had ever treated a woman with the TEs-then-rads combo. I was so worried that I had my Breast Health Coordinator (social worker) call the head of Rads Onc in another area and discuss my situation with him, plus I got a 3rd opinion outside of my network. Both of those doctors said they would not treat me any differently than if didn't have TEs. Being fully expanded was the key because you don't want to try to stretch the tissue after rads.
I used Emu Oil 2-3x per day (brought it with me to treatments and applied it in the dressing room too) and even though I am lily white I only ended up with what I would call a mild "sunburn" -- mostly under my arm where I don't really have any feeling any more. I got the Emu Oil through Amazon and I would highly recommend it. It was about $25 for a 4 oz. bottle and that lasted my full treatment. BTW, after I applied the oil to my chest I would run my oily hands over my bald head and now I have really thick hair about 2 inches long (finished chemo in July). I really think the oil helped with the hair growth too.
Also very important to stay hydrated. Drink tons of water.
Anyway, all you lovely ladies, you are not alone. Rely on each other for support and feel free to PM me too if I can be of help.
Jen
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Thanks for the info on Rad with TEs. I have the TEs and they didn't think I would need Rad but thought I should have a consult. Have had 1 te fill and going for only one more. Had my first round of chemo today no real side effects so hopefully they will stay at bay. So with TEs and rad does the ps just wait to do the exchange till rad is complete and does anyone know if you can do herceptan and rad therapy together? Have 5 more cycles of tC and than the remainder of the year with herceptan. If I need rad therapy would hate to have to wait an entire year. thanks for any info
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Hey everyone! Like SherryC I was supposed to start Rads in Nov. But I couldnt lift my arm past 30 degrees because I had a frozen shoulder after my Bilat-Mast/rest of nodes out (already had axillary nodes out in May) with TE. I had neo-adj chemo from May to Sept 5th and was on Tamoxifen for 3 wks, but was taken off due to my body not tolerating it at all. Its been kind of scary knowing that the cancer could still be growing in me during my wait. I went in today for my Mapping/tattoo/bolus making today. They said that I was a challenging case. My arm was still very low which made it difficult. Plus, I have TE in and they need to miss my heart, and get my nodes under my arm and above my breast (i forget what that area is called). The Rad onc said that I will be getting 28 treatments. He wants to start me ASAP but need the advise of some other experts to finish the planning. So for now I am starting on the 15th. He said that he will try really hard to get i done quickly and get me in sooner. By the way, how many tatoos or marks did everyone get? After today I have 10. And yes they are tattoos and they did hurt. Hopefully they dont have to give me more when they have the final plan. At least they were all very nice and willing to do anything to help with the pain. The mapping alone took 1 hour and a half. Staying still was soo hard and painful. I should have taken pain meds and anxiety meds first. I already had muscle relaxers in me and the Dr prescribed me vicoden for the future. Good luck everyone!
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I also had my TE filled before I started Rads. Actually my PS filled them a little bigger than what I wanted to take into consideration the skin tightening during Rads. My Rads Onc told me that the amount of rads given actually goes down with them compared to without them, or with a lumpectomy. Its also a little more complicated when it comes to the planning. If they are filled too much they may have to have some saline taken out. But that wasnt a prob for me. I was also told to use Emu Oil. And a friend of mine who just finished rads gave me her left over samples of Xclair cream. She said it worked great. But just make sure you tell your Rads Onc what you are using beforehand.
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Hi- id love to join this forum. I just finished chemo, Will be having a stimulation in a few weeks. Then 1st rad is jan 4th. Im nervous. We are doing rads because of my age (36) and also the tumour was about a cm from chest wall, and also just in case of any lost cells.
I am hoping my skin doesnt go bad (or if i can get lots of advice to keep it in good shape) as im having DIEP in Sep (if my skin is ok).
SO im getting some EMU oil today
Is anyone putting any stuff on right now. Ive had a masectomy already so, any advice? Yes lots of water to stay hydrated...........
Im so nervous!!
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By the way someone mentioned herceptin and Radiation, i have a port and will continue every 3 weeks until next sep. it doesnt affect it.
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tammyg - I ended up with 3 tattoos. One on each of my sides and in the middle of my breast line just below the bra line. These were used to line me up with fixed lasers on the wall and ceiling. They did additional marks with a sharpie each day and I look like a coloring book. Those are almost gone since I am doing boosts now. My lump scar is on the bottom side of my breast and I now have a "bulls eye" Will finish rads tomorrow.
Nancy91355 - Here is a kitty for you.
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Wow this board is active, how exciting. I am like Jo with my tatoos. Had three they were not painful. It is 10:40 and I have not heard from the rad clinic so that is a good sign that I am on for today. They did mark me with sharpies on Tuesday and I am sure will get more marks today. I used my xclair cream this morning so will have to see how it works. Welcome to ebann, michelekb, packjen, lexyloohoo,tammyg,redninrah. Glad you all have joined us here.
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Yikes! I'm with you Sherryc - This thread has really gotten busy! So glad to see so many of my November sisters here too!
Today I got for number 4! I got 3 tatoos too. Didn't hurt at all. I can't even find them they are so tiny. I don't feel any skin issues so far, just hoping if I keep using my cream it will stay ok.
Hugs to all! Love the ktty pix Jo!
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Sherryc - I am keeping my fingers crossed. If your facility is like mine, plan on getting remarked everyday. Thank goodness it is not swimsuit weather. They would be hard to hide.
Glad to see this thread busy. Sorry for the circumstances but we are good for each other.
starling - How many rads are you getting? You may have said before - don't remember seeing it. I chalk it up to rad brain.
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I have an appointment on Monday at 12:20pm to have my first radiation treatment. I have a pit in my stomach ever since they called this morning. It is nice to hear from others with TE that had no problems with radiation.
I have heard good things about Miaderm and emu oil for radiation skin. I ordered some Miaderm and am getting some emu oil. I don't know which one I should use or can I use both. My RO is no help. I am going to use something on my skin. I am not just going to wait for a problem to develop.
lexyloohoo,
I am also on herceptin every three weeks. you can continue while getting radiation. My PS said he will wait at least six months after radiation before exchanging TE for implants.
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michelekb - At first, rads can be overwhelming. Lots of stuff going on all at once with lots of people around. After the first couple of treatments, you will settle into a routine and things will go well. Skin care should be your first priority.
Sit back, take a deep breath and relax. You will do great. Let us know how your first appt goes.
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i bought some emu oil- i can not believe how expensive it was!
Im using going to get some BIOTIN 5000 mg to help my hair grow.............is this too strong?
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Despite the expense, I can vouch for Emu Oil's effectiveness. My son (blonde, blue-eyed) was very badly sunburned on his entire back a few years ago, resulting in huge blisters and so much pain that he missed a week of school - could not wear a shirt and laid around on his tummy for several days. The blisters would fill to the point of bursting on their own. I feared skin cancer right away. I heard about Emu Oil on a radio commercial so I went and got some. I had to dilute it and spray it on because he couldn't even stand to have me touch him. Once the blisters subsided, he healed up just fine without any scars, just eleventy billion freckles. I have a friend who suffers from severe dry skin and excema, and she uses it in addition to her prescription creams. I think it's worth the money in severe situations. My RadOnc told me it was okay if I want to use it, just to be sure there is nothing on my skin before each rad session. She also gave me an rx for something but I haven't filled it yet and can't remember what it's for.
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hello ladies
its time for me to join the Dec.Rads. I joined the Nov.rads but family issues came up and the tx were put off. Now i have an appt. with Rad.Onc. on the 7th. I am supposed to do every day for 6 wks.I hope my body is stron enuf.I hate this bc.
please sign me up.Good luck everyone.
hugggggggggggggggggs
K
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Hey ladies hope everyone has minimal side effects . I had Boost # 3 today, I will be finished on Wed. next week . Please keep your skin hydrated with what ever your RO recommends . I was pink after my first treatment and did not have bad side effects until last week . I started the aquaphor late in the first week, applied it only at night because it is so greasy. Durning the day I used fresh aloe, ( I buy it at the vegetable store, I saw it at stop& shop last night in the veggie section). About three weeks in I needed hydrocortisone for the itch , On Tuesday I had the RO write a rx for silvadene cream . Whatever you do don't apply anything four hours before . I cant wear a bra at all now with out a telfa pad under my boobie.
Jo1955 -this ones for you. Thanks for the sparkle it helped.
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grannydukes - Glad to hear you are finally starting rads. I did every day for 6 weeks and if I can do it so can you. The hardest part for me was the drive everyday in spite of the skin problems I had. I found dealing with traffic was more stressful than the daily zaps.
YOU CAN DO IT! WE ARE STRONG LADIES.
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DebbieLynn - Way too cute - Thanks.
What's the website - gotta check it out.
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grannydukes glad you decided to join us here and that you are going ahead with your treatment. You will do great.
MrsNice-what did you dilute the emu oil with to be able to spray it?
Jo I am so happy that you will be finished tomorrow.
I did #1 today (33 more to go) and no problems. After I finished I drove to Target on the way there I felt a little warm tingly for a few seconds and then it went away. Others have talked about how many zaps. My machine is pretty quite it just hums. I have four angles and each one last about 15 seconds. They only marked my tatoos, they made a circle around them but no other marks. I used the xclair cream this morning and after treatment, will use it again before bed. That is what they said to do so I will be a good patient. Debbielynn my doctor said fresh aloe is very good to use also. He recommended that if I wanted to stretch the prescription at first to alternate with fresh aloe. It felt good to finally get started, now I can see a light at the end of the tunnel.
[Sherry--lumpectomy left breast 9/30/10. No chemo, oncotype score 23 with 14% recurrence rate. 28 reg rads and 6 boost for a total of 34
Diagnosis: 9/27/2010, IDC, 1cm, Stage Ia, Grade 1, 0/3 nodes, ER+/PR+, HER2- -
Coming over from the November thread. I started this past Monday, so #4 of 33 today. No SE so far other than I feel tired today, but that may be just that I am not used to getting up at 6:00 am, which I have to do to get to radiation by 8:30, so I haven't been getting quite enough sleep. I am using Miaderm lotion, which I really like because it is not greasy and smells good. I haven't been at it long enough to know how well it works, but the nurse said the doctors were seeing better results since they started recommending it. I have three small tattoos just like Jo's, but I only had magic marker for the sim appt; I don't get daily markings.
I'm drinking lots of water, as recommended, and eating more protein. I hope it works!
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Jo I went to satisfaction.com and I can't seem to be able to copy those cute things. It just copies the code and does not show a picture. Have any ideas what I am doing wrong?
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I finished treatment #16 out of 36 today. I do have a TE which has been a great concern for me. I have a bolus treatment every other day which makes the skin react quicker from what I am told. So far my skin is holding up ok. I am pink and have some itching but no peeling or breaks in the skin. I am noticing that the TE is feeling a lot tighter in the last couple of days and is very uncomfortable. I cannot wear a bra any longer. I have been using Miaderm and Udderly Smooth. I cant wait to get this over with. The days are going by so slow. Good luck to everyone. This board has been a life saver for me.
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Sherryc - I sent you a PM for the pics.
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Jo good luck today I will be thinking about you. After I said everything was great last night I had some irritation. Felt like chauffing but my skin looked fine. I put some talc powder on and that did nothing for me. So I finally put my cream on and went to bed. It was better this morning when I got up but after I got in the shower in came back. Once I put my cream on it went away again. Caught me kinda off gaurd. I really did not expect to feel anything after my first TX
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I am not due to finish chemo until early February, but wondering how soon after last chemo do rads normally start? I am ready to get this all over with!!
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elaineg, don't really know since I did not have chemo, but seems that I have read others starting pretty quickly. Maybe someone else here can answer that for you better than I can.
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