June 2007 Chemo
Comments
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Happy New Year!
Melody, thanks for the picture info. Everyone goes back to work and or school tomorrow so I'll have more time to play on the computer. I'll have to check photobucket out and see if my chemo numb brain can figure it out.
Linda, congrats on finishing rads with minor discomfort! 2008 WILL be a good year for all of us!!
Dawn, sounds busy at your house! Is your son a graphic designer? I've always regretted not taking more art courses but I do some now at the local Gilda's Club. Watercolor is my choice of medium....well, I attempt to do watercolor. LOL
Hope your daughter and her little dog (I feel like I'm in the Wizard of Oz) do well in their new place. It's always scary when they first move out on their own and wondering if they'll be able to make it this time.
I hear you about the hair. I quit wearing head covers about a month ago and my hair is far from long. It's straight, gray and short but I don't care anymore!
Here's to a great 2008 for everyone!
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Hi TerryNY , and anyone else that would like some very good instructions on how to download pics. Go to "Moving beyond Cancer" thread , on page 14 , Timtam's post "how to download pics to forum". Click on that!
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Terry - Mike is specializing in 3d! cool stuff. hoping to see his name in the movie credits one of these years! Water colors are so pretty - I am glad you are taking classes. My artistic abilities end with decorating cakes - lots of tricks to use!!
My daughter actually graduated from college, married a week later, divorced a year later, moved back home for a year and a half and is now moved out again. She qualified for the apt by herself and a friend from England just moved in with her. I'll miss her and her little dog (definitely Wizard of Oz!!) but I know they'll all be over for dinner often!! Lisa has about 4 dishes that she likes to make!
Go Linda for finishing rads!! I had #24 today and my rad onc will reassess tomorrow - she wants to do more whole breast rads depending on my skin which isn't too bad. couple of places are bothering me. Guess we'll see. I can see the light at the end of the tunnel!!!
Happy New Year everyone!!
Dawn
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Just had to share, the surgeon's office called and I am negative for the BRCA 1 and 2 mutation, hooray for me!! However, just to temper the good feelings, he wants to schedule an MRI of my good breast..sigh...and away we go.....
Dawn, too funny about your daughter's cooking abilities. My daughter is dating a guy that likes to cook, thank heavens, because she's a dial-up-the-pizza-delivery kind of gal.
Let us know if your son gets any movie credits, that would be exciting!Melody, I have yet to check photobucket or that thread. Thanks for the suggestion though.
I tried spiking my hair this AM and it's stubbornly refusing to do anything other than lying flat against my head. At least it's hair, right?
Hope everyone is doing well!
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go Terry! I was negative as well, but I think it's a relief just to have ANOTHER question answered. My rad onc ordered an mri of my good breast and my reconstructed one. Weird laying on that table with your boobs in different holes............................hoping your test will be negative like mine was.
I'm hoping my daughter's room-mate (friend from England) has some cooking ability - Lisa has been known to each cheez-its for dinner........................
It is hair!! Maybe you should be glad it wouldn't spike - I think I might feel more like a chia pet if mine did!!
Today is the first day I've gone out of my house (except to the trash/recycling of course!) without a scarf or crocheted cap!! I feel kind of naked. One guy at work said I look about 17 - Not sure if that's good or bad!!!
Saw my rad onc today after tx #25 for reassessment - she wants to do more whole breast rads instead of boosts since my scar tissue is extensive from the first surgery and then the recurrence. Luckily I won't need the bolus and she's going to target a smaller area so my underarm, above/beside/below my breast can start healing. My underarm is almost raw - OUCH!! Not sure how many more tx but at least the area is fairly numb already so hopefully I won't feel it!!!
Oh well. Onward we go.
Hope everyone is having a good week. Last "short" one for a bit!
Dawn
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Hi All!
Just checking in; getting ready to start CNA classes on Monday, feeling pretty good although still a little fatigued towards the end of the day.
Terry and Dawn: Why the MRI's? Anything going on that I missed? Or is it a standard thing once treatments are done? I haven't gone back yet for a checkup, that happens towards the end of January. Just wondering.
It's been freezing (I kno it's winter!) cold here the past couple days, now they're saying we'll be in the 50's and 60's next week! Already I can't wait for spring..... the older I get, the more I hate the cold!
Hope you're all feeling well!
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Bonnie - my surgeon mentioned in July that I should have an MRI (on both) as well as mammo (on the healthy one) every year. My rad onc told me that chemo doesn't do anything in the breast tissue since it's mostly fat unless there is a tumor etc so she wanted to make sure there were no other issues lurking.
Interesting stuff that I never really wanted to know about!!
Good luck with your classes Bonnie!
Dawn
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Bonnie, I haven't had an MRI on my other (good) breast since I was dx last Feb. (I can't believe it's been almost a year!)
I mean, I've never had an MRI on that breast, only my right...now why they can't do both at the same time while they're in the cups, I don't know. Like a lot of medical mysteries, this one stumped me too. <sigh> So, he just ordered it for safety's sake as the guidelines recommend women who have been dx get yearly MRIs along with their mammos.
But I so don't want to deal with this, too close to my dx date and it's kinda freaking me out...the what ifs are having a field day in my brain.
Good luck with your CNA classes! I'm happy you found something to pay it forward. Let us know how it goes for you.
The weather has been unusual! I, too, am looking forward to the warmer temps next week.
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Hello all. I'm continuing to recover from surgery (Dec 3) - no more pain and almost complete range of motion. I do get tired every afternoon about 3 PM and have to take a 2 hour nap. I hope this is normal. I saw 3 doctors yesterday (BS, onc. and radiologist - mapping for rads). I'll be on Xeloda during rads due to the large number of positive nodes found. I asked the doctors if they had patients with 21 pos nodes who lived. Each of them said yes but they hesitated for a minute. So my rate for recurrence is high (70%). Good thing I'm taking Effexor or I'd start crying all over again. Next week I'll be getting bone scans and CT scans of my liver and lungs to see if the demon spread. At least my blood tests turned out OK. I imagined I had leukemia since I felt so tired. This is what happens when you have too much time on your hands.
My hair is about an inch long all over and mostly white. Eye lashes have grown in but are pointing almost straight down. Eye brows are a little fuller than they were before but that's good. They were too thin.
Hope you all are enjoying the new year. Good health to you all!
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Hi Shrink , so good to hear from you. After my surgery , I took afternoon naps too. Thats completely normal. I wish I could remember the thread I was reading here the other night... The ladies were talking about having so many nodes positive. And some of the ladies were survivors , and had more than 21 nodes positive. There is always hope Shrink. Always believe. I was wondering how much Effexor you are taking. I am taking 20mg for hot flashes , but it doesn't seem to be helping. I wonder if the doc can up it. You are always in my prayers ,and I will pray for clear , b9 scans. Good luck to you Shrink. Melody
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Thanks, Melody, for the support and prayers. I'm taking 37.5 mg of Effexor. Lots of people require more to reach a therapeutic dose for depression.
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Howdy all.
Shrink, the onc said "yes" to your question so just focus on that. Do do all you can to take care of yourself, nap as long as you want, read, knit, or start some plants indoors. By spring you could have stuff to put outdoors. Try anything that will take your mind off bc for a while if at all possible. I will also be praying for clear scans.
My hair is really wierd looking, too. Mostly gray now and going about 14 different directions. It reminds me of the swirlling fur of a certain type of guinea pig my daughters had many years ago. I'm still not ready to give up my wig when I go out. Besides, it's warm.
Dawn, how fantastic that your son graduated from an Art Institute. I taught art in high school for many years (retired now) and I always had a representative from AI make a presentation to the kids. Many wanted to go the 3D route but very few could actually do it. Kids will wear you out won't they? My oldest turned 30 last July and is a free spirit, traveling, working, belly dancing, sky diving (that one really freaked me out). About the rads - be sure to use alot of that prescription cream and get more if you need to. It sure helped me.
Bonnie, great to hear you are taking CNA classes. That should be fulfilling work - plus you are virtually guaranteed a job. I am gls to know that you aren't experiencing any side effects from Tamoxifen. I think that is supposed to be the next step for me, too.
Terry, that is so terrific you are taking watercolor classes! Just enjoy the medium and experiment a little. You can do so fun much stuff with it. I just ordered alot of oil paint and acrylic paint online. Hoping to get regular studio time going for one of my new year's resolutions. That is wonderful news about testing negative for Brac 1 and 2 genes. I will be thinking about you for your MRI. You know we have to face down this these tests for a quite a long time. Need to find a way to cope with them.
Melody, I enjoy the cool pics. Maybe I can figure out how to do it. Boy, have I rattled on. Stay well all.
Linda
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Shrink, I continue keeping you in my thoughts. Sounds like your drs have it all mapped out and you're on your way to beating this beast!
I think napping is very normal for what your body has been through the past year, emotionally and physically. It needs that down time to regroup. I still find myself napping about once or twice a week and feel so much better afterwards.
Linda, I hope you get your studio time. Do you enter art shows or sell your paintings? I think we could all take a cue from your oldest and be more daring! I'm not sure I could do the skydiving though. LOL
I realize the first few times we get follow up testing it will be nerve wracking, I'm just hoping it isn't as bad as the years roll by. My twin had bc 14 years ago, and she still gets a bit apprehensive around mammo time.
Hope everyone has a grand weekend!
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Cripes -- I just found this group too -- I started chemo in June 07. I wish the most recent posting were at the top!! I thought it was all "old" postings.
Here's the background -- lumpectomy in May, A/C June and July. Margin cleanup August. Taxol (oooh, the pain, eventually had to go on oxycontin!!), now have only 6 rads left (of 33). Very red boob, crispy clavicle (yuck). And I'm obsessing about my hair. Oh yeah, a couple of weeks ago it was confirmed that I had mets to my liver but the chemo cleared it up -- it's gone...
My big problem is that I never told my Mom. I haven't been back home since Feb 07 (I moved from Canada to the US Nov 06) and keep telling her work is keeping me too busy. It has been the lack of hair that has kept me away -- wouldn't be able to hide that!! She's bought it so far. She's in her 80's, a terrible worrier and starting a bit of Alzhiemers but still pretty sharp and simply a lovely woman. Anyway... I always remember her saying she would drop dead if anything happened to one of her kids -- hence me not telling her. My sister, an MD, at first said I should tell her but then agreed that it is better that I don't give my Mom that sadness and grief. Even though I'm 45 years old, there are days I would just love to crawl into her arms and cry.
My hair is slowly growing -- and am finally visiting her the first weekend of Feb. The story is that my goofy short hair is all the style and I just got a bad haircut.
Has anyone been in this situation of trying to hide their cancer? It's awful -- wanting to see my Mom but not being able to.
Sorry for the long-winded posting -- wish I found you all earlier...
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Gee, it was nice to see all the posts this morning! Welcome, konakat! This is a great group of gals and I don't know what I would have done without them over the last 6 months. I'm sorry you didn't find us sooner. I don't have any answers for you about your mom. I expect she might suspect something, but no matter what she will be so happy to see you!
Guess what I did yesterday?? I got a hair cut! Hah!! My hair was so shaggy around the ears and on my neck that I went in and had it shaped and trimmed. It looks soooooo much better, still very short but now it looks more like I wanted it that way. It was sure a strange feeling to be in the hair dresser's chair.
I received an email the other day and wanted to share it with you all as it really expresses how we have all helped, supported and felt about each other over the last many months.
Time Passes.
Life happens.
Distance separates.
Children grow up.
Jobs come and go.
Love waxes and wanes.
Men don't do what they're supposed to do.
Hearts break.
Parents die.
Colleagues forget favors.
Careers end.
BUT - Sisters are there, no matter how much time and how many miles are between you. A girlfriend is never farther away than needing her.
When you have to walk that lonesome valley and you have to walk it by yourself, the women in your life will be on the valley's rim, cheering you on, praying for you, pulling for you, intervening on your behalf, and waiting with open arms at the valley's end.
Sometimes, they will even break the rules and walk beside you, or come in and carry you out.
Girlfriends, daughters, granddaughters, daughters-in-law, sisters, sisters-in-law, mothers, grandmothers, aunties, nieces, cousins and extended family all bless our life.
When we began this adventure called womanhood, we had no idea of the incredible joys or sorrows that lay ahead, nor did we know how much we would need each other.
Every day, we need each other still.
Hugs to each and everyone of you!
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Thanks Debbie , I haven't read that in awhile , I got goosebumps all over again!
Welcome Konakat!
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Hi, my son is teaching me how to upload pictures from Photobucket and you're the guinea pigs. :-)
Here goes:
Me, at my last chemo, 9/26/07: (edited to remove HTML lingo)
LOL, we're obviously having difficulty...removing other stuff....
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There, it only took us 10 minutes to do the above picture. LOL
Konacat, welcome to our group. Sorry you had to join but we're a supportive bunch although a bit quiet these days. I hope you enjoy visiting your mom. I haven't had to travel in your shoes so I really can't pass along advice on how to handle that particular situation.
DebbieK, get outta here..a HAIRCUT?! LOL I'm tempted to get mine trimmed around the ears and neck, I feel like I'm growing sideburns.
It is WARM here in western NY today, very odd weather for January. I had the windows open for a short time while I cleaned house this morning, it felt heavenly, the fresh air, NOT the cleaning. :-)
I'm going to my first exercise class this afternoon for the local dragon boat team. Hope I'm able to do something but my feet neuropathy is acting up again so I'll see....
Hope everyone is doing well!
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Hi all...Welcome Konakat....I was warmly welcomed and sort of fell off the map but I wanted to respond to your mom question. I too dreaded that conversation since my mom is a chronic worrier and tends to the negative. I had no choice but to tell her and she handled it pretty well. I insist that she only talk about my prognosis in the most positive way. So far so good. I have a feeling that if your mom figures out that you've been going through more than a busy work schedule, she'll handle it okay. Blessedly the cancer diagnosis of "their" day is much different than today. Good luck with your visit! I wish my hair was long enough to look stylish! I still look like a balding man...ugh.
I've loved keeping up with everyone else. Just started rads and since I'm a warm NYer (Hudson Valley) no snow days yet!
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Linda - the Art Institute has been a wonderful choice for Mike. I think I'd have a heart attack if any of mine actually sky dived!!
welcome Konakat - glad you finally found us!! Good luck with your mom - let us know how it goes.
Congrats on the haircut Debbie!! thanks for the poem.
Go Terry!! no one saw me bald except my DH and kids.............
let us know how the class goes!
I had my #28 rad treatment on Monday, was supposed to have my #1 boost yesterday but my underarm is peeling so they skipped it and I had it today. Tuesday will be #5 and I should be done. My treatment has been very aggressive since this is a recurrence; I have peeling in several areas and I hurt so I'm whining big time! Rad onc suggested percocet so I can at least get some sleep. I can't wait till this is over. Sad to say, but for me, 3 months of chemo was easier than 1.5 months of radiation. I am supposed to see my surgeon and my plastic surgeon for follow up this month - NO WAY!! I think I'll schedule them for February and give my side time to heal.
Hope everyone is having a good week!
Dawn
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Hello All!
Welcome to Konkat! We are a great bunch of gals ....if I do say so, glad to have you here! Hope you come to a decision about what to do with telling your mom. I lost my mom 3 yrs ago and how I wished she was here for some of my down days!
Debbie, I had to get around my ears trimmed up as well; I just had my son's gf do it for me, she's such a sweetheart! They are both almost 21, been together 3 yrs......I know they're young still but I hope she's the one
!
Dawn, I have to agree with you, the 3 months of chemo was a breeze compared to how the rads treated my skin. Thankfully it's all cleared up now!
Terry, you looked great in that pic! Did you get that awful wind last night and today?? From one extreme to another in old WNY!
Well, today was my 3rd day of classes. I'm not as exhausted as I was on Monday. Yesterday we had our first test (really cramming it at us, it's only a 4 week course, not 6) anyways, I was the only one in the class that got 100%,pretty proud of myself!
I think I'm going to like it!
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100%!! Go Bonnie!!
As I was reading your post - I kept rolling "3 months" over in my head - well, duh, 3 months of A/C and 3 months of T/H = 6 months of chemo that I had, not 3 months!!!!
Either way, for me it was easier than these radiation treatments have ended up being. I can't wait till I can put my arm down when my armpit heals!! (see, it just doesn't take much to make me happy!!! )LOL
Time for pain meds!!
Goodnight all!
Dawn
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Dawn, I'm sorry to hear your rads tx is more than you bargained for. Hope the burns clear up fast. My sister had rads 15 years ago and she burned all the way through to her back. :-/
Bonnie, great news on your classes and especially the test, you go, girl! Show those young whippersnappers who's what. LOL And yes, we had horrible winds for almost two days. The temp has returned to normal too, back to winter.
I had my follow-up with the genetics testing and I did come back negative, yippee! I have to get an MRI next week and then mammo and US in May, all for follow-up scans. Methinks this is going to be our lives from now on.
She was giving me instructions on care and mentioned monthly breast self exams...ha, ha, ha...I told her I couldn't even touch my breasts yet for fear of finding another lump. I figure as many times I'm being prodded still by every dr, then I'm safe for awhile. She told me she's four years out and still can't do them for the fear and yet, there she is telling the patients to do them. Man, what a struggle for her, huh? Being a survivor and dealing with all the patients coming through the office..I'm not sure I could distance myself emotionally.
Enough of my rambling...hope everyone has a great Thursday!
Oh, as far being bald, I was in a private room for chemo that day and took my hat off...so just my husband and the chemo nurses saw me. But I never wore my wig, just baseball caps anyway.
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Terry - I can't imagine what your sister went through 15 years ago! I keep hearing how much better rads is now.................... I have one area of reaction on my upper back but it hasn't been too bad. 3 more boosts to go. I am getting the bolus with these just like I had everyday for the other treatments.
I'd love to see what you are working on - maybe you could upload a picture of your watercolors?
I understand not wanting to do monthly exams again but at least be mindful when you are doing lotion - that's how I found my recurrence and even my surgeon thought it would be scar tissue.
Hope everyone is having a good week!!
Dawn
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Some good news at last! All of my post-mast scans (bones, liver, lungs, etc) were negative! Guess that makes me NED for now. I am so relieved considering the number of positive nodes found during surgery. Thanks for your support along the way, Ladies.
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That is awesome news shrink!! Great way to end the week!
What is your treatment plan now?
Dawn
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Hi Dawn. I'm having radiation for 6 weeks along with Xeloda to catch and destroy any remaining cancer cells. How are you doing?
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Shrink, that's awesome news! I'm so happy for you and I know you're beyond relief!
Good luck with the rads and xeloda.
What are you doing to celebrate??
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My SO and I just had a Baily's on the rocks and toasted each other and our health. Since I rarely drink, this was a big deal for me. I'm thinking of some other celebratory behavior later this evening.
Some other good news - I'm fitting into my skinny jeans as a result of weight loss due to nausea due to pain killers and antibiotics due to surgery.
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Shrink , YIPPEEEEEEEEEEEE! This is great news. I'm drinking coffee , but heres to you Shrink. Have "fun" later on this evening
. All this AND your fitting into your skinny jeans. I'm sooo jealous. Although , I'm sure you didn't enjoy losing weight that way! I'm still praying things just keep getting better and better for you xx Melody
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