Raising Awareness About Dwarfism
Another family, The Hugos, had organized a benefit event to help Potentials Foundation, which is an organization which brings people with primordial dwarfism closer. They make annual trips to the National Little People of America conference, where people suffering from dwarfism get the chance to talk about their condition. Hannah got to express her view on this issue, and she talked about her health issues and medical treatment. It’s really important for people with special needs to get in touch with other people diagnosed with the same condition.