Winter 2013-2014 Rads

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  • MinusTwo
    MinusTwo Member Posts: 16,634
    edited March 2014

    Mimi, TeamKim & Lily - Thanks for your good good wishes.  I'm treating myself to a few days in Galveston on the beach after I get past the 2 weeks post rads when it's supposed to keep getting worse.  Tomorrow I get to start back on Herceptin infusions again.  Yay!!. (not)  I bought myself a bunch of daffodils on the way home and my kitchen is brighter just looking at them.

    Kim - I have you to thank for the Miaderm recommend.  Glad it's working for you too.

  • SallyS70
    SallyS70 Member Posts: 947
    edited March 2014

    Thanks to all of you who have posted.  I finished rads late in February.  Although I haven't posted much, I have read a lot.  Your posts have helped me both mentally and physically, so I wanted to say thank you and wish you all well.

  • dfwmom70
    dfwmom70 Member Posts: 14
    edited March 2014

    I finished last Wednesday.  I had my week after followup yesterday afternoon.  Thought I would have to go once a week for a month for skin checks, but I am healing up nicely.  I only scheduled a 90 day appointment.  I was actually surprised at how little redness I had, except for the boost area.  I had one area they seemed a little concerned with at my collar bone, but that is just slightly noticeable now after 2 weeks of no radiation to that area.

    My radiation oncologist also told me when I have any scans (mammogram, MRI, chest x-rays, etc.) to make an appointment 3 days after the scan to go over the results.  He said 50% of the time after someone has radiation the results are misinterpreted.  He said it would be a quick no charge meeting.  Interesting.  Come to think of it, I don't remember handing my credit card over during any of my visits there. Hmmm.

    Now on to lose the weight I have gained through this process.  UGH!  But My 10 (almost 11) year old daughter wants to go to the gym with me. I can at least have a workout buddy now!  And she is my motivator to be a good example.

    Happy First Day of Spring!

  • checkers
    checkers Member Posts: 95
    edited March 2014

    TeamKim,

    Glad to hear you're doing so well. I'm still getting those "zingers", too.  My RO said it's actually the nerve endings trying to repair from the surgery. My MO confirmed this. They said it can last for months and sometimes even years. Have fun in the cold NE.  

    Been on Arimidex for a week and so far no SE's. YAY!  

    This battle has been really difficult for me since not only have I been battling cancer, so has my husband. The support I've received from this board has helped me cope and vent which, in turn, has helped me heal so much faster than I thought I was capable of. I really hope everyone progresses as well as I have because it feels so wonderful when the end is in sight. THANK YOU!!!

    In fact, I'm feeling so good I started a Relay for Life team "Forward March!" We
    walk through our local zoo by the shores of Lake Michigan every June. It's a long night but well worth it. It truly is a wondrous sight to behold. 

  • annika12
    annika12 Member Posts: 433
    edited March 2014

    checkers - I'm doing a Relay for Life team too Kicking it with friends :) 

  • SallyS70
    SallyS70 Member Posts: 947
    edited March 2014

    Walking through a zoo ... how neat!  Good luck to all Relay for Life walkers.

  • RedReading
    RedReading Member Posts: 2,143
    edited March 2014

    Ladies (drumroll please)............ I'm officially done!!!! Got my grad certificate signed by all my techs and the secretaries and my smoking councillor.  

    Gosh it is bitter sweet. I am so happy to be done, yet I had a routine for the last 5 weeks. Rads at 3pm. Every workday. Now, no joking with the techs, no hugging my Linda, just done.

    I wore my Post Tit Note on my boob thanking my techs. They laughed so hard. Said that was a first for them. Please slip your arm out of the gown. Bahahaha

    Took in chocolates for them, more for the secretaries and candies for my non-smoking coach.

    But now it's nothing till may. Wow. OK. Guess I'm done. Yayay!!!!! 

    Love you ladies. Minus Two congrats on being done too. TeamKim and Checkers thanks for the info on what to expect now!

    ((((Hugs'n'kisses))))

  • TB90
    TB90 Member Posts: 992
    edited March 2014

    Red:  Way to go!!  I am right behind you.  I too have thought about my schedule change.  I have been commuting, but have sort of gotten into a rhythm and have started to enjoy my music, lunch with friends, etc.  I go right back to work, so will likely soon forget about the days of radiation and commuting.  Funny how there are things about all of this that we will miss.  Who wud of thought? 

    Love the post tit note.  I am certain that they will all miss you too :)  xxxxx

  • LanaM
    LanaM Member Posts: 142
    edited March 2014

    Congrats to all you radiant ladies who have finished or are close to finishing rads!  Life does get back to normal - well at least a new normal. I also have a Relay For Life team with my family - our team is called Walking With Angels. We started back in 1998 after losing my mother to lung cancer. The we lost my father in 2009 also to lung cancer. I was on the RFL planning committee for several years and even chaired the event one year. I'm never thought I'd be on the other side if you will wearing the purple survivor shirt!

  • Rlsteadman
    Rlsteadman Member Posts: 76
    edited March 2014

    Thought  I would update the group on my 1 month post rad checkup. I saw my RO today and she said it looked great. I feel almost back to normal. The first 2 weeks post treatment were the worst. Mostly around the nipple since that was where the boosts were given. It was swollen and sore but not to bad. I liked wearing my men's baggy Hanes t-shirts. I bought a three pack and they were soft and comfortable. If I went out I had a soft sports bra I wore.  My RO said she wanted me to come back in 6 months. I was surprised that I needed to go back. I also met with a new medical oncolog

  • Rlsteadman
    Rlsteadman Member Posts: 76
    edited March 2014

    sorry accidentally hit submit. I met with new medical oncologist. We reviewed my treatment and decided I would not do any other treatment. She said for me to come back in 6 months to the breast center for follow up mammogram.  What type of follow up care is everyone else getting? It is so hard when active treatment stops.  Hope everyone is getting back to their new normal!

  • MinusTwo
    MinusTwo Member Posts: 16,634
    edited March 2014

    RED - great news.  Congrats.  Now we just have to get through the next two weeks while the burns keep accellerating. 

    I have to go back to see my RO at 6 months and one year.  She suggested I set up the schedule to alternate with the MO. 

  • checkers
    checkers Member Posts: 95
    edited March 2014

    In 4 months I have a appointments for a mammogram, labs, my SO nurse and my MO all on the same day. My RO wants to see me in 8 months. She also suggested alternate appointments with my MO.

  • Lilyluv
    Lilyluv Member Posts: 160
    edited March 2014

    Congrats to all graduates!!!     

    OK, so has anyone sudddenly developed a raw infected burn spot 3 weeks post rads?  When I left treatment they said 7-10 days is when the burns peak.  I was sweating a lot yesterday and kept dabbing my boob with under my tshirt.  It looked pink and started burning, so I put cornstarch on it to keep the skin from sticking.  When I went to shower the cornstarch was all gunky and yellow so I put Neosporin on my skin and left off the cornstarch.  This morning, there was a raw patch of bright red skin along with bright red dots.   Dabbed at it with tissue and again yellow gunk on the tissue.  Put more neosporin on.  At last check it was covered with this whitish grey wet coating and again there was yellow.  So I called the nurse.  She said this is the time when burning peaks and that's normal to have a reaction this late in the game..  OK, so which is it?  7-10 days is a lot different than 3 weeks!  She said ust to keep putting neosporin with gauze on it.  

    How do you keep the gauze on without using real sticky tape?  The gauze won't stay put and the tape keeps peeling off (don't want to put heavy tape on it out of fear of ripping off more skin by accident.  I put my big  granny rads bra on to keep the gauze from falling off, but it's really hot and I'm afraid that will make it worse. In this cold weather I'm not going to walk around with no top on in here.  How do you keep gauze over a wound under your boob?  I tried cutting a strip of tshirt and tying it around my chest underneath, but it either was too tight or fell off.   Nurse said call back Monday if it's not better.   Mammogram and seeing the RO is 6 mo. for me.

  • Rads14
    Rads14 Member Posts: 8
    edited March 2014

    congrats all of you who are finishing and planning fun things ahead!! I just joined this board last week, and I only have 3 more treatments to go as well! Looking forward to a trip to Puerto Rico in April!! Haven't had really bad reactions to radiation but this week feeling the tiredness like a truck hit me an also tonight some nausea and dizziness. My friend who is also one of my nurses told me I'm probably dehydrated. Drinking a ton of liquid now to try to feel better. Have a great weekend everyone. <3

  • RedReading
    RedReading Member Posts: 2,143
    edited March 2014

    Hi everyone. I have an appt with my RO and my MO at the end of May. That's only 2 months post rads, but the do a lot of stuff different in Canada. 

    My Post Tit Note was a hit so if you want to borrow the idea TB90 go right ahead. To be honest, I got the idea from someone else, so, pay it forward. Lol.

    My boobie is bright red from collar bone to about 2" below my breast. The thing I've found that helped the best were 2 baths per day with the proper amount of Epsom salts. Did you know it calls for 2 cups per bath. I've been doing it wrong all these years. So I buy the big 9 lb jug for $8.99 and it does me about 4 days. 

    Ttyl. Gotta make dinner. (((hugs)))

  • TB90
    TB90 Member Posts: 992
    edited March 2014

    Red:  I thought about stealing your idea, but I do not have a tit!  Had a mx, so guess that does not work so well :)

  • RedReading
    RedReading Member Posts: 2,143
    edited March 2014

    TB90, sure it does. More than one meaning to the word post. As in, after/used to be/done. Lol. Your boob used to be! I think it still works. 

    :-)

  • AndreaJ50
    AndreaJ50 Member Posts: 889
    edited March 2014

    Lilyluv, Ouch!! I am so sorry to hear what you are going through. I hope you get relief soon. 

  • Miminiemi
    Miminiemi Member Posts: 340
    edited March 2014

    Lilyluv - I found that gooping the aquafor on pretty thick under the breast made the dressing stick to the aquafor. I'll bet vasoline would do the same thing. You could do the neosporin first.  I used those non-stick dressings that were smoother than gauze.  (Telfa pads?).  I had to use two to completely keep from having skin on skin rubbing. But my girl is pretty large and the shear weight of her helped hold the pads in place.  Also those Domboro soaks helped lots. They were soothing and help keep that layer of old skin in place while new develops. Hope that triggers some ideas that you can try.  T

  • lovewins
    lovewins Member Posts: 881
    edited March 2014

    lilyluv...they make a bandage that is non stick called telfa.  I just put cream on it and stuck it on and then put my bra on.  I bought a really stretchy bra by Bali called comfort revolution bra and I also got some SSD cream from the RO that really helped.  Hugs to you I know you are in pain...mine is just healing.

  • Mayanne
    Mayanne Member Posts: 108
    edited March 2014

    I have only two boost to go - Monday and Tuesday.  My redness/soreness/tenderness has turned into a tan and just peeling slightly.  I'm not yet fatigued. 

    But, I did want to ask if anyone has had indigestion/acid reflux?  It's that feeling that there's a bubble of gas in your chest that just won't release?  I didn't ask the doctor or nurse because until this weekend, I'd only had it a couple of times and thought it was from something other than radiation (don't want to blame everything on that!). Although I've read that the esophagus can be irritated from the rads.  It happens most often when I'm lying down. I'll be asking tomorrow - just wondered if anyone else has had this - I'd never been bothered by this before treatment.

    Also, I KNOW that slight chills must be a SE.  I've often felt them when I'm sitting and reading and just realized this morning that they're coming directly from my breast that is undergoing rads.  I'd read that there can be weird sensations and I'd thought it referred to the zingers, but the isolated chills must be another one.

  • Lilyluv
    Lilyluv Member Posts: 160
    edited March 2014

    Mayanne, I don't know about the  acid reflux but I also had chills (felt like when you're starting to get sick).  It kept happening, but the nurse and doc said they never heard of it being a side effect.  But I really do think it's a side effect too!   It happened when I first started to feel burning - almost as if you put Ben-Gay or Icy Hot on.  Kind of an odd sensation like a chill without shivering. 

  • Lilyluv
    Lilyluv Member Posts: 160
    edited March 2014

    LOL mimi I love the way you put that about your girls.  Is it OK to put that Aquaphor over open skin? (it's raw but it doesn't look infected anymore).

    lovewins I recall the nurse saying to use Telfa but I just thought that was a brand name for gauze or a band aid.  So I looked it up and found out it's the stuff that you're describing.  Yesterday after searching around neither Walgreens or CVS carried it, so I had to order via internet with express shipping.  Probably won't be here until Tuesday.  I found a couple of those huge bandaids - looks like Telfa is what they use.  So I cut most of the tape off of it and it's at least staying on well enough if I don't move around a lot.  I never had reaction to tape, but every kind of tape - even the paper stuff causes itching now and takes off more skin. I bought this huge bra for rads and it was working pretty good until I moved a certain way and the gauze fell out and the band touched the icky skin.  It's due for a hot water wash today.  

  • TB90
    TB90 Member Posts: 992
    edited March 2014

    I am so glad to read about all the SE that supposedly never happen!  I definitely get the chills without an actual temperature and the feeling of a bubble when I lay down.  I thought that may be due to all the carbonated water I have been drinking, but it only happens at night.  Also, I thought I had a tickle in my throat/chest but it also seems to be GERD.  I have never had this before either.  Very minor things but I am convinced they are all related to the rads hitting my chest. We should document our SE's and provide this written info to our radiology centres as I cannot believe we are the first to present with these symptoms.  My radiology nurse had never heard that taking vitamin C may not be recommended during rads as it works against what the radiation is trying to accomplish.  Sheesh! 

  • Mayanne
    Mayanne Member Posts: 108
    edited March 2014

    TB90, that's just what I experience, too.  It feels like a pressured bubble when I'm lying down and actually, today I have it even when sitting or standing.  It's very annoying.  I'm going to ask the nurse about it tomorrow, so I'll let you know what she says.  

    And those chills, Lilyluv and TB90, are definitely real, too. Just like chills when you're starting to get sick, but you can tell with these chills that you don't have a fever.  

    Thanks for sharing SE's. 

  • Miminiemi
    Miminiemi Member Posts: 340
    edited March 2014

    Lilyluv - My nurse told me to use the aquafor on my skin even when it was pretty raw.  I think they use it in actual burn units when people have been in a fire.  

  • RedReading
    RedReading Member Posts: 2,143
    edited March 2014

    TB90, Mayanne & LilyLuv the chills you feel are perfectly normal. I know because I am a redhead. How does that signify? I have had many, many sunburns! Sunburns are accompanied by chills, sweats and often fever, indigestion and diarrhea. Trust me on this one! You are getting one heck of a sunburn on your boob right now. Your body is reacting accordingly. All the good stuff races to the boob leaving the rest of the body to find for itself. 

    Sorry for right this minute. But it will go away. (((hugs)))

  • MinusTwo
    MinusTwo Member Posts: 16,634
    edited March 2014

    TB90 - my RO said no strong antioxidants - Vit A, C or E.  Now I'm seeing some studies that these same wonderful things which I've taken for years are on the "no no" list for BC.  I plan to discuss this issue w/my MO when I see him again the end of April and hope to find some research to talk about.

    I'm using cortisone on my really raw skin, covered with Miaderm.  Also use Aloe gel occasionally.

    Like Red, I've had some really bad sunburns and always got the chills.  Good call on the SE.

  • TB90
    TB90 Member Posts: 992
    edited March 2014

    Minus Two:  From what I had read, I even stopped my multi-vitamin for awhile.  And I too have read that taking supplements is not a good way to address or prevent bc.  Maybe Vitamin D would be an exception?  I have always been uncomfortable with the fact that our bodies could not get what they need simply from the food we eat.  If we all followed Dr. Oz, we would do nothing but eat and pop supplements in order to get "enough" of everything.  Maybe this theory needs to be challenged, finally. 

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