Forum Discussion
Recurrence in lymph nodes
Hi everyone,
I was diagnosed with TN Inflammatory BC in late Oct 2017. Treatment was 5 mths of Chemo ( 8wks fortnightly A/C, followed by 12 weeks weekly Taxol) then modified radical mastectomy (rt breast and 3 lymph nodes) which showed only a tiny amount (1.3mm) of residual disease with excellent margins. There had been evidence of activity in the lymphnodes. Surgery was followed by 5 weeks radiation and then I had what I refer to as my bonus chemo - 4 months of Capecitabine (Xeloda). That all took me to Christmas 2018.
Since then I have been feeling better each day and looking fabulous (according to my dear friends and family!). On an o/s trip in early June I noticed the onset of lymphoedema in the right arm - sad but not completely unexpected after the radiation. As soon as I got home I booked in to see my surgeon, who is wonderful and always says to see him asap if anything changes. He sent me for an ultrasound, having said he didn't expect anything sinister. Unfortunately the ultrasound shows at least three lymphnodes appear enlarged and diseased - I go back on Wednesday for a Fine Needle Biopsy, but the radiologist made it pretty clear she thinks it's not going to be good news. I have to wait until next Monday 22nd for the results and to know what I'm looking at in the way of further diagnostics/prognosis/a treatment plan etc. I know there's not much advice anyone can give at this stage, but am just having a little freak out and trying very hard to stay calm for my darling husband, so I thought you would all understand if I had a little figurative scream in this forum!!
I am searching my self for the inner strength to do this all again - in some ways easier when you know what it entails, and in some ways so much harder for the same reason.
Worried and sad, but trying to be strong.
Sally
I was diagnosed with TN Inflammatory BC in late Oct 2017. Treatment was 5 mths of Chemo ( 8wks fortnightly A/C, followed by 12 weeks weekly Taxol) then modified radical mastectomy (rt breast and 3 lymph nodes) which showed only a tiny amount (1.3mm) of residual disease with excellent margins. There had been evidence of activity in the lymphnodes. Surgery was followed by 5 weeks radiation and then I had what I refer to as my bonus chemo - 4 months of Capecitabine (Xeloda). That all took me to Christmas 2018.
Since then I have been feeling better each day and looking fabulous (according to my dear friends and family!). On an o/s trip in early June I noticed the onset of lymphoedema in the right arm - sad but not completely unexpected after the radiation. As soon as I got home I booked in to see my surgeon, who is wonderful and always says to see him asap if anything changes. He sent me for an ultrasound, having said he didn't expect anything sinister. Unfortunately the ultrasound shows at least three lymphnodes appear enlarged and diseased - I go back on Wednesday for a Fine Needle Biopsy, but the radiologist made it pretty clear she thinks it's not going to be good news. I have to wait until next Monday 22nd for the results and to know what I'm looking at in the way of further diagnostics/prognosis/a treatment plan etc. I know there's not much advice anyone can give at this stage, but am just having a little freak out and trying very hard to stay calm for my darling husband, so I thought you would all understand if I had a little figurative scream in this forum!!
I am searching my self for the inner strength to do this all again - in some ways easier when you know what it entails, and in some ways so much harder for the same reason.
Worried and sad, but trying to be strong.
Sally
68 Replies
- I love to sing classical choral music - I sing in the Tasmanian Symphony Orchestra Chorus and it’s the best thing ever! Also my lymphoedema therapist says it’s really good for you!!
- @sallylovestosing, I haven't anything further to add to what everyone else has said.
Just thought I'd throw a little distraction in. I love your "name". What do you lave to sing? - @sallylovestosing I have everything crossed for you, I know how hard the wait for results is, I hope it’s good news for you
- Thanks Tonya and everybody who has commented on this thread - I really am taking heart from your presence ! Every cheery comment and positive story has helped restore my equilibrium!! You’re all gorgeous to take the time and energy xxxxx
- Hi Sally, we always jump to worst scenario which is a normal reaction. I had a recurrence in the same breast 7yrs after first cancer diagnosis so had to jump through all the hoops again.I was so worried it would be in the bones but it was all clear. That was 9 yrs ago and I’m fine- no more cancer scares.I have a lady in my bc support group who had a recurrence in her lymph nodes and that was 17 yrs ago. She’s been on various meds and her oncologist keeps her monitored.The cancer stays put and hasn’t travelled for 17yrs! Sometimes nodes enlarge when you are fighting a virus.I hope you are cancer free but if not,take heart from all our positive stories.xx
- You’re you welcome and I have everything crossed for you to.
🤞🙏🏻🤗 - Oh Paula thanks for messaging - I so needed to hear your good news story! Keeping everything crossed that I can be as brave as you and be encouraging someone else in eight years time 🤗
- Hi @sallylovestosing,
@primek is right. I had a recurrance 6mths after completing treatment for TNBC (lumpectomy, chemo and rads). 1st diagnosis one positive node 10mm! Went on to have mastectomy and removal of more nodes. More chemo, so I know exactly how you are feeling. I was so gutted. However once I had my cat and bone scans which fortunately were clear I just put my head down and got on with it. I won’t lie, it wasn’t fun doing chemo again, but however as it wasn’t that long since the first lot so I soon got into the swing of things again. I am now 8 years clear of that second diagnosis so hopefully you can get here too. It’s not fair, but it is what it is.
Sending you hugs.
Paula xxxx - Thanks for thinking of me @primek. Great to know it’s not an impossible dream!!
- @mum2jj had a recurrence inside 2 years and now 8 years free tnbc (I think) We all get how devasted and how gutted you feel given treatment not finishing long ago. Please keep us up to date on what's happening next. Hopefully it's still considered locally advanced and chemo again may be the option.
