Fall 2013 Rads
Comments
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Congrats kika! Upward and onward! One more thing completed. -
Thanks, all. Keep the faith. -
Gracer55: Did your docs give you any static about doing IMRT after chemo? Mine is reluctant because she says there is no data about how the two interact -- she's afraid the side effects might be greater because of residual effects of the chemo. Apparently most of the studies comparing IMRT with 3D did not include patients who had had chemo first. I've been trying to find any info on the subject, but so far no luck. Can you point me to anything helpful?
Thanks! -
I know everyone's experience and tolerance for pain is different, but I just wanted to report my experience: Just got my tattoos this morning, and I have to say they did not even hurt as much as a flu shot. So if anyone out there is dreading that part of the experience, don't. -
Hey ffranny - you are so right. I was quite scared of getting the tattoos and although I felt them it was really fine.
I think maybe we toughened up a bit what with going through surgery and all!
It seems that 9 times out of 10 the waiting and worrying are worse than the procedure itself.
Its the 1 out of 10 that scares us!
When do you start rads? I start on Monday. -
I don't exactly know when I can start. It depends on whether I decide to go with the standard 6-week-plus program or the 3-week program -- which depends on whether I can find evidence to convince me and my RO that there are minimal additional risks to doing the 3-week version after chemo. She's reluctant to do it, but I see Gracer is doing it and would like more info. -
Talking about sugar, weight, what causes cancer etc, I'll chime in. After my diagnosis I consulted with a nutritionist. She diagnosed me with insulin resistance. I've never before been diagnosed as pre-diabetic or anything else, but according to her, that has been my problem - and why I've been overweight most of my whole adult life. (my fasting insulin measured 9 - which my internist thought was fine, but my nutritionist said she'd like to see it around 5) I was a grazer - eating small frequent meals - and I was always hungry - I'd eat breakfast at 7:30 in the morning, and be ready for a snack at 10. I'd eat supper at 6 pm and by 8 I was ready for a snack. Her solution: time restricted feeding. I now limit my eating to an 8 hour window in the day and fast the other 16 hours. (I have breakfast at 10:30, lunch around 2 and supper at 6.)
My nutritionist said that I should of course concentrate on protein and potassium (her claim is that if you get enough potassium you are eating enough fruits and vegetables to give you all the other vitamins, etc., that you need... and that carbs weren't necessarily bad (of course not junky sugary stuff, but things like brown rice), just not of much value nutritionally. the problem with someone with insulin resistance is that eating all the time causes you to produce a lot of insulin - and your cells don't recognize it so you keep producing more - and there is something called "insulin-like growth factor" that feeds cancer. Fasting for 16 hours a day causes your pancreas, and whole digestive system to rest - not produce insulin. I've lost 25 pounds in the last 5 months... still need to lose more, but I don't feel like I'm on a "diet" - I feel I can eat what I want, when I want, as long as I restrict my eating to my 8 hour window (and of course, I try to choose healthy things.) -
I am having number 6 rads today and I am already red and irritated around the nipple area. Is that unusual to have this happen so early? It sure has me concerned. It doesn't hurt much, but it is quite read and has itched. Oh dear....
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Kika congrats!! Pizza and sleep, what could be better?!
I am hoping for some tricks tonight. ;-) Although everything will be covered up until further notice!
Happy Halloween! Halfway done! 14 out of 28!
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Kiki, congrats! I just finished 4 of 33. It seems so far away. The techs are great at keeping up our spirits. Today they had a painted pumpkin for each patient. Then had a table of hot cider on this cold rainy day and pumpkin pie, cupcakes, candy to celebrate Halloween. Tomorrow everyone is to wear their team colors for the Michigan vs. Michigan State game on Saturday. A local church has donated an overflowing basket of knitted hats and a huge rack of those lacy looking knit scarves for the patients to take. I feel very fortunate that I switched MO's and found this group of very compassionate docs, nurses and techs. The techs wrapped me in a heated blanket today because it was cold in the room today. I so wish Bluebird could have her treatments here. -
RainyDay - Do you have a tape allergy? My nipple got red after treatment number 2. When I mentioned it to the techs, they asked if I had a tape allergy. Since I developed a tape allergy this year, they started putting a piece of gauze over my nipple when they tape it down. It worked! My nipple was better within a day. ... of course, it's red and painful now that I'm farther along but it's bearable. I'm 13/26 done - halfway!!! -
Girl on fire by Alicia Keys!! Best radiation song out there!! -
Kirklandgirl - no, they don't tape my nipple. So I doubt that I have a problem with that. Looks like I am one of the lucky ones with early redness. I do have sensitive skin, but I don't know if that is a factor.
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Today was my 4th of 33 treatments. My breast was pink after my first treatment, which I've read is way too early to be pink. It calmed down by the next morning, but pinked right up again after the 2nd treatment. I mentioned this to the tech at my 3rd treatment (yesterday), and she noticed my back was pink as well. Her only comment was that it's too soon for me to be pink.
I've been using Aloe Vera gel (100% pure with no fragrance, coloring, etc) and emu oil. I've just started using Aquaphor on the area between my breasts because it's just starting to look like lizard skin.
Any suggestions would be greatly appreciated. I'm terrified about what shape I'll be in in another week, much less three or four weeks from now. -
Yahoo kika! Happy Dance for you!
MsP - You shine. Love how you wore red everyday for a week.
rhcp66 - ask the techs or onc nurse if they have Radiaplex. That really seemed to help me more than the aloe or Aquaphor. We all react differently but it is worth trying various creams to see what works for you. I called my dermatologist to see what she suggested and she told me Radiaplex. I didn't listen and then on a fluke that onc nurse gave me some to try.Worked like a charm and I am still using it 2 weeks later to help with healing.
Take care radiant ladies. -
I finished rads today! 44 total. My skin has fared very well especially with more aggressive treatment. Honestly, I've barely put anything on it. Organic aloe gel or an organic balm (with coconut olive shea and some essential oils). All that dang tape I had to avoid made it a pita to apply anyway. My tech helped me rip off all the tape. Now I can slather. My PA reminded me that i have no oil glands, forever, in the radiated skin. I rang the bell. With all my other treatments I never rang the bell. This time I did! I drive back home to St Louis over the next 2 days. I can.'t wait to be home!!! Next I get the monthly shot Zoladex to shut down my ovaries an I will take arimidex. I already took tamoxifen and it did not work for me (hence the 2nd and 3rd bouts of cancer). I found out I have osteopenia (age 42) so I need to find out how to deal with that one. And I have lymphedema. Boooo! On to the next chapter! -
Vw... perfect song!
Cider, 44! Wow! Congrats on being done!
I have just 4 more boosts & feel good about being done!
My kids brought our grandkids over tonight....
This is Jaxon. Born on my birthday, 3 days before I started chemo & this "adventure" ive been on...,

Happy Halloween!
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I have PM'd flaviarose for more info on her nutrition.
She raised a lot of interesting ideas that might be very relevant.
cider8 - I am so glad you have finished and are headed home. Good also to know about not having oil glands! RO didn't mention that to me. All the RO told me when I asked about side effects is that if I wanted to climb Mount Kilimanjaro when I am finished rads I can. WTF!
Ladies - I can't scroll up and remember all that was said but thanks for names of creams that have helped. On Monday after my first treatment I meet with a nurse who will recommend some cream. I will see if it resembles any of the lotions and potion mentioned on this thread.
Keep the song titles coming. - Loved the idea of swopping the focus of Another One Bites the Dust and making it super good instead of super bad.
Hugs -
im adding toxic by Brittany spears to my playlist, for those Who have gone through chemo. I'm actually considering making a pick me up mix fr my friends who were diagnosed after me and starting their journey now! -
Kika,im so happy you are done!!! Also Cinder8 so glad you are heading home. What a great feeling it must be!!!
They took off my one sticker they had on my chest (i have no booby there) and said I had tape allergies. Not pretty skin under it. So I got a new tat. No more tape for me !
Itiiswhatitis,great pic of you and your grandson. Thanks for sharing it. My grandkids are not close by. Boy I wish they were.
Well its almost the weekend so hang in there every one. Two days to heal and rest. Hope everyone has a great weekend.
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YEA for finishing cider8! Now you get to go home! Congratulations
Annie -
Kika and Cider congrats on finishing. Go relax and recover. Can't wait just 8 more for me. -
Cider that is awesome! 44 has to be some kind of record!
Ititwhatitis, thanks for sharing the cuteness! Great photo!
Rhcp, it almost sounds like an allergy. Your back should not be pink if no rads there. Could you be having a reaction to the detergent they use on the gowns or sheets? Or even aloe, emu oil or your skin is flaring up due to a combination of things. Talk to your doctor about it.
Girl on fire is a great song!
Jo, I want to have rads with you!!!
Have a triple RRR (Rest, Relaxation, Radiant!) weekend everyone!
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Congrats Cider! Safe journey home. -
Cider, congrats! Have a safe trip home to your own bed...best feeling isn't it.
Bluebird, Oh how I wish you could do rads with me.
Itiswhatitis, cute photo! Time flies by when you are watching your grand kids grow.
Cakes, things are still on schedule. 5 of 33 done.
Have a triple RRR weekend everyone. -
Kika and Cider8....congratulations and all the best for your healing! Cider8, just so very happy that you will be home with your family.
Itiswhatitis....Your grandson is adorable (and so are you, by the way!!!
Keep shining, radiant ladies!!
MsP -
I am new to this group - and to this site. Had a lumpectomy and lymph biopsy last week - appt with onc next week to learn about my rad future. Something to look forward to! Anyway, it is very helpful reading all your posts about what bras and lotions and potions work, and how to manage through working full time. thanks! -
Sarigal55 - sorry you have to join us but that being said you will learn so much from these radiant ladies. I live in a rural area and these boards have been a real blessing. After you get the results of your biopsy be sure to post them under your profile and then ladies who have the same diagnosis will really be able to help you. This is a very scary time for you and the waiting is almost unbearable but it does get easier once you know what you are dealing with. (((Hugs))) -
Welcome sarlgal! Congrats on reaching the finish line Kika and cider!
I made it through my first five rads yay! No issues yet.
I wanted to add "Roar" by Katy Perry and "Brave" by Sara Bareilles. Both inspiring warrior songs! -
Sarigal55, welcome! Nobody wants to join this club. But if you have to, there are some really wonderful people that everbody else will never meet. After all they have thrown at us, rads is just one more thing to get us closer to getting done with the active treatment. I have done 7 rads so far. December 13 is my final one. It seems so far away, but we have to concentrate on today. Let us know what your rads schedule will be. Have a great weekend! :-)
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