Stage 2 endometrial cancer

Hi, I'm sorry I can't give you any advice as I'm at the beginning of my possible diagnosis. A mass was seen on a CT when it was done because they were thinking it was appendicitis. I then had a TVS, a biopsy which unfortunately wasn't a large enough sample to test. I had an MRI on Tuesday so waiting for the report on that. Like you I just want it done and to move on. I'm not afraid of the surgery (I've had several ops over the years) I just want to be alive to see my grandsons grow up.

I hope you get your surgery soon. Take care, Deb

Hi Gelisdefleury,

I was only Stage 1A when diagnosed so only needed the hysterectomy, which was not bad. I dreaded the operation even though I have been in hospital a few times. I was also worried about my age, 72 at the time. I had keyhole surgery and I believe the recovery is quicker than if you have to be cut. I only had 3 tiny incisions. The worst bit was that my bladder took some time to settle afterwards, but not everyone has that problem. I am coming up to 4 years post op and am fine.

I think your chemo might be the worst thing. I nursed my daughter through it for breast cancer, and she was pretty rough at times. However, its stopped anything else as she is now 7 years post op. 

My best advice is keep busy while you can as you will have to take it easy after the operation. It will  also help to take your mind off things.Any questions, just ask here. We are a friendly bunch and someone will have an answer.

All the best. xxx

Hi Gelisdefleury and welcome to our spot in the Online Community. We've all been shocked by the "C" diagnosis and are now at the beginning, the middle or the end of this rollercoaster ride. It's good to know worldwide once the diagnosis is in, the wheels turn really quickly!

It was this exact date last year I had a telephone consultation with my GP about unexpected spotting and she said she'd put me on the 2 week wait cancer pathway - I was shocked rigid - not me! 

It’s always helpful to others if you write a little something (or a lot) about yourself and your journey to date. You can enter it into your profile (click on your username and select “Profile”) It’s helpful to other members with a similar diagnosis who can then hopefully answer your questions. It also means that you don't have to keep repeating yourself. You can amend or update it at any time. If you’re not sure what to write, just click on my username.

If you read through the posts you'll find a wealth of experience here - If you want to ask any of us any questions please come back and do so. There's always someone around and we can offer a shoulder to cry on, a hand to hold or listen to a rant, we’re here for you.

It might also be a good idea to download this booklet Understanding Womb (Endometrial) Cancer I found it invaluable in my journey. 

There is also an Ask an Expert section, but you should allow two working days for replies from our expert team.

To find information covering diagnosis, treatments and pages covering most types of cancers can be found on our Online Information and Support Section. 

Sending you welcoming hugs, B xx 

Update. I have now had full open surgery. Surgeon said the tumour was confined to the uterus, and the washout returned a negative result. He removed lymph nodes as well. Results of histology in about a month. All healing well. Have been in hospital a couple of days longer than usual, as I have to fly home - I ended up having the surgery in Athens and I live in Crete.

Will be home on Tuesday; I can't wait!

Hi Gelisdefleury and "kalosorises xana" . Good to hear surgery is over and you're healing well.  The wait for histology is the pits but that's what this rollercoaster ride is all about!

Take it very easy, no lifting heavy cases and enjoy the sun, which we've had quite a bit of in the UK for a change!

Take care and come back whenever you want to chat.

Hugs, Barb

PS I confess I cheated, I do speak French and Spanish but had to look up the "Welcome Back"

Thanks for the welcome back, @MrsBJH! I'm now home, and gradually feeling more like myself, though very achy at times. Have had a few bowel issues, as hospital food very, very bland, and no veg. Have been told to gradually re introduce veggies, and take it slowly, which I'm doing. Difficult when my normal diet is mainly veg!