Lindsay is an eight-year-old little girl, who was diagnosed with Pitt Hopkins Syndrome, at the age of two. At the time, no doctor her family encountered had ever heard of it. It is a rare disorder, that little is still known about. Primary complications include being non-mobile, nonverbal, having seizures, and being completely dependent. Since it is so rare, it is also something that Lindsay’ s family’ s insurance company does not acknowledge in most cases. Even with insurance, costs can be astronomical, to cover the therapies, equipment, and support Lindsay needs on a daily basis. Lindsay is ready for a new wheelchair, but doesn’ t qualify for one yet. The Jiselle Lauren Foundation has been able to help Lindsay’ s family grow her current chair to expand the life of her chair and help Lindsay reach her full potential.