TRIPLE POSITIVE GROUP
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Congrats Fluff! 5 years! Looking forward to mine in either November 11-11-11 dx date, or December 12-8-11, sx date. Although dx of I'D was at sx. Crap, even figuring out time is screwed up with BC. Sigh. LOL. But I'm so happy for you Fluff.
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Congratulations Fluff! Excellent milestone!
Right there with you SpecialK - I've never know when people count from. I like lago's formula!
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I had a bad mammogram right before Thanksgiving of 2010. Had a surgical biopsy on December 3. Was told I had lcis, see an oncologist. And take a pill. My NP friend said she wasn't buying it. Hauled me to two breast specialists . Settled on one, had an MRI after Christmas. (Original mammo. Folks said that wasn't necessary...just get the biopsy). MRI showed something. Had an ultrasound biopsy. Got an all clear and come in the next day. Went in and she said she talked to the radiologist and didn't feel like they got where they needed to be.
Had another surgical biopsy on January 27....found it, removed it with clear but close margins...so that's my day that I became cancer free.
At BMX a month later, she and radiologist said all good and there wasn't any change. So I decided to stick with the January 27 date.
Thanks for all the great wishes! I have to admit I was kind of sweating it out. I was having some issues in the lady garden...twinges and paint and general discomfort. Kept thinking if I find out two days before my five year mark I have a problem, I Would get really pissed off, lol. Tried uti meds that made no difference so got in to my ob/gyn on Monday. I've had fibroids for decades. My small one that is low, grew a little and he thinks that is causing my problems. So...I may be looking at a hysterectomy this year if it doesn't improve. It is some better this week.
His comment was that if he could guarantee that they do the surgery, I could go home that day with problems resolved and live thirty years, he would recommend it in a heartbeat. But, they are big enough he isn't sure he can do it laparoscopically, which would mean a much bigger surgery and risks that come with that surgery.
So for,the moment, we are going to wait and see.
It's always something isn't it
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I'm wearing a 30 day heart event monitor, anyone else ever have one? It's nerve wracking. It records heart arrythmias, which can range from harmless to serious.
The problem is I know when it has recorded and transmitted an event, it shows on the monitor, but I don't know what the events are- the harmless type or serious. Apparently if its very serious you get a call telling you to go to the ER.
I feel fine, but I'm only 10 days into this, 20 more to go! Its making me anxious.
I'd appreciate any words of wisdom on how to survive the waiting period till I see the cardiologist and learn what is happening.
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I have never worn a 30 day monitor but have worn the halter monitor 2 or 3 times for arythmias. Thirty might drive me crazy, but it will be good for you to have some answers,so hang in there!
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Ugh, debiann, sounds stressful! Do you have to sleep with it on? That would drive me batty. No experience here, but hope that the monitor is just picking up harmless events.
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Yep, I sleep with it on too. It recorded a bunch of "events" today, whick made me kind of anxious, but I feel fine. Only 17 more days to go! Ugh.
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debiann! I'm surprised you get any sleep! Yup, only 17 more days for you. Let us know if the monitor picks up any real problems.
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debiann I had to wear it for only 48 hours. As it was the adhesive got me and I had square red itchy patches when they took it off. Not the best thing but could be worth it. It did not pick up my problem but mine was only less than 3 percent so no wonder it never got picked o. I now have a pacemaker for slow heart rate.
I ope your problem is easily found and corrected.
Much love
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Hello ladies!
Just dropping by with an update. After my second opinion I decided to move forward with TCHP which will start next Tuesday. I will have 6 sessions 3 weeks apart. I've got some nerves and look forward to being on the other side of this anticipation and anxiousness! Sending out lots of love to you amazing ladies!
Congrats fluffqueen and good luck with the wait and see!!!
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33triple we are here for you if you need us. Hydrate, hydrate, hydrate.
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Jersey girl is right; hydration is very important! I got so sick of water, though. I ended up drinking a lot of low calorie juice. Good luck, 33triple!
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for all you hot flash folks out there, ran across this post of Facebook. There are some things I wish I had found a couple years ago!
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and don't forget hotpeals: http://hotgirlspearls.com/ (might be cheaper on Amazon)
or make your own out of plastic ice cubes and an old nylon: http://www.craftster.org/forum/index.php?topic=382728.0#axzz2Wbg645CT
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I have one of these also:
http://www.mycoolingstore.com/mission-enduracool-towel-regular-size-blue.html
It seems counterintuitive because they are microfleece and I live in Florida, but I have found these sheets to keep me in the Goldilocks zone - not too hot, not too cold.
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I've had good results by wearing moisture-wicking T-shirts to bed. It really does make a difference; on nights I wear those, I only wake up once or twice drenched in sweat, versus 3-4.
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Speaking of moisture wicking... Target is having a sale on the the long sleeve tops!
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Happy February Everyone! Since the groundhog didn't see it's shadow, I am psyched for an early spring although this coming weekend the forecast is a high of 23 and a low of 12. Correct me if I am wrong...that is not warm weather!!
I have a question - I've completed 4 Herceptin and Perjeta treatments. My nose is constantly dripping and sometimes bloody when I wipe it. My Primary MD and MO told me to try Flonase but it hasn't really helped. My nose was very sensitive during chemo. It would burn and I had an acute sense of smell. I am wondering if my nostrils are healing from the chemo ( my last treatment was in September) or if I should consult and ENT? I just want the dripping to stop.......
Birdysmom - I also did neoadjuvant chemo, however at the time my initial biopsy was HER2- so I didn't have herceptin or perjeta. After my surgery, the tumor biopsy came back HER2+ which now I am doing both drugs- herceptin (1 year) & perjeta (6 months). I have completed 4 treatments thus far and luckily have had no SE. I go every 3 weeks for IV and I do get Benadryl first. After I am done I have to sit for 30 minutes to be monitored for any reactions. On a positive note, the neoadjuvant chemo shrunk by tumor substantially and my BS did attain clean negative margins, which was the outcome we both wanted. I hope your doctors find something for you to take to help the rash because itching is not fun!!
FluffQueen - Congrats on 5 years!! You must be over the moon!!
33Triple - Welcome to these boards...everyone I have crossed paths with have been amazing!! We are all here to support each other. Many times I had questions in the middle of the night and I knew if I reached out on the boards someone was always there!! I wish you all the best in your journey and stay positive!!
JerseyGirl927 - Where are you located? I am in Central NJ . If you are not too far we should try to meet if you are interested?
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Sharapril, I have a constant runny nose on Herceptin; I think it's a pretty common thing. I had the same thing you describe from hard chemo (I did six rounds of TCP), too--my nose was crusty and gross the entire time! Now, the crust is a wee bit better, but my nose still runs, especially during the first week following infusion.
I have Aquaphor for rads; I've been putting it in my nose, and it seems to help. It's not the most natural substance in the world, not by any stretch, but I'm okay with that at this point.
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Sharapril, I have a constant runny nose from Herceptin only, as well... I was in the same boat as Kate with My TCHP chemo... my nose was horrible... It got better when I realized that the hair in my nose is growing back and helping with the sniffles a bit more... not much, but a bit...
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I'm expecting to lose my hair, this is more than likely, yes? I see the medical oncologist for the first time on Wednesday 2/10. But we all end up with one of the add-ons (so to speak) that causes hair loss, true?
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Sharapril I had some really bad bloody noses when I was doing both chemo and Herceptin. My MO said it was from the herceptin. I would rub vasoline on it at night.
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So. . . I was denied for extra life insurance (no surprise there). But on the denial letter, there's something that troubles me. It says I'm denied because I'm on Herceptin and because my last echo showed "mild mitral valve regurgitation."
Here's the thing: my LVF has been fine--60-65%. When I was a teenager, I was diagnosed with mitral valve prolapse, but then as an adult was told that I didn't really have it. Here's the other thing: if I DO have MVP, I should be pre-medicating for dental appointments and surgery! Is this an oversight by my MO? I will of course call tomorrow, but thought I'd poll the experts first. . . .
My RO has told me to stay off of CoQ10 during rads. I take it for heart health. Should I try to talk him into letting me take it?
Do I need to worry about this? And why don't I KNOW if I need to worry about it?
Sigh. It's always something, or at least it feels that way today.
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wait till you are off herceptin and apply again. The problem is herceptin can make the issue worse. It's all about risk and your risk is higher on herceptin. (My husband used to be in insurance and is still licensed. That's how I know)
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lago, does the heart go back to normal when Herceptin is discontinued?
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Kate, my EF slowly went from 65 down to 52. My MO wouldn't let me get my scheduled Herceptin treatment until I saw a cardiologist. I had an Echo about two weeks after the Muga that stopped my treatment and I was back up to 57. There were a couple Echos that showed mild mitral valve regurgitation. An updated Echo in December showed my EF back up to 65 and my heart back to "normal". Assuming your heart was "normal" to start with, it should go back to being "normal". Permanent heart damage on Herceptin is very low.
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Thank you, Mommato3; that's reassuring. I'm going with this explanation: my MO (who is wonderful) didn't tell me because she didn't see anything to worry about. I'm getting another echo in March, and we'll go from there. I'm not sure why I had such a meltdown over it. Yes I am: there's a lot going on in life other than being denied for insurance!
As always, sending gratitude to all of you.
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I have had mild mitral valve prolapse for years. None of my doctors are ever concerned about it at all. I was freaked out when I saw it too. But it's apparently not a big issue if it's mild. Hugs.
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KateB, my MO's nurse told me today that it is normal for the heart function (EF) to decline and that it will return to normal once I'm done with herceptin. I however still won a future trip to the cardiologist because my pre surgery ekg yesterday indicated that i have had a heart attack at some time. That was a compete shock to me.
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Wow, twiggyOR! That is shocking news. My heart function didn't decline at all while on Herceptin. It was pretty much the same throughout treatment.
Kate,
Getting rejected for life insurance is what it is. I was able to increase my life insurance coverage in small increments over time through work because the small increments didn't require health exams.
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