We are 219,480 members in 81 forums discussing 155,301 topics.

Help with Abbreviations

Topic: Perspective

Forum: Stage IV/Metastatic Breast Cancer ONLY —

A place for those managing the ups & downs of a Stage IV/metastatic breast cancer diagnosis. Please respect that this forum is for Stage IV members only. There is a separate forum For Family and Caregivers of People with a STAGE IV Diagnosis.

Posted on: Sep 18, 2018 07:10PM

finallyoverit wrote:

I’ve been having a rough week.. nothing in particular happened- I’m just tired. Tired of appointments, feeling like crap, the constant “has it moved further” worry, the never ending paperwork and worry over how I’m going to pay for all of this. I know you guys get that

So, that said, I had my monthly MO appointment today. I swear, he’s become a good friend. He treated me when I was first diagnosed and was just as upset as I was when the crap came back.

I was talking to him today about how tired I am, physically and emotionally. And how I feel guilty about feeling blah because I’ve been incredibly lucky and blessed through this whole mess. Anyway, he did his best to comfort me saying that we just don’t know what’s going to happen. He told me he had the hospice talk with a 39 year old man with pancreatic cancer last Thursday; he passed away on Saturday.

Note to self: suck it up and carry on. Things could be so much worse.

Dx 10/2011, IDC, Stage IIA, 0/4 nodes, ER+/PR+, HER2- Dx 5/2017, Stage IV, metastasized to bone
Log in to post a reply

Page 1 of 1 (7 results)

Posts 1 - 7 (7 total)

Log in to post a reply

Sep 18, 2018 08:52PM Bigbhome wrote:

Finally - Am I wrong or does it seem as though just when we really need it, we are reminded of just how lucky we are. I know lucky is a strange word to use in regards to what is going on, but I bet that 39 year old man would say that you are lucky. A friend of mine reminded me that when I was first diagnosed with Mbc, I was told 18 - 24 months. That was over six years ago, so yes I am lucky!

My Dh was in a horrific accident in January. We are lucky he was not killed however, it has forever changed his life forever. We are so grateful that he was not killed. Unfortunately, there was a couple in a pickup truck this morning who were in the exact type of accident, who did not survive. It jerked me right out of my "oh woes is us" mindset.

Do we have tons of issues to deal with, hell yes! Are we lucky to still be here, hell yes! Excuse my French, but it says it best!

Hugs and prayers,


Log in to post a reply

Sep 18, 2018 09:08PM finallyoverit wrote:

Claudia ~ you are absolutely right. We are reminded exactly when we need it. I really wasn’t feeling “whoa is me”.. just more of a “I’m tired of all of this crap.. tired of thinking about cancer.. tired of being ‘that girl’”.

I bet that man would say that I’m lucky, and you know what, he would be absolutely right. I am.. my scans have been great and as my MO says I’m “at the front of the class” as far as how I’m responding to treatment. 99.9% of the people in my circle have no clue. My MO has told me before that if he passed me on the street and didn’t know, he would have no clue that I’m a stage iv cancer patient.

Usually I’m a pretty easy going person and take this stuff in stride.. but this week I’m struggling.. I appreciate that my MO put it in perspective for me. I hate that I have to have a relationship with him, but I love that man and feel incredibly lucky to call him “my MO”.

Hugs to all of my stage iv sister

Dx 10/2011, IDC, Stage IIA, 0/4 nodes, ER+/PR+, HER2- Dx 5/2017, Stage IV, metastasized to bone
Log in to post a reply

Sep 18, 2018 11:40PM illimae wrote:

“Things could always be worse” has been my mantra for as long as I can remember. My husband, who had always been a glass half empty guy uses the term himself now and I love that it’s rubbed off on him. When diagnosed de novo at 41, I still felt lucky knowing things could be worse and when brain mets were found (which I thought would be the worst), I soon realized it wasn’t. So today I feel good and very lucky.

I appreciate this post because although cancer is devastating, we don’t have to spend the rest of our lives in darkness.

Diagnosed at 41 Stage IV De Novo Dx 11/16/2016, IDC, Left, 5cm, Stage IV, metastasized to bone, Grade 3, 3/13 nodes, ER+/PR-, HER2+ (IHC) Targeted Therapy 1/1/2017 Perjeta (pertuzumab) Chemotherapy 1/2/2017 Abraxane (albumin-bound or nab-paclitaxel) Targeted Therapy 1/2/2017 Herceptin (trastuzumab) Surgery 6/26/2017 Lumpectomy: Left; Lymph node removal: Underarm/Axillary Radiation Therapy 8/10/2017 Breast, Lymph nodes Dx 10/5/2017, IDC, Left, Stage IV, metastasized to brain Radiation Therapy 10/19/2017 External: Brain Radiation Therapy 4/18/2018 External: Brain Hormonal Therapy Tamoxifen pills (Nolvadex, Apo-Tamox, Tamofen, Tamone)
Log in to post a reply

Sep 19, 2018 02:52AM finallyoverit wrote:

Illimae~ You are absolutely correct.. it could be so much worse. What’s that saying, “if everyone threw their problems in a pile, they would scramble to pull their own out after seeing everyone else’s?”

It’s true, we don’t always know what others are dealing with. As I told my MO tofay (well, yesterday now), I’ll snap out of it.. just having a tough time with it this week. I’m so very grateful not only for a great response to treatment but also to have you ladies who really get it.. it’s so comforting to me to be able to talk to someone who has been in my shoes and knows the feelings first hand.

Dx 10/2011, IDC, Stage IIA, 0/4 nodes, ER+/PR+, HER2- Dx 5/2017, Stage IV, metastasized to bone
Log in to post a reply

Sep 19, 2018 12:19PM pajim wrote:

We forget that in the pre-cancer days we also had weeks where we were down in the dumps, feeling totally inadequate, the weather sucks, I suck, everyone hates me, I can't get out of bed in the morning. . .

It's just that now all of that is bound up with having cancer and it's hard to separate it from the disease. Because of course it's always the disease's fault, LOL. And sometimes (often!!!) it really is the cancer's fault.

I hope your week improves. And I hope your oncologist's week improves. I promise it's no fun having a patient die on you, even when you know it's going to happen.

Dx 4/20/2008, IDC, Right, 4cm, Stage IIIA, Grade 2, 1/15 nodes, ER+/PR+, HER2- Dx 2/1/2013, IDC, Stage IV, metastasized to bone, mets, ER+/PR+, HER2- Hormonal Therapy 2/26/2013 Femara (letrozole) Hormonal Therapy 4/21/2013 Faslodex (fulvestrant) Targeted Therapy 2/24/2016 Ibrance (palbociclib) Chemotherapy 6/18/2017 Xeloda (capecitabine) Targeted Therapy 8/14/2018 Verzenio Chemotherapy 1/1/2019 Halaven (eribulin)
Log in to post a reply

Sep 19, 2018 08:07PM MuddlingThrough wrote:

finallyoverit, I could have written your first paragraph word for word today.

I am very sad for that young man who died from pancreatic cancer. I truly hate cancer especially when it affects children and young people.

I am "lucky" and I'm better than I was at dx, but something this week really has me down. Maybe it's the earlier sunsets? I don't know. I'll probably turn around but I'm so tired of being tired and hurting.

Diagnosed stage 4, de novo. It was quite a shock. Dx 1/4/2018, IDC, Stage IV, metastasized to bone/liver/other, ER+/PR+, HER2- Hormonal Therapy 3/28/2018 Femara (letrozole) Targeted Therapy 3/28/2018 Ibrance (palbociclib) Chemotherapy Taxol (paclitaxel)
Log in to post a reply

Sep 20, 2018 05:54AM finallyoverit wrote:

Muddling~ maybe that’s it.. the earlier sunsets. I just haven’t felt myself this week. Hoping it will pass soon for both of us.

Pajim~ you’re right.. I probably did have these off weeks before.. they just seem more intense now, which i guess makes sense because we have a lot more on our minds and plates now. I am appreciative that there are great treatments out there and that I have access to them, because I know there are those out there that don’t. I don’t take that for granted. I just need to remind myself to stay in the “now” and not think about how this will go on for the rest of my life.. the appts, the needle pokes, the meds and side effects.. just allof it. <sigh>

Dx 10/2011, IDC, Stage IIA, 0/4 nodes, ER+/PR+, HER2- Dx 5/2017, Stage IV, metastasized to bone

Page 1 of 1 (7 results)