April 2011 chemo
Comments
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Such a lot of chalenged we face in the lives we live. So many strong and wonderful women here!
Yes, yesterday was my last chemo. Because I had a reaction last time they dosed me up with the hated benadryl and ran the rtaxotere really slowly so it was a very long day. My wonderful daughter Christina always goes with me - she made me a shirt to wear - bright pink with Warrior written across the front and a flap for the port! She has been so great through all of this. Luckily she is a teacher and has been off for the summer! My other daughter will come to town to help around surgery.
I am blessed in so many ways - as we all are! Sometimes it is just hard to remember that part.
Sending loving and supportive thoughts to all my long distance friends!
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Sarah--I'm so sorry. It's so true--it's such a large decision in life, and it's hard to confront how you really feel about it until you start talking about it. I once told my husband that it didn't matter if I'd had one or ten, the day I knew I was done having kids would be a sad one. As it turns out, it was one. And I was on bedrest for my pregnancy! I really wanted to have another, but hubby was never that keen on the idea--not that he isn't absolutely in love with our son! I was in musical theater before I returned to grad school, and I admire the artists who stuck with it. I really made the choice in my late 20s that I wanted a family and I knew I wasn't headed there where I was. We all make our choices, and I really do admire yours.
Determined, there was something I wanted to say to you and now can't remember since it was on the last page....argg...chemo brain!
Artie--AWESOME shirt! My mom and I are great friends, and she's come up most weeks to watch our son as my hubby takes me to treatment. Mom went with me twice though when Larry had something for work. I feel awful to have put her through this...she loves me as much as I love MY son, and I know it would kill me to watch him have a battle like this, so I know it's hard on her. But then, that's the price for loving so much, eh? It sounds like you two have that loving relationship.
Gotta run...my son is home from school--first day and last day of this week since he was home sick Mon-Weds. I vomited last night and still don't feel 100%. I just have 2 more days of Lapatinib pills to take for this round of chemo, and I'm wondering if I should call and say I'm not sure I can hold them down. I may just WARRIOR through and give it a try. I think it's just how my body reacts to a bug while on the chemo. It seems if Jack has any bug at all it leaves me vomiting. That wasn't one of his symptoms at all, but maybe my stomach is just more sensitive since the chemo treatments. I don't know. Okay, really gotta run!
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Ah, Determined--a friend of mine with Alopecia swears by wig caps. She says it really helps with the sweat and even with a bald head it helps so that you don't feel scratchy. Anybody else know ways to beat the wig sweat?
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just checking in to say that after 4 rounds of taxoterre and cytoxin, my tumor has halved in size and satellite tumor cant even be seen anymore...just passing on how chemo does work...and for me, now comes the surgery...sigh
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Louis, thanks for sharing that. We all need to hear that.
Hugs
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hi everyone!! internet was down yesterday
so i missed alot! everyone needs a great big HUG!!!
i had my daughter at 19 so i feel that i grew up with her somewhat...and i only had one because we could never afford more. i think we did pretty good by her since we were babies ourselves!! it just sucks that cancer has to come up and crash your dreams of more children
but big hugs to all!!!
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Carla - thanks for sharing your moment in the car. I can feel it and imagine I'd do the same thing. We constantly have moments like these that takes our breath away and teaches us how to breath and move on.
Today I got news about my MRI - some good some not so good. The right breast mass has shrunk down to 2.4 cm from 5 and the lymph node is smaller. However, the left breast still has the cancer in it plus a suspicious 7mm satellite mass that wasn't there before but no lymph node activity on that side. So having an ultrasound next week on the left breast to rule out more cancer. I guess either way, both breats are coming off on Aug 16th so does it really matter?? Long as the surgeon gets clean margins right? I am confused to say the least. Thought the chemo would work on all the cancer, the left breast was prog pos and the right breast was estrogen pos, 2 different cancers going on. Oh well, time for me to take that deep breath I was talking about.
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Warrior on Ranger Mom!!!! Sending loving supportive thoughts!
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I'll take a deep breath with you RangerMom.
I'm feeling down today ... for some reason I keep thinking about my prognosis and it's doing my head in.
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Kiwimum: Yeah, I've had days like that. You and I have very similar stats, and sometimes I get a little freaked out too. *Hugs*
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Thanks guys - How'd you like the Look good feel better class KiwiMum? I had a good time playing with the make up. Free make up is a good thing!
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Look Good Feel Better was good. Heaps of free makeup and quite fun.
I enjoyed talking with the other women and being able to share "our normal".
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Gals, thanks for listening and offering your shoulders. I did not realize how much I was carrying on this baby topic. It was good to address it here. Felt safe.
Hope everyone has a good weekend.
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Everyone have a great week end. Stay cool
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I went on a rant with a friend a few days back - cancer is awful for all of us, but IMHO it's obscene when it attacks children and you young women who might have chosen to have (more) children. At 60, I've been blessed with health and children, so I can cope with this fork in the road. My heart goes out to you.
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I'm in the chair for my last taxotere, hurray!
And no last Carboplatin due to how it's been affecting my hearing!
So no more chemo, double hurray!
Just good ol' Herceptin until April 2012.
Nails: women pay good money to get the design I currently have on my fingernails: 5 white rings, one for each taxotere, and sure to be a 6th ring by next week. I've iced each time, so figure it might have been worse, but who knows. And I know the damage keeps coming till they grow all the way out. But still, today, they're looking designer... -
Merilee, that picture is hilarious! Thanks for all your upbeat words and images!
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So happy for those that are near or who have finished thier chemo! I have two more to go but am going to ask for a two week break so I can go to Casting for Recovery retreat and Atlantic City without being in pain! I don't think it will hurt anything. Just delay my radiation a bit. I hope the Dr. says its ok. I don't think they can force you to do it if you want some time off anyhow!
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Yay for finishers! I will join you on Tuesday! As far as nails go, try Shellac, the nail polish that stays on for 3 weeks. I put it on before I started chemotherapy then have it changed during my good week of each cycle. I have gotten so many compliments on my nails! Between that and me eyelash extensions! I feel less yucky!
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My eye lashes and brows are coming back.... so is my leg hair...sigh
I am 5 weeks out from my last TC. Fuzz on top still increasing but not enough to take off the scarf yet.
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Hi All,
Looks like I have some reading to do!
It's been a tough week, I ended up in the hospital watching an infection Wed/Thurs and came home last night.
I'll catch up on all the activity here....I had my tablet with me so I could read what was going on, but I can't post from it..it was frustrating.
Glad to be back amoung you ladies...
Sue
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i haven't lost all of my eyebrows or lashes!! they are thinner but still hanging on!! i guess that is a good thing! my friend did a special on folding chairs at dicks sporting goods on my last treatment!! i'll try to upload the photo!
have a great weekend ladies!! i hope you all stay cool and least amont of SE!! now if i could just taste something!!! lol....
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Welcome back, Sue. Glad you're on the mend.
The eyelashes and the hair on my legs came back first for me. (Though I am going to lose all my hair all over again in September.)
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So Sorry Sue to hear you were sick with an infection. Be good to yourself and take it easy.
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Did everyone do ok over the week end? Windlass how much hair do you have now? I am 5 1/2 out from my last chemo and have fuzz but I am impatient and want it to accelerate so I can at least ditch the scarves
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merilee do you have to take tamoxifen? and have they started you on it?i was wondering about cost also?
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Paw
I was on tamoxifen 2 years ago and did not have a good result. I am now post menopausal and will start on Aremedex after radiation is done. My plan is to start with a small dose ( against Oncs wishes) and see how I do. My insurance covered the Tanoxifen.
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I've got about an inch and a half of hair, since it's been a while since the AC. (The TDM1 I am on does not cause hair loss.) This pixie cut is actually kind of cute, though it ages me a lot.
The bummer is that I will lose it all again when I start Taxotere in September, but at least now I know it does grow back.
On another topic, I have a word of advice to all: GOOD DENTAL CARE. I went to the dentist today for my six month cleaning and discovered that I have new decay. Ack!
I have always been really careful with my dental hygiene, brushed, flossed daily, etc. but I have apparently slacked off a little lately because of the tender, bleeding gums, which was bad enough. But apparently the dry mouth caused by chemo makes it especially easy to get a cavity.
So be extra careful with your teeth, keep your mouth hydrated with non-sugary drinks, and don't put off a cleaning if your white cell count is high enough to do it. I may have saved my teeth today!
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Thanks for the teeth tip windlass. I've got an appointment for my 6 month clean and check next week and I was wondering if going to the dentist was ok. I'm in the chair today for Taxol #4 and will ask onc about my white blood count and hopefully get the ok.
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Hi everyone. I haven't had a chance to catch up with the posts. I have been so busy and sick as well. After the last chemo, I got very sick with fungus, bone pain, nose bleeds, blurred vision, blood under fingernails, diarreah, weak and exhausted. I have my sixth chemo session coming up. Can't believe it's my last one. Hope I don't get as sick this time. Everything after that moves down to Herceptin every three weeks, along with radiation five days a week. Don't want to get to far ahead of myself. Just want to get this last chemo in and recover from that. My thoughts and prayers are for everyone who is fighting this cancer demon. Lets warrior on. Hope to get caught up on the posts and enjoy my day tomorrow before treatment starts.
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