Tag Archive for: childhood cancer

Dear JEM Project: Thank You For Being the Team Who Kept Madison’s & ISF’s Mission on Course

It’s hard to put into words how grateful we are for the impact The JEM Project’s $250,000 donation to ISF is creating for kids fighting rare pediatric cancer and for our community.  Follow along this week as we share ‘Thank You’ letters from many of those who feel the incredible significance of their gift.

Madison’s Mom shares what this donation can do for other families fighting pediatric cancer…

Dear JEM Project, 

“What do you want to be when you grow up?” – the all too common question asked to kids when they are little.  My answer was always “a teacher”, but in my heart I just wanted to be a mom.  When Mickey and I got married we talked about having a big family, and would have been perfectly happy with our own reality show “Fedak’s Fab Fifteen”, but God had other plans.  In 2009, Riley was born.  She was beautiful and healthy, and you couldn’t tell me the world didn’t revolve around her.  We were blessed again when God gave us Madison in 2012, and immediately I knew how lucky I was to be a mom to two of the most beautiful, precious little people.  Our “parenting” story would stop with Riley and Madison, and we were both perfectly happy with that.  Our lives were going great, until they weren’t.

Neither of my babies ever went to the doctor unless it was a regular checkup or the occasional ear infection.  We rarely had fevers, no broken bones, and no extreme injuries.  But on April 5, 2018, Madison’s pain took us to an emergency room that gave us the most devastating news any parent could receive.  I’m pretty sure you know that story by now, but what you don’t know is that in my mind, I kept questioning, “What did I do wrong?”.  My thoughts immediately went back to my pregnancy with her.  Did I stand too close to the microwave?  Did I use my cell phone too much?  Was a computer too close to my belly?  What did I eat?  Did I eat the right things?  Did I eat something wrong?    For two years I have argued with myself that I could have done something to have stopped this before it even began, but I have just recently realized that it isn’t about what I did before she was diagnosed, it’s about what I am going to do now.  Now that I know this disease can steal a child from her momma without warning, I have to be a part of something that will look to the future and figure out a way that no other Madison will ever lose her life to this ugly disease. 

When I talked to Rachel, ISF Marketing Director, in early January, she shared that the ISF team was furious.  They were all so angry and disappointed that the work they were doing was not enough to save Madison.  She shared that they were working on raising funds for research trials in Madison’s honor, and I was thrilled!  My first thought was, “Madison might not be here anymore, but she is still affecting people!”  Madison was a tiny little girl who can still make a difference, and I had to be a part of continuing the fight she began.

Rachel asked if I would be willing to speak at a breakfast/coffee event for ISF, and truthfully I had mixed emotions.  It wasn’t that I was scared to speak in front of so many people, I was honestly scared that my words wouldn’t be powerful enough to raise the money.  I was worried that I would fail the entire team, or worse that I would fail Madison.  I wrestled with the idea because Madison had only been gone for a few weeks, and at the time of the event it will still be so fresh and raw.  But I also knew what better way to make an impact than to share those raw feelings.  Knowing how important that week was for ISF in terms of fundraising, I was devastated COVID-19 had cancelled the event.  Not having this event meant not having the money. 

But then Rachel called me again in early April and shared the unbelievable news that you and your team pledged $250,000.  There hasn’t been a word created yet (and I’ve looked) to adequately describe the overwhelming feelings of gratitude I have right now. Through your more than generous donation, I have realized there is no way I can fail as long as Madison’s story continues to be told.  I’ve shared recently that my biggest fear no longer exists. I feared for two years that osteosarcoma would take Madison from me, and it did.  I can’t hold her or tuck her in at night.  I can’t pick out her clothes or run to her when she calls me in the middle of the night.       

Cancer stole so much from me; it stole from my family.  But because of your donation, there will be less cancer families who will know this statement even exists.  You didn’t even know Madison, but I so wish you did.  She was beautiful, inside and out.  And when I say she loved everyone, I mean EVERYONE.  She welcomed everyone into her room, even when I wanted a break.  She made people happy, and unfortunately she will no longer be able to share that love with the world.  But thankfully, we can.  Because of what you have so selflessly done, the team has the money to begin the search.  They can now start finding an answer.  They can find a cure so that no other mom will never know the pain of losing a child.

Thank you.  Thank you for the donation, but for so much more.  Thank you for allowing me to share Madison with the rest of the world.  Thank you for being a part of something huge.  Thank you for being the team who kept Madison’s and the  ISF’s mission on course.   I can hear her saying, “Look mom, I got some more soldiers for my army!”  

With all my love, 

Laura, Madison’s Mommy

Isabella Santos Foundation Receives $250,000 Gift by The JEM Foundation

Dear JEM Project: Your donation is Giving Children Fighting Cancer Time

Thank You to our Breakfast at Tiffany’s Sponsors

Although our Breakfast at Tiffany’s coffee events were canceled this week, we wanted to brag on our business sponsors that not only support us, but support so many others.  We spent months planning for these two inspirational packed mornings and we couldn’t wait to share it with nearly 600 attendees. Many generous business sponsors in the community were equally excited to help us make an impact this week and we are incredibly grateful to each of them for their support.

During this time more than ever community support is critical.  We are thankful for those businesses who have been with us since the beginning, as well as so many new ones who believe in our mission.  We are in this together and know we can help kids fighting beat cancer, grow hair and live their dreams.

PRESENTING SPONSOR

A new relationship for us this year is with The JEM Project and we couldn’t be more grateful.  This team of women and their passion inspire us and we appreciate them stepping into the presenting sponsor role for our breakfast events.   

JEM Project is dedicated to improving the welfare of children and women, along with preserving wildlife and the planet. This organization empowers organizations in these areas through charitable giving. 

GOLD SPONSORS

SILVER SPONSORS:

BRONZE SPONSORS:

SUPPORTERS:

It’s Isabella’s Birthday Month

Isabella Santos, 2005-2012

It’s March, Isabella’s birthday month!  On behalf of a little girl who should have been 15, thank you for supporting her foundation.  Thank you for helping us continue her legacy and make an impact on other kids fighting cancer. It’s March Madness around here, we have something going on all month long to help celebrate our founder.  We hope you will join us in one of the many ways during March. And don’t forget to help us share on our social channels!

Donate & Help us Fund A Wish

It’s our 3rd annual Isabella’s Birthday Wish Fundraiser and we can’t think of a better gift than to honor another child’s wish on what would have been Isabella’s 15th birthday in the month of March. 

We are excited for one of our cancer warriors, as she heads to Disney World to meet Minnie!  Brinn Andrew, 2 ½ years old, is coming to the end of her neuroblastoma treatment plan and continues to thrive. What better way to celebrate than to head to Disney with her family!

If Isabella were here today, we know it would be her wish to pass this experience on to another cancer fighter. Make-A-Wish granted Isabella her wish to go to Disney and gave her the most joyful days of her life. Help us do the same for a kid like Isabella and Brinn.

Donations of all values will allow us to collectively reach our $6,000 fundraising goal and will be gifted to the Make-A-Wish foundation to go towards a child’s wish. Donate

Schedule Blood Donation Appointment With ONEBLOOD, MARCH 7-9

This is our annual gift of life that we are so proud to be a part of. This year, our blood drive will run three days and in multiple locations, making this our biggest one to date!  As a thank you, OneBlood will make a $10 donation to ISF for each confirmed blood donor! It’s a win-win… saving local lives and raising funds for pediatric cancer! Check locations, times and appointments and make your appointment.

Eat Jersey Mike’s Subs All Month Long

March is the 10th annual Jersey Mike’s Subs Month of Giving. Make sure you mark your calendars for Wednesday, March 25th for Day of Giving when 100% of sales are donated to ISF and pediatric cancer. Schedule lunch with a friend, pre-order lunch for your office… every sub counts!  Since 2018 the greater Charlotte area Jersey Mike’s Subs have donated over $300,000 to ISF! Details, March coupons & 43 greater Charlotte area participating locations.

Create a Facebook Fundraiser

You can help celebrate Isabella by setting up a Facebook fundraiser in her honor.  Have a birthday this month? Set up a fundraiser. Or simply set one up in honor of Isabella’s birthday!  Set up Facebook Fundraiser.

Order Sweet’s Elderberry Syrup During Sweetgiving, March 1-7

Sweet’s Syrup’s  annual outreach in celebration of their company’s birthday is the first week of March.  During this week, March 1- 7, 20% of Sweet’s Syrup sales will be donated to ISF. Visit Sweet’s online store and purchase their elderberry syrup.

PROVIDENCE PLASTIC SURGERY BOTOX CHARITY EVENT, MARCH 30-APRIL 4

50% of Botox & Dysport in store and onlines sales go back to ISF during the week of March 30 – April 4. Online pre-purchase opportunity starts March 25, keep an eye out on our social channels for details!

Purchase Checkers Hockey Tickets, APRIL 5

Join us at Bojangles’ Coliseum as the Checkers take on the Hershey Bears on Sunday, April 5th. Tickets are just $16, with $5 from every ticket purchased going directly back to ISF! A fun family afternoon.  Purchase tickets.

Simply Donate

3rd Annual Isabella’s Birthday Wish Fundraiser

We featured Brinn and her family during our September Through My Eyes Campaign, learn more about Brinn’s cancer journey.

Isabella (L), Brinn (R)

It’s our 3rd annual Isabella’s Birthday Wish Fundraiser and we can’t think of a better gift than to honor another child’s wish on what would have been Isabella’s 15th birthday in the month of March.

We are excited for one of our cancer warriors, as she heads to Disney World to meet Minnie!  Brinn Andrew, 2 ½ years old, is coming to the end of her neuroblastoma treatment plan and continues to thrive. What better way to celebrate than to head to Disney with her family!

Over the last 2 years, you have helped bring so much happiness to kids like Sydney and Madison.

If Isabella were here today, we know it would be her wish to pass this experience on to another cancer fighter. Make-A-Wish granted Isabella her wish to go to Disney and gave her the most joyful days of her life. Help us do the same for a kid like Isabella and Brinn.

Donations of all values will allow us to collectively reach our $6,000 fundraising goal and will be gifted to the Make-A-Wish foundation to go towards a child’s wish. 

FEATURED WISH CHILD:

  • Wish Kid: Brinn
  • Age: 2 ½ 
  • Illness: Neuroblastoma
  • Wish: Disney World to meet Minnie
  • Favorite Things: Brinn is a daddy’s girl and loves all things pink, sparkles, and anything girly! She also loves Minnie Mouse and bunnies (she has a TON of stuffed ones😊). Lucky Charms and waffles are her favorite food.

New Decade. New Look.

New decade. New look. ISF is evolving and growing.  Just like Isabella would be if she were still here. She would be thinking about her future, getting ready to drive, maybe even getting a job… she’d be growing up. 

And The Isabella Santos Foundation is too.  We are beyond excited about the direction ISF is heading. Every detail from our logo and the colors we use, to our mission and our giving program is evolving with intention and purpose behind every element.   

Hello new logo…

As we evolve as a foundation and honestly as a team, we are feeling a little emotional as we say goodbye to our little girl logo. She has been with us from the beginning and she has shown up in all that we have done to get to this point. 

Over 12 years ago we started with our first logo, an innocent and childlike stick girl, a simple representation of Isabella as she was first diagnosed with cancer. What started out as a stick figure little girl in which Isabella could easily draw and color, became a symbol of her legacy. 

In the beginning it was only about her.  That simple logo moved and shaped into a life of its own.  We have seen her running, drawing and perched up proud at every event and fundraiser and has occupied a front row spot on everything we would print.  Our little girl evolved to a ‘Girl on the World’ because that is how we saw Isabella.  And while It started with her, she is still changing the world. But as we grow, we have realized it has become about others. Others just like her.

It was Isabella’s dream to “Beat cancer, grow hair, and live my dreams.” ISF was founded in her name and dedicates itself to expanding its impact to others, so kids with rare cancers have a fighting chance. It has become about all of them. It is so they can run, draw and take a front row spot at their favorite event. Isabella is the legacy and will always be our little girl. In order to continue changing the world…she would want our focus to be on them.

Updated mission, updated purpose…

You never know you need a foundation like ISF, until it’s too late. As parents focus on fighting for their child, we are working to bring change.  

Over the past 12 years ISF has granted nearly $4 million toward expanding the scope of research and treatment, and supporting families dealing with cancer in a variety of ways.

  • $1.9M+ donated to Levine Children’s (tag)
  • $1.2M+ donated to National Pediatric Cancer Trials & Studies
  • $500K+ donated in Family Support

Our relentless pursuit to help kids Beat Cancer, Grow Hair and Live Their Dreams in Isabella’s honor requires tremendous support from the community and from our donors. Our vision is to inspire a 360 degree impact for kids fighting rare cancers… from diagnosis, to treatment and ultimately, to survivorship.

Introducing the Beat. Grow. Live. Targeted Giving Program which will give you the ability to directly support how you want to impact the fight against pediatric cancer. Whether you have a tie to a specific cancer, a strong feeling to help fund a trial in tribute of a loved one or simply believe in donating to give pediatric cancer lasting change. Whatever speaks to you, we want you to feel the impact of your donation.

Beat Cancer, Investing in Rare Pediatric Cancer Research, 70% of our Mission

Grow Hair, Improving Trials & Studies, 20% of our Mission

Live My Dreams, Supporting Families Affected by Cancer, 10% of our Mission