Herceptin / Port Question
I have my first oncologist appointment on Friday. My surgeon did say I would go on Herceptin which means that I would need to get a port - I originally decided not to get a port since I have decent veins and thought one less incision would be a good thing.
So here's my couple questions (knowing everyone is different) I wanted to know what restrictions there are if you have a port e.g. exercise, swimming, etc The second question is if you're on Herceptin did you get it for a year & is it every week.
Thanks !
Comments
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Hi there!
They will start your Herceptin with you Taxol or Taxotere drug. The first infusion takes a bit longer..about 90 min. The rest are about 1/2 an hour. Once you have finished the T drug you then will have Herceptin every 3 weeks for 1 year. This infusion is 1/2 an hour. It's really fast!
I finished my Herceptin this past November and had my port out 1 week later. I am glad I had my port. You can still swin and do whatever you want. But you have to wait for the port incision to heal first before swimming. Ask your surgeon how long they recommend . Good luck!!!
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My herceptin was every week for 20 weeks with chemo. Herceptin portion of treatment was 30 minutes. Since I finished chemo in November....I get a triple dose of herceptin every 3 weeks which is a 90 minute infusion until I have a total of 52 weeks. I have a port and highly recommend it. My only complaint is that it sticks out so I have to dress to cover up. Cami's and bra straps rub across it and make skin red. I look forward to getting it removed but it has definitely served its purpose and I would get another if needed. No physical restrictions given.
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I think Lexis covered all the bases. I am finishing up chemo and then will do herceptin every three weeks until Jan. 2010. I had my port put in during the bilateral mx surgery. Since I have not begun expander fills yet, I am thinking of getting my port taken out during my exhange surgery which will probably be in early Oct. Then I would have no scar at all and only 3 Herceptins through my arm veins.
Best of luck to you in your journey.
Ellen
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Just a quick thank you - I'm thrilled that there aren't any restrictions with the port - I'm looking forward to the Oncologist appointment - so I can "get a move on"
Thanks again
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Hi Min - Just a quick "ditto" to the info above - I got my port before 6 treatments of Taxol/Carboplatin/Herceptin, and have used it since then to get Herceptin every 3 weeks. I've also used it for scans and a colonoscopy
. It's sure better than getting poked every time, especially since I have "no veins." I've been swimming in the ocean, in hot tubs, etc. etc. etc. It's been a blessing, but now that I'm done with Herceptin, I can't wait to get it out!
Best wishes to you!
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I had a port put in Dec. 2008. It was tender for about six weeks. Now, I can snorkel and it would be fine. I like it. At times, I can feel it but it has been great for infusions. I suggest you have your Doc. suscribe a cream that will deaden the skin.
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Hi. I definitely recommend getting a port. It has made one thing in all of this easier. When you guys are getting just the herceptin part the two weeks in between are there any side effects?
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Another recommendation for the port. I have a small port and it's not as bad as what I thought it would be. I am grateful for it everytime I go into the infusion center and I have Emmla cream on and I don't feel anything but a push on my port and I am done.
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I too was against the port since I have amazing veins. Guess what?, a nurse drew my blood for pre-surgery screening and jabbed me a little too hard. It was bruised and sore for 7 days.
That alone convinced me that even though I have amazing veins, I would rather not be a pin cushion during this time.
My port surgery was a breeze. Other than minor soreness, I am able to pick up my children like before. Of course, I keep them away from the port side.
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Hi....I had my port for just over a year and there were no restrictions...only time it bothered me a bit was when I was the passenger and the seat belt rested right over it. Oh...and the summertime some of the tops with the smaller shoulders somehow just hit it wrong...so I didn't wear those!
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I was more terrified about getting the port than anything else they told me when I was diagnosed. Crazy, but true! But as I learned more, and met several wonderful women who showed me theirs and let me touch them, I got better about it.
I will say that it was somewhat painful for a few days after they installed it. More than I thought it would be, and I wish I had known that. I remember saying that I could not imagine ever being able to forget it was in there, but several days after I said it, hours were going by where I forgot about it entirely.
I have lost a little weight since the dx and it does stick out somewhat. Someone told me to ask the surgeon to place it a little lower so it wouldn't interfere with my clothes as much, and I did ask her. I don't know if it is placed differently than anybody else's, but it hasn't interfered with any of my clothes yet. In fact I put on a tank to to exercise in the other day and wondered if it would show, and it didn't at all. Some bra straps press against it, but it is more noticeable rather than painful.
I just had my first tx and they used the port. I was so excited - all that fear and pain and concern was about to pay off. AND IT DID. It was quick, easy, totally painless and no tricky trying to hit the vein thing. I am having Herceptin for a year, so I needed the port and now I am SO GLAD I have it. (And I can't believe I am even typing these words!)
But don't get me wrong, I will CELEBRATE when they take it out, for sure!
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Hi Just had my first treatment on Tuesday and also have the port. I too am glad I decided to have one. I was wondering, does your doctor have you taking any blood thinner meds since you have the port in? My onc has suggested taking a 1mg tab of coumadin daily to keep things flowing properly. I too will need the port for a year as I am on herceptin also.
Thanks
Debbie
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I am on Herceptin every 3 weeks and will continue to get it as long as it's still working. It takes about 2 hours for my infusion, I also get zometa via the port and they used it for my mastectomy, much better than an IV in the hand! No restrictions once healed.
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