Painful or not?

Hi

Having my first chemo on Wednesday. Been experiencing a dull ache and tingling pain in the tumour area. What has confused me is that most posts I have read say that breast cancer is painless.

When I first went to the doctors I was convinced I did not have cancer as my breast was painful. I thought it was a cyst.

 I keep thinking the pain I am having now is the tumour growing and will the chemo ease my pain. Has anyone else experienced this?

Best wishes

Parents
  • Hi Sandradee, just wondered how it went with your first chemo on Wednesday. Hope you are feeling OK. Xx

  • Hello feeling dreadful as in a hospital bed as I type. Thursday the chemotherapy helpline told my partner to contact A& E as I was experiencing terrible headaches and vomiting. I was blue lighted and put on drips and intravenous sickness as could not keep anything down. Ward doctor wants me to stay in for another night and hopefully can go home tomorrow. Had injection in tummy to fight off infections but will cause aching bones.

    Round one of six over unless Oncologist changes plan.

    Thanks for checking on me. How are you?

  • Please keep in touch and let me know how the 18th goes. What number chemo is it? 

  • Next chemo is number 6, then last one on the 9th of July, which happens to be my wedding anniversary! Will definitely keep in touch, would like to know how you get on. If you have any questions, don't hesitate to ask. Xx

  • Number six! Well done you. Keep in contact. X

  • Thank you, will definitely keep in touch. Xx

  • Met with consultant yesterday and he acknowledged my sickness problems. I now along with the other anti sickness tablets need to take 125mg Aprepitant capsule an hour before chemo (this is tricky as last time I was kept waiting for over an hour) and a further 80mg on day two and three to control sickness. Consultant seemed confident that these will help me enormously. I asked if they were that great at controlling sickness why the tablets were not given out straight away! The reply was they are an expensive drug.

    Noticed today that I have hair shedding despite cold capping at first chemo session. Not sure if I will continue as had an awful headache after treatment. Consultant said the headache would have been chemo related and not the cap.

    Still feeling a dull ache and prickling sensation in tumour area.

    Best wishes

  • Just thought I would let you know I had my hair cropped today. Went ahead with second cold capping 9 days ago but headache during my treatment was horrendous plus losing so much hair.

    The sickness tablets worked but I have been in bed for 8 days as so weak.

    How are you doing?

  • Hi Sandradee, great to hear from you. So pleased the aprepitant worked for you. I took this during my EC part of the treatment, it's annoying they didn't give this to you straight away. I think I have one before my docetaxel treatment ( it certainly looks the same shape) , but now don't need them afterwards. Sounds like you're still having a bit of a rough time, not great having to stay in bed so much. My main side effects at the moment are bouts of diarrhoea, which they've given me tablets for and metallic taste in my mouth, which I have for several days. I also noticed I get a bit more tired when out for my walks, hubby sometimes has to hold my hand, to help ne up the hill. Have my last chemo on the 9th of July, which happens to be our 41st wedding anniversary, can't wait to ring that bell. My hubby has started training to give me the phesgo injections at home, which will save a lot of hospital visits. He went through the paperwork at last session and all the safety side of things. He also observed them giving me the injection. They now have to observe him giving me the next two injections and then we can start doing them at home. Good idea getting your hair cropped, I think it is less stressful when falling out. Mine has actually started growing back already. Have you decided whether to continue with the cold cap? I didn't try it as I was already prone to headaches. I actually get fewer headaches now that I've upped my water intake. Good luck with your next treatment, hope all goes well. Xx

  • Hi

    Sounds as though the 9th July is a big day for you. My next chemo with EC is the 10th and no more cold capping for me. 

    Still so tired and woke up with lower back ache today and a delicate tummy to say the least. So much flatulence which is embarrassing ha ha.

    Cycles 4,5,6 I will receive the Phesgo injection. I will look to administering it myself if I can as my partner is no good at those sort of things.

    Meeting with oncologist on Wednesday and having a scan to see if tumour has started to shrink so fingers crossed otherwise not sure of the plan of action if it hasn’t.

    Have still not told my children yet (ages 22, 25 and 30) as can’t bear to see the fear in their eyes and the thought of them thinking am I going to die, but I will tell them after the scan.

    Best wishes 

  • Forget to ask Pippin24 whether you are finding the cycles 4,5 and 6 more doable without the EC (Red Devil intravenous chemo) and comparison in side effects.

    Best wishes 

  • Hi Sandradee, I had been told during my pre chemo review, that docetaxel is brutsl and stronger than EC, which really did worry me.  However,  I have not actually noticed much difference, apart from diarrhoea and taste changes. I had been told about possible nail issues and peripheral neuropathy, but have not had issues with either. I have been using a product called polybalm on my nails since starting chemo, so think this has worked well for me. I also wear thin cotton gloves when outside, as apparently the uv light can affect the nails. Hope this helps. Xx

Reply
  • Hi Sandradee, I had been told during my pre chemo review, that docetaxel is brutsl and stronger than EC, which really did worry me.  However,  I have not actually noticed much difference, apart from diarrhoea and taste changes. I had been told about possible nail issues and peripheral neuropathy, but have not had issues with either. I have been using a product called polybalm on my nails since starting chemo, so think this has worked well for me. I also wear thin cotton gloves when outside, as apparently the uv light can affect the nails. Hope this helps. Xx

Children