Saturday, September 11, 2010
Thoughts from Mia Mercatili......
Tuesday, September 7, 2010
With reverance and hope......
Monday, September 6, 2010
Have I hit my word limit for today???
Labor Day - a day of rest and parties, often symbolized as the end of summer, according to Wikipedia. Uncharacteristically, I did not attend any parties today, am in denial about the end of summer (but Fall, you have a very special place in my heart, also) and am experiencing writers block. Nevertheless, I vowed to pen a blog for each day of Childhood Cancer Awareness Month. So, I am going to use this entry as journal, a place for my thoughts to rest while I slumber for a few hours!
This morning seemed full of promise - sun shining, no set plans, and my ever present bowl of Kashi!! My sister and I planned to have laid back day, with a few hours of Cancertacular™ housekeeping for good measure. As we played dueling laptops checking e-mail and Facebook, I felt compelled to send a text. As I picked up the phone, there were 3 texts and a missed call waiting for me. All were from our fab web designer, Matt. The attempts at communication (as I slumbered peacefully with my ringer turned off) were to announce that our website re-design was ready to go live at 12noon! Woo hoo! Amazing news! Wait, it's Labor Day, a day of parties and rest. Okay, Matt, twist my arm, make our website live and then you have permission to take a break!! Jill and I anxiously awaited for the 20 minutes to pass for our new masterpiece to be unveiled!
In the meantime, I sent that text to Janet Donovan. I knew that Emily (pictured above) wasn't feeling well and was likely hospitalized the night before. In response, Janet shared the devastating news that Emily, 4, was nearing the end of her battle with Medulloblastoma. Docs approximate that she has about 4-8 weeks left on earth. My imagination does not stretch far enough to begin to fathom Janet's feelings. Tears were shed, and then Jill and I began to formulate a plan.
In the meantime, the website went live! It does need a few tweaks, but it is amazing! Cancertacular™ is growing, and my confidence is soaring that the new and improved site will be an amazing vehicle to promote Childhood Cancer Awareness. Flashback to Emily, speaking of that monster....Currently aware that Em is in the hospital with a grim prognosis, do we visit her? We should send her balloons. We will send her balloons. We can't send her balloons - it is Labor Day, and while docs are feverishly working on Em and Matt is breathing life into our website, balloon delivery is unavailable.
In the meantime, Jill and I critique our newly enlivened website - a tough task considering the amazing job that Matt did. Did I mention he did it pro-bono?? So, we picked apart his largely unpickable work, and sent our critiques off in a tiny e-mail. In the meantime, we called Uncle John, bowing out of the party at his house, and got back to the most important business of the day, Emily.
It was decided that, since Emily loves all things Disney and Princess (especially Sleeping Beauty), we must find a Disney Store. We found 2 options, Rockaway, NJ, and Whitehall, PA. Opting for Whitehall, PA, we made few stops before leaving the Scranton area around 3PM. Of course, we hit Labor Day traffic! People apparently were neither at parties nor were they working - they were sitting in traffic on I-80! Clarification - people do work onLabor Day, just not balloon delivery people.
We called ahead to the Disney Store, so Brandon, Jill, Joann, and their team of Cast Members awaited us. If only we had a more lighthearted purpose for shopping, it would have been a truly amazing experience! Cast members - who decidely work extra hard on Labor Day, likely to make up for the balloon people - lead us around the store showcasing all things Sleeping Beauty for Princess Emily, and all things Belle, for 5 year old sister Princess Lizzie. After spending a small fortune, and stopping at Wawa for Em's beloved chippies and Mountain Dew, we made our way to Janet Weiss Children's Hospital.
Emily was actually a little frightened by the sheer number of gifts we showered upon her. You see, the Disney Store shopping spree is on the heels of Em's 4th birthday, and that combination of gifts were all bestowed upon her tonight! Before long, each gift was opened and scrutinized, and 20 feet of signatures and well wishes made a boarder around the hospital room! Guess what? Emily had a balloon tied to her bed when we arrived. While balloon delivery people don't work on Labor Day, apparently the hospital gift shop staffers do!
After coloring, drinking Mountain Dew, eating chippies, getting medicine in her tubies, painting, and lots more during our 2 hour visit, we kissed Em goodnight. As I fought back tears, I couldn't help but wonder if that was the final time I would kiss her little bald head. Now, I'm thinking that Emily never got a chance to mourn the passing of summer, or curse the balloon delivery man. This day, for me was more Thanksgiving than Labor Day. I am thankful for the honor to share in the life of Princess Emily Paige Donovan. And, while Wikipedia sets Labor Day aside for parties, none will compare to that of the angels when Emily gains her wings!
Fabulously yours,
Tina
Sunday, September 5, 2010
Royal Dancetacular 2011!!
Good evening friends. On September 6, 1989 I entered Valley View Junior/Senior High School - for the first time - as an 8th grader. Back then, the school housed grades 7-12. Seventh grade was spent in my living room, with a home-bound tutor, when I wasn't in Heshey, PA. No, I was not a chocolate/amusement park savant training to take over the empire from Milton Snavely Hershey. Contrarily, I was in The PennState Milton S. Hershey Medical Center fighting for a chance to live my life.
As a reference point, here is a short time-line of my cancer treatment. My parents and I made our first trip to Hershey on July 22, 1988. My leg was biopsied on July 25, 1988. High dose chemotherapy began to course through my veins on July 28, 1988, and I returned to a house full of people in Peckville, PA on August 1, 1988. On October 12, 1988, I endured a limb salvaging complex surgery. After completing 11 more months of chemo, I began my final treatment on September 7, 1988.
Why did I choose to include that specific timeline in this blog post? Simply because all of those events listed were expensive! But, guess what, payment never entered my 11 year old head. And, truthfully, it was not at the forefront for my parents either. But, it was a reality. Fortunately, all medical expenses not covered by my parents medical insurance were eradicated by Four Diamonds Fund. This charity helps any family being treated by PennState Hershey Children's Hospital, Pediatric Hematology/Oncology. They have helped more than 2,000 families since 1972. Currently, approximately 100 new families receive support each year.
The four diamonds are courage, wisdom, honesty, and strength, as described by Chris Millard. He became on angel in 1972, but the legendary strength with which he fought his cancer battle live son through Four Diamonds. Penn State Dance Marathon, or "Thon," is responsible for a large chunk of their funding source. Four Diamonds made my cancer journey more bearable for my family, and will forever hold a special spot in our hearts. As such, I have always had a pipe dream of having a dance marathon to benefit local kids battling cancer, but lacked the know how.
While at the University of Scranton, I became very involved with volunteer work. Pat Vaccaro was a driving force behind my desire to make a difference through local projects, many service trips, and school projects. Pat and I reconnected last year through Cancertacular™'s first intern. After weeks of debating what-if's and should we's, Royal Dancetacular was born. It is based very loosely on Thon, as it is about 1/100th the size of Thon!
Our first try, February 20-21, 2010 was a screaming success. Below, please find some words from a junior at the University of Scranton regarding Royal Dancetacular, 2011:
"Hi everyone! My name is Sarah Phillips and I am this year's overall chair for Royal Dancetacular. Royal Dancetacular is Cancertacular™'s 24 hour dance marathon that takes place at the University of Scranton in February. Its purpose is to raise money for kids in NEPA facing cancer. Last year, we raised over $8,600 for the kids. My connection with this month, one about raising awareness for childhood cancer, is Dancetacular. Through Dancetacular, we not only raise money to benefit the families of Cancertacular™, but we continue to raise awareness among the campus community, in hopes of spreading Cancertacular™'s message. Ultimately, it is this awareness that will draw attention to the need for a cure."
In a nutshell, Royal Dancetacular is very representative of the greatest and most meaningful aspects of my life. It is a priviledge and honor to excite students at my Alma Mater about my life's passion - childhood cancer. Pictured above is the newly created shirts for Dancetacular 2011. They are currently on sale for $10, of which all proceeds will benefit local children battling cancer.
As the back of this year's shirts say, "It's kind of fun to do the impossible!" Join us on February 19-20, 2011 to be part of the magic that is made for childhood cancer on the campus of the University of Scranton!
Fabulously yours,
Tina
Saturday, September 4, 2010
It takes a village.....
Our current Secretary of State and former First Lady, Hilary Clinton wrote the book, "It Takes a Village to Raise a Child." While I wholeheartedly agree with Mrs. Clinton's sentiment, I further believe that it also takes a village to survive cancer. That statement is multi-faceted. Typically, before a cancer diagnosis, you undergo a (hopefully)thorough battery (or village) of tests. Those tests are (hopefully) read and conferred upon by a team (or village) of docs, who further conference (hopefully) before they present your options for treatments combinations (you get it - chemo, radiation, surgery all live in the same village).
After all is said and done, decisions are made and treatment plan is in place, it is time for YOUR village to shine! Truth be told, there is only one person in this world who has the luxury to drop everything and put you first. That person is you. Side-stepping my soapbox - almost - a support system ranks right up there with positive attitude and faith, meaning both spiritually and an unwaivering trust in your medical team. A support system may be at the ready as soon as word of diagnosis spreads. It may also need to be coddled and carefully constructed. Regardless, please never feel that cancer is something you must go through alone.
In the upper right corner of this post, you will find a picture taken today of my sister Jillian, our faithful volunteer Alivia, and myself. We're standing in the parking lot of the very church who organized the sole fundraiser for me about 22 years during my battle with Osteosarcoma. The church came together again today, for a man who I have known my entire life. He's battling kidney cancer. Selfishly, I feel like today brought my journey full circle yet once more. This day was a true priviledge and honor to have the opportunity to be on the giving end of my village.
Another fact also deserves mention. The small non-profit that I founded, Cancertacular™, has a mission directly correlated to the heroic efforts of my village. Cancertacular™ serves Lackawanna County in Pennsylvania, and the 10 surrounding counties. Yes, we do have limited funding, and some other constraints to work around. Years from now, as a well oiled machine of hope, we will still serve those same counties - the ones that are central to my village. For me, home is truly where my heart is - and where is it continually nurtured on a daily basis!
Have you hugged your village today?
Fabulously Yours,
Tina
Friday, September 3, 2010
Some wake up calls come at 8PM......
On August 31, 2010, I pledged to raise awareness for childhood by writing a blog each day. To date, I have done so. However, I feel the burning desire to qualify my statement. Blogs will be written by the end of each of my days. For instance, right now, it is 1:43AM on September 4, 2010. My day has not ended yet, so this blog counts for September 3, 2010, not September 4. 'Nuff said.
Now, kindly direct your attention to the picture placed to the right of the words that you are currently reading. Thank you. That is Persie. He is the driving force behind another project that Cancertacular™ has concocted to raise awareness for childhood cancer. Persie was named by fans of Cancertacular™ on our FB page. He had a Bon Voyage party at the University of Scranton on Tuesday, August 31, 2010. He will travel the world before returning to the University at the Royal Dancetacular on February 19-20, 2011!! Check the blog for updates on his escapades!!
After a fabulous day of frolicking with friends (including Persie), my sister and I had a truly life changing experience. We witnessed a swiftly moving vehicle in our small town (several stop signs, no traffic lights) literally crush the hind legs of a rabbit. The sweet animal was still very much alive, but made a paraplegic by a reckless and thoughtless driver. This brought us to a crossroads. What to do? Well, it was obvious for us that NOTHING was not an option. Jill pulled the car over, I exited and guided Buddy (that's right, we named him) to the side of the road. He breathing was labored and right eye bulging. We briefly left him safely nestled on the shoulder of Main Street, and fled to the nearest supermarket for a sturdy box.
Upon return, Buddy was actually attempting to crawl back out into the road. The rabbit had some get up and go, so we got up and got out our cell phones! We enlisted the help of friends, called the humane society, even a vet. Ultimately, we loaded Buddy into that box, and drove him to the river in hope of a peaceful respite. As I drove and Jill held the box, Buddy's movement slowed and finally stopped. We left him on the banks of the river after saying a few words. We took solace in the fact that he did not die alone and we did everything within our knowledge and power for him.
We did shed tears and mourn the life of a rabbit that crossed our paths just minutes before he left this world. Why didn't anyone else help him?? It is impossible for me not to connect this event to my life's passion, childhood cancer. Remember those 46 kids that are diagnosed with cancer each day?? All of them have parents, guardians, siblings, grandparents, and friends that love, adore, and live for them. Those children have rights - and they have voices, just like the adults that love them. However, it is the adults who must advocate for those children - guide them to safety as they face the fight of their lives. Is it okay to sit back when you just can't shake the feeling that something is wrong? Is it okay to "settle" for a doctor or a treatment? Is it acceptable to "tolerate" anything, especially when it involves the well being of a child who is counting on you to raise your voice for him or her?
But, where do you start? Every parent, guardian, or loved one of a child who is facing cancer has undoubtedly faced the darkest days of their life. Usually within days, maybe hours, your entire world becomes topsy turvy. Plus, anything that you thought was stationary suddenly becomes moveable. Your child becomes a statistic (#1 of 46.) Your home becomes the hospital. Your job becomes an impossibility. Realistically, the only steadfast entity in your life - your future - now lies in a hospital bed, completely relying on you to advocate for him.
There is only one option - fight! You ask questions. You take notes. You take on the starring role in your child's medical team. Below is a link for keeping a journal of your child's cancer treatment: http://http//www.beyondthecure.org/cancers-impact/medical/parent/medical-journal.html. And, after the need for all of that hell raising has ceased, you continue to fight in her honor or in his memory. You tell their story. You wear gold in September. You crawl up Capitol Hill if you have to, sharing your story with the Pediatric Cancer Caucus. You cry. You laugh.
The bottom line - I have never rescued a dying rabbit before. A laughable comparison to some, maybe even me on some levels, as you have never held the life of a child with cancer in your hands before. My sister and I had abolutely no idea what to do for Buddy. Neither did you on that fateful day. We followed our instincts, and did the best we could. So did you! I shared many tasks, ideas, and examples. This entire blog is hogwash and invalid UNLESS you believe it and it makes sense for your unique situation. I am not a parent, I am a childhood cancer survivor - we learn to fight. Please resist blaming yourself or feel guilty for not doing "enough." If you have a burning need to know more, do some research. Below are two advocacy agencies that can help guide you through the most difficult time of your life, while you summon that fight inside of you and teach your promising child through "GOLDEN" examples!
Childhood Cancer Ombudsman Program
National Children's Cancer Society
In the coming days, parents who have lived this battle will share their story on this blog. Not so long ago, I came to realize that while I endured the surgeries and chemo, they came with far less suffering than the emotional pain that my parents endured - still do on some levels. Their every minute was devoted to protecting me from the monster that dwelled INSIDE my young body. This blog is dedicated to my parents and their comrades in the childhood cancer world. I salute you. Extra special thoughts and prayers tonight for all that are facing this monster. I am beside you in this fight, if only in spirit!!
Fabulously yours,
Tina
Thursday, September 2, 2010
Blog Post #3, of 30!!
With approximately 35 minutes to spare, the writing of the September 3, 2010 blog post has commenced. Yes, I am tired. Yes, I should have removed my contacts before I started writing. And, yes, I could have started writing this entry sooner. But, 46 children in the US have been diagnosed with cancer in the past 24 hours. They are fighting for their lives. I am blogging, as a 22 year childhood cancer surivivor, for them - and for the 46 more that will join our 450,000 strong club tomorrow, and the day after that. My contact dilemma really isn't such a bother after being put into perspective.
This morning I awoke to warm temperatures, enjoyed some Kashi GoLean and Soy Milk, and tended to some tasks. Armed with two of my go-to Cancertacular™ cronies, Jill and Richie, we set out to promote awareness for childhood cancer around 12noon. With stops at no less than 5 confirmed penny collection sites, and a tasty lunch at another, Haystacks in Wilkes-Barre, we headed to Hershey, PA.
It is noteworthy that the owner of Haystacks is the dad of a fellow childhood cancer survivor, Keith Perks. Also noteworthy is the fact that we were both treated for cancer at the "Milton Hilton," or Penn State Hershey Medical Center.
While I underwent high doses of chemotherapy in the hospital, my parents took turns staying at the Ronald McDonald House just across the street. Back in 1988, only one parent was allowed to occupy the uncomfortable recliner that perched next to hospital bed. More often than not, the recliner dweller was my devoted mom, whose mission quickly became guarding my childhood and keeping a smile on my face at all costs!
The very same Ronald McDonald House has been unable to fill the demands necessitated by the growing rate of sick children. Last year, they turned away about 1100 families. After receiving a letter to announce a new expansion project, my heartstrings began to feel a tug. It became clear that the time had come to give back to the House that was our second Home for 14 months long ago.
The progression was slow for me. While it has to be said, the obvious is wickedly true - the entire town reminds me of being a broken child. Hershey took away - in just a few hours - everything creature comfort that was familiar to me, with the exception of my parents - thank goodness! On the flip side, without that experience, I would not be me. I was grateful, and indebted indeed. But, how to comfortably proceed?
First, I added the Central Pennsylvania Ronald McDonald House as the beneficiary on our original Facebook "cause" for Cancertacular™. Then, I visited the Hotel Hershey for an overnight stay and discovered what nostalgia I felt for that little chocolate town. Finally, on April 29, 2010, a contingent of Cancertacular™ volunteers cooked an organic dinner for the approximately 40 people staying at the House. Today, we did a return visit.
We served a "patriotic labor day picinic" supper! Such fun to make and eat the BBQ chicken, hot dogs, garden burgers, turkey burgers, pasta salad, fruit salad, mac n cheese (for the kids and kids at heart), chips, corn on the cob, vanilla cake, carrot cake, and brownies!!! It was utterly a pleasure to interact with the families and children. In a way, I played the "big sister" to them all - a living breathing reminder that there is a light at the end of every tunnel!
Brenna and Kade are infants battling heart problems. Kade has never been home, and neither has NICU buddy Keith. Meeting Ariana and her dad, Mike, was a great gift for me. Ariana, 15, has synovial cell sarcoma, a tumor that reared its ugly head just below her hip. She is a true surivor, and will be free of the "Milton Hilton" after just two more chemotherapies!! Of course, Persie stole her heart, and persuaded her to capture many ingenious photographs of our traveling bear. In fact, she is now the proud owner of Cans, the Cat - inspired by Persie!!
The bottom line is that this long day was filled with gifts, laughs, and memories. As we stare the end of summer 2010 square in the eyes, let's remember not to take any day for granted. Remember those oft referred to 46 children? 1/3 of them will not see tomorrow.
Fabulously yours,
Tina
Wednesday, September 1, 2010
Together We Can Make a Difference!!
Positivity: the state or character of being positive.
Positive: Tending towards progress or improvement; moving in a beneficial direction.
As a 22 year childhood cancer survivor, I credit the quality of my life to a positive attitude - an attitude that was instilled and fostered carefully by my parents. During chemotherapy, I rarely interacted with other children, because they were "sick." In reality, I was "sicker" than some, but not in my mind. Eventually, my body followed suit and recovered! Living with my heart open to positivity works for me, serving me well in every day. As such, it is highly uncharacteristic to start an entry with negative facts. But, these sobering truths must be shared.
1. 46 children are diagnosed with cancer each day.
2. 25% of those children will die within 5 years.
3. 50% will survive 5 years, but develop long-term health difficulties.
4. Since 1975 about 450,000 children were diagnosed with cancer.
5. 100,000 are now angels.
6. About 12,500 children in the US are diagnosed with cancer each year.
7. Every child has a 1 in 300 chance of being diagnosed with cancer by age 20.
1988 and beyond........
To kick off Childhood Cancer Awareness Month, below you will find the long awaited continuation of my first blog entry. After a lengthy hiatus and much comtemplation and learning, please check here for a new blog each day in September to promote awareness for Childhood Cancer. Most will be written by me, some by volunteers, others from professionals, survivors, parents, or siblings. All are individuals whose lives have been touched and forever changed by childhood cancer.
Part 2: As the ensuing days brought a total of 14 months of chemotherapy (including Methotrexate, Vinchristine, Bleomycin, Cytoxan, Dactinomycin, Adriamycin, Cisplatinin) and 5 surgeries, I whiled away the precious hours at home surrounded by love - and Nintendo! Too sick to attend 7th grade, a tutor was delivered to my door a few times a week. I excelled in academics, seemingly the only thing I had any control over.
Armed with a new Benetton book bag, a new outfit, and a strawberry blonde shoulder length wig, I attended Valley View High School on the first day of 8th grade! I missed the 2nd and 3rd days, as I spent them at Hershey Medical Center celebrating my final chemotherapy treatment! I returned to school on day 4, and never looked back. If I had, I would have seen my Mom and Gramma wiping their eyes as I entered the hallowed halls of learning, cancer free!!
Save a few nasty colds due to a compromised immune system, I sailed through high school. Proudly, I spoke at commencement in 1994, graduating with honors after serving as yearbook editor and attaining the title, through Future Business Leaders of America, of PA State Champion in Impromptu Speaking. My last truly carefree summer played host to a trip to California, before returning to academia at The University of Scranton. At Scranton, I was somewhat of a "legacy". I continued a long line of "Royal" students, which my paternal grandfather began with his graduation in 1935! I flourished on campus, serving as an orientation aide and resident assistant, before being bestowed with the Jesuit Community Award for School and Community Service at graduation in 1998.
May 31, 1998 was a melancholy graduation day - a day filled with promise, hopes, memories and tears. June 1, 1998 was my first day at my first "real" job at Scranton Counseling Center. It was undoubtedly hard, but what an opportunity for experience! Four years in, I started to feel sluggish, short of breath, dizzy, and gained 8-10 pounds per week. Difficulty grew to find clothes in my closet that fit, and my ability to walk distances was quickly shortened to 10 feet or less. After 6 months and several doctors, I was diagnosed with Dilated Cardiomyopathy. As pediatric chemotherapies are sparse, in 1988 I was treated with adult chemo at age 11. The very same chemo that saved my life had damaged my heart. My heart was functioning at about 30% off its capacity. After peeing out 42 pounds in 3 days (yes, I admit that I have fallen asleep on the toilet), heart transplant evaluations at Temple and Penn, and several weeks off of work, my heart was deemed stable. Miraculously, my heart stabilized further and regained some function. My heart will always be damaged, but it works hard enough to keep me quite active and quite happy! My second miracle happened shortly after the milennium in 2001.
Due to strenuous job requirements coupled with a 24 hour on-call component, I traded the Scranton Counseling Center for a 20 month stint as an Intake Coordinator at Allied Services. Another amazing experience with wonderful new friends ended in tears as I left in search of greener pastures with the Federal Government. September 2003 marked the beginning of my career at Social Security. As a Title 2 Claims Representative, I processed disability and retirement claims. This was, hands down, the most difficult task of my work life. In 3 years of training, I'm wagering that I studied enough to earn 2 more bachelor's degrees! I hit my stride as my 4th year commenced, and really began to feel as though I was making a difference.
On Sunday, February 17, 2007 I stumbled out of the shower around 10:30 AM. Feeling a little "off", I tried to comb my hair, but failed to remember what to do with a comb. My underpants lay on the counter, but I didn't recall what to do with them. Seconds (maybe minutes) later I stumbled out of my bedroom, and uttered my last word "help". I woke up 3 hours later in the ER at Mid-Valley Hospital in Peckville, PA, unable to speak, read, write, add, smile, or move my right side. Scared and frustrated, armed with only receptive communication, I was transferred by ambulance to Intensive Care at Community Medical Center in Scranton, PA.
3 days and one more ambulance ride later, I found myself in the Cardiac Special Care Unit at the Hospital of the University of Pennsylvania. After titration of coumadin (a blood thinner), physical therapy, speech therapy, and occupational therapy, I was discharged on February 27, 2007. Upon return home, reality set in with a short bout of depression, anxiety, and "why me's"? Throughout that, I strived for recovery to the best of my abilities, and returned to work at the Social Security Administration only 2 months post-stroke, albeit part-time. Throughout summer 2007, I felt somewhat sub-par; however, what was I supposed to "feel" like just 5 months after a massive stroke? On August 30, 2007, I left work and began the climb to my car, parked on floor 3. After completing 3 of 6 flights of stairs, I began to pray. Realizing that passing out was imminent, aloud I repeated "please God, let me make it to my car." My prayer was not specific enough. I did in fact make it to my car, but never made it inside, instead passing out next to my car. After regaining consciousness, I searched for my cell phone - of course to postone my dental appointment! My second call was to my dad. After his strong urging, my third call was to 911.
An ambulance ride delivered me to Mercy Hospital - where it all began (again)! Within 48 hours, on August 30, 2007, I again found myself at Penn, this time the proud owner of an internal defibrillator. I named him Charlie, like Charlie's Angels - he watches over me. His croney, Bosley, is a care-link monitor that sleeps next to my bed, recording data each night from 1-4 AM, then transferring the information to PENN weekly.
The last paragraphs have chronicled what some will, no doubt, call tragedies. I believe they are miracles. In fact, I believe that I am living proof that miracles actually do exist. God left me on this earth for a reason, and since September 2007, I have been hunting for that reason feverishly. As of November 30, 2007, I am officially retired from the Federal Government - initially a large blow, both economically and psychologically. Since then, I have realized it to be a gift, the ability to reinvent my life. I would not trade any experience that paved the way for retirement at age 31, and have no regrets, for they afforded me the opportunity to become the person I am today.
One year after Charlie was "born", my quest was completed. Hillary Clinton tells us that, "it takes a village to raise a child." I believe that it also takes a village to survive Cancer. NEPA is "my" village. Further, childhood cancer patients are not typpically treated in NEPA. Instead, they travel to New York, Hershey, Philadelphia, Danville, and Delaware, in pursuit of the best care possible. While there, they form a new "family" to aid in saving their young lives. At home, few understand what they are going through. That is where my non-profit, Cancertacular™, Inc, comes into play. Cancertacular™, Inc. became official on August 18, 2008. We are NEPA's neighborhood for childhood cancer. Our mission? No child should feel alone during treatment, and neither should his or her family. Optimally, no parent should have to choose between working to pay bills and accompanying their child for life saving medical treatment. Thus, all monies raised by Cancertacular™, Inc. remain in NEPA to support Golden Families, as gold is representative of childhood cancer.
What's next for me?? Medically, I honestly have no idea, as there are few childhood survivors who have lived longer than me. With a few of my contemporaries, we are traversing unknown paths. Paths that can be studied, affording prior mistakes to evolve into progress and pages in Journals of Medicine.
The moral of my story?? I am STILL learning, while surrounded by love and happiness. I have learned that attitude can make or break you. You need to be your own advocate. Please listen to that tiny voice when you have a concern! Above all, I know that I can handle whatever comes my way. For you see, I am a survivor!
Please follow the happenings of Cancertacular™, Inc. on Facebook at http://http://www.facebook.com/home.php?#!/pages/Archbald-PA/CancertacularTM-Inc/199555207023?ref=ts.
Fabulously yours,
Tina

