Help! What should I do?

Good luck @CathyMac, I was diagnosed nearly 2 years ago and my surgery was a week before Christmas .The wait seems intolerable as you just want the cancer gone but your surgery date will roll around soon enough. I wrote all my worries and concerns down when I received my BCNA journal and that helped.I went public and was going to use my health insurance if it meant I would be operated on quicker but when the theatres (both public and private) are full, there's not much you can do but breathe and wait. All the best x

This is a game of learning patience , patience with all the tests , scans and app. you have to see, I was similar to you , but when I saw surgeon , the scans showed it had spread to a few other places , so chemo first 6 months ,wait to be a bit stronger , more scans , then surgery , wait again to get a bit better , radiation next.
  So trust me and all the ladies that are on here, just do one day at the time and don't stress ( i know hard not to) when what you want isn't what your oncologist and surgeon have planned for you.

  Breathe ......Good luck .

Yeah i had immediate reconstruction and don't regret it. However i have heard if you need radiotherapy its not always a good option. Good luck @CathyMac this time is very overwhelming, so many decisions. Big hugs to you xxx

@CathyMac If you have a bit of time to think, do look into immediate reconstruction when you have your mastectomy. Depending on your treatment plan, you get better results with an immediate recon. Check out the website @primek linked you to. K xox

Thank you for all your advise. I saw my GP this afternoon and have a bit more of a plan now. I will have scans this week and blood tests. So the surgeon will have all that info when I see her on the 23rd. I think I have reconciled I will just have a mastectomy straight up and consider what to do about losing a breast when cancer is gone.

Hi @CathyMac,  the waiting is just the worst but hang in there. I was also invasive ductal carcinoma  Grade 3 as well as high grade DCIS like you.  I found out in April this year and my first surgery was in May.  I had a lumpectomy then re excision in June to widen safety margins.   They decided then for me to have chemo to mop up anything left from the invasive carcinoma tumour then for me to have the mastectomy due to the high grade DCIS they found on scans after the second surgery. Cancer is so individualised now and treatment plans are different for each person.
It was a good 4 weeks before any surgery plans were made for me and like many on this forum will tell you waiting is the hardest as your mind goes into overdrive thinking of the worst case scenario's.  But as the others have said deep breath.  
Let us know how you go.  I decided against reconstruction as I just wanted to concentrate on getting rid of the cancer. These are decisions you don't have to make straight away and again everyone is different but it was the right path for me. big hugs to you. xox

In the big picture of breast cancer it takes some time before it really spreads out so 11 days won't make much difference, just make you worried of course.
On your previous post I added a link about different types of breast cancer so armed with your pathology have a bit of a look at that.
As with all breast cancer...the final pathology once removed is the one they plan on. Mostly they do surgery first but sometimes they offer chemo first depending on its location to chest wall or size overall.
Use the time to look at different surgical options and if you would want reconstruction  or not if you had a mastectomy. All very relevant things to think about and help you plan surgery at time of your appointment. 
Reclaim your curves. ..is a good site  to look at with what surgical reconstruction is available also.

https://www.reclaimyourcurves.org.au/breast-reconstruction.html

@CathyMac - sorry to see you here - but you are in the right spot for support & advice from those who have gone before you.

Sadly, the waiting is the pits!  :(   In the meantime, try not to overthink it - it will do your head in  :(    Have you checked out the 2 surgeons you are tossing up as 'the one' for you?   I googled the 2 suggested for me - and one was a clear 'winner' over the other (they sort of do a "Trip Advisor'' on surgeons now!!)  

Where abouts are you based?  Others nearby may be able to help you with all things BC, including surgeons!  Do you have private Health Insurance?  If yes, you 'could' be done earlier .... tho often there is a bit of a  'financial cost'!   I went private for surgery & public for Radiation.  If I needed another surgery - I would probably go public next time, even tho there may be a wait! 

When my GP found my lump last Nov - it was the start of the 'Big Wait' for me (I live in a rural town up the mid north coast!)  I had to wait 2 weeks for an ultrasound/mammogram (early Dec), then wait another 2 weeks for the biopsy (between Xmas & New Year) and got my actual diagnosis a week later on Jan 5 (I was still hoping it would be cysts!) .... then all the surgeons were on holidays til mid Jan ......  so surgery wasn't til Jan15th - 2 months from 'detection'.

As @Zoffiel says - Deep Breaths (lots of them!) and maybe put the Big Girl's pants on ...... You could start by getting bits together for your hospital stay ...... ear plugs, eye mask (hospitals are notoriously noisy & bright!), sudoko or magazines (don't take a novel - just too much going on to be able to concentrate), a front opening nightie makes it easier to show the nurses & surgeon your 'bits' ..... slip on slippers ..... maybe some treats (lollies or chocolate ...) 

All the best as you await your surgery & results  xx

This might be a useful place to start. If I was in your position I'd read it and then make an appointment to see your GP to clarify the bits that you don't understand. This might help settle your mind while you wait.

Giving the BCNA helpline as suggested above is a good idea. It's staffed by nurses who can help you decode.

I had my mammogram on the 4th Novembet last year. It was three weeks before I received my callback letter. Don't stress about the wait more than you can help. If they see something truly urgent you'd be seen immediately. K xo 

@CathyMac I have noted others have recommended the BCNA  helpline - 1800 500 258. You can talk to someone about your concerns and your diagnosis,maybe get info about other supports in your area. 🙂