May 2010 Chemo
Comments
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I am doing yoga with my former instructor, who is working with me individually on a protocol for breast cancer patients. It is wonderful. I did not have reconstruction, but a modified radical mastectomy of my left breast. Yoga has really opened my chest/heart area, and helped me to regain full range of motion, as well as emotional calm. I work once a week with my instructor and daily by myself. I am including part of the theory behind yoga for breast cancer patients. The literature is very compelling " Yoga helps people with breast cancer by reducing stress and managing side effects. Pranayama (breath work), Meditation, Restorative asana, and Yoga Nidra (guided imagery for relaxation) can be both energizing and calming. These same techniques are useful for pain management as well. In addition to pain, nausea, and hot flashes, many cancer patients feel out of touch with their bodies. They may feel betrayed by their bodies. They may be frustrated that so many medical treatments are happening “to” them and feel like victims of a medical system over which they have no control. They may be repressing or ignoring emotional or energetic signs that arise. Yoga creates an opportunity for people to get back in touch with their bodies and find serenity with the process. The program allows the student to be a perceptive self-observer of the physical body, the flow of energy and breath through the body, of feelings and emotions, as well as to create awareness of these experiences." Personally, t has been the most useful thing I have done for myself thus far. It is not "power" yoga or pretzel poses, but gently gets the lymphatic system going. Hope this helps someone to consider finding a way to work it into your healing plan.
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fotopet, redness and itching just means there's inflammation, which can mean any number of things. Could be just a minor skin irritation, but there is a possibility it could signal infection, or a spot where chemo drugs leaked out of a vein, possibly due to improper IV placement. You should definitely call and talk to a nurse about it.
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Hi All,
Just checking in with everyone. Unfortunately, not feeling great today..stayed home. Good news is survived #2 infusion of T/C on Monday. This time I did not have the allergic reaction (think thanks to benadryl and steroids) but did get severe lower back pain so they gave me more steroids and slowed the drip. So made for a long night...but just so glad to be halfway done.
Fotopet- Thanks for your well wishes. Check in with your nurse about your arm. I have Thrombophlebitis...where the vein hardened and looks like a bruise above the injection site from the first infusion where I had the allergic reaction. I have to put warm compresses on it and they won't use this vein again.
Patricia48- Yoga sounds like just what I need..thanks for sharing!
CTherese- Thanks for making me laugh...I love the idea of A Big Wig Party!
To All: Thanks for your posts! It really helps. PMA!
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Hello everyone. I am doing much better after TC #2 than I did the first time. Except for the all-around exhaustion. I'm signing up for a yoga class this summer--I used to do yoga relgiously but I have fallen off the wagon. I love it, though, and I look forward to it making me feel better! (I know it will!)
Fotopet, sorry about that reaction, hope it gets resolved soon.
Sacphotomom, congrats on being halfway done. Sorry you're not feeling great today, hang in there!
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Alright ladies... question for those doing neoadjuvant chemo... anyone else experience cramps or pains in their tumor?? I have been - more last week than this week. My appt with onc is next Thursday, so will ask her then - but curious if anyone else has been 'feeling things??"
3rd treatment today... 25% done with taxol and herceptin! Hair not falling out, but those that I pluck are not being held in by much... they come out very easily and I haven't had to shave my legs... hairs on head come out pretty easy if pulled on... going to be a slow out process with the taxol I think... gives me time to get a wig still. I have turbans and found a website last night that had 27" bandanas for $2 a piece!! Hoot!!!!
(((HUGS))) all... we are tough, and we can do this!! Screw this cancer.
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Hello everyone and best wishes
Checking in day 7 after 1st round of chemo. Had 1st blood check yesterday and WBC is dangerously low at 1.0. Being super careful to not get sick. Onco gave me prescip. of Cipro anti-biotic as precaution.
When I was feeling anemic (fatigued and short of breath) my nurse suggested slow-release iron pills. They are called Slow-Fe and I took one every day with 1 colace stool softener. What a difference! I felt so much better and now my blood tests determined my red blood cell count is back to pre-chemo "normal" levels. Now I don't need to take them anymore. Hope this tip helps any of you feel better.
Love to all...
Victoria
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Hi ladies; Welcome to all newcomers. Sorry you have to join us, but it is a great group to be with.
I am so sorry for all you guys having mouth sores. I have had some off and on. I have gargled with salt water and used the malox/benedryl mixture. They have both really helped.
Well this weekend is the weekend for the head shaving party!! I am inviting a bunch of my close supporters over for munchies and drinks and getting a buzz( not shaved just short). It is time. I am on day 15 and the hair comes out very easily.
Last night at my sons championship baseball game one of our players made an error in a tie game with 2 outs, last inning. They other team scored and I grabbed the back of my hair and ooops! I pulled a chunk of my hair right out. I just started to laugh. That's when I decided it was time to buzz. I just hope it holds off until then. I have a party to go to on Saturday at 2:00 and then people are coming over at 7:00. I will let everyone know how it goes.
Jeanna9: Can you let me know the website where you found the bandanas? Also where did you get your turbans? The concert was excellent! My kiddos did a great job. It's hard to believe a full year has gone by already,
Sacphotomom: Congrats on being halfway done!!!
Talk to you all soon. Remember STAY POSITIVE!!!!!!!
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RedBarb: GL this weekend, sounds like fun, no fun, fun.... Argh!!
Are you gonna do the mohawk pic before you take it all short??
Bandanas: www.tansclub.com - click on paisleys for 0.33, and then scroll down to the 27"x27" - they're on sale for $2 each. My turbans were from: www.topsyturban.com - I liked the 'elegant' ones, they hang down in the back - most are $20/each but many are on sale for $15/each. I already have them, and they are awesome - elastic, pre-tied- super!!!
Victoria - great idea about the iron... reminds me I need to go take my multi, vit d, calcium, vit b and iron! Mmmmm, mmmmm, good!!!!!
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Hi All, I'm getting ready for TC#2 tomorrow, as well. I've been drinking lots and lots of water and have packed my little bag of chemo goodies already. I feel strangely nervous even though the first treatment went fine. I am trying to focus on being halfway done tomorrow and not thinking about any SE's. I meet with the radiation onc next week to start planning the rads to follow the chemo. It seems like there is always another doctor's appt to go to! I'm not sure I had been to the doctor as much in my life as I have in the last few months since diagnosis!
I went to a friend's father's funeral today. He had liver cancer years ago (but he passed from something totally unrelated) and one of the stories they told was how, after his chemo was done, he had his port removed then took it with him to happy hour, put it on the bar and toasted the end of chemo and cancer. I can't wait til I can do the same (though not sure I want to look at the port on the bar)!
Welcome all the new joiners, sorry you are here, but it is a great group! Hope everyone has an enjoyable Holiday weekend!
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Hi Everyone and welcome all newcomers:
haven't been around for awhile so had to catch up on all the posts. Unfortunately my mom was rushed to hospital so this consumed me.
On positive note,I can now hold my grandaughter again. It has been 7 weeks. I had been barred from holding her from ps...she got so big...so hard to believe how time passes
Sorry to hear about all the mouth sores....I had some 1st go round but mostly on cheeks. Funny I think I got every SE known first time. Had second infusion yesterday. If it goes like last time will be in bed this weekend...heck just in time to go back to work (oh yeah)
Hair update: On Day 13 I decided to get at wig. THe lady came to my house.. THis service was fabulous...She spent 2 and 1/2 hours with me picking the right wig for me. A little pricey but I know I will be wearing it for a year so in retropsect you want something that looks good. Anyhow she cut my hair very short. I had noticed strands coming out and when I pulled on it I got a fair size amount. I didn't want to see the clumps.
The onc. nurse gave me a good idea. Go to be with a turban on your head so when your hair falls out it will go into the turban and not all over your bed. I am going to start doing this tonight.
6 more treatments for me although I am not looking forward to taxol..that is a 4 hour drip..Can anyone on it now give me some idea of whe SE's are like? Are they comparable to the A/C or totally different.Nurse told me a little about how people get reaction from it and they have to take you off it, give you more meds and then start again...Any of you had this problem?
Wishing you all a wonderful holiday weekend. This will be the first year I am not going to the shore in 20 years...Hopefully next year...Anyone got plans?
For all going through another treatment this week....Good Luck
and oh yes I have gained 10 pounds in 2 weeks also...I eat everything in sight..I feel like a pregnant woman.. I even get cravings...I craved ice cream...Normally I don't ever ever eat ice cream. Anyone else eating foods they normally never do
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Thanks for the welcome. I am glad to have joined the group here. My first chemo has kinda prepared me for the rest I would guess. I learned how to get all my water in. As plain water was making me sick even with pills. Flavored water has helped. I also got mouth sours and got all the stuff to treat those. Bad bad hip and lower back pain. Out comes heating pad with moist towels. My mouth felt like fine sandpaper. And a few days I felt it was hard to raise my head off the pillow. And needed Husband to help for a week to get to and from the car to go get my shots.
So I am better prepared this next go round Tuesday.
My hair started falling out 13 days after treatment. So I shaved my head at that point. I had 2 friends send me different styles of wigs, 4 total. So I wear them with a cool cap when I go out some where. Otherwise I wear a turban or a happy face do rag. I have some pretty colored ball caps. But have not worn them yet. I have alot of time to change my look around. I can got brown hair,blonde or even as a brown with red head. What do I need hair for anyways?.
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Hi NJBHWGIRL - I'm on taxol now, but I am on it weekly - what is your schedule? I'm guessing because you said a 4-hour infusion that your dose will be higher and SE more. So far, I have had nausea (thrown up once) taste changes, tingling in feet and hands quicker than normal (i.e. if I cross my legs, they go to 'sleep' quicker than they use to). I've been tired, gained a few pounds, a little constipated and had runny noses... I'm also on herceptin, and can't say which SE may be a combo of both. Hope that helps. I'm still working full-time through the infusions and have 2 little ones at home, so it's definitely doable!
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Hey Tuck! I had to start drinking some propel water too - with the taste changes about day 2 after infusion, water tastes like dirt!!! Flavor definitely helps! Hope this treatment shows you less SE than the last! GL!!!!!
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Paxton, I too have a yeast infection, hard to believe all of this can go on in one body. Hope you are feeling better and happy to hear about your fun pot luck dinner.
Tuck welcome to you, Kim and Patricia. Tuck, you and I are on the same schedule, I too go on the 1st. For some reason I have to have 6 treatments, not sure why.
Day, how did your treatment go?
Fotopet, hope the sores are improving.
Tomorrow is the buzz night for me. At this point it will almost be a relief, I can't stand the feel of my head and the 'fear' of touching it and having it fall out. I will let you know how it goes.
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nanaof2, my treatment is tomorrow. At 11:30 to be more precise, so I won't probably be home before 5 or so (took 3 1/2 hours last time and the drive is almost 1 hour).
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OK so I had my first rude experience today while out for lunch...I had my new scarf on..was walking to my table and a very loud rude woman started talking to her friend ....WOW She must be having Chemo..will you look at that ...she really should get a wig when she is out in public..I felt like saying back ...You really need to wear a muzzle when your out! Then I wanted to take off my scarf and just have my head with all its nice big bald spots showing...
Some people just don't have a clue!
OK I have vented...moody yes ...and really emotional ....yup!
Having strange feeling where my left breast used to be... tight and like there is a tube pushing against my skin...haven't felt this before...call to surgeon .waiting for call back ahhhh not a good day!
OK it IS a good day... The weather but cant make up its mind sunny or rain sunny or rain.. and the air smells so nice... and I had lunch with my Mom and Dad ...talking to my 19 yr old son about camping, wishing I was going with him..but loving that he is going with friends and they are going to have a blast ....sent my daughter some little things she will need while touring Eastern Europe..cute little all weather jacket..had fun buying it for her...again wishing I was going with her..
OK I have talked myself back into a good mood...
Hope everyone else is have a Great Day!
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sacphotomom: I am so sorry for the rude comment. Sometimes I think I have been transported into a new universe, and it is so bizarre that I could never explain or describe it to anyone else. Heck with Mars and Venus, this is beyond that. Everyday brings new challenges and another body part that is malfunctioning. This is not for sissy's. Seriously, I love your change of attitude and the joy you find in your children! I have a 25 year old dau and my son is 38. He is the father of my lst granddaughter, in the pic with me. I sometimes feel sad that they have to experience Mom, and her illness. In between hair falling out, and nausea, and mouth sores, we all have to find those sunny places, if just for a moment.
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sacphotomom: You surely didn't deserve or need that woman's remark, and I can understand your desire to provide her with a muzzle. I am horrified at the actions of some of the inconsiderate folks who inhabit this earth. Having been in a similar situation when a stranger commented on my appearance, my reaction was to approach the person and in the sweetest and calmest voice I could muster asked, "I'm sorry, but do we know each other?" She responded no, and before she could get in another word, I again used my calmest tone and said, "Then why would you be even remotely concerned with what I'm wearing?" Turned, walked away, and never looked back. That was about 30 years ago...not sure I'd do it today, but, depending on the circumstances, it might be useful.
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Nanaof2 - (((HUGS))) will be thinking of you tomorrow!
Day - GL tomorrow for smooth infusion.
Sacphotomom - grrrr.... some people.... you want to just say, yes, cancer doesn't discriminate and just pick rude people, because if it did....... ha. I'm just truly amazed at what people will say. Has your surgeon called - what does he/she think? Sounds like your children are going to have lots of fun- and I'm sure thinking of you and missing you and knowing you can go with them later, when you've whooped cancer's butt!!
Patricia, your granddaughter is beaUtiful!! How old is she? You know your family going through this can be a very positive experience. The perspective they gain, the understanding, and maybe even guidance in life will amaze you. You might get a doctor/biologist out of this who helps to cure, or even better, prevent breast cancer one day!! But, they will never, NEVER, be that person in the restaurant who says something so rude and mis-guided!
Night, night all!! Got in my "at least 3 quarts" of water for the day... my stool softeners, vitamins, activia, sleep pill and I'm off to a happy place - be back tomorrow night if I have energy left after putting in a day on the Air Force base.
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sacphotomom: I am so sorry to hear about your experience. I can't believe how rude people can be. You know what they say, what goes around comes around. I'm sure she'll get hers.
Have a great night everyone.
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Victoria, thanks for the advice on the iron pills. I need some of those. I am getting my blood checked tomorrow, and I have a feeling it's going to show I'm anemic. I hope you can get your WBC #s up! Did they discuss neulasta or neupogen with you?
Redbarb, my son plays baseball too, and I can SO see myself doing that with my hair! ARGH! Have fun at your head shaving party. I am still kind of fascinated by my bald head. It's so surreal!
Leanna, thanks for the links!
GolferGirl, I was oddly nervous for #2, too, but it went fine. Hoping the same for you!
njbhwgirl, I'm sorry about your mom, I hope she's okay! That's cool about the wig lady coming to your house--what a great service. I'm having the weight gain and the odd cravings, too. Weird!
Sacphotomom, I really want to see that woman and give her a piece of my mind. I can't even BELIEVE she said that. That is beyond rude. Like what we're going through isn't difficult to begin with. I have some not-so-pleasant names I want to call her, but I'll stop there... I think I need to talk myself back into a good mood like you have! I'm having a weird feeling at my lumpectomy site--I wonder if all these strange feelings are normal...
Leanna and Tuck, I was drinking a lot of Propel too, but got nauseous once, and now I'm thinking I'm ruined for Propel forever! But it did sustain me for a few weeks there. Better than water, for sure!
Nanaof2, I had that same "fear" when I touched my hair. I'm sure you'll find the buzz a relief.
Patricia, you voiced exactly how I feel most of the time since diagnosis--like I've been transported into some bizarre alternate reality. I am about your son's age & have 3 young kids--your granddaughter is just precious!
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I wanted to add additional round of kudos for the Good Wishes program that France Luxe offers. MNLinda mentioned the program a couple of days ago. I received my scarf in the mail today and it is beautiful. The card they sent with the scarf brought tears to my eyes. It is truly a wonderful gift they offer.
www.franceluxe.com/i/goodwishesscarves/GoodWishesScarves.html
Merry
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Jenny - does "is this my life??" sound familiar! That's my joke around the house when it's something cancer-related that is going wrong... ie constipation... heartburn, etc!! We just HAVE to laugh about it! How old are your children? I have 3 also - they are 17, 8 and 3.
Spininfool - That's great - her scarves do look lovely - so glad you love it!! Hey, I just noticed you had 39 nodes... did you have BMX?
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Day and GolferGirl - Thinking about you and good luck!
To all - have a wonderful Memorial Day Weekend!!
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Hi guys,
Something wonderful happened to me on Tuesday and my first thought was "I can't wait to share this with my 'May Friends'... Not enough words to express how amazing the women in my life are! I went back to work Tuesday for the 1st time in a week and hanging from the ceiling of my office were clotheslines full of panties - each one had a note tag with the slogan "BRAS ARE OVER-RATED, UNDERWEAR ARE SEXY!".Almost 300 pairs of panties from family, friends, friends of friends, and people who don't even know me! I was touched to the depths of my heart.
Welcome to all our new friends, sorry you had to join us!
Leanna, thank you for the bandanna link!
Redbarb, have fun at your shaving party!
Question: I woke up this morning with crazy pain in my tail bone. It's been 9 days since my first treatment, is this pain from the neulasta shot 8 days later?
Hope everyone has a great holiday weekend!
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sacphoto - I admire your restraint. Don't know if I could have held my tongue.
I am off to the mountains for the long weekend so not sure if I'll be able to pop on again before Monday.
So to all - a happy and SE free holiday weekend!!!
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Summer38 - I had the same kind of pain - a littler earlier onset but the onco said Neulasta pain can be a week or so after the shot. They had me taking ibuprofin, which helped (600 mg) plus my leftover dilaudid as needed. The pain stayed with me for about 2 days then was gone like magic.
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Summer38... 7 day after my Neulasta I had the same pain only last till the Advil kicked in...its your white blood going into over drive after the fall....What a wonderful group you work and friends with....made my day just reading about it......
Thank all of you for all your support on my very bad day on Thursday... I am hoping that is going to be the last rude person meet....today is already starting out better...just sunshine an blooming flowers everywhere......
Fotopet have a wonderful time in the mountains..
Going to check out bandanas at the France Luxe 1
Have a wonderful weekend everyone!
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Summer, I'd say it's probably the Neulasta (though a little late, maybe?) Maybe call your onc just to make sure. And what an AWESOME thing you came back to work to. That is AMAZING! Since my diagnosis, I've found a lot of human kindness/goodness too that I didn't know existed before.
Leanna, Yes, that definitely sounds familiar. I got up this morning, looked in the mirror, and said, in a total tone of astonishment, "I'm BALD!" My husband just laughed.
My kids are 11, 9 and 5, and they're taking this pretty well, I think. My 11-year-old is the hardest to read, but the other two are rolling with it.
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Well, I didn't get my chemo today. Apparently the doc wants me to be pre-medicated with steroids (why in the world didn't they order that at the last chemo?) so I don't have another bad reaction. And if I still have a bad reaction then he will take me off the Taxotere and put me on something else. I am so glad that after the 7th of June I will not be seeing this oncologist anymore!
And get this: I go in, tell the receptionist that I cam ein for blood test, dr. appointment and chemo, she says "I'll chek you in for the blood work", I don'tgive it a second thought. The blood is drawn of course fast, after 20 minutes of me sitting in the waiting room, same receptionist comes to me and says "are you ready to see the doctor? Do you want me to check you in?". I'm sorry, but I guess I about had enough of incompetence, so I just told her VERY curtly - a smidge was missing for me to be practically yelling at her - "When I came in I checked in with you and I told you I need to have blood drawn, see the doctor and have chemo, are you telling me that you need repeating after each of these what I came in for?". She got a sour puss, said "Thank you" and went back behind her glass. Got called in to see the doctor 5 minutes after.
Anyway. I am so fed up with that place.
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