Corner cafe for the UK girls...let's have a nice cup of tea...
I couldn't find a thread to allow us UK girls to have a place to call home and swap treatment experiences, laughs and provide support...so thought I would start us up a cosy little corner cafe, put the kettle on and rustle up some cake and biscuits. There's an open sign on the door, cup cakes and scones on a stand and flowers in a jam jar on every table. Anyone want to come in for a cuppa?
Looking forward to meeting you all!
Hey Ho
Comments
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So I will start...with a classic one...cream teas are on offer at the Corner Cafe...so when it comes to stacking your scone, do you put the jam on first or the cream? I live in the West Country, home of the cream tea, and I'm a jam first girl myself but I know this is an area of hot debate. Your views welcome!
Also jam type? I prefer blackcurrant but am happy to go with Strawberry.
Not that I should be eating ay of this, you understand - I am grade 2, stage 2 but a whole armpit stuffed full of every single node full and busted open on one side, and fecking c on both sides so a BMX and the full treatment works to get me to where I am now...one year out, on hormonal therapy and working on my weight! Trying to adjust to the WTF year I have just come through, and to deal with the fears of it coming back...I'm told that my prognosis is "guarded"...eek...pass the jam...
Hey Ho
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Hi, this looks like a nice cosy cafe and I do enjoy a good cream tea. I go for the jam first as well, just seems to stack up easier that way. Jam type depends on my mood on the day. I quite like my own home made damson jam on a scone. Yummy!
I live in the West Midlands and I was first dx in 2009. I went through surgery, chemo and rads. At that point I thought and hoped that I was done with bc, apart from taking hormonals. I went back to work, got back to my usual exercise routine and increased my activity level, tried to stick to a healthy diet. Then in January this year I was diiagnosed with a recurrence. I have just finished 6 rounds of Taxxotere and need to have another CT scan in a couple of weeks, then see what is next for me.
2012 hasn't been a great year so far. My mouth is still a bit sore from chemo but I'm sure I could manage another scone.
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Hi Jayne, so glad that you could drop by for a nice cup of tea and a sit down. This cafe is a great place to recover from tough chemo like Taxotere, that is a big gun and I really hope that it has kicked the stupid reccurance to the curb. Please be sure to let me know! I am waiting on the results of a blood test and brain scan myself, and am looking for ways to distract myself until next Wednesday...which is why I opened this little cafe for business...
I am thinking of bringing in a shiny big Gaggia cappuccino machine as well so that we can offer proper frothy coffee here at the cafe, what do you think? May encourage a few more UK girls to drop by on their way out shopping or to or from treatment.
I am sure I remember seeing it written somewhere that cream teas are really good for chemo side effects...and your damson jam sounds lovely!
Hey Ho
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Hello.....Nice to meet both of you!
I am always up for a cream tea and could probably sit in this cafe all day.....
I am in London and was dx end of Oct 2001 - treatment was : mastectomy (unilateral), FEC x4 followed by Taxotere x 4, 25 rads, tamoxifen for 2.5 years , then aromasin for 5 years.....so far, so good.....
I gained weight after chemo and rads, mainly because I was so shattered that I just sat around for about 2 years; lost the weight after getting more active, but seem to have gained it all again (and more) since stopping aromasin 2 years ago. I have a theory that these endocrine drugs mess with your hormones.....I am planning to visit my gym more often, and eat fewer cream teas......well maybe next year....
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Hi Sam, nice to meet you too! I had FecT as well, but just three armfulls of each...I wonder why I only had six chemo doses when you had eight, and 20 rads when you got 25...I had ILC and loads of nodes. I guess the Honks know what they are doing and design our treatment to suit us all individually...
Hormonals are a challenge in themselves. I took Arimidex for 6 months and it made my joints ache like anything and the fatique was something else. I was then swapped to Aromasin, started taking it a month ago and the joint pain has really dropped away and I have so much more energy...so glad that my Honk switched me over, 5 years of Arimidex would have been tough. However there is no way I am going to stop taking that little white pill...
Obviously it goes without saying that all cream teas served up in our cosy corner cafe are fat free...so come here often and eat as many cream teas as you like!
Hey Ho
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Hi Sam, it's good to see another UK girl dropping into the cafe. Hi Hey Ho, nice to see you again. I don't usually drink coffee but I could just fancy a nice frothy cappuccino now.
I had FecT when I did chemo in 2009 and had 3 rounds of each. I asked at the time if they would like to give me an extra round for luck, but they wouldn't consider it. I only had 15 rads, so less than either of you. I was told that I would get the same total amount of radiation for my diagnosis whether I had 15 sessions or 20 or however many, they just divide the total by the number of sessions.
When my rads ended I was put on Arimidex and I had some joint pain afte a few weeks. I felt about 90 years old for a while there. It didn't last long though, then it just went away. Only trouble is that Arimidex obviously wasn't working for me because I had a recurrence. My onc put me on Aromasin while I was waiting to start chemo, so I would at least be doing something to treat it. I had to stop before doing chemo and I need to wait a few weeks now before I start taking it again. I'll have to see whether I get any side effects but I think I need a horrmonal that is going to work for me.
Well I hope you both enjoy the Jubilee weekend. I'll pop in again for another of these delicious fat free, guilt free cream teas.
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Hi Jayne, thanks for explaining the rt and chemo dose thing, that makes sense. I am so sorry to hear about the reccurrance - and another trip through chemo. Hope you were able to tolerate it OK. Has the chemo kicked the recurrance to the curb? I do hope so. It is amazing stuff - my second tumor was found after mx no 1, during chemo, so it was measured for response and it was nice to see it getting smaller on US after each armful. So I am hoping that the chemo has had the same effect on your reccurance. Hope the Aromasin works too. I am sure you will be closely monitored to make sure all is as it should be? How did you find the reccurance? I did not realise that a hormonal may not work, that is scary but useful to know. Am so glad you have got on top of it and dealt with it.
Did either of you ladies take HRT? I took it for about 2 years and I am convinced that it was what kicked my sneaky ILC off. The Drs say there is no way of knowing, but the tumor size and grade woud indicate that it had been slowly growing for about 6 years...which would fit with when I was on the HRT. Ugh. To think I may have inadvertantly bought this on myself does not bear thinking about.
Well it is Jubilee Sunday and I am off to see Elton John in a live open air concert this evening..looks like it is going to tip it down...oh well, no surprise really, this Is England, and it IS a bank holiday. Of course it is going to rain, its traditional.
Despite the Bank Holiday, the corner cafe will remain open all the time, welcoming alll UK folk, any stage and any grade. The tea, coffee and cakes are all organic, fair trade and fat free. But quite delicious. Try my favourite - coffee and walnut cake. Yum! What is your preferred cake of choice?
HeyHo
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Hi ladies, I'm just popping in to see how you are. Today I fancy a slice of carrot cake and a reviving cup of tea.
HeyHo I hope you enjoyed seeing Elton John in concert. We certainly had some typical bank holiday weather didn't we? I watched some of the Jubilee concert on TV and was happy enough to remain in the comfort of my own home.
I found that I tolerated the Taxotere better this time than I did when I took it in 2009. Partly because there seem to be more options available to help me control the side effects. I have stayed on the full dose and my blood counts recovered each time, so I musn't grumble.
I started to be concerned about a recurrence when I noticed a rash under my foob that didn't go away after 2 weeks. This was just before Christmas, so when the rash was still there at start of January I made an appointment at the breast care unit for someone to look at it. I started to feel very tired as well, which I also noticed before my original diagnosis, not just a normal sort of tired, this was getting more extreme, almost exhaustion. Well the rash turned out to be skin mets and the CT scan showed where the cancer had returned to soft tissue and lymph nodes. It has been interesting seeing the Taxotere shrink the skin mets to almost nothing. I also had a scan halfway through that showed it was working on the cancer inside as well. I will have yet another scan on 13th June to see how it all looks now I have finished my 6 rounds.
I was shocked too that this happened when I took the Arimidex every day without fail. I am highly ER+ so I thought it must be working for me. Well now I know better. I never took HRT, though I did take birth control pills for a few years when I was younger. I know they also affect your hormones, so who knows. It isn't good to think it may be something we did that caused this. We can only do our best, based on the information we have at the time.
I hope you get good news on your test results tomorrow. I'll be thinking about you, so do pop back and let us know.
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Hi Jayne and Heyho -
Hope you both had a restful Bank Holiday weekend - I just about managed to cut my lawn and do a bit of pruning and a little bit of work on my allotment in between showers; on Sunday - absolutely nothing , and today was pretty much a wash-out too. Flaming June, eh! Hpoe you enjoyed Elton John, Heyho; did you go to the concert outside Buck House? I saw bits of it on tv yesterday.
Hope you get 'negative' test results tomorrow, Heyho......and all the best to you, too, Jayne.
Nothing is certain with this b........ disease - and we cannot start thinking we did something to cause it; as the Americans say 'it is all a crap shoot'.
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Sam I'm impressed that you managed to get some pruning done and worked on your allotment. There is so much that needs doing in our garden, and it was always me that did most of it. Lately it seems that either I am not feeling well enough or it is raining too much to get out there. The greenhouse is sorted but not much else. My DH just doesn't seem to notice when things need doing. Don't get me wrong, he has been amazing through all this, just obviously sees things very differently to me. Maybe I'll have a chance to get out there today.
I've just seen this from Ann at Breast Cancer? But Doctor...I hate pink! and wanted to share it here:
Amazing words from Dr Erica D. Bernstein that mean so much today.
"Cancer is not a battle that we win or lose. It is not our fault or a sign of weakness. We are not responsible for our cancer outcomes. The crapshoot of cancer and recurrence can NOT be controlled. Celebrate yourself for each time you, despite all the trauma of cancer, treatment, and the mindfuck of "survivorship", choose to love, live, lust, laugh... We are not a success story based on our cancer progression or not. We succeed when we are courageous enough to keep walking forward even with missing parts, severe pain, addled brains, and broken hearts."
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Hi Sam and Jayne...sorry to have been absent for a few days, I have been out in the real world ...however i really do fancy a nice slice of fruit cake and an Americano right now...I would like to be out on my small allotment like Sam, but it is absolutely tipping it down so I am sitting in the kitchen instead. I dread to think what havoc the slugs are wreaking on my seedlings.
Jayne, thank you for sharing how your reccurance emerged and the treatment, that is good of you and very useful to know about, we all keep our radar up for anything out of the ordinary ...sounds like you are really vigilant and also that the drs have jumped on it straight away. Taxotere is amazing stuff, hopefully it will have melted all the internal feckers as well...it certainly did a number on my second primary and pretty much blew it out of the water. I hope you get a positive outcome too, I am sure that you will. Will you be able to have RT to the area after the chemo wraps up? Please do share with us how your meeting goes on 13th, I will be thinking of you and sending you positive support thoughtwaves.
Went to see the neurology consultant yesterday...all a bit complicated as I had peripheral neuropathy in my feet that started six years ago, and could / could not be a side effect of neurological response to anti gens produced by the body to fight cancer invasion...the timing fits in terms of how long the medics think the ILC was lurking. However nothing definitive can be proved. Not sure that proving a hindsight link really matters anyway, as that ship has sailed...Blood tests showed one marker slightly elevated, but apparently that can be caused by ongoing effects of radio therapy, apparently that carries on having an effect on the body for years after treatment stops..who knew? I thought that by the time the sunburn had faded that the rt had done its job but clearly not.
Anyway, I was not expecting to be told that the brain scan showed something up at the back of the cerebellum...but not a met according to the Dr. He did not know what it is (!!), but there is a small unidentifiable something lurking there. He is sending me for another MRI brain scan at the end of June to have a comparison scan to look at. Apparently it could just be an "artifact" which he explained as kind of the MRI version of dust on the lens...hopefully this is the case but means another month of not knowing and then waiting for scan results :-( I keep telling myself that there is nothing to worry about, but I kind of distrust the medics when they tell me that now, after I was told six uears ago that the neuropathy was idiopathic so not to worry, then three years ago when I was first sent to breast clinic that all I had was breast pain and not to worry, ha! and then after the left boob tumour was found last year, not to worry about my right boob, nothing there at all, then ok lets take a biopsy but nothing suspicious on ultrasound, and then oops, there seems to be another primary on that side...so will have my fingers permanently crossed until this next diagnostic is over...
All I can say is thank heavens for this little cafe...so much nicer to be inside with a coffee and cake on a cold wet day... whatever has happened to our summer?
Sam, I went to see Elton John at an open air gig at Taunton Cricket Ground, the day before the Jubilee Concert. It was great fun despite the rain, he really knows how to work a crowd. Was so tired the next day though! Duvet day! :-)
Cheerio, Hey Ho
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Can I visit every now and then? (You may want to keep this thread for Brits "at home!") I am a Brit living in the US and an "old" friend of Jayne's. We went through chemo together in 2009. I grew up in the Northwest, in the Rossendale Valley just north of Manchester. Cream teas are not something that happen here!! But I have been known to bake scones once in a while.
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Hi Gill, you are more than welcome! Hope the cafe brings you some lovely home thoughts from abroad. The cafe is open all hours and to all UK folk or international anglophiles...so that includes you too, Kayb! It would be wrong to be exclusive to any BC sister from anywhere who wants to touch base with a little bit of our islands, so just ask us if you need us to explain our peculiar UK ways...a cream tea, for example, is usually two scones, a pot of lovely jam, a big bowl of clotted cream and a pot of tea, all served up on a tray together as a mid afternoon treat. A very British indulgance, and usually very popular with people from all over the world, so make sure to try one when you visit us here!...and please do help yourself to the rain, e have far too much of it at the moment.
The cafe is looking very pretty right now. I have splashed out on some pretty printed vintage table cloths at a car boot sale, and there are small bunches of herbs from my garden in the jam jars on each table, mint, chervil, sage and rosemary. The scent from the herbs is very relaxing and theraputic. I have also added fresh mint, thyme and fennel tea to the menu. Lovely freshly brewed with a little bit of organic honey to sweeten if you so choose.
Looking forwrd to hearing from you all!
Hey Ho
PS Jayne, there is a fresh carrot cake here too, so you had better drop by for a slice before it sells out!
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This cafe is looking very welcoming today, and the smell from those fresh herbs is wonderful. In fact it's making me want a cup of herbal tea to go with my carrot cake. That sounds quite a healthy choice, doesn't it?
Hi Gill, fancy meeting you here, it's lovely to see you.
Welcome Kay, I'm trying to think of a way to give you some of our unwanted rain to take home with you as a memento. It has rained virtually non stop for most of the past week where I live.
Hey Ho I'll keep everything crossed that your 'artifact' from the scan does turn out to be dust on the lens. I can see why you don't trust the medics when they say it's nothing to worry about, although I hope that turns out to be the case. It's a shame you have to wait to find out. I often think all the waiting is the worst part of this business. No matter how much waiting I do it doesn't make me any more patient.
I have been told that I won't be able to have any more RT as it is the same area that was radiated before. Mind you, I thought radiation was supposed to help prevent a recurrence, well it didn't work on me so I'm probably OK with not having any more. On my CT scans now something shows up on my lungs that is described as being 'consistent with previous radiotherapy'. I assume it is damage of some sort. My onc said she would be concerned about it if I hadn't had the RT, but I don't have any symptoms from it and if I hadn't had a recurrence and needed a scan I wouldn't even know about it.
For the first time in ages we have had a day without rain. I took the opportunity to get a few things done in the garden, got some washing done and out on the line and also went for a walk. I'm tired now but I had a good day. I hope all you ladies had a good weekend.
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Hi every one. Jayne, we have been having horrible weather here. (Idaho) We still have the heating on and have had lots of rain. Tomorrow, the weather is supposed to improve. We are ready for some warmth and sunshine. My poor tomato plants etc are just sitting there doing nothing - waiting to grow.
A good friend of mine returns from a trip to England tomorrow. Her Dad's cousin lives in Halifax and she and DH were visiting and walking the Dales Way from Bowness on Windermere to Ilkey in Yorkshire. I am so hoping they had decent weather doing the walk - I think over seven days, and look forward to hearing all about it.
I will invite her over for tea, and might even make scones!!!
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Kay I'm sending tons of good thoughts your way for your MRI on Tuesday and your appointment on Wednesday. Really hoping all will be fine. Please come back and let us know how you get on.
Gill, my tomato plants sound similar to yours. Everything seems slow to get going this year. I hope your friend had better weather for her walk than we have been having. Mind you, they could always take shelter in a cafe or pub along the way.
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Hi Jayne, I have some lung scarring from rt too, so hopefully that is a normal position and nothing for you to worry about. Fingers crossed, stupid cancer. I also have rubbish tomato plants, in fact my whle allotment is just sitting there in the rain looking miserable. So frustrating!
KB, will be seding you lots of positive vibes on tuesday - I need to work out the time difference as when you have morning I think we are a few hours ahead of you? Anyway good luck and be sure to come back to the cafe and tell us when you got the results on wednesday. We will put a scone by for you.
Gill, I will go right now and dig out my favourite scone recipe and stick it at the bottom of this post. If you cannot find clotted cream in the shops, serve them with a nice thick double cream, that will do just as well. And some lovely jam. Yum!
This is a recipe that one of my best friends shared with me, it is very easy and works every time. Makes about 10 - 12 small scones, depending on how thick you roll out the dough and the size of the cutter.
4 fluid ounces of buttermilk, or 50/50 milk and natural yoghurt if you cannot get buttermilk. (I always use milk and yoghurt as always have some in the fridge!)
9 ounces self raising flour
1/2 teaspoon cream of tartar
2 tablespoons castor sugar (or less if you do not want the scone too sweet)
2 ounces butter
pinch of salt
Rub the butter into the flour till fine breadcrumb consistency, add the salt, cream of tartar and sugar. Mix in the liquid.
Turn onto a floured board and shape / roll out to about 3/4 an inch thick. Cut into scone shapes to the size of your choice. Small and dinky scones are very elegant but you can get more jam and cream onto bigger ones!. Place on a baking sheet and brush on some milk or a beaten egg. If you like a crusty top, sprinke with a little sugar.
Bake at oven pre heated to 220 for about 15 minutes until risen and brown on top. Take out of oven, ut on a baking rack to cool and see how long you can go without eating one...usually about 20 seconds...
To serve...place on a pretty plate and say Tah Da! as you present them to guests. Spit the scone accross the middle then stack jam and cream onto each half and tuck in...
Options: add sultanas, glace cherries, mixed spice or apricots to make variations. For cheese scones, leave out the sugar, add some grated cheese into the mixture and pile more on top before baking. Or add a few chopped herbs. Nice.
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You guys all ok?
It's been a while since I saw any activity on this thread......maybe you all ate too many cream teas and are sleeping it off somewhere.With the disgusting weather we've been having for weeks now, maybe you've just gone into hibernation??
But I am a bit concerned as I know a few of you had upcoming tests and appointments, and you have not come back to let us know how you got on.
Kay - how did your MRI go ? I hope you got good results.
Heyho - what about that unidentified something on your cerebellum? Hopefully something and nothing...
Jayne - hope all is ok with you.
Gill - how is life across the pond?
Best to all of you,
Sam
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hey Sam - thanks for posting.
Heyho, and thanks to you for your scone recipe - different from mine.
It's night time here and I'm having a cup of tea with a couple of digestive biscuits!!!! Not something I can easily buy, but we have this place called the Grocery Outlet and I think it's a place for products to go to before they expire. Anyhow, things are incredibly cheap and we found thise small packets with just 12 biscuits in for only 99cents. So I bought a ton of them.
It is very hot here. Bu we have been waiting a while for some heat so I won't complain, though I'm not really a "hot" person. It means the veggies are finally growing and flowers are looking well. DH and I and oldest son are off to California at the weekend with 2 cars in a mini convoy. Son is moving there in search of a job. He has just graduated with a degree in art. We have family in California to help him out. He has a lot of stuff to take!!!! I didn't have much when I finished college and starting m first teaching job. Took the train with a couple of bags to Carlisle and that was it.
Hopw you all wake up (shortly) to sunshine. I've heard there's been lots of rain.
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Hi Gill, good to hear from you! Was woken up today at 7 am by my daughter, 18 today...how did that happen? Cannot believe that my baby has now grown up, it all seems to have gone by so quickly. Anyway however "adult" she now is, did not stop her getting up earlier on the lookout for presents...now all opened and she has gone back to bed for a snooze!
Sunny here at the moment, although the last few weeks have been miserable, wet wet wet. My porr veggie plants on the allotment are all bogged down in mud, lokking shell shocked and not growing at all. It is a bit frustrating given the hard work taken to grow all the seddlings and shift huge volumes of weeds earlier in the spring. This has got to be one of the worst summers on record. However if I look back to last summer when I was going through chemo and having a pretty tough time with the side effects, I was quite greatful for the dull weather as the days when it was really hot made me feel even worse. So now I dont grumble about the weather because I think of other people currently going through treatment who might be quietly appreciative that it is not baking hot.
Am under instructions to make gooey chocolate fudge brownies instead of a birthday cake, so that is my baking task for today. I shall make some for the folk in the cafe at the same time.
Hey ho
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Hello ladies. Thanks Sam for getting this thread going again. It's lovely to hear from you Gill and Hey Ho. I suppose I have been hibernating in a way, just not had much energy to spare.
Last week I had an appointment with my oncologist. I still needed proper feedback on my latest scan and to see what is next treatment-wise. As far as the scan goes, the good news is that the blood clot I had on my lung has been dissolved and vanished. The chemo generally worked well but since my last round of Taxotere some of the remaining skin mets may have got slightly larger. There is still no sign of cancer in any internal organs. So, what to do about the pesky skin mets that won't go? My oncologist phoned my surgeon to see if she was free to come and join us. She was, and soon the tiny room was full with my onc and her registrar, my surgeon, two medical students, Nick and I! I was taking my kit off and covering up again every couple of minutes. It was a really good, useful appointment though.
We are all agreed that it is best to shrink the skin mets as much as possible before doing any surgery, so I will keep taking the Exemestane for now and give it a chance to work. We are aiming for remission, just not quite there yet. Meanwhile my surgeon will consult one of her colleagues and seek a second opinion and possibly a third opinion from someone who has worked on similar cases. She is keen to keep the surgery to a minimum, so as not to impact too much on my quality of life. We also want to avoid another recurrence in the future if possible.
Lots has been going on at work; basically the college had a massive cut in funding and has to make some savings. To achieve this they are making lots of people redundant, including me. I have had to attend several consultation meetings about this and I finally got my letter last week saying that I will finish on 12th September. I loved my job and will miss my colleagues, but I can't worry about it too much just now.
Take care ladies. I'll pop back again soon to catch up with you all.
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Hi everyone - Jane, well sounds like Exemestane is an even more powerful medication than i realised - I take it too. Fingers crossed that it does a number on the remaining skin mets. I wonder if there has ever been a competition to see how many experts can be crammed into one of those hospital consultation rooms? Sounds like you could be a record breaker. Anything to avoid surgery. I hope that you get more than remission - I hope that the skin nodules go away and stay away for ever. Sorry to hear about the redundancy though - a double whammy.
Sam and Gilly, what news form London and America? Hope all is well and that you are doing lovely summery things. It is raining and wet here and I have just riven my duaghter over to her friends house and come back home cold and tired so am snuggled up in bed with a cup of tea and chocolate and the dog and the laptop.
I am still waiting on an appointment next week with the nurology consultant to discuss my scans. Both MRIs showed the same weird thing on my cerebellum, but he does not know what it could be! I have decided to just not think about it any more as worrying was getting me nowhere. Once I go see him I will have a clearer idea about what on earth they are seeing inside my noggin, and if it needs treatment or not. I am hoping it will be a case of lets just keep an eye on it.
A rainy wet day here. So an organic egg and flour pancake filled with fresh raspberries and home made yoghurt, sweetened with a drizzle of local clear runny honey is the special for today at the cafe. (that really is what I have just eaten as a treat, and it was totally yummy.)
Time for a bit of a kip.
Hey Ho
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Hey Ho that pancake sounds delicious! I really should make pancakes more often. I hope all goes well with your appointment this week, do let us know.
I had my appointment with my second opinion surgeon this morning. It was an interesting morning. We took the opportunity to get my mammo done, since it is due about now. They fitted me in straight away. He examined me and could feel an enlarged lymph node on the opposite side. This could be cancer, but he said if it is, then where has it come from? He couldn't feel any lumps in that breast, but as I was having the mammo anyway he had an ultrasound and biopsy done as well. He suggested that I may be a good candidate for electrochemotherapy and that it would remove all the remaining skin mets in one session. He seemed positive that they can all be removed. I would have to travel to Manchester for this treatment, but it could be worth doing. I don't know much about electrochemotherapy yet, I'll have to investigate further.
It has been another day of rain here, just for a change. I have done my daily Clexane injection and now I am taking a break to enjoy a cup of tea. Hope you are all well and enjoying the summer, whatever the weather.
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Wow Jane it sounds as if the experts have been very thorough in checking you over. I hope that the mammo and biopsy results are all clear for that pesky opposite side node. I have never heard of electrochemotherapy, sure is a very big word though which in itself makes it sound important and thus I am sure it is ultra effective. I am going to have to go and look this treatment up now to see what it is! A trip to Manchester is surely going to be an acceptable journey - the stakes are so high in our position, I would travel anywhere to get treatment that the experts suggest would be of help.
Rain, rain, rain here in the West Country. I was visiting relatives in the Forest of Dean, usually such a lovely place but just as wet as anywhere else at the moment. Still, our lovely pub lunch has given me an idea for the cafe menu...anyone fancy a rosemary loaf cake drizzled with sticky melted honey?
Hey Ho
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I thought I'd try revive this thread! Happy New Year everyone. I have to brag I made real mince pies for Christmas. No Mr Kipling for us! Of course I bought the mincemeat (Crosse and Blackwell) but made my own pastry - a rich sweet version where you use eggs to bind the dough instead of water. I also made "sad cake" and flat jam cake if anyone knows what they are. They might be a northern thing, or even just a family thing.
Who did baking for Christmas?
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Nice to see you, Gill....thanks for reviving the thread.
No baking for me I'm afraid.....I have been spending the last 3 months visiting and looking after my 94 year old Dad, who collapsed and spent about 6 weeks in hospital.He now has much-reduced mobility and increased cognitive impairment, so it is hard-going,especially since he lives over 100 miles away.
I have been thinking about you all and hoping things are going well.It would be nice to hear how you are.
Wishing you all a happy and HEALTHY New Year!
Sam x
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- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team