What mental health problems are common in EDS? Research has shown that anxiety, depression, and other mood disorders are common in EDS patient populations. Somatoform disorders, where patients experience pain and fatigue without a known cause, are also common in patients with EDS.
Likewise, can EDS lead to depression?
Recent research has shown that patients with EDS have a higher prevalence of anxiety, depression, and personality disorders.
Moreover, does EDS Cause ADHD?
They found that 4.3% of all EDS patients had an ADHD diagnosis, compared to 0.8% in the control group. Siblings of those with EDS also had an increased incidence of ADHD compared to siblings in the control group. In those persons with hypermobility syndrome, 3.0% had ADHD compared to 0.5% in the control group.
Does EDS cause anxiety?
There is increasing evidence pointing towards a high occurrence of anxiety among those with hypermobile type Ehlers-Danlos syndrome (hEDS). There is also limited but growing evidence of a link with depression, eating, and neuro-developmental disorders.
Does EDS show on MRI?
MRI can help detect lesions in the brain containing collagen fibers, which are often seen in EDS patients who previously experienced trauma.
Does Ehlers-Danlos affect the brain?
Because EDS is a connective-tissue disorder, it is not commonly associated with the brain or the nervous system. However, there is evidence that some types of EDS can affect the brain. Studies have suggested that patients with EDS might be susceptible to damage to brain cells after even a mild traumatic head injury.
Does stress make Ehlers-Danlos worse?
Whether emotional, physical, or environmental, the impact of stress is felt more intensely in people with hEDS & HSD: This internal, and very real effect, is akin to feeling deafened by music that others can barely hear.
What is the life expectancy of someone with Ehlers-Danlos syndrome?
People affected by vascular EDS have a median life expectancy of 48 years and many will have a major event by age 40. The lifespan of people with the kyphoscoliosis form is also decreased, largely due to the vascular involvement and the potential for restrictive lung disease.
What is the life expectancy of someone with hypermobile Ehlers-Danlos syndrome?
Patients with the classical and hypermobility forms of Ehlers-Danlos syndrome have a normal life expectancy. About 80% of patients with vascular Ehlers-Danlos syndrome will experience a major health event by age 40 and the life expectancy is shortened, with an average age of death of 48 years.
What medications help with EDS?
Nonsteroidal anti-inflammatory drugs (NSAIDs), tricyclic antidepressants, and serotonin/norepinephrine receptor inhibitors (SNRIs) are commonly given to EDS patients. Muscle relaxants and magnesium can also relieve muscle spasms. For severe pain, opioids may be prescribed.
Why does hypermobility cause anxiety?
The experience of anxiety is greater and more frequent in people living with this condition than in the general population. Dr Jessica Eccles can explain this increase in anxiety by the fact that people with hypermobility are more sensitive to bodily feelings, such as changes in sensations like heart rate.