The good and the bad

Hi peeps

I have recently been diagnosed with breast cancer. Taking the excellent advice on this website I pretty much started by taking it one day at a time. This does indeed help. 

I thought to share the good and the bad and would love to hear anyone else's should they wish to share.

Today I had both a good and a bad moment. I received 2 letters in the post.

The first was from the hosp confirming my op date (my bad moment) cos my stomach dropped and I had that now familiar feeling of anxiousness take hold for a moment but shook it off cos I know it is needed. 

The good - my 2nd letter - as if... a tax rebate - boom  . Not half put a much needed smile on my face . Reckon a my treat family meal is in order.

Eeee it's the little things ain't it. 

Take care peeps 

Sandra x ️X

 

Parents
  • Just had the letter that the surgeon sent doctor.....I had a mucinous carcinoma which was ER + PR+ and HER 2 neg ( but for some reason it needs retest)  now what all this actually means I have no idea but when you read it in black and white it all sounds so real and scary.......

    Also just want to say what a lovely group of ladies you are....thank you all for being here....xxxx

  • Ooh Marlyn, that’s the same diagnosis as me! What are they retesting though? I’ve heard they check to make sure it’s pure mucinous rather than mixed with DCIS...

  • Hello mrsfingers, they said they were retesting the HER 2 - as it can sometimes change? Apparently if it changes from neg to pos it will mean chemo...so of course I am praying for it not to change. The letter also said there wasn't DCIS....

    what treatment did you end up getting? Xxx

     

  • Just read your bio....you were strongly positive? How did you get on with chemo....what meds you on ? Xxx

  • Hey ladies - been snowing down here in Kent. So glad I'm not working or commuting as trains will be buggered. This country makes me laugh as coming back from Canada with the amount of snow and freezing icy weather they carry on like normal. It really is cold tonight.  

    Had some pretty devastating news - hubby's brother who had cancer and has been fighting it well now has brain tumour. It has spread and prognosis isn't good.  Not a great start to the year. His was really far gone and in the thyroid gland, lung and back when first diagnosed so it is what it is and from day one were told it wouldn't be cured. He was in denial and I could see that. Sigh....it is what it is.

    We all have to keep fighting no matter what stage we are diagnosed at and yes cancer does suck but live, love and laugh to the highest degree every single day. Keep soldiering on ladies - you got this.

    Keep warm and keep well.x

  • They usually grade the ER and PR result and mine were 8/8 so the most strongly positive. This is a good thing as it means it will respond to hormone therapy as a means of preventing recurrence.

    mucinous carcinoma is usually Er+ Pr+ and Her2-. It’s typically slow growing and does not often spread to lymph nodes or other distant areas. However mine had gone to 2 lymph nodes hence chemo.

    if it isn’t in nodes you may get away with doing an oncotype test which will typically show a low risk of recurrence and hence no chemo. Generally speaking the prognosis for mucinous carcinoma is quite good.

    im on fec-t chemo and it’s gone pretty well overall. I had brain fog with the fec but not so bad physically. T has been no brain fog but various different pains. So mind or body takes a hit but all doable overall.

    after chemo I’ve got 3 weeks of rads. I’m also starting 3 years of zoledronic acid infusions (prevents spread to bones) and hormone therapy for 10 years...due to the strongly hormone positive thing this is another way of preventing recurrence.

Reply
  • They usually grade the ER and PR result and mine were 8/8 so the most strongly positive. This is a good thing as it means it will respond to hormone therapy as a means of preventing recurrence.

    mucinous carcinoma is usually Er+ Pr+ and Her2-. It’s typically slow growing and does not often spread to lymph nodes or other distant areas. However mine had gone to 2 lymph nodes hence chemo.

    if it isn’t in nodes you may get away with doing an oncotype test which will typically show a low risk of recurrence and hence no chemo. Generally speaking the prognosis for mucinous carcinoma is quite good.

    im on fec-t chemo and it’s gone pretty well overall. I had brain fog with the fec but not so bad physically. T has been no brain fog but various different pains. So mind or body takes a hit but all doable overall.

    after chemo I’ve got 3 weeks of rads. I’m also starting 3 years of zoledronic acid infusions (prevents spread to bones) and hormone therapy for 10 years...due to the strongly hormone positive thing this is another way of preventing recurrence.

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