Hello ladies, sorry to just pop in, im from the June chemo thread and was just having a thought about the nasty tongues and lack of taste buds due to chemo and remembered this tip. Get the vitamin c tables (the ones jn a tube which you disolve jn water) and let half a tablet dissolve on your tongue, it helpa cut through the sliminess, yoh ccan do a whole one but they are quite sharp. Juat a tip to pass on.
I can't really comment as I've not had surgery yet, doing chemo first but I would recommend you speak to your team about it asap. My lump Humphrey in my boob has a mate Patricia in the armpit. Both are hard, and the armpit one can hurt. I thought I could feel it growing recently but the BC consultant said that was due to the biopsy and poking and prodding. The armpit tumour is more sensitive apparently.
Get it checked out as soon as you can so it can be dealt with if necessary or, fingers crossed, it's absolutely nothing to worry about and you can just focus on getting through chemo.
Thinking of you 💪💪
💜 Fiona xxx
@pinklily I've had a picc line fitted... Was quite straight forward -had an ultra sound scan to check where my veins where and if they were suitable, I then had a local anaesthetic and the line was inserted, I then went for an X-ray to check it was in the right place and then you go back to the unit to have the picc line area cleaned and a dressing put on it... I couldn't really feel too pain afterwards, it's more like having a small cut...cleared up quickly and so much easier than having needles/canullas for treatment or blood tests! The district nurse comes out once a week to flush it and change the dressing! I would recommend it if you have the option! 💗💪🏼 x
Hi ladies, I just went for my follow-up on my mastectomy and the good news is that they did get clear margins. The tumor was 6 cm. Again, just saying...I don’t know how 14 consecutive years of mammograms could have missed that. Anyway, my doctors are saying eight rounds of chemo. Four rounds with epirubucin and cyclophosphamide and four rounds of docetaxel. My tumor is estrogen and progesterone receptor positive. Does anybody have any experience/advice on my type of tumor and the above mentioned chemotherapy? Thanks in advance!
I was hoping someone would say they could do walks, it helps me to think I might be able too as well, I know maybe the hills might be bit adventurous to start with, but it would make such a difference to get up there and see those views.
I'm not sure about using my ruck sack at the moment, I can't lift anything heavy with my right arm ever and I'm going to have the picc line in the left and I read I can't lift anything heavy with that arm, although what some people count as heavy, I don't. As you said, I will have to see how I feel, but the sooner I get walking, the better.
I got bitten by something two days ago, used the antisane cream and took a anti histamine tablet, but it's itching and still looks a bit angry, I'm worried that the chemo will cause it to become infected, I will have to see what they say on Wednesday. Good idea to carry a mini first aid kit, we've got one in the house, in the car and we both have one in our ruck sacks, hadn't thought about losing nose hair, but it must make a difference, just as well it's autumn and winter.
As I'm starting with the EC and the Zometa for the first four sessions, I'm hoping the side affects will not be too bad, it's when they start to add the Paclitaxel as well once every week for 18 to 20 weeks that worries me more.
@pinklily Take it as it goes with the walking -- and treat yourself as you can! My OH and I are keen walkers, and it's been hugely helpful to my spirits to keep it up. I've managed several 10-11 mile walks during chemo (at least one per cycle, often more), including a 3-day trip to the Wye Valley that involved carrying our "kit" on day 1 and 2 during week 3 of my 3rd cycle of FEC. It can be doable, though it all depends on how your body responds to each chemo regime.
I've found it best to plan a walk that allows for an "early out" in case I'm feeling tired or running short on water. This weekend, we did a 7-mile walk on both Saturday and Sunday -- late starts cut short by dusk/twilight. Both were on relatively flat ground, as I'm feeling it more now that I'm in cycle 5. I've found the taxane regime is harder, in terms of walking -- I'm more fatigued, whether from the specific drug (I've been prescribed docetaxel, not paclitaxel) or the cumulative effects, and I really feel the effects on my feet (soles weary, and a bit of peeling, but no worrying pressure blisters as yet). I also carry a little first aid kit with me -- antiseptic cream, plasters, antihistamines -- in case of bites/splinters/scratches, to reduce chance of infection and deal with extra sensitivity to any pollens in the air (losing nose hairs makes a big difference!).
Just wondered if having the picc line inserted is very uncomfortable and did anyone have any problems?
Also, I've got a Limbo arm cover that I used when I had surgery for golfers elbow, would this be suitable to use with the picc line when I shower or should the hospital give me something?
Hi @Sar_ah The advice I was given was not to bath because of the risk of infection due to the bath water not being fresh running water like a shower. If they tell you any different, or give you any tips when you see them, please let me know as I would love to have a bath again!
Which day to you have your 2nd chemo? My 2nd one is due on the 1st November.
Good luck for the port fitting, I had mine done with sedation, which helped with the anxiety of it all, and I didn't feel a thing
Well done for the 5k, that's amazing! I would have been exercising more but once I got this chest infection, I wanted to conserve my energy to help me get better, plus I don't think my lungs would have handled getting out of breath!
@Shi - thanks, sounds great! I'll get tuned into that jukebox now lol, and get on to the thread you mentioned straight after xxxx