thank you. It’s certainly helping speaking to you lovely ladies and knowing you’re going/gone through the same thing xxx

Hi ladies

Just found this thread and thought I would add my experience. I’m the other end of the journey from you and have just had my first post treatment follow up where I was told there was no sign of cancer. 

I was diagnosed in April 2018 with endometrial cancer after scans and hysteriscooy. I had keyhole surgery to  remove everything in May 2018 and stayed in hospital overnight. I had a second op to remove lymph nodes in July 2018 again an overnight stay. Fortunately they were clear and I had three sessions of internal radiotherapy in September. If you have any questions please ask and I will answer based on my experience. However everyone’s plan is different and suited to them individually. 

I hope everyone’s journey goes well Hugs to you all.

Sundial

hi sundial

appreciate your repsonse, x

Good to hear that you are doing well

How soon after the surgery were you able to do things like going out - i have a concert with VIP extras , 3 weeks after the surgery date , i will be attending the concert on my own, i know its not a necessity for me to go , bu i enjoy such events and am using it as my goal after surgery.

I also have other medical conditions that may contribute to a longer recovery - ME / CFS / FM, so hoping these don`t cause too many extra issues.

Post -op pain relief is one of my major concerns as the ME / CFS / FM causes chronic pain anyway and  am on maximum pain relief that i can tolerate for that - so wondering how that will go

After the initial key-hole hysterrectomy, how soon was the radiotherapy started, and i respect your privacy here, but did you have any side effects of internal radiotherapy

Am very concerned about `the menopause` symptoms, i am 47 years old and have had random symptoms for approx 6 months, but no proper `period`, 

tks for response and info, its much appreciated

xx

Hi

i recovered pretty quickly. It took me about four weeks to really be back to normal, I still got tired and outings were good but tiring so I made sure I rested the day before and the day after. I had a problem with one of my wounds infecting and had to go back into hospital overnight for IV antibiotics so that slowed me down a bit. I’ve also been type 1 diabetic for 57 years on insulin injections. However I managed to sort that out pretty quickly. I don’t drive so can’t tell you about when you’ll be fit for that so it might be worth considering other transport means if you can. Also a good tip is to do the exercises they recommend and try to walk upright. There is a temptation to lean forward which I did unspwiitingly and it left me with a painful lower back. 

As for pain I suggest you discuss that with your surgeon, I was fortunate in that I had very little pain and paracetamol was enough for the first few days. although I know some people have more pain so it’s worth discussing it, They gave me a spinal injections before the general anaesthetic which I think was intended to reduce pain. It certainly worked in my case.

i had internal radiotherapy which I believe is usuallly carried out at about six weeks after surgery.  Mine was slightly different because I had to have a seconded op. Internal radiotherapy has fewer side effects that re usually temporary. I had a few issues with constipation which was soon remedied, I believe there can be temporary uribary issues but I didn’t get any. The RT itself is painless. I hardly knew anything was being done. However it is a leave your dignity at the door occasion. Lol. It actually sounds far worse than it is.

i had already gone through the menopause so it wasn’t an problem for me. Again discuss it with a specialist nurse. There are meds’ they can give you if you need them, 

Will you see your consultant again before surgery or do you have a specialist nurse contact number? It might be an idea to write down these questions and ask them. I found that they are vary helpful.

I hope everything goes well. Please keep in touch. Don’t hesitate if you have more questions, I’m sending a virtual squeeze from my hand to yours. 

Sundial

I’ve sent you a friend request if you’d rather talk through private message. 

Sundial

sorry Subdial

ive had a break from the internet for a week, I don’t have a friend request. Hope you’re well xx 

hi Laney 

how you doing? Been thinking about you. Did you get your results? Xx 

I thought I would reply, as I’m waiting for a second scan, I’ve had some spotting on and off, then bleeding between periods. I put it down to stress, and then had scan and told one side of womb lining is very thick. I was over 2 weeks late with period which is not normal for me. They want to rescan and have one on the 9th May. I’m so worried. I lost my mum who is 64 7 months ago to uterine cancer, and then my dad died 7 weeks ago at 67. So stress has been full on so that’s what I thought. It’s just the not knowing. I’ve been having lower bk pain, niggly pains on and off in pelvic area, not sure if that’s just me over worrying though x I’m 41 this year. 

so sorry to read of your situation with losing parents. It is the waiting and unknowns that eat away at my brain and I have imagined all sorts of pains etc. I lost my father in Feb and then had a period. But I am post menopausal so that shouldn’t have happened but I put it down to stress and just “mentioned” it at GP appt for a persistent water infection - and that’s when it all kicked off. All womb lining is too thick and specialist talks about a “mass” in the womb - that worries me. However I know it could be other things too and that I’m on cancer pathway as part of NHS protocol. I hope your scan is positive - ask all the questions you can think of as that’s what I didn’t do and wish I had. 

X