In shock
Comments
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Dakota...seriously...I mean SERIOUSLY?????? I am so sorry you and your children are hostages of such a lowlife....!!! It sounds like you are backing off again, giving him the opportunity to continue to be abusive to you AND your kids. Exactly WHAT in his laundry/buddy actions makes you believe anything has changed in how cockroach will behave in the future. Building a life, certainly REbuilding a relationship is much more than dropping off some laundry and hanging out with the guys. I'm so so so sorry sweetie, but I really don't believe the issue is that you have "too much faith in him", I believe that you don't have enough faith in yourself. Pay the damn money right now, put the laundry on the curb, get YOURSELF some counselling and start believing you and your children deserve and can have a better life. If this nightmare was happening to your daughter, what would you advise her to do????? Do you truly believe this is an example you want her and your son to have in their lives..????? I know I'm ranting....I just am so FURIOUS that you keep giving him the opportunity to control and harm you. IMHO....this is truly what's happening....he is HARMING you and the kids. Get yourself some personal, counselling help, please.....you have the strength, you just need to have the belief in yourself!!!!!!!
movie....sorry the anti-sleep bugger got you last night. Thanks for the camping info, btw...I'lll forward it to my friend. Busy day yesterday...no mountains though!!!! (But there will be this week)!! Listen girl...weight loss is not about starving yourself and killing yourself in the gym!!!! You should know that!!!! You CAN lose 10 lbs, in that time frame without pretending to be a contestant on the Biggest Loser. You can't outsmart your body by starving yourself, you can't "out exercise" what you put in your mouth either.....balance, girl....it's all about balance. Eat right, exercise smartly....you'll good to go!
OK, obviously I'm in a lecturer mood....better stop here before I say what I REALLY want to say about cockroach!
Love you all.
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Nihahi -
Believe me I know. I know he controlling. And no I don't want her to ever live like this. The lawyer is 7500 I can pay by credit card I have to look at that all tonight and figure out how I am going to pay it it's all up front. I know it's what I have to do there is no alternative ! I can do it I know I can I have to starting appreciate the words trust me !!! -
(((((((((((((((((((x)))))))))))))))))))))
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Dakota, BIG HUGS to you! You can do it, the sooner the better.
Movie, no, I have never made pasties. What I would do, is type 'pasties' in on Google, and hopefully lots of recipes will come up. Then you choose whichever one has good ratings, and seems good to you. I always go for the ones that say 'Easy' - LOL. Have found amazing recipes - it's like a treasure trove. Hardly use a recipe book anymore, just so much easier with Internet at my fingertips. My laptop often sits open next to the stove, and has to be wiped from time to time - lol.
Traii, your bear story reminds me of Goldilocks, except the parent bears were not there! On a serious note, a 60-year old woman had been attacked in her yard by a cougar yesterday afternoon, and had been airlifted to Victoria. She is in critical condition, and her injuries are just horrendous. It happened near Tofino on the west coast of our island, not too far from where we live. Her brave husband fought off the cougar by stabbing him, he let go, then slinked off into the bushes. He has not been found, but is injured. This is very scary. Apparently the cougar has been hanging around that area for a month. I'll take a bear anyday. They don't stalk and attack you like this big cat does. Read just now that two thirds of cougar attacks in Canada occur on this island. So comforting to know . . .
Nihahi, you are quite feisty this morning - lol! Lecture? No. Good advice? YES, as always, wise woman that you are.
So yesterday I wrote a review of my rip-off experience on Tripadvisor. They will e-mail me as soon as it is posted, IF it is posted. I told it like it is, no holds barred - LOL. We'll see. Will probably be offered a free tapas meal there . . . lol. It made me feel better at least.
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Hi
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Wow didnt have a chance to catch up on here earlier and OMG the poop has sooo hit the fan !Dakota, Nihahi is one smart woman, a joke is a joke but that bxxxxxd aint funny. Cut arms out of tops and turn trousers into shorts and return bags of clothes pronto.
Of with his buddies ???? Who is he kidding.
Liefie, if you look up pasties, try Cornish pasties, flippin gorgeous ! They have a high pinched edge which the Miners held them by when eating to stop being poisoned by whatever they were handling.
They are like a meat dinner in pastry and sooo yummy.
Cougar story horrendous, hope poor lady survives her injuries.
You and DH be extra careful PLEASE.Movie, tummy tuck and perky foobs, YAY you will be gorgeous again very soon.
Been out with BC buddy, lunch then whizzed around the shops. Hit the health store and bought Turmeric capsules. Really good writeup on fighting the big "C".
I also bought a box of organic Yogi Tea, Womens energy type. Supposed to have great results and heaven knows I need a bit of oomph in my tank.
Had the strangest sensation this morning. DD rang second youngest GD not well enough to attend school so could I have her for the morning ? I jumped out of bed cleaned and tidied downstairs, folded laundry, then as I stood in the middle of the kitchen suddenly realised I felt NORMAL for the first time in over a year.
My friend rang whose husband is also a survivor told her and she said her hubby had the same sensation three months after chemo finished. I am three weeks out TOMORROW.
He has never looked back and I am Dam well no gonna do either.
She then offered us her caravan on the magical island of Anglesey free for our hols. DH wants to go so fingers crossed we will have a lovely break in a few weeks.
This island is off Wales and we spent many happy days there in our youth.Revving up to todays walk, on my own today, radio on, headphones in and look out here I come

Love to any sisters not mentioned but always in my thoughts. XX
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Edi, isn't that the same island where Prince William and Kate live? You may bump into them at the grocery store - lol.
Just came home from jogalates class. The exercise is okay, but the heat is something else, so I always try to get the coolest spot. Afterwards went to quickly practise some organ. Playing for a funeral tomorrow - not looking forward. Played for so many funerals, but it will always remain a sad occasion.
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Liefie, It IS the same island. The pub local to the caravan is where they liked to call in for a drink or a meal. Shame they are now moved away
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Prince William was based at the nearby Air Rescue base.
Kate used to shop in the local supermarket, would have been fun bumping into her there LOL. -
Well hello everybody. I'm back (yesterday), and somewhat jetlagged this evening.
I just spent lord knows how long reading all that I've been missing. I don't know why youall were concerned that the thread was dying!!?
Nihahi, great pictures from your hikes, and I recognized a few faces too! I didn't climb any mountains on my trip, but had some lovely long walks on the South Downs. Pub lunches. Walks by canals, wandered around Chichester and the beautiful cathedral. There's nothing like any of that here, but it was still wonderful to come home to Canada!!!
My parents were in fair shape when I left, so the parting wasn't near as painful as last year when I left Mum in hospital and we all thought she wouldn't make it out!
Today I went for the drumming circle at Wellspring. If you haven't tried it, and you get the opportunity, do go! It is indescribable, and a great healing experience. Our younger son just started his vet tech course at Olds, and they had drumming as part of the freshers activities. He was blown away!
I've signed up for the return to work sessions there, and also the brain fog sessions. I'm not sure if I really have brain fog, but I seem to be worse than usual on names and whatnot, so I thought I'd see how that goes!
I was quite sore and itchy from the rads while I was away, but now feel way better ... Peeling well. I don't really feel too fatigued, although not pushing myself overmuch.
Be great to join you and the girls on some hikes Nihahi???
How do you post pictures like that? "_" -
Dakota - what Nihahi said! Sending hugs ((()))
Movie - what Nihahi said
. Hope you sleep better tonight.
Traii - the news of those bears really travelled!
Liefie - what Edi said - be careful
Edi - the getaway sounds wonderful, yay for feeling normal!!!
Morwenna - good to have you back, glad you are healing well from rads, now to get over jet lag. Glad your parents are doing OK and easier to leave this time
I saw my Dr. again this afternoon. She is pulling back on my return to work plan - from four days a week to three days, maximum of 7 hours with a break of minimum 15 minutes every two hours - indefinitely, will reassess next month after Herceptin is completed. Honestly, I don't remember ever feeling so exhausted for so long as I have this summer, not after any of my surgeries or during chemo/rads.
Goodnight, lovely ladies -
websister.....the end of surgery, chemo and rads is the end of treatment, it is NOT the end of recovery.....that process, you are just beginning.....but stay strong....recovery has an "end" too....then it's look out world...here's to the future!!!!!!
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Hello all
Dakota, if CR wanted to make this work he would be dropping everything to work on his marriage and family. He obviously wants his cake and eat it to. Sounds to me like you are avoiding the inevitable. Don't waste another minute on a man who doesn't deserve you, it will not be easy but down the road it all works out and you will find someone who will treat you as you should be treated.
Morwenna, glad your trip went well,and that your parents are doing well.
Question about rads, does it feel like a sunburn? I will be starting in January and the unknown is killing me.
Liefie, be careful with all those wild animals running around.
Edi, yippie for normal can't wait to have that feeling again.It's so great you are getting out and about.
Movie, sounds like the healing process is a long one from Diep, take it easy and let your body guide you. Yes DH is very busy he has a full time day job as well as his comedy shows. He loves performing and it is his true passion.
We had quite the weather here today, they had to plow some neighborhoods because of all the hail.
Weird for September.
Dh and I got out of town for a night last Saturday. We had an early anniversary celebration, because I have treatment this Thursday which is the actual day.
Hope you all have a great week -
Morwenna I start rads in November not January dang Chemo brain
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Carla posted this on f/b put it on here for those of you not on there.
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That's an awesome picture!!!! I actually agree with everyone. I know in the beginning it will be rough but I know it will be better in the end !!! Thanks for confirming my thoughts ! Love u girls !!!
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and we love you Dakota.....consider us to be permanent pocket people for you!!!!!
benny....where the heck have you gone to now????
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Hi Maria.
The thing with radiation apparently, is that they cannot predict how or who will have a severe skin reaction. It seems that how one reacts in the sun has no bearing at all on the outcome. I have heard of fair-skinned red-heads who hardly react at all.
They did warn me, however, that because they used a bolus on me, I would be more likely to react. I had a left mastectomy, and so had very little tissue remaining over my ribs, and they use this sheet of gel-like stuff as "artificial tissue", which concentrates the radiation into the surface tissues and away from the heart and lungs.
I applied Glaxalbase cream to my chest and just over my shoulder, as directed, 2-4 times a day, and by my last (16th) treatment was noticeably reddened, especially in the bolus-covered area, and slightly sore. They told me my skin was looking exceptionally good at the last treatment, but warned me it gets worse for a couple of weeks before starting to improve.
This was the case, and over the next two weeks it became really hot and sore and itchy, with small blisters forming and disappearing. When it was at its worst I used Polysporin sometimes, which really seemed to help. It also helps to expose the skin to the air for an hour a day, preferably with a fan on it.
Eventually it started to peel, and only for the last couple of days has it felt quite comfortable, although still peeling a bit.
I have mostly gone without a bra, but if I did wear one, eg to go out, I used those soft "genie" bras. I got them in Bed,Bath and Beyond. I used my softee prosthesis, not my silicone one, but even so could only wear it for short spells at my worst.
I just bought a weighted foam prosthetic while I was in the UK, and its way more comfortable than my silicone boob or even my old softee, and also a swim-form, which I will be excited to try out once fully healed.
There, sorry, that was a rather long reply to a short question, but as they say, everybody's different. My sister-in-law just went slightly red, she said, then turned brown, like a deep tan, but she still had her breast, so maybe that helped as the radiation is less concentrated in the skin. -
Morwenna, glad to have you back, and that you had a fun trip to the UK, and a lovely visit with your parents.
((((((((Websister)))))))))
Edi, it was Movie looking for pastie recipes, but I will certainly try those Cornish pasties - sounds delish!
Maria, I had 25 rads. For me that was the easiest of all treatments. After chemo it was really nothing. Only pain was to go there every weekday for five weeks, including the week of my DD's wedding. My skin got a bit red and itchy towards the end, but I never peeled. Just liberally slathered on aloe vera gel (non-alcoholic) immediately after each session to cool down the skin, and then one more time during the day. The rest of the time I used Lubriderm Intense Dry Skin Repair. Over-the-counter hydro-cortizone cream helped a lot to calm the itching and redness that came later. My onc advised me to use it, and it worked so well. I went without a bra most of the time. It was more comfy, and my bra's did not become yucky from all the cream. Ruined a few T-shirts though - lol. Fortunately they are cheap at WalMart.
Feel pretty exhausted after a very busy day. After a funeral I always come home with a headache. No rest yet. Friend invited us for dinner at 7 tonight to meet friends of his, and I offered to bring dessert - what was I thinking? It's 4 in the afternoon already. . . still have some pears, maybe just bake them in the oven with some honey? And ice-cream? Lol.
Tomorrow I am going with DH to San Francisco for a conference till Sunday. Never been there, and really looking forward. Defo going to hike the Golden Gate Bridge. Don't know if I will post while there, but will 'see' you all next week. Keep well, sisters!
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I just got my pathology report back. Surgeon said if nodes are negative then no chemo. Today she says - nodes are negative amrgins are clean but her2+ - so you will need chemo. I'm angy. I don't know what to do with the anger. Been enraged since my biopsy. Don't know how to do this. I'm 52 and single with a daughter in college. Im on my own. How do you prepare for this? Please help me. I can't stop crying.
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Hi Michele !
You can do this it seems that way before you start, but trust me you got this!!!' I am a single mom of 2 very active kids I had 8 treatments and was able to do all the things I needed to for them. Ask for help when you need to and rest when you need too. One day at a time ! We are here for you !!! We will be in your pocket every step of the way ! Starting today !!!! You came to the right spot!!!! Hugs my newest friend
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Have fun liefie ! Thank you nihahi !!!!
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I made the mistake of taking a Trazodone an hour ago........so very sleepy here.....
Just wanted to pop in and tell you all that I appreciate ALL of the support I get from you......love you all!
Michele , welcome to the club no one wants to be a member of.......Dakota is right...you will find the inner warrior in yourself, and then you will rise up and destroy the enemy......you just do it one day at a time.......these women are the best, bar none, at making you feel like you can do it, and that they care.......hang in there, you CAN do it .....
Drowsy.....love you all!!!!! XO -
Michele, sorry you have to join our club. It is ok to cry. It is ok to get angry. I go through streaks of crying then fine for weeks then tears are back. It is a roller coaster ride for sure but you can do it.
My doctor told me right at the first meeting that if my tests came back Her2+ that I would need chemo. Didn't know what the heck she meant! I think we are bombarded with so much information while we are still in shock that we just can't process it all. I had my hubby with me and he understood some things that I just didn't and vice versa. Do you have a friend or relative to go with you to your appointments to be a second set of ears?
Just remember, this is not a death sentence. I have two sons who have been through cancer and two sister-in-laws who had breast cancer. All are doing very well and all have been through chemo and radiation. I also have two miracle grand kids ...my son was told he would not be able to have children after his chemo.
We can do this together. -
Michelle, Please, please cry all you need to. We have ALL cried rivers of tears and ranted about the unfairness of this DX.
You are new and we can ALL remember exactly how you are feeling even if we are months/years after.
Chemo is one of the treatments I too didn't expect. I walked out of Doc's office in a state of shock !
The day of my first one I was rigid with terror but all for no reason, it was over before I knew it.
Twelve more followed and at the end I cried again but only because of their kindness and compassion.
It is manageable, side effects ( if any ) are treatable. You will be looked after with great care at the hospital.
The warrior sisters on here will help and support you.
I logged on most days through this journey and they held me up, helped with side effects, and cheered me up so much.
I finished all treatments three months ago and it does fly past honestly.
Anything you need to know just ask. (((HUG)))
Edi x -
Hi
.Real dull and cold here today, brrr. This is my favourite time of year. Dark evenings and roaring fires, Halloween next month ( anniversary of my first chemo !!) then bonfire night, then Xmas !!
DH resigned from work yesterday. We need to sit and work out how we are going to avoid murdering each other in the future. LOL.Liefie, Enjoy your trip, looking forward to all the details on your return.x
Dakota, sure you will be big help to Michelle and she hasn't got a cockroach to put up with as well. How are things on the insect front ? x
Jo, good advice for Michelle too. Second set of ears plus notebook and pen a must on every appointment with the Consultants.
They are saying the same things to patients all day and they do forget that half the time we havent a clue what they mean. xMovie, glad you are chilling out,we LOVE you lots like jelly tots x
Mowenna, Glad your trip went well. great rads advice too. x
Bingo this afternoon, feeling good
hope all my sisters do too. xx -
Thanks to all for the rads info. I don't know what I would do with out all of you through this journey.
Michelle, welcome to this group of fantastic ladies. You will be bombarded with info for sure. My husband recorded every apt. on his cell phine so we could replay them as much as we want to.
Dakota, how is it going this week?
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Michelle and Jo......it does seem "unbearable and undoable" at this point....but you CAN do this. Clear nodes and margins is wonderful news....now your docs are trying to give you the best shot at putting this all behind you forever. Anger is part of the journey.....you wouldn't be human if you didn't feel that way. It will best serve you if you can turn it into "fighting back". Stay away from google, tv movies about chemo, etc.......the reality for most ladies these days, is NOT the horrific horror stories that are still "out there". Do NOT take advice from people who have not gone through it personally. We get it, we will help as much as we can.....stick with us.
movie....dang girl....still having sleep/pain issues???? Baby steps, good eating, realistic exercise.....hang in there. I bet you look damn "slinky" in that compression!!!!
Liefie....you have me chuckling...I noticed you editted your last post. Last night, when I read it, I thought, hmmm I didn't know they'd moved the Brooklyn Bridge???? Too funny. Have a great time....can't wait to hear about your adventures!
Edi....bundle up and keep up with those walks! Retirement with hubby can be a fabulous time....just keep the dialogue flowing at all times. So has he actually stopped working as of yesterday, or did he give notice???? Good luck at bingo...one of us has to win a jackpot so we can get that "group getaway" planned!!!!
websister....my neighbour was told she would have to go to Peter Lougheed to have the port inserted...SERIOUSLY....FROM OKOTOKS???? She refused, and is now waiting to be booked into South Calgary. Unbelievable access to healthcare sometimes, eh??? Thankfully, she was told that the tumor (lung cancer) is responding to chemo and shrinking. So she had a bad news/good news kind of day....we've all been there, eh!
I've sat on my duff too long this morning....gotta go ladies....love to all.
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Girl after my own heart ha ha.
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Edi-and this is EXACTLY why I love you! XO
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Movie Lovsya ,my mad yank. When you coming to see me ?? xx
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