Lois Watkins
Fundraiser launched for Brighton boy with rare genetic disorder
Description
Planning for her son's future is a priority for Brighton's Alicia Galambos, who has been caring for him 24 hours a day since his diagnosis with an extremely rare genetic disorder.
Four-year-old Mason Galambos is living with Allan-Herndon-Dudley syndrome (AHDS), which is also known as MCT8 deficiency, which requires his mother and father, Jared, to care for him around the clock.
To help the family with mounting medical equipment bills that are not fully covered through insurance, Jared’s aunt Kathy Jackson decided to start a GoFundMe campaign called Mason's Story: Living With a Rare Disorder, which can be found via gofund.me/6ef95416
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Lois Watkins
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community | other
2021-04-03