Thursday, June 12, 2014

She Asked For It

So it was just this week that I blogged about how I don't pressure those around me--well, not co-workers or almost strangers--into protecting their skin. I post what I have to say online, I share my story once I'm comfortable with you, and that's that. I don't comment on your obvious sunburn. I don't let you know I notice your brand new tan in the month of January when you haven't been on vacation. I smile and treat you just like I treat every other person. I'm not going to let my personal feelings towards tanning change the way I treat a person. Point is, I keep my mouth shut. No lectures.

(But I do post stuff like this.
Often.)

However, sometimes, situations just walk in to your office fall into your lap.

Today one of my co-workers began walking down the hallway, pushing one of the young X-RAY students towards my office. I knew, just by looking at which student he had by the shoulders shoving towards me, what was about to happen. "You need to talk to her, Chelsea." I started shaking my head, "No. I saw her tan. It's her body. I'm not going to lecture her." "You need to talk to her." He stood there, with his hands on her shoulders, preventing her from walking away. I was determined to be nice to this young girl who I don't even know by name and just give her the sweet smile, followed by the, "You really shouldn't tan" comment. But then she looked at me directly in my eyes and said, "I go to the tanning bed all the time."

I don't know what happened. I don't know why I let the poor girl have it like I did, but by the end of it, my hands and my voice were shaking. I don't have the slightest idea what I really said, but let's just say it went something like this:

Student: "I go to the tanning bed all the time."
Me, in a shitty voice: "You can go to my chemo sessions with me too."
Student: "No thanks."
Me: "And you're a RED HEAD! You're basically just asking for it!!!!!"
Student: "Stoooooooooooooop."
Co-Worker: "We've been telling her that she needs to stop. It's so bad for her!"
Me: "AND YOU'RE A RED HEAD!!!!!!! Statistically you're a walking melanoma patient!!!"
Student: "Stooooooooooooop."
Me: "Do you know that they said I had a 50% chance of being here in five years?"
Student: "Stooooooooooooooooooooooop."
Me: "If you don't catch it in time, it's not like you can just cut it out. There is no cure."
Student: "Stooooop."
Me: "The World Health Organization classifies UV rays from tanning beds as a class 1 carcinogen, just like tobacco. You might as well start smoking."
Student: "Guys, stooooooooooooop."
Me: "You have to know how bad it is for you. With all of the research that is available, every time you turn on the news they are talking about it. You have to know."
Student: "I obsess with sunscreen every time I'm outside!"
Me: "WHAT'S THE POINT?! 10 minutes in the tanning bed is just like spending 8 hours in the sunlight without sunscreen. What's the point in obsessing with sunscreen if you turn around and go to the tanning bed?"
Student: "I like the way it looks."
Me: "But that's the other thing! IT DOESN'T LOOK GOOD! It makes you look old!"
(This is when two of my co-workers chimed in with the changes they've seen in their skin after years in the sun.)
Student: "Stoooooooooooooooooooooooooooop."



And the convo went something like that. The student never said she would consider what I yelled said, but she did thank me. So while I doubt she'll cancel her tanning membership any time soon, I doubt there will be a time in the near future when she doesn't think about the mean girl in the scheduling office who told her that her tan isn't pretty.

(I swear, I wasn't trying to be mean. I realized right away that my tone of voice was abrupt, I was harsh, I said things that I usually only write because they are hard for people to hear, and I let her have it. I don't know why. It just came out! She is such a beautiful young girl with her whole future ahead of her and I hate to think about what she may face in her future.)


Maybe tomorrow, if she'll make eye contact with me, I will apologize for being a bully and encourage her to make better life decisions. Not only for her benefit, but because I don't want to be seen as the mean melanoma girl who throws scary info at the first tan girl that gets brought into her office.

Eh, whatever.

She asked for it.

;-)

(A big thanks to my co-worker who raised some serious melanoma awareness today! I appreciate you!)

Monday, June 9, 2014

In My Face

There once was a gal who valued a tan. She tanned before prom, graduation, and vacations. She tanned before summer break so that she would get a "base tan." She tanned to make her skin, as society determined was the prettiest, bronzed.




Y'all know all of that. I have never denied my tanning history nor have I ever played the victim because of my melanoma diagnosis. I know I screwed up and made some really shitty decisions that I will forever pay for. 

 You don't have to be a radiologist to know you're not supposed to glow like that.

While I am all about protecting my skin, my family members skin, and encouraging others to do so via the Internet, I am not pushy about it in my every day life. I don't pass a sunscreen bottle around the bleachers at my step son's baseball game. (Although I cheered a little when someone else did.) I don't lecture my co-worker about her obvious burn. Unless you're friends with me on Facebook or stumble upon my blog, chances are you don't know I go to NY every 3 months to see my oncologist. Unless you already know about it, you can bet I don't share my melanoma story with you until I consider you a friend. That's just not how I am. I don't want to be that girl who is always yelling at the co-worker she barley knows about his weekend at the beach.

However, if you are friends with me on Facebook, you know I preach sun safety and my true hatred for tanning beds. I try not to be obnoxious, but I'm certainly aware that I probably am. ;-)

Having said all of that, I can't help but cringe when folks come up to me and say, "I thought of you this weekend. I said to my husband, 'Chelsea's going to get mad at me for getting a sunburn" or "You are going to be mad at me, but I'm going to go to the tanning bed just for a few times." I never know how to react because I want to keep the friendly and professional relationships, but I really want to be like "Whyyyyyyyyyyyy do you tell me these things?!" If I saw your sunburn--and I always see the sunburns--I would never say a word. If I noticed your obvious fake and bake sessions, you can bet I wouldn't mumble a sound about it. While I like to raise awareness, I know there is a time and a place for it. But throwing it in my face? Making a point to tell me the things you know I will get upset about? WHAT DO YOU WANT ME TO SAY?! Ahhhhh!

So I started thinking about it today. Let's say I had lung cancer. Would my associate come up to me and say, "I thought of you today when I bought a new pack of cigarettes"? Would the stranger I see once a month say, "I only smoke when I drink" as if that is an excuse for her bad habit? Or would that be in poor taste?

Am I supposed to just be like "Oh OK!" because it's just a tan? Big deal?

If UV rays from tanning beds are class 1 carcinogens, just like tobacco, why can we make excuses for our poor decisions just because we want to look good at the country club?

I make a point to keep my cancer outside of certain areas in my life, but when I hear these confessions, I can't help but speak up. Obviously these folks know their decisions are poor choices, yet they make them anyway. And really, that's on them. It's their skin, their biggest organ. (And yet, the sensitive girl buried inside of me can't help but feel the sting. You don't have to make better life decisions just because I got melanoma, but you could refrain from telling me about those decisions. I had to learn my lesson the hard way which is why I put time and effort into sharing my experience.)

Maybe next time, instead of almost asking for my understanding, they will apply the extra sunscreen and cancel the damn tanning membership.

A girl can hope, can't she?

*Disclaimer: This isn't about a particular event. These types of comments are made weekly. DisclaimerX2: You should know by now there's always a chance YOU will end up on my blog. ;-)

XO.

(And yes, I realize it's been forever since I've blogged. PLEASE FORGIVE ME. Life is good--yet very, very, very busy!) 




Thursday, April 24, 2014

The Media Controls the Mind.


People in the spotlight have the great advantage of making a positive impact on society. They also have the disadvantage of upsetting a lot of people by comments they make. Today, I physically cringed while reading an article about Mike Schmidt’s cancer. The Ex-Phillies great, Mike Schmidt, was diagnosed with stage III melanoma last August. He is just now beginning to discuss his cancer with the public.
Mr. Schmidt has had numerous operations, radiation, and chemotherapy. The York Dispatch wrote that he is going through the third protocol of three different immune system boost treatments and is about a third of the way through the 12-week process. Obviously, he’s fighting melanoma with all he has. We all understand that, respect that, and we wish him well.

Here’s why I started cringing: the article states that the Ex-Phillies great is becoming an unofficial spokesperson for getting ones skin checked. OK, that’s wonderful. However, when discussing the new chapter in Mr. Schmidt’s life, he says, “I can think of a diagnoses that could be a hell of a lot worse. Cancer is a scary thing. Mine’s skin cancer.”
No joke. I cringed. My shoulders tensed. My jaw dropped.

Let me define stage III melanoma: According to the Skin Cancer Foundation, “At this point, the tumor has either spread to the lymph nodes or to the skin between the primary tumor and the nearby lymph nodes.” This means it has gone through the skin. In my opinion, if this has happened, the cancer can no longer be classified as “skin cancer.” It’s melanoma. Stage III malignant melanoma.
Mr. Schmidt also said, "I have to have scans every three months. Who knows what and when and where something's going to come up. That stuff travels around you microscopically. Until you have a year's worth of scans that show no residue and they tell you you're cancer free, all you can do is treat it."
We all know that he's going to always need to be followed, don't we? Sigh.
Please feel free to read this article yourself. Maybe I’m overly sensitive to it all and overreacting (wouldn’t be the first time!), but it sounds to me like Mr. Schmidt needs to be educated a wee bit more on the seriousness of his cancer. 

Maybe he wants to downplay the seriousness of melanoma to the public? Maybe he’s in denial? Or what scares me the most, what if he just hasn’t been clearly informed? But, he, someone who is speaking about his battle with cancer to the media, is doing our cancer, melanoma, not a lick of good. We’re fighting so hard to have melanoma taken seriously, and to see this article, well, it gave me a clear flashback to the many times I’ve been told, “at least you don’t have a real cancer.”

I do have a real cancer.
And, Mr. Schmidt, so do you.

Thursday, April 17, 2014

Bunk Beds and Backpacks

This is why I'm not as successful at this whole blogging thing as I possibly could be: I disappear for weeks on end. Forgive me. Life has been fun--and thankfully--melanoma free lately. I'm also having a major issue with my computer that even my IT degree husband can't fix. Anyone have any advice for a good laptop? Apparently I am now in the market. 

Since we last spoke, I turned 27 and my dog got diagnosed with cancer. I'll update you on all of that when I steal my husband's computer from him. Today I wanted to share this incredible article my new friend Kate wrote. I'm not sure how I came to read Kate's blog, but each post leaves me with chills, and usually tears. One day soon I'm going to take that 3 hour drive to DC and meet her in person.

In the meantime, please, my friends, meet Kate:



Bunk Beds and Backpacks


We were married when I was twenty six, and we held hands in a church in Arizona while I hoped the day would go off without incident.  Now I am thirty, and I hold his feet in my hands as I slather them in peppermint oil and massage, hoping he will rest.

"I was thinking on Saturday we could go look for bunk beds in the morning," I say as I sit on our bed, trying to create nightly "rituals"--as suggested by our holistic health practitioner--because we don't sleep.

"Sure," my husband says, reclined against the pillows, "we can do that."

A birthday gift for our soon-to-be-two-year-old, a big boy bed like his big brother.  But then I imagine their room without a crib, just two boys, no more babies.  I start to cry.

I begin to tell him that I want another baby, even though he already knows and even though I already know what he'll say.  He's not interested in having more children, and it kills me every time he says it.  He's too tired as it is, he will tell me, we can finally travel, the kids are finally old enough.  If we have another baby, we are back to square one, back to sleepless nights and non-stop nursing and no time for anything that we love.

And sure enough, he says all of these things.

"But they grow up," I tell him, "they're not babies forever--look how fast it happens," I motion to their room on the other side of our wall, the room that holds two towheaded boys.  They are enough, but sometimes, I tell my husband, I long to hold a baby, to know that we will have a house full of noise and toys and balls and dirty clothes for a long, long time.  That we will have millions of grand babies and great grand babies. 

I can't be left alone, I think to myself.

"I won't try to change your mind," I say, rolling onto my back, lying next to him.  "I wouldn't want you end up blaming me if something happens."

If something happens.  

He sighs so deeply that seems to unleash something in him.  He clears his throat, and I can tell, without looking, that he is holding back tears.

"There is nothing I want more in this world than to have a house full of kids with you," he confesses.  "But I don't know what our life will be like, I don't know if I'll be here in five years, or even two years, and just like you don't want to held to blame, I don't want to leave you with a big family if I can't be here to help you.  What if I get really sick again, and you're taking care of a newborn?  I can't do that to you."

He refers to his diagnosis--stage III melanoma--with a fifty percent survival rate after five years.  He is a year into his clinical trial, yet for some reason only recently has this statistic begun to haunt him.  It haunts him to the point of sleeplessness, to mental anguish.  It haunts him so relentlessly that he has started to change--he is not the same man I married four years ago.  So I massage his feet with peppermint oil, hoping it'll bring him back to me.

I am crying now, big tears rolling down my face, because I understand him, understand the truth that is finally escaping his lips, and my heart breaks for it.

"But for me it's different," I confess, "because I want more little versions of you, just in case."  Like an insurance policy, I think, a safety net, I want to surround myself with more little people that are just like him--if something happens. 

We lie together, crying slow-rolling tears down exhausted cheeks, silently understanding and silently struggling.

I roll towards him, wiping my tears on his shoulder and neck, burying myself in his smell.  "I'm so sorry," I whisper.  I'm so sorry we have to live like this, I'm so sorry that all of our decisions are based on the probability of life versus death, that his cancer won't come back, that he will win.  I think these things, but don't say them aloud. 

"I just want to give you everything you want," he whispers back, "I'm so sorry I can't."

Eventually, we fall into a sleep so deep it obliterates all possibilities of dreams.

Two days later I am seated in a coffee shop, watching ice skaters glide in circles on a DC ice rink though a big picture window.  I try to write, but my mind is blurry from lack of sleep and throbbing emotion, and so instead, I call my mother, because I know she will pick up, and I know she will listen.

"Why are you at Starbucks at nine o'clock at night?" she asks me from her vacation in Florida, knowing I would usually be at home in my pajamas, sitting with a hot mug of tea and my husband by my side.  Tonight, however, I am frozen and tired and cannot wait another second for my breakdown.

Surrounded by strangers working silently on laptops, with ear buds and the buzz of caffeine to drown me out, I begin to detail the latest emotional trauma in a slew of disturbances over the last fifteen months.  I tell her about babies, about statistics that she already knows, about my husband's thoughts of his own death.  I sob as I divulge my deepest fears, shivering uncontrollably--though from cold or from fear I can't decipher.

She is silent for just a moment before she speaks.  

"You are both making this decision out of fear," she tells me, "You are afraid he's going to die, and so you want a baby.  He's afraid he's going to die, and so he doesn't want a baby.  But both of you are using fear as your motivator.  That's no way to make a decision--especially one like this."

I watch an ice skater spin in circles in the center of the ice, faster and faster, until she almost loses control.  She stops herself just in time, then skates away.

With a brown paper napkin, I dab mascara stains off my face.  I glance around to see if anyone was witness to my breakdown.  If they were, they don't show it.

"Thanks, mom," I tell her, "I should go home now."

I find my husband at the computer.

"Did you talk to him?" I ask.  My stint at the coffee shop was an effort to grant him the privacy of a phone call in our tiny DC townhouse--so he could discuss things like dying without his wife around.

"I did," he gives me a half smile and a shrug.  Then he begins.

***

"Mmmmm," I say, glancing up from my computer, "smells good."  My husband shrugs and modestly tells me he hopes it turns out as he stirs the fragrant curry he's making for dinner.  I put the kettle on, then lean against the counter, waiting.  It has been a week since our baby breakdown.

"We've talked so much about having another baby, but have we come to a resolution?" I watch him.  "Will you ever feel comfortable enough with the statistics to move forward?"

He leans back, a dish towel thrown over his shoulder and hands in his pockets, thinking.

"You know, my friend told me it gets easier the further away you get from it," my husband says as I pour boiling water into my cup.  His cancer friend, his mentor, who is fifteen years from his diagnosis, was the phone call my husband made earlier in the week as I watched ice skaters through blurry eyes in a coffee shop.  "You have to live your life like you would without cancer," he told my husband.  "You can't let it run your life.  And it will get easier, you're still right in the thick of this."

But the further we get from this, the older I get, I think to myself.

He shifts his weight and I notice the dark circles under his eyes, his disheveled hair--reminders of a surprise visit from the side effects of his treatment and his weekend spent in bed, forgoing our ski trip because he was too ill to travel.  Another example of the utter lack of control he has over his--our--life.

"To be honest, I crave a little bit of stability right now," he tells me, his blue eyes misting.  He's right, we have moved three times in the last eighteen months, and we can't find things like birth certificates and passports. 

"I still haven't unpacked the backpack from Argentina," he laughs.  The backpack, storing his medical records from the hospital in Buenos Aires that biopsied his cancer-filled lymph nodes, that delivered the news that would change our lives, sits in a closet in our basement--a metaphor for how we've dealt with this disease.  For the last year, we worked through the physical trauma of this illness--cutting out the cancer, infusing medication into his body to prevent a recurrence, dealing with infections and subsequent hospitalizations until he was finally healthy--and now, at the year anniversary of his clinical trial, we are just starting to sift through the emotional wreckage. 

I watch him as he moves back to the stove, absentmindedly stirring the curry.  Another baby, perhaps, but right now, he needs someone to help him unload the backpack.  This wasn't what I expected when I married my husband on a 115 degree day in the desert four years ago.  But it's what I promised. 

"Let's go get that backpack," I say. 


Chills, right? Go read all Kate's post now: http://effthec.com/

And forgive me for being a horrible blogger. I needed a little break. XOXO!
 

Wednesday, March 19, 2014

Ripples of Healing


A few months ago I wrote about a man I met on a day when he "wasn't kickin' too high." The second time I ran into the stranger, he cried in my arms in the middle of a busy hallway and told me that after 8 years of being cancer-free, the cancer had returned. My heart broke for him as I watched the pure anguish on his face.

A few weeks after that very unexpected interaction, the fella came to see me. He wanted to apologize for breaking down in front of me, just a strange young girl who asked how he was. I cut the man off mid-sentence and asked him to hold on, that I had something for him. Ever since he confessed to me that he had already made up his mind to refuse treatment if the cancer had metastasized throughout his body, I knew what I needed to do. I ran back to my purse and grabbed the lucky rock Julie's mom had given me. I ran back into the room, grabbed the man's hand, and placed the lucky rock into his palm. I quickly said, as my voice began to shake, "I've been in your shoes. This was given to me by a woman who means a lot to me, it brought me good results. It's your turn now." The man began to cry. He hugged me and we said our goodbyes.



I didn't forget about the stranger. In fact, he crossed my mind a lot. I knew he was no spring chicken, but with an attitude like his, I had faith he would fight. I just hoped I would hear from him again.

This afternoon I received a call at work from the front desk secretary. She told me there was a man in the waiting room asking to speak with me. That's not really that unusual as doctors send patients down quite often to coordinate their appointments. She said it wasn't for a patient. Odd.

I walked into the waiting room and the stranger stood up. I immediately hugged him. We may not even know each others last name, but we shared a moment. I expressed how excited I was to run into him again. He cut me off and grabbed my hand. In it, he placed the lucky rock, and held my hand. "I was so touched the last time I saw you that I didn't comprehend that you had cancer too. I came to bring you the lucky stone back because I had my surgery, the mass was benign, the cancer is not back." I yelped and pulled him into a hug.

Even as I listened to him talk about how he's so much older than I am, how cancer is supposed to happen to people his age, not mine, I couldn't get over what was happening at that very moment. This stranger actually kept a rock given to him by some random girl he was likely to never see again. Not only did he keep it, he told me it brought him comfort when he needed it, but now it was time for me to have it back, that it's my turn for a little luck.

Honestly, when I gave him the stone I really thought that was the last of it. I figured he would remember me for a sweet gesture and that would be that. To see him today, to hear him say the words that the cancer is not back, to have that lucky rock returned after it brought him comfort during the months filled with fear, that was a feeling I won't soon forget.



Two strangers. One lucky rock. Two lives forever changed.

Life sure is sweet.


(To read the previous post about this man: click here)

Monday, March 17, 2014

Too-Much-For-One-Blog-Post-Title

Remember how I became really lazy in updating this blog? It is happening again.

Kick me. Throw something at me. Or just turn to Twitter/Facebook/Instagram and you can see that I haven't forgotten about melanoma awareness. In fact, I've been SUPER busy with it!

Prepping for an interview with the New York Post.

I love the months leading up to May. In just 3 years I have seen melanoma awareness grow. While we still aren't where I would like to see us, we are getting there. Alright, let me do a little updating.

Remember last year the American Academy of Dermatology launched the Spot Skin Cancer campaign in May? Remember how they asked the melanoma community, on Melanoma Monday, to wear orange? Remember the outrage from it? So does the American Academy of Dermatology. Many of us within the melanoma blogging community received an email a few weeks ago inviting us to a conference call to discuss AAD's plan for this melanoma awareness month. Instead of rehashing the conference call, especially because Al wrote about it so well, I suggest you read his post! We were all so thrilled that the American Academy of Dermatology read our emails, heard our frustrations, and reached out to us to apologize. I fully intend to support their efforts in raising awareness for this cruel cancer!

I also spoke with a drug company who plans to host a blogger conference in May! I wish I could share more info with you, but be on the look out for it in the coming months. I was so impressed with how interested the company is to promote melanoma awareness so I'm thrilled to see what happens!

This past Saturday was all about indulging in our city's St. Patrick's Day events. I lathered on the sunscreen and headed downtown with my husband to meet up with some of our friends. We had such a fun time!



 While enjoying the green beer, I received a message from my melanoma friend in Texas. She said that a reporter for the New York Post was working on an article regarding a donation made to Memorial Sloan Kettering Cancer Center. The reporter wanted to speak to patients who had been treated with Yervoy by MSK. Jennifer passed along my contact info and I was able to talk to the reporter Sunday morning.

So what did a reporter for the NY Post want to talk to this Virginia girl about? It's kind of ridiculous. Apparently folks in NY are royally pissed off at billionaire David Koch and expect New York-Presbyterian Hospital to turn down the $100 million donation he recently made. $100 million dollars, y'all. The reason they don't believe the hospital should accept it? His conservative political beliefs. (Insert eye roll here. It always comes down to politics, doesn't it?)

According to the NY post, Mr. Koch has given MSKCC  $61 million since 1992. This money was extremely instrumental in the development of Yervoy. Should Sloan-Kettering return that generous sum of money because Mr. Koch doesn't agree with Obamacare? Really? (Insert annoyed face here.)

You can read the article for yourself here; however, there are a few things I want to add:

1) The article's title this morning was "Cancer patients bash Koch hospital donation protesters." First, I can speak for Erin and myself, we didn't bash anyone, not even the protestors. When questioned about my feelings, I said that maybe I am selfish, but I'm grateful for the money that Mr. Koch donated because without money, there is no research. Without research, there will be no cure. I don't care where the money is coming from as long as it is used for the right reasons. I'm grateful for his donation.

2) The new title is "Koch hospital saved my life: Cancer patient." I think I'm just going to wait for Erin to blog about this because I'm sure she's going to have something to say. (Insert another annoyed looking face here.)

3) I remember the day Yervoy was approved by the FDA. I was sitting in my hospital bed at MSKCC, recovering from 2 full lymph node dissections, when my surgeon walked into the room. Dr. Ariyan sat down on the end of the bed and told me the news. She had tears in her eyes because she knew what this approval could mean for many of her patients: a new chance.

4) What would I say if confronted by Mr. Koch? Two words: Thank you.

5) So that's what it's like to be interviewed by the New York Post. (For the record, the reporter was SO nice and I enjoyed our 30 minute chat. I'm glad I introduced him to Erin because she was totally the right fit for this story. She's a badass melanoma warrior!)

**On a happier subject, I had the opportunity to chat with Robin over the last few weeks regarding articles for the website cancercommons.org  Talking with Robin, even about melanoma, was fun! She was so great to chat with and it was a pleasure telling her my story. Robin's article was published today and I am honored to be featured as a Super Patient! The article briefly touches on my melanoma diagnosis, why I said NO to interferon, and how I ended up in a clinical trial at MSKCC. Feel free to check out the article here. I encourage you to browse their entire site. There is a ton of important information.

Hopefully only one more time in this chair!

Oh, and by the way, my scans were A-OK! I was totally unremarkable! (The one time I strive to be unremarkable! Ha!) The lymph node remained the same size as it was in January. Scans 3 months in a row? I'm pretty much glowing. I'm so relieved to have a break until May!

I also had my second to last infusion! Can you believe it will be 3 years in May? My liver is apparently feeling it though. I received a call today from the oncology nurse that my liver enzymes--AST--are elevated. This happened after my last infusion as well. Maybe I really  am getting the drug. (Oh, and I promise, I had the bloodwork done last week, before the green beer! Hahaha!) I will go back this coming Thursday to have my labs repeated. Hopefully my liver will heal itself just like last time!

Alright, if you got through all of that rambling, THANK YOU. I'll try to do better about blogging, I promise.

XOXO


Sunday, March 2, 2014

Sweet Emily

You're going to have to forgive me this morning, but I'm going to share something that's not the slightest bit related to melanoma.



This is Emily. I had the honor of meeting Emily when I was waiting at Sloan Kettering for an appointment with my oncologist a year or two ago. Emily was waiting to see her oncologist as well. Drawn to her by her Virginia Tech sweatshirt, my mom and I began to chat with her. Emily had spunk. She may have been battling an incurable brain tumor, but the girl had one of the best attitudes I've ever seen. Over the last year, Emily's cancer progressively got worse. She was constantly in and out of the hospital, quickly losing her vision, etc. However, her spunk was still there. With the help of her friends, and even strangers, Emily was able to cross off a few items from her "to- see" list before her vision got worse.

In January I received a text from Emily asking me about Yervoy. Her doctors, with no other treatment options, and stating that Emily only had a few months to live, thought that they would do a trial with Yervoy. She wanted to try whatever she could that may possibly give her a few more months here with us. I shared my slim knowledge of the drug, told her how my mom and I continue to keep her in our thoughts, and Emily encouraged me to be healthy and well. I didn't hear much from Emily after that day in January.

I logged onto Facebook yesterday and saw the post I feared: Emily passed away yesterday at the age of 26.

Why am I sharing this with you on my melanoma blog? For starters, Emily was an awesome gal. She was a kind person, and even during her darkest moments, she cheered me on. Emily also had a way with words. I encourage you to check out her blog: http://www.emilyinthecity.com/

As an ending to this post, I want to share something Emily once wrote:

"Recently, two people have commented on all the fun I'm having on FB and in pictures. First, happy to trade--really, dying and relying on your parents, is not "fun." I'm just doing what I would encourage you all to be doing: live. Just live every day to YOUR fullest. In fact, because both your hands work and you haven't fallen three times in two days due to balance issues, YOU should be having more fun. If you're not; you're doing it wrong. If you hate something in your life --change it."

I think we can all learn a little something from that.

Rest now, sweet Emily.

"How do you live your life? I live mine with both eyes open – even if only one takes in the picture." 
Emily Morrison