Tag Archive for: Levine Children’s Hospital

MIBG Treatment Room Construction Begins at Levine Children’s Hospital

How satisfying is it to see your $1 MILLION worth in donations at work? To be able to touch and see the impact your dollars have on kids with cancer is immeasurable. Dawn (MIBG Therapy Program Director) and Lindsay (MIBG Head RN) stopped by the Levine Children’s Hospital ISF MIBG construction site to view the first steps of construction. Demo of the current hospital rooms where the MIBG treatment area will reside are underway, with the heavy demo starting today. We look forward to sharing progress photos and watching your impact unfold.

Levine Children’s Hospital will be 1 of 20 hospitals to have a MIBG Treatment room in the U.S. The two-room MIBG suite will provide targeted radiation to pediatric neuroblastoma patients and other rare pediatric cancers with minimal side effects. This will impact kids fighting cancer beyond the greater Charlotte region. Continue reading about the ISF MIBG room.

We are looking for individuals who want to be part of providing comfortable care for the kids/families that go through MIBG Treatment. Our new MIBG Ambassador Program gives you the flexibility of raising $5,000 the way you want to raise it… 100% of funds raised through this program will be distributed very specifically through our LCH partnership with this very targeted MIBG purpose. {You do not have to be located in Charlotte to participate, contact Tia for details}

ISF MIBG Ambassador: Tim McBride

We are excited to announce our very first committed ISF MIBG Ambassador, Tim McBride. The ISF MIBG Ambassador is a new program we have rolled out where each ambassador commits to raising $5,000 through his/her own network. We couldn’t think of the most perfect person to help us kick this program off. Tim fundraises 365 days a year for a variety of foundations and types of cancers, all while leveraging what he knows and loves best: running, bringing joy to kids at Christmas as Santa McBeast, and making whatever impact he can in ALL that he does.

Tim just retired. So we have to make sure he stays busy! And we love that he doesn’t take no for an answer as he fights to crush cancer every single day.

Funds raised through this program will be distributed very specifically through our partnership with Levine Children’s Hospital with a very targeted purpose. So get creative and fundraise the way you want to.

We hope you will join us at our MIBG Ambassador KICK OFF meeting on May 22 at 6:30 at the Santos Home.  Drinks and light appetizers will be available.  Please R.S.V.P. by Sunday, May 20th.  If you cannot attend and would like information, please contact tia@isabellasantosfoundation.org for details.
You do not have to be in Charlotte to participate!  Email Tia for more information.
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Date: Tuesday, May 22
Time:  6:30 pm
Location:  Santos Home

A New Way to Make an Impact: Isabella Santos Ambassador Program

Take your support of the Isabella Santos Foundation to the next level
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As the Isabella Santos Foundation MIBG treatment suite at Levine Children’s Hospital goes under construction, we want to ensure that we help plan for the kids and their families who will have to walk through its door for cancer treatment.  We have developed the Isabella Santos MIBG Ambassador Program, a new way of fundraising and making an impact.  As an Isabella Santos MIBG Ambassador, you agree to help raise $5,000 to provide a comfortable and customized experience for all families and children who undergo MIBG therapy at Levine Children’s Hospital.  This program gives you the opportunity to leverage your network and raise funds the way you want to raise them.  100% of your donation will go to help support patients and families by helping provide items and experiences that we will detail during our upcoming MIBG Ambassador kick off meeting.
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We hope you will join us at our MIBG Ambassador KICK OFF meeting on May 22 at 6:30 at the Santos Home.  Drinks and light appetizers will be available.  Please R.S.V.P. by Sunday, May 20th.  If you cannot attend and would like information, please contact tia@isabellasantosfoundation.org for details.
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Date: Tuesday, May 22
Time:  6:30 pm
Location:  Santos Home

Jersey Mike’s raises $135,000 for local pediatric cancer foundation during nationwide Month of Giving

37 Greater Charlotte area restaurants.  300+ smiling employees. 7,271 loaves of bread.  Countless paper sub bags.  Hundreds of community partners and long lines of volunteers, supporters and friends.  $135,000 RAISED.  Thank you for eating subs with us in March.  Thank you Jersey Mike’s Subs for your give back and make a difference attitude. It is these actions that create IMPACT.

Jersey Mike’s Subs joined forces with its generous customers throughout the Greater Charlotte area in March, to support the Isabella Santos Foundation (ISF) during the 8th Annual “Month of Giving” campaign.  The campaign raised an incredible $135,000 for ISF which will help fight rare pediatric cancer in the Charlotte region and beyond.  ISF recently committed $5 Million to establish The Isabella Santos Foundation Rare and Solid Tumor Program at Levine Children’s Hospital (LCH).  This program will oversee care for all solid tumors, rare tumors, MIBG therapy, and all related clinical and scientific research at LCH and it will be the first of its kind in the United States.

The month of fundraising culminated on March 28th with Jersey Mike’s nationwide “Day of Giving” where 100% of the sales, not just the profits, were donated to the local charities.

More than $6 million was raised by Jersey Mike’s around the country, impacting more than 170 organizations. Thank you for eating at Jersey Mike’s in March with us.  The funds raised for the Isabella Santos Foundation stay right here in the Charlotte community.  During times like these, we feel extremely humbled. Isabella has moved us and many others to take action for kids fighting cancer. Good things are happening because of Isabella’s legacy.  Thank you Queen City!

“Jersey Mike’s is very honored to be a partner with such a great organization like ISF who is making a huge impact on the fight against pediatric cancers.  It is truly amazing how many families the foundation touches and what a huge difference they are making in their lives.  We are so proud to be a small piece of all this and look forward to a long lasting relationship with ISF.” – Nick Smith, Jersey Mike’s Charlotte Franchise Owner

Charlotte Day of Giving Photos

Committed to Improving Pediatric Cancer Care in Charlotte and Beyond

Isabella Santos Foundation

Press Conference News coverage  |  Press Conference Video

Today we announced  the largest commitment we have ever made. We are a bit scared. Very emotional. The Isabella Santos Foundation commits  $5 million to establish The Isabella Santos Foundation Rare & Solid Tumor Program at Levine Children’s Hospital.  This program will oversee care for all solid tumors, rare tumors, MIBG therapy, and all related clinical and scientific research at LCH.  We are ready to take that next step by creating a rare and special pediatric cancer program that will be the first of its kind in the United States.

We might be scared. We might be emotional.  But we feel… Energized. Hopeful. Determined. Grateful.

Our partnership with LCH will allow us to continue the legacy Isabella left.  Isabella’s motto was: Beat. Grow. Live.  “Beat cancer, grow my hair, live my dreams.”  The foundation in her name dedicates itself to broadening that, so that other kids fighting cancer may Beat (the odds), Grow (awareness), and Live (without fear).

During the LCH press conference today for the partnership announcement, Erin Santos spoke about what this day means for her personally…

“First of all I just want to take a moment and thank the team of ISF that is with me today.  I always say after events like this to remember, every time you hear the word “Erin” it really means us.  I am nothing without all of you standing next to me and none of this would happen without the people here today.

October 6th, 2007 – this day has always meant something to me because it was the day my life changed forever.  My 2-year-old daughter was next to us in pigtails – wearing a pink t-shirt with a mermaid on it that we bought her at the Fort Fisher Aquarium that summer.  We weren’t sure what we were going to be told in that tiny room but in just moments we were introduced to a word we had never heard.  Neuroblastoma.  We were quickly taken to a waiting room in clinic that would become our home for 5 years and would soon meet our new oncology family, who I still see in the audience today.  

Sure, we may of known on that day that our life would change forever.  But what we didn’t know is that the little girl that just walked through their clinic doors would change their lives forever too.  The domino effect of that day is still falling.   

I look out into this sea of faces and I see lives that will never be the same because of her.  All of the people who were there from the beginning who made my cause, their cause.  I can see kids that like her will be walked into a clinic waiting room and will see and feel this domino effect of her life due to this gift and that gives me hope and inspires us to make this commitment.

For us to take on this huge milestone with Levine, it is more than just a check.  We are not famous or wealthy – we are just normal people who are doing amazing things.  The blood, sweat and tears that we will put into raising this money will keep us up at night.   But the faith that we have in Javier, Callie, all the doctors, nurses and administration keep us moving towards this goal because we believe in you.  I know this will be one of the best things you will ever do with your life, just like us.  We are in this together and we are beyond excited to watch this program grow into something that will receive nationwide attention and bring kids from all over the country to Charlotte to have the best chance of survival.  No pressure – but I know you feel the pressure.

So thank you for allowing us to be a part of the biggest thing to happen for kids with cancer in Charlotte region and beyond.  I can’t wait to see Isabella’s name on the center that brings new hope, treatments and cures to kids with rare pediatric cancers.  The only thing better would be to have here her alongside me, but in a way – I think we all know she is.”

With this $5 million 5-year initiative, we will be changing lives.  We will be the foundation of something special.  We will have the best pediatric cancer program, right here in Charlotte, North Carolina.  And we need your help.

MORE:

The Isabella Santos Foundation Commits $5 Million to Create Rare & Solid Tumor Program at Levine Children’s Hospital

Levine Children’s Hospital gets $5M for cancer fight

Atrium Health’s Levine Children’s Hospital announce $5 million donation from Isabella Santos Foundation

$5 Million Has Been Donated to Treat Childhood Cancers by a Foundation Set Up by Parents

New specialized treatment room coming to Levine Children’s Hospital, care of Isabella Santos

Levine Children’s Hospital Gets One Of Its Largest Donations in History

$5M donation will create ‘rare and solid tumor’ program at Levine

Pediatric cancer care gets $5M boost from Isabella Santos Foundation