Skip to content
Story about Congenital Sucrase Isomaltase Deficiency .

A Congenital Sucrase Isomaltase Deficiency story

Apr 11, 2016


My son has CSID. Diagnosed at 5 years of age. It's been a long journey to get to this point. 

As there is no access to sucraid in Australia, we are purely trying to manage by diet alone. 

As a mother, I will always be a voice for my young son and get the CSID awareness out there, as this disorder is so much more than dietary restrictions. 

Know someone who should read this story? Share it

0 comments

Login or register to leave a comment