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Our daughter Maggie was born with a very rare genetic difference. When she was first diagnosed, we were told that many children with her condition face significant challenges, including delays in walking, talking, eating, and other developmental milestones. Despite these predictions, Maggie has already overcome so much in her young life. She is a social butterfly who loves making people laugh, playing with her sisters, and spending time with her baby dolls and pretend kitchen. We know really well that joy and sorrow often walk hand in hand. Amidst all the miracles we have seen, Maggie still faces daily challenges and developmental delays which impact her life currently and will in the future.
Since Maggie was just a month old, our family has been committed to doing everything we can for her, attending physical, occupational, and speech therapy to give her the best possible start. We have come across the opportunity to take Maggie to a neurological clinic in Asheville, North Carolina for an intensive weekly treatment. This therapy includes light therapy, hyperbaric oxygen chamber sessions, and cellular therapy. We believe this treatment could help Maggie resolve her primitive reflexes and most importantly, open the door for her to advance in various milestones. In addition to the therapy, we are also raising funds to purchase equipment for long term therapy at home, including a violet/green light laser ($18,500) vibration plate, etc.
So many people love Maggie. We have seen that over and over again these past 3 years. Any way you would like to support Maggie on this journey would be so appreciated by our family!!
Much Love,
Tyler, Ashleigh, and the Girls

