Showing posts with label malignant melanoma. Show all posts
Showing posts with label malignant melanoma. Show all posts

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!
 

Monday, February 3, 2014

Words From a Friend

Sometimes I receive emails from people that I automatically know I'll become friends with. This was one of those situations. Having read her story, I knew that it was one that needed to be shared with all of you.  I'm so thankful she agreed to let me share it! So please, meet Chelsea, and share her words with someone who needs to hear them.


 "When I ran across Chelsea’s blog, I knew I wanted to know her. You see, not only do Chelsea and I share the same name, we also share an unfair diagnosis, which for both of us, is oddly in the same spot on our backs. I saw the picture of Chelsea’s scar that looked exactly like mine and felt an instant connection to this stranger miles away. When she asked me to share my story, I was a little nervous, because before now, I’ve never put it on paper. The feelings of it, well, they are just overwhelmingly strong, but the truth is, it needs to be told.
I’m one of the lucky ones, they say.  I never had to undergo chemo or radiation, and all my lymph nodes are still in place, but the truth of the matter is that melanoma changed me completely.  I was diagnosed at 18 during my freshman year of college.  The year prior was full of events that required me to be in evening gowns. There was prom, then the yearly pageant my school held, and don’t forget about those awful vocal music dresses that surely looked better on me when my skin was tan. Those moments in a tanning bed, defined my future.  While my friends were vacationing during Spring Break, I was undergoing a wide excision surgery to remove six inches of skin on my back all the way down to the muscle. This surgery was my cure, but it wasn’t completely healing, because the emotional scar runs a bit deeper and has lasted far longer.
The misconception associated with the word melanoma is that it will simply be cut out and everything  will be fine. I can’t tell you how many of my friends spoke those exact words to me when I shared my diagnosis with them.  Quite frankly, until I had my doctor tell me that there may be a chance that I could only have five to seven years left to live depending on my test results, I didn’t understand the severity either.  My friends couldn’t understand the situation I was in and it wasn’t because I had surrounded myself with people weren’t able to feel empathy; it was because they simply weren’t educated.
My family, they became my saviors, the people I laughed with to distract me from the constant terror I felt in my stomach, the people who held me when I cried, and the people who found strength  for me when I couldn’t find it in myself. In fact, it was my mom, who saved me. She was the one who had noticed the mole on my upper back that had gradually became dark black and she was the one who called me with the information from the doctor of my diagnosis. Often times, I still wonder how she found the strength to call me, her only daughter, to tell me I had cancer.  My melanoma diagnosis didn’t just emotionally scar me; it scarred every person in my family.
Life after melanoma is different to say the least. I’m far more cautious and I’m often fearful of reoccurrence. For the rest of my life, every six months, I will visit my dermatologist. I sit undressed in a brightly lit exam room while my doctor goes over every inch of my skin. These checks, more often than not, end with a biopsy of a something that looks suspicious leaving an open wound on my skin that takes weeks to heal. I then prepare myself to tell my loved ones that we are, yet again waiting on pathology reports. The chance of reoccurrence for me is 2% and while that may seem like a very small number, it is actually quite large in relation to melanoma.
I never dreamed that before I graduated college and said I do, I would be a cancer survivor, but it is my reality. I often have to remind myself to slow things down because facing a diagnosis that could have ended in death caused a horrible sense of urgency for me. Sometimes I have to take a moment to remember that I don’t have to live life so fast because God has given me more time and a chance to leave a legacy. I wasn’t lucky, I was blessed and I feel strongly that I am meant to educate others on how to care for your skin.  Unfortunately, I wasn’t educated on the effects of tanning, but don’t let that be your excuse. Don’t be like me. Your desire shouldn’t be getting tan. Your desire should be to stay alive. Educate yourself before you find yourself in a situation that educates you."  

Please take Chelsea's words and educate someone else on the true dangers of tanning. A big thanks to you, Chelsea, for sharing your story with others! I know it's scary to put yourself out there, but by telling your story, I know you'll save lives. XOXO

Wednesday, December 18, 2013

"On Particularly Rough Days..."

I've had some time to process the idea that melanoma may have shown her ugly face again. How do I feel about it? Frustrated. Scared. Angry. But I've also decided that I can't obsess about the possibility. I gave myself a week to work through my emotions, but now I want to enjoy the holiday with my new little family. What happens in January will happen in January!

I saw this one Facebook yesterday & I knew I had to share. I figured someone else may appreciate it too!


Have a great week, friends. 

XO

Tuesday, August 27, 2013

Moments.

I had a moment this morning. You know, one of those moments that you're almost embarrassed to tell anyone about because it's so out of character for you. One of those moments where you say to yourself, "OK. Get it together, girl!" Yeah, I had one today.

 I was driving out of my neighborhood this morning when I had to stop for a school bus. I sat there and watched a family prepare to send their baby girl to school. It was obviously her first day of kindergarten. She had her big book bag, both parents, and her baby sister cheering her on. The parents put her on the bus, the school bus driver sat there while they waved to each other, then the doors closed and baby girl was off for her first day of school. The parents continued to wave for a few seconds, and before I could even drive away, both parents started crying. Both of them, in the middle of their yard, sobbing. Naturally, I started crying too. It was like watching a damn Hallmark commercial. (Seriously wish I had recorded it for the family. It was special.)

Ah, special moments...

...Moments I want to have one day.

Thinking back on this special moment  made me remember I haven't shared my special moment with you! My bridal shower last weekend!

 My mom came in on Friday night as a complete surprise to me
as I thought she had to work!
I should have known,
mom doesn't miss milestones!

 My awesome cupcake dress cake!
(Thanks, baby sister!!)

With the amazing hosts:
 my baby sister Cara,
and the gal who introduced me to my future husband!
They threw a great--totally me--shower!

Apparently there is an old wives tale that says the amount of bows
you break indicates how many children you will have.
The one bow I broke--even though I tried not to--
was on the present my future husband wrapped!
How appropriate.
And hilarious.

I can't wait to use these October 18th!

It was such a special weekend. My mom was in town, my mom's best friend from Canada drove in for the shower, Mr. Spots' family joined us, and a few women who are special to me joined us for a great shower. It was personal, relaxed, and sweet. Absolutely perfect.



It was a day I once wondered if I would get.

When the reality of cancer started sinking after they diagnosed me with stage 3 malignant melanoma, everything I may not get to do ran through my head. Days when my anxiety levels are high--cough SCAN DAYS--cough--It still runs through my head. Would I get to marry my guy? Would I be a Momma? Would I get to grow old? 

To be able to marry my guy on October 18th really will be a blessing for so many reasons.

Non-existent bucket list item, Marry the love of my life, will be complete.

...and I can't wait.

Monday, July 22, 2013

The Balancing Act



It was only a few months ago that I was directed to a blog post that had been written about me. In that post the blogger said I need to move on with my life and stop writing about my experience. I needed to stop trying to get attention for something that happened years ago. I needed to move "the fu*k on" according to this fellow blogger. I didn't write about the post then because the blog was an immature example of the internet bullying that many of us have sadly experienced. However, I thought back to her post this weekend when I realized how out of the loop I am sometimes in the melanoma community.

While I try to update this blog from time to time I am much better these days at quickly uploading the latest melanoma article or a quote that hits home for me on Facebook, Twitter, or Instagram. I sometimes take a break from reading fellow warriors blogs. I don't always check my blog email the very next day. There are times I try to take a full fledged break--it doesn't last long--from Facebook because I need to live my life melanoma free for a while. It does not mean that I don't care about my fellow warriors or don't want to participate in all things melanoma; however, it takes an emotional toll to be too consumed every single day. This sounds incredibly selfish but I've had to be picky when it comes to what groups and events I want to be a part of because when I'm in, I'm fully in, and all of my emotions become invested. 

This isn't always a good thing for me.

I guess what hurt me the most about the post is that there was a time I was fully consumed by melanoma! Every single day I was writing about it. Every single day I was sharing my deepest fears with each and every melanoma warrior who would listen. Every single day I was living in fear instead of living. It took time, tears, encouragement and true effort to find balance.

Yet, sometimes I don't get the balance right. 

This weekend when I heard unwanted news about a dear friend from another friend, I realized maybe I've been too consumed by my own personal life these days. I have been so busy being a  live-in-soon-to-be-wife, a 50% full-time soon-to-be step mom, and a full time employee that I haven't been around enough to cheer on my friends. I felt like a Mole Mate failure.

There is no guidebook on how to balance life & cancer. I've just had to wing it, and sometimes, no matter which extreme I take, I fail.

How have you found balance in your life?




 

Saturday, March 23, 2013

Healing


Thank you all for your kind words, emails, and texts this week. While my new primary melanoma was quite a shock to us, my family and I truly appreciate the support you continue to send our way. We will head to New York in just a few days for scheduled CT scans and to evaluate the situation with my doctor. He has been on vacation this week, so he doesn't even know of my new excitement. I just hope he doesn't have anything exciting to tell me....I prefer boring scans, Dr. D. Please.

Thank you again for your well wishes and prayers. You've helped make this week easier.

Monday, February 11, 2013

Using My Voice


Sometimes you needs to sit back and listen.
Other times you gotta make some noise...


If you follow me on Facebook or Twitter you know that I was very upset on Friday night. I am a Virginia girl & I love my state. What I don't love is our lack of laws protecting our teenagers from tanning salons. There is currently a bill SB1274 that will hopefully pass that will prevent teenagers 14 and under from using public tanning beds & will cause kids 15-17 to need parental consent in order to use the coffin-like beds. While I truly wish this banned all minors from tanning like the law that forbids minors from smoking, I realize that this is a start in the right direction for my state. 

On Friday RVA News posted an article that discusses SB1274. The author, Allison Landry, writes, 
"For example, California banned teens under 18 from indoor tanning. Virginia is unlikely to go that far, state officials say. To many people, other environmental health concerns in Virginia that take precedence over tanning, said Gary Hagy, director of food and environmental health at the Virginia Department of Health."

Then I read the part of the article that interrupted my peaceful & lazy Friday evening:

“There is only so much you can do to protect the youth of an area,” he said. For Virginia, “indoor tanning is not as much of an environmental threat as it might be for California.” (Source.)

I was furious.

So, I wrote a letter.


Dear Mr. Hagy,

My name is Chelsea Price. I'm a 25-year-old Virginia native, a graduate of Radford University, and an employee of the Department of Veterans Affairs. I am also battling malignant melanoma.

I was 14-years-old the first time I used a tanning bed. I had been invited to prom by a cute older guy and wanted to be sure to look my prettiest. Tan was beautiful and I wanted to be beautiful. After those first few sessions I began to tan before major event like graduations, vacations, and weddings. I wanted to have that 'healthy glow' people referred to.

I was 23-years-old when an oncologist told me that malignant melanoma would not kill me "right now."

As you should expect, the statement that you gave to RVA News recently has me quite upset. In case you have forgotten, you said, "...indoor tanning is not as much of an environmental threat as it might be for California.” Excuse me, sir, but how is indoor tanning more of a threat to California than Virginia? Are the teenagers in Virginia less important than California? Do you have a daughter you allow to absorb the UV radiation that is classified as a class 1 carcinogen, just like tobacco smoke and asbestos? Why are the tanning beds more of a threat in California? I'm quite certain the beds are manufactured the same way. (Please don't tell me they are more popular in Cali than in Virginia. Have you seen the young girls lately, Mr. Hagy? What about the women who look ten years older than what they are due to the leather-like skin?)

While I am truly disgusted by your comment and your obvious lack of interest in saving Virginia's minors, I understand that this may not be your area of specialty. To give such an ignorant comment about a truly important subject seems insensitive and dangerous. Do you realize that melanoma in young adults is now considered an epidemic?

You may think that we cannot control our youth; however, isn't that what we attempt to do? Is a minor allowed to walk into a store and buy a pack of cigarettes? We control their inability to buy cigarettes. I will remind you once again that tobacco smoke and UV radiation from tanning beds are both classified as class 1 carcinogens. Why is it OK to give them one and not the other?

I cannot change your opinion. I cannot force you to retract your statement. I am quite certain I will never hear back from you or have the opportunity to speak to you in depth on this subject, but I can ask you to do three things before you make another comment regarding tanning beds and minors. I beg you to read my story. I ask you to take five minutes out of your day and view my surgery pictures. Then I ask you to dig deep and ask yourself if you would be OK with handing your teenager a pack of smokes and sending her on her way. It's the same thing, Mr. Hagy.

I truly hope you never have to see firsthand how dangerous tanning beds really are...even for Virginians.

Sincerely,

Chelsea Price
Stage III Malignant Melanoma Warrior
Author of http://adventurewithmelanoma.blogspot.com/



I wanted someone to know I was not OK with that type of attitude being shared at public level so I sent a similar email to other members of Virginia's Department of Health. Simply put, I couldn't stay silent. I washed my hands of it Friday night & figured that would be the last of it all.

It wasn't even 10:00 AM this Monday morning when I received an email from the manager of Risk Communication & Public Health Information:

"Dear Ms. Price –

At your convenience, I would very much like to speak with you about your email regarding a quote from Mr. Gary Hagy that appeared in an article in RVA news."


You can imagine my shock.

 I called, and shockingly enough, we had a pleasant conversation! According to Mrs. Brewster, the author of the article is a college student who interviewed Mr. Hagy last November regarding California's bill that banned minors from tanning. He has not spoken to her since then. Apparently the quote was taken out of context and twisted to fit this story. Mrs. Brewster said that Mr. Hagy was "touched" by my email as he has a 14-year-old daughter and that they would be responding to my emails; however, she wanted to speak to me on the phone for two reasons. First, she wanted to let me know how they were all "touched" by my heartfelt emails (I sent 3 separate types of emails to numerous people at the Department of Health), that they are truly sorry the twisted words of Mr. Hagy upset me, and to let me know that they have already contacted the student's faculty adviser regarding the article. She also stated that neither Mr. Hagy nor the Virginia Department of Health share the opinion that California's teenagers are more important than Virginia's. 

Then they wanted a favor from me. They wanted permission to share my emails. They are going to use my emails to show the college student just what personal damage can be caused when you take things out of context. Not only was I upset, according to Mrs. Brewster, Mr. Hagy was visibly upset after reading my email. I gave them permission.

While I have no idea if this will change the minds of anyone within the Virginia Department of Health regarding teens and tanning, I do hope it will spark an interest to do more education for our teenagers. Too many lives depend on it...

Just Friday someone told me that no one would read my emails. I'm thrilled to say that they read them, they responded, and I feel certain that at the very least, they had an interesting conversation about teens & tanning today. 

Progress.




Tuesday, January 15, 2013

Girl Talk: Skin Care Version 2.0





Y'all know I'm a fan of sunscreen.
You also know I hate tanning beds.
When given the opportunity to participate in a link-up
that will possibly open the eyes of other young women,
you know I have to do it.

Plus, I can never turn down an opportunity for girl talk!

1) What's your daily skincare routine?
     I wash my face twice a day with Clearasil Daily Face Wash. My skin is super sensitive and it's the only face wash that doesn't cause me to break out in a rash. I've tried...trust me! ;-)  Depending on what my skin is doing that day--it goes from kind-of oily to dry--I apply DDF weightless defense oil-free hydrator that has SPF 45 and Ole Henrisken Total Truth eye creme. I fell in love with Ole Henrisken after the eye creme was included in the Skin Cancer Foundation's goodie bags at the gala!

2) A skin product you could never live without?
    Sunscreen. My doctors would probably personally kill me if I showed up in their offices with a sunburn! Oh, and face wash...I can't sleep until the make-up and yuckiness of the day is off my face!

3) Have you ever used a tanning bed?
   Yes, I loved being tan. I started tanning when I was 14 and continued to tan before all major events until I was 21. The last event I tanned for was my college graduation. When I met my oncologist for the first time he said I was not the typical melanoma patient. I have no family history, I have dark hair and dark eyes, and I do not have a history of bad sunburns. 

Then the convo went like this:
Oncologist: "Do/did you use tanning beds?"
Me: "Yes."
Oncologist: "Ah..."

Ironically, I stopped tanning at age 21 when I realized it wasn't worth the risks. Sadly, I had already done the damage and was diagnosed with stage 3 melanoma at age 23.

The Tanning Days

The Cancer Days


4) Thoughts on spray tanning?
    It isn't for me. Having said that, I would much rather my friends go get spray tanned than step foot in a tanning bed! I feel like going to get a spray tan after everything I have been through and will continue to go through for the rest of my life totally goes against the message I'm trying to share. Plus, haven't you heard, "Simply put, paleness equals class. And it's sexy."

5) Favorite brand on sunscreen?
   I'm a big fan of Aveeno. It's great for my sensitive skin!

6) Biggest skincare splure?
    I use Bare Minerals so I do splurge on that every few months. I don't mind spending money on quality products. I've been lucky that I've been able to try a lot of high priced items firsthand before actually purchasing them! I will definitely buy Ole Henriksen's Total Truth again and again!

7) Celebrity with the most perfect skin?
     Have you seen the celebrities lately? The majority of them have stunning-PALE-skin! 







8) Feature you're most self-conscious about?
   Probably my teeth! I can tell they are shifting!

9) What do you think about botox?
     I make 1030232 facial expressions per day.  already have laugh lines. They remind me of happy moments. Ask me again in 10 more years! Ha! 

10) I feel most confident when...
    I'm wearing a tiara! Duh!
             (Thanks, Rev. Carol!)

"Melanoma Survivor...
And I plan on staying one!"

   
I hope you'll link-up and share your skin care routines too!