Ellie Strong

Ellie Strong This page was created for anyone who would like to follow Ellie's journey fighting leukemia.

We were asked to share Ellie’s story in the Why Me Annual Magazine this year. Click below to read and see some beautiful...
07/12/2023

We were asked to share Ellie’s story in the Why Me Annual Magazine this year. Click below to read and see some beautiful pictures of our brave Ellie. Why Me has been an absolute blessing to our family and I encourage you to consider donating if you have the means! ❤️

November 2023 Dear Friends, Why Me’s story is one of resilience, starting with a few dedicated volunteers, a handful of families, little money, and first-hand knowledge of the support services that would be most helpful. We persevered through the years, building Sherry’s House while the need for...

Ellie is off to preschool! ❤️
05/09/2023

Ellie is off to preschool! ❤️

02/09/2023

🎗️C H I L D H O O D C A N C E R
A W A R E N E S S M O N T H 🎗️


As we approach September, which is Pediatric Cancer Awareness month, I can’t help but think back to where we were a year...
31/08/2023

As we approach September, which is Pediatric Cancer Awareness month, I can’t help but think back to where we were a year ago. Some days it feels like it was all just a nightmare, but other days it feels like we’re still living it. Ellie’s cancer will forever be a part of our journey, I just pray that it is in our past. I’m so grateful for how far Ellie has come and how brave she has been.

She is one of the lucky ones.

Globally, approximately 400,000 children are diagnosed with cancer each year. 1 out of 6 children with cancer in America do not survive five years. Only 4% of the billions of dollars the government spends annually on cancer research is directed towards treating childhood cancer. These children need options for treatment that are not as toxic and won’t cause so many terrible and longterm side effects.

Help us spread the word and raise awareness that Pediatric Cancer research and treatment deserves more. The kids deserve more than 4%.

Nana and Doda joined us for this month’s visit to the Jimmy Fund Clinic! Ellie did a great job and her labs look good! S...
31/07/2023

Nana and Doda joined us for this month’s visit to the Jimmy Fund Clinic! Ellie did a great job and her labs look good! She will be back in Boston in September for her 1 year post-transplant bone marrow biopsy. ❤️

29/07/2023

Today marks one year since Ellie’s leukemia diagnosis. One year since we answered the phone and heard the word, “cancer.” One year since our lives were forever changed. One year since Ellie has been able to be a “normal” kid.

The past year has been filled with so many struggles, worries, days we didn’t know how we would survive, if Ellie would survive. Our whole world was put on pause so that we could focus on Ellie and be there by her side. Ellie, a two year old who had no idea what was happening. Who experienced so many things that no child, or person for that matter, should ever have to experience. We were forced to make decisions no parent should ever have to make, all while wondering if our decisions were ones Ellie would agree with as she gets older.

To say Ellie is a warrior is an understatement. While I was weak, she was strong. All of my strength came from her and I am still blown away every single day by how strong she proves to be. Her strength is the reason we are where we are now. Ten months out from her bone marrow transplant and no sign of leukemic cells returning. She is walking, talking, and playing again. This summer she has finally been able to be back out in the world with all of her friends and family. The moments I catch her doing “normal” kid things warms my heart and makes me weepy. I will never take these moments for granted as so many children who suffer from cancer don’t get these moments back. I keep telling myself: we are the lucky ones. Ellie made it through, when so many other families we met or shared stories with were not as fortunate. I have to remind myself of that on the hard days.

I wish I could say I was less worried today than I was a year ago, but it’s just not that simple. The fear of relapse, infections, side effects is still crippling. Every clinic visit, every blood test, every bone marrow biopsy causes an anxiety that only cancer families can understand. Will her labs be good? Will today be the day something comes up? What will her future hold? I hope as time goes on that some of these fears will quiet or become more distant, but right now it is still so fresh.

Thank you to Ellie’s Village, who has been by our side through it all. The texts, messages, phone calls, visits, donations, gifts to Ellie, home cooked meals, every generous act has meant so much to us. You all rallied around us when we needed you most, and we will never forget that.

Today, Ellie is happy and healthy. Today, we are winning the fight against leukemia. Today, we celebrate how far Ellie has come and today, I allow myself to take a breath and enjoy the moment.

Tomorrow begins the 100 Mile Ruck March, a fundraiser for Why My Sherry’s House. This organization has been absolutely i...
20/07/2023

Tomorrow begins the 100 Mile Ruck March, a fundraiser for Why My Sherry’s House. This organization has been absolutely incredible for our family, as well as many other local families who had experienced childhood cancer. Our whole family enjoys attending events and support groups here, especially Ellie! 💕

Here is the link if you would like to learn more about this organization and fundraiser or make a donation! https://whyme.org/event/100-mile-ruck-march-challenge/

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450 Brookline Avenue Smith 308/309

02445

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