#strangebuttrue Archives

Strange But True — The Walking Dead?

Posted on October 19, 2015 by Sage Robinson

Do zombies really exist? Walking Corpse Syndrome (also known as Cotard’s Syndrome) is a rare neuropsychiatric disorder in which the afflicted person believe he or she is dead, missing their soul, organs, blood or other body parts, and being in a state of existence denial. Conversely, some patients may have delusions of immortality.

For people with this condition, entertainment like cable TV’s “The Walking Dead” may be too close for comfort.

Studies indicate that the disease is more prevalent in older patients and women with depression. It is also more likely to occur in patients with disorders such as:

Schizophrenia
Bipolar disorders
Brain injury
Brain atrophy
Seizure disorders
Depression
Brain tumors
Stroke
Migraine

Lesions in the frontal and temporal regions (front and sides) of the right hemisphere of the brain have been associated with the disease. However, Cotard’s Syndrome is so rare that it is difficult to pinpoint the mechanisms that cause it.

Tests are used to diagnose associated diseases and rule out other conditions. Current treatment for Cotard’s Syndrome involves medication with antidepressants, antipsychotics and mood stabilizers. Electroconvulsive therapy, in combination with medication, has been reported to be more effective than medications alone.

Fortunately, patients with Cotard’s Syndrome can experience a complete recovery, even in severe cases.

All content of this newsletter is intended for general information purposes only and is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Please consult a medical professional before adopting any of the suggestions on this page. You must never disregard professional medical advice or delay seeking medical treatment based upon any content of this newsletter. PROMPTLY CONSULT YOUR PHYSICIAN OR CALL 911 IF YOU BELIEVE YOU HAVE A MEDICAL EMERGENCY.

Strange but True — Alice in Wonderland Syndrome

Posted on August 31, 2015 by Sage Robinson

Alice in Wonderland Syndrome is a rare, but real condition, but it doesn’t involve the Mad Hatter or the Cheshire Cat.

Alice in Wonderland syndrome (AIWS) is a neurological condition where the sufferer has temporary episodes of a distorted perception of their own size and the size of things around them. People with this condition visualize themselves as big as giants or as small as insects. The objects around them also appear abnormally large or small. For instance, someone with AIWS will perceive a teacup either as big as a car or as small as a thimble.

This hallucination-like state typically lasts anywhere from five to 30 minutes. People with AIWS also may experience an impaired sense of space, with objects suddenly seeming very close or far away. In some cases, the sense of touch and sound may also be distorted.

The syndrome references the adventures from the famous novel by Lewis Carroll, where the title character Alice experiences strange events in Wonderland. Many believe that the Carroll himself suffered from this disease and was the inspiration for the story.
The cause of the condition is unknown, although the episodes have been closely associated with the onset of migraine headaches or epilepsy. AIWS can affect anyone, but it is most common in children and young adults. Episodes stop for most over time, but those who experience symptoms are recommended to see a doctor immediately.

Strange but True – Werewolf Syndrome

Posted on August 12, 2015 by Sage Robinson

Werewolf Syndrome does exist but it is not what Hollywood or science fiction depicts it to be. Werewolf syndrome is medically known as hypertrichosis. It is a disorder that is characterized by excessive body hair. Typically the entire body with the exception of the palms of the hands and the soles of the feet are covered in dense hair, which can resemble fur. In some cases hair growth can be localized to a specific body part such as the back, elbows or ears.

Hypertrichosis can be classified into three main subcategories: congenital hypertrichosis terminalis, Naevoid hypertrichosis and congenital hypertrichosis lanuginosa.

Congenital hypertrichosis terminalis- Is often associated with gingival hyperplasia, which causes those that are afflicted to have very few teeth or soft voices.
Naevoid hypertrichosis – Symptoms may include excessive beard growth (men and women), a heavy unibrow, hairy ears and in some cases with underlying spina bifida-a tail on the lower back.
Congenital hypertrichosis lanuginosa- This form of hypertrichosis is extremely rare and is characterized by excessive hair at birth. There have only been about 50 cases reported globally since the middle ages.

Some possible conditions believed to cause hypertrichosis are metabolic disorders or genetic disorders caused by spontaneous mutations. The recommended treatment for this condition is hair removal because it is usually considered a cosmetic problem.