here it is xx
Srilata, sorry you've had to change mets but hopefully you will do well on fulvestrant, others seem to. As for skin cancer, I have had 7 cancers removed from my face and head last year so maybe we have a similar cancer that goez to the skin. Stay well and stay brave
Hello everyone...yes am on fulvestrant and was very apprehensive as I don't like injections...but these have so far been fine..do join the thread Carolyn mentioned...it's so lovely to have buddy's to Travel with xx
but keep up on this one too...it's a great thread and we all have such fun togetherxx
Glad to hear you’re feeling a bit better. I asked and was told, my trigger finger is nothing to do with my bone mets, but is almost certainly due to the Letrozole. It’s very difficult to be sensible and positive all the time, I got my scan result on Wednesday, appointments were running late and the HCA asked to speak to me, my immediate response was, what’s wrong?? Poor woman kept apologising as she thought she’d panicked me, fortunately I’ve seen a lot of her over the last two plus years and reassured her she’d only have to look at me and I’d assume the worst when waiting for results!! At least you don’t have too long to wait now, take care, Kxx
Thank you all for your reassurances, I'm feeling a little less scared now. Sometimes it's hard to be positive & sensible all the time. Most people seem to think my thumb problems are unrelated to cancer. Still it's a bit annoying as I have quite enough pain to get on with without other bits of me falling apart. Sometimes I just wish for a break in all the pain. The reflexology is good for that, roll on next thursday.
Srilata, I get a slight rash here and there from this treatment. I'm also very itchy on my legs, back, arms. I scratch myself in my sleep and wake up all clawed up. Onc told me it doesn't look like a rash from these drugs. Well, I disagree with her bc I didn't have this before these drugs. Also, I stopped this combo for 2 weeks to see if my back would quit hurting and I wasn't itchy anymore. Back on it and itchy. I didn't notice any difference in my back. My onc said she never heard of back pain as a SE for this. She needs to read! The two weeks I stopped it to see if the back pain would ease up might not have been long enough. When letrozole failed and I switched drugs it took about 2 months for my knees to quit hurting. Good luck! FF
Thank you Carolyn, Dragoncarine and Rosie, I love Thanksgiving. It doesn't involve all the decorating and pressure of presents. The food and company is awesome. I find it very relaxing. FF
Hi dragoncarine, afraid I can’t offer much help other than appreciating how uncomfortable trigger finger can be, as I get it from time to time but not as badly and haven’t needed any treatment so far. I know it’s a side effect of Letrozole but not one of the more common ones, I’m on Letrozole so assume mine is down to that. I knew treatment is steroid injections, as I asked my GP in case I should need any and I heard a doctor talking about it on the radio who’d said the same. That makes me ask, would they use them if they encouraged mets??? I really don’t know but would certainly hope not, or at least they would make patients aware of it.
Sorry I’m not much use and appreciate it’s easy to say and hard to do but do try not to worry too much, do you have any idea when the MRI will be? Btw thank you again for the book recommendation, it arrived yesterday and glad I ordered it. Take care, Kxx
Hi everyone. sorry to be a bit negative but I'm feeling really down at the moment. Went to see Orthopaedic chap today about my thumb because 2 oncologists and 1 radiographer were quite convinced that the pain is nothing to do with my bone mets. and more likely to be a returning of the trigger thumb I had diagnosed, and successfully treated in feb (before I knew I had bone mets). Feeling is different this time and specialist decided that my hand needed an X-ray which shows up something on the bone, so now waiting for MRI scan appointment. All sorts of questions:
1) was the original trigger thumb diagnosis actually wrong and it was cancer all along?
2) could the cortisone injection I had to treat the triggering have someone "encouraged" the cancer to go into that area?
3) Why is everyone so sure it can't be another bone met - what is it then?
4) And I know the answer to this one: should I just try to relax and not worry and wait for MRI result?
PS most of the time I'm really thankful for my life and the good things I have. I think thanksgiving day is one of America's better ideas 🙂
Thank you Bon and Moijan! We are going to my daughter's FIL. He is about 2 1/2 hrs away.I work tomorrow but I'm making a turkey and all the sides on Saturday.I love having the left overs for a few days. I'm trying to be good though. I'm down 95 lbs. and would love to make the 100 lb mark. We are about ready to leave and I just went to put on my dress coat. OMG, I can't wear it.It's so big the sleeves are hanging past my finger tips.Not to mention I would need to tie the waist with a rope to cinch it in. It's hysterical. Guess I will be wearing a fleece jacket. Hubby bought me a new ski jacket type coat for Christmas and said I can have it if I need it, but I'm trying to wait. I never gave my dress coat a thought. I will have to look for one on sale. FF
Yes FF, so do I. Love to you.
Bon, have pm'd you xx
best wishes to everyone...btw, I've started carrying the blue strepsils around in my handbag now as everyone I meet seems to be coughing and spluttering..went to see my go today and the poor receptionist couldn't speak..said there were loads of staff off with it.
i tend to carry' first defence' around in my bag always too as it does clot any bugs which reach the nose and stop them multiplying.... has worked for me for about 16 years....only get colds when I forget to squirt it into the sides of my nostrils,.... well worth a try.
love and best wishes
Silrata, When I had ny scan in Aug my Inc said that it mentioned an enlarged lymph node above my collar bone. She said she looked at my scan herself and didn't really notice it. I was freaked but didn't want to ask questions. When I had my scan results 2 weeks ago she didn't mention it and I decided not to ask. She also didn't elaborate on my scan as much as she usually does. I kind of didn't ask since it is holiday time and granddaughter to arrive in Jan.My next appt and scan is in Feb. I will ask more then! FF
i understand how scary this is for you. The only thing I would say, is that Consultant Oncs are, by the time we see them, pretty experienced physicians, and altho oncs can get things wrong....I think that if he were certain it was due to bc he would hopefully act to treat them....also, if they are painful, that would sound like they could be due to infection...let's hope so. Have you checked your temp?
nowadays, these very expensive pet scans can pick up cancer much more expertly than before and with any luck it's an infection. Yes googling can be very scary...and make things sound definite.....I did that in the summer, thinking I'd got skin mets round the scar, but they turned out to be from the rads I'd had yonks ago.
very best wishes for some good news.
I really don’t know anything about this Srilata but just as a suggestion, did you have any bloods done? Only with infection often your white cell count will be raised. Not saying if it isn’t it isn’t infection but it is an indicator. Sorry I can’t be of more help. Have you tried asking your breast care nurse? That said, ones I encounter never offer me much support! Or your GP? Hope you get things sorted soon. Kxx
Hi Juma, believe it or not, oncs are often very pleased when patients seek a second opinion...the job carries a load of decision making responsibility and they welcome patients just exploring wether there are other options.
just to say tho, Cape IS a very effective drug and if you look on the 'Capecitabine your top tips please' thread, you will find that some people, like Barton. Have had their bc controlled on it for a long time. I had it for about 21months before having to change but there are some who find it works much longer. You are also fairly needle free as it's a tablet.
best wishes and good luck
''see how well you managed her!.. yes it's very unheard of for that to happen......maybe she has had her own troubles (been wrapped up in them)and your feedback gave her just the kick in the *R** she needed
I think you might find she is very different now.....hopefully. I realise you probably feel a bit awkward in seeing her after your 'frank feedback' but it could be a good idea to give her one more chance before changing.....I know doctors can be missing the rapport gene....but you could change and then find your new onc is worse in some other way......just a thought.
i know the Christie is excellent and loads of oncs, but In your place, as you say, I'd give her another chance...it is really very hard changing and a lot of internal stress - I have a feeling she may now turn out to be very responsive.....they worry about getting complained about .
best of luck
Hi Juma, I am interested to read your post because I was told I had a spread to the lung following a ct scan. I was in a lot of pain in my hips, shoulder, could barely move my arm. So I got an opinion from a different hospital who looked at the same scan and said no lung spread but extensive bone mets. I got a gp to refer me to that hospital where I have had a lot of radiotherapy to save my spinal cord. I don't want to mention the names of the hospitals just to answer your question-for me it was the best move I have ever made.
Oh and Rosie,
try setting out all your questions on paper or your iPad, you can then hand it over. I'd also take a advocate with me...a hubby, friend etc to note down replies,xx
You know what Rosie, well done! I changed my surgeon because his bedside manner was appalling.
i found it a relief, but also a bit stressful because I wondered if the next guy would then worry that I would complain about him! However, the surgery bit passes quickly and now I'm under a lovely onc and I guess they know too about the change, but it's about 16 years ago.... so I may have lived it down!
As you have tackled your doctor, you might find she is completely different next time...you could go along and just see...are there loads of hospitals near you? I mean maybe do a bit of research first before acting.
in the south we have quite a few options, but I still asked a senior nurse friend who worked in the field and she recommended my new surgeon as she had heard from quite a few ladies, just how very nice he was....and he was too. Sadly he died a few years after that.
best of luck with it xx
And you ff, hope you're improving.my mum does armchair aerobics at her home, maybe your people could try that, not too taxing on the back.
Thanks Bousy good to hear that, mine was in 10 vertebrae so I shall try to stop feeling so anxious for 2 weeks at least. Thanks for replying. Hugs
I had rads to L2 of spine last Christmas and was told 8 weeks for pain to go and it was 8 weeks exactly. Hasn’t recurred since. Good luck , Hope pain goes.
Hi there, has anyone had radiotherapy to thoracic spine, I finished this treatment 6 weeks ago and am in more pain now than I was just after. Am on painkillers but getting very anxious that itshould be better by now.
Hello, ff, I am glad to hear you haven't got compression fractures, but it still leaves the mystery of what is causing your pain. I do hope your pain is sorted out soon and proves to be nothing sinister.
Carolyn, I'm still going to work. I missed 2 days when it was real bad and last Friday when the ulcers were bad. Not sure if they were from meds or a virus. I'm just careful what I'm doing at work. I have limited the active activities. No balloon volleyball, parachute or waving ribbons and ties. Lol as simple as these sound in involves a lot of twisting and me bending to pick up a ball every few seconds. I'm going to start putting them back in the program, but for less time. I need to build myself back up, but not til I get my MRI. FF
Thanks Silrata and Barton, I have improved over the last few days. I have kept moving but being careful what I do. No stretching or twisting! X-Ray showed no fracture. CT said no changes but was compared to the x-ray. Should have been compared to previous CT! Having an MRI on the 28th. Possible bone scan after that. I feel it could even be a small change that might have out pressure back there. Before I got real bad off and on I had burning feeling there sometimes.
I know not everything shows up on scans.When I first started with mets I had a ton of post nasal drip, coughing from it, and this weird sneeze. If I was active I would clog up so much I would get sick. The sneeze I had would start as a tickle in my throat and I would sneeze out my mouth not my nose. I'm not exaggerating! I could sneeze a 100 times a day. Onc told me he didn't know what was going on but that the lung mets couldn't cause this. I read on-line that lung mets can cause post nasal drip. I went through this for 7 years until they decided I needed radiation bc a tumor had almost closed off my bronchus. After about a week if radiation to my bronchus the lis t nasal drip and sneeze were gone! It's been 5 years! My onc said the radiation couldn't have fixed it. Radiologist said she doesn't know what it could have done but maybe it did. Lol! I know it did!! I don't know how either but how else did it get fixed! So, I believe we are each unique and these drs. don't know everything.Test don't show everything either. FF