New TNBC Diagnosis Disbelief

I am newly diagnosed last week and just met with a breast surgeon who referred me to start with Chemo.  I have an appointment scheduled Monday Aug 16th.  First , let me say that no one in my family has ever been diagnosed with breast cancer.  When they told me last week my biopsy was positive for Triple neg breast cancer,  I really felt like they made a mistake and mixed up my results with someone else.  Not that I wish this on someone else, it just seem unreal to me.  I’m a planner.  I had everything figured out as I plan to live a healthy life (mind, body and spirit).  Even as I write post, I feel like I’m talking about someone else.  I’ve been reading everything I find and trying to plan things out before I even meet with the chemo team.  All I know thus far is what I’ve read and Chemo sounds very scary. 

I’m 57 years young, Clinical Director of a Behavioral Health team and the sole caretaker of my 80 year old mother who lives with me.  I haven’t told my mom because she will freak out!!  I plan to tell her after I meet with the Chemo team on Monday, so I have a better idea of how to move forward, keep working to pay the bills and take care of us both.  I’ve heard that many people are able to work while getting Chemo.  Can anyone attest to that???

Dear @Starr1  , I am so sorry you have found yourself in this situation. I understand the utter devastation and shock. There seems to be no rhyme nor reason to this terrible disease. My friend is a consultant and she said people get it who are fit, unfit, healthy, and unhealthy…. It does not discriminate.

Like you, I have no family history at all of breast cancer and discovered my lump by chance (mine is HER2+ and wide spread DCIS). I was 45 when diagnosed in Nov last year. I have had a mastectomy and 12 weeks of chemotherapy - I finished 6 weeks ago.  I have a 7 year old son and husband and am an Assistant Headteacher in a secondary. Words simply cannot describe my utter shock, terror, fear and panic when I was diagnosed.

I am no expert but I found my breast unit nurse to be an amazing support. She rang me regularly and I could phone to ask her any questions. I also asked to be referred for help at the hospital, so had six sessions of reflexology and mindfulness at our local cancer care unit. I see a counsellor, I pay for privately, and a clinical psychologist at the hospital. I have found once I started chemo that joining the monthly group of others starting chemo at the same time was extremely helpful and supportive. Breast Cancer Now and Macmillan have helplines.  I think it is so important to look after your mental health when going through this, as I am sure someone in your line of work can understand. 

Everyone’s journey and treatment plan is individual. I suppose you won’t know if you can work until you are going through it. My work were very supportive and I went off work from the day I was diagnosed. Mentally, I just could not cope. I get 6 months full pay and 6 months half pay. Yet, I sat with a lady at chemo, who was a bank manager, who worked right the way through. She said work were very understanding and flexible. She could work from home and if she was not well she could go and rest. I managed to play tennis quite a lot through chemo on my good days but it will depend on your treatment plan. I had weekly Paclitaxol, which, I understand, reduces the side effects. Other treatments seem to have a lot more. 

When I heard I had to have chemo I was devastated and fearful but from my experience it was manageable. 

When I was panicking about work when I was fist diagnosed, my breast nurse took my hand and said to me, ‘You are now in a fight for your life and you and your health have to be a priority.’ She did not say it to scare me but to make me put work on the back burner for a while.  

You will also find you have a lot of appointments coming up. I can’t imagine how worried you are about telling your Mum. When you have the full picture you may find it slightly easier to explain. She may be your biggest support and will just be concerned for you. 

Use all the help and support you can get and look after yourself. I hope you get a full treatment plan soon. Take one step at a time, stay off Google (easier said than done) and listen to the professionals and your body. My friend warned me that a lot of data out there on Google is outdated, as there have been so many new developments in breast cancer treatment, or based on American statistics.  

I am sending you lots of strength, support and love. Nicky xxx

I was also diagnosed with TNBC 6 years ago, aged 50, and felt exactly the same as you. I felt as fit as a fiddle, couldn’t believe it, thought they’d misdiagnosed me!!

I had local wide excision, followed by FEC-T chemo, 3 weeks of radiotherapy and finally 3 years of Zoledronic Acid infusions. I am now absolutely fine, no lasting side effect, back to how I was before really :slightly_smiling_face: .

Regarding working through treament, I think maybe it depends which chemo regime you having. For me personally there was no way I could have gone to work. I work on a hospital ward and during chemo you’re more likely to pick up infections etc, and after the second cycle of chemo I wasn’t fit for work. That was me, people are react differently.

Let me know how you are getting on, and whether you have your treatment plan. 

Take care of yourself .

Julie :two_hearts:

Hi there.  I am just out the other end and finished treatment three weeks ago. I did a few hours here and there at work through my chemo. Apart from a bit of energy loss I felt okay to be able to do it. I guess it depends on what type of job you have. Happy to help and answer any questions that you have about the treatment. xx