Mucinous ovarian cancer

Hi everyone.

Any positive stories out there in respect of recurrence of mucinous ovarian cancer?

My story.... 2021 surgery for stage 1a ovarian cancer. Hysterectomy and removal of mass.

2023 ...recurrence. Debulking surgery and spleen removal. Just finished 6 chemo treatments.

Will now be checked via blood every three months.

Really struggling with emotions as been told i am high risk of recurrence.

Also told my cancer is rare mucinous.

Any help or stories you can enlighten me with.

Thank you x

  • Hello Cah60

    I'm sorry to hear about your diagnosis in 2021 and that despite initial treatment you had a reoccurrence last year. I hope that since you completed this most recent round of treatment you're recovering well. 

    I know that many of our members will understand the fear that comes with being told that you are at a high risk of recurrence. It's good to hear that the hospital is keeping a close eye on you with regular monitoring and hopefully, you will get some replies from others about their coping strategies for living with this anxiety. 

    As you've said, mucinous ovarian cancer is rare. I've had a look through the forum and I can't see that we've any other members who have posted about this diagnosis within the last few years. I'd suggest having a look at the website for Target Ovarian Cancer as it may be that you're able to connect with other women who have this diagnosis via their support options. 

    If it would help to talk with one of our nurses about how you're feeling you're welcome to call them on 0808 800 4040, Monday to Friday 9am to 5pm. I know they will be happy to listen and offer any advice and support they can. 

    Best wishes, 
    Jenn
    Cancer Chat moderator