hi im 36 mother of 3 n diagnosed dec 23. ive had 2 ops n 5 of 6 chemo n finding it very hard at mo. feel so peed off n cant get rid of that feeling. would love to chat. x
hi im 36 mother of 3 n diagnosed dec 23. ive had 2 ops n 5 of 6 chemo n finding it very hard at mo. feel so peed off n cant get rid of that feeling. would love to chat. x
Hi everyone its been a long time since Ive been on AGAIN because the computer has been playing up AGAIN and its made me very . could do with a new one but this time of year its an expense we can't afford! I've been reading back a few posts but it will take me forever to catch up so wondered if you could all just update me on how you are all doing!! Its lovely to be back in the community I've been on a bit of a rollercoaster last two months and am waiting for the straight jacket to arrive lol!! Seriously does anyone else get really angry!! My anger has been uncontrollable at times with me even smashing a wall and it has really upset me!!
Please be intouch
LOTS AND LOTS OF LOVE TO YOU ALL
Louise
Hi Louise
Sorry to hear you are having problems with your computer and your emotions.I dont get angry because I find it just leaves me feeling worse in the long run,plus my last treatment has damaged my heart so at the moment I cant get stressed.Waiting to see the heart specialist in 2 weeks and when he gives me a magic pill I will be fine.You have been through so much for so long.Can you have some sort of therapy or a massage or reiki treatment to help?Being on here should help to unload so rant away and let us help.No more wall hitting!!!
Stay strong
Rose xx
Hi everyone!
Uhmm interesting topic...like everyone here..mine is secondary breast cancer spread in the pleural of my lovely lungs! I had chemo 2 years ago and my gud feelings thinks i will have more next year.Is a tough journey for everyone...partners,family, friends...I just hope they find a cure for every single cancer. I dont call it cancer ..i call it..."small C", Is so many topics that i can talk about this subject from trying to find a new job living with small c, to check ups and ct scans, hormone medications, etc I am a fighter like everyone here..but sometimes we have blue days....We need to keep being positive guys and I think this is why i coming here too..doesnt matter if i get scared of the b c words...I thinking to start to write a diary but i am lazy...at least for the past 6 months but i am going to try to back to be the active person that i was before...will see....
Hi Nina and girls,
It seems like things are getting on top of us all.Nina you sound like a mirror image of me at the moment.Christmas is my thing,I am like a child and I love it but I am sitting on the settee in my P,J,s because dressing takes up too much energy chomping at the bit .I know I cant expect more as 10 days ago I had emergency heart procedure but I find it soooooooooooo hard to slow down,even after 3 1/2 years of this.We really must be kinder to ourselves and accept these changes but it is so difficult.
Have you tried changing the anti sickness tabs?There are a few different ones and be sure to take them before because they dont work once the sickness has started.,which sorry you probably know.I hate what I am doing to my family as well,I want to be helping my daughter with the grandchildren while she goes shopping but I cant even lift the one year old.But we will all get there.Poor Lonie has been going through terrible symptoms since i can remember.being on here/
We must all get ready for a joint Christmas drink at a set time over Christmas and dont feel bad about coming on here and ranting ,it is why we are all here and as you say it takes the pressure off family.
I hope you get your meds sorted,it drags you down so much feeling low all the time.
Good luck to all lovely ladies.
Rose xxx
Hello and welcome to the place no-one wants to be.
Have you tried writing a blog.If you go onto other topics i will try to bring it to the top .It is really helpful to read and keep note of what you have gone through.Are you on treatment now?
Keep posting .
Rose xxx
Happy birthday tomorrow Colly,Make it a good one.
You could try aloe vera after sun on the redness,i found it worked well.
Rose xx
Hi Rose, its sat my birthday, but thanks very much. I did mention using aloe vera but hosp really against it, they only want me using simple soap and aqueous creme, until at least 2 weeks after treatment is finished, cant believe how quickly my treatment has went by, im blessed to have been in touch with so many nece people on this forum xxx
hi nina
just wanted to say no 5 was my worst time, n was when i started this page. so glad i did. it might help if you go back to the beginning of this thread. it might help you understand more about the way you are feeling. wish i had a magic wand. or a cure would do!
feeling sad myself n fed up with it all n bit teary. n my chemo finished months ago. roll on january n the end of chemo.
lots of love leonie xxxx
Hi Colly
many happy returns for tomorrow, hope you get to celebrate in style, dont forget to post a pic when you get your first hair cut, its so exciting hearing how well you are doing, and dont feel guilty because this site is not just to share our sorrows, we all love to hear how well people are doing as it gives everyone hope, god bless you and may you have a wonderful christmas xxxxxxxx
beautiful, truly beautiful and I have loved looking at your gallery, your an inspiration to others.
Lots of love
lee xxxx
Hi there Rose
so glad to hear your feeling a little better, onwards and upwards I say! you really are an amazing lady you give so much strength to everyone even when you are struggling yourself, if angels walked the earth you would definitely be one of them, have a wonderful christmas and a healthy new year.
Lots of love Lee xxxxxx
Hi there Rose
so glad to hear your feeling a little better, onwards and upwards I say! you really are an amazing lady you give so much strength to everyone even when you are struggling yourself, if angels walked the earth you would definitely be one of them, have a wonderful christmas and a healthy new year.
Lots of love Lee xxxxxx