Living with Fibrous Dysplasia/McCune Albright Syndrome

Call to Action for the FD/MAS Alliance to help those affected by the rare bone diseases Fibrous Dysplasia and McCune Albright Syndrome. Visit the foundation's website: fdmasalliance....
Created as a project in 2017 by students at Georgetown University.

[@annapatriciabunacruz4318]

Hi!I am a mother of a 7year old boy named alfred james bunacruz who was also diagnosed to have mc cune albright syndrome.you might help us also with the condition of my child.thank you!