Candice Chilton was diagnosed with Stage IV Breast Cancer at 28.

Showing posts with label las vegas. Show all posts
Showing posts with label las vegas. Show all posts

2 for 1 Blog Post this week!


Hi everyone! Sorry for the extremely long 34 min video. Just think of it as two blogs in one, since I haven't blogged for a couple of weeks. <3

This edition includes:

Frustration


  Here we go again! 2nd installment of the video blog. Sorry guys, it's kind of a long one. Lots to talk about including my doctor appointment, Kellie Pickler, The Dallas Cowboys, and I received my first hate mail. Must mean I'm really popular if I'm getting fan hate mail, right? LOL

Here's the links as promised:

Melatonin Study (one of many)
http://www.breastcancerchoices.org/melatonin.html

Birch Box - Samples
http://www.birchbox.com/

Fight Like A Girl decals
http://www.ebay.com/itm/Fight-Like-Girl-Pink-Breast-Cancer-Ribbon-decal-/150377882369#vi-content

Kellie Pickler Shaves Her Head
http://abcnews.go.com/blogs/entertainment/2012/09/kellie-pickler-shaves-head-for-breast-cancer-pal/

First Chemo!

So everyone is asking me how I'm doing since my first chemo treatment and the answer is so far so good! My chemo was Wed and after an hour wait in the waiting room and an argument over co-pays, we finally got in to see the doc. Well, actually the docs assistant because he was out last week. She prescribed me two anti-nausea drugs, Compazine to try first and if after I take that and if I'm still sick, to take Zofran.
Then I walked to the back and picked a recliner to sit in. A nurse came over, accessed my port by sticking a tack looking needle in it and proceeded to give me an IV of saline and premeds including a heavy dose of Zofran. West sat with me and held my hand as they did the needle and premeds but I was disappointed when they told me he couldn't stay for the two hours because it was a HIPPA voilation :( but he was allowed to check on me as often as he wanted so he went back and forth from the lobby.
The first drug they gave me, they told me straight out they call it the Red Devil. It's actually called Adriamycin but its known as the red devil because it causes all the side effects: hair loss, vomiting, fatigue, and general crappy feeling. That lasted about 45 minutes in an IV drip and then they gave me something called Cytoxin which lasted another 45 minutes. According to Livestrong.com:
Adriamycin is an anti-tumor drug that attacks the part of a cancer cell responsible for synthesizing RNA and DNA, according to Chemocare.com. Cytoxan is an alkylating agent, and as such works by breaking DNA strands while the cancer cell is in its resting phase before cell division, according to the Core Curriculum for Oncology Nursing.
I felt nothing different during the infusions...and after it was over West and I went to Subway and I ate an entire meatball sandwich lol I hung out the rest of the afternoon with Momo because I was afraid of being alone and violently throwing up but I felt fine Wed night, felt fine Thursday and now today, today I felt just ok. I woke up fine but West helped me take a shower and after the shower, ugh it felt like I ran a marathon and I slept for two hours after. The rest of the day today I just watched West play video games, settled in front of the TV and just took it easy but I can't say the tiredness is any different than the way I felt during radiation nights...
Tomorrow will be the test. My Aunt went through chemo for ovarian cancer and the third day was the worst for her, thats when it really hit her, so we'll see how I feel tomorrow!

Last day of radiation!!

So just a quick note today. Today is my last radiation treatment! I would be more excited but I've been kinda feeling like crap yesterday and today. Today is not so bad, did take a lot to get out of bed this morning and even more to choke down oatmeal but I have to remind myself that I should be thankful I can get put of bed, that I can make myself breakfast.. As there are many worse off than myself!
So as much as I can, I'm going to celebrate my completion of radiation and look forward to my sore throat healing and the fatigue going away. My radiation tech said that radiation works in your body two weeks after the last treatment so it could be awhile until my throat feels normal.
Now my celebration is short lived because tomorrow at 930 is my first chemo dose. I'll go in and spend 15 min with the doc and doing bloodwork to make sure my white count is healthy enough, then they will give me about a half an hour of iv premeds for nausea etc and then it's two hours of the actual chemo. West is being a trooper and sitting with me and then when he goes to work I'm going to hang out with momo bc I'm just not sure what the chemo is going to do so I didn't want to be alone. All in all the chemo should last 3 hours so I should be home by 1.
In other news I saw dr lee yesterday who said my wound on my neck is healing slowly but should start to close after radiation. He also said I've got 6 more weeks in the god awful brace and that's if the radiation didn't slow down the healing but he doesn't want to do X-rays for a few more weeks. I go back and see him on the 23rd.
In other news I don't think I mentioned in any of my posts that I've lost 37lbs with all of this. Now trust me I had the pounds to lose but I don't recommend doing it in this fashion. The problem is, between my sore throat and all of my meds/radiation upsetting my stomach, I have zero appetite. I've been taking nausea meds but they just settle your stomach, they don't make you hungry. I'm drinking ensure, taking a multivitamin and trying to choke down breakfast at least so I can take my meds but if anyone has any ideas to stimulate appetite I'd like to hear them. I feel like I have the stomach flu and the sight of food makes me want to throw up...
Well off to my final radiation! I hope the side effects this afternoon are better than yesterday bc yesterday I came home and pretty much napped from 3pm on...

Radiation, Bactrim, Tamoxifen and incisions don't mix.

So I haven't posted in awhile which makes everyone worry lol so I'll post an update :) I haven't been posting because well, the radiation is actually making me lazy. I'm not going to say tired because its not a nodding off need a nap tired its a OMG I have to find my laptop, plug it in, sit in the office, find a pillow for the chair and then attempt to type - oh hell no do I feel like getting out of this chair feeling :)
I have 4 treatments left. Thu/Fri/Mon/Tue. They were going to do 15 but after seeing Dr. Nyamuswa (chemo) last Wednesday, he spoke with Dr. Dean (radiation) and decided the important thing was getting me to chemo ASAP and 12 treatments would do.
Thank goodness because I have a wicked sore throat. They told me I'd get one but man its worse than strep. You never know how much saliva your mouth produces until you can't swallow! My teeth are sensitive too. At night my eyes burn like allergies and my skin gets super hot. I've been sleeping with a refrigerated ice pack on my forehead and eyes (or at least falling asleep that way) which does help. If this is the worse of it, well I'll take it. It can always be worse!
The other thing thats not helping is I'm back on Bactrim (antibiotic). Last Tuesday West noticed the incision on the back of my neck was starting to open up. Wednesday at my chemo appointment the doctor put me on Bactrim to prevent infection and the stuff is hard on your stomach and gives you a nasty taste in your mouth. My appetite has decreased a lot since I've been on it so its kinda like being sick to your stomach, hot, and have a sore throat all at the same time. Thank goodness today is my last dose! I missed radiation on Friday because they didn't want to radiate an open wound so I went to see Dr. Lee (surgeon) on Monday who said to treat it with a wet/dry dressing and continue radiation, eventhough radiation was the cause of the wound breaking open. He insisted that most important thing was getting to chemo which means getting through radiation ASAP and said he doesn't mind wound care just don't skip radiation, even if it makes the wound worse.
Speaking of my appointment last Wed, Dr. Nyamuswa set me up with a treatment plan. They took a CBC to check my white blood cell count and flushed my port. Did I mention in all the madness I had a port surgically inserted underneath the skin of my right arm? Theres more info on what a port is here: http://powerportadvantage.com/about.html but basically instead of having to poke you with a needle every time they need to take blood or admin chemo, they use whats called a port. Its a plastic implant that is hooked to a catheter that leads into the major vein near my heart. When they need to draw blood or give me something through IV they stick a needle into the port and its instant access. It came in really handy in the hospitals because I didn't (usually) need to get stuck for lab work and it made admin morphine really quick! Anyway, for some reason at the docs office my port would take meds but wouldnt release blood for blood work so they had to do it the old fashioned way. The nurse said sometimes that just happens and the next time they try it could work perfect- that its real positional. My CBC came back really good, or at least thats what the doc said. Not sure if thats really good for a cancer patient or really good for a healthy patient but if he's pleased, I'm pleased.
The doc said we can't start chemo during radiation, that with me healing from spinal surgery, it would just be too much on the bone marrow so we have to wait. In the meantime he put me on Tamoxifen, a drug that stops estrogen production which is the chemical that is feeding my cancer. It mimics menopause so I'm having heat flashes, mood swings, sick to my stomach, sore throat, hot skin, an incision that won't heal..all at the same time. Yuck! Again, though...if this is the worse of radiation, I can handle this...this isn't so bad. I start chemo next week. Next Wed at 9:30 if I remember right. They said it will be about a 3 hour process, an hour for blood tests and premeds and 2 hours to administer the chemo. I can't remember the names of the chemo drugs right now but its pretty strong stuff. Its the hard hitting make you lose your hair and feel crappy kind but if it kills cancer, I'm on board. I'll do that every three weeks for 4 treatments and then they'll assess how that's working and then go into a weekly chemo regimen with a drug that's not as strong.
So, all in all I'm hanging in there. The mornings are good. The evenings, around 7 and later are the I'm tired and started to feel crappy times but I'm pushing through and am looking forward to being done with this radiation!

Setting up for radiation!

Hello world! :) Day 3 at home and I'm feeling pretty accomplished! I have a doctors appointment every day this week which means getting up and getting for the world each day. I have succumb to the fact that for the next 8 weeks I will be living in skirts. I hate skirts. *sigh* but this stupid brace covers my pants line which means if I wear jeans, button them, get into my suit of armor on theres no way to unbutton the jeans to go to the bathroom. I tried yoga pants and on special days, when I just cant find the stomach to wear another skirt, I suppose they'll work but it takes ten minutes to get back under the brace at the right pants line so they don't fall off my ass :)
I'm so thankful for so many things right now. Today mom and momo took me to payless to buy some flats. Here in Vegas, in the 100 degree plus heat I've been living in flip flops and what a difference a few months in the hospital makes because now I'm out and about I am the crazy girl wearing skirts and flip flops in Vegas winter (not that its cold lol but you still get weird looks) and my love for heels has back fired. I discovered I didn't have a single pair of closed toed flats!! My momo Betty Stafford bought me three pairs of beautiful shoes that I can actually walk in ♥.
After that we went to Fashion Bug where mom (@Kim Fletcher) bought me a new skirt and THEN we went to SuperCuts and got my hair cut. I don't want to post pics yet because I think I can style it better than the hairdresser did but its an a line bob really short in the back and long in the front. Pics coming soon!
Did I mention this was all done after two doctor appointments? I got marked for radiation today. The people were so nice and gentle. The appointment was easy, I just laid on a cat scan table while they took pics and they marked my body for the machine with a sharpie and covered the marks with waterproof stickers. There was one semi-tattoo mark that they stabbed me in the chest with a needle but that was it. My first radiation treatment is tomorrow at 1. They are radiating from the top of my neck to the middle of my shoulder blades not only to prevent the tumor from coming back but also because they couldn't find clean bone in my hip to replace in my neck bone so they want to kill the cancer in the new bone graphs. I will go to radiation every day for 3 weeks. The side effects will include fatigue, sunburn, sore throat, and of course ya know, poisoning my body lol but the cancer won't come back in that spot and thats all that matters. I'm prepared to fight! I am a little discouraged it might slow down my voice coming back - which it still hasn't done yet but I'm trying to be patient.
After the markings we went to another office to consult with the radio-oncologist himself. My mom and momo had never met him and we had questions about radiation, nutrition, side effects, prognosis, etc. Dr. Dean spent 45 min with us and answered every question and every side effect and was matter a fact. The last time I talked to this man I was extremely depressed at his attitude. I was emotional and alone in the hospital room and he came off to me as if he was there to tell me that statistics are I have two years to live and his job is to make me comfortable and prevent bone tumors in what little time I have left. That his job wasnt to save my life just make it more comfortable. I was devastated. Today he re-explained. He said what he meant was that radiation can't cure cancer. His job can't save my life. His job is to get in there, stabilize the horrible things the cancer has already done and then get the hell out of the way so that the chemo doc, the guy that can save my life, can get in there and do its job and softly said he was there to remind us that the statistics are metastatic breast cancer patients have a two year life span, thats the rule but there are plenty exceptions...but as a doctor he has to state the rules, not the exceptions blah blah. Realistic but....
Anyway for 3 days out of the hospital I feel like things are quickly going toward normal....and I'll report on my first day of radiation tomorrow! ♥

Save the date!


SO! I FINALLY HAVE A SURGERY DATE!! After a little over a month of talking talking talking....we're finally going to take some action. I talked to my surgeons office today and I finally have a surgery date. I will be having my double mastectomy on Wednesday September 28th at 10:30am. The whole surgery will take between 3 and 5 hours.They are going to:
  • Make an incision
  • Remove the tumor and send it off for testing
  • Remove breast tissue from my collar bone to my arm pits to my back
  • Remove the nipples (but save as much other skin as they can)
  • Do a lymph node biopsy and remove lymph nodes if they contain cancer
  • Insert tissue expanders behind the muscle
  • Fill those tissue expanders as much as my muscle and skin will allow
  • Close everything back up
 The surgery will take place at Spring Valley Hospital. I think it's on the corner of Rainbow and Hacienda but I haven't been there before. Apparently, I'm getting a packet of information sent to me in the mail but sometime next week I have to go for a bunch of blood tests and a chest X-Ray. Then I have to go down to Spring Valley and pre-register as a patient for surgery. I don't know how long I will be in the actual hospital for. That depends on how smoothly the surgery goes and how much pain I'm in after. I've talked to a lot of people who have told me they stayed anywhere between just overnight to as much as 5 days in the hospital so....I guess we'll play this one by ear. As with any surgery, I won't know my room number and all of that until I come out and get assigned so I'll post that when I'm awake again lol

Mastectomy Scar Tattoo
Now the first question I got asked to was if I was excited? Now excited probably isn't the right word. I'm relieved to have a date and know action is on the way. I'm comforted knowing that soon this tumor that is reaking havoc in my body will be gone and I'm just plain ready to have the whole thing over with. The flipped side to that coin is it finally makes it real. It's happening. The inevitable is happening and I'm getting all those nerves and jitters that come with any operation. I trust my doctors, I know things are going to be fine but it's now a week and a half of anticipation to deal with. I am watching surgery videos to be informed and now finally connect what I'm seeing on the screen to what is going to happen to my body. I'm going to wake up and the breasts I've had for 28 years are going to be gone. They're not going to grow back. It's not like cutting my hair. A piece of me is being taken and looking in the mirror, no matter how much I complain about their size, how they hang, how I can't ever find any bras for them, they are still my breasts and I prefer to keep them. I'm devastated knowing that I will never ever ever feel the sensation of my nipples being touched or rubbing against fabric, that I'll never have my real nipples again. I can take pictures of my breasts to remember them, I can make a mold of my breasts to remind me of their size and shape but you can't bottle a feeling, a sensation. It's like a part of me is dying and I'm in mourning in a way.

The second question I got asked was if I want you there? Well of course. I could always use a visit from you. I'm speaking generally but seriously, I welcome anyone who wants to come down for the surgery, who wants to come down to visit me after the surgery, to come on down. The more the merrier! I'm going to be bored out of my mind at the hospital. I would love to see each and every one of your smiling faces. Now I probably can't go clubbing with you in the evenings and show you around the city but...if you want to play a bored game, or catch a movie on TV, I'm your girl :) Speaking of visiting, that means that I will probably have my Boob Voyage party the weekend before, the weekend of Sep 23 so if you're interested in going to that, let me know......the more the merrier to that also!! Would be nice to party it up before I start to feel like crap! :)

Now is as good as any time to mention that I'm going through a lot of anger this week. I'm mad at my breasts for rebelling against me. I'm mad at stupid people. I'm mad at people that do things to their bodies on a daily basis that cause cancer but yet they don't get cancer. Yeah. I'm talking to you, you people that smoke. Most of my family, some of my friends, and even my roommate smokes. I'm mad at you. I'm angry at you. I don't mean I personally have a vendetta against you...its not personal...but I'm severely upset with you people as a whole. You smokers. You people use a product that ON THE FUCKING LABEL says it causes cancer yet you continue to use it. Some of you have used it for more years than I'm alive. The product is a known cause of cancer and you know this is the consequence when you light up yet apparently to you guys it's more important to get that hit of nicotine than it is to stay alive. You do something all day every day that SHORTENS YOUR LIFE SPAN yet you guys aren't the ones that end up with cancer. I do. I get cancer. I don't smoke, I've never done a single drug in my life, I don't drink excessively. I stay out of the sun. I do everything to PREVENT cancer and this is my reward? Meanwhile you guys do the shit that causes it, YOU ASK FOR CANCER EVERYDAY and I'm the one that has to go through this. I'm the one that suffers. How is that right? How is that justified? How do you guys get to be selfish but yet my life hangs in the balance? I mean I had anger before this. I have asthma and some days breathing for me is so difficult it hurts. I cherish my lungs and wish every day to just wake up and have the disease gone and you guys take two perfectly good lungs and RUIN THEM selfishly in front of me while I watch hopeless, helpless. You should be ashamed of yourselves. YOU SHOULD HAVE THIS CANCER - NOT ME. I don't deserve this.

Not all who wander are lost

Before I can go forward with this blog, I need to take a step back for all ya’ll that missed the party bus a couple weeks ago. If you’ve been with me for the whole trip, take a nap and I’ll wake you up at our next destination. If you’re just joining us, well, have a seat, pour a drink and listen up because I’ll be your tour guide for the next few months…

Yup. I have the cancer. Obviously. See all the pink? I’m not much of a pink fan (expect for Pink herself, for which I have the upmost admiration for), I’m more of a purple kinda girl but the color is growing on me quickly. Candice, Candice! We have so many questions…I know minions, drink your cocktail and have a listen. I’ll answer this as if I’m being interviewed, by…myself…because I am…because I can’t think of a better way to do this so I’m just going to compile all the questions I get asked on a daily basis and you can read it as if you were reading one of those teen magazine pull outs of Justin Timberlake when you were 12 (or Nick Carter, I suppose if you were THAT kinda fan).

Cliffnotes version, how did this all happen?

Here’s the timeline so far:

7/6/11 – Went to see my gyno about birth control (oh yeah and that pesky lump)

7/17/11- Had a breast ultrasound done because my gyno didn’t like the look of the lump

7/27/11 – Had a biopsy done of the lump, a marker placed, a mammogram done to check the marker placement

8/3/11 – Called down to the breast care center and was told I have breast cancer

*Dates are fuzzy here but I’m pretty sure I had to go for a blood test and something else then:

8/22/11 – Had MRI done to see if cancer had spread to other breast

8/24/11 – Met with plastic surgeon

8/26 – Met with surgeon again to go over MRI

Then this Thursday I meet with a different plastic surgeon (because my surgeon doesn’t like the guy I saw the first time)

Are you ok?

Yes. I’m fine. Really. I am one of those people that says it like it is and if I wasn’t ok…you’d know it. Ask West (my bf) what it looks like when I’m not ok. He’ll tell you. You can’t miss it. Really. I don’t feel sick, I’m not losing sleep, I’m not worried about the cancer (I’m worried about other stuff as a result of the cancer like $$$ and work and all that crap) I’m not crying every day and I’m not wallowing in my own depression or planning my funeral. I am the same person I was before the diagnosis and I’ll be the same person after I kick cancer’s ass.

How did you find out you had cancer?

Uh. Well. I didn’t. I mean…I’m 28. I don’t do mammograms, I rarely do self breast exams unless you count reaching down into my bra to pull my boob back up into my bra a breast exam. Breast cancer is for old people lol. I know that’s not true NOW of course, but…in short, West found it. One night we were (insert goddy laughable porn music here) and he said uhhh…stop. What’s this? Where did this come from? (Things you say when someone pulls out a sex toy for $200 Alex) I felt what he felt and realized I had a lump that I swear was not there before that very moment, like him touching my breast put it there. As they say…the rest is history…

Does it hurt?

No. Well actually that’s a lie. It phantom hurts sometimes. Your brain does strange things when a doctor tells you, you have a tumor. You body starts giving off these phantom pains, your mind starts playing tricks on you…oh and around that time of the month it hurts but that’s almost every woman. Boobs in pain + Cramps + Blood + I hate the world = period.

Which boob? How big is the tumor?

Left. Which I think is odd because I’m left handed so it’s almost like I overworked that boob and its fighting back or something. The tumor is a little over 3CM X 1.5CM which on a ruler doesn’t look that big but apparently, the size along puts me at a stage II.

So you know what stage you are?

No. Not really, I know what stage I’m at least at. I’m at least a 2 because of the size of the tumor but it could be a 3 depending on if it went to my lymphnodes. What we’re hoping for is NOT a stage 4 which means the cancers spread and theres tumors elsewhere. We’ll know this “staging” after surgery.

What kind of cancer is it?

Haven’t you been reading? It’s breast cancer? JK – I know what you mean, its called IDC – Inductal Carcinoma or plainly boob cancer that starts in a milk duct. It’s the most common type of cancer which I’m told is a good thing because rare+cancer = no bueno in most cases. Wow I need to stop blogging after math homework. I’m doing a lot of equations here. Besides that, I’m pretty sure I heard the docs say it’s HER2 negative and Estrogen positive. If you want to know what that means, google it, cuz I’m not a doctor.

Has it spread?

I don’t have an answer for that. Surgery needs to be done to check my lymphnodes. If there’s cancer in my lymphnodes then yes, its spread, no cancer in my lymphnodes means there’s a pretty good chance it’s just in the breast. We’ll know after surgery.

Are you ok?

Yes, thanks for asking…again.

What are they going to do?

A double mastectomy. Yup…both boobs coming off, chopped away, removed…and the cancer with it!

No, seriously, what are you going to do? Isn’t there another way?

There is. I could have just the one infected boob removed…and have no left boob, or have a fake left boob and a healthy right boob….and when I’m seventy my upper body will resemble a teeter totter. Or I could have a lumpectomy but I’ll lose my left nipple and pretty much half my breast and insurance doesn’t cover lumpectomy reconstruction (the insurance company won’t buy me a new nipple)…. I could make millions on fetish websites who like women without matching breasts, save up some cash and get reconstruction later..but I’d like to not find out what the online porn industry is like.

To be serious for just a sec, it makes the most sense for me, for my age, and for my risk factors. I read a study today that said that women have a 1.5% chance per year of breast cancer reoccurring after once having the disease. That means if I live till I’m 80, that’s a 78% (52 X 1.5) chance I’ll have a reoccurance in my lifetime. It’s bad enough I have to go through this once, I don’t want to hold my breath my entire life for the other boob to drop, as they say. Plus, the reconstruction will make them match and I’ll never have to do self-exams, mammograms (for cancer, they’ll still do them for implants) or worry about breast cancer ever ever ever again…and who knows where I’ll be in life when/if I keep a healthy breast and it re-occurs. Maybe I won’t have insurance, maybe I’ll have a billion kids and won’t be able to sleep and recover like I can now etc. etc. lets just get it done and over with, as extreme as it may seem.

How are you feeling?

I feel fine. I don’t feel sick, I’m not tired, I don’t have pain…if I didn’t have a lump, I would have never known anything was wrong.

How is your family/boyfriend/friends handling it all?

It’s funny how people react to cancer. I had a co-worker I was pretty close too and she had a first hand account of cancer so I when I got my diagnosis I immediately wrote her a novel on my feelings/fears/medical advice etc. etc. and was just sure she was going to be a great support tool. She never wrote back. She got it, she just hasn’t answered yet apparently. On the other flip of the coin I have a friend from high school, we didn’t hang out much so I don’t know if she calls me a friend but anyway, we knew eachother, we talked occasionally but our relationship wasn’t necessarily memorable…but ever since I was diagnosed she writes on my facebook wall and sends me wishes just as much as my best friend. I have an aunt that sends me greeting cards in the mail. She writes inspirational messages in them and being a cancer survivor herself, it makes it fun to check the mail finally J All in all everyone is dealing with it in their own way but it’s been positive and that’s all that matters to me. No negative JUJU!

Are you scared?

Hell yeah I’m scared. For someone to tell you they’re going through something like this and not scared is full of bullshit with a capital B. Point them out so I can kick them in their babymaker. The thing is, fear can be a motivator or a paralyzer and I choose to let it motivate me. All fear really is, is the feeling of not knowing. I fear what surgery is going to feel like. I fear what the pain is going to be like after. I fear what chemo is going to be like, if I have to lose my hair. More than anything I fear this whole experience will leave me with the inability to have kids. That is my greatest fear…but you press on and you take it day by day and you face it because the true character of a person is what they do when they are faced with a great challenge, and I don’t intend to have stories told of me of how I lost my battle with cancer. Nah ah. Not me. Not this girl. Breast cancer has no idea who it’s messing with.

Do you have to have chemo? Radiation? Are they going to take out your ovaries? Tell me more tell me more:

I don’t have answers for these questions which is why I grouped them all together. We won’t know these answers until after surgery and as for the ovaries, it seems pretty common with estrogen positive breast cancer but I am going to fight tooth and nail to find another way.

Are you ok?

Ask me again. Really. Find out what happens. IM EFFING FINE!


Ok…now we’re all on the same page? Good! Glad we took this trip down memory lane :) Moving right along…..

Just a LUMP in the road...

Just a lump in the road…

Ehehmm…is this thing on? Testing….testing…ahh ok. Well. I suppose since I have your attention now, I should introduce myself. My name is Candice Chilton and you’ve reached my blog…leave a message at the tone and I’ll get back to you when I can/feel like it/if I love you…er…wait…wrong message. Focus…focus… I’m a 28 year old Vegas livin, music lovin, smart ass. I am originally from Carson City born and raised but I’ve been in Vegas now for a little over a year. I live with my boyfriend of almost 4 years, West, and his brother Evan…and my three cats, Bella, Tara and Neka in a two-bedroom (why-does-the-whole-place-smell-like-cat-litter-eventhough-I-bought-a-$80-effin-electronic-cat-box) apartment. I am an office manager for a restaurant group on the Vegas strip and I’m a student at CSN pursuing a degree in event management. When I’m not working, going to school, fighting/bantering/bickering with the people I live with over who’s turn it is to do the dishes, or blogging, I’m usually helping my mom run her part time jewelry company (insert cheap advertising space here) called Neon Skullworks (www.neonskullworks.com). Oh yeah, and I have breast cancer.

Jesus! I know, right? You found this blog/know me/reading because you know I have breast cancer and you want to read all about it, and here I go writing a whole paragraph NOT about breast cancer. Ya know why? Because of all the things I’ve done/doing/about to do, the last thing I want you to remember about me is that I have breast cancer. Yeah, yeah, I’m writing a blog about it so it’s hard to forget, I’m not saying pretend I don’t have it, I’m just demonstrating how A) there are a lot more pieces to me than my cancer and B) that I refuse to let this stupid effing mofo $#%#$^#$^#$% disease define who I am. So while yes, this is a blog about my experience with the disease I also plan on incorporating my daily life in the mix too.

Here’s what this will not be. This will not be a pity blog. This will not be a blog all about woest me, feel sorry for me, pity me, and give me that look when you see me. Ya know that look. We all do it, that “oh poor thing has cancer, and she’s so young look”. This will not be a blog for the weak, thin skinned, easily offended people who like to read pity blogs. Here’s what this blog will be: A tell it like it is, exactly like it is, probably too many details than you ever wanted to know about the entire breast cancer experience and then some blog with so much humor added in, you’ll probably forget cancer is such a scary thing. Ladies and gentlemen, I’m going to post pictures of my boobs. Go back and read that sentence again. Yep, I know. Shocking. A breast cancer blog with boobs…and don’t worry all my fathers/brothers/uncles/sisters/etc. that don’t care to see my boobs. I’ll put a warning before aforementioned post so you may skip to the next chapter before being flashed – and maybe blogger might take my post down and say that its porn…to which I’ll laugh hysterically but I do feel its important to put this out there in this way because if I help someone my age battling the same disease, put them at ease, let them know what to expect, then this blog has done its job.

So hang in there with me and please post comments. Seriously. I don’t mean read and just close, like interact! I want to know what you think/feel/saw/react etc. because this disease isn’t just about me. It effects everyone around me, yep yep, that’d be you…you reading….and as such you get a say in the whole shebang. Get ready to laugh, cry, be disgusted, be amazed, celebrate and repeat. Maybe not necessarily in that order but more importantly get ready to smile with me….because when you smile, you’re less likely to give me “that look” J

--Candice--

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