Hi takeadeepbreath , I am due to start rads a Preston soon . So oncologist on Thursday and he said I will be starting in the next few weeks just waiting for planning appointment . My treatments been delayed due to infections . Was you at preston on Thursday afternoon as I was in the que for a drink and a lady handed a green tea bag over to the lady serving . Hope all goes well .
Also jill how did you get on today was going to post to wish u well at your planning appointment . but Iv had loads of problems logging on ended up with 2 sign on names last night only just got on now . X
Hi everyone I just started rads at ,Preston if anyone else is? I even got in early today and didn't have time to finish my green tea. It was all over in 10 mins. No side effects as yet but feel tired....could be the tamoxifen flushes waking me up early.
Glad you Rads went will Whitejasmin, have a lovely weekend x
missmore, when I had my first CT scan, they said that if they couldn't see my heart on the scan, they wouldn't call me back for the 'Heartspare' one so, perhaps no news is good news for you? They said yesterday that is just a precaution and that the heart can actually take some radiation without any side effects
Hi Maggie haven't caught the man flu (I've warned him if he passes it onto me he can look out). Rads was OK better than I thought, feeling OK. Just lined up with tattoos keep still for a couple of mins and then, see you tomorrow. Got all 5:30 appointments which is great for me as John will be home (he insists on taking me). Glad you had a lovely time with your grandson, going over to see mine on Saturday. Wondering if I'm feeling a bit like you at the moment ( when John says about going off for the day/weekend I say great it'll be lovely to get out, then I get up in the morning and I don't want to go). Joyce x
Appointment went well thanks missmore although I could never actually get used to people drawing on me!
I have to hold my breath for 20 seconds six times during the Rads. They said that the new CT scan showed that my heart is now well away from where the beams will go. My Rads will now run from Monday until 7th September. Good luck to everyone who is having treatment x
Hi Joyce hope your day is going ok and you not caught "man flu" Hope this hasnt stopped your first rads, let me know what it was like.
I have felt ok yesterday Had my Grandson for morning rained most of it but we had fun in house, my Daughter is having him where I cant at moment so she had him for the afternoon. His daddy has him today but always needs company around 2pm.
We are going away for the weekend have been getting things together. I am not as happy as I would normally be, but it is "away" my Husband's treat so need to buck up a bit. Then it will be rads.
I still havent had my planning letter - they said Monday - I am giving them a call later.
Once I get started on Rads then all this wondering/headaches will go I am sure. take care Maggie xx
Hi Tweasel Glad you got your meeting, did the tatoos hurt? I havent had my planning appt letter yet? take care.
Just had a call from the Radiology Dept. to say that my Rads, which were due to start on Thursday have been postponed as they were not happy with my CT scan (which I had on the 9th July). I now have to go in tomorrow morning to have another CT scan whilst holding my breath for 20 seconds. She said it was because it is left side and they could see my heart on the scan(?). My Rads will now start on Monday instead and still run for 25 sessions with new appointment times. I hadn't realised that all the appointments would be at different times of the day, luckily I work in a school so 20 of them are in the holidays but they will now run into the first two weeks of September too.
Hi amberstone, consultant told me I'd be on tamoxafin for 5yrs when I finished rads. Had a good weekend pottering in the garden Saturday, weather has put paid to any more work out there. Think I may be in for a hammering with my husband he's come down with a cold (sorry I mean man flu) awe Bless. Soon be Wednesday just wanna get started now. Joyce X
Hi Joyce thanks for reply. glad someone has same thought process like they say "two heads better than one." Can I ask what tablets? no-one mentioned tablets to me that is why I was wondering,I will ask when I go to the planning appointment - not got letter for appointment they said would be here Monday!!
Hope you are ok and your weekend was good for you.
Can anyone tell me if you have any medication/tablets with Radiotherapy??
Hi Tweasel just catching up -- my results were Triple Negative ER negative HER2 negative so they said I would not be able to have Herceptin or Tamoxifen just Chemo and Rads but now I am only have Rads (not started yet). Did you get answers you wanted from BCC. Have a nice weekend Maggie XX
Morning Joyce I am fine thanks you hope you are having a nice weekend. So you are same as me? Does it mean they have sent us away with no treatment and we keep fingers crossed, or does it mean the percentages are low and really good - in other words we have got off lightly??? I am so confused. Does it make sense what I am trying to ask. I am waiting for post Monday should get date to go for first planning appointment.
Morning Sheena just having thoughts - like they never stop do they. Can I ask what your percentages were for you to decide against Chemo I am not sure I understand mine if good result for future or not? Mine were Chances of it coming back without Chemo 4% Chances with Chemo 2-3% I am sure we all feel "thick" at times butlike someone said we need a Doctorate after this lot. I am waiting for letter to give me first planning appointment should come Monday?? Have a good day today everyone. Maggie XXXX
My rads run from 30th July - 3rd September. I had two WLE's the first one on 1st April and the second on 7th May. It has been a long wait to start the final stretch! 40 mile round trip for me.
Whitejasmin
I'm also starting on 29th but not til 4pm so the day will drag. Also 15 sessions which seems standard. Are you being zapped left or right?
Hi ladies. I'm not on any hormone tablets, just Herceptin as my results were HER2 positive. What factors determine if you need hormone tablets, e.g. Tamoxifen?
Hi All mine is a different hospital to where I had op. It's about a 30 mile round trip. Like so many of you I just want to get started and get some normality back in my life. Not looking forward to the tablets though been told by a friend she had terrible mood swings on them (tamoxifen). Joyce X
Morning ladies. It's great that there will be a few of us in this merry band so we can support each other and compare experiences. I'm feeling a bit nervous at the moment but I'm sure I'll be fine once the treatment starts. Are you all having rads at a different hospital from your other treatment? I will have a 50 mile round trip for mine, which is not too bad. Hope everyone is doing ok at the moment - have a lovely weekend all xx
Morning ladies!
I'm starting on 6th August x15. So will join this happy band and hopefully we will have a laugh and a moan together and get to the end of this without too much sizzle x
sheena xx
Hello whitejasmin you wont be far in front of me so maybe we can help each other together with Tweasel. I will have to remember to be on Rads of August thread. speak soon hoefully Maggie
Hello Tweasel I also had op about 5 weeks ago (15th June) had lumpectomy and 2 lympth nodes removed, all ok. Been tld I am Triple Negative was told Chemo and Rads was the plan but visited Onc. yesterday and she wasnt recommending Chemo - With Chemo 2-3% chance of it returning Without Chemo 4% so not going to have it. Have a wobbly ticker so not worth putting me through side effects, especially if I got an infection could be in trouble with heart.
I should get a letter Monday for my first planning appointment and then bit like you should start the following week.
After all the anxiety about Chemo, in a way I am happier today - I can deal with Rads, how do you feel about it all? My Surgery was ok only had trouble sleeping properly had the flippin' drain in 8 days though, my breast is hard/lumpy but doesnt look as bad as I thought it would be - so that part is forgotten now in a way.
Hi all. I have started this thread because it now looks as though my rads will be starting in early August. I will be having my planning meeting next week and I'm hoping the treatment will start the following week. I will then be 5 weeks post-surgery. I am having 15 sessions and will also be having the clavicle area done too. Is anyone else expecting to start rads in August?