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


Latest progress of Congenital Sucrase Isomaltase Deficiency

What are the latest advances in Congenital Sucrase Isomaltase Deficien...

Congenital Sucrase Isomaltase Deficiency symptoms

Which are the symptoms of Congenital Sucrase Isomaltase Deficiency?

Is Congenital Sucrase Isomaltase Deficiency contagious?

Is Congenital Sucrase Isomaltase Deficiency contagious?

Do I have Congenital Sucrase Isomaltase Deficiency?

How do I know if I have Congenital Sucrase Isomaltase Deficiency?

Congenital Sucrase Isomaltase Deficiency cure

Does Congenital Sucrase Isomaltase Deficiency have a cure?

Congenital Sucrase Isomaltase Deficiency causes

Which are the causes of Congenital Sucrase Isomaltase Deficiency?

ICD9 and ICD10 codes of Congenital Sucrase Isomaltase Deficiency

ICD10 code of Congenital Sucrase Isomaltase Deficiency and ICD9 code

Congenital Sucrase Isomaltase Deficiency advice

Which advice would you give to someone who has just been diagnosed wit...