CMF Question
Comments
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Good Evening fellow CMF ladies,
Just trying to catch up on all the posts. It's amazing how much you miss in a couple of days.
Carol and I had a wonderful visit!! Beautiful weather, great dinner (thanks to my dh) and great company. It felt like we have known each other for years. It was nice being able to share our stories, and as the pictures show my kids (puppies) enjoyed the conversation too! We both agreed that this board has definately helps us through this bump in the road. Thanks everyone for your support. 2 more treatments for me!
Harley- Will be praying for you on your scans. It will I ask my ONC when he will order scans to make sure this treatment is working and he said after chemo. I hope and pray that it is. The SE's of this treatment are so much easier to handle and sometimes this worries me. (it's amazing how we all think alike!)
Well off to bed for me, my dh and I will be planting our first garden tomorrow. Should be alot of fun!
Have a great weekend everyone and Carol and Kent have a safe trip home!
Jill
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Jill, just spent about 40 mins trying to post on this thread, it went "belly up" before I submitted...
in a nutshell just wanted to say thanks so much again, Kent and I would be thrilled if Craig and yourself would like to make a trip to the great Pacific Northwest, our home is wide open to have you stay!
We'd suggest the summer months, just called home yesterday and it was a rain mixed with snow, yuck.
I'll be hitting the txt regimen again on Tuesday, just told the dh, not looking forward to the reality of my "real life", this vacation has been just what the doc ordered. I've felt like a million bucks all week, must be good co, great weather, which adds up to no worries.
Harley, Annie, Rita and others, I'll be back to actually take some time to read whats been happening come about Tues afternoon, until then, hope all is well with each of you and you've been getting and receiving the great support we all know from this great site.
Take care all, Carol
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Jill, Thanks for your message.
I slept better last night, but I took an Ambien before I went to bed. I guess since I haven't been sleeping very well for the past couple of nights, it knocked me out, and I slept all night... only when I woke up this morning, my hand was VERY NUMB!!!Now I am REALLY worried....
Harley
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Hi all:
Jill, good luck w/ last (!!!!) two treatments! I am sure it is working, I am delighted you are doing so well..good for you!
Carol: You sound great, glad you had such a blast! I'll be thinking of you during your next treatment and knowing it's doing the job it is supposed to be doing...getting you all healthy! Remember, we are cancer free ladies, getting preventative treatments, right? I'm going with that!
Harley: Oh, you've had so much!!! Do you think you slept so deeply with the ambien that you turned on your bad arm again? That is why it may be numb? If it's getting better, that's most likely it, if it doesn't as the day goes on, prob. worth a call to onc/general surg.?
Good luck!! I'd say try not to worry, but none of us are good at that one, so try to distract yourself a bit? use the arm and see if it doesn't improve? Maybe it's an ambien se? I am of no use here, but hope you feel better very soon.
love to all
annie
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Annie,
ALL these se's are on the LEFT side of my body, and I can't help but think it's bc...
I will call my dr. tomorrow, and maybe they can order the tests sooner, but... I am just too scared!
You know, when I decided to get the chemo, it was 'cause I said "I am NOT going to do this again, EVER....If I can help it!" I am NOT strong enough to go thru this again... ...especially since I am thinking if IT IS bc.... then.... game over.Harley
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Harley- I'm a nightly user of Ambien and have been since starting this BC journey. I tried to stop but it wasn't worth it. I thought the same thing about the whole chemo thing (having to do it again) and did everything in my power so it wouldn't return but was surprised when it did 14 months later! Was not happy, but am hoping this treatment will put it in remition. (I would love a long dance with NED). This is a game and we all play to win! Hang in there, you ARE strong, we are in this together.
Jill
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Harley:
It's so easy to go off on this thought process, and I do it too, we all do...but as of right now, you have nothing going on but some admittedly scarey things that can be caused by other things than bc...I know, believe me, I know, bcuz mine came back as well...six years later, and not one single sign or symptom anyway.
For tonight, why don't you just be. Try not to think about it at all, do something nice for yourself, watch a movie, have a drink, anything but sit there and be scared. Since you've had some back pain, moved a mattress, it honestly does sound like perhaps you've pinched a nerve somewhere. Most likely your neck from the sound of it. Or there is a muscle in spasm impinging on a nerve. And remember, you said pain killers like tylenol helped. So often, things that are happening are caused by little things we did not notice at the time like Rita's band aid. Moving a mattress and having it drop on you ain't little! When I get a new ache or pain these days I usually look at what I've been doing over the past week or so....can almost always find the answer. Also, you look so young, you can't be more than 40 tops and you wouldn't have a whole lot going on yet would you. Wait til 50! (52). JK!
Go and see what the dr. says tomorrow. We can have alot of symptoms that have nothing to do with bc...but it's only natural to assume it is, as we are all part of the "knee Jerk Reaction" club now.
The good news is: this does go away in time!! the bad news is: it takes awhile and a few freak outs before that.
You will feel better when you see the dr. Look at it this way: If you had not had bc, and went to a dr. with these symptoms, well, what would they do. Prescrible tylenol/advil, etc.? If they persisted (and like rita said, the word is "persist") then they'd go to an MRI to rule out pinched nerves, see what got hurt and where....you've had treatment for bc, but how recently was it? It's doubtful it'd be back so soon, it does happen, but not too often. Most people get a remission for quite some time I believe if not for always
So for tonite: Unless you really need to, why not take a tylenol and look on the bright side? It's most likely something else, but you know what? Good for you to be cautious and check it out with your onc. it's your body! but try to view it as being the responsible person you seem to be and not the chicken you keep calling yourself.
That you are not!!! Love to you, sending good vibes and big hug ( ) and a positive
white light to surround you with protection!
xoxo
annie
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Annie
Thanks so much! I know you are right, but I can't help worrying. I never had pain to last this long... it has been going on for about a month, on and off... it got better, then we flipped the mattress, and it took TWO weeks before it came back! Also, it's been since Mid March or so, that we turned the mattress...shouldn't this get better by now?
My dh is getting mad at me. He said I should go get the MRIs, but he doesnt' want me to keep going on and on like this. He said that he just wants to go back to riding the motorcycle and laying on the beach! I know he wants things to be normal again.
Actually, it isn't my neck, it is my lower back...like my butt, and my left leg that hurts.You are too funny! I will be 45 next month. Now, though I feel like an 88 yr. old woman!
So you are right...I will just try not to think about this again until I see my dr. on Friday, because otherwise, I'll drive myself crazy!Thanks for letting me rant...
You are SO sweet!!
Harley
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Hi everyone....
I feel like a total idiot... I've been so scared, I had just about decided that all these pains were bc... I am so sorry for obsessing and bothering all y'all so much.
Thanks Rita, Jill, and Annie for all your kind words of advice.
I will tell my surgeon about these pains when I go on Friday, but I saw what my constant worrying and obsessing was doing to my dh, and I just can't keep doing this to him. I saw what happened to him when I was dx'd, last year, and I saw what happened to him when my FIL had kidney cancer with bone mets. It was horrible! I guess that is especially why I am so scared about my pains.
Anyway, thanks so much for all your words of wisdom!
This is a wonderful group of women!!
Harley
P.S. I just realized that it has been raining here for the past couple of days, so maybe that is why these old joints are aching so much!
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Hey Gals ...
Back home to the Pacific NW, the shorts are back in the closet and the fleece in layers is back on the ol' body. YUCKY-YUCKY!
I'm watching the Mariners play a home game, they just showed it snowing/hailing at the ball park. I'll the AZ sun over this anyday.
Had myself a meltdown on the plane coming home last night, the reality of 3 more months of txt and rads following that ,was not the most pleasant thought. I guess I just enjoyed myself too much for the short 8 days we had to relax, and the reality of it all hit me between the eyes.
Any whoo ... looks like each of you has been supporting those who need it right now.
Harley, you hang in there gal, I know its easy for the mind to get carried away (I bet we have all done it a time or two), so try your darndest to turn off that worry button on your brain. I'm with Jill on the approach to sleep, I take a Lorazepam to turn my brain off at bed time. Hoping some day it won't be needed.
Annie, your words of encouragement are priceless.
Jill, so is the garden planted? I bet its fun trying to keep your four legged kids out of that one! Oh, how I'd love to have a home in AZ, atleast for 9 mo out of the year. Its amazing to me how the sun took away every little ache/pain that I had. We're hoping to go back down in the fall (Oct), our friends have invited us for another stay, kinda hard to turn that one down!!!
I'll be off to the chemotini bar tomorrow, oh how I'm not looking forward to the GI tract getting itself into a knot. Atleast I'll be over the hump, and I know from you all that the next 3 mo will be behind me before I know it.
Time for dinner, take care you great ladies,
Carol
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Carol, welcome back!!
It must have been wonderful...but to have chemo a day after you get back? Girl, talk about rubbing it in...ow! I wish you could have had a little more ease into it time for re entry. Altho I do like the chemo tini bar, perhaps our se's could qualify as a "hangover"?
remember what they all say tho, that after the middle treatment, it kind of gets easier, if you are a little more tired? Like your body gets "used to it" sort of? I will wish that for you tomorrow and send good vibes that is how it will be the day after for the tummy troubles. I am devoutly hoping for myself too cuz it hasn't been working in that department at all vis a vis se's. I could use a break from this squeezing in midsection and swollen feet, stiff neck, etc.
At least I'm not throwing up!
I'm thinking you were very smart to schedule a nice "break" in the midst of all this....I think I am going to do the same, can't get away, but something nice for each chemo, bunch of flowers, new book to read, (preferably funny) I don't know, but something like that. Even a drive elsewhere than to a drs. Lunch with a girlfriend, etc. We should and can reclaim our lives in little bits and pieces all around this. You were wise, I think. Again, no worries with rads, it honestly and truly is soooooooooooooooo easy compared to this. I hoped so much to be able to do that again vs. chemo, but nope.
You'll be thru that like a breeze, I promise. You won't even notice it.
One step at a time tho.
On the sleep issue; from someone who has seen this twice (and hopefully nobody else will go there, and this is it for us all now), the sleep issues and the worries do go away...it took me about three years, maybe three and a half to be able to sleep without worrying and over thinking. I started leaving the tv on and that helped so much. turned the volume way down, but it really helped alot. that and working out, felt I was doing as much as I could. So then you get to a place where well, dammit, what else can you do. Might as well relax. I hope it works for anyone that wants to give it a shot.
(A "shot" would work too, and I can't drink ha ha)
Anyway, welcome back, you've been missed, but so glad you had a blast. Must have been great to meet Jill and see her adorable fur babies. What cuties!
Harley, I hope you are beginning to feel a little bit better? I was chatting to a buddy and mentioned a friend was having back and leg pain and they said it sounded like classic sciatica. Worth a question to the dr, maybe?
We've all been there tho. I hope you are feeling braver and calmer,
and that your visit on Friday goes smoothly and eases your mind.
Good luck Carol! Kick Butt at Chemotini "happy hour"!!
love to all
annie
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Carol,
Thanks for the wonderful advice! I have used Ambien a time or two myself, when I just can't sleep for a couple of nights in a row, I will take an Ambien, and it helps me to sleep. Don't know if I can take it on a nightly basis, though. I think it would help...especially since I sleep only about 2 hours, before waking up, with hot flashes... geez, seems like I wake up, and I feel like a wet dishrag...Sorry you have 3 mo. more of tx...followed by rads! Oh, I feel so lucky, since I didn't have to have rads, and I only (did I say ONLY?) had 4 txs of Taxotere & Cytoxan... I was very tired at the end! It definitely IS cumulative!
Strange, but somehow, it was easier for me when I was going thru tx, but now, all I do is take this little pill every day... somehow, this part seems worse to me.
You will get through tx! You are strong!
Hugs,
Harley
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Annie,
I really feel like a fool for obsessing so much! This morning, the pain seemed to go away, after I got up and started moving around. But, at night, it seems to come back...and then I toss & turn all night! Tylenol doesn't seem to help me when I take it at night...hey maybe I need to take Tyleno PM at night??
I will mention the back pain to my surgeon on Friday, and see what he says. Knowing how he has been so far, he'll probably say that it can't hurt to have the MRI... just to be sure there isn't some other problem, like a herniated disk or whatever... I don't know much about back problems, and I don't know if an MRI would show sciatica. I think my dr. will know, though. Funny, my aunt had a very bad bout of sciatica at Christmas, and she was even in a wheelchair for awhile, and in rehab. At least this isn't that debilitating.
You are such a trooper, you are getting through tx...just chugging along...
You know, it seems to me, now, looking back on it, that the tx was alot easier than this period for me... Now, I just take Tamoxifen every day, but the se's... of course, I didn't have that gorilla hug pain after tx!! You are one strong woman!
Thanks for all your words of advice! You are so very wise!
Hugs,
Harley
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Carol's back! So glad you had a nice trip. Those reality checks sneak in when we lease expect them. We've all had a meltdown and it's not fun. You're on the downslide now, Carol. Good luck tomorrow. By this time tomorrow night, you can mark off another one of the chemo cocktail parties! Hang in there. You can do it!
Hi Annie, Jill and Harley. I hope you had a good weekend.
Hi also to Susan, Ginny, Candie, SoCal Lisa, and all you other greart CMF ladies.
I had a busy weekend and I'm beat. I'll get caught up on the posts again tomorrow.
Take care...
Rita
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Hi all:
Just popping on to wish Carol luck and best wishes today!!! Sending big hugs ( )and a big "YAY"
that she is now on the down swing of chemo after halfway!!!
Harley, sounds like you are figuring this out pretty much..I am so sorry you are having se's with your tamoxifen, I can't help there I had nothing with it. They must have advice for those, isn't there even a web thread on here about it?
Good luck everybody!! Hello, Miss Ritajean(I love your name) hope you are feeling good! Interesting to read everyone's diagnoses, and evals, I don't know much about mine, but Ritajean, I think it was mostly like yours, no nodes, a little over a cent., no HER2N and estrogen positive. It's interesting how much they know now about it, I hope they come out with a vaccine against it, I know it's in the works right now, according to another onc. in the office who is in the front line of cancer research and heads up the lymphoma dept.I personally cannot wait, hope it's soon! He said prob. within 5 years.
We can all go get it and celebrate. Kick butt Carol, I know you will.
love
annie
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Carol,
Hope your tx goes well today... thinking about you!
Hugs
Harley
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Annie,
Yep there IS a thread about Tamoxifen, but I have noticed that everyone's reaction to it is different.
YAY...A vaccine would be nice!
Hugs
Harley
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Annie, did you take anything after your first treatments? Tamoxifin or any related drug? Were such things available to you at that time if you were er positive?
I'm really interested to learn that a vaccine is actually in the works. That would be a pure blessing, wouldn't it?
Hello to all you gals. I hope your side effects are minimal this time. I'll be back later. The sun is shining here (a strange sight!!!) and it's calling my name. I also need to meet a friend for lunch so I need to get hustling! I'll catch you all later.
Rita
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Hey Rita,
Have fun at lunch with your friend!I am also very glad to see the sun today!
Harley
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Carol, How did your treatment go and how are you doing after it?
Jill, my feeble brain is not registering when your next treatment is. Are you ready for #5? You and Carol look so good in the pictures that it's hard to believe you are going through this.
Annie...missed you today!
Harley...the sun makes everything a little brighter. I had a good day. I got several things accomplished around here and had a nice lunch with a golfing friend. How'd your day go?
Hi Ginny, Susan and Candie. We miss you gals! Hope you are enjoying this lovely weather and getting outside some.
I'm off for the night! Take care ladies!
Rita
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Rita,
Hi! I'm doing ok, hanging in there. My surgeon appt. isn't til tomorrow, so this week has been a long one, filled with anxiety. I thought that most people who have back problems usually have them ALL their life. They don't just start when we get old, but I really don't know. Last year, at Christmas, my aunt had sciatica so bad she wound up in the hospital, in a wheelchair and in rehab.
Annie, where are you? I think I remember that you told me you took Tamoxifen the first time around, but you had no se's from it. I am not sure whether this back pain is from the Tamoxifen, but it seems unlikely.
Everyone have a great day!
Harley
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Harley...I'll send out extra special good vibes and say a special prayer for you before you go tomorrow. How well I understand your anxiety! I've had my back problems since I was in my 40's. At first they were few and far between (maybe a bad spell every 4 years or when I did something stupid to aggravate it) and as the years went by, they reappeared more frequently, probably from excessive use and stress. Just keep taking deep breaths when you really begin to feel anxious today and think positive thoughts. There are SO MANY other things that this can be! HUGS TO YOU ACROSS THE MILES!!!
Rita
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Good AM ladies!
Carol I hope you are feeling well today after last treatment.
Jill, good luck w/ treatment #5, boy you guys do look awesome in you photos..and having alot of fun!
Rita, hi! I did indeed have five years of tamoxifen and not one single solitary side effect, except for losing 20 lbs. and feeling great! The 20 lbs. seemed effortless coming off, but could also be attibuted to that fact that I kicked my own butt and said "OK, no more junk food, missy!". That it came back anyway? You know, they said it's a different cancer, but Sloane kett. in NYC said it must have been a tinsey calcification they never saw the very first time, and then it was "held in check" by tamoxifen, grew when I stopped it. Makes alot of sense. It was very close to chest wall, hidden from mammos and unpalpable. For some reason unknown to myself, I decided to have that MRI...wasn't going to as all mammos were clear. Thank god, I did, it found it! I would have been one of those "uh oh" stories
I think otherwise by the time it showed up on a mammo.
Moral of this admittedly rambling tale is I think everyone should have an MRI cuz yeah, they do catch things that are not found in mammos!
Harley good luck tomorrow...
Alot of times sciatica is just literally a passing pain in the butt and that's it. And I'm not a dr. for sure either, just musing on what it may be, so let's not go there til a dr. takes a look..
Your poor aunt sounds like a very extreme case. And I am sure you will be reassured by the visit, and feel much better very soon!
I'd love a vaccine too, this onc. group is amazing!
love to all
annie
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p.s. Harley:
My sister was going thru a very very bad divorce and her back was so bad, she was in a wheelchair.....got rid of the guy/anxiety and bingo! Perfectly fine....she now does everything, and she was at the point where she couldn't even take a car ride without a bag of ice.
Back stuff is sooo exacerbated (as all connective tissue is my Fibro doc tells me) by stress....
Read your line in there..."this has been a week filled with anxiety"....
Sending humoungous hugs that it is just that......... stress ( ), praying for that to be "it", and nothing else!!!!
I know everything our bodies have been thru is stress enough to choke a horse! It can be so so many things other than cancer....
so easy to have that "knee jerk" of course, our minds go there, and they will for quite some time to come. This does pass, I promise.
love to you and a big big good wish for tomorrow.
Annie
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Hello Ladies,
First off, thanks for the well wishes for #7, so far so good on the se's front. My WBC was low again 2600, but no change in txt or the ugly n-lasty shot, Whew!
I had txt on Tues and spent all day yesterday at a free retreat for cancer patients and their caregivers. I synopsized my day to share with the Jan 2008 group I chat with and thought I'd copy it to this post ... kinda lengthly but I was pretty jazzed up about it!
Had a great day at Harmony Hill, walked in a little nervous, and was greeted by a very nice facilitator. The setting was in a "Yurt", never even heard of a Yurt before today. It was very cozy, with chairs all in a circle. Blankets were placed on each chair, many took there shoes off to get comfy. There we're 8 of us undergoing txts at this time and three spouses in attendance. A very personable sized group. I was the only one with bc, four women had non-hodgkins lymphoma, and I thought bc was the popular cancer. Unfortunately two of the attendees we're dealing with stage 4 cancers. It was pretty hard to hear their stories and then share my own, quite a few tears we're shed by all in the first hour.
Things lightened up with some breathing exercises, and then some basic yoga stretches. All new to me, never knew I was supposed to be doing deep breathing through my nose and not my mouth. I did have to ask how the heck you can do that when your nose is stuffed up like mine is half the time.
Lunch was interesting but good, very organic and free of just about everything that is supposed to be "bad" for you. It was served in the main building dining room. The grounds are quite large, with accomodations for there 3 day retreats as well, there was a nurses retreat taking place on the grounds for these 3 days. Thats probably why we were in the "Yurt". There is a scheduled 3 day retreat for bc patients, but unfortunately they scheduled it the same weekend as the Komen 3 Day, which I plan on being a cheerleader at this year.
Had time to just visit with one another for about an hour after lunch, I spoke in length to a gal with lymphoma, who was also diagnosed with thyroid cancer within the last 6 months. She had a great fighting spirit but was just tired of not feeling "normal". I had very little to complain about after hearing her story.
We returned to the Yurt, and learned about some self facial massage, and then listened to a tape on Relaxation and Wellness, by Belleruth Naparstek. We we're each asked to get as comfortable as possible, many took blankets and pillows to the floor, I noticed the sun coming through the window and decided to pull my chair into the warmth. About 10 min into the tape my head was bobbing, and I literally missed the last half of the tape. I'd say it put me into relaxation mode with no problem.
I thoroughly enjoyed my day, it was definitely not something that I would have ever thought I'd be a part of, but then again I still have a hard time believing that this isn't all a dream.
Harley, I bet you'll be happy when tomorrow comes, isn't that your day to see your doc in regards to your back aching? Try to hang in there for one more day, stay relaxed as possible, "breath through your nose"!!!
Annie, I like what your posting on Tamoxifan. Losing weight (albeit with diet), and having no se's. I still want to talk to a couple of docs about having my ovaries removed vice taking Tamo for 5 years. And I'm with you on the MRI vs Mamo, I'm not too confident with the mamo as it showed nothing 7 months prior to my diagnosis. I'll be demanding a MRI in the future. Refresh my memory but did you have rads as well?
Rita, always appreciate your popping in for so many well wishes, got those clubs dusted off yet? I sent an e-mail to my surgeon thanking him for the numb underarm and missing boob, my golf game was unbelievable!!! Gotta love the roll your ball gets in the desert. You could literally putt from a 12-15 foot fringe. I missed the opening of Women league on Tues (had chemo) and now I'm scheduled for next Tues as well. I need to see if they will change my txt day starting in May.
Jill, how you doing gal friend? I'm off work today, trying to get caught up around the house from being gone last week. Oh how I miss the AZ sun, send a little this way would ya!
To all, refresh my memory, but did your hair continue to thin about the same amount throughout all 6 mos? Mine seems to have kinda kicked it up a notch in the last couple weeks.
Okay, better motivate to complete a few things on my to do list today.
Take care my friends,
Carol
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Hi all, just a quick check in to see how Carols'doing...glad to hear all went smoothly this time!
Your retreat day sounds very cool. I'm not too good with hearing others' scarey stories, as hard to keep positive head when i do, but that sounds like something interesting...good for you!
Yeah, I did have rads, 7 1/2 weeks of it, intensive too! (got radiation poisoning effects and got stark white hair and a burned boob). However: it was very very easy compared to chemo! The only thing I noticed (well, beside the white hair, hard to miss that) was that I was more tired than usual at the end of it...flat out lambasted. You might want to think about a leave of abs. from your job or cutting back hours towards the end of rads bec. both chemo and rads are cumulative. On the other hand, you have such great energy!!!
I don't know on the hair front, I had a huge shed after the second treatment and now it's kind of settled down. I think it's different with everybody and your treatment regime is different than mine, and your drugs too. Maybe ask somebody on the board who has the same regime as you could be helpful? Look, with that face of yours, no one's gonna look at your hair anyway, hon. You're good to go!
I too, am going to buttonhole my onc on why he won't take ovaries out. Little damn cancer factories, I don't want them!! I'd rather yank the stupid things out and be done with it, he wants to do Lupron which is AWFUL...took it for fertility cycle and oh my god, anything else but that again.
I'd be interested hear why these drs. try so hard to keep those ovaries....we are saying take them out, we don't want them, etc.?
hmmmm....
but so glad you are doing so well. That sunshine must have been sheer heaven.
Stay well everybody.
love
Annie
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Carol,
Thanks for the positive, warm thoughts! Oh, and BTW, I have done yoga before, so I know about the breathing!! Sometimes I think "How the heck am I supposed to do the exercises and breathe?" That is, I can only seem to concentrate on ONE thing at a time...either doing the exercise properly, or breathing properly... LOLOh, I am starting to try some of the easier yoga poses again, and I am alternating them with walking. Since it's been so cold and rainy here lately, I will probably be doing more yoga than walking!
Thanks again!!
I am so glad to hear that your tx #7 went well today. YEAH!!!
Hanging in there,Harley
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Rita,
Thanks for the prayers! They are what got me through everything so far... the bc dx., the surgeries, and oh...let's not forget, the tx!
In my good moments, I know that this is probably 'just a back ache', but at other times, all rational thought goes out the window!
I'll try to pop in again after my dr. appt. tomorrow, but I will probably be scheduled for the MRI next week!
Harley
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Annie,
Thanks for the hugs! I really need them!!
Oh, Annie! I don't trust Mammos, either! I will be fighting with my surgeon, 'cause he says I still need to have mammos, to screen for recurrence, but... I don't trust 'em! Plus, I am afraid I'll get a blow out! with my implants!
Well, the stress...if that is the case, then no wonder I have been feeling worse! I can't seem to turn off that worry gene! Sorry about your friend, but glad that she's feeling better now.
Thanks for reassuring me that it will get better. I sure hope so... I am driving myself and my dh absolutely crazy, with my constant worrying.Thanks
Harley
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Good luck tomorrow Harley!!!! I'll be with you in spirit. Please let us know how it goes ASAP as we will be anxiously awaiting your news.
Annie, that sounds logical to me about the recurrence. I wonder why they don't continue with the Tamoxifin and Arimidex after the five year period if it's been proven to keep the beast away. Maybe there will be improvement in that area soon, too.
Carol..your retreat sounds like it was SO neat! I've never heard of anything like that but it sure would be great for anyone. So glad that you had the opportunity to attend.
Well...just wanted to wish Harley good luck tomorrow. I'm off to the recliner for the night.
Rita
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- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 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