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Stage 3c

wlkdnose
Posts: 45
Joined: Jun 2011

That was what we heard from the gyn/onco appt for my sister today. The types were mostly squamous cell and they did find a few clear cells which he said were so small in amount that it was irrelevant. She will have six cycles of taxol and I think Cistplatin? She will have to stay in the hospital overnight while one of them is being infused...I can't remember which one. Good thing my sister wrote it all down! She already has the IP port and she is debating on getting a chest port. What is your advice/experience on that one? She will also be the first person to receive the IP chemo at our local hospital because of her lack of insurance Mass general is not an option right now even though her gyn/onco. is from there. I am telling you, our healthcare system is messed up...again thanks for reading!

leesag's picture
leesag
Posts: 625
Joined: Jan 2010

I love my Chest Power Port! I am one year out from chemo (undergoing radiation for a recurrence in another area), but I plan to keep my chest port as long as it works. It's a dream for blood draws, chemo was easy (I could use my arms freely!), and I just have to have it flushed every 5 - 6 weeks. Make sure your sister has some tight sports bras to hold the girls in place, (I'm fairly well endowed and the jiggling of the jugs was a bit painful)but other than that, it's an easy install!

I'm sorry that she's been staged 3c, sadly that's usually the norm. There are a lot of long term 3c and even IV survivors out there, I plan on being one of them!

Hugs and Healing!

Leesa

Hissy_Fitz's picture
Hissy_Fitz
Posts: 1869
Joined: Sep 2009

The chest port is THE way to go. Chemo trashes your veins, and once they're gone, every subsequent blood draw for the rest of her life will be an ordeal.

Be sure she gets a script for the numbing cream. Apply it one hour prior to chemo (or blood draws). Nobody gets extra points for pain, so take all the "helpers" you can get.

Carlene

LaundryQueen's picture
LaundryQueen
Posts: 682
Joined: Mar 2011

Nancy707: Where was your IP port located and how long did you have that?

I think Carlene is talking about IF chemo trashes your veins, then you would get poked over and over again for blood draws. Now THAT would be an ordeal!

LQ

Tethys41's picture
Tethys41
Posts: 1057
Joined: Sep 2010

Nancy,
So do you receive all of your integrative IVs via a peripheral vein?

Tethys41's picture
Tethys41
Posts: 1057
Joined: Sep 2010

Thanks Nancy. This is good information. My IVs are going to taper off over the next few months, and I've been debating as to whether to keep my port or not when I'm down to 2 IVs per month. Sounds like getting rid of it won't be a problem.

MK_4Dani
Posts: 318
Joined: Sep 2009

I love my chest port. The chest port does not hurt or feel as uncomfortable as the IP port. It is a piece of cake and so much easier to receive treatments via chest port. I had IP treatments and did very well. I was dx Stage 3C and I have been NED for one and half years...tell your sister there is hope and she will get thru these treatments.
Good Luck,
Mary

tjpt16's picture
tjpt16
Posts: 27
Joined: May 2011

Got my chest port about three weeks ago and I'm loving it. Much better than being stuck five times to try and find a vein.

Teresa

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