welcome to oneEDSvoice
- a positively charged Ehlers Danlos Syndrome community.- join today!
- login
Ivar the Boneless: Did a Disease Cripple the Infamous Viking
Ehlers-Danlos syndrome is a connective tissue disorder that causes unusually broad joint mobility. EDS also weakens the joints and may increase the likelihood of developing painful joint conditions.
Whereas Ehlers-Danlos syndrome affects connective tissues, Osteogenesis imperfecta is a genetic defect that weakens the bones themselves. Although Osteogenesis imperfecta can cause damage to the joints and muscles, the most common symptom is fragile bones that are prone to break and fracture “from little or no apparent cause.”
It has also been suggested that Ivar was nicknamed “Boneless” because he was impotent. Although there is little, if any, evidence that Ivar the Boneless suffered from erectile dysfunction, he is not known to have fathered any children.
If Ivar the Boneless had a disease that left him physically deformed, it did not deter him from becoming a powerful and ruthless warrior. As reported by English Monarchs, some sources describe Ivar as a “giant” who “dwarfed all his contemporaries.” He was also labeled as a “berserker” who had a reputation for “exceptional cruelty.”
expertly curated content related to this topic
-
21st Century Ehlers-Danlos Syndrome (EDS) Sourcebook: Clinical Data for Patients, Families, and Physicians – C...This comprehensive ebook provides author...
-
Coeliac Axis Thrombosis After Surgical Correction of Spinal Deformity in Type VI Ehlers-Danlos Syndrome: A Case Repo...STUDY DESIGN: An unusual case of postop...
-
Life-Threatening Large Subcutaneous Hematoma after Minor Head Trauma: A Young Female Patient Who was Suspected of ha...Life-threatening large subcutaneous hema...
-
Hospital PrincessThese are the ramblings of my chronic, 2...
-
Ehlers-Danlos Syndrome – A Reference Guide (The Hill Resource and Reference Guide)The Hill Resource and Reference Guide se...
-
Brave 26 year old, Sara Geurts, is launching modeling career while having Dermatosparaxis Ehlers-Danlos syndromeA woman in her twenties with a rare skin...