Tag Archive for: pediatric cancer

Why I Ask

Written by Erin Santos, Isabella’s Mommy & President of The Isabella Santos Foundation

ISF Backdrop Quote Sept

Why I ask.

A couple of weeks ago, I was enjoying a casual dinner with friends. We were eating our weight in chips and salsa and conversation turned to ISF, as it usually does. We started a conversation about a new concept I was trying out on Facebook to help raise money. It’s a simple idea based off our #isftagteam concept.  Each day I ask 5 people to support children’s cancer research by tagging them on Facebook.  It’s just a simple tag, asking you to take a minute and give to the cause of children who DIE from cancer. I don’t make you pour buckets of ice on yourself, you don’t have to do some silly dance or even do a single push-up – and you don’t have to tag others to do the same. You just have to support children’s cancer research.  Make a donation of $5 or make a donation of $500.  I don’t care what you donate – just support it.

I got pushback from my dinner companions for this concept immediately.  “People don’t want to be called out publicly”, “You can get away with doing something like that, but I would never do it.” I kept explaining that I didn’t really think it was offensive.   If someone directly asked me to give to something they really believed in, I would give. But, the looks on their faces told me that it was too “in your face”. Even though the conversation changed topics, I kept bringing it back to the simple question of whether or not I’m offending people by asking them publicly to support something that means everything to me. I couldn’t swing their opinion.

So I stopped doing it.  My goal wasn’t to upset anyone or push them to give when they didn’t want to. That was 2 weeks ago.

I hated that I stopped.

The more I thought about it, the more I realized something. I don’t give a F*ck if it makes people uncomfortable.

There, I said it.

Do you know why it killed her?  Because people are too nervous to ask someone to donate.

Not anymore.  So I’m sticking to my guns here.  Guess what, if I ask you – you don’t have to give and it won’t make me hate you.  But if you do give, it will make me love you.  It will make me love you because you get it.  You understand that nothing will be done unless something is done.  Someone once told me, “You know… I would give to ISF more if someone just asked me to do it.  But lots of times no one asks, so I forget and I don’t donate.”  I about choked when I heard that from someone recently.

So I’m making it my mission to just ask.  No harm in asking.  Things can only change if people take action and MAKE them change.  My goal isn’t to put you on the spot.  But sometimes you do things when you are on the spot.  And I’m hoping that what you do when you are on the spot will bring change and save lives.

Let’s do this.  Prepare to be tagged.


Erin Santos, President of the Isabella Santos Foundation and Isabella’s Mommy



Isabella Race Picture

We Should All Want to be Like Her

Written by Erin Santos, President of The Isabella Santos Foundation

Ib_Magnolia BakeryI saw this picture of Isabella in our new video and it stopped me in my tracks.  One of my many awesome abilities is my long and deep memory.  In the memories of Isabella, it is a a blessing and a curse.  Many of you will look at this picture and think of how happy she was.  And you would be right.  She was happy here.  She was one of the happiest children you ever met.  What you don’t see in this picture is the struggle.  This was Monday, September 19, 2011.  We were in New York City for dreaded quarterly scans.  We tried to make our time in NYC exciting for her and this day was no different.  We were given a private tour of Magnolia Bakery and private cupcake decorating party.  She brought her American Girl doll with her who also liked to decorate cupcakes.  She and her doll, Lanie proceeded to decorate cupcakes with hot pink icing and every color of sprinkle in the rainbow.

Behind the scenes she had every symptom imaginable.  Headaches, vomiting, stomach pains, dizziness and blurred vision to name a few.  I was anxiety ridden because I knew something was wrong.  I took a call during this cupcake session from a nurse who told me she was scheduling a neuro consult for Isabella the next day.  I felt sick.  I found out the next day that the cancer had spread to her brain, her bones, her bone marrow, areas in her chest and abdomen.  She was dripping in cancer.  The disease in her brain was bleeding and we should be expecting seizures any day.  We should go home, be with our family and call our home health care nurse.  This was it.  Just yesterday she was decorating cupcakes with a smile on her face.

Look at her face.  Then look at it again and tell me if you see cancer in that picture.

That’s the thing about Isabella.  She chose to dance in the rain instead of waiting for the storm to pass.  She lived every day like she was happy to be alive.  As a matter of fact, 4 days after this picture was taken – we held the 4th annual 5k for Kids Cancer and she danced and partied until the sun went down.  She lived 282 strong days after that death sentence we received.  

The longer she has been gone, the more I have gotten to know her.  I watch Sophia become obsessed with her in her daily life.  It gets scary at times to watch her be so consumed with everything in our house that is Isabella’s.  She wears HER clothes, she watches HER High School Musical Movie on HER iTouch, and listens to HER Taylor Swift CDs as she falls asleep in her bed, on HER Pillow Pets, with HER blankies.  I have to go to Isabella’s room each morning, open her door, and hear that same creak in the door that I heard for years when waking her for the hospital.  I have to go over to her bed and see a little girl in kitty pajamas, covered in pink little blankies and wake her.  But instead, this healthy little girl has hair… this time it’s Sophia.

For Sophia, Isabella has become the ultimate role model.  She sees pictures of her doing amazing things with this bright red hair and her big smile.  She sees her enjoying every minute of her life in pictures.  Sophia doesn’t know Isabella with cancer or being defeated.  People talk so positively about her with admiration.  The story of Isabella has been built up over the years so much that Sophia wants to be just like her.  I struggle with that because I want Sophia to be her own person, and then it hit me:

I want to be like her too. 

I want to leave a lasting footprint.  I want to inspire people.  I want to make a difference in the world.  I want to leave a lasting legacy and live a life that is fulfilling and rewarding.  I want to think that my time in this world was used towards a greater purpose and lives were saved because of actions I made.  I want people to see my picture and think I was truly happy and no matter what was going on in my life, I was going to fight through it and do something monumental with my day, my year, my life.

We should all want to be like her.

Her fight and her face inspire me every day and for this reason I choose to continue raising money to make a difference and do what she would be doing if she were alive today.  She would want to save her friends and make the world a better place.

They told her she was done and she wasn’t.  And I’m not done either. 


Please give to this amazing cause and ask your friends to do the same:  http://www.firstgiving.com/fundraiser/isabellasantos/8th-annual-5k10k-for-kids-cancer

Register for the race: www.5kforkidscancer.com 

[youtube_video] sH3nELoFQHU [/youtube_video]

Fight Cancer. Run with us.


By Tom Patania

On March 9th, we unveiled the details for Isabella’s Dream Team – 2015. This date was picked specifically because it would have been Isabella’s 10th birthday. Not only is she the Founder of ISF, she is the inspiration behind this team. Our focus is about Isabella, and following her dream of creating a world with “no more cancer.” We continue the fight for her and the many children that are also battling cancer.

Last year, in our inaugural year, the team was filled with passionate and selfless individuals that came together to surpass our wildest expectations. The 2014 team raised $34,000. This program continues to be a volunteer based, grassroots effort without the high overhead of a large charity.  We ask each participant to fundraise a minimum of $500 (but our hope is that each will shoot for much more than that).  What we lack in advertising dollars we make up for with heart and community.

 “Though she be but little, she is fierce.” – Shakespeare

IB in race tIn an effort to grow our team and our impact, we are recruiting runners and run/walkers that want to join our mission of helping make a little girl’s dream come true.

This year each athlete has a choice. We will be training for two races:  Rock N Roll Savannah (Nov 7th) or Thunder Road (Nov 14) half or full marathons.  With this being a volunteer effort, we ask that each participant sign up for their race of choice. Our hope is that the athletes that choose to run RnR Savannah will take part in supporting and cheering for those that are running Thunder Road, and to support our Charlotte community. The ISF10K/5K for Kids Cancer (Sept 26th) will be a part of our training program, so each team member will want to sign up for that race as well.

Official team training will start the week of July 13th and training schedules will be available for both distances. Included in the training schedule will be speed & hill workouts (Blakeney area) and Saturday long runs (various locations – early morning). I highly encourage all of you to attend as many team runs as possible.


dream teamHow to join the team?

  • Email Coach Tom at tom@isabellasantosfoundation.com with which race and distance you’re interested in and your t-shirt size.
  • Create your First Giving fundraising page by selecting: Isabella’s Dream Team 2015
    • Be sure to make this page personal. We do not ask you to cover the difference if you cannot hit $500.  We only ask for your best effort.
  • Register for your race and distance: RnR Savannah or Thunder Road
  • Get Social: tag five friends to let your network know you’ll be running with us this summer.


…A Princess Superhero?

Hero: n. Someone who faces challenges bravely and lives with a smile despite problems and shortcomings.

Qualities of a Hero:   Bravery. Confidence.  Determination. Dedication. Endurance. Perseverance. Selflessness. Sacrifice. Humility.

Princess: n. A noble young lady who carries herself with poise and dignity. She is compassionate, humble and is always thinking of others.

Qualities of Princess:  Strong. Unique. Independent. Loving. Curious. Fighter. Humble. Determined.

Ariel, the iconic princess from The Little Mermaid, has long beautiful red hair and loves the color purple. She is kind to others no matter what their circumstances, and is always looking for ways to help them in any way that she can. She is determined, fun to be around and known to follow her heart.  Sound like anyone you know?

superhero_ibAriel was Isabella Santos’s favorite princess. If you knew Isabella- there is no question as to why. This was her.  Plain and simple. The description of Ariel, down to the red hair and love of purple, fit her to a tee.

As children, we grow up fantasizing about what it would be like to be characters like Spiderman, Batman, Ariel and Elsa. We grow up learning to love these iconic personas in our life and want to do everything we can to be just like them. We dress like them, talk like them and even run around with a gown, a crown, a shield and cape just to play the part. In fact, even as adults, we secretly still want to be one of them.  We want to have abilities like teleportation, invisibility, time travel and superhuman speed just to get through our everyday life. But, in reality- we are human. We can only do what we can do.

So, what if you really had to transform into one?  And we mean REALLY had to transform. It is one thing to be Superman in our childlike imagination, but when real life throws us a ball of kryptonite- we have no choice but to fight back.

But here is the interesting part. If you have ever known a child with cancer- the resemblance is uncanny.  They are the bravest people you will ever meet. They are the most determined kids you will ever know. And…when push comes to shove- they fight with superhuman strength, they love with the most selfless of hearts and they teleport to places during dark times that most adults could never comprehend.

They are the real superheroes. They are the real princesses. THEY… are the real deal.

Throughout the month of September, we want to honor these incredible kids. We want to show that although they are just like every normal kid out there- they are heroic and deserve some serious recognition. They have fought battles worthy of Thor, shown the strength of The Incredible Hulk, and had to become invisible to the outside world like The Black Widow.  Much like Cinderella, they do not let life’s circumstances keep them down and continue to keep a positive outlook. Similar to Belle, they look past the masks and see the true beauty in people within. They live their own life… in their own way…regardless of being different.

Throughout the month of September, we will honor heroes once again that are just like Isabella was and will call them “Ibby’s Heroes”. She would like that.

Some… are in the middle of the fight. They have their armor on and ready to receive potions of every kind, with great hope that the next one will be the magic one. Others… have overcome their battle, yet continue to wear their shield close, so the cancer villain cannot attack again. And then…we have our Angels. The ones we honor that have traveled to another time. They have gained their wings, become invisible to the naked eye, but fly around and protect the ones they love most.

Ibby PrincessWe want to know through the imagination of a child- “What SUPERHUMAN POWER would you use to rid the world of cancer?”  Would you shoot it with a laser fighter, zap it with hot lava, cast a spell on it…use a healing wand? Whether you prefer to live in a castle and adorn a crown of sparkly jewels or wear a mask to combat super villains- we want to know. Kids are insightful and very creative. It’s no wonder that we look to them for their innocence and their honesty. We will be using this theme in an engaging way, throughout Pediatric Cancer Awareness Month, to help bring attention to the real faces of this disease. Our hope is that through more awareness…will come more action…and will rid the world of cancer forever and give children the opportunity to live their dreams.

…And back to that one special princess known as Ariel…AKA “Isabella”?

Well, she is special. She is a metaphor of love and transformation. She epitomizes what love is and wanted so desperately to experience what she had so longed for. For Isabella, this was a life without cancer. We may not be able to do it alone, but with your help, we can fight the battle- with gloves of white, a glass slipper and a cape to match!

Now is your turn…become a superhero for a child with cancer.  Register for our 5K for Kids Cancer or donate today.

August Firstgiving Promotion!

Ready. Set. Go!

Ready. Set. Go!

August can feel like December with the ramp up of Back to School – the calendar books up in the blink of an eye and summer seems like a distant memory before it even ends.  Plus, we’ve been busier than ever getting ready for our September 21st 5k (Go to www.5kforkidscancer.com to register!) We can’t wait!!! Those are our excuses for posting our August FirstGiving Promotions almost halfway through August!

We’ve mentioned in previous posts just how important FirstGiving is to ISF. Last year we raised over $100,000 through pages YOU created. We’re officially halfway through 2013, and we’ve already raised $33,000 through FirstGiving – our goal is $100,000 (33% to goal!). We know we WILL get there thanks to the constant support from old AND new friends.  August and September are always our highest giving months so we are excited to see where we will end up!

To thank you for all of your efforts this month, we’ve set up some pretty fabulous prizes – we like to call it the ISF 5K Swag Bag (drumroll, please…):

If you raise at least $1000 on your Firstgiving page by August 31st, 2013, you will be entered to win:

  • A $100 Dicks gift card (did we mention it’s Back to School AND ISF 5k time?? How many tennis shoes are YOU buying this month!!);  Thank you to Dicks Sporting Good for donating this to us!
  • Two entries to the ISF 5k for Kids Cancer; and,
  • Five raffle tickets to use at the race.  You will NOT BELIEVE the items that are coming in for the raffle and silent auction so these could be your winning tickets!

Even if your name isn’t pulled from the hat, just by raising $1000 you will have access to our Firstgiving VIP tent that will be at the race.  This includes a delicious hot breakfast, piping hot coffee, time to socialize with new and old friend, AND bragging rights for the entire day.

For every $1000 you raise, your name goes in the bucket for these prizes again and again. That’s your incentive to go beyond your monthly goals – how many times will your name be entered??

Remember that raising money has never been easier. Use Facebook, Twitter, Instagram, Pinterest – whatever social media site you adore this month to get the word out. Tell all of your friends just how easy it is to set up a Firstgiving page for ISF. Let’s do this together – spread awareness and beat this Big Bad Thing for good.

Thank you from everyone here at ISF and as always, Happy Fundraising!!