Evening. Very pleased to report made it through my appointment at hospital with make up in tack. No blubbering today. I have not been to one of the make up sessions yet. I will have to look into it. I know they do a great one at Maggie's in Glasgow. Normally I would just drive up (only 45 minutes away) but don't think my chemo brain could handle city traffic at the moment. I have turned into a bit of an inside lane hogger the past few weeks. Taking me twice as long to get to work. Hope se not too bad tonight for everybody. I am FEC3 tomorrow. This is my first treatment without other half here. My two sons are here though. One of them lives here and the other one has come home to look after his Mum even though he has just had surgery and is in a fair bit of discomfort. Feel guilty!!! I should be looking after him. Downside is got music going somewhere in the house, someone is on the x-box fighting WW2 and the dog is barking at the gun shots. Sooooo restful.xx
Congratulations Lainie, what a relief to be getting home!
Just had my first T&C combo and feeling pretty good so far. From my googling i have seen that day 4 is the one to watch out for as it feels like being hit by a sledgehammer/bus/small building so I guess I need to make the most of the next 3 days!
Bettypoppit hope FEC 3 went ok today
So pleased for you LainieG. Have they not suggested a PICC line for you. I don't like it at all but if it is a toss up between this and needles every time I will take it. I had bloods today. They have decided my PICC line is okay for treatment this week. That made me feel so much better. Might not last until number 4 though but will worry about that next week. Enjoy being home.xx
Great news LainieG, so pleased for you. Hope the bloods go well on Weds.
Strange to think we are all now desperate to have the treatment and not have it delayed!
Great news LainieG, so pleased for you. Hope the bloods go well on Weds.
Strange to think we are all now desperate to have the treatment and not have it delayed!
Hi Jingo-X , I hope it goes well today - really interested as to how you get on as I'll soon be on T.
Peta, goodness me - I hope you have a lot of help moving house, I'm not sure I could do it.
Lah21, I hope you made it through without ruining your make up today.
Had my bloods done today, neturophils at 3.3 so all stations go for FEC no 3 on Wednesday.
NanaJane hope your bloos are ok too...
Good luck to all of us having treatment this week......and hope everyoone who had treatment last week or the week before is feeling a tonne better
xx
Re useless arm...
I had so much nerve pain in the weeks following my surgery that I was too scared to let a physio near me. But when it was obvious that it wasn't getting any better and indeed cording was setting in I found this video on the web
https://www.youtube.com/watch?v=5bfCG0Fg-Sk
It's a health professional from a unit in America with a set of exercises for after surgery.
I did these exercises multiple times a day for several weeks and they made a HUGE difference (still do them now and then to keep limber). My pain went away eventually but by that time I had made so much progress I decided not to bother with the physio. I found the key was to push and hold when you feel the stretch but NOT when you feel pain. I have almost full range of movement back, and that's still improving, and I'd say the numb and sore bits are feeling fairly normal now (or as much as they ever will I expect). Massaging the cording (sometimes bits of its made a popping sound LOL) and numb parts also really helped.
You should DEFINATELY ask for a referral to the physio, as they are miracle workers (taught me to walk again after a nasty car accident a few years ago) but I thougt I'd post this as you might find some of these exercises can begin to help you whilst you wait for your appointment. The video is for folk without reconstruction (not sure if that fits you) but I guess a couple of months down the line that part probably isn't so crucial. I think one thing that IS crucial is that when you get a referral to a physio make sure its from the breast unit to a physio who is familiar with post-breast-work as a non-specialist physio won't be nearly as effective (also found that out with my leg, when the first physio admitted to googling my injury to see what to do with me needless to say I got myself a second physio who was the one who got me walking again).
Morning everybody. Good luck today Jingo. I have not slept much. Getting up soon to go in to get bloods done and see about PICC line. Lying here listening to the bin men outside. So resentful that life just goes normally all around. Having a bit of a why me time. Anyway decided I am getting dressed up today with full face on. The nurses won't recognise me. Well at least till I start crying as usual....xx
Thanks for your good luck wishes ladies. Had 8 steroid tablets today so not expecting much sleep.
Peta so glad to hear you will be moving at least - rubbish timing, but when you're in t will feel so much better even if you are on the floor! Re physio I ask my breast surgeon to refer me after my node clearance surgery left me with almost no use of my right arm. Have only seen the guy 3 times, but movement in my shoulder and arm is a lot better and he got me to start massaging all my numb areas every day to try and fire the nerves and I have definitley had an improvement and some sensation returning. Worth doing I would say.
Wish I could say the same for my chemo brain - twice this weekend I have called 'the hospital' 'the hotel' instead...now how could I get those two mixed up!?
The DN comes in to change the dressing she always measures the line that is exposed. It was originally 3cm. Moved to 4.5cm for a couple of weeks but is now 10cm. My sister-in-law who is a nurse says that it is not uncommon for them to move. Due my blood test at hospital tomorrow and have been told it will need x-rayed as it sounds as if it has travelled too far. I know getting it in wasn't the worst part of this adventure but could really do without it. Now worrying they might not do chemo until it is replaced/ worrying about getting it in the back if the hand if they do go on with it. I have only had one go with the hypnotherapist about my needle phobia. It involved a story about somebody confronting a dragon with the words needle,sharp, quick etc. Still petrified of needles but not so scared of dragons anymore.
Hello everyone not posted since last week so hope I have not lost the thread must try to keep up!!!
Debtex the chemo brain! I didnt really believe it could happen until I misjudged a cupboard door to put my boiler on bent down to wrong cupboard cut my eye and now have lovely bruise to match flushed face! Been doing all sorts of weird stuff tried putting the kettle in the fridge the other morning!
Zelda Thank you for your kind words as you say its always a sad time remembering a loved one, we never stop missing them but all the emotions seem to be so heightened while we are going through treatment.Hope the anniversary of your dad passing passed peacefully and you were able to recall happy memories. How is your hand now? its so painful when they can't get the cannula in love and hugs to you Xx
Lainie G Thank you too for your kind words, our pets become such a big part of our families! Dont think I will get anymore so upsetting when they go! I'm so so sorry to hear you are still in hospital and have had such a dreadful time of it Hoping you can rebook your mum and dads special anniversary dinner soon. Don't worry about having a good cry it makes you feel better and helps you to relax down. Hoping by the time you read this you have had some good news xx
Nicnac 15 We sure do get attached to our pets dont we? Glad to hear that your treatment went ok last Monday hope your doing well. The hair loss is so upsetting I can't believe how much I cried but do feel much better now that its shaved, hope your coping a little better now. lxx
Peta So good to hear your news about the house exchange good luck with the move how does the date fit in with the treatment? Hope your doing well XX
Murphy 1963 Thank you for your kind words re my rotten day feeling much better about it now. Did you get over your UTI that can be very nasty hope its cleared. I have found less nausea and more tiredness this time. I know what you mean about leading a normal life again sorry to hear you have been feeling down sometimes the UTI contributes to that as well. All of the treatment and talk of the BC takes over your life rant away we have to get through this anyway we can. It must be very hard with young children its hearbreaking what they have to worry about! My children are both grown up and married but both have young children my 10 year old grandson couldnt see me the other day because he had a bug and could not stop crying not because he was unwell but because he could not come to see me. Anyway thinking of you take care xx
Betty poppit Thank you I am feeling much brighter than last week emotional wise had 2nd treatment friday just so tired lack of sleep through blasted steriods! As you say its all part of lif'e rich tapestry. Hope you are doing okay xx
Jingo X Is it tomorrow you are switching to T and C I know its always harder worrying about the unknown its far more scary than knowing what to expect. Will be thinking of you I know its hard but try not to worry let us know how it goes love and hugs xx
Hi Lah 21 welcome I joined a little late on but group are fantastic and excellent support. Hope when you read this you are feeling much better. It does help to share with people outside of your family I find I have to filter quite a lot its better to let it out here than bottlr it up! I admire you so much for working.
I feel your pain like you I only had one lymph node involved just seems so unfair and so frustrating but we must look at the chemo as a preventative for the future and a battle against this nasty disease. Hugs xx
Nana Jane Welcome to a lovely group its really helped me a lot looking forward to chatting in the coming weeks.
To everyone out there and apologies to anyone I missed have a good week and good luck with those having treatment Im off for a sleep sooooo tired love nd hugs xxx
Nana Jane
Hi NanaJane and welcome to the group - I hope you find it as useful as I have and it sounds like you have done pretty well so far!
Zelda I have been using Ibuleve to rub on to my sore veins in my arm, it does relieve the pain a bit but cant say that the vein looks much better to be honest!
I was due FEC 3 tomorrow but it has been switched to Taxotere at the last minute and I am struggling to get my head around that. Have been taking steroids today to help with any allergic reaction tomorrow (!!?) and been reading anything I can on Docetaxol/Taxotere - Have failed to find much good news unfortunatley so I am preparing myself for a miserable 12 weeks with no 'up weeks' like the FEC. I do hope all the info is wrong and that I can give all you ladies on FEC-T some good news next week!
AMDriver seriously impressed you played golf! I still can't move my right arm enough to even imagine swingng a club gain, but my physio says I have every chance of being able to at some point if I keep doing my exercises.
Good luck and lots of love to everyone for this week. Keep your chins up and take care xx
Hi NanaJane,
you are on the same cycle as me then. I have my bloods checked tomorrow for FEC No 3 on Wednesday. I too have to have the injections after each cycle, though I am told they would be given as a matter of course for the last 3 cycles of Taxotere.
Lah21, how do you know your PICC line has moved? I have one too which I am really grateful for when I hear of the number of blood tests LainieG is going through. So far my line has been blocked but they did manage to unblock it, but said if they hadn't managed it they would remove it and put in a new one.You can do it, we are all here to support you
I hope all the ladies here have had a good weekend - I even managed a round of golf yesterday! - and that we have a good week to come
xx
Hi NanaJane. Like you I followed the conversation for a while before I joined in last week. Made me feel part of something as I have been keeping myself very much to myself. I am due for my 3rd FEC this week. Really nervous about it. My PICC line has moved so I have to go for an x-ray tomorrow but have already been told it will probably need to come out and another one put in. I was in 'bring it on' mode this morningas I walked the dog in the sunshine but as the day is wearing on my bravery is swirling down the plug hole as fast as my hair. I feel for you LainieG. Nothing seems to happen in hospitals at the weekend. Which one are you in?
I feel that I owe everyone an apology for eavesdropping on your conversations for the last few weeks and not making a contribution. I too started chemotherapy in October following surgery and I amexpecting dose number 3 on Wednesday if blood tests are OK on Monday. Unfortunately I turn out to be hopeless at making white blood cells and have a course of injections following each treatment which leave me feeling exhausted just as the nausea is wearing off and end up with back ache. However I don't have a young family to look after and I do have a lovely husband who is taking excellen care of me, so I really feel for those of you who have family responsibilities.
I hope that everyone managed to enjoy some sunshine this weekend, it makes everything so much easier to cope with.