March 2011 Rads
Comments
-
thegood5 - I know...go figure! Actually my cardiologist feels that there is more harm/danger from the additional radiation being injected into you for the MUGA and it's not worth the value of the test. I'm happy to agree as I figure the less pokes the better! My 2nd MUGA produced a false reading so who knows. I am glad that here, for the most part, our medical expenses are covered by the province so I don't have to make treatment decisions based on what the insurance company is willing to pay for. I am very lucky in that regard and anything that hasn't been provincially covered has actually been picked up by my work benefits (drugs and neupogen shots).
-
Geez! FATAL! I can't imagine, after all the treatments, he looks at you and says...take it easier your treatment side effects could be fatal for you. Maybe you'll just need to lily dip in the dragon boat from now on?
thegood5: the insurance business just makes me crazy. Wouldn't it be better if we could just deal directly with our doctors? Third parties suck! Could you imagine if we did have nationalized health care? We'd have even less choices! I would love to do yoga but I'm having issues with my pec muscle. I can't really push or pull with my right arm without shooting pains...it feels like my muscle is ripped!
msjag: It's hot up here no matter if you're on the water or not...I would think next weekend will be a perfect beach weekend! My beau and I have been heading down for a date night picnic and walk...maybe we can bump into each other!
-
Lily dipping. Blech.
-
Pardon my ignorance, but why the MUGAS and echoes? Are they preventative scans or cause chemo messed up your heart?
-
cmblastic~the Herceptin can weaken the muscle around the heart so they have to monitor it.
-
Yes and some of the chemo drugs (epirubicin and adriamycin) are very heart toxic. After every chemo I would have severe shortness of breath and heart palpitations for about the first 4-7 days which meant that my heart was struggling. Looks like I may have suffered some damage but it's not going to be able to correct itself until herceptin is done. It is a little fruststrating because I made sure to tell my onc about my symptoms, but was told not to worry about it. Ah well.
GirlFriday - just curious, why do you think that you would have less choices with nationalized healthcare? I don't think we have any limitations here, but I do really feel that the system is abused. People take advantage of the system where I think if they had to pay even a share of their medical expenses they would stop and think first. That's just my opinion anyway! Did yoy have radiation? My pecs, shoulder and in general the whole radiated area are very tight and painful to try and stretch. I am starting some physio that I hope will help.
-
margie: The only way insurance works is to have the pools of the insured great enough that there are more healthy people than ill people. I figure between me and my employers I have paid at least $30k into the some insurance company over the last 10-15 years. I think my personal medical bills, and the use of my insurance was under $5k in that same time period.That $25k easily went to pay the bills (that are negotiated at a lower rate with the health care providers) of someone who was ill. Insurance companies balance this healthy person vs sick person ratio very carefully. One of the management techniques is to limit choice and procedure. I'm pretty sure no matter who administers the insurance, this will be the case. When Hilarycare was introduced in the 90's it was based on our SS act (1967 I think) The current proposed Obamacare is even worse in terms of setting limits on patient choices. Insurance stands between you and your doctor. For example: My insurance would not cover an MRI (multi thousand procedure) so I did not have one prior to my surgery. The BS said "it's not necessary and I've been doing surgery without MRI's for years." She was trying to save me money, but looking back now, I wonder, do I have anything growing in my left breast? Did my the fact that my insurance refused to pay for something leave me at greater risk? And yes margie...I did have radiation...that's how we met
-
GirlFriday - yes, LOL, I checked and saw that! Mind Fart!! Anyway, I've been really lucky with my standard of care so far and that may not be the case with everyone, For me, I really feel that they've gone above and beyond in most cases. Ofcourse, my cancer centre is also a research centre and I think that perhaps they go a little further because of that.
-
Girlfriday, once again well put and I believe you to be very acurate. I was lucky in having an MRI before surgery (dense breast), but the reason I was able to have one was I got into a study at umass breast center in Worceter to see if having MRI instead of mammo, ultrasound before surgery would help w/diagnosis/finding cancer in other breast, or in same one. I felt lucky to be one selected to have the MRI, but the results showed no signifcant difference. If it was their breasts, they would feel a very significant difference in piece of mind.
GirlFriday, Iwould be honored to bump into you one beach bound weekend!!
-
Marjie - Sorry to hear you're having a hard time. It just doesn't seem fair for some people.
I've been blessed. I feel better than I have in years. Our women's health advocate gave me information about Vit D3 being better than Vit D2, which is what is in the prescription so I take the equivalent dose in over the counter.
I had my first fill since before rads and it was really painful on the rad side, but just for that day. Today it feels fine. After all the problems I've have the PS was practically thrilled to see how well things are going now. She did tell me to skip Zumba for a few days, so I'm going to try to do the rest of the fills on Fridays. She said I'm up to 480cc's. I don't know when we got that high. Last I remember was 380 and then 50 yesterday. I guess she knows what she's talking about. All I know is I'm not flat anymore. WooHoo
-
Sandymess, how was your appt yesterday?? Hope all went well!!
TheGood5 and Marjie--sorry you have to add heart worries to your list of concerns. Just not fair.
Tonia--Wonderful you are feeling great!! Glad to hear the fills are working out for you!
I went and colored/cut my hair for the first time since this mess started. I turn 50 in a month and I was tired of looking way older. Everytime I look in the mirror, I have to do a double take to make sure its really me. . .
-
cmblastic - How did your hair turn out?? I just went and had my second trim PFC. I'm sure some of the ladies in the salon thought I was crazy, but when your hair is so short it needs to be trimmed alot! I was getting little wings over my ears and I needed to get the top thinned out a bit.
Thanks everyone for the good thoughts - I'm not too worried about my heart, but I do really need to listen to my body. I am just hoping that things stay as they are and don't degenerate over the rest of my Herceptin treatments. I'm still training to be able to get a db race under my belt this season but I'm not going to kill myself for it. Last race of the season is in September so we'll see.
-
Marjie--its darker than I remember. . .oh thats right, no more gray!!
I need to go get some wax so I can spike it. I too had wings over my ears--looked like the flying nun!!
I can't believe you are going to DB. that is so awesome!! Does it help with the stiffness from rads??
-
Claire - I have been dragon boating for several years so after diagnosis I just switched over to the breast cancer survivor team. It is good exercise for the rads stiffness, chess muscles, and lympedema for sure. My team are the Canadian National Gold Medalists for two years running - we're a tough bunch of survivors for sure!
-
Marjie - I love the new avatar. You look gorgeous!
Claire -- Thanks for asking.
My mammo went okay. It was more uncomfortable than usual but nothing I couldn't handle. They were supposed to do an additional magnified pic of the surgical site, but because of the tenderness in my breast and the fact that I just finished radiation in May, the tech talked to the RO and they decided it could wait till next time. Now I just have to wait till Thursday to see the MO for results. Unless, like last year, they see something and call me right in to have a sonogram. I'm hoping that doesn't happen!
Spent a couple of days at Popham Beach in Phippsburg. Loved just enjoying the weather, reading, sketching and taking pics. I did get a sunburn on my chest though and I thought I was being so careful! I used tons of sunscreen and wore a linen shirt for part of the day. I'll be more careful next time, for sure. Don't want to experience skin cancer next!
Hope you are all feeling good and having a wonderful summer.
-
Sandymess - thanks! I have a mammogram next week and I'm a little nervous about squishing my poor radiated boob. Maybe they will decide the same for me!! I'm glad you said it wasn't too bad though...
-
Sandymess-the beach sounds sooo nice!! Wish the beach here was as relaxing--right now just too darn hot, and the water is not cool enough to be refreshing. i'll have my fingers crossed for you on Thursday, here's to a clear mammo!
marjie--hope your doc visit is a painfree as possible. Haven't we already been thru enough??
-
Thx Claire - I guess I might as well suck it up, I have just passed my one year since diagnosis so I'm definitely noticing lots of appts over the next month or so.
Has anyone else started any physio? My rads area has stiffened up quite a bit and it seems to have really affected my shoulder. I am going to physio to get it worked out and more flexible again. I had to go to my family doctor for the referral.
-
I have my 3 month follow up with my RO at the end of this week, as well as the results of genetic testing. And then I see the MO in two weeks. I don't think my first mammo will be until December, and I asked who would be scheduling it (my MO) but I have not asked when it will be. I definitely have scanxiety over it, so I'm just going to ignore it until it's time. I blush to disclose that although I am not quite a sloth, I have not been back to the gym since my dx. I haven't even been walking/running either. I found my lump because of lifting,and trying to increase my bench press. I just don't have the energy I used to have. I'm gardening, and cutting the grass, and yesterday I loaded the truck three times with wood, and then re-stacked it, but going to the gym has just not been on my priority list. At first I was scared, because I didn't want to injure something that was so sore...and now it seems like it hurts more than it used to. It's like my right arm and pec are crunchy, and i can never seem to stretch them or work the into being smooth and lubed. I'm not nearly as strong as I used to be either. Even my legs don't have the endurance (use it or lose it, I guess). I believe part of it is Tamoxifen, because even my knees and hips hurt now. I think I'm just kind of frozen in place. Waiting to see what's lurking around the corner. I wish there was a Dr. Seuss book to explain this crazy better!
-
marjie -- I had physical therapy for my arm and shoulder before rads. I developed LE but since doing the exercises faithfully, it seems to have gone away. I do still have the 'crunchy' feeling as GirlFriday so eloquently (as usual
) put it. I do the stretches all the time--I even have more movement in the bad arm than in the good, but it still does not move smoothly. Feels stiff all the time.
GirlFriday -- I'm taking Anastrazole, the generic for Arimidex ('cuz I had a hysterectomy a few years ago), and I'm getting a lot of the same symptoms you are.I am achy just about everywhere and exhausted most of the time and sometimes I really feel like an old woman. I have NEVER felt like this before and I don't like it one bit! But we shouldn't be too hard on ourselves. We're doing the best we can. I'm hoping it will get better with the passage of some time. Either that, or we'll get used to it? What a crazy trip!!
-
Sandy I too do the exercises three times a day. I went to see a LE therapist, just for a baseline, and learned so much. I posted alot in the After rads thread. I think we all have days of feeling like we are 100, and all our muscles/joints are awake! (even though it can't be from rads...ohhh noooo) Swimming felt great, therapist said its great for avoiding lymp.
Girl Friday, sound to me like you are doing lots! I got tired reading everything you have been doing! My rads nurse was soooo honest, she said, don't even think of feeling like yourself for at least a year from the end of rads. She said you will feel better because the physical stuff will fade, but the emotional side/aches and pains, will stay with us for many months.
I just checked out a couple of gyms, because I know reasearch has shown exercise is thought to be so important to keep reoccurances at bay. I think working full time thorugh chemo/rads has kept me active, and kept my mind/emotions in tact. I carry the insurance so I gotta work, thought I would take alot of the summer off, but I think in the back of my mind I'm afraid to use my sick days/ vacations days in case "something" should come up. Every now and then I worry because I don't have anything to take (triple negative).
I do wish we all lived closer and could get together, somewhere in Hawaii, would be nice!! I think being at work with such a great group of friends, coworkers, supporters makes such a difference in my day. They don't expect me to be 100% just because I'm walking and talking!! I feel blessed that way.
-
I would be ashamed about not working out--but I really didn't do too much before my DX. We belonged to a gym and I would go occasionally, ok, not that often!! But I work at a bookstore, and run the circles in an 8 hour shift, plus lift boxes, and books--huge stacks all day. By the time I get home from work I am exhausted. A couple of weeks ago, we bought an eliptical machine. I've used it twice. Ache at night, can't get motivated in the a.m. Well, that's a whole other thread!
I think I need to see a physical therapist again, my insurance would only cover therapy 60 days after BMX. Have to see if one of my lovely docs will refer me again, but I don't see my MO until the end of Aug and my RO until mid Sept. My rads side is still pretty stiff no matter how much I stretch. Everyday it seems to get tighter. Oh well. . .
Msjag, you are so lucky to be surrounded by supportive co-workers. It truly is a blessing.
-
Ugh! Remember how I said I have the appt with the MO on Thursday, unless they call me in right away for a sonogram? Well, they called today. The RO is concerned about a spot in the same breast as last time. He can't tell what it is, so I have to have another mammo tomorrow and if he still can't tell, I'll have a sonogram right away. I know I don't have to tell you ladies how terrified I am right now.
-
sandymess: He's being overly cautious. They shouldn't do the mammo a second time, they should just go right for the US...see if you can skip the second mammo. Why put yourself through that when they US will be a better diagnostic? If you have to get the second mammo, push to have it read while you wait. You don't need the additional stress caused by the wait. Also, I can be there in 1.5 hours if you need entertainment in the waiting area! I'm more than happy to travel!
-
Sandy, I totally agree with Girlfriday, being overly cautious, which is a good thing, just get to the US, skip the mammo!! I will be thinking of you and sending you lots of positive energy. I'm hearing more and more of scar tissue issues coming up as "spots". Hoping that is what you find out.
I'm heading to Saco tomorrow, I can accompany girlfriday for that entertainment!
(((((((((((((((((((Sandymess))))))))))))))))))))))))))) we are all here for you.
-
Sandymess-I agree with everyone--hopefully he is just being cautious, its just scar tissue and you'll be at home eating chocolate before you know it!! i am sending the good energy your way and I will be thinking of you!! ((((((group hug))))))))
-
Sandymess - I am cheering for you!! I have my first mammogram since dx and treatment today...I feel like running away and hiding
-
Marjie, how long has it been since you finished rads? also will you have a mri?
-
Marjie-- ---->>>>>good thoughts>>>>>>your way!! We're all in that waiting room with you!
-
I finished rads in mid-April. So far they haven't said anything about an MRI...would be much easier! I'm not so worried about the outcome as I am about the discomfort of the test itself. I can't even stand a manual exam yet! Not that it hurts so much as I just don't want anyone touching that boob!!! As I posted elsewhere...my DH is pretty sure I'll try to kick someone, lol.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team