“Trichotillomania (TTM, also known as trichotillosis, or more commonly as trich) is defined as "hair loss from a patient's repetitive self-pulling of hair" and is characterized by the repeated urge to pull out scalp hair, eyelashes, facial hair, nose hair, pubic hair, eyebrows or other body hair, sometimes resulting in noticeable bald patches. Trichotillomania is classified in the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) as an impulse control disorder, but there are questions about how it should be classified. It may seem, at times, to resemble a habit, an addiction, a tic disorder or an obsessive–compulsive disorder.” (Wikipedia)
Trichotillomania leads to severe and noticeable hair loss, distress, and social or functional impairment", and is "often chronic and difficult to treat". Trich can present as early as infancy but peaks between the ages of 9 to 13. Depression, anxiety, obsessive–compulsive disorder, posttraumatic stress disorder, and stress are common triggers for Trichotillomania. Many with Trichotillomania hide their disorder due to the social implications and embarrassment so it is hard to give a reportable prevalence of this disorder.
Part of the criteria in diagnostician Trichotillomania is an increasing sense of tension before pulling the hair and gratification or relief when pulling the hair. However, some people with Trichotillomania do not even realize they are pulling their hair, that after time it becomes habit or ritual.
Trichotillomania is usually "confined to one or two sites", but can involve multiple sites: "the scalp is the most common, then eyebrows, eyelashes, face, arms, legs, and pubic hairs". Children are less likely to pull from areas other than the scalp. It has been noted that the higher the stress level of a person with Trichotillomania, the more pulling they do.
Psychological effect can be low self-esteem, increased isolation, and increased depression. Medical complications that can result from Trichotillomania are infection, permanent loss of hair, repetitive stress injury, carpal tunnel syndrome, and gastrointestinal obstruction as a result of trichophagia. Trichophagia is when people with trich also ingest the hair that they pull.
Treatment is approached based on the age of the patient. Parents are counseled to ignore the behaviors in pre-school age children, as these children frequently outgrow it. In pre-adolescents to young adults, establishing the diagnosis and raising awareness of the condition is an important reassurance for the family and patient. Non-pharmacological interventions, Habit Reversal Training, including behavior modification programs, may be considered; referrals to psychologists or psychiatrists are considered when other interventions fail. When Trichotillomania begins in adulthood, it is often associated with other psychiatric disorders, and referral to a psychologist or psychiatrist for evaluation or treatment is considered best. The hair pulling may resolve when other conditions are treated. Medications may also be used, especially when there is dual diagnosis.
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How truly awful this must be. I've never known a person to actually eat hair. I thought that was something only cats did and then it's not on purpose. I'm glad to know there is help for these people.
ReplyDeleteI've never heard of TTM so I'm guessing it's not a prevalent disease. I agree with Jude, it sounds awful.
ReplyDeleteThere is a little boy, probably around 6 or 7, who sees the same doctor as my daughter who may well suffer from this disease. I watched him playing with her and he reached up and pulled out several pieces of hair from his head. He played with it for a few minutes and dropped it on the floor. He was a cute little guy. I really felt sorry for him and his Mom who looked totally stressed as she watched him.
ReplyDeleteI've heard the term trich, but certainly never knew the devastation it can cause. I'm glad it's not a common disease and I wish it didn't exist at all. I can't imagine watching your child doing this and not being able to help them.
ReplyDeleteI went to grade school with a boy who had this disorder. I'm not sure at the time that they realized what it was as that was nearly 50 years ago. There was a lot of speculation about why he had no hair and eventually his Mom took him out of school and he finished his education at home. I've often wondered what happened to Joe. He was a nice kid.
ReplyDeleteThis sounds so devastating. I'm glad I've never seen anyone who suffers from this.
ReplyDeleteThat's horrible! I've never heard of this before and I hope I never do again. It upsets me to think that youngsters hurt themselves like this for any reason.
ReplyDeleteAh, I've been at this for about 6 years or so now and I found this a really good description of the condition.
ReplyDeleteOne of the biggest things has to be the ongoing fear of discovery - at someone catching you in the act, seeing exposed patches, seeing under a wig; especially being a female sufferer, when hair is really tied into perceptions of femininity. It wasn't until I finally came round to the idea of wearing wigs after years of bandanas that I finally felt beautiful/acceptable/normal again. Well, partially. ;]
And Sandy, if it makes you feel better, it doesn’t necessarily hurt? It’s more like there are certain no go areas that are like…OUCH but you don’t go for those, you go for the most part where it’s like flicking an elastic band - the twang/snap is what you’re going after. The “hurting” bit is more the social anxiety - the sense that pulling your hair out makes you a freak that especially in school, people will judge you for. So hearing about it is actually good? It makes it that bit more understood by the people undergoing it and the collective circle around them.