Recent diagnosis and new to the group

Hey Jenny,
I have the same diagnosis as you( Hormone +, Her2-).  Mine was grade 3, stage 3( I’ve used past tense as my hubby insisted that my tumor has been removed and I have completed all the active treatments, I.e. lumpectomy, chemo and radiation). I was diagnosed in Jul 2023.
I think with chemo, you’ll likely be on AC and then weekly Taxols. There’s heaps of ladies who have shared their experiences here. If you have any questions along your journey or anything you like to share with us, feel free to post it here.  
I’m so glad to hear you have accepted it and learning to live your best life with this diagnosis ( I’m still getting accustomed to my new ‘normal’🙈.
Wishing you all the best with your treatments. 🤗.

p.s. I noticed your location is Hervey Bay, we will be heading there for a short holiday in July!
💝💝💝
Gin

Hi @Madimack, So sorry to see you join our select little group and glad that you've found us.   I was lucky & dodged the chemo bullet, having lumpectomy, Rads & still on the Tabs.  Yes, it is a real roller coaster ride, so well done on feeling OK with it all xx

Congrats on getting thru your surgery and  I wish you all the best with your upcoming chemo.  I nursed my husband thru his chemo - Drinking lots of water after each infusion helps 'clear it' from your body.  Not everyone loses their hair - so maybe ask your Medical Onc about a cold cap ... it has reduced hair loss with some members.  (Tho it may be a tad uncomfortable in Winter?)  Taking rests if/when you need them, eat whatever you like, WHEN you like (it may not fit into regular meal times ...). If you start cooking up some of your favourite dishes now & freeze them in meal size portions, it may make  
it easier on those days you just can't be bothered cooking. xx. I hope you have good family & friends supporting you xx 

Consider recording all your team meetings, so that you have 'back up' - as it is easy to miss bits when you are still pondering what has just been said.  Also take a trusted friend/relative with you as physical support & an extra set of ears  ;) 

Feel free to jump onto this thread that has a lot of 'general' info on the Forum - and some 'off topic' threads that you may like to check out, if you have pets, a nice garden or are into art & craft xx.  We also have some funny threads too (we all need a laugh now & then!)  At the bottom of the main thread are some 'tick sheets' for self assessing how you are going, physically and mentally!   Sometimes it is easier to tick or write things down than to talk about it .... and if you feel a bit 'down' and want someone to physically Talk to .... jump onto our Helpline (Mon-Fri, Office Hours) on 1800 500 258
https://onlinenetwork.bcna.org.au/discussion/23477/a-big-welcome-to-all-new-online-network-members#latest

Terrific that @GinGin will be in Hervey Bay in July - you might be able to catch up for a coffee & a chat!  I am sure we have other members up that way too xx

Take care and all the best xx

@Madimack  welcome to the club noone wants to join.  I had same diagnosis as you.  Im 4 years down the track of lumpectomy,  mastectomy,  chemotherapy and radiation.   You sound like you are in a good head space.   Look after yourself. Remember to breathe.  One step at a time.  If people offer help accept it.  Prepare a few meals for the freezer.  Chicken broth or vegetable soup in the freezer will be helpful if you have days you are not up to cooking.

Hi Jenny, I am also a Jenny (located adelaide).  I was diagnosed 22/12/23 IDC, and the process of scans, tests, biopsys etc lead to surgery 28/2/24 partial mascectomy, chemo ( Ive just completed the x4 dose dense over 8 weeks and about to start weekly x12 weeks.  Then to come still radiotherapy and hormone blockers (for er/pr +).   I had 14 cancerous lymphnodes also removed in anxillary clearance, along with idc tumour.  I was offered, but didnt worry on cold cap (its hit and miss with red devil and I didnt want to be in infusion suite longer than I had to). About day 18 hair started breaking off, so I got it buzzed off by my hairdresser.  Had it neatened to a zero the other day, its weird but fine, its winter so beanie/head covers and scarf do the trick till I look into wigs.   Side affects are very individual.  It hasnt been easy, Ive had various issues, but talked about them with oncologist each appt to get advise to get through.  I am quite open and honest with family and friends on things happening,  and one day at a time conquering this crazy time.  Ive got a trip coming up Im doing in all this (7 days to auckland), which is still possible with precautions, and I pick the good days toward end of each cycle to do a few things (reward things like see a musical, lunch with friends etc).  While there are up and down times, acceptance and positive outlook definately will get you through.   Goodluck with starting chemo 🩷, 

I also did the Look good Feel good Workshop today, that was quite good to get out, put make up on as part of morning, and there was a wig demo so of course I volunteered to model a couple! 

 

Good morning Jenny

congrats on the results! Such a 😅 relief! You may wish to consider creating a new discussion for this topic. 

@madimack I used the socks gin gin mentions for taxol. I do believe they helped me.  I did have some neuropathy in my toes but I feel it would have been much worse if I didn't do it.  I did have my big toe nails lift which was very painful.  Podiatrist said I did very well and thought the icing saved the other nails.  We brought towels to treatment.  Nurses were helpful showing us where to get ice for my hands.  I would double glove my hands.  Brings jugs from home and try to keep my hands in the jugs for as long as I could.