I was diagnosed with ductal carcinoma a week ago today. I have two tumors in my right breast about 2mm each. We still don't have all of the test results back so I don't know if the tumors can be shrunk with chemo or if I'll lost the breast. I've already seen the oncologyst and surgeon, but without those last results (Her-2) for one - we're still in limbo. My only daughter's wedding is on the 23rd and the good news is I will get to attend before any surgery is done.
I know that I will have to have a chemo pump and that really scares me. I still don't know what to do. I will probably try to save my breast if they think the tumors can be shrunk but then there's the radiation to follow chemo.
There's been so much information thrown my way in the past week that my head is spinning. I don't know what to expect with the chemo. I've heard of women who went back to work and didn't miss a day and others who were miserable. I plan to fight the fight, but I'm still really scared.
Thanks for listening out there!
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karenmary Joined: Mar 2006 Posts: 102 |
May 13, 2008 07:59 pm
karenmary wrote:
Susie Q ... just take it one step at a time. You aren't the only one who starts reeling after being diagnosed. The information overload is so overwhelming, I know. Once you have a treatment plan in place you'll start to feel more in control of things. You just have to get through these early days with prayer, venting whenever you need to, and deep, deep breaths! www.pinkribbonreview.com
Dx 4/2006, IDC, <1cm, Stage I, Grade 2, 0/1 nodes, ER+/PR+, HER2- |
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FitChik Joined: Sep 2005 Posts: 4189 |
May 13, 2008 08:21 pm
FitChik wrote:
susieq....karenmary is right....you need to take it a step at a time and, before long, it will all become much more manageable. I promise! Your first step is to get all of the facts about your cancer and the options for addressing it. You'll need to make some choices here & there, based upon the specific characteristics of your tumors AND what your heart & gut tell you to do. And then you just do it....one step first and then, later, the next, then the next, until you finish treatment and hear your doctor tell you it's all gone. And that day will come...it really will! So hang in there, girl, and stick with us here. We hold one another's hands and help to get each other through. I don't think I'd have made it without these women. Oh, and btw, I'm pretty sure its not a "pump" for your chemo but, rather, a port which is a small, quarter or half-dollar-sized piece that is implanted close to the skin in your chest and through which the chemo goes, making it incredibly easier and less toxic. When you're done with chemo, they simply take it out. So please don't worry about getting a port. I'll tell you that I became so attached to mine that I named it ("Portia") and even waited nearly a year before letting them remove it. But I'm sort of starnge.... You're gonna be completely fine, susieq. ~Marin I can't change the wind, but I can adjust my sails!
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susieq23 Joined: May 2008 Posts: 5 |
May 14, 2008 09:49 am
susieq23 wrote:
Thanks for the great advice. It sure helps having the support. I've found that out already. I think once I know the results and which way to go with the treatment I'll be better. I wake up at night with my heart racing. It helps to know others have gone thru this and have come out on "the other side" stronger and a lot wiser. :) |
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FitChik Joined: Sep 2005 Posts: 4189 |
May 14, 2008 12:54 pm
FitChik wrote:
Susie...Some women find it necessary to ask for a sedative to get through these initial days, so you might want to consider that. Alternatively, practicing some calming behaviors like yoga or guided meditation (I use CDs) and drinking chamomile tea can help too. ~Marin I can't change the wind, but I can adjust my sails!
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BinVA Joined: May 2007 Posts: 1204 |
May 14, 2008 08:16 pm, edited May 14, 2008 08:17 PM
by BinVA
BinVA wrote:
Hi Susie, Oh geez ... it is hard to catch your breath, isn't it. I asked my doctor for Ativan to help me through my anxiety between the time of my diagnosis and surgery. That is the worst time ever. Once you have a plan in place and move forward ... all your energy and attention is focused on that. You mentioned two 2 mm tumors. 2 mm is very small. That's very good news. Please keep writing and let us know how you're doing. You're in our thoughts and prayers, Bren |
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susieq23 Joined: May 2008 Posts: 5 |
May 15, 2008 06:53 pm
susieq23 wrote:
Thanks for the calming ideas. I found out that I'm having chemo first and then the lumpectomy so I'm really one of the lucky ones. I'm having the port put in, lymph nodes removed and the marker clips inserted on June 4th and then the chemo begins. That scares me, but since everyone seems to handle it differently, I will just wait and see. Thanks so much for your support. It really means so much. SusieQ |
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susieq23 Joined: May 2008 Posts: 5 |
May 15, 2008 06:55 pm
susieq23 wrote:
Can anyone give me any ideas about where to start looking for a wig should I need one? Will the doctors have resources? Also, have you gals been able to work while taking the chemo? |
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