FF - Great news re Stable Mabel!
I've just taken my first dose of ribociclib, am officially on the trial!
love JT xx
I am on the same meds as you and have been for 4months now. The pain I have in my right hip turned out to be arthritus, this was found after a scan. Ask your oncoligist for if you can have a scan just to put your mind at rest, I did. I have secondry bone cancer on my scull and spine.
I had a bit of a blip with my blood test 4 weeks ago as the cancer markers had gone high. Oncolygist said it could be that the med are not working, but good news the next blood test shows the markers had gone down and she said that this happens sometimes and said meds are working. What a relief.
It's not plain sailing all of this but we have to get on with our lives. Some days I feel so well and forget I have it and others, like today , I feel good for nothing. I had a great day yesterday and got quite a lot of jobs done I had out off and today I am suffering for it.
Sending Love, hugs and kisses to you all out there,
Such wonderful news funny face, what a relief. I had scan on Tues so I am now in worry land !! Enjoy your weekend and let's think positive you will have Christmas etc off from all these appointments xxx
That's fantastic news Ff. What a feeling it is as the anxiety floods away! Enjoy your new job - sounds good.
Yay. A stable Mabel 😊, We all know the strain that scanxiety gives us so I'm hoping you had a fantastic nights sleep and ready to face everything in the morning. Your new job sounds great as well. As to planning ahead around the next scans that's my type of gal - treats and celebrations 🎉🎈🍗🎄
Stable Mabel has her elbows on the table!! Trying to hold my head up. I haven't been sleeping well and I'm not allowing myself a nap! Maybe I will settle down now that my stress is getting less!! Dr thinks my post nasal drip is from whatever I'm allergic too. Lung mets were either stable or a little smaller. She did say this radiologist said that the lymph node in my clavicle had reduced in size. She said she went to look at the CT herself and do a comparison. She said she really couldn't tell any difference in size and wasn't convinced it was in it. Will be watching it. I get to go back in 3 months!! She is keeping me on the same dose. Crossing my fingers that when I go back in 3 months that I'm stable again. My appointment is Nov 9th and if I could go another 3 months I wouldn't have to come back til Feb. I would be free from appointments for Thanksgiving, Christmas, New Year, and hubby 's 60th. One can dream!! FF
Good luck Jellytot! You have been through a lot and I'm hoping things calm down for you. Hopefully this drug works as well as pablociclib has for others. I'm not sure if I have ever had a panic attack or not, but I have been frazzled and completely twisted!! I'm betting your hormone level through you into it! I will be holding your hand! Hugs!! FF
PMOL, good news! I had my ovaries and tubes removed on 17th July, so please ask if you need any information.
I'm a week into letrozole and so far, not too bad. Combined with the immediate menopause from my oophorectomy, I thought I was going to be a total wreck but I'm actually doing ok. I did have an awful panic attack on Sunday, I've never had one before, it was crushing and terrifying and lasted for about 2 hours. I'm not sure if it's a side effect from my meds or if it's just my body's way of going "holy hell you've dealt with a lot in 10 weeks", either way, it was not nice at all.
Tomorrow I'm off to see my oncologist about my trial drug Ribociclib and all being well with the scans I had last week (CT and bone), I'll be starting the treatment. When I had my bone scan, I could see the images of my skeleton. My ribs didn't look as lit up as before, so hopefully that means the radiotherapy did a good job. I could see my hips lit up though and they weren't like that before, but having not been on any systemic treatment (until last week) and knowing I've had a lot of pain there, I'm not surprised. What I saw could have been the new spread in the lumbar region my onc told me about. He said that treatment will remain the same and if the pain gets too bad, we can discuss rads there too.
Anyway, please cross fingers for me for tomorrow, I'll let you know how it goes xx
We can't tell whether we should worry about pains or not but they are not always symptoms of progression. Didn't have much pain with tamoxifen but have more with exemestane, Earlier this year I developed new hip pain, shoulder pain and in my head (the fact that my routine appointment had been postponed didn't help) but a scan showed no progression and i started to feel better. It's hard not to but don't assume the worst..
Wendy, Enjoy yourself! Then you can return relaxed and ready to get answers!
Mollymop and Carolyn, Thanks for the support. Today went well at the job. Went around and talked to a few residents and got them to engage in conversations, coloring, bingo marker painting, bean bag toss, kick ball, and a ball toss. I'm off tomorrow! I do think it is going to be a fun place to work. The more I'm there the more I realize how relaxed of a place it is! I'm ready for my results tomorrow!
PMOL That's fantastic that the cancer isn't spreading quickly! Good luck with radiotherapy! We all have So much on our plates.
Hello ladies! Some kind of good news!! Today I had a call from my onc who said that after speaking with other 3 MDT's they have decided that I am on the right path BUT the best news was that they reviewed the scans and the cancer hasnt progressed as fsast as they had originally thought 😁😁😁. So still on exemestane and zoladex, will have radiotherapy on spine and a chat with spine surgeon anyway...
also he mentioned about having the ovaries removed by surgery so will probably need more info abuot that too!!
anyway, good night 😴😴😴😴😴❤️❤️❤️❤️
Wendy, Yes we all experience new pains. Sometimes it just goes away, sometimes it's something else and sometimes it is progression. No way of knowing until it's checked out. I would call and see if they want you to come before Sept. Good luck.
Renee, That is a dreadfully long day for a two hour appointment. You are a saint being so patient!! How sweet of you to make lunch for your DIL. It's good for both of you. Wish I lived closer so I could take you for your appointments.
Carolyn and Bon, Sounds like a great setting for lunch! That's great you can get together.
I know I need answers, but not looking forward to results. I just don't
think I feel right. Feel that my breathing isn't as good. Unless my imagination is working in over drive. I will say though that my knees have calmed down a lot!
I finished two days of training! Ten hours of watching movies and signing papers. Today I actually start learning the job. I'm sure I will be fine. It is only 3 hours a day, 4 days a week. I figure I can get through 3 hours. My old job was 4 hours a day, 3 days a week. I'm going to miss my Tuesdays off! Thinking positive! I got this!!! FF
hi carolyn ,
pleased you enjoyed yesterday,and yes the weather is dreadful here as well ,terrific rain showers then hot sunshine ,very strange to say the least.
went for my treatment monday ,best said soonest mended ,i went from the house at 11am and my son brought me back at 8 30 ,this was for a two hour treatment ,just waiting around the rest of time,so i was not amused at all,as you can imagine,apparently they have amalgamated two clinics into one.?.
go to onco on friday so will mention my knee and see what he thinks and will let you know .
will depart now as have daughter in law coming here on her lunch break ,i just do her some soup and a sandwich,plus a yoghurt so she is easily pleased
take good care
thanks forr your comment ,i do try to keep cheerful ,but hard sometimes ,just waiting for the ambulance to arrive and take me for treatment .
your wedding sounds wonderful.
take care .
Ff, good luck with your new job. You'll be great, lucky clients! Hope you get good news from your scan and your dobts about e&e are unfounded. Will be thinking about you Bon x
Hi girls! Excited and nervous! I start with orientation for my new job tomorrow and Tues. I start work Wed . I will planning programs for dementia clients. I was hoping to get away from "dementia" but the hours are perfect and weekends. I figure I will see what happens. At least I got my foot in the door.
Tues morn I have my scan. Thursday results. I really don't think this treatment is working. God news is the rash and itching is calming down.
Had a great weekend on the bay. Twelve of us got together for a party day and 6 of us stayed. Blew up air mattresses and slept in the living room. Felt like a bunch of giddy teenagers. Was good for the soul.
Kirky, I have a lot of foot pain from exemestane, have been walking round London, ouch, but went to a fabulous wedding, my nephew's at the House of Commons, reception on the terrace (has a marquee roof). Another side effect for me is chronic insomnia. The hotel where we were staying promised a good night's sleep or your money back. I didn't think it was fair to penalise them for my sleep problems but at 2.30 this morning i heard what sounded like very heavy rain. It wasn't, there was water pouring through the ceiling. Perhaps I'll get a refund.
I only found out about my bone mets because I had a CT scan for a gut problem which turned out not to be a problem. Goodness knows how long they had been there or how long it would have been before I noticed something and then whether any doc would have taken it seriously.
Suze, a slipped disc is no joke, Iv'e had one and ended up having an operation. Hope you get the treatment you need soon.
Renee, hope you get some reassurance at you appointment, you are truly inspiring and lovely to know
Hugs to all Bon xx
hi again carolyn,
i have just read your last post and how right you are about people being in a chair and others thinking you are deaf ,some even think i have dementia as some nurse was explaining something to me ,she was on her knees ,talking so slowly as if i was a child ,then said ,would it be better if i wrote it down for you,arghhhhhhhh how i didn't hit her i dont know,but now if anyone attempts in the slightest i just say,hey i have lost my leg plus have cancer ,but not lost my mind ,it does so annoy me .
Hello ladies. Thank you for all your lovely comments about my good news. Pippin, I did leave like a bat out of hell but my heart is still on this site. I keep up to date every few days because in such a short time I got to know you all so well.
It has been an experience joining this site and tbh I still wonder whether the doctors are right.
I'm no longer on Letrozole and can tell you that my aches and pains have reduced considerably so Carolyn was right about that causing the most pain.
Still waiting patiently for them to deal with my slipped disc and yesterday attended my first music festival using a mobility scooter for the first (and hopefully last) time. That was an eyeopener as well. Spent quite a bit of time being ignored and feeling lonely because couldn't get in with the crowd. But I blinged up the cart, covered my head in flowers and once I'd mastered the controls, shot through the crowds with a huge smile.
I know I'm lucky and I've had an insight into how secondary breast cancer feels but I still belong here albeit as an outsider looking in. I still feel your triumph, scanxiety and pains. And I will be watching, laughing with you and crying from frustration that I can't help.
Much love and cyber hugs to you all. Sue xx
i had to have someone in to decorate for me as could not manage from wheelchair,and didn't tell family until had arranged a decorator ,or they would have said they would do it ,but i get my disability benefit so pay from that ,i had my staircase done and wet room ,ceilings ,walls and 8 doors ,he charged me £ 200 which i was amazed at so having him later in year for kitchen and lounge ,but as you say it's the upheaval for these rooms.
dont know what to think about my treatment carolyn ,have had 8 out of 18 sessions but breast gives me pain now ,not a lot but there and dont know if normal or trearment not working,but see onc on friday so shall ask him and also mention my stomach and back which my doc said was the cancer spreading in his opinion,so shall be pleased when this week is over .
take care and thanks for your on line company.
a happy sunday to you too,we had rain all night long so everywhere soaking ,hoping it stays away now as have my treatment tomorrow then oncologist on friday ,not looking forward to tomorrow as an hours drive each way ,but hey no other choice ,my appointment is 1pm but have to be ready for ambulance by 11 am and usually quite a wait before the actual treatment comes to the ward,
hope you are well and feeling ok ,have you chosen your new carpets yet ??or did you say in the future ,my memory is like a seive at the minute down to old age i suspect haha.
take care of yourself .
Thanks Carolyn! Now on exemastane. Had an emergency mri as question on stability on my spine; going to speak with spine surgeon as they decided it was not urgent, having radiotherapy and trying to get into palbociclib trial... and been signed off from work for 4 weeks so 'enjoying' the summer holidays 😅🌧🌧 xxxx
Hi everyone, haven't posted on this forum for a week or so, as I mainly use another forum now. However, I missed all of you lovely ladies so have caught up with the last few pages. Has anyone been to a breast cancer meeting ? They're having one in Maidstone on Monday, came across it by chance ( pressing wrong button on IPad).
Ive got extensive mets in my skeleton including my entire spine. I'm fortunate in that I have no problems in my spine. The reason my spread was found is that my GP thought I had Piriformus syndrome. Eighteen months later it was found that I have extensive bone mets. Apparently, the original treatments hadn't worked so I'd been walking round about 8 years, without any real symptoms.
Funnyface, congratulations to you. I told you there would be a new pathway for you. You will be sorely missed I'm sure.
Welcome to newbies, you'll find loads of support on here with these gorgeous funny ladies.
Now then.....yesterday, after I struggled home(well, hobbled actually)
I Sent an update on my trek to the RA Summer Exhibition....and lost the lot!
anyway.....sadly Ramade stood me up! hadnt got my spiky ball with me, I had to keep
prodding and kneading My left cheek in order to be able to keep going......goodness knows what the hordes of other people thought! Anyway, I just knew Carolyn would like some pictures, as it was an exhibition....so here below, we see in first place.....the spiky ball, next ..the RA, and lastly,...the welcome very very welcome, sight of my bus appearing, to take me back to Victoria station! Boy Was I grateful to see