For those of you who don’t know me, I have an affinity for old-school professional wrestling, or “wrasslin'” as it’s colloquially known around here. One of my favorite lines from Dusty Rhodes, better known as “The American Dream,” was how he described his life was when trying to win the world heavyweight championship: like “living on the end of a lightning bolt.” Dusty had quite a way with words. But he was trying to explain to all of us out in TV land that his career was the world’s biggest roller-coaster ride, filled with earth-shattering turns, excitement, power, and something that rivaled a celestial explosion.
I feel like the Me Fine Foundation is living on the end of a lightning bolt right now, and believe me when I tell you that it’s quite an amazing feeling.
We wrapped up 2017 with our first-ever expansion into a new hospital, launching service at WakeMed Children’s. Although that growth took a few years of work by a lot of dedicated folks, it has already produced incredible response from families who are thrilled to have Me Fine’s help along their child’s journey at that hospital.
As much as I want to take a moment and reflect on this major accomplishment for our community, I find myself repeatedly feeling charged to move immediately forward because of this event. Harness the energy, the excitement, the GOOD in helping an entirely new population, and bull-rush our way forward. How could I even think about slowing down from that?
The short answer is: Me Fine is NOT slowing down. The organization enters 2018 with some amazing momentum, goodwill, and motivation and also large aspirations for internal improvements and organizational evolution.
To our DONORS: you’re going to hear from us more regularly. We’re working to put our value of stewardship into action so you know how much we appreciate you and for you to stay abreast of ways you can continue to help us deliver our mission to the children and families who need us most.
To our CORPORATE PARTNERS: we’ve got multiple opportunities coming your way to partner with Me Fine’s mission in new and innovative ways. We want your customers to know how much you mean to us and how powerful of an ally you’ve become.
To the HOSPITALS where we operate: we’re adapting to the challenges in the healthcare landscape. Me Fine aims to be a smarter, broader, and more reliable partner to enhance the patient experience of care that you so dependably deliver.
Finally, to our KIDS & FAMILIES: we hear you and you’re not alone. We’re working harder than ever to raise more money and to be more of what you need as you navigate your treatment journeys and hold your families together. Me Fine is going to continue to be on your team and in your corner to strengthen when you need us.
2018 is going to be a remarkable year. We hope you’ll consider how you might fit into Me Fine’s story this year. Whatever way that might be, we’ll save a seat on the lightning bolt for you.
All the best,
Joey Powell, Executive Director
Written by Melissa R. Johnson, PhD
The world of the newborn intensive care unit is a hidden world, a place of both daily miracles and heartbreak. In the past several decades, advances in both medical and developmental care have led to major improvements in survival and long-term outcomes for babies born as early as 23 weeks. But for most people who are excited to discover that they are pregnant, what goes on in the NICU is a mystery that they would just as soon not think about.
For the majority of parents, the birth of a premie or a sick baby comes as a real shock. Sometimes there are a few days or even weeks of warning, if mom is experiencing complications or signs of early labor, though these complications themselves are often very stressful. In other cases, the first indicator that a baby is coming early is a sudden onset of labor months before the due date, or even the precipitous delivery of the baby at home or in the ambulance on the way to the hospital. All of these circumstances catapult the young family from anticipating a normal birth in a number of months, to an encounter with a tiny infant (or infants in the case of multiple birth)surrounded by technology in an overwhelming, complex setting.
Typically, parents feel as though their baby’s life is in the hands of others, and though these doctors, nurses and therapists are typically warm and caring, they are also total strangers. In my thirty years of working in a NICU as a developmental specialist and psychologist supporting families, I was always amazed by the courage, resilience, and love shown by families who often had no idea a few days earlier that their lives would be turned upside down. NICU staff members over the years have come to appreciate more and more deeply how critical parents are to the medical and developmental recovery of the baby, and how important emotional support of the parent is to facilitate the parents’ success in functioning effectively in the NICU and after discharge.
While the relationships among parents and the doctors, nurses, therapists, social workers, chaplains, medical secretaries, and all the other professionals in the unit are critical, there are many other ways that parents need support. The more parents can remain by the bedside, the more they can understand and advocate for their baby’s needs. Every hour spent holding a premature infant skin to skin (“kangaroo care”) benefits the baby’s developing body and brain.
But virtually every family faces unexpected obstacles. Practical issues such as parking costs, fuel expenses, food while visiting, child care for siblings, clothing for a tiny infant who will outgrow outfits rapidly, and life expenses when maternity and paternity leaves are not available or inadequate, add to the stress and sadness that families experience. Assistance with such needs are much more then optional extras – they can be critical to a young family taking their baby home feeling capable of facing the future.
I’ll never forget giving some parents gas cards made available through donations to our hospital, during one of many gas crisis periods when costs were especially high, and having both mothers and fathers start to cry tears of gratitude for what was basically one tank of gas to come visit their child. The work of organizations such as Me Fine, addressing the social and practical support needs of families whose children are in medical crisis, is critical in so many ways. It can truly make a difference in the long-term outcome of children and their parents as they find the strength to recover, grow, and develop together.
A HUGE THANK YOU TO ALL OF OUR SUPPORTERS!
We are proud to announce that the 2017 Me Fine Gala, held at City Club of Raleigh on September 23rd, raised over $210,000 for the children and families we serve. The Gala, presented by Centrifuge Media, celebrated Me Fine’s accomplishments over the last year and served as a thank you to the amazing team of donors, allies and advocates who helped in that success. The many local businesses that sponsored the event ensured a magical evening for all in attendance. The Gala is the nonprofit’s annual signature fundraiser, raising funds to help provide financial assistance and emotional support programs to parents and caregivers whose children are receiving critical medical treatment from Duke and UNC Children’s Hospitals.
The “Hero for Life” Award is the Me Fine Foundation’s highest honor, recognizes those who go above and beyond to help critically ill kids and families, specifically with respect to Me Fine’s mission. It is presented annually at the Me Fine Gala. This year’s recipient, Jordan Wright, is a two-time cancer survivor and longtime foundation ally who donates his time and talents as a professional photographer to the foundation.
“Once again, the community has shown us just how much they care and we’re incredibly thankful, “ said Joey Powell, Executive Director of the Me Fine Foundation. “Our sponsors and supporters ensure that we have an enormous impact on the children and families we serve.”
Photos are available HERE:
A massive thank you to the AJ Fletcher Foundation for helping build out the Teen Resource Cart at Duke Children’s Hospital! The cart carries fun supplies for teenagers receiving treatment to ensure that they have access to engaging material. The cart includes items such as books, movies, games, coloring books and art projects.
Neat, right? Read what some of the teens and staff have to say about it:
“The gel pens and adult coloring from the teen cart helped me relax and pass the time.” -Lea, age 18
“It is great for our teens to have a special space to choose activities that appeal to their age.” – Katelin, CCLS, Child Life Specialist, Duke Children’s 5300 Unit
“The teen cart is an awesome way for our teen patients to make choices when many things are out of their control.” – Jess, RN, Duke Children’s 5100 Unit
“We are fortunate to have teen carts that we can utilize for teen patients on adult units. These units often have fewer resources to normalize the environment so the rolling teen carts provide comfort to these patients.” – Susan, Child Life Specialist, Duke Children’s (Hospital School Coordinator)
Stories like these allow us to show our community the impact that their donations can have. We aim to have a real and tangible impact on the lives of children receiving care and their families. Interested in speaking with someone to contribute? Visit our website to learn more and get in touch.
Hello there fellow Raleighite! Here’s your guide on how to show up for the Me Fine Foundation Gala in something you’ll enjoy yourself in all while making a statement! You’ll be helping children with illnesses and their families battle through their journey so you’re already a star in our book! Continue reading
TICKETS ON SALE FOR 2017 ME FINE FOUNDATION GALA
Raleigh, N.C. (August 21, 2017)-The 2017 Me Fine Foundation Gala presented by Centrifuge Media will be held on Saturday, September 23rd at City Club Raleigh downtown. The gala will be a night of celebration with food and drink, a live and silent auction, and music performed by local favorite Crush. Proceeds from the gala will benefit families facing medical crises while being treated at Duke and UNC Children’s Hospitals.
As you know, we recently completed our Christmas in July campaign at UNC Children’s hospital. We want to thank each and every one of our supports for the kind words, thoughts as well as the gifts that we distributed. The children all had smiles on their faces, which was very rewarding to see! Here are some images for you to see how the day played out as well as information about our upcoming local gala. Continue reading
A recent college graduate recounts his story during his illness. Read about the wonderful and caring staff that helped him through his journey. A great example of social good in practice. Continue reading
On July 20th and 27th, the Me Fine Foundation will once again spread some cheer to kids who really need it. Thanks to the thousands of dollars and hundreds of toys donated by our supporters, we were once again will bring Christmas in July to the children at Duke and UNC Children’s hospitals. Led by the one and only Santa Claus, volunteers will distribute toys to the sickest children in the hospitals. Christmas in July is important in that it fills a recreation and activity gap in the summer when so many volunteers, staff, and students are away. Continue reading