New here, have no idea if my story rings any bells with others.

Former Member
Former Member
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Had a biopsy in June, get a phone call in 2nd week in August to come to a hospital appointment the next day and to bring someone with me, I ask what is it regards to. They answer " Your biopsy you had in June."

Right there and then I knew it was cancer, I got told stage 1 and I had 3 choices. 1, do nothing (you'll be surprised how many patients do nothing) 2, have chemo and radiotherapy. 3, Have a Full hysterectomy and bilateral salpingo oophorectomy ( means cervix, womb, tubes and ovaries gone) all 3 run the risk of death. Told them I'd rather die under the surgeons knife than to die in pain.

After a cancellation, I'm a 11 days after the surgery and I don't know where I had the strength to have a positive  outlook to it all, either I'm amazing or I had an outer body experience lol, just waiting to see if I need further treatment and outcome of staging. Wanna do things and go places but son's a tad overprotective and slightly overbearing, I love him but wanna bat him with a pillow. I realise I have another 6 weeks of who's the parent and who's the child. Does anyone else have these little problems?

  • Former Member
    Former Member

    Hi Trippy,

    sounds like you’ve been on one hell of a ride!! It seems a long wait from June to August, I would have been a total wreck of worry, I had my biopsy one week, and telephoned the next week to see the consultant the day after, much like your call, you know it’s not going to be great news, it’s not going to be everything’s fine. I wasn’t given any choice at all, it was a case of you have to have surgery, and it will be done quickly, there isn’t a choice. I had my surgery 2 days ago, so it’s very early days on the road to recovery. I had total hysterectomy and bilateral salpingo  oopherectomy, the doctors said everything went as planned, and histology takes 2-3 weeks and I have follow up with consultant in 6 weeks. I just hope and pray there is nothing ‘lingering’ , but as all other ladies gone before on this mad journey, will face that when I need to. For now it’s taking it easy, it’s frustrating, but necessary. I completely get the out of body experience feeling, I can’t believe I have just done and been through what I have, I still feel as though it’s someone else! Madness I know, but maybe it’s the speed this conveyor belt moves that does this to us, who knows! My husband is chief cook and bottle washer, and is like your son over protective, but honestly Trippy, let them! It’s not forever, it’s for this time we need to heal, and if that’s how they cope with this then go with it. I don’t think we realise the stress our loved ones go through when the control is taken away, my husband said to me the look of fear in my eyes when the nurse took me from the door will stay with him forever, so I would say let your son do what he feels he has to. It’s a measure of the love he has for you, and his own coping mechanism . Sending lots of love, Emm xx

  • Hi and welcome to our spot in the Online Community. I love it when a new post on here makes me smile. Normally when we all check in we're shaking with fear and climbing the walls and only calm down after we've had a chance to connect with others who've all been there and know what we're gabbling on about! Then we realise we're not alone on this scary journey and gradually calm down. My only difference is I went through all of this last year and had to go everywhere alone due to Covid, and didn't have my hubby with me when the bombshell was dropped. Looking back it was surreal, I felt like I was on the outside looking at it all happening to someone else.

    I went back to see my Oncologist approx 5 weeks after surgery & he discussed my results. Up until then I took it easy not lifting or bending, got away with hoovering for ages LOL. So don't overtax yourself even if you feel great, listen to your body! I was back to walking my little dog ( with an adapted poo picker) in about 3 weeks and gradually back to 3 mile walks within 5 weeks over


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  • OOps, sent before finishing!

    I drove myself to my Brachytherapy, exactly 6 weeks after the op - don't forget to check with insurers when you can drive.

    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 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’s always good to talk and the Macmillan Support Services provides lots of information, support, financial guidance or just a listening ear. It's free to call on 0808 808 00 00  8am to 8pm, 7 days a week. Have a look to see what is available by Clicking here .

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

    Sending you welcoming hugs, Barb xx 


    Community Champion Badge

    Womb cancer forum

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm

    "Never lose hope. Storms make people stronger and never last forever” - Roy T Bennett