November 2009-Starting Chemo
Comments
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Melinda: or should I call you rodent mom
I got no premeds with the herceptin. I drove myself - the only annoyance was the seat belt over my port even though I have lambswool seat belt covers. It doesn't like it just after it's been accessed. It's not nice seeing what chemo can do to some people. I remember visiting the pharmacy in an oncology ward for my work (software engineer) and saw a girl who was little more than a skeleton and they were treating her. It made me so sad. I think we are lucky that we have come through all this relatively well. Life isn't fair.
Good news, the tech seemed pleased with my echo today. Apparently my first one was normal - no one told me (that prick of a bs - I never want to see him again!!!). They were running late and I waited over an hour but it's done now, hopefully I won't need one for a while.
Sue
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Suepen: congrats on the echo! My tech always says he can't tell me how things look, but that I look good (wink, wink).
LOL about the rodent Mom! I rub my head on my OD's arm since it creeps her out. I am tempted to shave it off and see if something better will grow out, but I figured I will at least wait until I finish chemo. I am hoping real hair will grow in the thin spots, I can buzz it off even when I fill out a little.
But I do have a morbid curiosity as to what is up with the see through hair (I refuse to call it gray). Even my eyebrows are see through. They are still there (for now) they just lost all there color.
Sue: Thanks for reminding me about the seat belt thing. Since my Mom always takes me to chemo, I forgot that my port is on the drivers side. When I can drive myself like a big girl, I will keep the Barbie pillow I stole from the kids handy.
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Melinda: I have (as I said) seat belt things made out of lambswool - got them on advice from another bc friend. Check out your local car accessory store, you might have them over there. I don't have to drive far so it's tolerable coming home from the treatment. My hair is looking reasonable - not good enough to go topless yet but it's certainly getting thicker. I started using Nioxin last week - might as well give it the best environment to grow in. I'm now 5 weeks PFC. Maybe by the time rads are finished I'll be able to lose the head coverings.
Sue
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Michele, I was pretty much told no to implants, as I too will be doing rads to my lymph nodes and chest wall.
Sue & Melinda, I get my Herceptin (3X/3 wks) over a 30 minute infusion. I have Benedryl, and that's it. No side effects to mention.
Have any of you heard about only having 2 lymph nodes? My surgeon said he did a complete axiliary node disection (I don't know how to spell this crap), but he only found 2 nodes. Neither one was cancerous, but the biopsy showed they were. Therefore, with good margins, I had a "complete pathological response" to chemo/surgery. Meaning...no cancer!!!
(((Hugs))) to all.
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Well, you, guys, have had me dizzy with the talk of DIEP's and...oh, I'd have to go back and see what the other acronyms are and if I did that, I'd lose my posting. I have looked up these procedures in the past, but have forgotten what they are, but I'll check them out again so I can keep up. (I have only a lumpectomy, and am very fortunate that the surgeon had to take only the bottom 1/3 of my boob, so I can wear a bra with a separate insert that takes up the space that's missing.) The fact that your body still sees the abdomen fat as just that even when it has been used for the reconstruction is weird, but I guess it makes sense. How would it know otherwise?
I have only 2 rads left. (woo hoo) Redness isn't too bad, though the area is occasinally itchy. I have been doing the "boost" (the smaller focused area) this week, so the redness from the large area radiation should start going away now. I never did get use to going to the rad sessions: I was anxious for every one of them, though I only took Ativan on Tuesdays when I met with the dr.
Melinda41: that poor man you saw in chemo. That would have broken my heart, too.
Re: hair growth...Everyone who sees me without my wig says that I have enough hair to go without the wig...that I have as much hair as Jamie Leigh Curtis, but I beg to differ, so I'll wait a while. Plus, I have to wait long enough for my hair length to cover a birthmark I have on the back of my head that is the size of a quarter and has only a couple of hair follicles. I knew it was there prior to buzzing off my hair, but I'd never seen it. Was extremely obvious when I had no hair!
All of you Warriors still getting chemo, or Herceptin: hang in there! For those of you looking at surgery now or in the future, I wish for you only the best outcome...and symmetry!
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Linda: You get Benedryl with H only, that blows, as that is the only reason I can't drive myself. Regarding lymph nodes: I just happened to ask my lymphedema therapist how many lymph nodes in an axilla. She didn't have an exact number but said the most she has heard removed was 32. You only have two lymph nodes sounds odd. But I am glad you are all clear now!!
Nette: Congrats on almost finshing rads, so are you done with treatments when rads is over?
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Melinda: Yep, as of Friday, I'm donedone. BrendaShar should be done that day, too. Not sure what I'll do with all my free time after I'm done. I did tell the secretary at school that I would be ready to return to subbing after Friday, though I plan to only do half days for a while. I've been extremely blessed not to have to work during the last months of hell. I don't know how others have done it, but I guess you do what you have to do. I know they get a lot of respect from me.
It still amazes me when people tell me how brave I am to make through everything and I figure, the only other alternative would have been to crawl into a hole somewhere. Not much of a life that way, though there were plenty of days that that would have been easier.
Everyone have a good evening.
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Yah Nette, you are almost over the fence you little monkey...remember we are monkeys climbing over a fence to the finish line.
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Nette,
I am as thrilled as you. I do finish my rads the same day as you and glad of it. I had a total of 34 rads the last 9 being the "Boost" I'm not too tooo bad although my breast is getting a little red and for sure tender in the nipple area. I was told yesterday that even though I'm done with the rads they are not done with me. The effects are to last for approx. 2 weeks to a month. (I'll still be cooking from the inside out so to speak). My nipple is even black in some areas. Very strange looking and very sore. I am totally exhausted, I believe in part due to the long 3 hour drive to and from the treatment center each day. They are very efficient, I'm in and out. BUT, the drive sucks!
Melinda,
The see thru hair!!!! Oh yeah!!!
Does yours look like just maybe another colour is under all that baby duck fuzz?
Well ladies it's coming to the end:
Began August 13, 2009 diagnosis cancer of the left breast, biopsy confirmed as well as mammogram and CT scan, etc.
From surgical lumpectomy Sept. 3, 2009, surgery again Sept. 17, 2010 for a 23 Node Axillary Dissection, to chemo treatments from October 28th 2009 thru Feb. 10, 2010, then onto radiation for 34 treatments March 2nd thru April 16th 2010, along with physical therapy for Lymphedema in between. Well, I'd say I've earned my degree and the right to celebrate this weekend.
To all "Warriors" (((((HUGS)))))
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Brenda,
Congratulations on being finished with treatment!!! You have done such a wonderful job keeping up with all of us - thankyou. Now you can get your life back - almost. There are still a few ladies left to watch over.
((((HUGS)))) to everyone
Sue
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BrendaSharon: Congrats on getting done, I hope you have a great weekend!!
My hair looks darker than the first fuzz. When I look straight on, it is like dark with white tips. Very weird, I am tempted to shave it and start over, but I figure I will wait until chemo is done and then see.
Speaking of chemo, I am so sick of bloody booger stew in my nose. The weirdest stuff comes out of my nose, at then it wants to bleed for awhile and it always feels dry or chunky or drippy. I want my old nose back.
But I guess I should be grateful my pubes are growing back, at least I can pee straight now. I would hate having weirdness at both ends.
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Brenda, kudoos to you for being done....another monkey over the wall...
Melinda, glad to hear you are peeing straight...
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Melinda,
My pubes don't seem to be coming back at all. My leg hair is just a faint prickle from last time I shaved them. At least the head hair is doing something.
8 rads down heaps more to go.
Sue
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My pubes, pit hair, and leg hair are coming back too, but DAMN...are they white! What is up with that? Please tell me it will darken up!! At least on my hair. Alas, I still pee crooked. Some women have all the luck
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I have hair down there, but it is not pubic hair. It is like the hair on my head. Started out clear and is gradually darkening. But it in no way looks like pubic hair. It is like I am going through puberty again. Trying to grow new boobs, getting hairy...
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Warriors,
Thanks for the thumbs up everyone!!
What a celebration I will have this evening.
Planning to out to dinner and see a movie.Then tomorrow go out in our boat to the Island in our area near our home and just enjoy a gorgeous day with friends and my dear sweet hubby who bless his heart he has endured this entire journey with me.
Bless all the caretakers that have dealt with each of us as their job was long and hard, but not unappreciated ~~~ Each one of you are special to us each day and each hour.
I really can't wait to see the outcome of the "Hair Colour" :-)
I will continue to watch as the final few come to their finish, I wish everyone the best life can offer and continued good health from here in. We have made it and I know each of us will cherish every minute of our lives from here in. I will pop in and out of this thread probably once a week, just to see how everyone is getting along with their lives. And once a year on November 1st, I think we should all come on board to say hello and to let each other know how we are getting along. I will miss each and everyone of you and I want to thank each and every "Warrior" for sharing your journey with me. I know we are truly blessed to have made it though this.
Together as "Warriors", we won our fight against Breast Cancer
((((((((((WARRIOR HUGS))))))))))
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Brenda, you make this sound so final.....I think we warriors should still check in on a daily bases.
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Oh ya Brenda, sounds like a fun celebration.
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Brenda ~ CONGRATULATIONS for finishing RADS ~ woo HOO.
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Hi girls dropping in to read and give updates. Glad to see some of you are finishing up with rads a celebration is definetly earned. I am still getting herceptin every 3 weeks until Nov 23rd so far ok seem to tolerate it better each time. My infusion takes 30 min with no premeds. I finally could put some mascara on my lower lashes and brows are coming in nice, the hair on the head is going slow and was pale at first but now seeing the dark brown and filling in so trying to be patient. Its starting to get in the 90's in AZ so wanna go wigless soon. Almost done with my tissue expander fills probably 2 more then I will be good. Wanted to go a little bigger after all this shit I deserve some good cleavage.
Wishing you all a great weekend
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Please Sisters...DON'T LEAVE ME YET! I have just had surgery and am headed for rads. I still need you. My journey is almost over, but I still have a little bit to go. 6 1/2 wks of rads and a liver ablation. I can't go to the Stage IV forum...too depressing. I don't fit there. I can't deal with the sadness there...it gets me down.
Even being stage IV, there are a lot worse sisters than me...I have one stupid spot on my liver that is the size of a pea...
I know I'm rambling, but if the chemo did so good on my chest and lymph nodes, I can't wait to see what my liver did. I plan on living a long, happy life with my family, grandchildren, and friends.
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Girls, Girls, Girls!!!!
I'm not going anywhere!!!! I could never leave y'all. You have been my strength through this entire journey I have been on. I just was hoping everyone else would as well continue to check in and chat every now and again. Michele, I'm not sure about daily (I will daily till all "Warriors" are over the wall) but I will check often to see how everyone is doing each and every week.
Sue, said there are a few to still watch over and that I shall. Sue nor I will let you down. We will be "Warrior Sisters" forever and ever.
The only thing final is that we each make the finish line to our journey. BUT~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
I would love for everyone at least in November on the 1st to check in give an update on their life and how they are doing in general, health and or otherwise.
Love all of you
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Hi Warriors,
I am so happy for all of you that have recently finished your tx's. I have been away for a while due to an unexpected turn of events in my journey. I have been staying busy with work and school and my hair is coming in really well. Basically, I feel fine just different. New back pain prompted me to see my PCP a couple of weeks ago and x-rays revealed two lesions on my back. Had a MRI yesterday and I hope to have the results today. Found out from blood results that I am still pre-menopausal so it will be Tamoxifen for me even though I haven't started it yet. It sounds like all of you are doing well and I'm so very happy for each and every one of you. You all have truly been such a blessing in my life and you will always be my "sisters" in my heart. I am participating in the Relay for Life tonight and I'm walking the survivor lap in honor of all the November Warriors!
HUGS ~ Toyah
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I'm not going anywhere. You have all become such a part of my life. There are many of you I feel like I know in a small way ~ We have shared a major hardship in our life and we will be sisters forever...... I truly care for each and every one of you and wish you a life full of happiness ~
GROUP HUG !!!!!!!!!!
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Toyah: I hope you get your MRI results soon and it is all clear so you can have a great weekend. Please let us know what they say.
Alicia: your hair in coming in nicely, good coverage!
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Toyah, good luck with your MRI...let us know when you can. I'm sending positive vibes your way!!!
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Hey hey, All you warriors!! I had my last rad session today!!! woo hoo!! The radiation techs call your last day of radiation your "Graduation Day." When I was there yesterday, one tech jokingly said, "Don't forget your cap and gown tomorrow." Well, that got me to thinking... I found my daughter's graduation robe, my old high school graduation cap, and my son and I figured out a way to make a pink tassel. So today at rad, after I was called back for my final session, I put the robe over my hospital gown, put on the cap, and waited in the holding area. The doctor's assistant walked by the room and saw me waiting, laughed, and ran and got a camera and said, "This is going in your chart, my dear." A few minutes later, when Candy, one of the techs, came to get me from the holding area, she went nuts when she saw me...laughing and saying oh my gosh!! The 4 other techs went nuts when I walked into the treatment room, too. They said no one had ever done that before The head tech took my picture, then the 3 techs that have actually been doing the treatments got my son to come in and take my picture with them while I had the robe and cap on. I'm really glad I did it. Was lots of fun. During the session, they played the grad. song, "Pomp and Circumstance." Afterwards, they gave me a "diploma," a picture of me taken the first day I started rad with a grad. hat superimposed on the pic, and the pic the head tech took today, with a note card signed by all of them congratulating me and wishing me luck. (I hope to get a copy of the pic of me with all the techs when I go back for my follow-up in May.) I actually did the cap and gown thing to lighten up a very emotional time that otherwise, I would have reacted with lots of tears: of happiness, but still tears. Instead, we laughed a lot.
My DH took me to the session today and I let my son stay home to go with us. Afterwards, DH brought us home and he went on in to work. My son and I went to the Cheesecake Factory for lunch. During lunch, I received 9 text messages responding to a text I sent out saying, "I'M DONE! I'M DONE! I'M DONE! WOO HOO!!" He and I were laughing every time my phone buzzed with a new text! After lunch, we walked around the mall and he surprised me by buying me a very pretty ring with some sapphire-colored stones as a congrats gift. I also had enough car wash punches on my card to get a free car wash while we were out. Came home and I got a call from the school to sub a half day the week after next. Whoa, what a great day.
So, I'm relieved it's all over. I'll miss the fantastic staffers I've met along the way, as they have all been compassionate, kind, and caring, but I'll see them at times during follow-ups with the various specialists over the next several years.
Thank you for letting me share this epic day with you, my Cyber Friends, my Rocks, my Encouragers. And I'm not going anywhere either.
Cheers (with sparkling grape juice) Annette
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Nettie ~ so glad YOU had such a great "last" day of rads ! You are too cute wearing the cap and gown in. Sounds like they loved it~ And a nice day with your son, lunch, a car wash and a new ring. woo HOO ~~~
Hugs,
Alicia
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I'm not going anywhere either. I can't imagine how I would have coped without all of you. You all have been my rock.
Nette, congratulations on being done with rads, I still have 22 to go - eeek!!! What a great way to graduate.
Toyah - fingers crossed for you - (((HUGS)))
Alicia, wow you have hair!! Mine is so pale you can hardly see it.
Linda J - good luck with the liver ablation - we won't desert you don't worry.
Sue
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Nette - Congratulations!!
My onc nurse just called to tell me that the MRI showed some stuff going on with my blood vessels in my back but NO EVIDENCE OF METASTATIC DISEASE!!! Now I finally feel like I can put this shit behind me and celebrate living! In case I haven't told you lately, I love each and every one of you! Have a great weekend, I gotta go get my Relay on
Oh, pic is horrible but wanted to show my hair growth. I will be replacing it tomorrow (if I remember..LOL)
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