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"Born with a rare congenital heart defect, Grace Wheeler required surgery just days after birth and ongoing monitoring t...
04/05/2026

"Born with a rare congenital heart defect, Grace Wheeler required surgery just days after birth and ongoing monitoring to survive. Thanks to Cleveland Clinic Children’s Infant High Risk Home Monitoring Program, her parents, Randi and Ken, learned to care for her at home, tracking vital signs, medications, and weight while connecting with her care team via telehealth.

Grace successfully recovered from her Glenn procedure and has thrived at home, enjoying playtime, books, and learning, showing remarkable resilience. Her story demonstrates the power of parental involvement, innovative care programs, and teamwork in giving children with complex heart conditions the best chance at life.

Grace’s journey inspires hope for families facing similar challenges, proving that even fragile hearts can thrive with love, guidance, and technology.

📌 Full story in the comments.

"

"The EEG is done, and Ivy’s family is finally enjoying the best snuggles, holding her close and cherishing every magical...
04/05/2026

"The EEG is done, and Ivy’s family is finally enjoying the best snuggles, holding her close and cherishing every magical moment. 💞 Even the days when they cannot hold her feel heavy, reminding them of how precious each second truly is.

Her tiny hands, gentle sighs, and quiet presence turn ordinary moments into extraordinary memories. Every cuddle is a celebration of life, resilience, and love, showing that even amidst medical uncertainty, joy can be found in the simplest connections.

Ivy’s journey is a reminder that love, presence, and family are what make life beautiful, no matter the challenges. Each embrace teaches gratitude, patience, and the power of hope in action. 🥰 Celebrate Ivy’s magical moments with her family and hold onto the wonder she inspires.

📌 Full story in the comments.

"

"At just four months old, Josephine Gilmore was diagnosed with SMA, a rare genetic disease that attacks motor neurons an...
04/05/2026

"At just four months old, Josephine Gilmore was diagnosed with SMA, a rare genetic disease that attacks motor neurons and threatens the ability to walk, eat, or breathe. Her family faced heartbreak and uncertainty, but thanks to a $2.1 million one-time gene therapy injection called Zolgensma, she now shows signs of movement in her hands and legs.

Her journey is documented on the Strong Like Jo page, giving hope to families facing similar struggles. Every tiny movement is a victory, and her parents celebrate each milestone with gratitude and love.

Josephine’s story shows that early intervention, innovation, and unwavering parental dedication can make miracles possible. Her life is a testament to resilience, hope, and the power of love.

📌 Full story in the comments.

"

"At just 1 pound, 7 ounces, Ford Sutton entered the world already fighting for his life, spending his earliest days in t...
04/05/2026

"At just 1 pound, 7 ounces, Ford Sutton entered the world already fighting for his life, spending his earliest days in the NICU surrounded by machines and monitors. Every breath, every ounce gained, and every tiny movement became a victory for his family who celebrated every milestone.

Despite setbacks, fear, and uncertainty, Ford never let go, showing that true courage comes from willpower and determination, not size. His story is about resilience, hope, and learning to treasure the smallest victories because they matter the most.

Ford’s tiny hands and quiet strength remind us all that even the tiniest fighters can have the strongest hearts. Celebrate his journey and be inspired by his perseverance.

📌 Full story in the comments.

"

"Livia was only six days old when a routine checkup revealed her tiny heart didn’t sound right. Her parents were thrust ...
04/05/2026

"Livia was only six days old when a routine checkup revealed her tiny heart didn’t sound right. Her parents were thrust into the cardiac unit, learning their newborn had two holes in her heart and would not survive without surgery.

Five months later, she faced open-heart surgery, and her parents held her close until the moment they had to trust the medical team completely. Waiting hours in silence, fear and hope intertwined, every heartbeat a reminder of how fragile life can be.

Today, Livia’s story is one of resilience, love, and courage, showing that sometimes the hardest part of love is learning how to wait and hope when everything feels uncertain. Every parent, caregiver, and loved one can feel the weight of that moment and the power of faith.

📌 Full story in the comments.

"

"“‘He was blue and frail, barely alive.’ 💔 Easton, a 2-month-old shaken baby survivor, was given a second chance by fost...
04/04/2026

"“‘He was blue and frail, barely alive.’ 💔 Easton, a 2-month-old shaken baby survivor, was given a second chance by foster parents who refused to give up. Through endless love, therapy, and care, he overcame trauma to thrive as a happy, resilient toddler 🌈. His story proves the power of family, hope, and miracles.



📌 Full story in the comments.”"

"MIRACLE BABY: Sophia recovers quickly after rare surgery 💛Born with Down syndrome and a rare duodenal obstruction, Soph...
04/04/2026

"MIRACLE BABY: Sophia recovers quickly after rare surgery 💛

Born with Down syndrome and a rare duodenal obstruction, Sophia underwent minimally invasive surgery just one day after birth. Thanks to Dr. Guelfand and the Cleveland Clinic team, she recovered fast, started feeding within days, and left the NICU in just 14 days. Sophia’s courage and resilience inspire families everywhere 💙



📌 Full story in the comments."

"Fern was self-conscious about her hands, noticing her gloves didn’t fit and saying, “I don’t like my hands” 😢💔. With he...
04/04/2026

"Fern was self-conscious about her hands, noticing her gloves didn’t fit and saying, “I don’t like my hands” 😢💔. With help from a kind stranger and artisans, she received four-fingered gloves, transforming her confidence and joy 🌈✨. Now she proudly exclaims, “I love my hands,” embracing her uniqueness with smiles and play. Representation matters, small acts create big change, and Fern’s story inspires inclusion and empowerment every day.



📌 Full story in the comments.**"

"Samantha Hatch and her husband welcomed twins during an already overwhelming year, only to discover William had a sever...
04/04/2026

"Samantha Hatch and her husband welcomed twins during an already overwhelming year, only to discover William had a severe heart defect and their daughter Penelope was diagnosed with high-risk neuroblastoma.

💔 While William underwent multiple heart surgeries, Penelope endured chemotherapy and emergency procedures that left her temporarily paralyzed. 🏥 Despite the immense challenges, the family found strength, love, and hope, celebrating each milestone and recovery.

Their journey shows that resilience, faith, and unwavering parental dedication can overcome unimaginable medical adversity. 🌟 Samantha and her husband inspire others to advocate, support, and fight for their children.



📌 Full story in the comments."

"Janai Smith faced the unimaginable when her identical twin daughters were born prematurely, each fighting for survival ...
04/04/2026

"Janai Smith faced the unimaginable when her identical twin daughters were born prematurely, each fighting for survival in the NICU. 💔 From life-saving surgeries while awake to endless ultrasounds and transfusions, every day was a test of courage and endurance.

One twin battled necrotizing enterocolitis, the other needed constant monitoring, pushing Janai to her limits. 🏥 Through therapy, family support, and unwavering determination, she overcame fear, trauma, and postnatal depression. Her story is a powerful testament to resilience, hope, and the strength of a mother’s love.

🌟

📌 Full story in the comments."

"🔥 Zachary Sutterfield survived a burning apartment, losing five friends and suffering burns over 70% of his body.Now, a...
04/03/2026

"🔥 Zachary Sutterfield survived a burning apartment, losing five friends and suffering burns over 70% of his body.
Now, at 27, he walks into surgery number 36, a neck and mouth release, continuing a journey filled with pain, hope, and incredible courage.
His mom asks for prayers for his comfort, the medical team, and for her as she supports him through this milestone.
Zach has spent years turning tragedy into purpose, advocating for burn survivors and inspiring hope.
💛 Send him your support and leave a message he can read after surgery.

📌 Full story in the comments.

"

"💛 “TEN FINGERS, TEN TOES?” The answer was NO, and it changed everything.Our son Cade was born with limb differences, a ...
04/03/2026

"💛 “TEN FINGERS, TEN TOES?” The answer was NO, and it changed everything.

Our son Cade was born with limb differences, a left hand with two digits and a tiny flipper-like foot. Fear and uncertainty filled our hearts, but love and community lifted us through.

From prenatal scans to NICU care, every milestone has been a victory. Cade now walks, explores, and thrives, proving that beauty is not defined by convention.



📌 Full story in the comments."

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