maldives, sorry to hear your news. Hopefully the chemo will blitz the blighters. Let us know how you get on. x
Geezzzzzz Juicylucy, You sure are filling your schedule up with operations! I hope you can get them out of the way before summer! FF
Sorry not replied sooner had a few log on issues and been mega busy with work, wedding planning and appointments. I'm in one piece thankfully after my hol, no broken bones either lol .Thanks for asking...Loved the hol just what I needed but was full of cold last few days But hey ho....
I'm sorry to hear your cancer has spread chicken, but try stay positive and active too ....I find the longer I sit/lay down the more pain I'm in so I'm having to keep active / walking moving about etc....
I see the Spinal Surgeon end of Feb, As well as the Secondary Breast Cancer in my bones I have something else called Myleopathy (Compression of the spine) I think he'll hopefully be talking to me about operating on that....I got my date through for my gynaecologist too which is end of March to talk about hysterectomy....
Keep me updated with how you get on with Chemo, hope it works and chases the little swines away (cancer cells) stay positive (if you can) & active all the best I'll be thinking of you.
Good for you jet setting off around the world, you do right lass.
I am still working at the moment to try keep a bit of normality, but part of me thinks I should just pack everything into a camper van, including my furry babies (My Cats lol) and our lad (My Partner) and bugger off exploring anywhere and everywhere.... The main thing stopping me sadly is finances, but having said that I have been extremely lucky in where I've been in the world work wise for free and what I've done so it's not all bad....
I've been to China, India, Kenya, Dominican Republic, Canaries, Spain, Balearics and done soem amazing things witha nd for my work so I know I've been exetrmely lucky in that respect and I'm very thankful for my experiences.
Keep me updated with your travels & take care
Yes originally they put me on ibandronic acid which gave me bad stomach acid now I'm on monthly Zomat drips..
I am managing at the mo but I know the pain is gonna get worse so I want to try & cope or use lesser pain killers as much as possible where I can before going onto hard stuff.
Thank you for your info
Hi Mulan (only joking - Moijan)
Love your username, Chiropractor is quite a good idea, before I was diagnosed I had deep tissue massages & they worked loads.. unfortunately my oncologist has suggested I avoid massages / swimming / yoga / Pilates etc in case I break anything..
I will speak to him about chiropractor though maybe they can help with my pain too ?
Thank You so much for suggesting it..
Thank you so much for your info.. I'm managing at the Moment with paracetamol during the day and cocodamol at night. (Thankfully this is working-although I do know it's gonna get worse so don't want stronger pain killers at the no) I have been suffering from shoulder/ back pain, but luckily not enough currently to stop me living my life. I'm currently in Austria snowboarding, don't get me wrong I'm a lot more tired than I previously have been & I'm a hell of a lot more careful than I would have been, but other than that I'm currently enjoying every minute of it, whilst I can & I'm ensuring I take my pain killers at the correct time.
I've now been put on the Zomat drip as the Abondronic acid was affecting my stomach acid..
I've also asked to be referred to a bone specialist to see if they'd be willing to operate as my cancer is low grade according to my oncologist ( I also have myleopalacia in c4/C5 of my cervical spine which they say they'd operate on - my question is why not operate on the other affected areas of my spine too ?)
I've Never been one to follow the rules & I've never liked being told what to do & this is no exception! Lol
I'll see what the bone specialist has to say about things & take it from there, I doubt he can do owt, but if you don't ask you don't get..
Welcome Juicylucy, I'm not very helpful with bone mets. I only have one which doesn't bother me. It remains stable. My issue is lung mets. There is a lot of peeps with bone mets on here. I'm sure you will find a wealth of info. FF
it seems the others have got this all covered, good advice I cant really add to xx
i just thought id butt in and say that I have bone mets too and I often go to my chiro..she usually sorts out my pains...which appears not to be related to the mets...but to my posture both during the day and in bed.., which gives me sciatica quite often!
anyway she does sort it and has given me lots of tips too. Often my pains are due to added stress.
Hi Juicylucy (what a great login!) and welcome to the secondaries part of the forum.
Youve had some good advice from Snoopy and, like her I'm assuming you are on one type of bone strengthener? This in itself can help with mild bone pain but other medications such as pain killers might be needed if it's bad. I've had bone mets for nearly 9 years now and mine have never caused a problem with pain, just the odd tweak every now and again so it doesn't mean just because you have bone mets that pain will follow. If it is really bad then radiotherapy to that specific spot can help and a few ladies have had this. The pain tends to increase for a while after the rads but usually it settles down and has obviously helps the ladies that have had it.
If you want to join in with the wider Bone Mets community on here there is a thread called Bone Mets please join in, which is very active and therefore informative and supportive.
I've recently been diagnosed with secondary breast cancer in the bone and need some advise on pain relief. Idea of what to expect with radiotherapy, what has / has not worked etc...Basically anything and everything....
Can anyone help ?