for individuals with 22q 11.2 deletion syndrome. Our mission is to connect families and individuals affected by 22q (Velo-Cardio-Facial syndrome, DiGeorge Syndrome) and related disorders. Our son Jonah was diagnosed with 22q 11.2 deletion syndrome when he was 21 months old and is our inspiration for starting this support group.

This is Landon Steele Sands' adventure with 22q11.2 Chromosome Deletion (Digeorge syndrome).