Asher Blake Jay, age 2, was recently diagnosed with a rare and incurable genetic disorder. His care requires frequent travel and ongoing support, creating financial strain on his family. Please consider donating or sharing to help ease the burden and support Asher’s journey. 👉 Donate now to help ease travel
🧬 What’s happening in the body SDS commonly involves exocrine pancreatic insufficiency (EPI). That means the pancreas doesn’t produce enough enzymes to break down food. Key Dietary Issues 1. Poor Fat Absorption Fats aren’t digested well Can lead to: Greasy, loose stools Poor weight gain Low energy 👉 This is one of the biggest concerns 2.Malnutrition & Growth Challenges Difficulty absorbing calories and nutrients Children may: Struggle to gain weight Fall behind in growth Especially fat-soluble vitamins: Vitamin A – vision, immune system Vitamin D – bone health Vitamin E – nerves, muscles Vitamin K – blood clotting 👉 These require fat to absorb, so levels can drop 3. Higher nutritional demands due to chronic illne May need: Extra calories Balanced protein intake Abdominal discomfort Bloating Frequent or bulky stools Pancreatic Enzyme Replacement Therapy (PERT) Taken with meals/snacks Helps digest fats, proteins, and carbs Very important for SDS 2. High-Calorie Diet Nutrient-dense foods Frequent meals/snacks 3. Vitamin Supplementation Especially A, D, E, K Often prescribed in special forms for better absorption 4. Specialized Nutrition Support (if needed) High-calorie shakes Feeding support in some cases