August 2011 rads

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  • katehudson25
    katehudson25 Member Posts: 2,467
    edited August 2011

    I had my first radiation treatment today and I am very frightened of having skin problems, especially since I am going to get breast implants when the effects of radiation heals.

  • Merilee
    Merilee Member Posts: 3,047
    edited August 2011
    2 more then boosts next week
  • justmejanis
    justmejanis Member Posts: 1,847
    edited August 2011

    Merilee way to go!  I know I will be doing a happy dance when I get that close.

    I have some redness/irritation under my armpit, but my breast so far is okay.  Of course I have only had two treatments! 

    Kate don't worry, I believe it is different for everyone and you could easily get through with no skin issues at all.  I hope your treatments go well for you.  No worries!

    I have thrid rads today, then have to see my Onc...and a couple hours after that I have an appointment with my primary care doctor.  Whew!  I;ll be busy today.

    I hope you all have a wonderful day, free of worry!  Hugs.....

  • MamaV
    MamaV Member Posts: 907
    edited August 2011

    shays37 - Chemo kicked my butt!  I had 4 AC treatments (every 3 weeks) which were the WORST!  I was in bed for days 3-5 after each, lost 20 pounds, basically didn't eat for 3 months, lost my hair (of course), had my WBC down to 0 a few times (managed to stay out of the hospital by the grace of God), and major chemo brain and basically felt like I was being poisoned to death. 

    Then I had 12 weekly treatments of taxol - not as bad as AC, but didn't gain any weight back, had no appetite, lost all my eyelashes and eyebrows, lost 2 toe nails, almost lost 4 more fingernails, had major hot flashes and pretty bad bone pain towards the end and MAJOR Taxol depression mixed with anxiety! 

    It was so much fun - Ha!  But praise God I made it through it and it's a little like childbirth - or maybe it was the chemo brain, but I seem to be forgetting how bad it was already :)

    So far I am breezing through radiation - I'm going for #20 today.  I have 8 more after today then just the boosts.  I use Fruit of the Earth pure aloe on put it on liberally 4-5 times per day.  It's sticky and yucky but if it works, I'm all for it!  I think we are all different and our skin type/color makes a difference.  (I have olive Italian skin - but not very dark - but tan easily).  Also, my RO told me that thin women (I'm 5'8" and weigh 125-130) usually don't have as much skin effects b/c the radiation goes right through - or something like that?!?  Oh - and also, I have not worn a bra since I started rads (I wear tight camisoles under my shirts - with the liners from my swim suits put in there to keep the girls who stand at attention all the time under wraps).  I am lucky with that - I know some girls have to wear bras b/c of their size.  I am actually large breasted, but have a tiny rib cage - my custom fitted bras are 28G - no kidding - but if I buy at the department store I can work with a 32D or DD.  Somehow the girls are still perky enough that I can get away with just a camisole and liners (I'm 41)

    Good luck to all starting, in the middle, finishing or whatever.  Big hugs of encouragement to all!

  • sweetcorn
    sweetcorn Member Posts: 188
    edited August 2011

    I see my RO every Wednesday during rads.  Just finished with #16 of 25, then 5 boosts.  No ill effects yet, just a slight tan.  I use the aloe vera gel that they gave me, plus maybe some Curel and Lubriderm for damaged skin.  They said they would give me more stuff when I need it.

    Keep up the spirit ladies!

    Jane

  • justmejanis
    justmejanis Member Posts: 1,847
    edited August 2011

    sweetcorn, you are halfway there.  Congrats!

    My visit went fine today, just routine.  Onc said I will see him once a week.  I forgot to ask about deodorants that are safe.  I made the mistake of coming home and putting my regular under both pits.  Rut Roh!  Found out really quick that was a bad plan!  Any suggestions would be appreciated!

    For me, 3 down, just 30 to go!  Hurray!

  • Merilee
    Merilee Member Posts: 3,047
    edited August 2011

    Happy to report that the Emu oil has brought the itch down to a tolerable level.

  • sarahbob
    sarahbob Member Posts: 131
    edited August 2011

    justmejanis: I go for #3 this afternoon. I am also 3 down, 30 to go! So far no redness, no irritation, nothing. I hope it will continue!

     Sarah 

  • MamaV
    MamaV Member Posts: 907
    edited August 2011

    Good to hear Merilee!

  • Merilee
    Merilee Member Posts: 3,047
    edited August 2011

    Thanks, I felt like I was being ant tortured or something worse. Much better now.

    By next Friday I will be done! I have to tell you I am dragging ass to the finish line hear gals LOL

  • Cyborg
    Cyborg Member Posts: 848
    edited August 2011

    18 down. Monday they said I was half way through. Not on the boards much cause of work. It consumes all of my energy. Thank you , Merilee for the wonderful energy to carry me through the radiation.

    Xoxoxoxo to all of the ladies.

  • Merilee
    Merilee Member Posts: 3,047
    edited August 2011

    Does anyone else have thoughts like " why was I allowed to live while other's did not?"

    It makes me feel like I have some mission or something, just havn't figured out what yet.

  • justmejanis
    justmejanis Member Posts: 1,847
    edited August 2011

    sarabob.....looks like we are on the same schedule basically.  Today I have a little more burn and discomfort, especially in the underarm area.  I got Calendula Gel from my techs and have been using it a lot today.  Hang in there sara...I am with you!

    Merilee I am so glad to hear that the Emu oil is helping.  Yes, I have those thoughts a lot.  My biggest weird emotion is guilt.  Why is my cancer less evil than so many of the women on here?  I was spared both mastectomy and chemo.  Clearly we have no control over the disease we are given.  Still, I wish everyone had it easier.  I too sense I have some new purpose.  My navigator says that Angel Care really needs volunteers...I told her once my treatment is over I will be happy to.  She said with my attitude she knows I can provide great comfort to a newly diagnosed and scared person.  So maybe that is part of it, but far from done.  Cancer changes us profoundly.  I am betting most of us here have asked many similiar questions.  Lots of soul searching happening for me.  I am still a work in progress!

    Love and hugs to all,

    Janis

  • Merilee
    Merilee Member Posts: 3,047
    edited August 2011

    Janis you are so right. Tons of soul searching in this process and every emotion under the sun. Glad to hear I am not the only one.

  • justmejanis
    justmejanis Member Posts: 1,847
    edited August 2011

    Merilee.....I totally understand your feelings about all this.  I know that I am just now beginning the start of my emotional journey through this.  There is a purpose.  It will come to us in time I believe.

    Big, big hugs! 

  • Cyborg
    Cyborg Member Posts: 848
    edited August 2011

    Merilee---Yes. I have those thoughts frequently.

  • sarahbob
    sarahbob Member Posts: 131
    edited August 2011

    has anyone experienced other SE besides skin issues (fever, lung inflammation, etc).  Just wondering. I have read the list of common SE with rads to the chest (per www.cancer.net): 

    Chest. Side effects from radiation therapy to the chest may include difficulty swallowing, cough, fever, shortness of breath, breast or nipple soreness, and shoulder stiffness. Some people may develop a cough, fever, and fullness of the chest that is diagnosed as radiation pneumonitis, an inflammation of the lung occurring between two weeks and six months after radiation therapy. Left untreated, radiation pneumonitis could cause radiation fibrosis (inflammation of the lungs from radiation), which is associated with more serious heart and lung problems. Radiation lung fibrosis (permanent scarring of the lungs from radiation) can occur, as well. The dose of radiation associated with fibrosis is well known and the radiation oncologist accounts for this in the planning process to minimize symptoms from fibrosis.

  • sarahbob
    sarahbob Member Posts: 131
    edited August 2011

    @ justmejanis. I am a little achy tonight in the armpit, but nothing bad. No redness yet. I saw the RO today (will see him every Thursday). He was pleased so far. I also got my appt changed to the mornings (was3:30 and will be 9:10 starting next week). This will be much more convenient, as I have kids to get off the bus/homework/stuff in the afternoons. I will go to the gym and then right to rads and then home. Today was a busy day.....1st day of school (have one in 10, 7th, 5th) rads this afternoon, my youngest had an appt and then home to start dinner, etc. PHEW! 

  • katehudson25
    katehudson25 Member Posts: 2,467
    edited August 2011

    Hi Janis and Sarahbob,

    It looks like I started one day after both of you. Today was my second treatment. I have 13 to go and then a week of boosts. So far I don't have any side effects. I am applying miaderm cream three times a day.

  • justmejanis
    justmejanis Member Posts: 1,847
    edited August 2011

    sarabob....WOW!  You sure have a busy schedule.  My "baby" is 32 and lives in Colorado.  No kids here for ages.  I am glad you got your appointment time changed to fit your schedule better.  I go every morning at 9:30 so not too bad.  I get up very early, so I could go earlier bit that was the time slot they had open.  I think I will see my RO every Thursday as well. 

    The side effects you listed sound kind of scary.  So far I am good, but I do have that sunburn thing going on today.  A bit sore.  This too shall pass.

    Kate....everything sounds great for you!  I hope you get through all this with very few problems!  Hang in there and please stay with us.

    Always...hugs! 

  • Elizabeth1889
    Elizabeth1889 Member Posts: 1,036
    edited August 2011

    Hi Merilee:  Yes, I often ask myself what is my purpose now that my active cancer treatment is coming to an end.  Like eyeryone, I have been profoundly changed by the experience.  My plan for now is to become a Make A Wish volunteer.  Whatever happens next, I will leave in God's hands.

  • Merilee
    Merilee Member Posts: 3,047
    edited August 2011

    If  I were doing rads over again I would try to schedule them right before bed time.

  • Merilee
    Merilee Member Posts: 3,047
    edited August 2011

    Last regular week for me. Boosts start next week, I can see the rainbow all ready

  • bb226
    bb226 Member Posts: 102
    edited August 2011

    Today is my last treatment! I am a "free" woman after 1000. I will be free from going everyday. I am seeing the skin nurse in 1 week because you peak with skin reactions 1 week post rads.

    Merilee you bring a real good thought to this board. Why us? How will this change us for the better? For me I told my husband at the beginning that God gave me cancer so I can help someone else through the journey. I didn't think it would be so soon. As you know my sister had an excisional bilateral breast bxs yesterday. I am extremely worried for her but do not tell her. I know so much more now then pre-cancer. I have been very helpful to her with suggestions. Her results come in Tuesday. You probably don't know this but I am a pediatric nurse that has the pleasure of working with cancer kids. How has my cancer experience changed me? God I hope I am a better nurse for those kids and their families! I didn't ask God for cancer but I am going to use this experience to make a better person of me.

    sarahbob-Yes those side effects can happen in a very few number of patients. I think I was quoted 1-4%. It is dose dependent. In other words the more rad to your lungs, the better chance of possible having a problem. My co-worker's mom who went through rads in the last 2 years did get rads pneumonitis. It was easily treated with antibiotics. With all these treatments we all weighed the pros (decrease chance of a recurrance) and the cons (long term side effects or medically termed long term toxicity). We all will have rad fibrosis (scar tissue) when we are done. We won't notice it in day to day life but if we ever need a chest xray it will show up. Again this was mentioned during my initial appointment. I saw 2 RO before starting treatment with my 2nd one. I also had my husband along and wrote notes. This helped when I finally made the decision. But now I can refer back to the notes and let you know what was mentioned to me. 

    If I went back to the time before I started rads and was able to change anything, I would tell my self that rads was not as bad as I imagined. It was very doable. Alot of people come through with minimal SE. And what SE there are, the doctors and nurses are on top of them and have treatments to help. Ladies just starting please keep this in mind. These boards sometimes highlight the people that have severe problems. Not many people tell you that it is doable and you will get through it!

    So sorry for rambling but it is the anticipation of being done in 4 hours. I am so happy but kinda sad. Can you believe that??

  • justmejanis
    justmejanis Member Posts: 1,847
    edited August 2011

    bb226......you weren't rambling at all, I enjoyed reading your post.  HUGE congratulations on finishing up today!  I too have the feeling i was given cancer for a reason.  I do plan on volunteering for AngelCare...but I don't think I am done.  It is all still a process for me.  I am so sorry about your sister...but the timing is amazing and you will be a strong shoulder for her to rely during the confusing days ahead.  Big hugs to you both, and sending lots of kove as well.  I hope she gets good news.

    Elizabeth...that is wonderful that you have chosen such an amazing charity!  I know they will love to have you, and there is so much good to be done.  I am so happy to hear your treatment is just about done!

    Merilee....I love your rainbow and I will be reaching for it not too far down the road.  Sending lots of healing and happy thoughts your way.  I am thrilled you are nearly finished!

    Day # 4 rads for me today...counting down. 

    Worried about Irene and all of you up the east coast.  I will be anxious to hear your experiences.  Just be safe.

  • lynniea
    lynniea Member Posts: 611
    edited August 2011

    Well I am about to start mine.  We are suppose to be direct hit for the hurricane.  I got through chemo I heard Radiation is not so bad.  I start my real thing on Sept 1.  I just want this all over with.  Hope everyone has a nice weekend.  Ours will be nice and wet.

  • sarahbob
    sarahbob Member Posts: 131
    edited August 2011

    @ lynniea: I am in NC and we are getting a direct hit at a category 3/4 later tonight/tomorrow. We have already started getting rain from the outer bands on the coast. I pray the storm weakens dramatically by the time it gets to you in CT. Stay safe! 

    @ bb226: I know they list ALL possible side effects on websites and that sometimes freaks people out. The internet can be a wonderful resource and also be the worst place for information. Sometimes you get TOO much info! LOL! I am a PT, so I have a degree in healthcare. I am getting most of my "cancer education" from boards like this....people who have BTDT and learning what is most common. My RO told me about the scarring also and said I will probably always have to inform drs whenever I have a chest xray that I have had chest rads. He also mentioned the possiblity of pneumonitis. I really like my RO. His personality is not the most outgoing/energetic, but he seems very supportive. He told me yesterday not to wait until Thursdays if I have an issue/problem.....he will see me whenever I need him. His nurses are great too.  

    I was wondering, for those of us who had a MX, would we get some of the lung SE more easily b/c there is less tissue for the rads to go through? I am sure they adjust the strength accordingly, but this thought still went through my head. Also, does anyone get a "bolus" (gel pad they tape to my chest) with treatment? I get it every other day. The "odd" days are bolus days for me (#1, #3, #5, etc).   

    Sarah 

  • sarahbob
    sarahbob Member Posts: 131
    edited August 2011

    BTW, yesterday was 6 months since my surgery and 8 months sicne my dx. WOW! How my life has changed in the last 8 months! I was thinking last night (as I was rubbing aloe gel on my boob stump) that a year ago, I had no clue how drastically my life was about to change. 

  • Merilee
    Merilee Member Posts: 3,047
    edited August 2011

    Sounds like many of us are moving from thoughts of no fair and "being picked on" to being "picked out" instead. It takes a while to figure this out. I plan to live my life in almost a completely different way. Not so much on the fast forward work treadmill. I think I prefer poor over worn out to the point of getting sick. Big change for this lady. I gave notice at my work place this week and am going to live for a while on a small disability policy until I feel I am at optimal health again. First time in my life since I was age 14 that I will not be working. I am almost 52

  • Elizabeth1889
    Elizabeth1889 Member Posts: 1,036
    edited August 2011

    bb226:  Congratulations on finishing today.  I had that strange mixture of joy and sadness when I finished chemo, but when I finished rads, all I felt was joy.  I hope your joy will be abundant, too.

    Merilee:  Best of luck with your new life away from work.  I think everyone is at peace and deeply satisfied when they follow their gut feelings. 

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