Ovarian cancer treatments

I was diagnosed with stage 4 ovarian cancer September 2017 after ultrasound,CT scan,blood tests and 3 biopsies. I started chemotherapy 1st October using paclitaxel and carboplatin, I had 4treatments to shrink the tumour,then I had surgery 3rd January 2018 to remove my ovaries Fallopian tubes and the fatty apron of the abdomen, I’d already had a hysterectomy 23 yrs ago leaving behind my ovaries. My surgery went well,the surgeons got everything they could see with the naked eye. I resumed my chemotherapy 6 weeks ago,having been told I needed 3 more treatments,I have my last one tomorrow, I’m also being started on Avastin (Bevacizumab) at the same time, this will be given every 3weeks intravenously for 12months, I’m wondering if anyone of you on this forum have had Avastin or still having it, and can let me know how your getting on with it,and if you’ve had any issues with it.

  • Hello Jayboo and welcome to Cancer Chat,

    You might be interested in reading [@Pauline12]‍ 's post here. Pauline posted today on the forum and seems to be in a similar situation having been diagnosed with Stage 4 ovarian cancer last November. She doesn't mention whether she had Avastin but she also had chemotherapy and an operation four weeks ago. I will make sure to mention your thread too so that you two can connect and share your experiences as I am sure you will have a lot to say to one another!

    We also have some information on Avastin our website here which may be useful to you.

    I hope others will be along soon to tell you how they have been doing on this drug.

    Best wishes,

    Lucie, Cancer Chat Moderator

     

     

  • Hi lucy ,Great to hear from you ,no jayboo ,would be ahead of me on treatment ,im only starting back on my chemo this week ,providing they have a bed,im going for skintest in morning to see was the same chemo jayboo was on; cause when i was getting both i had side effects,the only Thing is my chemo doc mentioned another chemo,but i didnt get name ? she said it was intense ,but looking at me she thought 'd be fit enough lol she'd want to see me at home ,their's times my head would climb a mountain ,but you need a trailer for my body ,really appreciate you keeping me intouch with ladies with familar cancer love hearing about it,also if you come across anyone that has started hotflushes after full hysterectomy ,but im not sure if it was op now!! As when i was only on second chemo these started! But omg since op alot worst ,im currently taking sage evening primrose and id be lost without ice drinks & ice packs im on evening primrose since last wed ,but today im finding im constipated ,i seem ok when i was on sage only ,im also drinking peppermint tea ,as after op ,i went through hell with air pockets in intestines , if you see anyone that has come up with anything for hotflushes will you let me know? I cant take anything perscriped as chemo doc is reluctant as she said she doesnt want anything to interfer with this chem 

  • Hey there, have you had a laparoscopic surgery after the 3rd chemo to explore the abdomen before the "real surgery? My mum is stage for as you are, hope to find it if it's normal