Is this the normal process?

Hey Guys,
I posted recently that I was diagnosed last Friday with triple neg breast ca stage three. All this week I’ve had the CT scans, bone scans, tomo the PET scan then Friday I’ll meet up again with the doctor that is looking after me and also meet my oncologist.
I received a call today from the genetic councillor and my appointment with her is not until next Thursday. Apparently it takes the councillors up to four weeks for my results to see how I’ll be treated.
I posted recently that I was diagnosed last Friday with triple neg breast ca stage three. All this week I’ve had the CT scans, bone scans, tomo the PET scan then Friday I’ll meet up again with the doctor that is looking after me and also meet my oncologist.
I received a call today from the genetic councillor and my appointment with her is not until next Thursday. Apparently it takes the councillors up to four weeks for my results to see how I’ll be treated.
I have never felt this kind of anxiety before. Four weeks? Omg this thing has grown so much in four months.
Is this normal?? I thought I’d be getting treatment as of next week. I’m beside myself with worry. I know my surgeon is a good one but far out. I thought I knew what stress was but this thing is a whole new level.
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Comments
Genetic testing is a relatively new component, it does take a couple of weeks to get the results. Realistically, that extra time is not likely to be a major factor--unless, of course, it is. If there is any urgency, you will be informed.
Whatever is going on under your shirt didn't start yesterday, so there is every chance that the short wait to get a better idea about what is going on is well worth it. It sounds like you are getting the full gamut of tests, which is a good thing. Mxx
I only had one cousin with ovarian cancer and they passed at age 56. I also had a cousin who had breast cancer and an aunt with cancer of the cervix. I had another cousin with liver cancer and another with bowel cancer and lots of relatives with various skin cancers.
He recommended i get tested because of the ovarian cancer in the family. He also wanted me to get tested because I had 3 malignant melanoma which were successfully removed but there is a link with breast cancer and melanoma in brca2. He did say that there was only a very small number of people with the mutated gene of Brca 1 or 2. He said most breast cancer has nothing to do with genes.
I had to order the test online as it came from America. He had approved it. It arrived by courier it is a saliva test. I gave the saliva, called the courier to collect it and waited 4 weeks I received a negative result 4 weeks later via an online report and a letter from my dr.
Here in Brisbane there is alot of work going into genetic testing and using the gene results to target the breast cancer treatment. I guess your team of medical people are looking at this for your treatment. When you have your appointment go prepared with your family cancer history. Write down any questions you have for them. Take a support person if you need to as well.
Good luck with it. Sending you a hug x
Been thinking of you
First sess was yesterday. Geez it's gon be a long road and I try not to think too deeply about it cos I'd get angry.
Thanks for thinking of me @irb_o3, that's lovely. Ok, soup and try and exercise time. At least it’s a lovely day in Melbourne today. ❤️💕❤️