I am 39 and New Here. First round of Chemo

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Catoklyzmk
Catoklyzmk Member Posts: 12
edited June 2014 in Just Diagnosed

Hey Ladies,

I just wanted to introduce myself.  I am Cat and I live in Canada.

I am 39, married and have an 8 yr old daughter.

My journey began on July 6th when I discovered the lump in my right breast..........

It has since been a rollercoaster of waiting and having so many doctor visits and tests.

I started my first round of chemo last Thursday and I am so confused by everything I read on the internet about what is right and wrong to eat and about symptoms.  It's enough to make anyone's head spin.

So I found myself here looking for comfort from those who understand and are perhaps maybe feeling the same way I am.  Looking forward to meeting you all and taking comfort from being there for one another.  I think this will do my emotional well being a lot of good.  Hope I can be a comfort to someone out there as well?

Looking forward to talking to you all soon ;)

Cat

Comments

  • lizylu
    lizylu Member Posts: 9
    edited October 2013

    Hi Cat, Im new to this forum, but its a great one. It was a roller coaster for me too, and im a nurse. What i learned about chemo,was all on my own, not from Dr's,drink lots and lots of water, i like smart water,take anti nausea pills, before you get sick or you may not,i never got nausea and vomiting, just got tired alot. I exercise but not a whole lot, walking in place, bend and stretches. Eat small meals and fruit,soup goes down well for some. My Dh is retired, so he cooks. These women here will help you more than google, just ask. Please keep one calendar for your dr. Appts.

    Chemo will go by fast, nice to meet you, im from illinois, usa. My last chemo is oct. 15 ,then radiation, ask anytime you have questions.

  • melmcbee
    melmcbee Member Posts: 1,119
    edited October 2013

    welcome Cat. I was 42 at diagnosis. Im sorry that this hppened. Go to your profile and complete as much as you want and set it to public so it will show under your post.. That way people can help you who have similr diagnosis and treatments.

    Also there is a ton of threads on here that covers just about anything. You might like to read some or introduce yourself to specific grou

    ps. Pm me if you need anything and again welcome

  • fredntan
    fredntan Member Posts: 1,821
    edited October 2013

    The first one is the hardest. So yeah for getting that crossed off



    My appetite was so crappy during AC I just ate when and what I could. If you want a milkshake then have it.

    Put blinders on. If you have 16 chemos, etc etc. Only focus on what you are on at present.



    I drank 33oz three times day everyday during chemo.

    You will learn all the other stuff.

  • Catoklyzmk
    Catoklyzmk Member Posts: 12
    edited October 2013

    The part that has surprised me the most is that my appetite has doubled!  I feel like I am pregnant again.  I am always hungry and craving comfort foods.  I read that the steroids I took before my chemo can cause that but it certainly isnt what I had expected.  I normally drink tons of water per day and I am easily able to maintain that pace.

  • Moderators
    Moderators Member Posts: 25,912
    edited October 2013

    Hi Cat, and welcome to Breastcancer.org.

    You might also want to connect with others who are at the same stage of treatment with you, by joining the October or September thread in the Chemotherapy - Before, During and After forum.

    • The Mods

  • mdg
    mdg Member Posts: 3,571
    edited October 2013

    Hi Cat, Sorry you have to deal with BC.  It's no fun but the gals here will help you through it! Post questions or ask for information...or just come here to chat with those of us that "get it".  I hope chemo goes quickly for you with minimal side effects.  Hugs!

  • alcb70
    alcb70 Member Posts: 166
    edited October 2013

    Welcome Cat! You're in good company! Definitely look and see if someone has started a Sept. Chemo group...that made all the difference for me. Steroids do make you hungry. It was a strange mix for me...hungry & nauseated at the same time. Grrr Drink lots!!!!

    Post questions, fears & milestones! This is a great place. :)

  • Hannariggs
    Hannariggs Member Posts: 137
    edited October 2013


    Hi Cat,


    I am from the July firecrackers group. Glad you started the October group for sisters unfortunately about to join in this fight with you. They will bring you strength and comfort, and to let you know you are not in this fight alone. We are from all over the world unfortunately with one common goal. To beat this b(&(&( of a disease. It may be hard at times, but you will get through it to the other side. I know when I was first diagnosed I was SO scared and afraid of the unknown, but you are stronger than what you think. Take one day at a time and try not to look so far ahead(something I still have trouble with). God Bless you and the other sister in this board. You WILL get through this and you WILL beat this disease. A positive attitude will help us all WIN.......

  • Cristen002
    Cristen002 Member Posts: 5
    edited October 2013


    Hi Cat,


    Wow, very similar stories except I am a little newer diagnosed than you. I am 39 as well, right breast. Diagnosis was IDC, stage II, grade 3, 3.1cm. I just got done last week with all the testing (BRCA, MRI and first Onco appt.) and awaiting results from BRCA to make the lumpectomy vs mastectomy decision. The Oncologist dropped the chemo bomb on me last week and I was NOT prepared for that. When I found out I was told the tumor was 2.1cm and no lymph node involvement. After the MRI, it changed. Lymph nodes are swollen (Surgeon said maybe from the biopsy) and the tumor was bigger than they thought. Honestly, I am scared to death to do chemo. I work full time and live alone so I can't see not working and going bankrupt. I read so much and Googled everything under the sun but nothing prepared me to have to go thru chemo, as I was told lumpectomy and radiation before the MRI test. How many treatments do you have to do? How much time in between? How was your first one? I want to know everything so I can mentally prepare myself for this part of my fight. The one thing I keep hearing at every dr. apt is "You are so young". I keep thinking well, I can happen to anyone right?

  • Julie99
    Julie99 Member Posts: 12
    edited October 2013


    Hello Cat from a fellow Canadian, I'm sorry you have to go through this. You have certainly found the right forum for information. As many have said, stay away from Google and ask questions here. Like you were, I'm in the waiting period after finding out my biopsy results last week...until MRI and surgical consult next week. Stay strong girl, you can get through this.


    Julie

  • YoungTurkNYC
    YoungTurkNYC Member Posts: 334
    edited October 2013


    For all of you about to start chemo - please do not fear it. It gets a bad rep, but at least for me, it was much easier than expected. Just remember that the chemo is killing any cells that may have come off your tumor prior to/during your diagnosis and trying to set up shop somewhere else in your body. Once those cells set up shop somewhere else in your body, you become a Stage IV patient, and although treatable, you are no longer curable. I did dose dense AC - for me the worst side effect related to the GI tract - I could not eat very much because my GI tract was hit hard by the chemo (burning, etc). I had only very mild nausea. I actually hate nausea, and it was one of my biggest fears, but those anti-nausea meds are really strong. Do not be afraid to take them! I also worked during the entire chemo regimen (except a couple of days for each infusion) while also taking care of two young children. For AC, you may want to take off 2 days after infusion. Taxol was a breeze compared to AC, and I could literally get the infusion in the morning and be ready to work that evening. One thing that was easier for me though was the fact that I could work from home (and go to the office as needed). If this is not an option, it may be more challenging to work, at least during the AC portion of the ACT (if that's the regimen you are doing).


    Also, it is sickening to me that there are so many really young women who get hit by this beast. And there are so many of us. Just the other day at my oncologist's office; I met three women who all had children under the age of 10 (just like me). One of them had just given birth (had a 3-month old) and was there for her post-op appointment.

  • JenSF
    JenSF Member Posts: 45
    edited October 2013


    Hi Cat & everyone, I m 43, married and with our 9 yr old. I found a lot of strength through this forum. Just started my 1st TC tx last Thursday. Did the first Neupogen shot at home this morning. Managed it well. That was a relief. One SE I found was actually "being lost"....I didn't feel as much from all that was described and explained during prechemo class. This weekend was the first one that I decided to stay home. (I went out almost everyday after surgery in mid Sept). I was workaholic in my previous life and this "laying low" and "getting rest" effects are really hitting me.....while there were not many other friends or families that I can vent this feeling, my gratitude goes to all of you who will just understand exactly where I am....opps...water drinking time.....chat soon.....Love, Jen

  • msphil
    msphil Member Posts: 1,536
    edited October 2013

    hello Cat, I was 42 when diagnosed and planning my wedding when I found the lump, during my chemo I took anti vomit pills, and on days when I received chemo I had only soup, which worked great for me, it "TOO shall past"so hang in there and come here often, we are here for you, take it from a 19yr Survivor,i,m here telling of long survival for "INSPIRATION" to others.

  • Kathy04
    Kathy04 Member Posts: 5
    edited October 2013


    I am 44 with a 13 year old son, diagnosed late Aug, did my first round of chemo Oct 9 (TC) and tolerated it quite well. Days 4-9 was a little yukky (sore throat, fluish and diarrhea) but not too bad, still walked 5-10k a day and ate normally. Chose neupogen daily shots over the neulasta one time shot (just in case I had too many symptoms). Shaved my head last week, hasn't started to fall out yet....still the hardest part for me. Luckily here in the Yukon its pretty much winter so I wear a toque but feel very selfconsious when inside and I have to go without headcover, so far have only revealed my shaved head to a few family members. I'm not looking forward to the bald look, I'll probably wear a beanie even when inside (not doing a wig) Fortunate to be off work since day of diagnosis (long term disability insur). The other hardest part for me has been people's/friends/family reaction - or lack of. SO disappointed in people....but I have to get over it or I'll end up even more alone in all this. At least husband and son have been good. Good luck to all of you, so wish we could get together in person.

  • Kalonis52
    Kalonis52 Member Posts: 134
    edited October 2013


    Hi honey, First, I am so sorry for your diagnosis. Yes, everything can be pretty overwhelming. However, you came to the right place here. These women here are so helpful and supportive. I turned here when I was diagnosed in 2006. Yes, you came to the right place. Get some rest. If you have any questions, feel free. I am here.


    Take Care, Kaloni

  • Catoklyzmk
    Catoklyzmk Member Posts: 12
    edited October 2013


    Gosh Ladies I feel so bad for not getting on here as much as I had hoped to.


    Things are going ok and I haven't really had any issues except constipation. That has been the worst thing for me.


    I am so honoured and glad to have you all to lean on and stay in touch with.


    Cat

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