As of April 2, 2012, this blog became the place for documenting our New Adventure called Breast Cancer. Basically it's all about our Cancer ParTay.
As of Oct 2013- our 18 month Survivor mark- the ParTay's pretty much over. Treatments are done, my hair is back and I am healthy & cancer-free!
As of today- I want you to know that the trick to living a happy, healthy and wonderful life in the future is to remember where we've been, what we've learned and how much we've been blessed! That's exactly what I hope you find here.
Showing posts with label Breast Cancer. Show all posts
Showing posts with label Breast Cancer. Show all posts
Wednesday, April 2, 2014
2nd CANCERversary
Wow! Time flies when you're not fighting cancer! LOL
I seriously can't believe that it's been 2 years since my "Big C" phone call.
I have a hard time remembering it all anymore. I am very grateful for that, actually.
I am happy to report that I am living on
Even if I am occasionally whiney about the mundane- it's awesome to feel NORMAL!
Se trata de:
Breast Cancer,
Cancerversary
Wednesday, March 12, 2014
Young & Healthy
I had a 3 month follow-up visit with Dr. Thomas today. (Technically my "7 month-post mastectomy" visit or my "23 month since diagnosis" visit)I met the Nurse Navigator, Pam Sasser. She was super sweet and helpful. She sat in on the appointment today and even took notes for me. Where was she for my whole cancer ordeal? LOL
Dr. Thomas asked me how I was doing and tried desperately to find something he could do for me. Unfortunately for him- I am Young & Healthy. It was funny to see him try to come up with anything he could do for me. He said he could have my cholesterol checked if I'd like. LOL
* He did listen to my heart and offered an echo if I felt I needed one. (which it doesn't sound like I do- it's just that the info on cancer patients says that they usually check it after your treatment. And I had mentioned to him that Dr. Panwalker had never had it checked)
* We talked again about Tamoxifin which I still feel strongly about NOT taking. He said that he would keep bugging me about it but leave the decision to me.
* He also brought up Genetic Counseling which I also still feel is a waste of my money. Now that I've been diagnosed with cancer and I already have children- my kids will automatically get checked early. Getting genetic counseling (in my opinion) would only benefit the industry and pocketbooks of someone other than me. ;)
* He told me he doesn't see any reason to see me back for another 6 months. (unless I decide to take Tamoxifen- then he'll get me in right away!;)
* I did get a High-5 for being my young & healthy self.
* I asked about getting labwork done. He said if I'd like- they could do it next time. I would just have to fast beforehand. Basically- I'm not sure if I want labwork done but I'm not sure how else they would ever know if my cancer came back. It's not like I can find a lump in my breast and get it checked out. LOL We'll see what the next 6 months bring.
Dr. Thomas is really great and I appreciate him as my Oncologist. But I do admit- it's nice to not need him.
Se trata de:
Breast Cancer,
Doctor Appointment
Wednesday, December 4, 2013
Cancer Survivor in Montana?

Do I have to be a cancer survivor in Montana?
Can we just pretend that it was someone named Shay in North Dakota that had it?
Probably not. Dang!
I figured I should be a good girl and at least show my face at the Cancer Center here in Helena.
Lots of people recommended Dr. Justin Thomas. He is an oncologist at St. Peter's Cancer Treatment Center. So I set up an appointment for this morning.
He was way nice. He read over my chart beforehand and then we chatted about how I've been doing. I've actually been doing great! It feels like it actually never happened but I guess I understand the importance of getting checked.
Then came the topic of Tamoxifen. Let's just say- It's not been my favorite topic. ;) Here's a few explanations- See Posts- Discussion with Panwalker and Herceptin # 8. By the time we were done- Brett was laughing at us. He said he could see that both of us felt strongly about the issue. And he also could see neither of us were about to budge on where we stood.
My biggest thing is that I did everything "right" to get rid of my cancer. I am now cancer-free and doing very well. I am NOT a drug-fan. It comes down to that -for me- there's not enough evidence that Tamoxifen will keep it away. And the possible (even if they claim they are very few that get them) side-effects are not worth the risk to me.
In his defense, he said that he has a similar patient. She did everything "right" and was doing well. She choose not to do Tamoxifen as well. Then several years later- it came back and the diagnosis is not good. He said she hasn't said it but he suspects that there is a tiny bit of regret that she didn't do the Tamoxifen when she had the chance. He said if I was his wife- he would want to do everything possible to keep me healthy and cancer-free for as long as possible. I appreciated his honesty.
We left it with-- He asked me to pray about it. And he would support me in my decision of whether to try it or not. He said we could just try it for a month and see how I react. Then maybe a month more. And another... until I had a reaction. (He was hinting to the fact he didn't think I'd have a problem and he'd get me to take it for the full 5 years. Oh! He is a sly one. LOL)
He said that if a reaction came up- we'd stop. OR- for the most part, any side-effect I would encounter- they would have another drug to deal with it. My anti-drug-self had to chuckle. I could start Tamoxifen, drug free and walk away in five years a full-fledged drug addict. Wahoo! Sounds fun, right?
The tricky thing is that there's no "RIGHT" answer to Cancer. [That sounds like a catchy slogan!] Dr. Thomas was absolutely right though. It has to be a matter of prayer and then just have faith it will turn out like God has planned.
Se trata de:
Breast Cancer,
Doctor Appointment
Wednesday, October 2, 2013
Is this ParTay over?
It has been 18 months since I got the phone call labeling me as a Survivor.And to tell you the truth- it seems like it was a phone call that was made to someone else.
The whole Cancer experience seems like perhaps it was a movie I remember watching and not something I actually went through.
Is that weird?
I feel like the only proof there is that I ever went through all of it- is this blog.
..O.K. and the little fact that I no longer have boobs. Guess there's that. LOL
Sometimes I feel like I'm doing this Cancer Survivor thing all wrong. There are survivors that attend support groups every month. There are survivors that worry every day that it might come back. There are survivors that never feel back to normal. There are survivors that continue to raise awareness. There are survivors that support other survivors. There are survivors that start foundations. There are survivors that are changing the world. Then... there's me. I just want to pretend it never happened. I don't want to spend my days consumed by any of it. I paid my
So I can't believe I would ever say this but-
Is this ParTay over?
{Let's hope so}
Sunday, September 29, 2013
Remember the Walk
I thought this was fun. I got this email from the Fargo YMCA this week. We participated in this event last year, And here's my little family [top picture on the flyer] on the advertising for this year's Walk. We're so cute!!! Too bad we weren't in Fargo to participate.
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Se trata de:
BC Events,
Breast Cancer,
LiveStrong
Thursday, August 1, 2013
A Head Full of Hair: Part Two
This was me and my nearly bald head- one year ago today....
And here I am today (O.K.- that's a lie but this week at least)...
I can't believe the difference this year has made. In some ways, my hair growth has taken FOREVER! But in some ways, I am amazed at how thick and curly and long it's getting. CRAZY! It's been really fun to document it's growth.
I did this a while ago (see it HERE) but thought I would update the remainder of my hair growth journey. It's like a Hair Style magazine personally made for me. I can look at any length and know exactly how I would look. Pretty neat!
And here I am today (O.K.- that's a lie but this week at least)...
I can't believe the difference this year has made. In some ways, my hair growth has taken FOREVER! But in some ways, I am amazed at how thick and curly and long it's getting. CRAZY! It's been really fun to document it's growth.
I did this a while ago (see it HERE) but thought I would update the remainder of my hair growth journey. It's like a Hair Style magazine personally made for me. I can look at any length and know exactly how I would look. Pretty neat!
The Back
The Sides
The Top
Tuesday, July 16, 2013
One Year Surgeon Checkup
It's been almost a year from the day I became an Amputee. ;) Today was my one year check-up with my Breast Surgeon, Dr. Bouton. It was like a five minute meeting. Seriously, what a pain these check-ups are!!! Dr. Bouton was his normal, friendly, Texan self. He asked how I was, took a look at my scars, and wrote me another prescription for some more foobs. That was about it.
It was however, the last time of doing anything "CANCERy" in Fargo. No more big, fluffy white SANDFORD robes for me! LOL
P.S. I had forgotten to take my camera with me. Not that there was anything to take a picture of! But I did snap a picture with my phone of my last white fluffy robe! But then I forgot about it. By the time I got around to writing this post, I had switched phones. No longer can I send myself the picture. LOL Oh well! You get a picture of the picture. Better than nothing, I say!
It was however, the last time of doing anything "CANCERy" in Fargo. No more big, fluffy white SANDFORD robes for me! LOL
P.S. I had forgotten to take my camera with me. Not that there was anything to take a picture of! But I did snap a picture with my phone of my last white fluffy robe! But then I forgot about it. By the time I got around to writing this post, I had switched phones. No longer can I send myself the picture. LOL Oh well! You get a picture of the picture. Better than nothing, I say!
Se trata de:
Breast Cancer,
Doctor Appointment
Saturday, June 29, 2013
Volunteering at the Run or Dye
Since my diagnosis, I've had several of opportunities here in Fargo to participate in Breast Cancer Awareness Events. One of my favorites has been the Run or Dye. ***At Run or Dye, you get showered with safe, eco-friendly, powdered dye all throughout the 5K course...turning you into a technicolor canvass of fun! *** I think it was my favorite because it was something I got to do with my family.
I'll just copy the day's events from my Family Blog:
The members of this Seamons Family are NOT runners!!! But this particular Run or Dye teamed up with Fargo's YMCA to help fund the local LiveStrong Program. The Livestrong Program has changed my life. I am extremely grateful (and continue to be because of the very generous discount my family receives at the Y for the next year for completing program). I have wanted to be able to give back somehow and this looks like their last big event before we leave. But instead of running, my family and I decided to volunteer.
Unfortunately, that entailed being at the Fairgrounds at 6:45 AM. Holy Moly! That is WAY early for our family. But they were all quite the troopers. Lucky for us, we live 3 minutes away and got to park in a special Volunteer parking lot. They did feed us donuts and we all got a Run or Dye T-shirt so people would know we were volunteers. We were excited to see Katelyn and get a picture with her. [She was my LiveStrong Trainer and we LOVE her!]
Then, we joined Volunteer Team 9 which was assigned to handing out Waters at the Finish Line. Our team was great! They were way friendly with the kids. We had a lot of fun and really had the best seat in the house for the race. It was awesome! Liberty and Dad handed out waters at the finish line the entire time. (like from 9-12) The other kids helped keep waters stocked, painted each other and helped clean up. I was way proud of everyone for being willing to serve so early and so long!
Run or Dye's signature quality is the color dye they throw at the crowd before, during and after the race. Right next to the finish line, they had a stage for the After Party. They played music, danced and did lots of "Color Throws". Because we volunteered right there by the stage, we got to see and participate in a lot of them. They were crazy!!! So gorgeous at the beginning and then a big huge cloud of dust for several seconds after. *Cough*Choke*Blindness*LOL* And then of course.... being covered in color. Lots of fun!
One of the ladies in our volunteer group had bought the kids each a packet of dye. They spent hours painting each other and throwing dye. We will be lucky if we ever get all the color out of the girl's hair! LOL By the end, we were all covered. We even got Katelyn to stay with us for the last Color Throw. So fun!
We definitely had one Color-rific Day!
Thanks Run or Dye & LiveStrong!
Se trata de:
BC Events,
Breast Cancer,
LiveStrong
Wednesday, June 12, 2013
3 Month Post-Herceptin CheckUp
I went to my 3 month post-Herceptin Checkup today with Dr. Panwalker.
Nothing to report. Everything looks fine. I think they were just missing my bubbly personality and my money. LOL
As a side note: This is probably the last time I will visit the Roger Maris Cancer Center here in Fargo. It's weird to think about. Not that it's a sad day to bid farewell forever just surreal that this part of my Cancer journey is done.
I need to see if I can find a Cancer Center in Montana just for checkups but it's like I'm closing a chapter on my life. Strange.
Nothing to report. Everything looks fine. I think they were just missing my bubbly personality and my money. LOL
As a side note: This is probably the last time I will visit the Roger Maris Cancer Center here in Fargo. It's weird to think about. Not that it's a sad day to bid farewell forever just surreal that this part of my Cancer journey is done.
I need to see if I can find a Cancer Center in Montana just for checkups but it's like I'm closing a chapter on my life. Strange.
Se trata de:
Breast Cancer,
Doctor Appointment
Tuesday, April 2, 2013
One Year CANCERversary
"'Cancerversary' is a word lots of survivors use to describe the day you find out you have cancer. It is a pivotal life altering moment in time that seems as big as the Grand Canyon, but far less Grand. Not sure how to celebrate such a moment, but it's certainly hard to forget it." -Rhonda Radliff (breast cancer survivor)
I found the following letter on a blog from a Cancer Survivor named Ann. She's an amazing writer. (See her original post HERE) It was almost exactly how I feel about my Cancerversary. So I added a couple thoughts and specific memories/events that pertain to my own story- and wanted to share it here with you. It's what I wish I would have known in the beginning.
I found the following letter on a blog from a Cancer Survivor named Ann. She's an amazing writer. (See her original post HERE) It was almost exactly how I feel about my Cancerversary. So I added a couple thoughts and specific memories/events that pertain to my own story- and wanted to share it here with you. It's what I wish I would have known in the beginning.
A Letter to the Newly Diagnosed
on my One Year Cancerversary
on my One Year Cancerversary
Dear Newly Diagnosed Breast Cancer Patient,
I was diagnosed with breast cancer one year ago
today. April 2nd, 2012. On this cancerversary, I thought I would
share some wisdom with you.
The first thing you need to learn about a diagnosis
of breast cancer is that you have to learn stupid terminology such as
"cancerversary."
Why an
illness has its own terminology is a mystery - but you will learn it.
Instead of recovering, you are a Survivor. You don't heal,
you have a "New Normal." You have foobs and fipples, experience chemobrain and get chemo curl. I don't know if any other illnesses have their own
phrases. But my suggestion is to learn the vocab so you won't be out of the
loop, but try not to use it in polite conversation. Discussing your foobs
with your mailman is only going to lead to confusion.
The next thing I would like to share with you is
that the fear and shock you feel right now will pass. One year ago today, I
felt it too. I know it doesn't seem like it will ever go away, and I
know you feel like every nerve ending in your body is made out of high voltage
wire. You will eat, sleep, dream, and think about nothing but Cancer for
quite some time.
I'm sorry to tell you that you will become a bore,
because it's all you will talk about. Heaven help anybody who asks how
you are doing, because you are likely to tell them. In detail. If
somebody cuts you off in traffic, you will be outraged, "How dare you?
Don't you know I have CANCER?"
But, as they say, this too shall pass. It
will gradually become just a disease you are dealing with, like diabetes or
high blood pressure - an inconvenience, but one you can manage. It's hard
to understand that during the early days, and I know you don't believe me now,
so you'll just have to trust me.
The worst part of a cancer diagnosis is the
uncertainty, and the worst part of the uncertainty is at the beginning. You are
facing an illness that can take your life. You are facing medical
procedures that are unknown and pretty darn scary. You may be facing the
loss of a body part or two, or even three, counting hair. You don't know
what any of this is like: how you'll feel, how you'll react, how your family
will deal with it. All you may know is what you've seen in the movies or
on TV. You likely will have many sleepless nights, and be on an
information hunt/overload for weeks, if not months - all to try to know what
will happen to you - to see into the future.
At some point though, you will come to terms with
the fact that knowing the future is impossible, and living with the day you
have is all you can do. You will find peace in that.
Looking back on my cancer treatment, do you know
what I remember? I remember my hubby and my kiddos shaving their Mommy
bald for family night. (How often does that ever happen?) I remember Kristen
and me laughing until we cried in the infusion room with tubes stuck up my nose.
I remember getting treats from the volunteers and catching upon my blog for hours every 3 weeks on my borrowed iPad. I
think of my oncologist's smart comments and rolling eyes as I challenged all
his treatment suggestions (I'm sure he was glad when all my treatments were
over). I think of heart-felt conversations accompanied by a few tears with Carrie,
my fav chemo nurse about what it's like to really live through cancer and how
if you haven’t experienced- you just don’t get it. I know it sounds funny
but in a way, now that it's over, I will miss going there.
I also think back on the support of so many people
- finding surprises like a new hat or a pink basket full of treats on my
doorstep when I got home, or the meals my friends contributed towards. Thinking
of heartwarming events like that take away any exhaustion you may feel at the
moment.
I wish I'd known when I started that the loss of a
breast (or two) is meaningless. They were a part of me for as long as I
could remember. Granted they were a little smaller and hung a little lower than
in my pre-Momma stage but they were mine. It was devastating to lose them. But
even losing them both, I still feel every bit the woman I did before. Now
I just get to choose what size I’d like to be each day. LOL My missing breasts
nursed my babies but in losing them, I find I can be with my babies longer.
I don't feel, as many do, that my breasts tried to kill me and so they
had to go. To use the omnipresent war
comparison - I felt that they were the battleground which had to be sacrificed
for the greater good. The land is scarred but the soul survives.
There is a lot of controversy about having a
positive attitude. A positive attitude will not change the course of your
disease, nor will it cure you, nor should you feel required to put one on all
of the time. Someone asked me if a pessimist can beat the disease, and the
answer is yes. For the most part -it's medical science that cures cancer, not attitude.
However, if you can learn to see the positives, the
humor, the blessings even, that come from this disease, than your treatment
course will be easier on you. I believe that without a doubt. Some of the
treatment won't be fun. Some may have long-lasting side effects.
But, life goes on, and you have yours. Dwelling on the negatives,
overlooking the good things, is, in my opinion, wasting your new life.
A diagnosis of cancer will change you. It may
always be in the back of your mind, and yes, nervousness and fear will again
pop-up around testing times, but you will learn to manage it and eventually
take it in stride.
And, here's the thing: it's up to you whether
cancer changes you for the better or not. It's entirely in your control.
You can't alter the fact that you have the disease, but you can choose
how you react to it.
I want to tell you that I'm very sorry that you
have to go through this. But, as horrible as it seems now, it will bring
blessings to your life that you never expected. My advice? Look for them,
even if it seems impossible.
Especially if it seems impossible.
Because, they are there.
Love, Shay
Se trata de:
Breast Cancer,
Cancerversary
Friday, March 15, 2013
Ringing the Bell
The sound of a ringing bell has different meanings in different circumstances. Often they're rung for religious reasons, at times to commemorate a momentous event, or in remembrance. At the Roger Maris Cancer Center, the ringing of a bell signifies that a patient has completed treatment.
Ring this bell
Three times well
Its toll to clearly say
My treatment's done
This course is run
And I am on my way!
DING!! DING!! DING!!
I'm done!
Se trata de:
Breast Cancer,
Herceptin,
Humor
Herceptin #16: DONE FOREVER!
Brett came with me for my appointment with Dr. Panwalker this morning. Which was way nice of him since I admit that I had a mini-freak-out this morning, ended up crying and told him I would just go by myself. Going to bed late, getting kids up and off to school, making breakfast, getting Glory ready, shoveling part of the driveway (yes! It snowed AGAIN this morning), getting myself ready, trying to do something with my ugly hair, driving in the freezin' cold and snow-swept roads to drop Glory off to the Gills (in the opposite direction and in a truck that isn't running well lately), picking up Brett at work on the way and making it to the RMCC by 9:10 AM (not to mention that I am so tired of treatments I could scream) was a little too overwhelming for this non-morning-loving Cancer patient. So... a big apology and thanks to my amazing Hubby for putting up with me and coming anyways. XOXO. Luv ya, Honey!
Our appointment with Panwalker, our Oncologist went well. I was not as melancholy as last time so I didn't freak him out as much. [My old tease-y self made a semi-comeback] The doctor did his regular questioning, examing and discrediting any of my symptoms. (I like to tease him because the things that I feel I have as side effects like my brittle nails, my heart racing for a couple days and my urine smelling like mouse ovaries I guess are NOT real symptoms. What do doctors really know anyways? LOL)
He did say everything is looking great! Well, except that my weight is up by 5 pounds. Grrrr! Not that he cares or is worried about that [In fact, I'm the one that brought it up] but I did inform him that it is because I did Pilates yesterday and it's ALL muscle. He completely agreed. LOL
Then, we discussed how my treatment is almost over. I told him that today was my last Herceptin that I had scheduled and was wondering if I needed to set up one more. OR..... If this could be my last one? He totally surprised me but he said it could be. WHAT???? You mean I can be done? Hallelujah! Today is my LUCKY DAY!!!! [I told him I actually wore my "LUCKY" shirt today, just in case it would help. Looks like it did! Wahoo!]
* It looks like for follow-ups we will meet with him every 3 months until next year and then every 6 months after that until the 2 year Cancerversary from my surgery. But no more infusion so I am so ecstatic!
Back in the Infusion Center, Theresa was my Herceptin nurse for today. She was awesome! I have been really lucky to have some amazing nurses on my journey. I actually feel bad that I didn't do anything BIG to celebrate my last day. You know, gifts for all my nurses or throwing a party or something. LOL But then, the fact is that I was trying not to get my hopes up just in case I had to do one more treatment. {This is a first for me that things have gone my way so I was completely caught off guard!} So... perhaps I'll have to do something and take it in sometime. Any ideas?
I did think it was ironic because I actually forgot my camera today. Can you believe that???? Figures! It's my last day and I am without a way to document it properly. Grrrr! Thanks heavens that I decided to throw my iPod in my bag. Crappy pictures are better than no pictures if you ask me!
Despite my lack of preparedness for this momentous occasion, I sit here in my own little, secluded room at the Roger Maris Cancer Center Infusion Center for my final Herceptin treatment, taking inventory of all the things I will do for the last time. Nothing bitter-sweet about it but for the record, this will be the last time that I...
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| Honey- Are you "leaning"? You must love me! LOL |
He did say everything is looking great! Well, except that my weight is up by 5 pounds. Grrrr! Not that he cares or is worried about that [In fact, I'm the one that brought it up] but I did inform him that it is because I did Pilates yesterday and it's ALL muscle. He completely agreed. LOL
Then, we discussed how my treatment is almost over. I told him that today was my last Herceptin that I had scheduled and was wondering if I needed to set up one more. OR..... If this could be my last one? He totally surprised me but he said it could be. WHAT???? You mean I can be done? Hallelujah! Today is my LUCKY DAY!!!! [I told him I actually wore my "LUCKY" shirt today, just in case it would help. Looks like it did! Wahoo!]
* It looks like for follow-ups we will meet with him every 3 months until next year and then every 6 months after that until the 2 year Cancerversary from my surgery. But no more infusion so I am so ecstatic!
Back in the Infusion Center, Theresa was my Herceptin nurse for today. She was awesome! I have been really lucky to have some amazing nurses on my journey. I actually feel bad that I didn't do anything BIG to celebrate my last day. You know, gifts for all my nurses or throwing a party or something. LOL But then, the fact is that I was trying not to get my hopes up just in case I had to do one more treatment. {This is a first for me that things have gone my way so I was completely caught off guard!} So... perhaps I'll have to do something and take it in sometime. Any ideas?
I did think it was ironic because I actually forgot my camera today. Can you believe that???? Figures! It's my last day and I am without a way to document it properly. Grrrr! Thanks heavens that I decided to throw my iPod in my bag. Crappy pictures are better than no pictures if you ask me!
Despite my lack of preparedness for this momentous occasion, I sit here in my own little, secluded room at the Roger Maris Cancer Center Infusion Center for my final Herceptin treatment, taking inventory of all the things I will do for the last time. Nothing bitter-sweet about it but for the record, this will be the last time that I...
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| Borrow an iPad to blog during my visit. And get a hole poked in my left hand to insert plastic tubing. |
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| Get a warm blanket and a treat bag of Chex mix, pretzels, cheesiest and m&ms. |
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| get hooked up to an intravenous (IV) infusion pump in a Cancer Center |
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| Get my blood pressure taken with an IV in the same arm. Ouch! |
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| walk down the hall connected to a machine to use the bathroom. And have to flush twice! |
| Wrap my Hand up like a Boxer so I can go home! |
Also (without photographic evidence), it will be the last time that I:
* sit alone in an Infusion room for hours.
* tell the Nurse that I didn't have lab work done because Dr Panwalker says, "I'm fine!"
* spend a week having my urine smell like mouse ovaries. [You can't even photograph that anyways!]
* whine about having to take drugs that may or may not keep my cancer away.
* tell the Nurse that I didn't have lab work done because Dr Panwalker says, "I'm fine!"
* spend a week having my urine smell like mouse ovaries. [You can't even photograph that anyways!]
* whine about having to take drugs that may or may not keep my cancer away.
Good riddance to all of that! Wow! What a year! No words can say how happy I am to be done with Herceptin FOREVER! Farewell you stinky, icky mouse ovaries!
Se trata de:
Breast Cancer,
Doctor Appointment,
Herceptin
Thursday, March 14, 2013
Freedom from Treatment!!!
(In my latest bout of blog-stalking other Cancer patients, I found these thoughts from a blog called The Funny Thing about Cancer. Every word was exactly how I am feeling so I changed the amounts, took out what I didn't experience and added a few of my own thoughts. Thanks to Cynthia Ericson for putting my feelings perfectly into words. I've been saving this post for a LONG time. I'm so excited to be able to finally share it.)
Tomorrow is possibly my last Herceptin.
It is my sincerest hope that tomorrow will be the last time I:
- ever visit an infusion room. For any reason.
- see a nurse in a special gown that is supposed to protect her from the poison she is about to pump into someone.
- have to wait (and wait... and wait) for the lab to release my meds. Seriously. Takes forever sometimes.
- have to pull an intravenous (IV) infusion pump down the hallway to use the restroom.
- have to wrap my hand like a boxer with a cohesive bandage so I don't bleed all over the floor on my way home.
- spend my Friday morning in an infusion room.
Bottom line is that I hope tomorrow is the end of my cancer journey.
Sure there will be follow-up visits. But even with those future appointments, tomorrow FEELS like the end of all of this craziness. It feels like the chains are coming off and I'll finally be free! Free from the appointments and the waiting rooms. Free from the physical annoyances that are "side effects". Free from the constant scheduling that all the appointments require. Free from the insurance forms telling me the price that they think mouse ovaries cost. Free from ALL of that.
Did you know it's been THIRTEEN months since I've gone more than 3 weeks without a doctors
appointment of some kind? For the last year, I have seen a medical professional at least once every 3 weeks. Prior to cancer, I saw a doctor exactly once a year (except for when I was pregnant) and even less after my little one hit 3 years old. I am so unbelievably excited for that to be over.
After tomorrow, I won't have to go see my oncologist for THREE MONTHS. By then I am hoping that God will let me in on his plan for the future and I will officially put this part of my life behind me.
Now, I know I will never be truly free from cancer... any survivor will tell you that cancer will forever be a part of your life, even when you're "cured". But to be free from the responsibility of the constant appointments and treatments will be divine. I can't possibly tell you how exciting that is for me.
So here's to celebrating the end of treatment and ALL the freedom that comes with it :)
Tomorrow is possibly my last Herceptin.
It is my sincerest hope that tomorrow will be the last time I:
- ever visit an infusion room. For any reason.
- see a nurse in a special gown that is supposed to protect her from the poison she is about to pump into someone.
- have to wait (and wait... and wait) for the lab to release my meds. Seriously. Takes forever sometimes.
- have to pull an intravenous (IV) infusion pump down the hallway to use the restroom.
- have to wrap my hand like a boxer with a cohesive bandage so I don't bleed all over the floor on my way home.
- spend my Friday morning in an infusion room.
Bottom line is that I hope tomorrow is the end of my cancer journey.
Sure there will be follow-up visits. But even with those future appointments, tomorrow FEELS like the end of all of this craziness. It feels like the chains are coming off and I'll finally be free! Free from the appointments and the waiting rooms. Free from the physical annoyances that are "side effects". Free from the constant scheduling that all the appointments require. Free from the insurance forms telling me the price that they think mouse ovaries cost. Free from ALL of that.
Did you know it's been THIRTEEN months since I've gone more than 3 weeks without a doctors
appointment of some kind? For the last year, I have seen a medical professional at least once every 3 weeks. Prior to cancer, I saw a doctor exactly once a year (except for when I was pregnant) and even less after my little one hit 3 years old. I am so unbelievably excited for that to be over.
After tomorrow, I won't have to go see my oncologist for THREE MONTHS. By then I am hoping that God will let me in on his plan for the future and I will officially put this part of my life behind me.
Now, I know I will never be truly free from cancer... any survivor will tell you that cancer will forever be a part of your life, even when you're "cured". But to be free from the responsibility of the constant appointments and treatments will be divine. I can't possibly tell you how exciting that is for me.
So here's to celebrating the end of treatment and ALL the freedom that comes with it :)
Se trata de:
Breast Cancer,
Doctor Appointment,
Herceptin
Sunday, March 3, 2013
Feeling Unspectacular and Unanswered Prayers
It's been a rough couple of weeks for me emotionally. I'm sure it's partly a Winter Blues issue but it's also an "angry at cancer" thing. I should start out by saying that I will probably be struck by lightning for my bad attitude since I have been blessed more than my fair share through this past year. But regardless of my fear of being fried to a crisp by 300 kilovolts---these past few weeks I have had a hard time not focusing on all the things cancer has robbed me of and the frustration of unanswered prayers.
As most of you know, my family had big plans to have a once-in-a-lifetime experience. Long story short... Cancer robbed us of that! Many have said that perhaps giving us that opportunity was the only way that we would have found the Cancer in time. But I can't agree. There was lots of other things that could have happened to help us "discover" the cancer. I wish I could say that I understand why they would say that but we had prayed so long & so hard and had turned the issue completely over to God and everything was starting to fall into place when we were diagnosed. I know without any doubt that God had told us to go. Even after the diagnosis, we prayed with open hearts (although heavy at the time) that if this was all for finding out about the cancer that we would give it up. But time and time again more things fell into place. Then after EIGHT long months of continuing down the path we felt we were directed to go-- CANCER made our Dream and Big Adventure over. Why?? What happened to all the answers to prayers we felt we had received and how do I get past that???
I am NOT doing a very good job, I'll tell you that. I have tried to make CANCER my new Adventure. After my diagnosis, I worked hard on making it a positive experience for our family and having some fun along the way. It worked for a while. But after finding out we were staying stateside, I really don't see the point. My point was to beat the cancer and then go on an amazing Adventure. But NO!!!!!!!! Instead, I may never even get out of Fargo! {Where it feels like Winter 11 months of the year!!!} Grrrr! While we were fighting our way through chemo and surgery, we passed up opportunities to go other places because we were sure that Bogota was where God wanted us. And now we don't have any clue where we should go or where God even wants us. None of our prayers seem answered as of late. I actually torture myself by having the temperature for these other places on my iPod. I check it every morning. [I know it's pathetic but that's how I roll these days] So like this morning at 7:30 am when it read- SLC: 39 degrees, Helena: 43 degrees, Bogota: 54 degrees, Fargo: -6 freezin' degrees- I almost wanted to swear. You gotta be kidding me!!! "WHY do I live here????" has become a question I ask myself a zillion times a day lately! What is the purpose of me being stuck in this frozen place?
In the past couple weeks, I also started reading a few Cancer blogs- perhaps for a little sympathy or to get some perspective. That has backfired! One blog was such a fun-loving positive blog. I felt like I connected to her words and her spirit but then she died suddenly! A complication from the drugs or something. Man! Cancer sucks! Another lady has made her cancer diagnosis into a business. She started a foundation and travels all over the world promoting awareness and making a zillion friends. So... I pretty much hate her! LOL A few have posts about how family and friends rallied and threw big, huge fund raisers in their behalf to help them offset their medical bills. Did I need that? No. Brett and I worked really hard for the last several years to save for a rainy day. We were prepared! Does that change the fact that it hurts my feelings a little that no one did that for me. You bet. Cancer sucks! Most of the cancer blogs that I read have tons of followers. At the conclusion of each post, a handful of friends leave comments and words of encouragement. Me? I'm not sure that anyone reads mine at all. Guess that's my unspectacular cancer life. Oh well! Two other blogs I read are of women who are on their SECOND time through cancer. Both did drastic measures to "take care" of it the first time but years later, it's back and it's fatal. What the.....ll?? Cancer SUCKS!!!!!
So what is the purpose of all this dramatic and pathetic whining?? I don't really know. But that would be a really sucky way to end a post.
So... the other day on a most unspectacular day of mine, my little family was doing some scripture study when we came across this quote. I have a bit of a love/hate relationship with it but I am trying to make it speak to my heart. Perhaps by typing it here it will sink in a little.
So is that my answer???? Who cares if Cancer sucks, Shay? Who cares if you use all your savings to pay off your medical bills? Who cares if you want to leave this crappy, freezing place??? Who cares if you are boobless and have a really ugly hairdo? Who cares if you feel like your life is NOT the Adventure you want it to be? Just be serviceable, woman!!!!! Is that my answer?? ..... Perhaps.
P.S. As I was being my whiney, pathetic, unspectacular self these last couple weeks, I did receive this email from an old friend. Funny how people can do/send things when they have no idea how much it will mean to someone. Thanks, Heather! You'll never know how much I needed it! XOXO
As most of you know, my family had big plans to have a once-in-a-lifetime experience. Long story short... Cancer robbed us of that! Many have said that perhaps giving us that opportunity was the only way that we would have found the Cancer in time. But I can't agree. There was lots of other things that could have happened to help us "discover" the cancer. I wish I could say that I understand why they would say that but we had prayed so long & so hard and had turned the issue completely over to God and everything was starting to fall into place when we were diagnosed. I know without any doubt that God had told us to go. Even after the diagnosis, we prayed with open hearts (although heavy at the time) that if this was all for finding out about the cancer that we would give it up. But time and time again more things fell into place. Then after EIGHT long months of continuing down the path we felt we were directed to go-- CANCER made our Dream and Big Adventure over. Why?? What happened to all the answers to prayers we felt we had received and how do I get past that???
I am NOT doing a very good job, I'll tell you that. I have tried to make CANCER my new Adventure. After my diagnosis, I worked hard on making it a positive experience for our family and having some fun along the way. It worked for a while. But after finding out we were staying stateside, I really don't see the point. My point was to beat the cancer and then go on an amazing Adventure. But NO!!!!!!!! Instead, I may never even get out of Fargo! {Where it feels like Winter 11 months of the year!!!} Grrrr! While we were fighting our way through chemo and surgery, we passed up opportunities to go other places because we were sure that Bogota was where God wanted us. And now we don't have any clue where we should go or where God even wants us. None of our prayers seem answered as of late. I actually torture myself by having the temperature for these other places on my iPod. I check it every morning. [I know it's pathetic but that's how I roll these days] So like this morning at 7:30 am when it read- SLC: 39 degrees, Helena: 43 degrees, Bogota: 54 degrees, Fargo: -6 freezin' degrees- I almost wanted to swear. You gotta be kidding me!!! "WHY do I live here????" has become a question I ask myself a zillion times a day lately! What is the purpose of me being stuck in this frozen place?
In the past couple weeks, I also started reading a few Cancer blogs- perhaps for a little sympathy or to get some perspective. That has backfired! One blog was such a fun-loving positive blog. I felt like I connected to her words and her spirit but then she died suddenly! A complication from the drugs or something. Man! Cancer sucks! Another lady has made her cancer diagnosis into a business. She started a foundation and travels all over the world promoting awareness and making a zillion friends. So... I pretty much hate her! LOL A few have posts about how family and friends rallied and threw big, huge fund raisers in their behalf to help them offset their medical bills. Did I need that? No. Brett and I worked really hard for the last several years to save for a rainy day. We were prepared! Does that change the fact that it hurts my feelings a little that no one did that for me. You bet. Cancer sucks! Most of the cancer blogs that I read have tons of followers. At the conclusion of each post, a handful of friends leave comments and words of encouragement. Me? I'm not sure that anyone reads mine at all. Guess that's my unspectacular cancer life. Oh well! Two other blogs I read are of women who are on their SECOND time through cancer. Both did drastic measures to "take care" of it the first time but years later, it's back and it's fatal. What the.....ll?? Cancer SUCKS!!!!!
So what is the purpose of all this dramatic and pathetic whining?? I don't really know. But that would be a really sucky way to end a post.
So... the other day on a most unspectacular day of mine, my little family was doing some scripture study when we came across this quote. I have a bit of a love/hate relationship with it but I am trying to make it speak to my heart. Perhaps by typing it here it will sink in a little.
"Not everyone is going to be .... fill in the blank with some important responsibility. Not all are going to be like ...fill in the blank with some more-than-amazing leader... catching the acclaim all day every day. No, most will be quiet, relatively unknown folks who come and go and do their work without fanfare. To those of you who may find that lonely or frightening or just unspectacular, I say you are "no less serviceable" than the most spectacular of your associates. You, too, are part of God's army."- Howard W Hunter
So is that my answer???? Who cares if Cancer sucks, Shay? Who cares if you use all your savings to pay off your medical bills? Who cares if you want to leave this crappy, freezing place??? Who cares if you are boobless and have a really ugly hairdo? Who cares if you feel like your life is NOT the Adventure you want it to be? Just be serviceable, woman!!!!! Is that my answer?? ..... Perhaps.
P.S. As I was being my whiney, pathetic, unspectacular self these last couple weeks, I did receive this email from an old friend. Funny how people can do/send things when they have no idea how much it will mean to someone. Thanks, Heather! You'll never know how much I needed it! XOXO
I was checking out your blog today. (It has been awhile since I was on.) I am truly amazed by your out look and attitude. You have always been an inspiration to me and I miss talking and sharing with you. I have thought and prayed a lot for you and your family. I am truly blessed for this experience. I know it can't be easy and life is difficult on its own, then to add such an illness makes it more difficult. I hope you know of my love for you and that I miss you terribly. Thank you for sharing your journey, I love hearing about it. You have a great sense of humor and it is always entertaining to read.
Keep your chin up and know that you are loved, Heather Parry
Se trata de:
Breast Cancer,
Friends,
Humor
Friday, February 22, 2013
Herceptin #15: Almost done!
Another three weeks have flown by, and I headed up to the RMCC for my Herceptin treatment. I haven't felt the best this week- (not Cancer stuff but lady and headache stuff) but nothing to keep them from drugging me up. LOL Although my blood pressure ended up being a little lower than usual. Maybe that's why I've wanted to stay in bed all week? [Not that it was low enough to do anything this time]
I've never had problems with my blood pressure before even with having all four of my children. Because of that, I've never taken the time to understand what it means. I actually have no clue what it even measures (HaHa...ok- I know it's the pressure of my blood, at least) So for my own benefit, here's a little info about blood pressure. Always interesting to find out how much I really don't know. LOL:
Blood pressure is typically recorded as two numbers, written as a ratio like this:
SystolicThe top number, which is also the higher of the two numbers, measures the pressure in the arteries when the heart beats (when the heart muscle contracts).Diastolic
The bottom number, which is also the lower of the two numbers, measures the pressure in the arteries between heartbeats (when the heart muscle is resting between beats and refilling with blood).
How Is Blood Pressure Measured?
Blood pressure is measured with a simple, painless test using a blood pressure cuff -- doctors call it a sphygmomanometer. It consists of a small pressure gauge that is attached to a cuff.
The inflatable cuff is wrapped around your upper arm. Some blood pressure cuffs wrap around the forearm or wrist.
When taking your blood pressure, your doctor will use a stethoscope to listen to the blood moving through an artery.
The cuff is inflated to a pressure that’s known to be higher than your systolic blood pressure. As the cuff deflates, the first sound heard through the stethoscope is the systolic blood pressure. It sounds like a whooshing noise. When this noise goes away, that indicates the diastolic blood pressure.
The systolic blood pressure number is always said first, and then the diastolic blood pressure number is given. For example, your blood pressure may be read as "120 over 80" or written 120/80.
Blood pressure is measured in millimeters of mercury (mm Hg).
My Herceptin Nurse today was Janae. She was great! She got me in and out super fast! I was home a whole hour earlier than I usually am. Yeah! Thanks to my dear Hubby for helping me out with little Glory today. One or two more treatments and then we'll put this chapter behind us! I CAN"T wait!
Thursday, February 7, 2013
My Final Word on Wigs
I probably should have wrote this post a long time ago but life keeps flying by so quickly it's hard to keep track of it all.
I haven't really worn a wig at all since the end of October {almost 4 months ago}. Looking back at pictures of when I stopped wearing one, I can't believe I ever left the house like that. It was SOOO short! But I do remember that as it was growing back and I was still wearing the wig, it was smashing the new fuss and stunting the growth in some places. Brett kept encouraging me to let it do it's thing and go natural. At least that was the mentality behind the abrupt stop to the fake do.
A few things that I did learn about wigs from my experience. Take it for what it's worth!---
* Get one really great wig! You'll end up spending a few bucks but it's worth it. It doesn't necessarily have to be made of real hair (and in fact I enjoyed NOT having to fuss with styling it. "Slip it on, smooth it down and go" was the best for me!) But get at least one you really LOVE! Getting more than that would purely be for fun!
* Make sure you try it on before you buy it. Best advice ever! Wish someone would have told me that! I bought a couple online but neither of those are my favorite. Such a bummer! So... Try before you buy! My two cents from first hand experience.
* I would spend the extra money and get a monofilament cap (and possibly with a lace front). That way it looks like the hair is coming from your scalp. Have no idea what I am talking about? LOL Well, while I was researching for wigs at the beginning, I came across this WIG GUIDE on wigs.com. It's really helpful!
* Buy yourself a soft "Cancer Turban". This 3 seam cotton one was my favorite. Cuz let's face reality. Wearing a wig ALL the time is a pain (and itchy)! I wore this a lot!!!
* Take a deep breath. Hair grows back. Maybe not as fast as one would like but you won't be wearing a wig forever!
I haven't really worn a wig at all since the end of October {almost 4 months ago}. Looking back at pictures of when I stopped wearing one, I can't believe I ever left the house like that. It was SOOO short! But I do remember that as it was growing back and I was still wearing the wig, it was smashing the new fuss and stunting the growth in some places. Brett kept encouraging me to let it do it's thing and go natural. At least that was the mentality behind the abrupt stop to the fake do.
A few things that I did learn about wigs from my experience. Take it for what it's worth!---
* Get one really great wig! You'll end up spending a few bucks but it's worth it. It doesn't necessarily have to be made of real hair (and in fact I enjoyed NOT having to fuss with styling it. "Slip it on, smooth it down and go" was the best for me!) But get at least one you really LOVE! Getting more than that would purely be for fun!
* Make sure you try it on before you buy it. Best advice ever! Wish someone would have told me that! I bought a couple online but neither of those are my favorite. Such a bummer! So... Try before you buy! My two cents from first hand experience.
* I would spend the extra money and get a monofilament cap (and possibly with a lace front). That way it looks like the hair is coming from your scalp. Have no idea what I am talking about? LOL Well, while I was researching for wigs at the beginning, I came across this WIG GUIDE on wigs.com. It's really helpful!
* Buy yourself a soft "Cancer Turban". This 3 seam cotton one was my favorite. Cuz let's face reality. Wearing a wig ALL the time is a pain (and itchy)! I wore this a lot!!!
* Take a deep breath. Hair grows back. Maybe not as fast as one would like but you won't be wearing a wig forever!
Wednesday, February 6, 2013
A Head FULL of Hair
My journey from Bald to Beautiful is gonna be a LONG one! But keeping track of it almost every week has allowed me to realize how far I have come! It's fun to actually see the slight changes that happen. And having hair again is nice! It's coming in WAY thick with quite the wave. I'm not sure what you would call the color? And... often I have wondered how people describe me? LOL Especially because I still categorize myself as the "blonde chick". Weird, I know! It's definitely darker than before but the tips are getting lighter. Only time will tell what I really am! ;) I [and especially my girls] are looking forward to having "girl" hair again but I will admit- having short hair has been SO nice in the getting-ready sense. What used to take me HOURS to dry and do- is completely done (straight out of the shower) in like 3 minutes. Wahoo! Maybe short hair will become my norm? LOL
Here's to slight changes!!!!
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| P.S. As of beginning of Feb, I finally am able to tuck my side burns behind my ears! |
Friday, February 1, 2013
BOOBLESS- My Surgery Recovery: (with Pictures)
This post is dedicated to living BOOBLESS! LOL
It's been six months since my surgery to remove both my breasts. I have hesitated to include this post due to it's graphic and possible offensive nature BUT this is the reality of breast cancer with a bilateral mastectomy. And afterall the reality of My Breast Cancer Adventure is why I am keeping this record.I have mentioned it before but another reality of Breast Cancer is that time passes, the shock and worry for those around you fades and everyone "moves on" from the craziness surrounding your diagnosis. But MY reality is that it will never go back to normal. Whatever NORMAL is, right? Taking a shower will never revert back to cleaning a body with a female chest for me. Getting dressed each morning and having to make the decision whether to wear "boobs" or not will always be a part of my life. Not that it hugely matters but it is a daily reminder that Breast Cancer has changed me forever.
My decision to NOT do reconstruction was a personal one. One that seemed natural and less complicated for me. It was one less long-drawn-out-process to avoid. Before I started this adventure I was unaware that reconstruction takes a minimum of 4-6 months depending on the size you want. And then an extra surgery! um....No thanks!
Another logical reason for me was due to the fact that foobs don't last forever. What? I guess nothing really does, right? The doctors informed me that because I was young I would need to have them replaced once maybe twice in my lifetime. That was not an appealing option for me. Besides, I am an "options" girl and how fun is it that I have so many choices of breast sizes now that I gave myself a flat canvas to work with. ;) Shopping for new breasts was way more fun that I thought it would be! And bonus- I technically could get a new pair of perfectly perky boobs every year for the rest of my life. How many women can say that? LOL
One thing that I did NOT expect was the fact of how often I would choose to not wear anything. Now that I am a worker-outer, it is way more convenient to be boobless. "Boob sweat" is a thing of the past for me, my friend! Besides running on the treadmill and bouncing in Zumba- piece of cake for me now! ;)
One thing that has been a little disappointing was the fact that I had in my head that after my surgery, I would have a perfectly flat chest. The harsh fact of scars never even crossed my mind. Stupid, I know. But it wasn't something I was expecting. Before my surgery I had came across this elegant black & white picture of this woman that had a bilateral mastectomy She's beautiful and flat chested-- flawless. That's what I was looking for. Well, at least at first glance and to an untrained (a non-mastectomy participant) eye that's what she seemed to me. Now six months down the road and with a more-than-I-ever-wanted-to-know knowledge, I can see her scars and the fact that her arms stretched up and it being printed without color gives a false impression of perfection. Interesting how we only see what we have the ability to comprehend. {Back in July, I even thought about taking the picture to my surgeon so he knew what I was expecting. I never was brave enough to take it in to him. Maybe I should have??? Oh well! Too late now. Bummer!}Anywho-- regardless of my pre-amputation expectations, flawless & flat chested is NOT my reality. I had two different surgeons on my big day. Not sure if that added to my certain outcome but in my opinion, one took off too much and the other left too much. Over time and a little beefing up some muscle (LOL), I hope that they will even out a bit. However, regardless of time, two 5 inch scars (and two tiny poke holes from my drains) are now permanent features of my front side. Like I said--- Breast Cancer has changed me forever!
As I talk to (or read) others, it seems everyone has a different opinion about the importance of breasts and whether to reconstruct some resemblance of a former life. Some women (and some husbands:) actually have very strong opinions about breasts. Imagine that! ;) I guess I can understand how people would feel somewhat "attached" to them. LOL But for me, boobless is an ok option!
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| 6 days after Surgery: With Drains in |
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| 17 days after surgery: Sterry strips off |
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| 1 month after surgery: Healing |
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| Six weeks after Surgery |
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| 6 Months after Surgery |
Se trata de:
Breast Cancer,
Health,
Humor,
Mastectomy
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