Starting Chemo March 2015
Comments
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I'm here sitting on the ledge too...now that treatment is over I'm having a hard time coping with the fear of it coming back, every little thing I feel must be mets...I'm trying to keep myself distracted but it feels like it's on my mind 24/7. It of course doesn't help that the holidays are here and my cancerversary date is approaching.
I don't know how to move forward with my life like this. I'm thinking about trying therapy, but wondering if that will help. I find comfort here on BCO and like being here where everyone gets it, but at the same time wondering if being on here is holding me back. This year really sucked with all the treatments/side effects etc. and it kept me busy trying to stay on top of taking care of myself physically, but I've heard that the year after treatment can be more difficult dealing with all the emotions and fears. Trying my very best to enjoy each day as it comes, but it's so hard.
Sharon and Amber...thinking positive thoughts for you both that your lumps turn out to be nothing to worry about.
Theresa...sorry to hear about the car break in.
Eileen...have you considered melatonin? I've heard it's good to take especially with Tamoxifen and might help with insomnia. It's been working for my insomnia.
PB
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Well, it's nice to see some company on the ledge (not really!) so I know I'm not the only one. Thanks for the spanking...just what I needed! I will stay away from those boards and try to just move on. 2015 cannot be done soon enough
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Bekah, r u back to work?
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I just went back to work today. I'm doing 3 days a week for now. Probably will keep this schedule until done with Herceptin and then back to full time
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I went down the rabbit hole a bit this weekend, but I quickly recognized the warning signs. It is so weird that a few of you have a memory block for 2015. I have the same thing! I think it's probably a psychological coping mechanism. I know things happened, but they feel surreal - almost like they happened to someone else.
So, it turns out that I kidnapped my neighbor's kitten.
After spending $350 on a crate/self-cleaning litterbox and housing her for several days, I ended up locating the owner through our neighborhood FB page. (I use the term loosely since the kitty isn't vetted or spayed, and she's left outdoors to sleep in an outdoor shelter.) I felt sad having to return her. Let's just say that I have a 2-strike policy with lost animals. She won't be returned again.
I'm still feeding about 4-5 strays and trying to establish trust to see if they can be adoptable. We've done dog rescue for many years, but this has been my first adventure with cats. My big, fat, stupid, bleeding heart misses sweet little Penelope so much (my name for her).
Funny enough, this wasn't my first catnapping, but the last one was about 7 years ago and involved a LOT of liquor.....
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Lee - can't wait for the drunken catnapping story!
Bekah - what kind of work do you do?
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That's weird...I posted a reply but it didn't post.
Anyway, I'm a Physician Assistant and I work in Occupational Health.
I know, I know...I should be more rational about things being a medical provider but hey, I'm human - don't judge me!
Bekah
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Hello to everyone hanging in to th cliff's edge. It seems to be pretty crowded here - I've been stuck in this dark place since September, but I am starting to be a bit hopeful. I don't know. The end of active treatment seems a very hard transition, particularly after a lost year, where the whirl of diagnosis, surgery, chemo/rads, and pervasive illness has made a hash out of any sense of normalcy.
I, too, have some difficulty populating this year with memories. I think there are lots of reasons for that, but one of the biggest is the merciful nature of human memory. I remember being very sick during chemo, but the physical memory of exactly what that feels like is fading somewhat. Because I was feeling unwell much off the time, I have big gaps in my day to day memories.
Also, so much of what little energy we have was engaged in very personal pursuits. When we are very sick, we,don't have energy for the other things we normally would do, whether that is our close relationships, our jobs, or even our leisure pursuits. In "normal" times, for example, I used to have three or four books on the go at once, and when reading light material, like novel, I would grind through at least 150 pages an hour. During chemo, I had some vision "changes" and my attention span reduced me to picking through one or two paragraphs at a time. This means I don't have the mental images from a year of reading that I would otherwise have. Being alive and focusing on recovery uses it all, but doesn't leave much in the way of milestones to measure progress.
The transition from tending to your illness every day, with medical people following you and watching your every symptom, to being basically on your own to monitor your own symptoms is very jarring to me, and more than a bit frightening. I'm trying to learn how to function "with the fear", and while I can't claim success, there's a little piece of me that is hopeful.
I've had my second consultation and workout with a trainer today. My lymphedema didn't explode after the first one, so that's a good thing. I'm cleaning up my diet, and have lost 3 pounds already. I have quite a way to go, but I'm doing something. Maybe after the pathology Tumor board has weighed in on the DCIS and LCIS in my "prophylactic" mastectomy tissue, I will feel better. Right now, that appointment is scheduled for December 15
I'm reminded of a little plaque that my son got when he was a teen, though I can't remember the quote exactly. I'm going to track it down tonight when I get home, and will post it then. It's about courage.
Hugs to all of us hanging from the cliff....
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make room on that crowded cliff. I found a lump at the incision from my exchange surgery. I found it a week ago but hoped it was just inflammation from rads. I ignored it for a week and hoped would go away. It is more prominent now so I messaged the surgeon. They can't get me in until next Wednesday. Ugh. I am hoping it is just scar tissue. My body likes to make scar tissue. But my body likes to make cancer too. In my 2014 Christmas letter, I had just finished all reconstruction, so my last line of the letter was that my goal for 2015 was to stay out of the OR. I did not even make it past January. My year started with a cancer diagnosis and I am scared to death it'll end with one too. I hate this.
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Oh Karen! You just can't catch a break!!! I'm praying for scar tissue. We know physically that waiting 10 days wont make a difference but mentally it makes a big difference. Hang in there!
Bekah
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Thanks Bekah! I am hoping you get good news on your lump too. I hate that our bodies do this to us! Like we don't have enough to worry about! I should add that I did have several lumps that formed very soon after I had fat grafting in 2014. I hope yours just comes back related to that.
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That's good to hear since I just had fat grafting 2 weeks ago...
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I had several that formed around that time frame. The biopsies came back as inflammation, not fat necrosis, but my body obviously did not like it, so I never had it done again!!!!
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Karen, Sharon and Lee- my arms are around you all. I hate it that you have to wait. We are all here. Please let's all just hang out on the cliff for a couple of days. Much love. 🙏🏼🙏🏼🙏🏼
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I will lean out the window, set one foot on the ledge, and start passing out bourbon and chocolate for those who need it. DON'T LOOK DOWN (which includes looking at the Stage IV topics).
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think I will be imbibing some bourbon tonight. And feeling myself up real good. And living in the fear locker for a bit. With ex husband stroke, friend breaking collar bone, mom in hospital again, getting ripped off at beach, coming home and having husband say our dog about got hit by a car today, and all the posts today, life is a scary place right now.
Karen, I am in disbelief. Yours has to be fat necrosis, what else could you have done to prevent a new tumor from growing? Gotta go find a star to wish on for you. And for everybody else too
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Thinking of everybody going through tough times right now
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Thanks ladies. I did this twice and got through fine, but the mere thought of having to do this a third time literally takes my breath away. I just want my life back for a while! I appreciate all of the good thoughts. I am working tonight, so that is good distraction. I am hoping for good weather tomorrow so I can go for a really, really long walk or run to try and clear my mind. I did a good job burying my head in the sand last week. I need to find that hole and bury my head again!!!!!
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This is actually a picture of you, Sharon, Bekah, lee, kbeee, and theresa.
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we need Lake Arrowhead now! I need to see all my sisters. I miss you all so much right now
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that would be so nice..... 💗💗💗.
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I'm so sorry for everything everyone is going through. I promise to keep you all in my thoughts. I also understand about the pervasive anxiety. I find if I stay busy, meaning overbooked and never saying no, I stay back from the ledge. Being so social can be exhausting for me being an introvert, but exhaustion seems to help keep the demons at bay. Sometimes the better part of a very busy day will pass and I've not thought once about the cancer. I consider that progress but the ledge is always there.
This weekend I had more than the usual time alone and I did some shopping, was coming up from the basement of a sporting goods store and my foot caught the last step and I face planted. I am someone who never falls down so of course I unraveled over the next 24 hours about how the end must be nigh, I'm becoming an invalid, etc. Etc. A year ago I would've laughed at my clumsiness and not given it another thought. We are coming out of a fog of a year and it's up to us to be vigilant with our bodies while not obsessing about every ache and pain. That's a tall order.
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Kbee - I don't know what to say besides you're in my prayers and that I'm hoping so much this time it's merely scar tissue.
Bekah - I know u r returning to work with your same passion and compassion. You're too awesome to waste your skills.
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Thank you Sue. It's hard (physically and emotionally)going back to work but I love my patients and it's good for me to go back!
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Karen. It's too cruel to even comprehend. I'm so sorry.Eileen, Thankyou for asking about Ashlee and for your very generous donation. She is overwhelmed with the support she has received. She is going to stay at her aunts for a while. I'm catching up on the weekend. I'll give her a hug from all of us.
I'm throwing myself into work and running. Thinking of you all. I know we are all going through stages of trying to stay on top of our fears. And I'm so glad I can share with you all.
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avmom I'm so proud of you!
Pb I'm throwing over a rope. Hopefully we can all help to pull each other into safety.
I'm cheering for your successes. You just can't see it because I'm hanging onto the cliff tightly.
I can't tell my family what's going on. I'd hate to worry them. I'm so grateful for all of you.
Time for me to go to sleep. Have a lovely day xxx
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Thinking of you, Karen. I agree with Bekah. Waiting can drive you mad. I am carrying you close to my heart while you are going through this worry and limbo.
Sharon, let us know when the bracelet arrives I can't wait to see pictures of it going to all of your favorite places. I love the fact that it is traveling well. What an awesome symbol to unite us all.
I think it's time for a Jack and Tutti pic today! (My auto-text tried to convert Tutti to titty. Must be a hot topic in my conversations.)
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Checking in to say I am thinking of all of you! Esp Karen, Bekah, Sharron.... All of you facing and waiting for crazy situations!!! I want to say that i am soooooo with everyone of you with the crazyness of this post treatment life!! One minute I am fine and not at all thinking of Cancer, glad I am feeling good and moving on... then the next thing you know I am diving down the rabbit hole of recurrence. I lost some weight.... I feel great.. I worked really hard to lose it, i gave up sugar and yummy carbs....... then i let myself think that maybe I lost it because there is something wrong, there is mets somewhere.... It's maddening that I do that to myself!!!!! But I can't stop thinking it!
On a positive note... including today I have 3 more Rads!! I have made it through with little incident. I am a little burnt and itchy but nothing more than a bad sunburn.
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Is there room for one more on the cliff? Alan & I met yesterday to start dividing assests/transferring properties/making a list of next steps....he showed up bawling. Both drank too much.....had frank conversations about our past. Blech. At one point he had to check on a work e-mail & I checked the board. When I saw Karen's message I lost it. I was telling Alan about her previous recurrence, etc. I was reminded that people don't understand that it's not like you take off your boob, get chemo & call it a day. He didn't realize you could still get cancer. I broke down & was telling him how much I worry about recurrence.
Ledge ladies, keep in mind we have been so freaking strong over this last year. We can do this. Let's hold on tight - to the ledge and each other.
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Oh, wow. I am sorry to those of you who are going into the pit now. I am sure it will my turn. Right now I guess I am on a sugar high from being done with radiation and having my itching start to ease up. Hugs to everyone.
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