Congenital Sucrase Isomaltase Deficiency
A Congenital Sucrase Isomaltase Deficiency story
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.
Find people with Congenital Sucrase Isomaltase Deficiency through the map. Connect with them and share experiences. Join the Congenital Sucrase Isomaltase Deficiency community.