With a soft tissue sarcoma diagnosis I feel in total meltdown. I live in Italy and have a caring supportive family but I just really don't know what to expect.
Hi Sarah
I have just replied to your post to me on the other thread.
I hope you pick it up
the nurse Said today when I Spoke to her that there was still nothing back but... she did say they've not yet got tomorrow's in yet so it's possible they could be back later today. She said they're chasing. I asked is the delay due to COVID and she said no it's because it's a very rare biopsy because of where it is etc and so they need to do lots of extra tests to clarify exactly what it is
Try and stay strong to fight it sarah
keep in touch
Tracie
Morning and thanks for thinking of me
No nothing yet, if I don't hear anything at 1pm Today I will phone to ask the nurse, I am finding myself doing this every other day now.
it's four weeks today since the biopsy was taken, like the nurse said on Monday it's a strange one because of were it is as in my deltoid muscle, trust me to get a strange one
how are you did you look at the sarcoma uk website?
The waiting is hell. As I said I found out after 19 days. I have this sarcoma on the front of my thigh in the muscle. I had a full body scan yesterday and the results came back immediately. This morning I had to get some paper work to not pay for all these tests and visits and the fact I don't have italian citizenship ( been in the country thirty odd years) the woman said she would just have to check. Thanks again Brexit!! Everything was fine as I am a law abiding citizen , married , mother of three. I think I was ready for meltdown. The scan was fine but will have a more senior person check it. I shall keep everything crossed for you. Bye for now. Sarah66
BTW I don't know how the hell I put MOT as a nick name?? Brain isn't with it.
Hi Sarah
how are you? I hope things have settled down and you can now get on with your treatment.
I am still waiting on my results, I spoke to the nurse yesterday and it's because one test has lead to another and then another!!
i don't really know what to think anymore
I asked the nurse that if they confirmed it was cancer would I then have to have a CAT scan, the nurse said if there was any more tests this would not impact on my treatment plan and they would be done there and then at my consultation.
I couldn't bare any more waiting for tests!!
stay strong and focused on beating it sarah
Had the call!!
It's a Nodular fasciitis it's a tumour but not a cancer one
I have to now wait for an appointment with the consultant to see what he is going to do about it
It mimics a cancer that's why all the testing
Not so long ago they treated as sarcoma cancer
stay strong sarah and take care
Tracie
So pleased you got an OK diagnosis. I completed my first chemo course. I have become a patient. My consultant says I have gone into depression because of this outside event. You don't need 12 years of medical studies to understand that. I was kept in the hospital as the stuff they gave me is pretty potent. I got home yesterday evening. I had a provisional port put into my cava vein as there wasn't a surgeon available for the other one. My friend is coming to cut my hair today as the nurses say it is less traumatic if your hair is short falling out. I have a shoulder length Bob. Silver streak at the front as I never dye my hair. I have been able to eat a bit of weetabix and a kiwi. Hard going to say the least. Take care. Xx
So pleased you got an OK diagnosis. I completed my first chemo course. I have become a patient. My consultant says I have gone into depression because of this outside event. You don't need 12 years of medical studies to understand that. I was kept in the hospital as the stuff they gave me is pretty potent. I got home yesterday evening. I had a provisional port put into my cava vein as there wasn't a surgeon available for the other one. My friend is coming to cut my hair today as the nurses say it is less traumatic if your hair is short falling out. I have a shoulder length Bob. Silver streak at the front as I never dye my hair. I have been able to eat a bit of weetabix and a kiwi. Hard going to say the least. Take care. Xx
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2024 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007