Politics
Community Unites for Heartfelt Send-Off of Young Dixon

A heartfelt funeral procession took place in Gore on November 4, 2023, as over 20 trucks, vintage cars, and various vehicles gathered to honor the life of 9-year-old Dixon Bangma. His mother, Elisha Bangma, expressed deep gratitude for the overwhelming support shown by the community during this difficult time.
The procession was organized by Southland Hug a Rig, a group that the Bangma family has actively supported. Given Dixon’s passion for trucks, the family felt it was a fitting tribute. Ms. Bangma remarked, “All these people, they showed such support for my baby boy. He was just ‘him’ and to see such support is overwhelmingly beautiful; it just means so much to us.”
Seeing the array of vehicles filled with supporters left a profound impact on Ms. Bangma’s two other children, who also have Dravet Syndrome. The display of community solidarity was both surprising and uplifting for the family, who had initially faced a bleak prognosis for Dixon. Diagnosed with Dravet Syndrome, it was once thought that he would not survive past five years, but he ultimately provided his family with “four more years of absolutely beautiful serenity.”
The event was not just a farewell; it was a demonstration of love and compassion that resonated throughout the community. Mrs. Elstob, a member of Southland Hug a Rig, expressed her appreciation for everyone who participated in the motorcade. She emphasized how the turnout illustrated the remarkable spirit of the community to support a grieving family.
Looking ahead, Ms. Bangma is determined to establish a foundation in Dixon’s name, aimed at raising awareness of Dravet Syndrome. She hopes to assist other families in accessing the best medical treatment and increasing visibility for the condition. “My son would have wanted nothing more than to help others,” she said.
The outpouring of support for Dixon’s send-off not only honored his memory but also underscored the importance of community in times of sorrow. The Bangma family’s journey highlights both the challenges of living with a rare condition and the power of collective compassion.
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