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
What great news! Really pleased for you spirits. I hope you start to feel better soon. As for the pain in your breast maki, it should get better with time although it can take months to feel more normal. I still have a lot of pain in my breast but I have lymphadema. I hope your app went ok today n I'm sure we will be able to help you through it.
I still feel quite strange n my energy levels keep nose diving! I did the race for life a week ago n I still cant move much. Haven't been out since n spend most of the day n night on the couch. I'm so tired n can't pick myself up. Starting to think something sinister is going on! Its over a year since I finished chemo n 6 months since I finished treatment altogether. Periods started again a few months ago to my dismay. I feel like poo! Felt better a few months ago than I do now. Any ideas why I feel so ill?
Hope this finds you all well n lots of love always.
Sorry to hear that you are feeling nacked, please don't ignore anytning, we know our bodies the best and if you think something may be wrong ask to be looked at. I hope that today your energy levels are higher.Please let me know how are you. I just hope that maybe you did too much and it takes some time to recover.
I was with the onco yesterday and it seams to me this will last forewer I will have 6x3 weekly FEC-T, Hamptum ( i think thats the name) 3 weekly x 17 that means for a whole year, RT and tablets
I went shopping yesterday and on my way back just burst crying. I am traying so hard to bottle it and be strong and carry on as normal but its hard at the mo.
Have a lovely day and again I hope you are feeling better
I went through exactly what you have got to go through last year, and I have 4 more herceptin treatments to go, my last one is in October. I have had the FEC-T and the rads and am now on the Femara tablets. The herceptin is not as tough as the chemo, it makes your muscles ache and you feel tired but nowhere near as bad as the chemo. I am not saying my body has returned to normal - it never will, but I am going to pilates, yoga and power walking now so things are much better. Yes you do feel knackered at times and a bit down in the dumps but I am having more good days than bad now.
I know it seems a long haul of treatment and I thought the same as you last year, but it has flown by and you will get through it just like I did and so many others do. One bit of advice ask for a PICC line - this is a line they put in your vein and it stays there whilst you are having your chemo, it will help your veins as the chemo can make them go tough and show up on your arm. The drugs are then administered through the PICC line. The herceptin is not so harsh on your veins and I now have that straight in the veins when I go. the oncologist said I shouyld feel better again once the herceptin has finished - cannot wait!
It is good to cry - it helps relive the pressure - so don't cram it up let it out.
I have just been catching up as I have not been feeling to clever lately, what with aches and pains, tierdness etc etc a bit like all of you so my oncologist has stopped my Tamoxifen for now and I had a bone scan yesterday. This was after having a Doppler scan blood tests and so on, I am so scared of the result but have an appointment with him on Friday, fingers crossed all will be okay. We think all the worry is over after all the treatment is over but it just doesn't seem to go away, I could cry and cry but I am determined that this is not going to beat me, I WILL NOT ALLOW IT TO. There I was looking forward to my reconstruction in January now that might all be put on hold.
Well sorry for that rant but I feel so fed up but I know I should be greatful for being here unlike some of our very good friends may they rest in peace.
Well what else has been happening with you all, I am hoping to book a holiday on Saturday for over Christmas if not to expensive otherwise it will be November and early December.
Tony where are you as I have not heard from you in a little while.
Lonie sorry to hear that you are having a difficult time at the moment as you are always so full of life on here
Caroline how are things with you, I did read your message is all okay still with you.
Well all you other lovely people out there a big hug to you all and take care
What a load you've been going through! Make sure you let us know how things go on Friday. I'll keep my fingers crossed for you, as will everyone else, I'm sure. Moaning is good ,as, at least it keeps you alive! We're all her for you,as you know. Got my oncologist appointment next week so sure I will undergo numerous tests as well, although I've been feeling a little (minuscule! I'll be back online tomorrow when,hopefully, I'll be a bit more alive!!
Well went back to the hospital for my results from Bone Scan on Friday and they were not there, not happy as you can imagine. My oncologist bless him was going mad and tried to get hold of them but unfortunatly the department was closed., I am now waiting for a phone call yes a phone call Monday morning from him. To play safe he has also booked me in for a full body CT Scan but am not allowed to go back onto my tablets yet, this worries me as my BC was hormone based.
I am so angry hence why it has taken till today to come back on here, how are you souppose to carry on, waiting for this phone call. The pains are just getting worse all the time, he is also checking my thyroid, he says it may be a process of alimination to find the problem. I have heard though that chemo can bring on arthuritus and ostioparois (sorry about the spelling), has anyone else heard this?
Well thats my moan of the day sorry about that
Lonie how are things with you, hope your feeling better
Tony I hope you are okay please get in touch
And all you other lovely people a big hug is sent to you all, please take care
I went for my 1st dose of my 2nd cycle 2 wks ago (hope that makes sense) & I was telling the Dr I had been having a lot of pain in my R.arm,she informed me it could be osteo whatsit(sorry can`t spell it)brought on by chemo I was puzzled by this but as she didn`t elaborate on it I didn`t push for more info,but as the prob is still there I`ll be asking her next wk she also said it may be the cancer from my shoulder,I`ll keep posting to keep you updated can you please do the same.Love Kathryn
Sorry that I have been neglecting you all....I have been a bit of a hermit and although I have a few illness related problems I am pretty much in denial for the moment. What with the ulcer in my colon that needs surgery and a permanent stoma...I am waiting on the results of my last CT scan to see how the chemo is going..Last time it was a 20% reduction and I am so waiting for similar or better....I hate this cancer and will do my best to keep my chin up however as I am sure you know it can be pretty tough at times.
Sis I hope you have had that phone call n had some good news. It's awful that you've had to wait but I'm hoping it will be fine n one less thing on your mind. I know you will let us know when you can. Thinking of you n wishing you the best.
Tony I hope the ulcer on your Tongue has gone or is going. Can't imagine how your other ulcer feels! You are always in my thoughts n I hope so much it's shrunk more. Keep up the fight big man.
I have oncology on Wednesday. I don't feel any better really. Energy is just non existant. Hope they can help me feel better. We'll see. Hope other ladies are feeling ok. Maki how are you?
Another newbee here. I was diagnosed 2 weeks ago after finding a lump. I have a large lump maybe 4cm on left side and cancer cells in several lymph nodes. Scans show rest of me is clear it's early at stage 2. I'm starting chemo tomorrow and I suppose I'm just scared. I think I know what to expect but until it happens i still feel in the dark. I'm 36 my boys are age 5 and 2. My husband is finding it tough. We were living abroad we've come home because of this and right now we don't even have anywhere to live we're staying with family I don't feel in control which I hate!
