Sweet Nectar Society

 

PHOTOGRAPHY WITH A PURPOSE

Lilianna :: Congenital Muscular Dystrophy SYNE 1 gene

Meet Lilianna! Lilianna was born with a rare form of Congenital Muscular Dystrophy SYNE 1 gene. For the first five and a half years of Lilianna’s life she went through numerous tests, therapies and equipment without having a specific diagnosis. She was considered severely hypotonic and failure to thrive. But she continued to fight through her first year of life and defied the doctors expectations. She crawled at the age of 23 months and after assistance of a Kid walk and K-walker she miraculously got up one Sunday afternoon at 3 years and one month and walked on her own. She has never looked back. God has given her a strong, stubborn personality that has overcome her physical weaknesses.
Join Sweet Nectar Society in encouraging sweet Lilianna to keep on breaking through others expectations!

Lilliana_1-3 Lilliana_1-2


PHOTOGRAPHY DONATED BY Angela Eller 

Session Info

SWEETIE SESSION

•A free photography session

•A digital gallery of images

•A keepsake book

•A platform to raise awareness

•Story shared for support

PATIENT SPOTLIGHT SESSION

Provides documentary type photography session to patients currently admitted to the hospital.

•A digital gallery of images

•A keepsake photo

FOCUS SESSION

Portrait session events designed to raise awareness to a specific diagnosis, build community, and celebrate Sweeties.

•A digital gallery of images

•A keepsake photo

(559)408.5969 | info@sweetnectarsociety.org

Sweetly rooted in California