The information available on the Breast Cancer Network Australia website is not medical advice and is provided for information purposes only. It should not be viewed as a replacement for a consultation with a qualified medical professional. Our website is designed to offer information and support to the general public. Be aware that we do not provide any medical advice, and for medical advice we recommend you speak to a qualified medical professional or doctor. 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I was diagnosed with \"locally advanced mul...","body@stringLength":"1735","rawBody":"Hi everyone,
I'm currently on a bit of a waiting game so thought I'd introduce myself as I'm new to this club that none of us wanted to be a part of!
I was diagnosed with \"locally advanced multicentric left breast carcinoma\" on my 46th birthday a couple of weeks ago. It was quite a shock as I'm super healthy and have zero cancer in my family!
I was diagnosed after me noticing a lump and strange dimpling, plus feeling discomfort. I was convinced it was a cyst that needed draining as it felt (and still feels) like I did when I was breastfeeding and parts of my boobs would fill up with milk! My GP referred me for a mammogram and ultrasound plus I also had two biopsies - one core needle, one fine needle - in to different locations of concern.
I'm going through Flinders Public here in Adelaide. Have meet with the surgeon for my initial appointment then at her request this last week I've had a bone scan, CT scan and MRI scan, plus a blood test.
And now I wait for my follow up with the surgeon for all the results and plan of attack on 1 July. The waiting is definitely the worst bit! (and to top it off, I've caught a horrid flu type lurgy off my kids so am totally down in the dumps!)
What I know so far (everyone seems to speak in such technical terms here - I guess we become pros in our own experiences!) is it's grade 2 and Invasive Ductal Carcinoma. It's also a Hormone Receptor Status type of breast cancer.
Just here to say hello really but also keen to discover other women at a similar stage to me, or anyone who's been through Flinders Public. Always just nice to know I'm not alone!
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I'm currently on a bit of a waiting game so thought I'd introduce myself as I'm new to this club that none of us wanted to be a part of!
I was diagnosed with \"locally advanced multicentric left breast carcinoma\" on my 46th birthday a couple of weeks ago. It was quite a shock as I'm super healthy and have zero cancer in my family!
I was diagnosed after me noticing a lump and strange dimpling, plus feeling discomfort. I was convinced it was a cyst that needed draining as it felt (and still feels) like I did when I was breastfeeding and parts of my boobs would fill up with milk! My GP referred me for a mammogram and ultrasound plus I also had two biopsies - one core needle, one fine needle - in to different locations of concern.
I'm going through Flinders Public here in Adelaide. Have meet with the surgeon for my initial appointment then at her request this last week I've had a bone scan, CT scan and MRI scan, plus a blood test.
And now I wait for my follow up with the surgeon for all the results and plan of attack on 1 July. The waiting is definitely the worst bit! (and to top it off, I've caught a horrid flu type lurgy off my kids so am totally down in the dumps!)
What I know so far (everyone seems to speak in such technical terms here - I guess we become pros in our own experiences!) is it's grade 2 and Invasive Ductal Carcinoma. It's also a Hormone Receptor Status type of breast cancer.
Just here to say hello really but also keen to discover other women at a similar stage to me, or anyone who's been through Flinders Public. Always just nice to know I'm not alone!
x "},"Conversation:conversation:68806":{"__typename":"Conversation","id":"conversation:68806","solved":false,"topic":{"__ref":"ForumTopicMessage:message:68806"},"lastPostingActivityTime":"2024-07-17T00:10:48.000-07:00","lastPostTime":"2024-07-17T00:10:48.000-07:00","unreadReplyCount":23,"isSubscribed":false},"ModerationData:moderation_data:68806":{"__typename":"ModerationData","id":"moderation_data:68806","status":"APPROVED","rejectReason":null,"isReportedAbuse":false,"rejectUser":null,"rejectTime":null,"rejectActorType":null},"Revision:revision:68806_1":{"__typename":"Revision","id":"revision:68806_1","lastEditTime":"2024-06-24T22:12:39.000-07:00"},"ForumReplyMessage:message:68813":{"__typename":"ForumReplyMessage","id":"message:68813","conversation":{"__ref":"Conversation:conversation:68806"},"author":{"__ref":"User:user:3907"},"revisionNum":1,"uid":68813,"depth":1,"hasGivenKudo":false,"subscribed":false,"board":{"__ref":"Forum:board:general-newly-diagnosed"},"subject":"Re: The waiting game...","readOnly":false,"editFrozen":false,"moderationData":{"__ref":"ModerationData:moderation_data:68813"},"parent":{"__ref":"ForumTopicMessage:message:68806"},"body":"Hi Gemini I am now in a similar boat. Saw oncologist yesterday.
I have the rest of my lymph nodes out on Monday. If more nodes found to have cancer cells , then scans.
On the 29th of July I start 5 months chemo. A break then radiotherapy. Then hormone tablets.
I am lying here thinking have I done the right thing saying yes. I think it's just fear of the unknown. I always said I would never have chemo. It's so different when you are affected by this hideous disease.
Anyway I am usually pretty positive. My calm place is the sea, even though it's cold at porties. It's my happy place. I was back in as soon as I could after surgery plus swimming is the best for moving arms. Plus my head.
@boy boy good luck with results. I saw a previous post of yours about exercise,totally agree so much research into exercise when going on this journey.
Funny I asked my hubby how will he be looking at me if I lose my hair. Well he doesn't have much anyway, boy did we laugh. Mind you I will go for the shaved look and rock those hats.
Might try and close my eyes before our cocker spaniel bounds in. Take care guys...
","body@stringLength":"1266","rawBody":"Hi Gemini I am now in a similar boat. Saw oncologist yesterday.
I have the rest of my lymph nodes out on Monday. If more nodes found to have cancer cells , then scans.
On the 29th of July I start 5 months chemo. A break then radiotherapy. Then hormone tablets.
I am lying here thinking have I done the right thing saying yes. I think it's just fear of the unknown. I always said I would never have chemo. It's so different when you are affected by this hideous disease.
Anyway I am usually pretty positive. My calm place is the sea, even though it's cold at porties. It's my happy place. I was back in as soon as I could after surgery plus swimming is the best for moving arms. Plus my head.
@boy boy good luck with results. I saw a previous post of yours about exercise,totally agree so much research into exercise when going on this journey.
Funny I asked my hubby how will he be looking at me if I lose my hair. Well he doesn't have much anyway, boy did we laugh. Mind you I will go for the shaved look and rock those hats.
Might try and close my eyes before our cocker spaniel bounds in. Take care guys...
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