Millie has a gene mutation called ~ mandibulofacial dysostosis with microcephaly -~ MFDM for short. It is a very rare condition with only 108 people world wide with this specific mutation! On top of the MFDM, she has another very very rare mutation. The second mutation has never been seen before. Sweet Millie is the only one who tested for this specific test.

With these rare conditions come hospital stays, medical bills and never ending financial stress. As a community we can come together to help support the Conran family!! For more information and updates on Millie, you can follow her on Facebook : https://www.facebook.com/Millie-Jolene-278707125965816/