In 4 days, I will make my way to San Francisco for a weekend to remember.
A weekend surrounded by teammates.
A weekend to remind myself of my TNT journey.
A weekend full of inspiration, full of heart, full of memories.
A weekend kicking cancer butt.
In 6 days, I will stand at the start line of Nike Womens, surrounded by 30,000 other runners.
Among them, thousands wearing the TNT purple jersey.
A jersey that represents so much:
Our Commitment to the Cause. Money raised towards a CURE for CANCER. Our TNT journey. Lives changed. Miles upon miles ran. Honored Teammates. Our incredible supporters. PUNCHING CANCER IN THE FACE.
I can't for the journey ahead.
To be part of the purple sea at Nike. For the memories to be made.
& for lives to be saved.
Thank you to all my supporters on this journey <3
Without you, I couldn't get this far.
Thank you for your love, support, and commitment towards a cure.
with love-thanks- & appreciation,
SAM
Whether you are training for your first race, your 10th, or your 100th, everyone needs a place to celebrate their accomplishments & to display what you trained so hard for.
As I train for The Nike Women's Marathon in October with Team in Training, I will be making customized Race Medal Hangers for a Suggested donation of $40 benefiting The Leukemia and Lymphoma Society.
All you have to do is:
1. come up with what you would like on your race medal hanger
2. email me your idea or any questions you may have at punchcancerintheface@yahoo.com
3. Make your donation to my fundraising page
4. Wait for your race medal hanger
5. Receive your medal hanger from me in person
5. Hang up your race medal hanger and show off those medals you rightfully earned!
I will be making every race medal hanger myself, so please be patient with the time it will take!
And if you would like to customize your own, join me at my RACE MEDAL HANGER MAKING PARTY this Sunday 9/15 RSVP here: https://www.facebook.com/events/626188207413519/?ref=3
"Every 4 minutes someone in the US is diagnosed with a blood cancer.
Every 10 minutes someone dies"
A few years ago, I didn't know what blood cancer was.
I didn't know there were so many types of blood cancer.
I didn't know anyone that had a blood cancer.
I didn't know there was a whole month dedicated to blood cancer awareness.
But then 3 years ago my dad was diagnosed with a blood cancer. He was diagnosed with Non-hogkins lymphoma.
And I researched blood cancers like crazy. The Leukemia and Lymphoma Society was one of the websites I often browsed
Blood cancer was my focus, and I searched non stop. Looking for answers. Looking for a cure. Looking for what could help my dad.
I found that september was blood cancer awareness month and made it my mission to raise awareness as much as I possibly could.
For 4.5 months I stood by my dad's side as he fought his battle with cancer.
I saw him go through chemotherapy.
I saw him get blood transfusions.
I saw him with every procedure.
I saw him weak and strong.
I saw him fight for his life.
I saw him in practically every unit of the hospital.
I saw him taken to the hospital in an ambulence.
I saw him in good days and bad.
I witnessed low white blood counts.
I witnessed the roller coaster that is cancer.
I sat with him for hours.
I felt a 5+ minute embrace with him on one of his last day.
I felt tears down my face.
I listened to doctors and nurses.
I listened to the machines stop beeping.
I listened to the sound of crying fill a hospital room.
I lost my dad to blood cancer. I lost my hero. I lost a piece of my heart.
As painful as it was to lose my dad, I do what I can so no other daughters have to face losing their dads to cancer, so no one has to wonder who will walk them down the aisle one day, so no one has to say goodbye to a love one.
I train, I run, I fundraise for a CURE.
"Every September The Leukemia & Lymphoma Society observes Blood Cancer Awareness Month as a way to raise awareness about blood cancers and the work LLS is doing to advance research to find cures and provide access to breakthrough treatments for blood cancer patients.
Since 1949 LLS, with your help, has invested almost $1 billion in research to advance therapies and save lives. We are working everyday to provide resources and improve the quality of life for patients and their families. Your funding is helping us save lives not someday, but today.
We are at an extraordinary moment in time. A time where cures are not out of reach. But we aren't there yet. It's your generosity that advances our mission to fund cures for blood cancers and provide access to the patients who need them." - www.lls.org
Please join me and make a donation for a CURE!
Today, it marks the day that my life and world was completely turned upside down. August 18, 2010, 3 years ago, marks the day my dad was diagnosed with Non-Hodgkins T-Cell Lymphoma. It is a day that I will never forget-- a day forever ingrained in my heart and my mind. I clearly remember sitting at the dinner table with my mom and having her tell me that my dad had been diagnosed with lymphoma. For close to 2 weeks my dad had been in the hospital for a cough that wouldn’t go away, in the hospital for what they thought was pneumonia and after multiple tests and consults from a Nephrologist, Pulmonologist, Infectious Disease, Rheumatology, and finally Oncology- the mystery had been solved. The cough and difficulty breathing was caused by the Lymphoma in his lungs as well as his spleen and abdomen. Oh, how my life was changed.
When my mom told me I immediately started crying --and crying. And as I tried to go to sleep that night, tears continually streamed down my face and I found myself screaming into a pillow so upset with the diagnosis. When I woke up that next morning I remember thinking that it was just a dream, that I was going to go visit my dad at the hospital that day for his pneumonia and soon he would be home with us and we could continue planning our annual family vacation to Pismo. But it was not a dream, and reality set in. We put our vacation on hold, came together as ONE to FIGHT and TEAM CELERA came together in full force! I even had bracelets made TEAM CELERA on one side and T.C.K.C.A (Team Celera Kicking Cancers Ass) on the other. August 18 will always have a place in my heart. It marks: the day of my dad's diagnosis, the day my life was changed, the day I began my fight for my dads life! It marked the start of chemotherapy treatments, X-Rays, MRI's, blood transfusions, dialysis, it marked up's and downs, seeing my dad bed ridden, to days my dad was able to get out of bed and walk those hospital hallways. It marks the start of drained energy, daily hospital visits, taking notes from the doctors when I was the one in the room with my dad, breaking the "only 2 visitors in the room at a time" rule, transferring to different rooms in the hospital: DOU, ICU, CCU.. Neutropenic Isolation. It marks family taking over the waiting room. It marks makeshift beds in the waiting room. It marks homecomings, family time at home, sharing an In-N-Out burger in the comfort our home together. It marks being able to spend our last Thanksgiving, Christmas, and New Years together. It marks the 911 calls for them to take my dad back to the hospital. It marks numerous tears shed. It marks low blood count, failing kidneys, high creatinine levels, low platelets, fever, fluid in the lungs, storming heaven with prayers. It marks a rollercoaster of emotion. It marks having loved ones surround my dad as he took his last breath on January 7, 2011, sending him with lots of love, prayer and tears. It marks my dad now being pain free and at peace. It marks my dads journey. It marks strength. A battle. My families journey. Our fight for my dads life. It marks a journey that has changed my life.
Losing my dad has been the HARDEST thing I have ever faced. When he passed away I had no idea how life would go on without him, how I would be able to go through each day knowing my dad wouldn't be there anymore, how I would no longer hear him singing songs as he got ready in the morning, how I would no longer be able to play a round of golf with him on his birthday, how I would no longer have In-n-out runs with him when he had a Friday off of work, how I would no longer be able to listen to him making up stories as though he knows the name and life story of everyone person we pass on the street, or how I would no longer be able to see his smile or hear his laugh. My dad's journey with cancer has impacted my life, more than I ever imagined. And it continues to change my life. And although my life is incomplete without my dad-- I continue to remember what he taught me. I remember the good times that we had. I remember our family roap trips, with his cassette tapes as the background music for our travels. I remember the laughs- the smiles- the hugs. I remember the golf lessons he gave me. I remember the sound of his voice as he sang songs around the house. I remember our trips to home depot when I was little, and having to watch the shopping cart full of supplies and wood, while he ran around the store. I remember pretending to be asleep so he could carry me up the stairs and put me in my bed. I remember his heart- his generosity- his love. I remember and cherish all the years we had together. The impact he has had on my life. The legacy he left.
He is my reason for running. He is the inspiration for my fundraising. He is at the root of my passion for a cure. He is FOREVER IN MY HEART and ACTIONS.
If you want to make an impact in the fight for a cure, and have a few dollars to spare, please consider making a donation towards a cure for cancer. I can't tell you how much it would mean to me. Especially today, the day my life has been forever changed.
Thanks for taking a read!
Live with PASSION,
Sam
As I was thinking of what I was going to write today for an update on my fundraising page, I looked at the date and realized that in 5 days (July 24th) it marks my dad’s birthday. This will be the 3rd year we won’t have ice cream birthday cake as we sing him happy birthday around the kitchen table. And that makes my heart sad.
I find myself a bit more upset than usual. I find myself extremely angry that he is no longer here. I find myself looking for an outlet to express these feelings, and the way that I know how, is by writing. So I decided to remind myself, and all of you Why I train, Why I fundraise, Why I choose to punch cancer in the face.
So here I have compiled my list of:
10 reasons why I choose to PUNCH CANCER IN THE FACE.
10. I have an amazing group of people fighting alongside me.
Through Team in Training I have personally met hundreds of individuals sharing my passion, my fire, my drive, my heart, my longing for a cure. They fight for a cure alongside me. Cancer survivors, runners, fighters and people who just want to make a difference.
9. Because I can.
I have the voice to spread awareness. I have the words to write about my journey and the journey of so many others. I have the ability to raise funds for a cure. And I have working legs, that will go as many miles possible, towards the ultimate finish line a CURE FOR CANCER.
8. To give someone else more days
Hearing of lost of loved ones, days cut short, moments unable to be shared. It breaks my heart. I punch cancer in the face, to provide more days for those fighting the fight. More days for them and their loved ones to cherish. More moments to be captured. More unforgettable moments to be had. More lasting memories for them to make.
7. I know what I do makes a difference.
Raising funds and awareness makes a difference. I know, with every fiber in me, that we are doing good, and making a positive impact in the lives of others. I will keep punching cancer in the face to continue making a difference in the lives of those I know, and those I will never meet.
6. To inspire others
By punching cancer in the face. By running. By training. By fundraising. By spreading awareness. By sharing my connection to cancer... Who knows, maybe I can inspire another. Maybe, my words can impact someone. Maybe the story of my dads cancer journey and my journey alongside him can touch someone else. Maybe, my actions can lead someone else on a journey towards punching cancer in the face, as well.
5. To help improve the quality of life for patients and their families as well.
I've seen first hand the lives saved by the money The Leukemia and Lymphoma Society has raised. I do this for more success stories. For more survivors. For a world with no more cancer.
4. I want to change this statistic: “Every 4 minutes someone is diagnosed with a blood cancer. Every 10 minutes someone dies”
I aim to change this statistic. That is far too many people being diagnosed & far too many lives lost. I will keep fighting, keep running, keep fundraising, keep pouring my heart into this until a CURE is found.
3. With every day that passes my list of those I train for, grows longer. The length of the list needs to diminish.
Every name I add to this list, I carry them with me. Every person that I know, those that I don't. Stories that I hear about others. Every honored teammate I have the privilege to meet. Every cancer jouney I encounter. For every person I will not meet. They all hold a place in my heart. Always. I won't stop fighting until the writing of names stops.
2. Because CANCER SUCKS.
Obviously. It's an asshole. End of story.
1. Because not having made any new memories with my dad for the past 2 ½ years is absolutely heartbreaking.
All I want is one more day, one more celebration, one more hug, one more smile, one more laugh, one more moment. I’d give anything to do what he loved, play golf. One more dad and daughter day at the driving range, one more birthday round of golf, one more large bucket of golf balls shared, one more lesson on my swing, one more day, one more hour, one more moment shared.
Let's PUNCH CANCER IN THE FACE together!
Rosa Celera | $250.00 |
Team Celera | $200.00 |
Gaudioso villagonzal... | $100.00 |
Van Garner | $100.00 |
Janet Celera | $100.00 |
Rebecca and Emil Enr... | $100.00 |
Virginia and Van Gar... | $100.00 |
Tan Tan Celera | $84.00 |
Rosalie | $50.00 |
Missi | $50.00 |
KT | $50.00 |
melvin santos | $50.00 |
Lily and Dylan Yu | $50.00 |
Jonathan Catap Celer... | $50.00 |
Roger and Nancy Klin... | $50.00 |
Veronica Garcia | $50.00 |
Tara Shochat | $50.00 |
Cassie | $44.76 |
Anita Kornick | $40.00 |
Rona Smith | $40.00 |
Liz Hamada | $40.00 |
Tina Pak | $40.00 |
Yanelle Gavina | $40.00 |
edith boulton | $30.00 |
LOLO LEE | $26.00 |
Katie Lee Stamps.com... | $25.00 |
Jessica Nerio | $25.00 |
Scott DoVale | $25.00 |
Denisse McCrea | $25.00 |
Tricia Thayer | $25.00 |
Bonner Meudell | $25.00 |
Edgar Bordeos | $25.00 |
Anonymous | $25.00 |
Liz Hamada | $25.00 |
Cheryl Lougen | $25.00 |
Judy Thomas | $25.00 |
Anita Kornick | $25.00 |
Erin Karahadian | $25.00 |
Lauren Plichta | $25.00 |
Conster | $15.00 |
Jamie Lee Mitchell | $10.53 |
Southside Roosters | $10.00 |
Andrew Bordeos | $10.00 |
SGV Fall Team | $10.00 |
Tawny Barin | $10.00 |
Adam Bernier | $5.00 |
DHRC Dodgers Day | |
Hot Trot 5K | |
Jessica Vaca | |
Pantipa & Roy | |
Lisa Furumoto | |
Team Lai | |
Lucia Serio | |
Challen David | |
Martha Orozco | |
Megan Olson | |
Jeff Thomas | |
The Lais | |
Shivali Bidaiah |
Do you have technical issues or questions about our website?
For assistance, contact us by email, or call us at 888-LLS-7177
The Leukemia & Lymphoma Society® (LLS) is a global leader in the fight against cancer. The LLS mission: Cure leukemia, lymphoma, Hodgkin's disease and myeloma, and improve the quality of life of patients and their families. LLS funds lifesaving blood cancer research around the world, provides free information and support services, and is the voice for all blood cancer patients seeking access to quality, affordable, coordinated care. The Leukemia & Lymphoma Society is a 501(c)(3) organization, and all monetary donations are tax deductible to the fullest extent allowed by tax laws. Please check with your financial advisor if you have more questions.