Best Of
Re: Just diagnosed
Hi @hope3736 waiting is the hardest part. After an April DCIS diagnosis that changed to Stage 1 IDC diagnosis after the lumpectomy surgery I know how scary it can be. Here if you ever need to talk. Always find it best to distract myself; exercise, yoga, meditation, walking. Making my friends come hang out with me as much as schedules allow.
Re: Just diagnosed
@hope3736 - Hi Kim, and welcome. We're truly sorry for what brings you here, but so glad you’ve found us. It's okay to feel scared and overwhelmed after a diagnosis; you're not alone here, and many, many members here have felt the same way.
While you're waiting for more details about your diagnosis and next steps, you might find these pages on our main site helpful:
Stages of Fear After Diagnosis
Hope this helps a bit. Sending you strength and calm as you prepare for your MRI and surgeon visit. We’re here whenever you need us.
The Mods
Re: Triple Negative BC & Older Women
I'll chime in as real newbie-- recently diagnosed TN 56-year-old the last of July. I had a CT brain scan and a neck to knee PET scan just today- to come up with a complete diagnoses and staging.. Now I have the weekend wait... having fun yet??? **sigh**
You bet it bothers me that "older women" seem to be the stepchild of the studies since the numbers of us appear to be smaller.. While my heart TRULY bleeds for these younger women, and right now I worry about my own grown daughter, it would be nice to have more studies for those of us who DO develop this later in life. I feel sick for such young women to be hit with TN, so don't get me wrong. This is uncharted waters for so many of us as it is. Surely older women should be considered since we DO indeed develop TN. Hello!? Here I am, and so are you posting in this thread.
My mother had early onset BC yet I have no idea of what kind. She had a radical mastectomy on her right breast after finding a very palpable lump.. Mine was easily found also.. like it popped up overnight. I digress. There's no other family history on Mom's side of the family, nor my Dad's who are all now deceased. Even my baby brother died of the chronic form of leukemia Mom had. I'm very familiar with cancer as it's hit my birth family with a vengeance. My Dad died of pancreatic cancer also 3 weeks after diagnoses.
In Mom's case she survived the breast cancer treated (at around 38 years old, I think).. About 30 years later died from complications of chemo to treat what I think was a late diagnoses for acute myloid leukemia. She lived 3 weeks from diagnoses.
All I know right now about my own diagnoses is a poorly differentiated invasive ductal carcinoma from 4 tissue samples acquired from a needle biopsy. I also had an MRI which only confirmed this diagnoses with no other findings.. And of course it's TN.
Discovering that own my own thru my path report was a huge kick in the gut. I was ready to fight breast cancer.. I'd never heard of this form though. And yes, It WAS confirmed by my new oncologist.
Everything has happened so fast.. but not fast enough after reading about the invasive nature and distant reoccurring rate of TN.
I plan to get tested for BRCA mutations as I have a 37 year old daughter and 3 beautiful granddaughters, one who is approaching her teens.
Even my oncologist was surprised I was over 50. It could be taken as a compliment, however in reality I think it had more to do with the fact that most of her patients are much younger. She does the most breast cancer cases in the state. What she can't handle, such as cases where her TN patients have mets she sends to Baylor. She feels the true experts for this particular cancer is best treated at Baylor, as the so-called-mother of TNBC doctor is there with her research team.
Filtering all this information in such short time has been a real kick in the behind, but I'm hoping and praying for clean scans and and a low stage to start.. as I'm ready to do what I can to beat the crap out of this nasty beast.
Sorry this turned into a novel.. my first post.
I'm so glad I found you! Peace of mind seems a thing of the past.. though I desperately wish it for all of us, at ANY age! Take care... ![]()
Need help anyone else had anything else come back on their pet scan
Hi I am 37 years old I have recently been diagnosed with IDC triple negative and went for a pet scan the scan come back and said that the area hasn't spread anywhere else but the scan did pic up something in my colon area they weren't concerned at all really but now I have to wait yet again before I even see oncology to have a colonoscopy done. I really thought after my pet scan I would get on with doing something proactive like getting treatment now I feel right back where I started extremely scared and frustrated just waiting to be told I have cancer in my colon as well. Has anyone else experienced this? And did you have a better outcome than what you thought I'm going crazy again I had excepted my breast cancer and was determined to get on with the fight this has set me right back and I feel deflated and I haven't even started any treatment yet the constant wait for scans then results is driving me mad because what am I waiting for the long I wait with no treatment the worse it's getting I am really frustrated any advice would be very much appreciated
