Is There A September 2011 Chemo Group?
Comments
-
Pinkshirt - I'm so sorry for your setback! I'm so glad you were able to get on and vent a little. Sending you warm, gentle hugs and hoping you are able to heal quickly and get back on track with your chemo.
Lee Ann - Good for you!! Fingers crossed for you to find a new, awesome Onc!
RJ - Good luck with Rads and your port removal. I'm glad to hear your port infection was caught early.
I've been working on a little photography project to try and keep my brain busy. I'm going to try to attach one here.
-
Mary: Glad your chemo is on schedule
Belleast: so glad your hand is better...you have had such a terrible time of things. ((HUGS))
Pinkshirt: (((Huge Hugs))), omg that is really awful and I can't imagine how frustrated you must be...hang in there...it absolutely has to get better:) warm thoughts and hugs coming to you.
RJ: So glad they got things drained and headed off that infection. Goo dluck with Rads!
Kelli: That is really beautiful...I hope you'll post lots of your projects

Good News! ChestCT and Echo came back good so final chemo is on for tomorrow. Yay for the last one...ugghh for the SE''s but at least this time I'll know that when they finally end it is over. Thanks for everyone's support about the doctor. I really do appreciate it
-
Kelliregi.... beautiful picture. You took that? Awesome. Wish I had some creative talent. Thanks for attaching.
rjbaby..congrats on getting that port out this week. I'm bummed to hear the posts stating your oncs want them to stay in. I am going to ask mine about this Friday when I see her. She originally told me she didn't care whether or not I got one. Since I was doing 12 weekly taxol plus the 4 AC I elected to get one. I still have to do the herceptin every 3 weeks for the rest of the year. I would really like my port out in the next few months prior to finishing the herceptin. I heard the herceptin isn't bad on your veins like chemo. Now that I have it, I'm sure I'll be stuck with it. Mine is in my arm and bugs me. I can always feel it. Just another reminder....
sarasowise..congrats on your last tac!
Leanne...good luck with your onc search. You definitely want to be comfortable with that person.
Curious.. do any of you that had surgery prior to chemo still see your bc surgeon at all? I only saw mine once after surgery but now have a few questions regarding an anterior margin. Thinking I need to make appt.
pinkshirtnow....I am so sorry you have to endure this. As horrible as it is, you will get through it. I hope you can have the surgery on Friday so that you can get it all rolling along, heal up and finish off those last two chemos I believe is what you had left. Keep us posted and know we are all here cheering you on.
maggie.... give us all the fun details of your trip so we can live vicariously through you. I love Vegas. I'm sure your staff loved it and congrats on the award.
-
lee ann, so glad you got some good news, you have had it rough! HUGS to you.
kelli, you've got talent,girl!! beautiful photo,i like the saying,too.
ccjj, i only saw my bs once after surgery, then he released me. i'm sure you could call your bs if you have questions.
-
Aw Pink, I see what you're saying, couldn't picture it getting worse, then...Wham. I just have this dumb question? Why did you fall in the shower? Were you weak on your legs? Did you just slip? I'm glad your parents were able to come and help you out during this. Are you worrying about bone healing and your BC treatment...I can just imagine. You know what, you will probably heal better if you're not stressed from worrying on top of everything else, so as miserable as it is, try not to overdo the worry because that's not going to help. I hope it doesn't hurt too bad. I never broke a bone so I don't know. BIG OLE BOOBLESS CHEST SQUEEEZING HUGS from your friends. Hang, buddy. What else can we do?
RJ - I am using the same Eucerin. There is no dry skin like Arimidex dry skin, turning into my memories of grandma overnight, or within 2 weeks of start. Well, let's say I feel bald and dry and leave it at that.
-
Pinkshirt, I am SO sorry for your setback. The fracture sounds pretty darn serious when they are saying you need a plate. Hang in there, sister, we are all here for you!
As for me, last rad tx is tomorrow!
-
OH PINK---so sorry about your accident. I can only imagine such a setback and how I sould feel. You have been such a positive influence on so many of us here...now let us do the same for you. You can do this. This setback is temporary and you are strong. Sending you healing thoughts and prayers for strength to help you through this. If we lived closer I would come to help you out....Anyone in the Portland Area??
Have 2nd rad consult today as insurance would not budge on the Local Cancer Center Doc so gotta head south for treatment....could be worse right! Rad may be a little delayed from this but not upset as body is just ravaged from chemo crap and could use a little break.
Maggie
-
CCJJ: I only saw my BS once and she told me I would see her again in about a year when I was done with all the BC crap for a checkup and another mammo.
I am sitting here in the cancer center getting my final chemo and I am both excited and a little scared to stop using a drug that is killing this BC....so weird to be afraid to stop and be desperate to stop at the same time. Oh well, rads are next so at least we'll still be frying those little buggers!
-
Pink Shirt - I am so sorry about your accident. I broke my foot 1 year ago and I was bummed about having to hop about one leg or use crutches. I did not have breast cancer at the time and I was still fairly mobile but it bugged the living H_LL out of me. So I cannot imagine the level of aggravation you must be feeling.
It will definitely be depressing and difficult but you can get through this. You are a strong person (you pretty much have to be to go through all this crap and still try to get out of bed in the morning). And in time the surgery will heal, the bone will heal and you will be back on both legs.
My thoughts are with you. I hope you have a speedy recovery from the surgery - Take care.
-
Lee Ann - Congrats on the chest CT and Mugga results! And congrats on your last Chemo! It will feel good to be done (after you get over the worst of the SE's.
I am in the same boat as you I guess (a 37.5 to 48% chance of recurrance after chemo). But my doctors have been nothing but positive. One even layed into me about the whole "Triple negative fear". She told me there are many different types of triple negative cancers and I should not be so negative about the one I have. One doctor told me a recurrance doesn't mean I would die from it just that I would have to treat it again.
I guess we have to remember that hopefully the chemo did it's job and the radiation will further benefit us (on a local basis) and pray for the best.
I am glad that you are finding another oncologist. That was incredibly insensitive and, if you believe my oncologist (which I am not sure I do!) not necessarily truthfull.
I get depressed about the whole thing sometimes but then I think what is the point. I am here today, I feel Okay right now - what is the point about getting worked up over something that may or may not happen in the future.
I will be switching my diet to a low fat diet (under 33 grams per day) and on the weekend we bought an elliptical machine for me to exercise on (5 hours a week is what they say). They say this combination can lower your rate of recurrance of TN by 42% five years out - but we still have to do the five years I guess. Beyond that the only thing we can do is get the regular scans (PET, CT, Mammogram) and deal with the results good or bad.
I will probably be going south of the border to get tests in the future because all of my doctors are united in saying "No more tests until symptoms". Although one did offer up am MRI on my liver just to ease my mind.
I hope you success with your new oncologist. Take care.
-
I got the news that my blood counts are high enough to do surgery on Friday so keep me in your thoughts. I am relieved and scared at the same time.
I am a bit overwhelmed to reply to everyone but I can say that we don't know why I slipped in the shower. Every health care worker has quizzed me on that one and I think that I just slipped. I don't think I lost consciousness and I didn't have a seizure. I could have been dizzy from the chemo because that is one of my side effects but it all happened so fast. I guess I can't answer the question with certainty.
People have started to bring my family food which is very nice of them but they are bringing so much that it is overwhelming. I asked one of my friends to coordinate it because I don't want to waste any of it but I my freezer is full. People all want to help but I truly don't know what they can do. They all have such busy lives and work full time so it's not like they can move in with me and take care of me. Sigh.
Take care everyone - I will be thinking of you even when I am not posting.
Linda
-
Kayrem: Thanks, it feels good to be done and it does seem like we are in the same boat.
My Oncoloby Nurse Practitioner informed me yesterday afternoon that the doctor I am leaving is usually more agressive than the other doctors but is more "medical facts only" in his practice. She suggested I might want to let him know that I felt let down about what he said and see what happens. The she said, "if he is still and a..hole then go to this other one." I had to laugh. I might talke to him before I fire him. She made a good point that sometimes we want to be such good patients that we don't speak up in order not to upset the doctor.
Linda: you will be in my thoughts and prayers on Friday. Your feelings about the surgery and all the extra food are totally understanduble but you will come through all this with flying colors, doing the happy dance! Just take it one thing at a time...(((HUGS)))
-
LInda, I am glad you are able to have your surgery.....the faster fixed, the faster healed!
You might want to tell your friend that there are websites available to help coordinate food....can't remember the name of it, but the one we used for a friend of mine was awesome. You can list preferences, and folks sign up for a particular day and show what they will bring. May help her get it under control for you!
-
Hurray to you Lee Ann for finishing up the chemo and on the clear scans.
Hurray Pink for being able to have the surgery as scheduled. Keep us posted. We are all pulling for you
Maggie
-
We are thinking of you Pink. Congrats on final chemo Lee Ann, hope you sort out the doc situation!

-
Everyone, I have been out of the loop because of rough side effects and will get around to replying to you all
Pinkshirt- I just wanted to say how sorry I am about your injury. I am sending tons of positive thoughts and prayers your way for an uneventful surgery Friday and fast recovery. Hope your incredible support network can help give you the physical and emotional support to get through this with the grace that you have everything else up to this point.
As for the thoughts about the cause of the fall, etc., I don't know, but I do remember reading last month a statistic about how many women have a fracture within a short time period after BC treatment, controlling for a bunch of factors. Anyone else see this research and the background of it??
-
went to see my sub mo today,last chemo next tues. did i ever tell you i don't like my sub mo, still don't so condescending!!!!!! thank god i only have to see him 1 more time in a month!!
also found out today trial is postponed til may 7th, now i have to call RO and tell them i can start earlier.
-
Belle---I feel so bad for you with this lousy sub MO...he sounds like an idiot. Glad that you can get on to rads quicker. My nephew was murdered 3 yrs ago and the young lady who did it only faced manslaughter charges. She was only 17 at the time so I think they wanted to go easy on her. Glad she get off easy...I think of my nephew every day with tears. May it go well for your family.
I go for mapping on Tuesday and start rads when I get back from Vegas in 2 wks. Can't wait til it is all done and I can get my foobies and put this whole mess behind me. Pet scan Friday. Feeling like this is a big one as the tumor was such a fast grower that if any "escaped" they should be big enough to see if chemo did not work. Feeling too good now with Se's going away as it has been 2 weeks since last tx. Positive thoughts.
Rae--missing you and hoping you are doing ok. This journey has been so rough on many of you for sure. Wishing you the best.
Maggie
-
CJRT - Noticed the increased fracture risk to BC patients due to the dual whammy of poor balance post chemo plus increased risk of break related to increased osteoporosis from anti-hormonals. I'm having theories that chemo has effects on the brain and balance, physical weakness and general debilitation, and a lot of us have numb feet and toes so we are not getting the sensory input a normal person would. I know my sister lost her balance and fell in the deep end of my pool with her winter coat on during her first year post chemo. I was talking to her during this and remember seeing her foot step where there was no cement and kind of watching her fall sideways in slow motion. Sisters, I'm telling you, middle of November, Wisconsin, in the deep end of the pool with your coat on is not good. I was so happy she was able to swim out because I didn't want to have to jump in to save her. That water was about 35 degrees. I also saw her trip and fall getting out of car on Wisconsin snow, which is kind of uneven at the curb, but still it is something we are used to. I know that she took a tumble at work going up some stairs, apparently misjudged the stairs, and got a nasty gash on her head requiring stitches, again, very near her chemo. I don't see or keep in touch up her butt, so these are only the ones I am aware of for that time, there might have been more. So yeah, in general I think the fall risk is real. Knock on wood, haven't fallen yet, but saw the numbers too, think of my sister and now Pink. Anyone else taken a spill since chemo? I try to be extra careful because I live alone. I admit the subject scares me a bit.
About Pink in the shower, I just know there were times during chemo I had a hard time standing long enough to take a shower, was that weak, and leaned against the wall for support during a lousy 5-minute shower, had to sit down to brush my teeth afterward and to step into my underwear. When your feet are numb, that's obviously an additional disadvantage.
Another subject, CONGRATULATIONS LEE ANN, Another one made it home through the chemo nightmare. Power on sister. Any SE are a little easier to bear knowing its the last.
-
Kimberly- Scary stories about your sister, but I can really see how those things happen with the dizziness, neuropathy, sleep probs, dehydration, stress, etc., of these treatments. Thanks for all the info. I know what you mean about feeling too tired and weak to feel safe even during a short shower. I feel the same way and like to make sure someone else is home. I'm trying to be extra careful since I was a clutz and broke my foot during my recent pregnancy. Being in a cast to my knee was hard enough with the big belly, but can't imagine the challenge doing it now with all that we are up against with our treatments. I plan to discuss the osteoporosis issue with my onc. once tamox starts up since the thought of menopause at 34 is daunting.
LeAnn- Congrats on being done. Hope the SE period passes quickly!
Mags- Good luck with the scan and mapping, and have a wonderful trip!
Belle- Yay for the last chemo nearing!
Rae- Thinking of you and sending positive thoughts your way!
-
Hello Ladies. I hope you all have been doing well. I am doing pretty good. I've had 4 radiation treatments and only 26 to go! Yippee! The hardest part so far is the drive. I did see a nurse today and we discussed skin care during radiation. She told me not to use anything on the skin and that if I developed problems to let her know and they would give me some cream to use. Ummm, okay. So far there is very little to report as far as skin irritation. I guess it will take a while before anything shows up. Hope everything goes as smoothly the next 5 weeks as it has this week. Not looking forward to surgery tomorrow, but I am ready to get the port out. Swelling has gone down some but it is still swollen from the fluid.
Hope everyone has a great evening and wonderful Friday. Talk to ya soon.
HUGS!
-
Linda - Good luck with surgery, will be thinking of you tomorrow.
-
linda, thinking of you! hope surgery goes well.
-
Good evening ladies. Just thought I would let you know surgery went well and I am resting comfortably at home. I have to take another weeks' worth of antibotics, but that's okay. I didn't get the pain pills filled cause I end up just throwing them away anyways. Tylenol works just fine for me for the most part. Sitting here with my ice bag on the surgery site. Should be fine by the time I return to work on Monday.
Linda - Hope you're surgery went well.
Take care and I will check back tomorrow.
HUGS!
-
rj--how do they remove the port? Are you knocked out or just a local? Have heard 2 different versions so was just curious. Mine comes out if scan comes back clean from yesterday.
Maggie
-
Haven't checked in for a while, but wanted to give you ladies an update. As of last Wednesday I finished rads!!!!! Treatment, except for aromatase inhibitor, is done!!!!! I see my MO on Monday as follow up, then onto my world of mamm in Feb, then breast MRI in August and then mamm again in Feb 2013.
Nails are still a mess, toes numb, hair slowly growing. Had to shave my legs!!!
KImberly, I too have noticed balance issues. Have to be careful, hold onto railings, etc.
Good luck to you all! May 2012 be our year of recovery!
-
Shelley, I am halfway through rads and cannot wait until they are done.
Maggie, when I had my port out a few weeks ago my BS used a local (lidicaine). She did the procedure in one of her exam rooms, and it took all of about 15 minutes. So, so glad to have it gone!
-
Mags, my port came out the way it went in...I had twilight sleep and don't remember a thing. Mine was in a hospital radiology dept though...
-
RJ and Linda, hope you are both recovering nicely. Hope Linda can recover from this and get back on track with chemo and surgery. I know it's a cause for worry but worry won't heal you one second faster. I hope you order a new freezer to hold the casseroles, take your pain pills, let family take care of you, and TIVO comedies for chuckles to take your mind off it. Hang in there sister.
Karen - Changing diet is difficult. I have been feeding the dogs all the salty food I can no longer eat. Perhaps that is not ethical but I hate to just toss it. They are getting ham and sausage and bacon bits and soup and some frozen pasta dishes, broccoli casserole as their treats. Pink's freezer may be full, but my refrigerator and freezer look emptier and emptier as I clean out all the no-no food. So far the dogs' paws are not swelling. They like my cooking because they don't know any better.
Congrats Shelley on finishing rads.
About falling, I always wonder about old people falling, because they break hips and so forth and so debilitating. I bet they think the same way I do before they fall....I don't fall. No worries. During chemo I was weak on my feet so I did worry. Now I don't worry as much, except that my bones are going to get crunchier on the AI's. I am aware that women with breast cancer fall more than average, no matter what the reason is. I feel steady on my feet, but I think it is something that I have to be aware of and more careful with than I was before BC.
I thought I would pick up Biotin to help hair growth. Ooops, picked up the 5,000 mcg dose, Way too much, should probably be 1/10 or less than that. I can't believe my hair growth is this slow because when I used to color my hair, all the white was 1/4-inch up and a problem 2 weeks after coloring.
Ha, ha funny. I thought the hair on my legs was not growing because they felt so smooth, but my hair is white on most parts except my forearms. For whatever reason, I was laying on the bed and put my leg up in the air, and the overhead light revealed the hairs. AHHHH. OMG. Some were about 3/4 inch long. I hadn't shaved them since chemo started. Guess I should wear my glasses in the shower for the state of the union, hair-wise.
-
Kimberly, that is exactly what happened to me with my leg hair. Thought it wasn't growing until the light hit it just right...no nubs, just long, fine, white hair!!!! Pretty funny.
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