Chemo May 2013
Comments
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Lorrie,
Hope you got that thing out if your eye! I think it's contagious sometimes!
A bunch if us Girl Scout leaders went out for dinner tonight. As we were waiting for the table one of the leaders says to me. "You look really good,it's all done, you are past it, life goes on". And in the next breath she says "my MIL had uterine cancer and had a hysterectomy and did the chemo thing. They discovered a nodule in her lung and now she is back in chemo doing that whole thing". Ugh. I sat in stunned silence the whole meal.
Sigh.
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uh.... WTF... ..
I don't know what to say to that...
I'm sure they didn't mean anything, but....IDIOTS
unfortunately, or fortunately....
This is where we can hate.. or dislike stupid people. ...
jeesh......
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Good grief. Ignorant. Just what you don't want to hear. Forgive them for they no not what they say.
Hang in there. ♡♡
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Patty - seriously??? People feel the urge to fill any silence with some stupid chatter.....
Happy New Year to you lovely ladies. We have to be proud of what we have endured!! And if nothing else, we'll never forget 2013.
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Oh Pat so sorry! People think telling us about other cancer victims that they think are in a worse situation then we are in their mind somehow will make us feel better! How stupid! I recently went to a christmas party, with my short hair, and a lady came up to me and introduced herself and said that we had not met...well we did, several times, before BC when I had long hair. I reminded her we had paddled together on several occasions, and then she quickly backtracked and raved about how much she liked my new haircut! I just stood there frozen, and did not know what to say.
Kate you are soooo right about feeling proud of all we have went through so far. We had no choice but, it really was an ordeal. We do have to remember to be good to ourselves still.
Lori: love you new motto! I will have to borrow that one! I am also go grateful for you ladies as this year closes. And you also have a very good point about our DH's divorcing us if they had to hear all of the stuff we have confessed to eachother! I am trying not to talk about it so much with my family, but am so thankful I can do it here!
May I make an early toast. To a better 2014 for all of us!!! May we keep in touch as we go though this next emotional year.
My MO says it will be a psychological rollercoaster as we find our way back to live as "normal"
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Gully! To us! May those who are unfortunate enough to follow in our footsteps take a look at the strong women from the May chemo board and know they they too will come out on the other side.
Pat
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klink. Happy New Year. Here's to feeling better physically and emotionally. Spiritually is important too. yes....Let's all stay in touch. It means so much to me.
Love - Carla
P.s. Not feeling very strong right now. .Maybe tomorrow.
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We made it girls! Happy new year!!!
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Happy New Year!!!
My Onc says I was cancer free once I had my mastectomy. The chemo and anastrozole is the insurance just in case of any cells that slipped by. Something like that. My blood levels were good. However he wants to see me every three months for two years on anastrozole. He will do blood tests each time. I am to let him know if my side effects get to be too much for me to handle because there are several options on meds. My body aches have been gone for a few weeks and hot flashes aren't too bad. So we continue with no changes at this time. The results from my bone density scan were good too.
I had a great New Years with my date and his youngest (15) daughter. We went to a friend if his' and played games. I got home at 3 am. It was fun and I even only drank water all night. Nice start to a New Year.
I have had some heartburn and a little acid reflux too. It seems to be a little worse when I drink soda but not too bad so far.
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Chiming in a little late....Happy New Year to all of you amazing, strong and brilliant women! I fully expect all of us to kick some major ass this year! Thanks to everyone for your support and listening ear throughout this adventure. Here's to a much healthier and enjoyable 2014.
Love to all,
Annie
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2nd opinion update.
Today I went for a second opinion. I can't say this doctor is "known in the field". She was recommended by one of my Girl Scout leaders (I later found out she is a stage4 survivor)
Anyhow, the doctor met with hubby and I and said she reviewed my file (I had dropped off a complete copy last week) and she felt confident that my oncologist did a good job. (Would they really say otherwise?-seriously!)
She feels that the CT scan in 3 months from first scan is the protocol required for my lungs. She reiterated that it is likely nothing, but must be followed. If it becomes larger we will discuss other methods..
She commented about following with tumor markers and circulating tumor cells (? I think that's what she said) tests ...both are blood tests. I was NEVER offered these before, often wondered why and I understand they are not "foolproof" but it's "something". I mentioned the "tender" area in my ribs (lower back) and she asked if I felt a PET scan would alleviate my concerns....YOU BET!
So, she also did a physical exam (and loved the DIEP boobs..they do look really good!).
I commented that I guess I need to "pick an oncologist" to stay with and she said I should. So I told her I picked her. I was never 100% in love with my oncologist. Hubby described her as flippant, I describe her as dismissive...I guess they are similar? I NEED someone who will make me feel my fears are discussed thoroughly without being rejected. I did LOVE my chemo nurses (one lives in my neighborhood and I see her at school things) and God forbid I need to do chemo again I will really miss them!
So they took a few vials of blood ...tumor markers and circulating tumor cells as well as CBC...which is the blood counts...I was disappointed my last one was done PRIOR to last chemo, why not check my counts after? and they are calling to get an approval for a PET scan.
The doctor did say that this period of time after treatment is completed can be most stressful for us. (As many of your docotrs have said). I told her it probably wouldn't bother me so much if they hadn't found the crap in my lungs! With that said she asked if I have gone to any support groups. I'm thinking maybe I should give it a shot. I am feeling better now that I spoke to this doctor , and I told her I LOVE this site, but maybe I need a little "therapy" to help me deal.
I am looking forward to getting the blood results and PET results. Hopeful that there is nothing and I won't regret asking for these tests! The chest CT will be in February (3 months from first one). Tamoxifen for 5 years and then a switch over to a aromatase inhibitor (I think that's what it is) for another 5 years.
That's all I've got for now.
Pat
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Pat so great that you found a good onc. Listens to you, takes you serious, has suggestions and has follow through. Excellent!
Teresa my onc also said the same thing about the mastectomy and cancer free. I think she said the chemo was to get any of the nasty little cells that slipped by. And I think the anastrozole blocks estrogen.?. Glad your bone pain is nill and thatyou are tolerating anastrozole....Was the date you had on New Year's the same gentleman you told us about before?
And Happy New Year to you too Annie and Gully ...and all.
Carla
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Pat,
What is the name of the test for circulating tumor cells? Don't think I've heard of that one before and want to see if I've had it. My cancer center has now puts all the lab and test results online for each patient so I can cruise my records 24/7........a little scary but easier than waiting to get them from the doc.
Ann
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Ann,
Here is a link in regards. It does not appear to be a "standard" test. This is for metastic breast cancer. No one is using that term with me. However they are keeping an eye on a lung nodule, I thinkit is prudent to do a bit more testing in my case. http://www.mayomedicallaboratories.com/articles/f...
Pat
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patty, I'm glad you went for that 2nd opinion and found a doc you feel good about. We have to be our own advocate
Dh and I started watching Breaking Bad. We didn't watch it when it was on tv but we are catching up. Some of the cancer stuff is hard to watch. Plus I was thinking that if I had started watching the show in 2010 when it began, my cancer journey would've been years away
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Happy New Year to all.
Patty so glad you found a MO you are comfortable with. I am not a fan of mine and think about switching. Received a letter from my insurance and it sounds like they will pay for herceptin. Have not heard from the doctor's office yet. Ok was kinda of hoping it would get denied so I didn't need to make the decision. I think I may call the MO who I went to for a second in May to see what he thinks. I really wish this would of been thought thru when I had my chemo.
Theresa...great to hear about your fun new years.
Good day to All
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Carla yes my New Years date was with the same guy I told you about before. I really like him, the weird thing is that he talks a LOT when we are together but when we aren't together he doesn't keep in contact.....I asked him about that when I saw him on Monday and he said he gets that from his Dad. So we texted for a while last night but I'm not going to text again.....going to wait for him to make the first move, but it's frustrating.
Ann all of my results are also online for me to look at whenever I want from the Oncologists office. I can check blood counts and all kinds of stuff on there, of course most of it doesn't mean anything to me. I am now back to my pre cancer weight, however I have quite a ways to go to get where I really want to be.
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Well... Happy New Year to all of you!!I think I'm feeling a little bit better now with the Tamoxifen... I'm less tired during the day and not quite as achy... Its either leveling off for me or its my new Sleep Number bed.... (I'm a 30-35 by the way, hee hee) either way, I'm feeling better and think I'll be able to stay the course with the Tam.
I'm following Peter Walsh's 31 Day Organizational Challenge.. and IT IS KICKING MY BUTT!.. Sure, you start off doing just the 10 minute challenge, but then you dig into other things while you're motivated & it turns into a couple hours each evening. I was shocked when I looked under my hubbys sink in the bathroom.... there must be at least 20 empty bottles of shampoo and conditioner... they may have a drop or two left in them... He says he hangs on to them just in case he actually runs out of shampoo. Well, they are in the garbage now and have been replaced with one new bottle of shampoo in case he runs out! Jeesh..
My hair is growing in REALLY thick & curly just like before chemo... but slow to lengthen. I went hatless for the first few minutes of our New Years Party that we hosted this year. I found myself getting anxiety until I put the hat on for the rest of the night... I'm just not ready... it's my bangs.. I need my bangs to be a bit longer.
Anyway... Feeling better everyday and I hope the rest of you are as well!!!!!!
Here's to a Kick-Ass 2014!
Lorrie
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My hair seems to be getting thicker but not longer to me. Others say it looks great. My concern is that there are a lot of days when my scalp is kind of tingly like when I lost my hair from chemo. It's kind of scary to know that I am just getting my hair back and the Anastrozole might make it get thinner or I could even lose it. So far I have noticed any hair loss just that weird kind of tingly sensation. Anyone else having this?
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Teresa,
I don't have the tingling but the top of my head still itches like crazy. I'm also on Anastrozole and haven't noticed any hair loss. Hair is coming in thick but taking *forever* to lengthen!
Annie
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My hair is taking forever to grow long and my eyelashes are falling out again!!! WTF????????
I saw my plastic surgeon yesterday and I'm going in for a revision surgery -some fat grafting!!! I hope he can lipo the shit out of me!!!
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Kate, good luck with the lipo!
Here is a link. I can relate to the "just feel them". Though I didn't make that offer to my girlfriend when a bunch of us went to Vegas. She was drunk as all hell (our flight was very delayed and she had the free drinks in the casino) and when she saw me (first time since diagnosis) she was excited and gave the girls a huge feel up! Lol. She never mentioned it the next day. I don't think I will remind her!
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My headis extremely it hy too... I thought cuz im constantly wearing a hat...
No hair falling out, really thich. But seems to get thicker instead of longer... haha
Im having somewhat of a meltdown (again) last couple days. ihate my moodswings, if the hotflashes dont do men, my moods will. Ill be surprised if my hubby comes home tonight after work.
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Lorrie! LOL, I've been really bitchy the past few days...I think my husband is done with me! Ha!
Called the new oncologist office today to ask about my pre certification for PET. Just so happens they got it today (hmmm....). Anyhow I booked for Monday. Never had pet scan before. I was told no food after midnight and only water if I wanted. the test is at10:30 am and I will be there 2 hours. Was also told to dress warm.? Damn, I'm going to be a real cranky bitch if I'm not allowed to eat...I could care less about being cold!
Well, I won't be dwelling on it until after the test is done. Keeping fingers crossed.
Pat
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Fingers crossed for you Pat!!!!!!
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Btw,,, hubby did come home tonight & saw him on my ipad looking at vacation spots in belise..,, not sure if u all remember, but he promised me a vaca after radiation. Well, his work got unusually busy for this time of year so no vaca...maybe it will happen after all. ?.
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Haha yes my eyelashes and eyebrows are falling out again too - booo!
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Lorrie, if hubby can't go with you I'm available!
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I watched a really good Christmas movie I recorded that was on the Hallmark channel. It was called November Christmas. It had Sam Elliott and John Corbett in it. It was about a family with a 9 year old daughter that has cancer. Excellent movie and fortunately had a good ending. I've been meaning to mention this for a few weeks but keep forgetting. I hate the chemo brain! Has anyone else seen this movie?
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Good luck on Monday Pat! My PET scan at the beginning of all this was a breeze...you'll do great. My eyebrows are falling out again (2nd time)...sheeze. Hair is thickening up and has finally gotten long enough to lay down on top of my head instead of sticking straight up. I've been without the wig and hats for over a month. Finally just said WTF!
Teresa, haven't seen the movie but will definatelyl ook for it... Netflix?
Annie
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