A Heber Springs family is asking for community support as they face an unimaginable battle with a rare and incurable brain disease.

Loree Garriott, known by friends and family as a lifelong caregiver and source of encouragement to those around her, has been diagnosed with Creutzfeldt-Jakob Disease, commonly known as CJD. The disease is extremely rare and currently has no cure.
After receiving a bleak prognosis in August 2024, Loree has continued to fight beyond expectations. However, the disease has progressively taken away her memory, speech, and independence, leaving her in need of constant, round-the-clock care.
Family members say Loree’s condition has continued to decline in recent weeks. She is no longer able to eat solid foods and now relies on smoothies and protein shakes for nutrition. She sleeps much of the day and shows signs of discomfort and pain.
Her husband, Michael Garriott, continues working full-time while also serving as her primary caregiver, creating emotional and financial strain on the family.
Loree’s daughter, Emalee Jaco, has launched an online fundraiser through AngeLink to help cover essential caregiving expenses, medical supplies, and daily care needs. The goal is to ease the burden on the family so Michael can focus on spending meaningful time with his wife during this difficult season.
Supporters say the fundraiser also aims to raise awareness about CJD and the challenges families face when navigating rare diseases with limited resources.
Community members who wish to learn more or contribute can find the fundraiser online HERE!
















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