Was SIA diagnosed with Ehlers-Danlos Syndrome?
“Chandelier” singer Sia has revealed she has a rare genetic condition called Ehlers-Danlos syndrome that results in chronic pain. The disease affects 1 in 5,000 people globally. It causes hypermobile joints, loose, stretchy skin, and ongoing fatigue, which makes someone more prone to injury and chronic pain.
Does Ehlers-Danlos make you skinny?
Ehlers-Danlos syndrome (EDS) is a disease that weakens the connective tissues of your body. These are things like tendons and ligaments that hold parts of your body together. EDS can make your joints loose and your skin thin and easily bruised. It also can weaken blood vessels and organs.
What mimics Ehlers-Danlos Syndrome?
Tnxb−/− mice showed progressive skin hyperextensibility, similar to individuals with Ehlers–Danlos syndrome. Biomechanical testing confirmed increased deformability and reduced tensile strength of their skin.
Do any celebrities have EDS?
Australian singer/songwriter Sia (born Sia Kate Isobelle Furler), 43, is known for wearing elaborate wigs and headpieces that hide her face. However, the “Chandelier” singer is not hiding the fact that she was recently diagnosed with the connective tissue disorder Ehlers-Danlos syndrome.
What syndrome does singer CIA have?
Oct. 7, 2019 — The singer Sia revealed that she has chronic pain, a neurological disease and a connective-tissue disorder called Ehlers-Danlos syndrome.
How is a diagnosis of Ehlers Danlos made?
A diagnosis of the Ehlers-Danlos syndromes (EDS) is typically based on the presence of characteristic signs and symptoms. Depending on the subtype suspected, some of the following tests may be ordered to support the diagnosis: [1] [2] [3]
Is there a genetic cause for hypermobile Ehlers Danlos?
Although hypermobile Ehlers-Danlos syndrome is regarded as a genetic condition, the underlying cause ( gene or genes responsible) has not been identified. [1] [7] Although the underlying genetic cause of hypermobile Ehlers-Danlos syndrome is unknown, it appears to follow an autosomal dominant pattern of inheritance. [1]
What’s the life expectancy of a person with Ehlers Danlos?
The long-term outlook ( prognosis) for people with Ehlers-Danlos syndromes (EDS) varies by subtype. The vascular type is typically the most severe form of EDS and is often associated with a shortened lifespan. People affected by vascular EDS have a median life expectancy of 48 years and many will have a major event by age 40.
Is there a cure for Ehlers Danlos syndrome?
Depending on the subtype, EDS may be inherited in an autosomal dominant or an autosomal recessive manner. There is no specific cure for EDS. The treatment and management is focused on preventing serious complications and relieving associated signs and symptoms.