Anyone from East Kilbride/Glasgow area?

Hi Girls

I feel like I’ve missed loads as I’ve not been about for a couple of days.

Had my 2nd cycle of chemo today, I can’t believe its come round so quickly. I’m feeling a bit sick and tired, so sorry if I’m not very chatty!

I had a really good time at the LGFB workshop and headstrong session on Monday. Fiona, I’m really pleased I was able to get on the same session as you, as it was great meeting up.

I’m probably won’t be able to make Lunch this week, John is working Friday & Saturday, so I won’t have a babysitter. But please go ahead and organise something as it would be lovely for you to meet up before Sharon’s op.I’ll come along to the next lunch.

Angela – take it easy back at work, no one will expect you to be back to full capacity straight away. I’m sure your boss would be horrified that you were trying to sign in at 12:30! Try not to get too stressed – although I know that’s easier said than done!

Hugs to all

Helen

Girls

Not long home after being out all day, message on answer machine from surgeons secretary need to call them in morning about Op, will need to let you know about lunch

Night night

Sharon xxxx

Hi i am a newbie from glasgow looking for any help and information to make this easier to deal with.
I have lobular cancer they originally thought it was very small before they operated on the 31/3 but it was 3cm grade 3. i was 4 nodes positive had the lymph glands removed its ER.
Have had bone scan ,ct scan and waiting for mri seeing the oncologist on the 6 may for results and what chemo i will be getting. know i will be chemo,radiotherapy,tamoxifen.and the big hair loss but any tips i would love to hear.

Hi Girls,

Welcome YvoYvo, Sorry you’ve had to join this club! Everything’s a waiting game isn’t it? This is a great site for help and advice and all the girls are really nice. we’ve all got different types of breast cancer and are on different stages and types of treatment. Once you’ve seen your oncologist and he’s told you your treatment you’ll know more about what to expect.

I had 13mm tumor removed in Feb, no nodes involved, but ER+ and HER2+. I’m 12 days into my first chemo and I’m on a trial for early breast cancer combining chemo with Herceptin… I’ll have radiotherapy too and Herceptin for a year and then Tamoxifen.

Anything you want to know ask away, chances are somebody will have a bit of advice for you… Are you going to recieve treatment at the Beatson? I had my op at the Southern General and treatment at the Beatson… Also have you been down to The Maggie’s centre situated at the western Gen? It is a great place to visit for any kind of help, support and advice…X

Sharon - hope all is well with op. hope you don’t get any set backs!!

Helen - Glad all went well yesterday, hope your sickness doesn’t last too long. Very hard to get plenty of rest with 3 small kids but listen to your body and stay horizontal!!! Had a practice with the scarfs yesterday, didn’t do too badly, I was quite surprised I managed to get them to stay on an they felt quite secure. X

Pauline - Good luck tomorrow with PS, hope all goes well. you’ll be exhausted after such a long appointment… can you tell me how I go about getting any alternative therapies from the Accord Hospice? Do I go along or phone them? It’s so near where I live, it would be really handy.X

Angela - you must be feeling good being back at work… Life must feel like it’s getting back to some normality. Hope you’re still taking it easy…X

Jo - It’s Great you’re half way there… Do you get chemo every 2 weeks or 3? It’s hard keeping up with everyone’s times… Because I never got my chemo when I was supposed to I’m now a week behind where I was!!! X

Sheila - Did you get mouth ulcers with every chemo? did they heal up in the 3rd week…mine are massive and I can’t chew at all now… had mushed up weetabix this morning, Yech!! felt like baby food!! also I’m eating smoothies and soups… I’ve used adcortyl in orabse for ulcers in the past and they heal up in a couple of days but not now! they’re not healing at all…X

Lost all the Hairs on my legs yesterday!! And my head is a bit itchy!! oh boy!!

Take care everyone

Hugs
Fiona xxxxx

Hi Girls

That’s me definately getting Op on Monday will be admitted Sunday.
Can’t make lunch as have to go in tomorrow for Pre-assesment, Frid I’ve to pop into work and Sat forgot I’m already going out.
Sorry girls I’m not going to get a chance to meet up before I go in.
Hope you girls manage to get a lunch organised soon.

YvoYvo - welcome to this thread, if you have any questions just ask away.

Jo - good luck for chemo on Frid

Helen - hope your sickness passes quickly, keep taking meds.

Fiona - Good luck with wig fitting.

Pauline - Good luck with surgeon

Sheila - hope you enjoy your Art Exhibition and seeing your friend.

Angela - bet your still thinking about work!!

Where is Ann?? Hope your ok.

Take care for now

Sharon xxxx

Hi
Thanks for your replies i had my op at the royal anyone got any info wheres better the royal or beatson or just the same?
Can you tell me where you got your wigs i saw a website for
second hand wigs in edinburgh anyone been?
I am hoping to visit Maggies today

Hi There YvoYvo,

If you’ve had your op at the Royal, chances are you’ll get your chemo and radiotherapy at the Beatson. The Beatson covers a large area and deals only in Cancer treatment, Situated in the grounds of the Gartnavel…

Once you’ve been told a date for your treatment you may go up the day before for a pre chemo assesment. I didn’t get one as I had blood tests done at the southern 2 weeks before, I turned up for my chemo and was given a NHS voucher for my wig that day,(this gets you a wig for free and you are entitled to one every 6 months) she also gave me a piece of paper with 3 names and addresses for city centre wig shops,(was advised not to go to one of them as sales girl not very nice). You then phone them up and make an appointment and go along for a fitting and to try them on. It takes about a week for it to come into the shop where you go to try on the one you’ve ordered. I go tomorrow to see mine, I went to extra Hair salon in sauchiehall street(across from watt bros), they were very nice in there and helpfull, there’s also Judy Plums, and another in st Enoch’s square.

Hope this is helpfull to you and enjoy Maggie’s, Tell them it’s your first time and someone will have a good chat to you, which is very helpful. They are all very experienced professionals with medical backgrounds so you know they know what they’re talking about.

Best Wishes Fiona xx

Yvoyvo - welcome to this forum. I just joined recently despite having great cancer for 11 years. Diagnosed with secondaries 4 years ago so am on and off chemo.
Sharon - all the best for your stay at the Royal. Will be thinking about you . Sure all will go well and you will be glad when it is all over. Look forward to hearing from you when all over.
Fiona - my mouth ulcers weren’t as bad as yours seem to be. Know what you mead about eating. Hope you get on OK with wig fitting.
Helen - hope all ok after 2nd chemo. Just rest as much as you can though not easy with a young family.
Jo - hope chemo goes ok
Have we settled on a day for lunch
Sheila

AFTERNOON AND WELCOME YVOYVO…

SHARON…BEST OF LUCK WITH OP ON MONDAY.ONE OF THE WOMAN FROM MY WORK IS GETTING HER OP DONE ON TUESDAY I BELIEVE AT THE GLASGOW ROYAL.I HAVE TOLD HER 2 LOOK OUT FOR U…HER NAME IS PAT CROFT.SHE IS AN OLDER LADY.WHAT WARD R U GOING IN 2…SO I CAN SEND A CARD.U CAN PM THIS INFO IF U WISH.
I KNOW U WILL B OK…GOD U HAVE DONE ALL THAT CHEMO PISH…SO KEEP HANGING ON IN THERE.U HAVE BEEN SO UPBEAT ABOUT THINGS AND I KNOW U R A FIGHTER.STAY STRONG.U MIGHT EVEN FIND SOME TALENT OVER THERE.

I AM GOING 2 C PS 2 MORROW AFTERNOON AT THE ROYAL BUT THEY WILL COME UP 2 THE RAH 2 DO THE SURGERY.MIND AND BRING IN WIPES …I AM OCD ALSO ABOUT CLEANING ESPECIALLY IN THE WARDS…REMEMBER UR IPOD. REALLY EXCITED FOR U NOW…LET ME KNOW HOW U GET ON AT PRE ASSESSMENT…ITS JUST FOR BLOODS,ECG ALL THE ROUTINE STUFF.
BIG HUGS 2 U
XXXX

FIONA…MY GOD…WHATS THE SKETCH WITH UR MOUTH.I GOT THEM 2 GIVE ME FLUCLONAZOLE(ANTIBIOTIC) TABS BEG ON DAY 3 OF UR CHEMO.I ONLY CAME DOWN WITH 2 ULCERS.I WOULD GO THE DOCS WITH THAT AMOUNT OF ULCERS…CAUSE U NEED 2 KEEP UR WEIGHT UP.BRING ON THE BLENDED SCOFF!!
HANG ON IN THERE…THEY WILL GO AWAY.FIRE INTO THE DIFFLAM.FRESH PINEAPPLE 2!!!
RE.HOSPICE…PHONE UP UR BCN AND TELL HER U NEED HELP COPING WITH THE SE OF CHEMO AND TELL HER U R STRESSED KEEPING IT ALL TOGETHER.
SHE WILL REFER U …TELL HER ACCORD H IS HANDIER FOR U AS OPPOSED 2 THE P &P.

SHEILA…WHAT ART EXHIBITION R U GOING 2…R U KEEPING OK JUST NOW?
HOPE U MANAGE 2 MEET UP FOR LUNCH THIS WEEK…ITS BEEN A LONG TIME COMING.

ANGELA…HOPE U R OK

JO…HOPE CHEMO GOES OK ON FRIDAY.

HELEN…HOW R U FEELING 2 DAY? KEEP POPPING THOSE TABLETS…KEEPING THE SICKNESS AT BAY.

ANNIE…HAVE U ABSCONDED 2 A FAR AWAY ISLAND…HOPE U R OK

YVOYVO…HOPE U GOT ON OK AT MAGGIES…GET URSELF ON LOOG GOOD FEEL BETTER DAY

TRACY…KEEP RUNNING

BIG HUGS 2 U ALL
PXXXX

Hi GIrls

I hope everyone is fine.

Welcome YvoYvo. So sorry you’ve had to join us, but as you’ll be discovering everyone here is really great and you’ll get so much support and advice, especially as we’re all at different stages in our treatment. I was dx on 24/2 with an 11mm grade 3 ER+ lump and with a 1/3 of a mm trace on my sentinel node, I was breast feeding at the time so was really lucky I found it when I did. I’m having EPI-CMF Chemo, radiotherapy & tamoxifen. I had my second dose of chemo yesterday. Do you have any family?

I’m feeling a bit better today, still a bit nauseous but spent most of the day dozing in bed with visits from the kids for a cuddle. I actually think the anti sickness tablets are making me feel worse, as about 5 mins after I take the domperidone(?) I feel really sick and can’t face food (same last time). I forgot to take them before tea tonight and feel so much better and tea was great. I’ll take them again tomorrow, but if I still feel rough after them I might mention it to the hospital and ask what they think – has anyone else has issues with anti-sickness drugs? - or is it all in my head - ha!.

Our house was like a hospital ward today, 7yr old was off school, as he staggered down the stairs last night in tears complaining of a headache and promptly threw up on the stairs and 4yr old was already down stairs rolling round in pain as the Dr thought he had gastrointeritious which was producing colic pain! So he was off nursery today, but seems a lot better now. Think baby is cutting another tooth too, so tiredness could just be down to being a mum and not all chemo! Thank god ‘nurse John’ was off to look after us all.

Fiona – sorry to hear your mouth is still really sore, have you been back to the doctors or dentist? Glad you’re managing to practice with the scarves. How is your hair? My hair is now coming out, not in huge chunks, but definitely a noticeable amount. I did wear the cold cap again yesterday, but I’m not sure how long my hair will last as it’s thin enough as it is. Good luck with your wig fitting, I’ll have to chase mine up if they don’t phone tomorrow.

Sharon – Are you getting ready for Monday? I think we’ll all be thinking about you on Monday and sending you good vibes, keep positive and keep being strong. Take Pauline’s advice and look out for some talent whilst you’re in – a nice dishy Dr would be good!. I hope it all goes well at your pre-assessment on Friday. I’d love to send you a card too, if that’s ok.

Pauline – Glad you had a good weekend away. Good Luck with your PS tomorrow. Are you cooking something nice for your friends on Saturday or is it just a coffee and chat?

Jo – Good luck on Friday, how are you feeling? How long do you have between your CMF treatment? As it doesn’t seem long since you had the last one. When I eventually get to CMF it will be day 1 & 8 with a 3 week break.

Sheila – I hope you’re keeping well and have a good time with your friends at the weekend. What art exhibition are you going to see?

Tracey – hows the training going?

Angela – how are you coping back at work? Are you really tired? When I went back after 9months Mat Leave I did a 3 day then 4 day week before this all kicked off and was totally shattered.

Annie – How are you? I hope you’ve not been ill again.

I was really brave tonight I rang the FPC and cancelled my coil fitting appointment and left a message for the doctor that the lump that she had told me was nothing to worry about, the one she was not at all concerned about as lumps/bumps were really common in breast feeding women, was actually BC. I’d just wanted to raise her awareness so she didn’t dismiss the next BF lady she saw with a lump. Anyway she rang back and said she was just in shock and felt awful she’d just dismissed it and was so apologetic. Anyway, we had a good chat and she admitted that she would’t normally refer a BF woman to the breast clinic, but would monitor the lump over some weeks, but she said she was so shocked that now she would reassess her approach – so hopefully that may speed up someone else’s diagnosis. I submitted an FOI request to NHS FV and only 9 women under 40 were diagnosed with BC last year and only 1 of them was either PRG/BF – probably explains why I don’t think the hospital have read the ‘standards of care for young women’! – What a moaner I am!.

I’ll end by apologising for such a long note, but as I haven’t been about since the weekend I feel I’ve missed out on loads and I’m having a catch up!

Hugs to everyone.

Helen
x

Morning all,

What a day!!! not keen on rain!!

Glad you’re feeling a bit better Helen…I had the same anti sickness tablets as you and I was ok. They made my friend sick too and the hospital told her she could try not taking them and she was fine without them!! Hope the Kids are all better too. If something’s going to go pear shaped it’s always when you least want it!! It was good that you informed your FPC doctor as I had a similar experience with my GP… she didn’t feel the lump was serious either and it wasn’t refered as an emergency… I spoke to her for the first time 2 weeks ago and she said she was shocked to hear that it was cancer. I hope it has alerted her to the fact that cancerous lumps don’t nescesarily come waving flags!! As it turned out I only had to wait an extra 2 weeks from that of an emergency referal so a big thumbs up for a speedy service!!

Sheila - Hope you enjoy your day out Today, Hope the rain goes off!x

Pauline - Good luck today… Go girl!! x

Sharon - Good Luck with the pre op assessment… x

Jo - Good Luck for tomorrow, Hope you don’t suffer any bad side effects. x

Yvoyvo - Hope you enjoyed Maggie’s yesterday. x

Tracy, Angela and Annie - hope you girls are doing good. x

Re Lunch - Everybody ended up really busy this week, only Sheila and me free for Lunch… Sorry not going to get together with you Sharon before your op. My mouth is starting to feel a bit better today and I’m hoping that’s it on the mend. Is anybody free next week for Lunch? I’m free any day… x

Hugs

Fiona xxx

hi eveyone

welcome to the site yvo/yvo it sad you had to join us!!!

I had a mastectomy and reconstruction done at the Royal in Nov and I am getting my treatmet at the Beatson. My chemo is EPI/CMF followed by Radiotherapy,tamoxifen. I an half way through my chemo just counting down every sessions its getting a bit much now just want my life back fed up going to hospitals. I whent to Andrea at st Enoch Sq for my wig the girl was really nice, I am going back now for my second wig think i will get a really short one this time. My hair has started to grow back in now so hopefully i will have some sort of hair do by the end of summer.

Sharon it was good to see you again on Tuesday the girls are asking when your coming back to see us… Hope all goes well on Fri and I will come and see you at the Hospital.

Got my bloods done yesterday and My chemo nurse said I cant get chemo this week because of the chickpoxs scare!!Still no sign of them so i will go back next week and see if i am ok for my chemo.

Helen hope your all feeling better in your house and are over the sickness bug!! How is your S/E iam taken dexamethasone, Domperidone and also ondansetron for my sickness.

Pauline good luck with your Plastic Surgeon today hope all goes well !!

Sheila hope your day out with your friend is good !!!

Angela hope your settling back into the work routine and your not too tired.

Fiona hope the sickness passes quickly and your feeling better !! I want the sun back too.

Hi Tracy Have you changed your mobile number text you a few times… hope your training is going good I have been out walking the last week done 4 miles on Tues and the same on thurs will try running next week now that i have no chemo this Fri.

Take care girls

lol jo x

Hi Girls hope you are all well and the s/es are subsiding a bit.I am skiving at work and thought i would log on quickly.Sharon i hope everything goes well for you sorry need to log off now will sign in later Tracy xxxx

Hi There,

Ok… How does the wig look? xxx

Fiona xxx

Fiona - wig looks good - its so traumatic at first. I have had wigs on and off for last 4 years and still feel self concious. I’m always looking at other peoples hair.
Helen - hope your coping with chemo. You are so brave to go through all this with such a young family. I am alone at home so can sleep and eat whenever i want. My daughter lives in the same street and she pops in all the time to see I am ok.
Sharon - How are you bearing up. Hope all goes OK
Yvo - hope all went well at Maggies. They are so helpful and kind and there is lots going on there
I was at the Art Exhibition at George Square today. It was really good and had such a good time with my friends. Really tired when I got home so will have lazy day tomorrow.
Hope we can get another date to meet up with everyone.
Sheila

Hi everyone

Hope it’s ok for another Glaswegian to join your thread. I was originally dx in Aug 07 and chemo then mx with ld recon followed by radiotherapy, tamoxifen and zoladex. I kicked around the boards quite a bit during that time but left for a bit and tried to move on. Unfortunately i was dx a few weeks ago with bone mets so i have came back to the boards as they were such a source of support first time round.

I made friends with a wonderful group of women and we still keep in touch. Unfortunately they are all down in England so regular meet ups has never been possible. If it is ok with all of you i would love to join in as sometimes only someone going through it can understand, but i am not sure how you would feel about someone with secondaries joining in. I fully understand if you would rather i didn’t as sometimes this is a place you don’t want to go when you have a primary dx.

I am 42 and i have 2 girls 12 and 9 who keep me really busy. I work full-time but i am off sick at present as having radiotherapy. Hopefully having been through lots of treatment i can be of use to you all.

Thanks for listening

Take care

F x

HI ALL…AND WELCOME FUZZYFACE 42…

FUZZYFACE…LIKE UR NAME…OF COURSE ITS OK 2 JOIN IN…WE R ALL IN THIS TOGETHER.SORRY 2 HEAR ABOUT UR BONE METS DX…BUT I HEAR GOOD REPORTS FOR THE TREATMENTS AVAILABLE FOR THIS.U WILL B A GREAT SOURCE OF INFO…WHICH IS GREAT FOR US.
LET ME TELL U A BIT ABOUT MYSELF…SAVE U TRAWLING.DX 31/10/08 IBC 7CM TUMOUR PR/ER POS HER2 -.STARTED WITH NEO-ADJUVANT CHEMO AND NOW AWAITING BILATERAL MX WITH ONE STAGE RECON.OVARY REMOVAL A BIT LATER.
NO RESULT IN FROM GENETIC TESTS YET…MUM ND DAD DX BC 2…AND EXTENSIVE HISTORY ON MY DADS SIDE …SO THERE IS A HIGH PROBABILITY I HAVE FAULTY GENE…EVEN IF IT IS NOT PROVEN.BLOOD SAMPLE DNA MAY B A BIT SKEWED AS THEY TOOK IT WHILST GETTING CHEMO.

HOW WAS UR REON AFTER RADS? THIS IS AN ASPECT WHICH I WORRY ABOUT AS JUST GETTING IMPLANTS AND THERE IS AN 85& CHANCE OF GETTING COMPROMISED.DID U GET SURGERY AT GLASGOW ROYAL…SPENT NEARLY ALL OF YESTERDAY AFTERNOON IN THERE…JOY.

ANYWAY…RU GETTING RADS 2DAY? HOPE U GET ON OK.

EVERYBODY ELSE IN THE GANG…HOPE U HAVE A GOOD DAY

TAKE CARE
PX

Hi Fuzzyface,

Welcome to the thread. Sorry to hear about your dx. The last few weeks must have been really tough on you. I agree with you that this forum is a great place for help and support and I have found it so important to chat to people that are going through the same as me. The fact that we’re nearly all young and most of us have young children and all we want to do is lead as normal a life as possible (especially in front of the kids)is a hard thing to manage…!! but a bleather, rant or moan on here really helps… I have found it invaluable…X

I’m 38, dx 18 feb 09. 13mm tumor ER+,HER2+…no nodes, lumpectomy. now receiving Tax+Herceptin x3 + FEC x3, Radiotherapy and Herceptin for 1yr. 14 days into first chemo and starting to feel more like myself again!!

Hope Everyone else is doing good… I’m off to buy some nice food seeing as I can eat again!!! xxxx

Hugs
Fiona xxxx

Hi All

Welcome Fuzzyface42 – sorry to hear you’re having to join this forum again, but I’m sure you’ll get a massive amount of support from everyone here as we’re all young and going through the same thing, but just at various stages. I have to admit I would of felt totally lost and isolated without the support of all the girls here. How are your girls coping with all of this?

Fiona – the wig looks absolutely fantastic – I would never have known it a wig as you look exactly the same as you did on Monday. I just hope mine looks as good as yours, when it arrives.

Jo – Good luck with your chemo today, I hope you’re feeling ok later.

Sharon – Good luck at your pre-assessment later.

Pauline – Take it easy, you must have a lot to think about after your PS appointment yesterday.

Sheila – Glad you had a good time yesterday with your friends. Take it easy today and get some rest. I compare my tiredness and breathlessness with being 10 months pregnant!

YvoYvo – hope you had a good visit to Maggies. Fiona & I went on the LGFB & Headstrong workshops on Monday and they were really good. Get yourself booked on them.

I’m doing OK, still feeling a bit sick and tired, but doesn’t help that 4 yr old was up for 1 ½ hr in the night with a sore tummy - again!.

Fiona - you’ve just confused me, think we must of been trying to post at the same time - couldn’t understand why mine wouldn’t post till I saw your new message below mine. Really glad your mouth must be better.

Hope everyone else is doing fine

Take Care
Hugs

Helen

Hi girls

Welcome to Fuzzyface, we are here for everyone.

Had pre-op assessment this morning all went well had a walk around the high dependancey unit (ward 49), nurse was really nice but goes on hols tomorrow, same as breast care nurse, everyone seems to be going on hols, last thing on our minds eh!!

Just had call from hospital saying op might not go ahead as surgeon (not plastic surgeon) had to cancel, then 10mins later got another call to say they have found someone else, THANK GOD!!! So it’s all go again.
Go in 3pm on Sunday, taken down for surgey at 8.30am.
I will be in Ward 47 after Tues, thats Glasgow Royal
Jubilee Building
Ward 47
Canniesburn Unit
Glasgow G31 2ER for Pauline and Helen as you guys want to send card.

Helen - your sickness will subside and you’ll feel back to your normal self in a few days, hope kids feeling better this afternoon.

Jo - Yeah was good to see you again, kids are adorable, so gorgeous, I will hope to see them again. Hope chemo went well

Fiona - Wig looks fab, really suit it xx

Pauline - hope your ok about yest

Tracy - I’m so chuffed you’ve been well enough to keep up the training.

Sheila - glad you’ve had good day with friends, take it easy

Ann - where are you???

other chicks i’ve missed hope your well.
I’m looking forward to Mussel Inn tomorrow night, yum yum
Just want this op and hospital time to be over now

Take care for now
Big hugs
Sharon
xxxxxx