Tag: Ehlers danlos

According to one study, up to 86% of patients with hypermobile EDS experience gastrointestinal symptoms, which can severely impact their ability to eat enough protein. While the core genetic issue in Ehlers-Danlos syndrome is flawed collagen production, not a lack of building blocks, adequate protein intake is still crucial for managing associated symptoms and supporting overall health.

While true scurvy, a severe vitamin C deficiency, is rare in developed countries, certain medical conditions are still known to mimic its classic symptoms like fatigue, bruising, and poor wound healing. This makes a thorough differential diagnosis crucial for proper patient care and treatment.

Up to 80% of individuals with hypermobile Ehlers-Danlos Syndrome (hEDS) also experience Postural Orthostatic Tachycardia Syndrome (POTS), a form of autonomic dysfunction. This common comorbidity often prompts the question: **Do people with Ehlers Danlos need more salt?** For many, increasing salt and fluid intake is a crucial, doctor-supervised strategy.

A high percentage of individuals with hypermobility also experience autonomic dysfunction, which is a key reason why people with hypermobility need more electrolytes. Addressing this need is crucial for managing symptoms like fatigue, dizziness, and palpitations, and improving overall well-being.

Individuals with Ehlers-Danlos syndrome (EDS) often experience co-morbid conditions such as Postural Orthostatic Tachycardia Syndrome (POTS) and Mast Cell Activation Syndrome (MCAS), which can significantly alter their physiological responses. For this reason, the seemingly simple question, **is caffeine bad for EDS?**, requires a complex, individualized answer.

While the Ehlers-Danlos syndromes (EDS) are primarily genetic disorders affecting connective tissue, many individuals experience secondary nutritional deficiencies that can exacerbate their symptoms. Understanding **what is deficient in Ehlers-Danlos syndrome** is a crucial part of a comprehensive management strategy, focusing on both the genetic and symptomatic aspects of the condition.

Over 86% of patients with Hypermobile Ehlers-Danlos Syndrome (hEDS) or Hypermobility Spectrum Disorder (HSD) experience some form of gastrointestinal symptoms, which can lead to micronutrient deficiencies. Understanding what supplements to take for hEDS can be a crucial part of a comprehensive management strategy, working alongside medical care to address specific symptoms like joint pain, fatigue, and autonomic dysfunction.