April 21, 2024, Saraeyah Rose Durocher, aged just 7 months, peacefully departed from this world, leaving behind love and resiliency in her memory. She passed away at home, surrounded by her loving family, capping a short but incredibly influential journey.
At the tender age of 3 months, Saraeyah was diagnosed with Gaucher’s type 2 Disease, a rare genetic disorder. Her perseverance and unwavering attitude never stopped astounding her family, even in the face of this disease’s difficulties. Her diagnosis only strengthened the bond within her family, as they rallied around her with love and support.
Saraeyah was born on September 4, 2023, in the serene town of Potsdam, into the loving arms of her parents, Jenalee Durocher and Spencer Konitsiotis. From the moment she entered their lives, she became the embodiment of joy and happiness, bringing light to every corner of their home.
What is Gaucher Disease?
Pronounced “go-shay,” Gaucher disease is an inherited lysosomal storage disorder (LSD) that results in the accumulation of fatty molecules, or sphingolipids, in the spleen, liver, and bone marrow. Sphingolipids cause your organs to grow and weaken your bones, which prevents them from functioning properly. Although Gaucher disease has no known cure, some treatments can significantly enhance the quality of life and reduce symptoms.
Types of Gaucher Disease
Gaucher’s disease comes in three varieties. They all result in comparable symptoms in your bones and organs. Certain variations of the illness also impact the nervous system and brain.
Gaucher disease type 1
Type 1 Gaucher disease affects your spleen, liver, blood, and bones. It is the most prevalent kind in the United States. It has no effect on your spinal cord or brain. Type 1 Gaucher illness has no known cure, however it can be managed. Some folks just have minor symptoms. Some suffer from significant bruising, exhaustion, and discomfort, particularly in their abdomen and bones. Any age, from early childhood to late maturity, might have symptoms.
Gaucher disease type 2
Gaucher disease type 2, a rare form of the disease, appears in babies under six months of age. It results in serious brain damage, an enlarged spleen, and mobility issues. The second kind of Gaucher illness has no known cure. Typically, babies with this illness die between two and three years of age.
Gaucher disease type 3
While type 3 Gaucher disease is the most common worldwide, it is uncommon in the United States. It causes anomalies in the bones, organs, and nervous system (brain). It usually manifests before the age of ten. Many patients with type 3 Gaucher illness can survive into their 20s or 30s with the help of treatments.
A Farewell to an Angel
As Saraeyah bid farewell to this world, she left behind a legacy of love, courage, and resilience. Those who were fortunate enough to have known her will always be affected by the effect she left behind, even though her time on earth was short. Even though she may have attained angelic wings, her cherished family and friends will always carry her memories forward.
Giving Back
In place of flowers or gifts, the family suggests contributions to the National Gaucher Foundation. Donations can be sent to their address at 5410 Edson Lane, Suite 220, Rockville, Maryland 20852. By supporting the foundation, we honor Saraeyah’s journey and contribute to the ongoing fight against Gaucher’s Disease, ensuring that other families receive the support they need.
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