chemo treatments
I am new to this site and have a question. I am 50 yr old and was diagnosed with invasive lobular carcinoma on 4-12-13. I had a bilateral mastectomy on 5-15-13. I was stage IIa, ER+, PR+ and HER-. All lymph nodes were clear. I had silicone implants put in during surgery. The surgeon said I will have to have chemo due to having 4 tumors, one which was 2.2 centimeters and is sending me to an oncologist. I am wondering how many chemo treatments I will need. Does anyone know this? Thanks for any advice/information.
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If you look around, you will
If you look around, you will see that so many of us have different chemo plans. Part of it is our own diagnoses while part of it is what our oncologists prefer.
I would have to go back and dig out my papers, but I know I was told after my surgery, which was the last part of February 2012, that I was Stage 3A. Tumor size had a lot to do with it, although I had one node affected. My oncologist had me do Adriamycin/Cytoxin four times, every other week and then taxol four times every other week. After that I had radiation therapy. I finished everything as of the end of last September.
What we share around here varies person to person. I know that how chemo affected me was different in most instances than it affected two other people I know. What they shared, though, gave me some idea of what I could expect. That did keep me from unnecessary concern I sometimes experienced.
Keep a positive outlook, as that helps a lot.
e
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Thanks. I have no idea whatdesertgirl947 said:If you look around, you will
If you look around, you will see that so many of us have different chemo plans. Part of it is our own diagnoses while part of it is what our oncologists prefer.
I would have to go back and dig out my papers, but I know I was told after my surgery, which was the last part of February 2012, that I was Stage 3A. Tumor size had a lot to do with it, although I had one node affected. My oncologist had me do Adriamycin/Cytoxin four times, every other week and then taxol four times every other week. After that I had radiation therapy. I finished everything as of the end of last September.
What we share around here varies person to person. I know that how chemo affected me was different in most instances than it affected two other people I know. What they shared, though, gave me some idea of what I could expect. That did keep me from unnecessary concern I sometimes experienced.
Keep a positive outlook, as that helps a lot.
e
Thanks. I have no idea what to expect and I am dreading it. Thanks again for your reply.
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Hi Doe1504
I had a lumpectomy last Jan. to remove an ILC tumor. I was stage Ic, ER+, PR+ and HER-, all lymph nodes were clear. I had 4 sessions of chemo; Taxotere/Cytoxan -one session every 3 weeks-.
When you have your treatment plan, you will be able to ask for more advice/information on this board. Members here are very helpfull.
Good Luck.
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Your doctor will know. He or
Your doctor will know. He or she will refer you to an Oncologist who will give you all the answers. My surgeion refer me to a wonderful Oncologist who answered all my questions. Take someone close to you to help you understand what you will be going through.
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Had my oncology appt. today.
Had my oncology appt. today. Found out I have to have 4 adrimycin/cytoxin treatments, 1 every 2 weeks with a neulasta injection to follow each treatment, then 12 weekly taxol treatments. He wants to get started by the end of the month as time is of the essence. He said chemo has a higher survival rate if started 90 days after surgery. Please pray for me.
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Hi Doe1504Doe1504 said:Had my oncology appt. today.
Had my oncology appt. today. Found out I have to have 4 adrimycin/cytoxin treatments, 1 every 2 weeks with a neulasta injection to follow each treatment, then 12 weekly taxol treatments. He wants to get started by the end of the month as time is of the essence. He said chemo has a higher survival rate if started 90 days after surgery. Please pray for me.
I wish you good luck in your treatment plan. I didn't take this combination but others in this group have taken it, and members are eager to help with advice.
Take care
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Doe .. prayers going out to youFaith_In_God said:Hi Doe1504
I wish you good luck in your treatment plan. I didn't take this combination but others in this group have taken it, and members are eager to help with advice.
Take care
My 2 cents -- keep a journal on hand write down any questions, or concerns you have regarding your treatment - time frame - side efforts, and any preparation you may need to do before starting your chemo therapy. A tape recorder is highly recommended to take with you to your Oncology appointments - this way you can go back and revisit what was discussed during your doctor session.
Strength, Courage and HOPE for a Cure.
Vicki Sam
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I have a busy 2 weeks ahead.
I have a busy 2 weeks ahead. I go tomorrow for my CT and Eco. On fri. I have my first saline fill then have my port put in on Fri. Next week I go to an oral surgeon to get some teeth out and have chemo education. The should start my chemo treatments on 6-27-13. I have a friend who just finished chemo and is going through radiation and a male co worker going through chemo now for cancer. I have heard about possible side effects but have no idea how I will do. I am really dreading this part of my life and the next 5 mos. of treatment. I am a single parent with an adult son who lives with me and is in college and the Army reserves and works evening shift. He is devastated by all this because he feels like I am all he has. I feel pressured to be strong for him, friends and family. If they think I am weak they smother me. Please keep me and my family in your thoughts and prayers as I begin this journey.
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You are already in my prayersDoe1504 said:I have a busy 2 weeks ahead.
I have a busy 2 weeks ahead. I go tomorrow for my CT and Eco. On fri. I have my first saline fill then have my port put in on Fri. Next week I go to an oral surgeon to get some teeth out and have chemo education. The should start my chemo treatments on 6-27-13. I have a friend who just finished chemo and is going through radiation and a male co worker going through chemo now for cancer. I have heard about possible side effects but have no idea how I will do. I am really dreading this part of my life and the next 5 mos. of treatment. I am a single parent with an adult son who lives with me and is in college and the Army reserves and works evening shift. He is devastated by all this because he feels like I am all he has. I feel pressured to be strong for him, friends and family. If they think I am weak they smother me. Please keep me and my family in your thoughts and prayers as I begin this journey.
You are already in my prayers and I will continue to pray for you. God Bless.
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God Bless you Doe1504Doe1504 said:I have a busy 2 weeks ahead.
I have a busy 2 weeks ahead. I go tomorrow for my CT and Eco. On fri. I have my first saline fill then have my port put in on Fri. Next week I go to an oral surgeon to get some teeth out and have chemo education. The should start my chemo treatments on 6-27-13. I have a friend who just finished chemo and is going through radiation and a male co worker going through chemo now for cancer. I have heard about possible side effects but have no idea how I will do. I am really dreading this part of my life and the next 5 mos. of treatment. I am a single parent with an adult son who lives with me and is in college and the Army reserves and works evening shift. He is devastated by all this because he feels like I am all he has. I feel pressured to be strong for him, friends and family. If they think I am weak they smother me. Please keep me and my family in your thoughts and prayers as I begin this journey.
Good luck and God Bless, please keep us updated.
Take care,
Faith
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How was it getting the portDoe1504 said:Got my port put in today. Now
Got my port put in today. Now to the oral surgeon next week to have some teeth taken out then on to chemo the following week!
How was it getting the port put in? I'm having mine put in Monday morning and my first chemo that afternoon.
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Coco, getting port was notcoco2008 said:How was it getting the port
How was it getting the port put in? I'm having mine put in Monday morning and my first chemo that afternoon.
Coco, getting port was not bad. Where I had the bilateral mast, I am kinda tender and numb in spots anyway. The area where the port is there is some bruising, but, not very sore today. I start chemo on the 27th. Let me know how your chemo goes. Prayers for you. Good luck! Keep us posted.
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