Welcome New Members - 10th October 2024
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You have found your way to Breast Cancer Network Australia's (BCNA's) Online Network. This is a forum where you are not alone and can engage with generous members who provide meaningful support to each other. You can share as much or as little as you feel comfortable with other members. Please explore our various Groups for members who are looking for greater peer-to-peer support.
The following links may also be helpful in getting you started:
If you would like to introduce yourself please read How do I post a new Discussion?
- Community Guidelines
- My Journey
Newly diagnosed? Listen to BCNA's Upfront About Breast Cancer Just Diagnosed - What's Next? and What I Wish I Knew podcasts
Metastatic breast cancer diagnosis? Webcast: Just diagnosed with metastatic breast cancer, what’s next?
When is your birthday? Head to this discussion thread if you would like to share your birthday (no need to include the year unless you want to). We love an online celebration and on the day you will receive a virtual birthday cake that we can all share!
Our long-time members (newbies too!) are a wealth of information regarding the useful discussion topics and information available through BCNA's Online Network, therefore please do not hesitate to post your questions. You have the option to add details about yourself to your 'Profile' (Update your profile image by clicking 'Change My Picture') and if you would like more targeted responses, you may like to add where you live (e.g. Sydney; Melbourne; Regional Victoria).
If you need help navigating the Online Network please message myself @Mez_BCNA or one of our other moderators: @Denise_BCNA , @Risha_BCNA , @Pat_BCNA, @Kate_BCNA , @Daina_BCNA
Please note: the Online Network is not moderated by staff/volunteers on the weekends, however if you need something actioned, the quickest way to resolve your query is to contact the Helpline Team via email helpline@bcna.org.au or phone 1800 500 258 Monday to Friday 9:00am-5:00pm AEDT
Comments
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Oh my goodness, it is sad to see so many new members. Welcome !
Please remember that no question is too small or too silly. If something concerns you then come on here and ask.
Try to take someone with you to appointments as a second pair of ears - and take a list of any questions or concerns that you think about. This is about YOU and YOU are the most important. You are also your own best advocate.
Members here have "been there and done that" so know what you are going through and will be happy to help you in any way they can.0 -
Hello everyone my name is susan I’m 51 and been diagnosed with HER2 positive a mth ago am now having surgery on the 29th then chemo and radiation0
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I am glad to see so many members found the way to the network to get support. However, it is so concerning to see so many women diagnosed with BC. Beginning of the journey is hard and challenging but we have to keep going, focus, take care of ourselves and liaise with medical team. Being informed and get some knowledge helped me to go and still going through. This is a great website with so many useful resources. I wish all the new members all the best through this unpleasant and scary experience. . And remember! There are no silly questions.0