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Juvenile Diabetes is also known as Type 1 Diabetes Mellitus, is a chronic autoimmune condition in which the pancreas produces little to no insulin which is a hormone essential for allowing glucose to enter cells for energy. Unlike Type 2 diabetes, it often starts in childhood or adolescence, but it can develop at any age. Managing this condition requires lifelong insulin therapy, blood sugar monitoring and lifestyle adaptations.
Frequent urination and excessive thirst
Sudden and unexplained weight loss
Extreme hunger even after eating
Fatigue and weakness
Blurred vision
Mood changes or irritability
Bedwetting in children who previously didn’t
Slow-healing sores or frequent infections
Autoimmune response mistakenly attacks insulin-producing beta cells.
Genetic predisposition plays a significant role.
Environmental triggers like viruses or dietary factors in early childhood.
Family history of Type 1 Diabetes increases risk.
Diabetic ketoacidosis (a life-threatening condition due to insulin deficiency)
Long-term organ damage affecting kidneys, eyes, nerves and heart
Growth delays in children
Increased risk of other autoimmune disorders
Skin and foot complications
Family history of Type 1 Diabetes
Certain genes linked to autoimmune diseases
Viral infections during infancy or early childhood
Early introduction of cow’s milk or gluten (being researched)
Geography – higher prevalence in colder climates
While Type 1 diabetes currently has no guaranteed prevention, these steps may help with early awareness:
Genetic testing in high-risk families
Monitoring for islet autoantibodies in children with family history
Breastfeeding for at least 6 months may offer protective benefits
Delay introduction of cow’s milk in infants when possible
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