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Topic: March 2008 Rads Team

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Grand Blanc, MI
Joined: Sep 2007
Posts: 120
  • Posted on: Mar 1, 2008 04:39 pm
brst26 wrote:

Hoping to get a group of March rads women together here...I will be starting sometime in March.  I see my rad onc on Friday.  Here's my history in a nutshell: I was diagnosed with IDC in July (yup...only 26 years old)...joined a clinical trial (B-40) which had me do my chemo first, followed by lumpectomy and ALND.  At the same time I am having rads, I will start up getting Avastin again (part of the trial) once every three weeks for 10 cycles.  I have no idea what to expect from radiation...but I've heard that it's a lot easier than chemo!

-Abbey, 27 yrs old...started Taxotere, Gemzar, and Avastin on 7-26...AC started 10-18. Lumpectomy on Jan. 23rd, followed by rads and 30 more weeks of Avastin.
Dx 7/3/2007, IDC, 2cm, Stage II, Grade 3, ER-/PR-, HER2-

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buffy2az
Joined: Feb 2008
Posts: 15
Mar 2, 2008 06:53 pm buffy2az wrote:

I'll join up with you.  I saw my rads oncologist last Friday and he determined that I need treatment.  I go on Wed. for the planning, mapping session, then a "dry run" session a day or so after - not sure what that is exactly.  I think I'll start the daily treatments the Monday after, lasting 6 weeks.

I was diagnosed in Jan. and had my lumpectomy on 1/23.  I don't need chemo because the tumor was only 6 mm, but my PR was positive so I've started Tamoxifen as of 2/22.

I don't know what to expect from Rads either, only what I've read the other women have experienced.  Let's start off together and see how things go.  I'm hoping for the best-case scenario. :-)

Good luck!

luckywife
Joined: Nov 2007
Posts: 404
Mar 2, 2008 07:36 pm luckywife wrote:

Hello all, 

I would like to join too. My radiation will be done to manage the bone pain I have due to metastasis in my lower back and pelvic area.

I had my mapping session on Friday and the first appointment is on Tuesday. I go on for 14 days of radiation Mon thru Fri.
I have been told that in addition to possible skin issues, I may be facing nausea and diarriah as side effects as my digestive system may be in the way of the radiation. I am most concerned about that. I wonder if anyone who has experience with this may give some tips. 

I am an almost 13 year survivor so did my initial lumpectumy and breast radiation 12 years ago.

Good luck all.

-luckywife 

brst26
Grand Blanc, MI
Joined: Sep 2007
Posts: 120
Mar 3, 2008 04:26 pm brst26 wrote:

Buffy2az...what do you know, we had our lumpectomies on the same date!

Luckywife...sorry to hear that you are having to go through rads for a second time.  Let us know how your mapping goes on Friday.  I have my consult on Friday...so hopefully, I will know when I will get my tatoos, simulation, and start rads after that.

-Abbey, 27 yrs old...started Taxotere, Gemzar, and Avastin on 7-26...AC started 10-18. Lumpectomy on Jan. 23rd, followed by rads and 30 more weeks of Avastin.
Dx 7/3/2007, IDC, 2cm, Stage II, Grade 3, ER-/PR-, HER2-
WellWater
Cedar Lake, IN
Joined: Dec 2007
Posts: 1823
Mar 3, 2008 04:51 pm, edited Mar 3, 2008 05:44 PM by WellWater WellWater wrote:

Well count me in too......I keep getting invited to these parties that I really don't want to go to but I'll keep on coming and since I'm here I'll keep on dancing.

I finish my T/C tx's on March 7th - am scheduled to be tattooed on the 18th with rads (33 total)starting on the 25th so you gals may be ahead of me in start dates.

My rad nurse said they will give me any creams I will need.  One deoderant hint I got that sounded good was a drop of Purell rather than the natural deos. 

I'll have to give up swimming and that'll be tough but I guess I'll join the gym rats and work out on the machines for as many months as it takes for my skin to heal.  I'm hoping we have good experiences and don't suffer bad s/e's.

Abby - sure sorry to see you go thru this at such a young age - I'll be 60 on April 2nd and I think I'm TOO YOUNG to be dealing with this!

Luckywife - So sorry to hear that you're a repeater......I pray that your s/e's won't be too bad and that they'll be able to manage your back pain with rads. 

Buffy:  Lucky you able to skip chemo - how is the Tamox s/e's?

Trina


Dx 11/7/2007, ILC, 1cm, Stage I, Grade 1, 0/0 nodes, ER+/PR+, HER2-
Nanstoys
Pierce, CO
Joined: Feb 2008
Posts: 51
Mar 3, 2008 05:39 pm Nanstoys wrote:

Well ladies, count me in.  I was diagnosised in Jan with DCIS, had a lumpectomy on 1/21 have changed oncologists, the first onoclogist initally said, I need do nothing additional I had a small tumor, 3 mm and 2 mm of clear margin.  I skipped home.  Then I got a call from the surgeon wanting to schedule another surgery.  HUMMMM Went back to the onoclogist who when 180 and said, surgery, chemo, radiation and Armidex. Went to surgeon who said, you don't need surgery just radiation.  HUMMMM  Went and a second opinion.  Best thing I did.  New onoclogist - went step by step through my pathology report with me.  Gave me the down and dirty.  No additonal surgery but yes to radiation.  NO Armidex as my tumor was too small to test, so unsure if it was pos or neg.  Anyway had my mapping and simulation down on Thursday and will start on or around St. Patricks Day. I have a great group of professionals around and a support group that is great. 

Trina- I'm with you.  I am 56 and feel that I am too young for this.

Well ladies it is All for one and one for all.

I am determined to live my life to follow my favorite quote

"Life in a banquet and most poor suckers are starving to death"  Mame Dennis 

darah58
Joined: Mar 2008
Posts: 42
Mar 4, 2008 12:11 am darah58 wrote:

Hello to you all, I have one more rad treatment to go.  I have been doing very well, so I thought I would send my best advice to you who are yet to begin. 

Skin:  I used calendula cream (marigold-extract cream from Whole Foods) three times daily.  My radiation oncologist recommended this and, after five weeks, my skin is still supple and I only now have some redness under my arm. 

Fatigue:  If you already have an exercise program, stick with it.  I have been doing pilates for six years -- continued during radiation 4x weekly -- and it has been so, so good for me.  I had lumpectomy for DCIS -- no mastectomy or chemo -- but stretch as much as you can comfortably do it.  Some of us have underarm stiffness, so work on keeping your muscles flexible.  Rest when you can, and don't try to be too brave. 

Deodorant:  I have been using Tom's of Maine Calendula deodorant.  It's been working well, and I have also been using cornstarch powder for my underarm and under-breast area. 

Shaving:  I bought a battery-operated razor at CVS, and I use it every Sunday.  I hadn't used an "electric" razor since I was 14, but this has worked well, and it has not exacerbated underarm irritation.

Bra:  Many people on this site have recommended good bras.  I've been using a Title Nine sports bra, but I only wear it for exercise.  If you can possibly do without it, do not wear a bra.

Hope this is helpful.  I'll post again if I remember anything more.

Darah 

buffy2az
Joined: Feb 2008
Posts: 15
Mar 4, 2008 11:47 am buffy2az wrote:

Hi all!

Trina - S/E from Tamoxifen haven't been too bad yet. I take it before bed because I wanted to reduce the risk of nausea - so far I've only had 3 or 4 mornings when I felt a little bit of nausea, but it went away quickly. I'm already dealing with the hot flashes off and on - trying to work my way into menopause - and I think the Tamoxifen is adding to them. I'm waking up 2 or 3 times in the night with them, and I've noticed them becoming more frequent during the day now. I've only been on it for 10 days, so I'm hoping there won't be any other s/e.

Darah - thanks for the suggestions. I was wondering about getting an electric razor and whether it would cause irritation. As for the cream you used, is it messy? My doctor recommended aloe vera gel, but that can be a little messy. I'm planning to work through all this so I'm hoping to keep the fatigue at bay. I'm dealing with some of that already and trust it doesn't get any worse. Still not sure what I'll do about the bra situation.

I have my mapping session tomorrow afternoon, so I'll post again after that.

Here's to keeping a positive attitude!
Buffy

Nanstoys
Pierce, CO
Joined: Feb 2008
Posts: 51
Mar 4, 2008 03:29 pm Nanstoys wrote:

Thanks for all of the information.  I am planning on exercising during my radiation treatment as much as I can.  I am a swimmer so will have to change up my routine.  My gym actually has a cancer treatment work out program that I am joining. It is twice a week for the duration of your treatment and they waive your dues for that time period.  I hope to work, but if it gets to be too much I will go out on short term disability.

The corn starch sounds good and will check with my nurse about the cream. 

I am large busted so going without a bra if I am working is not an option.

I am hoping to have enough energy to play with the dogs even if I can't run with them. (one Great Dane and one Gordon Setter/Shelti cross)They are what is helping me through each day.  You can't feel too sorry for yourself when you have a great big dog try to crawl in lap with his big blue toy and giving you kisses to make you feel better.  He just knows if he lays down beside me that I will feel better, and he is right.  Boyfriend and family also wonderful.

Life is a banquet and most poor suckers are starving to death!" by Mame Dennis
Dx 1/21/2008, DCIS, <1cm, Stage 0, Grade 2, 0/0 nodes, ER-/PR-, HER2-
pattis
Snellville, GA
Joined: Mar 2008
Posts: 5
Mar 4, 2008 04:39 pm pattis wrote:

Buffy, you and I are on the same path.  I had a needle biopsy on December 21st, a lumpectomy on January 3rd, and received my cancer diagnosis on January 8th.  I started radiation on February 21 and will do seven weeks total.  I'm on tamoxifin and it's not "agreeing" with me.  Hot flashes, insomnia, bloating, leg and foot cramps.  Please keep me posted on how you are doing. 

Listen for God's voice in everything you do.
Frenchgal
Joined: Mar 2008
Posts: 4
Mar 4, 2008 05:53 pm, edited Mar 4, 2008 05:54 PM by Frenchgal Frenchgal wrote:

Hello to you all,

First time I participate in an on-line conversation ever, but then again, first time cancer patient.  I've been diagnosed with BC à the end of September.  I have been operated twice since and started my rads on February 25th.  I should have 20 tx.  So far, so good except for irritation around the nipple.  Thanks for all the info concerning aloe gel and cornstarch that I have been reading about.  I intend to talk to my rad onc tomorrow and see if he is OK with this.   For you ladies that will be starting rads soon, keep in mind the  ink  used in marking will permanently stain your closes so I have been wearing dark close and an old cotton sports bra.  I have been told that no bra is better but being 50 and a 34D, I am certainly non comfortable without a bra.     Good luck to you all, I sure will be reading you ladies every single day.  Thanks    

brst26
Grand Blanc, MI
Joined: Sep 2007
Posts: 120
Mar 4, 2008 06:30 pm brst26 wrote:

Man...I feel for you ladies with the hot flashes!  I experienced them with chemo...since it haulted my periods.  I get to be oh so lucky and go through it all again when I actually get to the age of going through menopause...haha! 

Nanstoys-that is the coolest thing I have ever heard of (your gym's program)!  I am a high school PE teacher...so I'm a big exercise fanatic.  I'm finally starting to get back into the whole workout routine.  Chemo got to be too much to continue with an exercise program while working.

Welcome frenchgal!  Do you live in France? 

-Abbey, 27 yrs old...started Taxotere, Gemzar, and Avastin on 7-26...AC started 10-18. Lumpectomy and SNB on Jan. 23rd, ALND on 2-13, followed by rads and 30 more weeks of Avastin.
Dx 7/3/2007, IDC, 2cm, Stage II, Grade 3, ER-/PR-, HER2-
Frenchgal
Joined: Mar 2008
Posts: 4
Mar 4, 2008 06:57 pm Frenchgal wrote:

Hello Buffy2Az

I believe that a "dry run" is sort of a "make believe" tx so that you know what to expect at your first tx.  Personally I find that thinking of how I'm one step closer to the cure during the treatment helps to keep my nervousness under control. 

Good luck !

Frenchgal
Joined: Mar 2008
Posts: 4
Mar 4, 2008 07:05 pm Frenchgal wrote:

Hello Brst26,

I wish I was living in France, but I'm from up north in the snowy province of Québec. 

luckywife
Joined: Nov 2007
Posts: 404
Mar 5, 2008 01:25 am, edited Mar 5, 2008 01:29 AM by luckywife luckywife wrote:

Hello all,

I had my mapping session last Friday and tatooed today. They also did my first treatment today. Since I am getting radiation on my lower back and pelvic are for pain managment for bone pain, it was quite painful today to lie down still but people were gentle and quick. That helped a lot and I also took some pain meds just before starting. As the treatment progresses I am hoping my pain will reduce and I won't need to take the pain meds. I was told to take anti nausea meds as the rads may target my digestive system. I didn't feel any nausea. I am going to take the meds again tomorrow but going to try without them on Fri. May be I won't get the nausea? I am also expected to have diarrea but so far everything seems okay. Hope stays that way.

I am told not to put any cream on the area of radiation before the treatment. Since my appt. is in the morning, I will shower after I get back and then cream it so by next morning, it should be okay. Did they say anything like that you all for the breast?

I took tamoxifin for 5 years and it worked like a charm for me. Side effects were not too bad and the body got used to them over time. I used to put the corn starch and a fresh t-shirt on the night stand and changed middle of the night without even opening my eyes so I as to not interrupt mine or DH's sleep. I was in my mid 30's then.

Good luck everyone. Let us get through this with minimal side effects.

-luckywife

trigeek
Orlando, FL
Joined: Aug 2007
Posts: 641
Mar 5, 2008 11:33 am trigeek wrote:

Hey Gals,

Bilateral mastec with recon on 8/31/07 Finished DD chemo 1/11/2008 had implant exchange on 2/14 - happy valentines day !

Had my mapping yesterday, will get tattoos and get my first treatment tomorrow.

I do not know how many I will get forgot to ask the doctor. I think I will be getting the whole chabang, from collarbone down and maybe towards my back too, since I declined to have additional Axillary Node Dissection surgery.

I am nervous although I know this should zap any stray c cells that might have hidden from chemo I still have a hard time digesting exposing myself to radiation beams voluntarily.

Sigh...

Trina,

Why do you have to give up swimming ? I was not aware of that and thought it would be great to keep it up during radiation.

Live Deliberately ! http://www.aylin-yeahright.blogspot.com/
Dx 8/3/2007, ILC, 2cm, Stage II, Grade 2, 2/6 nodes, ER+/PR+, HER2-
frankrause
Joined: Mar 2008
Posts: 16
Mar 5, 2008 02:31 pm frankrause wrote:

Hi, my name is Fran and I should start my rad treatment next week.  I am nervous but ready to get started and over with.  I live in Baton Rouge, LA.  Good luch to everyone.

buffy2az
Joined: Feb 2008
Posts: 15
Mar 5, 2008 05:05 pm buffy2az wrote:

I just got home from my mapping session.  It wasn't bad at all.  My arms started going to sleep from having them over my head for so long - 1/2 hour maybe? - but they let me put them down as soon as they could.  I'm not claustrophobic so the CT scanning didn't bother me.  I had to get tattoos because I'm allergic to the adhesive on tape - otherwise they would have marked me, then covered the marks with tape.  The tattooing wasn't too bad - I noticed a little more "pain" on my sides than I did anywhere else.  Overall, I'd say it was pretty easy.

I go on Friday for my dry run.  Thanks, Frenchgal, for the explanation on that.  I think it will be nice to have them go through it all before actually doing the radiation so I know what to expect.

One of the technicians told me that it was fine to use the aloe vera gel after treatments, that it wouldn't help with the redness, but would make it feel better.  Have to wait and see I guess. I'm fair skinned so I'm sure I'll get pretty red.  I'll get the rest of my questions answered on Friday.

Buffy

trigeek
Orlando, FL
Joined: Aug 2007
Posts: 641
Mar 6, 2008 06:53 pm trigeek wrote:

Had my mapping on tuesday and today got the tattoos and the first treatment. I was about to jump off the table, I do not recall how long I was in that stupid position but had a really hard time staying still I think it took at least 50 minutes in the same position. My neck and my shoulder killed me.

Buffy I will put pure aloe (it is liquid) after treatments and will put on aquafor at nights.

1 gone 32 to go !

Live Deliberately ! http://www.aylin-yeahright.blogspot.com/
Dx 8/3/2007, ILC, 2cm, Stage II, Grade 2, 2/6 nodes, ER+/PR+, HER2-
sharona
Joined: Feb 2008
Posts: 31
Mar 6, 2008 10:03 pm sharona wrote:

I go tomorrow for the beginning of this treatment process.  I am so thankful to find a group of others in the same boat.  I have really been sad toda- I accepted that radiation (instead of mastectomy), is my next step.  I decided to take a medical leave from work, mainly for my "spirits "and my company is OK with it.  I am in sales and really need to be "on", this diagnosis has me far from it.

Sharon 


Dx 1/25/2008, DCIS, 1cm, Stage 0, Grade 3, 0/2 nodes, ER+/PR+
nicky36
Sudbury, ON
Joined: Aug 2007
Posts: 16
Mar 6, 2008 10:25 pm nicky36 wrote:

Hi everyone!

Finished 3 rounds of FEC and then 3 rounds of Taxotere on January 31/08. Man oh man I am glad that is done.  Tattooed and started Rads on Tues. Mar 04/08.  In it for the long haul as scheduled to get 30 treatments.  Using 100% pure Aloe gel.  Also started Tamoxifen on Feb. 25/08 and am getting some dandy hot flashes. Started swimming on Feb 27/08 and am trying to build up my strength and lose some weight. Scale is reading the same number as the past month but jeans and other clothes are getting real tight.

Will be seeing a LE therapist soon as my passion is driving my motorcycle and I want to do everything to be able to continue doing so.

Haven't been able to get much sleep over the past 3-4 months and am very annoyed by it so seeing another therapist to learn relaxation techniques so that "maybe" I'll get at least 5-6 straight hours of sleep every now and then.

So as of today (Mar 006/08) I am 3 down and 27 to go.!!

Nicky

"We are like tea bags, we don't know how strong we are until we are thrown into hot water."
Dx 8/7/2007, IDC, 1cm, Stage II, Grade 1, 1/14 nodes, ER+/PR+, HER2-
brst26
Grand Blanc, MI
Joined: Sep 2007
Posts: 120
Mar 8, 2008 12:22 pm brst26 wrote:

I go for my mapping and CT scan on Friday (3-14)...I just want to get this started...the sooner I get started, the sooner I'll be done :)  My rads onc told me that I'd have 6.5 weeks of rads...5.5 to whole breast, then 1 week of boost to just incision area.  Good luck ladies who have already started!

-Abbey, 27 yrs old...started Taxotere, Gemzar, and Avastin on 7-26...AC started 10-18. Lumpectomy and SNB on Jan. 23rd, ALND on 2-13, followed by rads and 30 more weeks of Avastin.
Dx 7/3/2007, IDC, 2cm, Stage II, Grade 3, ER-/PR-, HER2-
koshka1
Vancouver, BC
Joined: Oct 2007
Posts: 193
Mar 8, 2008 01:03 pm koshka1 wrote:

hello!

i'll join your group.

just started rads last tuesday......oh my!! i am so exhausted even after 4 treatments.  hard to believe how that 15 second treatment actually does something!!!

seriously, came home after tx yesterday and  just crawled into bed.

they did not advise chemo for me,,,my tumor was 4mm and grade 1, but i will be taking tamoxifin after.

i am having 16 treatments w/ 4-8 boosts after. I am in Canada and they are doing different rads now, shorter treatment/stronger doses.

anyway,,,hang in there ladies!!

kosh...   :)


Dx 12/2007, IDC, <1cm, Stage Ia, Grade 1, 0/1 nodes, ER+/PR+, HER2-
trigeek
Orlando, FL
Joined: Aug 2007
Posts: 641
Mar 8, 2008 04:26 pm trigeek wrote:

The second treatment was a lot better, and I was in and out in about 15 minutes.

I did feel as if my throat was achy afterwards and had a slight cough, I have been  prone to psychosomatic symptoms  and I think this is one of them. 1 hour after the treatment I was really tired, and was ok 5-6 hours later. Maybe cause I was tensing up a lot during the treatment ?

The nurse was not able to answer my questions which were:

- Why should we avoid hot and cold showers (I do hydrotherapy cold-hot showers everyday)

- Why cant' we swim ?

One would think that being a nurse she would know the answers ! she kept on repeating:

" you just have to avoid hot and cold and not swim for 7 weeks"

And I was repeating " i understand you but why ??? does it interfere with how radiation works ? Is it something with the veins constricting/contracting ?? "

Finally she  brought one of the radiation therapists to answer my questions, basically she said that they wanted to baby the skin during rads. Ok now we are talking I said.

So I will not do my hydrotherapy , but I will just protect the skin getting rads  by applying vaseline before going swimming.

She thought it was a good plan or she wanted to get rid of me.

In any case I will be swimming maybe not often but once a week, hopefullly the vaseline will seal out the drying effect of the chlorine, I was not able to swim after mastectomy then  during chemo cause I was afraid of catching infections from the gym pool, then  had my exchange surgery and finally thought I could hit the pool again.

I am also taking curcumin ( see the curcumin thread in alternative treatments) it seems to protect the skin and is stated to possibly enhance the efficacy of radiation and taxol ( but counteracts with AC)

Live Deliberately ! http://www.aylin-yeahright.blogspot.com/
Dx 8/3/2007, ILC, 2cm, Stage II, Grade 2, 2/6 nodes, ER+/PR+, HER2-
buffy2az
Joined: Feb 2008
Posts: 15
Mar 8, 2008 05:55 pm buffy2az wrote:

Trigeek - I'm glad your second treatment went better. That's encouraging.  It does seem odd that a nurse couldn't answer your questions, especially since she works in that area. At least you got a couple of them answered.

Abbey, I'm with you on wanting to get started!  I have everything done now and am ready to start tx on Monday. I'm armed with my aloe vera gel and Aquaphor.

I went looking for cotton camisols today...no luck. Everything is nylon and I'm thinking that would not be as comfortable.  It was suggested to me by one of the therapists that I wear something like that rather than a bra to avoid irritation to the skin. I'll keep looking.

I wouldn't think I'd need it right away.

6 1/2 weeks will go by fast, right? :-)

Buffy

sharona
Joined: Feb 2008
Posts: 31
Mar 8, 2008 07:15 pm sharona wrote:

I get started this week also.  My cat scan was Fri, markings on Monday and start the Tx on Wed.  They have not mentioned the gels and bras, is this irritation expected?  My doc acted like the 1st 2 weeks, very little change.  I wanted to do water areobics also, is that out of the question too?  I find it amazing that they don't tell you all of this before you start.  My primary care doc said these 6 weeks will fly by, I hope so.

Sharona


Dx 1/25/2008, DCIS, 1cm, Stage 0, Grade 3, 0/2 nodes, ER+/PR+
trigeek
Orlando, FL
Joined: Aug 2007
Posts: 641
Mar 8, 2008 07:44 pm trigeek wrote:

Sharona,

They are afraid of the irritating affects of chlorine on the skin and that in turn this might affect being able to complete the rads uninterrupted.

Intentions are good, we also need to use good judgment, so I will be limiting my chlorine exposure to 1-2 /week, and will put aquaphor before going in and will rinse immediately there(not waiting till I get home)

Live Deliberately ! http://www.aylin-yeahright.blogspot.com/
Dx 8/3/2007, ILC, 2cm, Stage II, Grade 2, 2/6 nodes, ER+/PR+, HER2-
luckywife
Joined: Nov 2007
Posts: 404
Mar 8, 2008 11:06 pm luckywife wrote:

I had 4 treatments last week on my lumbar spine and pelvic area. I had to use aquaphor on Wed. night as the second day my skin felt a bit of burning sensation on the lower back. I was very tired on Thursday and Friday and slept most of the afternoon. I am sure if I was out doing things I may have been able to but when I allowed myself to rest the body was ready to do so happily.

First time around radiation on the breast (12-13 years ago) I remember the nurse telling me that radiation is killing the bad (and some good) cells in the targetted area. Recuperating from that and flushing all the dead cells along with healing all takes energy. Therefore the body need rest and you feel the fatigue. If you can afford to rest, it will only help you in the long run. Next week, I am planning a nap every afternoon.

As for nausia, I stopped taking the anti-nausia meds on Fri and had no problems so don't plan to take next week. As for diarriah, no problems so far...keeping my fingers crossed for the next two weeks.

Brst26, good luck starting next week. You got ample feedback from those who have started so it should be a breeze Smile

Good luck everyone. Happy napping if you can.

-luckywife

luckywife
Joined: Nov 2007
Posts: 404
Mar 8, 2008 11:25 pm, edited Mar 8, 2008 11:26 PM by luckywife luckywife wrote:

Hello everyone,

I found another conversation on "radiation side effects" where other women have posted about their skin irritation and fatigue getting worse as radiation progresses.  You may want to take that into consideration along with the "babying your skin" advise. Same goes for resting.

Nurses told me that it is really not good to have to take a break in radiation schedule and rad. onc. will not continue treatment if the skin is not reasonably healthy and your blood counts are not too low. Radiation treatment has cumulative effects so skin irritation and fatigue get worse with time.

My rad. onc. meets with patients every week to review progress.

Trigeek, you are right in asking questions and should get the answers for sure and correctly from the oncolgist him/herself.

Goodluck and take care.

-luckywife 

WellWater
Cedar Lake, IN
Joined: Dec 2007
Posts: 1823
Mar 10, 2008 08:49 am WellWater wrote:

Trigeek:  I am a huge swimmer - not being able to swim is bumming me out more than the tx's themselves.

My rad onc said the chlorine will irritate the skin and we don't need another irritant.  When I finish my rads we are going to Gulf Shores AL for a week in a beach house...when I told my rad onc this lhe said "well, you know you CANNOT swim in the gulf because it's salt water". 

So until I finish my rads I will stay out of the pool.

Sorry it took so long for an answer - I just finished my last chemo on Friday and have been down for the count since then.

Trina


Dx 11/7/2007, ILC, 1cm, Stage I, Grade 1, 0/0 nodes, ER+/PR+, HER2-
trigeek
Orlando, FL
Joined: Aug 2007
Posts: 641
Mar 10, 2008 09:13 am trigeek wrote:

Thanks Trina, guess no swimming for me. ( can not run either cause not supposed to wear a bra and the implants are uncomfortable).. that leaves me on my bike I guess.

So lets say I slather aquafor at night, and then should I take  ashower to wash it off before I go to the treatment ?

Live Deliberately ! http://www.aylin-yeahright.blogspot.com/
Dx 8/3/2007, ILC, 2cm, Stage II, Grade 2, 2/6 nodes, ER+/PR+, HER2-

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