Tag Archive for: pediatric cancer foundation

ISF Funds Frontline MIBG Therapy with the Children’s Oncology Group

In this picture is Isabella in MIBG therapy at CHOPT in Philadelphia. Isabella not only received this as a end of life treatment instead of a frontline therapy… she had to travel away from her home and family to receive it. This will be a game changer for kids fighting.

In 2016, funded a Frontline MIBG Therapy project with the Children’s Oncology Group (COG). The purpose of this project was to determine the effectiveness of pulling MIBG therapy, which was traditionally used as an end of life treatment, to the frontline of therapy for children with high-risk Neuroblastoma. We are excited to announce, thanks to your donations – this trial is ready for children across the country. Starting in August of 2018, the COG will start the process of enrolling over 800 children with high-risk Neuroblastoma and will enroll children over the next 3 years. Tomorrow night, Dr. Peter Adamson, Chair of the Children’s Oncology Group, will be with us here is Charlotte to speak at a private event about the advancement of the program. Can’t wait to share more updates.

This is great news for Charlotte because as you know, ISF has agreed to fund the creation of a MIBG at Levine Children’s Hospital! We are inching towards our goal of $1 MILLION DOLLARS and anticipate breaking ground in 2018. What this means is that in just one year, our local children will benefit from a trial that YOU supported in a room that YOU built. This trial hopes to reduce the number of children who relapse and reduce the burden of late effects of therapy. Amazing.

This is due to your support. So thank you. Children of Charlotte thank you.

We were so proud to have been able to donate a total of $175,000 to the COG through three of their children’s cancer trials and programs.  Learn more about the programs YOU helped us fund through the COG.

First Quarter Fundraising Update

We are excited to announce that The Isabella Santos Foundation has raised $260,000 in the 1st quarter of 2017. We have set a goal of raising ONE MILLION DOLLARS in 2017 for our 10th anniversary.  Your support will help us get our message of hope to more people than ever before and generate much needed research and treatment options to eradicate childhood cancers.
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It’s amazing to look back on where we were 6 years ago before Isabella passed away…   “I’m proud of our team and what we have done. Not only do we have the uphill battle every day but we do it in our own style and manage to keep it together the best we can. Not to mention the fact that while running uphill we have managed to raise close to $150,000 for various charities, mainly Neuroblastoma research. My mom and I were talking recently and my mom was saying how hard it is for her to understand all the good that Isabella brings to other people’s lives but how she has to suffer in the process. I’ve always struggled with this as well as I watch other children get to do all the “normal” things of childhood while she is hooked up to toxic treatments. But after thinking about it, I think of all the people in history that have suffered. But through their suffering, it brought something good. Maybe she is just one of those people in our lives that takes the bullet to make us all better people. Or maybe her suffering will help raise awareness and funds that will one day CURE all children. Who knows.” – Isabella’s Mommy, 2011
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Thank you to everyone for their passion and support.  It’s pretty darn incredible how far we have come.  We can accomplish so much if we fight cancer together.

ISF Volunteer Opportunity: Auction Committee

We can’t believe that it is almost May.  We have had such a wonderful start to 2017 and excited to dive into bringing you the BEST 5K and10K for Kids Cancer Race in September that you have seen yet.  This is our 10th annual Charlotte 5K and 10K race event and we look forward to celebrating Isabella’s life in the best possible way while bringing our community together.

At the 5K and 10K for Kids Cancer Race we have become known for our SILENT AUCTION.  What started out as a fun idea of having 20 raffles baskets available years ago has blossomed into fantastic way to raise funds for neuroblastoma research and pediatric cancer.  In 2016, our ISF Silent Auction and Raffle raised $80,000!  That is incredible!  Our raffle and silent auction includes beauty/spa packages, sporting events, date night outs, vacations, jewelry and more.  There is something for everyone.  We are looking for new volunteers to join our Auction Committee to help us.  Not only is volunteering for ISF rewarding, we can guarantee you will have fun while meeting many great faces.

“When I originally became involved with ISF, I was a volunteer on the Auction Committee.  Every year we host a huge auction at our annual 5k/10k for Kids Cancer in September.  The auction has become a staple at the race and is responsible for a large percentage of the monies raised at this event.  I felt such pride in being a part of something bigger than myself with a purpose of helping children fight cancer!  I didn’t necessarily have as much time to devote as I would have liked, but I did what I could.  I can truly say being a part of ISF has changed my life in so many wonderful and fulfilling ways! Today, I am the Auction Co-Chair and I couldn’t be more proud to lead such a giving and fun team!   We have several needs for this important committee.  Anyone with a passion to help others who can dedicate some time to helping us create an incredible 10 year anniversary auction this year is welcome!  We have needs for individuals who are not shy to ask for donation from businesses, or who have connections in the community.  We also need those who have time to fill out applications for donations, help organize the auction items, and help us wrap the packages!  We have room for anyone who can help!”  – Andrea Isaac, Auction Co-Chair
We have our first Auction Committee interest meeting on Wednesday May 3rd at 7:30pm.  If you can’t make the first meeting, we can send you details!  Please contact Andrea Isaac for the meeting location, if you are interested in learning more or have questions!  If you are business who would like to donate an item, all items are welcome!  Its great advertising as our auction is in front of thousands at the event itself as well as online!

10 Years in 10 Minutes

10 years in 10 minutes. A glimpse of Isabella’s sweet soul, the legacy her parents fight to build to save children like her, and what the Isabella Santos Foundation is doing today in her honor to help kids with cancer.

 

February 23, 2017 – 7 years 111 days

When you lose a child, your life becomes a series of numbers, times of day, songs, and dates.  I don’t really know why we do it to ourselves.  Why do we look at the clock or the calendar and say things like, “this day in 2010”.  It’s just plain torture.  It’s especially bad around her passing day because the memories are so vivid that you can still recall every day of that month.  How she looked, what she said, who came to visit or even the haircut you got that month, which you always regretted.  Why would I leave her to do that?  The haircut always haunted me.

How old was Isabella when she died is a question I get all the time.  My immediate answer, or the one you will hear out of my mouth is 7.  But in my head I am saying 7 years and 111 days.  She wasn’t just 7 because of course like any tortured Mother, I remember the day she turned 7.  We had a full day planned to celebrate on that day, but we got a call from Dr. Kaplan who told us that she was in need of blood and platelets.  I had a small breakdown in the clinic about it because I was tired of having special days ruined for her.  She of course was clueless to missing out because her whole life was about missing out.  The staff decorated her transfusion room for her and got her cake, balloons and gifts.  It was sweet of them and I honestly think they did it more for me.

While we were there, we also got a call from NYC and were surprised to hear that one of Isabella’s four bone marrows tested positive for neuroblastoma.  This came out of left field for us because we thought she would be squeaky clean after her third MIBG treatment.  The amount they found was very minimal, but in the world of cancer, sometimes that is what will kill you.  This small evidence of disease was ultimately the cells that exploded and eventually took her life.  Go figure, the start of her death started on her 7th birthday.

Of course in Isabella style, we did have a wonderful birthday weekend.  We went to Great Wolf Lodge with her bestie Soleil and had a horse party with all her friends.  She asked for Target gift cards for her presents and then proceeded to spend every single one of them buying toys to replenish the oncology floor playroom.  Even on her last birthday, she was still giving.

That was her 7th birthday.  The good, the bad and the ugly.  She lived 111 more days.

Phia, 7 years 111 days

I saw it coming as I took a glimpse into my February calendar.  There it was.  February 23, 2017.  This was the day that Sophia would be 7 years, 111 days old.  This is also the day that Isabella would officially become my youngest child and daughter.

Of course my natural way is to push things down and try not to think about them.  But grief has a way of sneaking up on you.  Even this morning, the day before Isabella’s birthday, I find myself being a total bitch.  I’m overtired.  I’m cranky.  I want to be alone.  I’m snapping at my kids and want nothing to do with seeing Stuart.  I know what it is all about, I am just trying to deny it.

So I go about the days leading up to it and walk right into a memory a week before the dreaded day.  I had been trying to get back in the gym and my body was hurting.  I decide to take a nice relaxing soak in the tub.  We all know as mothers that kids hear that bath running from miles away.  Within 2 minutes, Sophia is stripped down naked and about to do a cannonball into the tub with me.   She is squirmy as usual and I can’t even get a word in edgewise.  Sophia is non-stop energy and it baffles me how she can be at a 12 all day every day.  She is making a Mohawk in her hair with bubbles and is putting a Santa beard on me all while telling me about her boyfriend and how he tried to kiss her on the playground.  I try to be present but I find my mind wandering as I look at her.

June 21, 2012 (One week before she passed)

“The days seem so long and often I ask myself, what day is it?  I seriously don’t know if it’s Sunday or Thursday.  The majority of my days are spent in the bed with Isabella.  I try to lay with her in the morning until around 4 each day.  We don’t do much in the bed.  Occasional meds, back rubs, small conversation.  I’ll get her up and put her in the bath with me to make sure she at least feels clean every day.  But with each bath, I look at this girl and can barely see my Isabella in there.  Her stomach is sunken, ribs showing every bone.  Her shoulders stick out like they want to punch through the skin and her spine shows each vertebrae.  I can no longer carry her with my hand on her back because it just upsets me too much.  

While we are all trying to come to peace with things, Grant is beginning to struggle.  He is having moments of tears that come from just seeing a picture of them together.  Nightmares, night sweats and the constant need to be right next to me, letting me know that he is grieving.  He misses her.  He comes and gives her hugs when he leaves and constantly says, “tell Isabella I love her”.  Even today he came in and sat next to the tub while Isabella and I took a bath.  Just talking about whatever came in his head… but it just felt normal to him for a minute.  They talk as if nothing is going on… he tells her that her hair is coming in good, or they talk about how library day will work next year at Marvin, what happens when people have surgery, his new Spider-man book…whatever.  He just wants to be there.  I’m amazed he doesn’t mention the look of the body he sees in the water…he notices it I’m sure.”

Just a couple of days later, we took our last bath together.  I laid her on top of me and not much was said.  I knew she wanted to talk to me but it was hard for her.  The words that were coming out of her mouth weren’t making sense.  She was trying to talk to me about a bunny or Grant but then said, “Mommy, that didn’t make sense did it.”  By this point the cancer was in her brain and it was taking over quickly.  It was the last conversation we had.  For the next 24 hours she was still there in her mind but this too would go soon.

June 26, 2012 (Two days before she passed.)

Her heartbeat is slowing down but sounding different because her heart is working harder.  Her oxygen is slowing down a bit too.  Her breathing is slowing down so much in fact that I just stare at her.  She will take a breath and then it will be so long until the next one that I find myself holding my breath until she takes one again.  She sleeps most of the day and gives me small glimpses of what is in her mind.  I lay with her so quiet and still and listen to the things that she says in her sleep.  She asks me if I see things or tells someone to wait on Mommy.  She will say Grant’s name but then it wakes her and she says that she was just dreaming.  She flinches and smiles, makes gestures with her hands and squeezes my hand softly.  It’s like she is talking to someone.  But the occasional smile let’s me know that it is not a conversation that scares her or makes her sad.  Each night Stuart and I snuggle in beside her and tell her things just in case she is not with us when we wake up.  We have been told by hospice that we are lucky.  She is relaxed, comfortable and not in pain.  

Two days later she died.  She died in the morning on June 28th at the age of 7 years, 111 days.

Phia, 7 years 111 days

So on February 23rd, 2017 I crawled into bed with my now oldest daughter Sophia.  We snuggled for a bit and then she got a piggyback ride downstairs as she got ready for school.  I dropped her off and continued to torture myself throughout the day.  I talked to my Mom on the phone and cried.  Then I sat down and watched “This is Us” and bawled my eyes out as the father I loved on the show died from cancer.  I visited Isabella’s site briefly.  I sat in the sun quietly and waited for Sophia to get off the bus.  I gave her a big hug and told her that today she was 7 years and 111 days old.  She shrugged me off as usual.

I took her for a haircut where the stylist walked right into my nightmare.  She asked Sophia how old she was, to which she responded “7 years and 111 days”.  The stylist laughed at how cute she was.  I knew when she asked her if she had any brothers or sisters, that we were in for it.  Sophia of course responded telling her, “I have a brother Grant and a sister Isabella who died of cancer.”  All this while zoned into watching Big Hero 6 on the TV screen.  The stylist turned and looked at me.  “Oh my gosh!  I’m so sorry.  How old was she?”

“7 years and 111 days.”  I replied.  I then proceed to weep on the couch of Pigtails and Crewcuts.  Welcome to my f’d up day lady.

Phia, 7 Years 111 days

I took Sophia back and we walked on the trail together, holding hands and laughing.  I would catch myself looking down at our hands together and thinking how unbelievably similar that view was.  Her hands are identical to Isabella’s yet so much is different.  She is healthy and running barefoot ahead of me in her purple dress with her blonde hair bouncing up and down.  I am looking at a child that Isabella should have been on that day.   Happy, cancer free, without a care in the world.

But instead she is gone and Sophia is now older than Isabella.  I am thankful this day is behind us and can thankfully say that I don’t have another day on the calendar for awhile that I’m scared of.  It’s crazy to think she would be 12 years old today.  I can’t even imagine.  But, as Sophia ages each day – it gives me a small glimpse into a piece of who she would have been on that day in history too.  I always say Sophia is a gift from Isabella.  Her little sister who has in one day, all of sudden, become her big sister too.

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