A Piece of Home 2016 “Sponsor a Tree”

It is nearing that time of year again, the time where everyone starts preparing for the holidays, whether you celebrate Christmas, Kwanzaa, and Hanukkah(these are just a few of the celebrations that take place). Although in some aspects different they have one thing in common and that’s to be together as a family and usually in the home enjoying the celebration. In the world of childhood cancer or any serious medical world that’s not always the option for those going through the treatments or the hardships, many spend their time of celebration in the hospital’s where they need to be at that time for whatever the reason it may be. Our mission at Nathan’s Story with “A Piece of Home” is to help ease that by bringing some of that home comfort to those in patient.
As many of you can only imagine being in the hospital over the holidays is no fun…now imagine yourself as a child fighting cancer, a new way of life for you and your family that you have just embarked on in the last month. Nathan started his chemo treatments on Thanksgiving day of 2010, what better day we thought to be thankful for a “beginning to and end”. The chemo treatments were three weeks out of four in the hospital as inpatient, he was pulled out of school and taught by the teacher in the hospital and a home teacher the schools sent to our home, when he was there. Nathan and our family spent every holiday in the hospital as in patient either for chemo treatments or fevers/isolation with the exception of Halloween. The staff did everything they could to help make this as joyful and painless as they could but when it all came down to it we were still in the hospital for the holiday’s; childhood cancer seemed determined to take from us those special moments that we as a family cherish.
We at Nathan’s Story C.C.O. wanted to help make it even more special, beings we could look at it from a different perspective then most since we actually were in the situation. We personally came up with the idea of bringing in “A Piece of Home” for the holidays. Our first year and within months of becoming an official 501(c)(3) we raised funds to get the children that would be in the hospital for the holidays their own holiday tree. The trees we chose were specifically chosen with the children in mind and with the help of Nathan himself. The trees are no more then 32-36″ with fiber optic lights, lights that change colors automatically and cascade through the room with soft soothing colors to be able to relax and and enjoy. The children as well as the family truly enjoy the soft glow of the tree and the changing of the lights, it offers a relaxed and peaceful moment.
We reached out to everyone with our “sponsorship program” last year for the first time to help us grow in our mission and make it even more special and there was a response that was truly amazing and helped not only provide the trees but we where able to provide a holiday dinner and gifts for ALL the children including the siblings, we had crafts and just all around a great coming together of everyone around enjoying each others company and conversation; all this on the unit of a hospital.
Won’t you please help us again by “Sponsoring a Tree”…

Sponsorship is $20.00 per tree; you can donate by secure check out below or with check,  Mail to: Nathan’s Story PO Box 213 Galena MD 21635

Thank You…

Nathan’s Story



**All donations are tax deductible as we are a Federally approved 501c3 non-profit and will provide receipt of donation upon request.


Broken Hearts and Tears of Children

alex While you see so many children with smiles on their faces there are many more you may not see… These are the children of the childhood cancer world, yes that’s right children get cancer too, and at to high of a rate at that.

Childhood cancer come in many different sub-types, it’s not just one disease…they get all the cancers adults get and some that adults don’t. The bodies of children inside and out are not fully developed yet, so as you can imagine chemo does unbelievable things to our children’s bodies inside and out. We see and hear all about the adult world as it’s discussed and talked about on a regular basis, but what people don’t like to talk about or discuss is children suffering, yes I said suffering, not only are the treatments they receive decades old and made specifically for adults and administered at high doses, but these tiny little humans are trying to grow both mentally and physically and these adult based chemo in high dose forms to try and take a lot of that away from our children, let alone everything else it does…BUT what many-many folks don’t realize again is that these beautiful children fighting to survive and to have somewhat of a decent life afterwards is they do a lot of growing up in the hospital(s) and cannot attend school because of their particular delicate situation(s). The friends and playmates they make are also children in delicate/difficult situations as well. The bonds between these children become very tight, they share moments, stories, dreams and encourage each other through hard times; they are some of the most bravest and strongest people I know. We/they all become one very close tight nit family/community, we share tears, shoulders, struggles, and yes at times we can find laughter.

Nathan has been in this world now for just about 6years and throught these years he has like many of the children met and grown very fond of many of the children that share his delicate life, they may not all share the same diagnosis but that don’t stop them from understanding and bonding. We have met so many families from all walks of life and Nathan being out of school for so long and away from so many has become very close to these children/families he shares so much with and they have filled voids in his life that may not have been created if he was not diagnosed with cancer, they have become his friends, close friends; along the way and in all this he has also had to say “goodnight” to many…Yes there again another world our children who are diagnosed with cancer have to endure that maybe they would not as much if there was a change and a huge difference in how they are treated with cancer… Part of getting the children through recovery is to keep their stress levels at a minimum, you they have toxic chemicals, can’t go to school, cannot be a regular actuve child, lives primarly in a hospital and the list goes on…we are to keep the stress level at a minimum..UM YEAH NOPE! This past week we, the childhood cancer community have lost yet another young life to cancer; this young man battled 3 different types of cancer, being diagnosed lastly with a terminal brain tumor; this young man has been along with us from the start for the most part, Alex was the first we met, that was diagnosed with the same type of cancer as Nathan, osteosarcoma; bone cancer. In our first meeting his words of encouragement he offered not only to Nathan but to me, an adult, were just so uplifting and encouraging that I will never forget that day, all while Nathan was dealing with his wonderful side effects of his steroids he needed to take his chemo, but as it was, Alex paid no mind to that; he said no worries that happens to us all; we all go through it, its part of the course.(unacceptable world for children) All week long I struggled to tell Nathan, as he has his own struggles going on as well and Drs cannot express enough just how imporatan it is to keep his stress at a very minimal very low level…feeling horribly, I decided not to share just yet as Nathan had an event coming up that he was invited to attend as a HERO, a hero: a child fighting, who has fought cancer, anyways he needed this desperately, I found myself extending sympathy and apologies all at once to the mother/a friend of the young man, who was laying her beautiful son to rest the same day. Our day went off beautifully for Nathan, all the while I was just agonizing if I did the right thing, with a very heavy heart and mind I participated in the day along side of my son who was just in his glory with the outcome of his experience, thinking of this young man and his family and all attending his services at the same time; I wept many times through out the day, I wept in pain and in joy, it was a emotional struggle, you see the event was for another little boy who is also fighting cancer and has quite a ways to go yet to be done with his treatments and who will as the parents just found out, spend the rest of his life fearing another diagnosis of another cancer due to a genetic disorder. Nathan understands all too well and too much for being 15, so does all the other children who are put into these situations. This morning as I knew in my heart I could not hold it any longer I explained to Nathan the loss of Alex, the whole week and why I waited…in return my son who understands beceause we’ve been here too many times before, got angry, very angry with emotion and expressed to me that this would not happen if people, those people who could truly do something listened and trey cared enough to do it, angry that there is so little done to help make this NOT happen, so very little known to the general public that CHILDREN GET CANCER TOO and to top it off he just can’t comprehend how little the children mean to the world…