My son is why! at 28 weeks pregnant, my husband and I were told that our baby has a Congenital Heart Defect called Tetralogy of Fallot and would require surgical intervention early in his life to survive.
At 3 weeks old, Mathew had open heart surgery and this will not be the last procedure he will endure because TOF is a life-long diagnosis
Please support us as we walk for babies like Mathew with the American Heart Association on September 28th. Mathew is Why ; Life is why <3