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desdemona22
Joined: Dec 2008 Posts: 557 |
Sep 15, 2009 08:46 pm
desdemona222b wrote:
Irishred - Have you told your rads technician/doctor you're using hydrocortisone cream? I don't think you're supposed to go anywhere near that stuff during rads, especially with your skin breaking down like that. I'm pretty sure it will only make things worse. No one has mentioned lidocaine gel, which my rads onc gave me during my treatments. It helps the discomfort quite a bit, and it is the only thing I used during rads. I don't think anything actually prevents skin breakdown, but I do know that one reason they tell you not to use ANY creams or ointments that are not prescribed is because they actually make skin breakdown worse and more likely. Diagnosis: 11/17/2001, DCIS, <1cm, Stage 0, Grade 3, 0/0 nodes, ER+/PR-, HER2+ |
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MTG Joined: Aug 2009 Posts: 287 |
Sep 15, 2009 10:03 pm, edited Sep 15, 2009 11:42 PM
by MTG
MTG wrote:
Wow ! I thought hydrocortisone/ cortisone creams were ok !!!! I've just completed my pre-radiation shopping and picked up a tube thinking that's what every uses to deal with itching. Now I'll be sure to check it with my doctor. Of course, I'm feeling a bit foolsh now since I already know that everything should be okayed by the doctor, I just thought this was like aloe and ok without asking. A dumb move but you ladies have my back (even without knowing it). M
Diagnosis: 6/30/2009, 1cm, Stage I, 0/1 nodes, ER+/PR+, HER2- |
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desdemona22
Joined: Dec 2008 Posts: 557 |
Sep 15, 2009 10:20 pm, edited Sep 15, 2009 10:24 PM
by desdemona222b
desdemona222b wrote:
This Post was deleted by desdemona222b.
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desdemona22
Joined: Dec 2008 Posts: 557 |
Sep 15, 2009 10:20 pm, edited Sep 15, 2009 10:23 PM
by desdemona222b
desdemona222b wrote:
Not trying to make anyone feel bad, MTG, just trying to help. But, there's a reason the docs tell you not to use any creams or lotions, period, for the duration of your rads therapy. For one thing, you can't prevent burns (or skin break-down, as the professionals call it), but you can definitely make it a lot worse by disregarding your doc's advice and using moisturizers, etc. A lot of women just can't or won't accept that fact - it's not like you're going out in the sun or anything. The radiation works by killing cells - all cells - but gradually. It kills both healthy and cancerous cells, and the healthy cells regenerate relatively fast. So, any itching is caused by that and goes way beyond the surface of the skin - the entire breast is radiated through and through which means the itching is also coming from the dermis. Also, moisturizers and creams tend to hold in the heat from the radiation. Lastly, the skin becomes so insulted from the treatments that even gently rubbing it can cause painful breaks and blisters, which is why they tell you not to wash the breast. You want to avoid even the gentlest rubbing on the skin, and they give you Lidocaine in gel form instead of cream form so you can just gently spread it without really affecting the skin. Hydrocortisone shouldn't be used on the skin on a regular basis even if one is not going through radiation therapy. It can clear up short-term issues like rashes and itching, but using it regularly is bad even for healthy skin. Diagnosis: 11/17/2001, DCIS, <1cm, Stage 0, Grade 3, 0/0 nodes, ER+/PR-, HER2+ |
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MTG Joined: Aug 2009 Posts: 287 |
Sep 15, 2009 11:41 pm
MTG wrote:
desdemona22 - Please, please, please, I appreciated reading the post about hydrocortisone and your follow up post as well. For me, feeling "dumb" is not at all the same thing as feeling "bad"; it simply means being reminded how much there is to learn and to keep straight and how thankful I am that I can rely on you and others who've gone down this path before me. I never expected this sort of education but I am learning tons ! M
Diagnosis: 6/30/2009, 1cm, Stage I, 0/1 nodes, ER+/PR+, HER2- |
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ccbaby Joined: Feb 2009 Posts: 506 |
Sep 16, 2009 10:05 pm
ccbaby wrote:
MTG...My radiologist told me today to use hydrocortisone cream if I start having bumps and /or itchiness. He said any brand will work. If it gets worse, he will give me a prescription for Silverdine. I have been using calendula lotion (homeopathic) and told him about it. He looked it up and said it was ok to use. My skin is doing really good so far and I have had 14 treatments and get zapped in 5 different places. ~Christy~ left side mastectomy with TE February 16, 2009 started TCH March 20, 2009 Finished TC July 6, 2009 Continue Herceptin until March, 2010
Diagnosis: 1/29/2009, IDC, 3cm, Stage II, Grade 3, 1/13 nodes, ER-/PR-, HER2+ |
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MTG Joined: Aug 2009 Posts: 287 |
Sep 16, 2009 10:47 pm
MTG wrote:
ccbaby - I also checked with my radiologist today and she had no problem with me using 1% cortisone if I have any itching and also offered me a prescription if I wanted something stronger. With that said, I still appreciate desdemona22's input re: the risks of overuse of hydrocortisone. The thing I love about this site is that there's tons of info and points of view; all of it gives me the tools to make informed decisions. For whatever reason, they didn't start rads today but simply did films. Tomorrow the process starts for real. M
Diagnosis: 6/30/2009, 1cm, Stage I, 0/1 nodes, ER+/PR+, HER2- |
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nonnie Joined: Sep 2009 Posts: 3 |
Sep 16, 2009 11:32 pm
nonnie wrote:
I finished 30 radiation treatments Dec.30. Sometimes, I would apply simple olive oil to my breast, especially after a bath at night. Very soothing. My instructions said not to use talc, but corn starch was okay. I never had more than a bad sunburn. What I found most useful was the lycra camisol. I always wear underwire bras, and was uncomfortable braless. The ones I found were shaped, with a "cup" formed into them. Sometimes, I would put on a bra over the cami! Another trick that helped, try wearing your bra inside out. The seams are smoother, and the fabric often is, too. I did that for a few months after treatment. Hope this helps someone! |
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ibjennifer1
Joined: Jul 2009 Posts: 54 |
Sep 17, 2009 10:42 am, edited Sep 17, 2009 10:43 AM
by ibjennifer125
ibjennifer125 wrote:
I am 3 weeks out of rads and used Silvadene, prescribed by my Dr. I tried a couple of sample topical creams they gave me but nothing eased my discomfort like Silvadene. I would slather the section that was raw and weepy with Silvadene then cover with a bandage ( the ones I had left over from my mastectomy) the bandages are meshy so the wound would still get air. That's the ONLY relief I found. Hang in there my friends.....it rads WILL end soon. There's no tougher gals in the world than breast cancer sufferers. You gain strength, courage, and confidence by every experience in which you stop to look fear in the face. You must do thing which you think you cannot do. Eleanor Roosevelt
Diagnosis: 10/30/2008, IBC, 2cm, Stage IIIa, 6/10 nodes, ER+/PR+, HER2+ |
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desdemona22
Joined: Dec 2008 Posts: 557 |
Sep 17, 2009 05:34 pm
desdemona222b wrote:
Okay, I stand corrected on the hydrocortisone 1% - I guess it's such a weak concentration that it won't affect the skin the way stronger concentrations are used. My whole thing is just make sure your doctor approves - I've seen women talking about using creams and lotions in spite of what their doctors tell them before and it really bothers me because there is a reason they tell you to stay away from creams and lotions. For what it's worth, I did really well during my rads too until maybe the last week when it got to be very painful. I wouldn't let them put tape on my breast (they wanted to leave it there throughout the treatment) and the last couple of treatments someone stuck a small piece of tape on my breast. The skin seemed to holding up pretty well, so a couple days after treatment I removed it and all the skin came up with it. Just a caution for you ladies. I would also like to strongly advise using cornstarch VERY liberally and often on the underside of your breast, especially once you have a burn. I ended up with a nasty keloid under there that is making me crazy - it bothers me so badly and it just keeps on growing, not to mention that it's just gross. Best of luck to all of you - this may seem like the longest 6-7 weeks of your life but you WILL be finished and when that happens you can breathe a sigh of relief. Diagnosis: 11/17/2001, DCIS, <1cm, Stage 0, Grade 3, 0/0 nodes, ER+/PR-, HER2+ |
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desdemona22
Joined: Dec 2008 Posts: 557 |
Sep 17, 2009 05:39 pm
desdemona222b wrote:
nonnie - I wore either extremely large athletic bras or extremely tight workout tanks (the kind with lots of spandex). This is SO important for ladies to know about when they're going in. Going braless can actually cause the kind of damage I was talking about that I have because of skin rubbing on skin, but bras are out of the question. So getting something long, like your camisoles without the shelf or the other stuff I mentioned is critical. Diagnosis: 11/17/2001, DCIS, <1cm, Stage 0, Grade 3, 0/0 nodes, ER+/PR-, HER2+ |
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LRM216 Joined: Feb 2009 Posts: 667 |
Sep 17, 2009 07:15 pm
LRM216 wrote:
CCBaby where do you get Calendula lotion? I am totally naive about anything related to the rads and will be starting in early Oct; however, my radiologist told me I could use aloe, or any "good" cream that I wanted. I don't know what to get or where. Thanks, Linda I have been put on this frightening journey against my will, but I do not have to travel it alone.
Diagnosis: 2/23/2009, IDC, 1cm, Stage I, Grade 3, 0/1 nodes, ER-/PR-, HER2- |
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ccbaby Joined: Feb 2009 Posts: 506 |
Sep 17, 2009 11:08 pm
ccbaby wrote:
LRM....You can find it at a health food store and you should buy your aloe vera gel there too because it will be pure and won't contain alcohol. Look for 99% or 100% pure alore vera gel on the bottle. You can also order either one at a online health food store too like the Vitamin Shoppe. ~Christy~ left side mastectomy with TE February 16, 2009 started TCH March 20, 2009 Finished TC July 6, 2009 Continue Herceptin until March, 2010
Diagnosis: 1/29/2009, IDC, 3cm, Stage II, Grade 3, 1/13 nodes, ER-/PR-, HER2+ |
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LRM216 Joined: Feb 2009 Posts: 667 |
Sep 17, 2009 11:49 pm
LRM216 wrote:
Thanks, CC, I will go this weekend. Appreciate your help. Linda I have been put on this frightening journey against my will, but I do not have to travel it alone.
Diagnosis: 2/23/2009, IDC, 1cm, Stage I, Grade 3, 0/1 nodes, ER-/PR-, HER2- |
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Irishred Joined: May 2009 Posts: 120 |
Sep 18, 2009 02:21 pm
Irishred wrote:
I had trouble finding any type of cream my radiologist or the people on here recommended. I order MY GIRLS Radiation Cream online, while it feels good dont think it really did much. I also order Pure aloe vera online, and keep it in the frig, it does feel good going on. My rad dr gave me samples of Miaderm, which is also nice. I have had one major problem under my arm, which kept me off rads for two weeks but silvadeen healed it nicely. |
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MTG Joined: Aug 2009 Posts: 287 |
Sep 19, 2009 12:11 am
MTG wrote:
Is anyone else having an issue with the creams semi drying on the skin and either flaking or just feeling gritty rather than simply absorbing ? I'm using calendula or sometimes aloe instead (also sometimes just Miaderm which doesn't seem to have the same problem) and thinking I'm appplying it too thicky. Or is it something else ? This isn't a problem now but may be if/when my breast starts getting sore and I wont want to wipe it down before rads. Thanks. M
Diagnosis: 6/30/2009, 1cm, Stage I, 0/1 nodes, ER+/PR+, HER2- |
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YoungOldMe Joined: Mar 2009 Posts: 1 |
Oct 20, 2009 10:22 pm
YoungOldMe wrote:
There are a lot of posts on this topic! But, I know that when I was in rads, I read all the posts, so I'll post some of my experience. To me, the worst part was never knowing how bad it would get. It got bad, but had I known I wouldn't have trouble with "wet desquamation," I would have been less stressed about the redness, itching, and pain that I did have. Once my skin started being uncomfortable, I spent as much time as I could staying home with my skin exposed to the air. I used a lot of products on it, too. I didn't want to use the petroleum products; oddly, all the ones the docs recommend have petroleum/methylparabens. These ingredients are controversial; probably OK but I still tried to avoid using them. I bought Boiron calendula at Whole Foods (though it does have petrolatum), Burt's Bees After Sun Soother (Walmart), Country Comfort Herbal Savvy (Whole Foods), Egyptian Magic (online), and My Girl's Radiation Cream (online). I used plain aloe gel and even tried my own aloe plant, but the consistency wasn't easy to use. I got tired of the calendula and other salves that were thick and greasy and felt bad with clothes on. Everything helped a little, but of course the treatments are powerful insults to the skin. My Girl's was my favorite toward the end when the skin was the worst. My Girl's feels cool and gets absorbed and I felt it had safe ingredients. I thought the amount in the container was generous, and I was comfortable using as much as I wanted to use without feeling the need to scrimp. I used that and Burt's Bees for several weeks after completion of treatment. I finished the My Girl's. Now, several months out, I use some Burt's Bees if my skin feels a little dry or itchy. About My Girl's and the advertising on this message board - I do think the owner made some mistakes on this website; but when I contacted her in June, she was very nice to me. She rushed a jar of cream to me because I was going on a trip for a few days and felt desperately in need of "something better" to deal with the skin getting worse and worse. She told me how she found/created the cream, and she seems sincere in her efforts to help people with this product that she happened to find. It's a good product. I think trying different things can be helpful, in that you feel like you are doing something for your poor sad skin. I was surprised and disappointed that the docs and nurses had minimal knowledge about products, but I was impressed with the docs about everything else. I guess they know what to do when the skin needs medical care. I introduced the calendula and My Girl's to the radiation oncologist. I hope this is helpful for those reading it at the difficult time of therapy. Be well... |
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kime Joined: Sep 2009 Posts: 92 |
Oct 21, 2009 08:00 pm
kime wrote:
I'm starting rads tomorrow, so went out today and bought some 100% aloe vera. I was also going to buy the Aquaphor I've seen mentioned, but noticed it had a warning about getting sunburned more easily while using it because it contains alpha hydroxy (I think that was what it was, but not 100% sure) so it said to make sure you had on sunscreen if you use it. So , I know that radiation and sunburn are different, but since many people describe radiation skin damage to be somwhat like sunburn it made me wonder if Aquaphor would make the radiation worse, or is it ok as long as it is washed off and not put on within 4 hours prior to radiation. As I haven't started the rads yet, I hadn't asked what they recommend at the rad clinic. Diagnosis: 8/13/2009, DCIS, <1cm, Stage 0, Grade 3, 0/2 nodes |
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bcamnb Joined: Jul 2009 Posts: 145 |
Oct 25, 2009 04:13 pm
bcamnb wrote:
Hi All, My first post on this site - for what it's worth.... I finished 16 rad treatments in early Sept. I used - * very mild soap in a WARM shower (Although Dove was recommended, I used a natural olive oil soap) * Glaxal cream (the base for most cream medications) applied liberally 2 - 3 x /day, given to me by the rad folk * a cotton bra (which, because I am/was a 38 DD, I wore the whole time with no problems, except for its becoming very multicoloured where I was marked each day ;-) and I aired my breast for at least an hour /day This was great and I had no skin issues BUT 7 - 10 days after the rad was over, when I was told it would peak, it did and I had all sorts of skin issues although never blistering the skin. These lasted for several weeks. Coincidently, I began using Dove soap (we were away). I was told to back off the cream. Almost two monthe later, my skin is good except for a new, worrisome mole that has appeared and we are watching. Good luck all. Caroline
Diagnosis: 5/2009, IDC, 1cm, Stage I, Grade 1, 0/2 nodes, ER+/PR+, HER2- |
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kime Joined: Sep 2009 Posts: 92 |
Oct 27, 2009 01:06 am
kime wrote:
wow Caroline 7 to 10 days after rads? just when you think you are safe huh? Thanks for the info, hope the mole turns out to be ok. Diagnosis: 8/13/2009, DCIS, <1cm, Stage 0, Grade 3, 0/2 nodes |
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MTG Joined: Aug 2009 Posts: 287 |
Oct 27, 2009 05:39 am
MTG wrote:
Caroline - Thanks for the warning !!! I'm starting boosts today and several people have warned me that boosts are esp hard on the skin and also that I need to keep moisturizing for 2 weeks after everything ends. As on woman put it, we keep "cooking". It's one of those warnings like "Look both ways before you cross the street"; one can't here it too much ! M
Diagnosis: 6/30/2009, 1cm, Stage I, 0/1 nodes, ER+/PR+, HER2- |
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bcamnb Joined: Jul 2009 Posts: 145 |
Oct 27, 2009 03:27 pm
bcamnb wrote:
Hi MTG, Good luck with the boost. I didn't have one - just the usual dose spread over 16 Rx - so maybe I was boosted all along! Anyway, although I was warned about afterward, I sort of scoffed at it - and should not have - that turned out to be my worst time skin wise - SO.....air, mild soap, warm water, and cream (but what helped me was to actually back off the cream)....whatever works for YOU - amazing how different we all are. GL again! Caroline
Diagnosis: 5/2009, IDC, 1cm, Stage I, Grade 1, 0/2 nodes, ER+/PR+, HER2- |
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Pill Joined: Sep 2009 Posts: 190 |
Oct 27, 2009 06:12 pm, edited Oct 27, 2009 06:13 PM
by Pill
Pill wrote:
YoungOldMe, I feel the same way you do about petroleum based ingredients. I haven't used products like this for years. It seems like during rads it's even more important to avoid parabens, synthetic fragrances etc. I don't start rads until Dec, but I've been giving a lot of thought to what I will use during tx. This thread has been very helpful! I'm really considering the suggestion to make a tea with dried calendula and comfrey, maybe I'll apply that in a base of 100% aloe. I'd like to follow it up with something oily/softening. Does anyone know if there is a particular reason to avoid vit e oil during rads? I'm thinking of adding a few drops of vit e to olive or coconut oil, to help seal in some moisture. If you have two loaves of bread, sell one and buy a lily - Chinese Proverb
Diagnosis: 3/2009, IDC, 4cm, Stage IIIb, 8/9 nodes, ER+/PR+, HER2- |
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bcamnb Joined: Jul 2009 Posts: 145 |
Oct 27, 2009 06:29 pm, edited Oct 27, 2009 06:31 PM
by bcamnb
bcamnb wrote:
"Hi Phil, Don't go near the Vit E. I even had to forgo my vaginal Vit E suppositories (for dryness...) while I was taking my rad. " Vitamin E is an antioxidant, a compound that blocks the action of free radicals (activated oxygen molecules that can damage cells).....Some scientists believe that taking high doses of antioxidant vitamins may actually interfere with the effectiveness of radiation therapy and some chemotherapy drugs." From the site: http://www.cancer.org/docroot/ETO/content/ETO_5_3X_Vitamin_E.asp Be sure to discuss whatever you want to use with your doc/onc nurse/rad therapist. They are the experts and will help yo figure out what's best for you. Good luck! Caroline
Diagnosis: 5/2009, IDC, 1cm, Stage I, Grade 1, 0/2 nodes, ER+/PR+, HER2- |
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MTG Joined: Aug 2009 Posts: 287 |
Oct 27, 2009 07:22 pm
MTG wrote:
Pill - Yes, be sure to ask your radiation team. Although I haven't figured out exactly why, the Dos and Dont very dramatically from place to place. Even Vitamin E isn't clear cut. My rad onc at least makes a distinction between topical Vitamin E (okay to use) and Systemic Vitamin E, as in supplements (a big thumbs down). I did a lot of research into topical antioxidants when I started radiation and was super surprised to learn that many of the commonly used radiation creams have anti-oxidants in them. Of course, the farther down on the ingredient list, the less quantity so that's also important to note. Here's what I found out: Biafine - contains Squalene (Fish oil; 7th Ingredient), Avocado Oil (8th Ingredient) Xclair - contains Butyrospermum Parkii (Shea Butter, containing both Vitamin A & E; 3rd Ingredient), Ethylhexyl Palmitate (a derivative of Palm Oil; 5th Ingredient), Tocopheryl Acetate (Vitamin E; 11th Ingredient ), Hydrogenated Castor Oil (12th Ingredient) Radx - Sweet Almond Oil (3rd Ingredient after Aloe and Water) Miaderm - Calendula ( 3rd and 4th Ingredient), Rosa Canina Seed Oil (Rose Hip Oil containing Vitamin E; 13th Ingredient) Alra Therapy Lotion - Vitamin E Jeans Cream - Tocopheryl Acetate (Vitamin E Acetate) By the way, Olive Oil is also a strong antioxidant Caroline - I had actually backed off the lotions as well; to me, they seemed to be aggravating and bringing out the bumps more than if I did nothing. Then the nurse showed me how burnt I was getting and suggested that the bumps might be better to deal with than the burn that would result if I went thru boosts using very little moisturizer. So, I started again M
Diagnosis: 6/30/2009, 1cm, Stage I, 0/1 nodes, ER+/PR+, HER2- |
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MarkeyGoW Joined: Nov 2009 Posts: 1 |
Nov 1, 2009 12:05 pm
MarkeyGoW wrote:
Hello.... although I am not dealing with radiation treatments a friend of mine is. She asked that Thank you for allowing me to ask this question and my prayers and thoughts are to you all. M. Martin |
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MTG Joined: Aug 2009 Posts: 287 |
Nov 1, 2009 04:07 pm
MTG wrote:
MarkeyGoW - You're a really good friend ! As far as I know, there's only been a bit of discussion about it on this site and they make a distinction between super market honey and pure, medical grade honey. Check out: Topic: Has anyone else used "MediHoney?" at http://community.breastcancer.org/forum/70/topic/741969?page=1#post_1547628 as well as another thread on this Discussion Board, "Honey heals wounds- Research to back it" at http://community.breastcancer.org/forum/79/topic/736964/1438443 For even more information and some direct feedback, why don't you also post your question on the natural girls site: http://community.breastcancer.org/forum/79/topic/730113?page=107#idx_3192 . One word of advice: If you're friend decides to use honey and lives in the US, she might want to do some research and find studies re: using honey to give to her radiation oncologist. From my personal experience, rad oncs here are hesitant to give their okay to use a "natural cure" that they're unfamiliar with, unless there's some empirical evidence that such a cure does work. I used Apple Cider Vinegar (10% ACV to 90% water) and at first my radonc said "No"; after I showed her my research, she not only okayed it but was rather intrigued by the whole thing. As for the use of honey, I found a very small Dutch study specifically on point, "The Effect of Honey Compared to Conventional Treatment on Healing of Radiotherapy Induced Skin Toxicity in Breast Cancer Patients" (see http://pdfserve.informaworld.com/892817__749296021.pdf ); it looked at 24 patients and found that those using honey actually had less pain, itching and irritation than those using traditional salves. However, I think that they used medical grade/sterile honey rather than the sort we put on bread or in tea. By the way, you might also find helpful a comprehensive list of lotions and creams used by the various women on this site: http://community.breastcancer.org/forum/70/topic/739663?page=1#idx_14 The ladies on this site are really quite helpful. Feel free to ask questions. M
Diagnosis: 6/30/2009, 1cm, Stage I, 0/1 nodes, ER+/PR+, HER2- |
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inforeffy Joined: Nov 2009 Posts: 3 |
Nov 10, 2009 08:19 am
inforeffy wrote:
My doctor gave me bottles of RadiaGuard to use during my treatment, and also for afterward. Following radiation, she also prescribed a medication and Vitamin E to treat the breast tissue. One year out almost, no problems. I have trouble remembering even, but I believe I had 38 treatments. Something that I thought I'd never forget, but time heals too. |
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minevicp Joined: Dec 2008 Posts: 17 |
Nov 13, 2009 07:52 pm
minevicp wrote:
Hi everyone, Just wanted to let everyone know that I used Aveeno cream for dry skin throughout my treatment (5 weeks) after it was approved by my rads team. I think it helped a lot; I never had skin breakdown, although the skin under my arm turned almost black and eventually peeled. The worst time was the 2 weeks post-rad (I finished Oct. 20), I couldn't believe how sensitive and sore my skin was. I bought Basics cotton bras at Walmart for a big $10 each, and they really helped during the treatment. Good luck to everyone, and I hope this helps. Cancer is a word, not a sentence!
Diagnosis: 1/14/2009, IDC, 2cm, Stage IIb, Grade 3, 1/15 nodes, ER+/PR+, HER2- |
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linnyk Joined: Nov 2009 Posts: 2 |
Nov 20, 2009 02:27 am
linnyk wrote:
I finished rads a month ago. In the beginning the nurses gave me Sensi-cream and told me to apply it 4 hours before treatment, then again in the evening. They worked fine for 3 weeks, then the skin started to redden under my breast and they gave me triamcinolone acetonide cream, but that wasn't helpful so they switched me to radiation relief cream. That was good. Plus they gave me a stretchy bra (made by DALE) and pads to stop any rubbing irritation under my arm and under the breast. After the first 3 weeks, on weekends, I left my breast clear of all creams and slathered my breast in pure aloe vera I bought at the health food store (AlBrey Organics). Very soothing. I am a light-skinned redhead yet the nurses said my skin did very well. Now, a month later, the redness is gone and the dark "sunburn" has all flaked away. No hardness either!. (I am still using the aloe.) The nurses were very good at skin care after every treatment. I hope this is helpful. Diagnosis: <1cm, Stage I, Grade 1, 0/2 nodes, ER+/PR+, HER2- |
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