Hi everyone, just thought I'd give you an update, as I had my post op assessment today. It was the best possible news I could have had. They took 20 lymph nodes out, none of which had cancer showing. There was no sign of either tumour and no cancer cells in any of the breast tissue. They still want me to have radiotherapy as a precautionary measure and to reduce the risk of cancer coming back. Hope you are all OK. Xx

Hi Pippin24   That's amazing news!  Well done you!  Radiotherapy will be a breeze after everything you've been through.  Do you know how many sessions you will need? 

All good here thanks.  Had a poorly pup for a couple of days but she seems to be much better today.  My last immunotherapy session is scheduled for 21 November - all being well (e.g. bloods are ok and they can find a vein for treatment!) I will be ringing that bell!  

I'm meeting up with the "Moving Forward" ladies on Monday evening for dinner and a catch-up.  I'm looking forward to that.  Am also out to dinner tonight lol. Thank goodness for my PT to help me work it all off!  He's gradually increasing what I do and I am definitely feeling better for it.  Yesterday he introduced light weights and I found out I couldn't quite straighten my left arm directly in front of me!  That was a new one lol.  So I'm working on that in between sessions too. 

Hope everyone is doing well.  

Carol xx

I did got boob pain also, a couple of weeks after my biopsies. Good to hear that your ct scan showed no spread, that is a big relief. I opted for a port instead of a PICC line, only because I didn't want to have to go and get it flushed every week. You will get used to having lots of appointments. I have 2 this week, one for a wound dressing and one with oncology. Hope your week goes well, take care. Xx

Hi Carol

i see you experienced poor mobility.  Was this the result of medication or just knock in effect of chemotherapy.  
everyone responds so differently it can be confusing.  

im pleased you found the course helpful and an ongoing support network.  I'm struggling emotionally so really looking forward to support around that 

xx

Hi Pippin 24 I have been following all you ladies on here from the very start of your journey's. I was diagnosed in March. I started my chemotherapy end of May finished that and just had my surgery yesterday got discharged the same day also got a drain too. 

How long did your drain stay in for? 

I am not liking it at all. 

Hi Nedb, sorry to hear about your diagnosis in March. It's great that you have finished chemo and had your surgery, hope you are feeling OK. My recent surgery was mastectomy with diep flap reconstruction and I was in hospital 5 days. I only had one drain, which was removed three days after my surgery, so before leaving the hospital. I know others have had drains in for longer, I think it depends on how much fluid is draining, I'm assuming you have to measure it. If you have any other questions, feel free to ask. Take care. Xx

Mine is less than 50ml yesterday it was 22ml in the morning it was 20ml and will see what it is the evening. It's only been one day yet. Yeah my husband measures it and we have to write it down on the paper the hospital gave us and date and time it also. 

Yeah it has to be less than 50ml yesterday it was 22ml today in the morning it was 20ml and in the evening need to see what that will be. You have to date, time and measure it and record it on the paper hospital gave. Don't like it at all can't sleep with it it always in the way of anything you are doing. Going to the bathroom is a mission. 

Hi pippin24 mine  has so far been below 50ml but it's only been 1 day yet. 

Mine has been below 50ml and it's been only 1 day so don't know how long they will keep it in for.

Mine has been below 50ml but it's only been 1 day so don't know how long it will be in for 

Sorry every time I would post it it wouldn't show so got multiple now on here sorry about this ladies.

Sorry every time I would post it it wouldn't show so got multiple now on here sorry about this ladies.

No worries. As far as I know it has to be between 25-30 ml, but someone else may be able to clarify this for you. As mine was removed before coming home  I didn't take too much notice. Hopefully, you won't have it in for too long. Xx

Thank you pippin24

Your welcome xx

Hi - D Day - arrived at hospital waiting for check in.  Terrified this morning- not about the treatment formalities but what the treatment will do to my body.  For someone reaching the ripe old age of 71 and do not take any medication (except for the odd paracetamol and very rare antibiotic) never had any operations - just given birth to two fine boys) skipped relatively easy through the menopause this is one hell of a day.  Never smoked but do enjoyed nice glass of wine, the odd G &T and of course our sunny holidays   Didn't have the best night's sleep so tired as well today but steroids should keep me going. Anyway no more moaning just need to get on with this and come out the other side.  Update to follow.xx

Hi Robin 

I had a double mastectomy.  For me I had two drains each side and a pump each side do six tubes in total.  Like you my husband had to drain and measure fluid but just once a day.  When my fluid went below 20 for two days they removed drain.  Took 10 days for all 4 drains to come out  xxx 

It seems every trust / surgeon has their own direction so be guided by yours. 

wishing you well with your recovery 

xx 

Hi NGS   I had my first session today - 6 planned all being well if no serious reactions.  You have had quite a journey.  I will have my mastectomy after treatment but cannot have reconstruction because it's inflammartory bc so all skin is removed so I will be flat.  Was wondering whether to ask Consultant when we meet if they could make the other boob smaller just to equalise it a bit!!!

Hi ROBIN71, sorry I must have missed your post and would have sent you a message to wish you, good luck. Hope everything went well for you today and that you're feeling OK. Try not to worry too much about side effects, Im 62 and my side effects were minimal. Let me know how you're doing, when you feel up to it. Xx

Hi NGS, just wondered how things went with your oncology appointment. I hope they were able to give you some reassurance regarding your pain and that you don't feel so anxious now. Have a good weekend. Xx

Hi Pippin 

all good here.  I had second bone infusion on Tuesday and have avoided a and e like before 

saw oncologist Wednesday who has reassured me cancer not spread to bones.  The second cancer although high grade was not invasive and had not spread so the mastectomy got it all out.  Such a relief to know.  He was concerned though by my level of pain and peripheral neuropathy.  Has stopped my medication - letrazole as certain it is that and to give my body a rest.  I’m going to move to a different medication in 4 weeks but honestly if pain is the price and it isn’t the cancer spread I’ll suffer it 

How is your recovery going ?  Hope you are improving with every day 

xx 

How are you feeling.  One down - keep focusing on that end goal.  I’m sorry to her you can’t have reconstruction.  Being cancer free if the main thing.  But just a thought. I have BRCA1 so had to have all tissue right up to skin removed.  My surgeon did tell me if he couldn’t save my skin or if there was cancer in the nipple there was a way he could make a breast from skin at my back flap and pull it round.  That said my cousin went flat and she absolutely rocks life.   
I hope side effects are minimal.  We are all here to help 

I second Pippin - Polybalm was brilliant.  I ordered mine from Amazon.  I also highly recommend look good feel better. You get lots of goodies and it was a godsend - look them up they have lots of courses on hair / eye brows and make up 

xxx stay positive - you’ve got this