Story about Congenital Sucrase Isomaltase Deficiency , Congenital Sucrase Isomaltase Deficiency.

Millie's Story

Apr 11, 2016

By: Millie


my name is Millie and I was diagnosed with SI at age 18 months as I didn't fall under the top four genetic mutations of CSID and it was too expensive to continue testing, but I follow the exact same diet and can't have sucrose or much starch. I have been sick since I was born and have to be vey strict with my diet.

We don't have access to sucraid in Australia so my mummy and daddy read every label to make sure I won't get sick but it's very hard and I still get sick sometimes and don't know why.

i am nearly 7 and learning to cook some of my own foods

Know someone who should read this story? Share it

0 comments

Login or register to leave a comment


Is Congenital Sucrase Isomaltase Deficiency hereditary?

Is Congenital Sucrase Isomaltase Deficiency hereditary?

Prevalence of Congenital Sucrase Isomaltase Deficiency

What is the prevalence of Congenital Sucrase Isomaltase Deficiency?

Congenital Sucrase Isomaltase Deficiency causes

Which are the causes of Congenital Sucrase Isomaltase Deficiency?

Celebrities with Congenital Sucrase Isomaltase Deficiency

Celebrities with Congenital Sucrase Isomaltase Deficiency

History of Congenital Sucrase Isomaltase Deficiency

What is the history of Congenital Sucrase Isomaltase Deficiency?

Congenital Sucrase Isomaltase Deficiency is also known as...

Congenital Sucrase Isomaltase Deficiency synonyms

Natural treatment of Congenital Sucrase Isomaltase Deficiency

Is there any natural treatment for Congenital Sucrase Isomaltase Defic...

Living with Congenital Sucrase Isomaltase Deficiency

Living with Congenital Sucrase Isomaltase Deficiency. How to live with...