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Are there mild forms of Ehlers-Danlos syndrome?
Symptoms range from mild to very severe, and vary with which type of EDS you have. Milder forms of EDS are often not diagnosed until early adulthood, as it can take some time before the symptoms and signs become noticeable. The more severe types, however, are diagnosed mainly in childhood.
Why is EDS skin soft?
It is caused by genetic mutations or errors that affect the collagen protein. Collagen contributes to the flexibility or elasticity of connective tissue. Problems with collagen can lead to a looseness and possible fragility of the skin and blood vessels.
What supplements are good for Ehlers-Danlos syndrome?
We therefore hypothesize that the symptoms associated with Ehlers-Danlos syndrome may be successfully alleviated using a specific (and potentially synergistic) combination of nutritional supplements, comprising calcium, carnitine, coenzyme Q(10), glucosamine, magnesium, methyl sulphonyl methane, pycnogenol, silica.
Does hypermobile EDS have stretchy skin?
If you have hypermobile EDS, common signs include unusual joint flexibility and slightly stretchy skin. The reason for this is because EDS is the result of defects in the type of collagen your body produces.
Should EDS patients take collagen?
Bottom Line: No established research or clinical experience has proven that collagen supplementation is helpful for persons with EDS! Theoretically, a diet adequate in glycine, proline, lysine, and vitamin C (or supplementation) would support collagen biosynthesis.
What is velvety skin EDS?
Patients with EDS often have skin that can be describes as “velvety”, “loose”. This skin characteristic predisposes patients to problems with wound healing. Patients will often note that they develop “paper-thin” scars. Patients also have excessively flexible, loose joints.
Is there a cure coming soon for Ehlers-Danlos syndrome?
There is no cure for Ehlers-Danlos syndrome, but treatment can help you manage your symptoms and prevent further complications.