At just seven years old, Noah Quish from Monaleen, Limerick, has endured a series of complex medical challenges that would test the resilience of even the strongest individuals. Born in March 2017, Noah was diagnosed with multiple health conditions, including a congenital heart defect, severe obstructive laryngomalacia (a condition affecting the airway), Chiari malformation of the brain, severe sleep apnea, scoliosis, and a chromosome deletion. These diagnoses have necessitated numerous surgeries and continuous medical care throughout his young life.

Noah Quish History of Surgeries

Noah’s medical journey began early. At just four months old, he underwent open-heart surgery to address his congenital heart defect. This was followed by surgery on his airway to alleviate breathing difficulties. As he grew, the challenges compounded. In a span of six months, Noah endured six brain surgeries due to complications arising from hydrocephalus—a condition characterized by an accumulation of fluid in the brain. These complications included severe infections, such as meningitis, which further jeopardized his health. Additionally, Noah has undergone procedures on his lungs, appendix, and stomach, bringing the total count of his surgeries to 15 by the age of seven. Despite these relentless medical interventions, Noah’s spirit remains indomitable.

The Battle with Scoliosis

One of the most pressing issues Noah faces is severe scoliosis—a condition where the spine curves abnormally, leading to significant discomfort and potential complications with internal organs. The curvature of Noah’s spine has progressed rapidly, exerting pressure on his lungs and stomach, which has resulted in chronic pain and respiratory challenges. His mother, Una Quish, has expressed deep concern over the impact of scoliosis on Noah’s quality of life, noting that he often experiences fatigue and discomfort, making daily activities increasingly arduous.

Challenges in Accessing Timely Care

The journey to secure appropriate medical interventions for Noah has been fraught with obstacles. His scheduled scoliosis surgeries have been canceled multiple times—three times in a single year—due to various factors, including the unavailability of his surgeon and Noah’s own health complications. These repeated cancellations have not only delayed critical treatment but have also taken an emotional toll on the family. Una has voiced her frustration and concern, emphasizing that the delays exacerbate Noah’s condition, leading to further deterioration of his health.

Seeking Specialized Treatment Abroad

Given the challenges faced domestically, Noah’s family is exploring options for specialized treatment abroad. They have identified a medical facility in the United States that offers advanced therapies tailored to Noah’s unique needs. However, the cost of such treatment is substantial, with estimates reaching €20,000. This financial burden is beyond the family’s means, prompting them to initiate fundraising efforts to ensure Noah receives the care he urgently requires.

Community Support and Fundraising Initiatives

The local community has rallied around Noah, organizing various events to raise the necessary funds for his treatment. One notable initiative is the collaboration between the Morning Star Vintage Club and other local organizations to host a tractor, truck, and car run. This event is scheduled to commence from Ballylanders GAA club, traversing through Galbally to Lisvernane, and returning to Ballylanders. Such events not only aim to generate financial support but also serve to raise awareness about Noah’s condition and the broader challenges faced by children with complex medical needs.

In addition to community events, an online GoFundMe campaign titled “Noah’s Long Road to Recovery” has been established. This platform provides an avenue for well-wishers from around the world to contribute to Noah’s medical fund. The outpouring of support has been heartening, reflecting the collective compassion and solidarity of those touched by Noah’s story.

A Mother’s Plea for Her Son’s Future

Una Quish remains steadfast in her determination to secure the best possible care for her son. She has been vocal about the systemic challenges within the healthcare system, particularly concerning the delays and cancellations of critical surgeries. Una emphasizes that time is of the essence, as prolonged delays could lead to irreversible damage to Noah’s health. Her advocacy underscores the need for timely medical interventions and the importance of a responsive healthcare infrastructure that prioritizes the needs of vulnerable patients.

Conclusion

The journey of young Noah Quish is a testament to resilience, hope, and the unwavering love of a family determined to overcome daunting challenges. As they navigate the complexities of securing specialized medical treatment, the support of the community and compassionate individuals worldwide plays a pivotal role. Through collective effort and generosity, there is hope that Noah will receive the care he needs to lead a healthier and more fulfilling life.

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