Why are psychiatrists so ignorant about eating disorders?

ShameScale

I recently accompanied a friend to an intake appointment at our local eating disorder treatment centre.  The program operates out of a psychiatry program at a major hospital in our city.  It’s a medium sized city, and a fairly well known treatment program which is publicly funded and free to access.

I was completely disgusted by a good portion of what the Dr said.   Sadly, many of the things he said were things I have personally heard from other doctors.   I found it pretty triggering and it wasn’t even my appointment.

Let me share a few thoughts about what NOT to say to someone in recovery from an eating disorder (especially if you are a Dr who is supposed to be an expert!):

  1. Do NOT ask people about their history with traumatic events and then proceed to tell them that their abuse is connected to their eating disorder, but that your eating disorder program does not treat trauma.   This makes absolutely NO sense.  If aren’t willing to help someone address the roots of their coping techniques, don’t bother asking intensely personal information.  It comes across as invasive, asking questions for the sake of personal curiosity rather than to actually help someone.

Instead:  All eating disorder programs and specialists should be willing to help patients cope with the traumatic events they have survived.  If they hadn’t experienced those traumas they likely wouldn’t have turned to eating disordered ways of coping in the first place!  You don’t have to be a trauma expert, you just need to be trauma informed.  Validate!  Believe people!  Let them talk about the links between their traumas and their eating disordered behaviours.   I can almost guarantee that nobody will achieve lasting recovery without addressing the root causes of their problematic coping techniques.  Conversely, do not refuse to allow people with eating disorders to access PTSD services.  Do not forbid patients from discussing addictions either.

People don’t exist in boxes.  Someone often copes with PTSD, eating disorder AND addiction.  They shouldn’t be forced to lie about some things to access services for other related issues.   Services NEED to be intersectional or they are borderline useless and can further stigmatize vulnerable people.

2.  Do NOT shame people about their weight, body shape or the foods they eat.  People of ALL shapes, sizes, genders, races and socioeconomic statuses can suffer with eating disorders.  Do NOT promote restrictive eating by underestimating what a healthy amount of food is.  Do NOT set goal weights so low that someone will still be underweight when they finish treatment. Conversely do NOT assume that everyone who has a BMI over 25 is unhealthy.  Fat people can be healthy.   Encouraging someone who is fat to drastically restrict causes shame and further disordered eating.  All bodies look different, people can be healthy at different sizes.  The goal should be to reduce body shame and increase normalized eating.  This will NOT look identical for each person in recovery.  Do NOT place moral values on food such as labeling certain things as “junk” and “unsafe” or off limits.  Believe me, the person with an eating disorder has enough of these nasty thoughts in their head already.   This attitude needs to start with children from a very young age, where they can be taught that food is not something that makes them good or bad.  Our value as humans is not correlated in any way with the food choices we make.  All people have inherent worth or value, no matter their body shape, size or food choices.

Instead:  Promote body positivity within eating disorder treatment.  Do not assume that all recovered bodies will be a certain size.  Encourage people to gradually learn to return to intuitive eating, and trusting their bodies.   Explain that some people in recovery from restricting eating disorders may be extremely hungry while they restore their weight.  This is normal.   It’s okay to eat slightly more than your meal plan if you are genuinely hungry.   Focusing only on BMI, weight and portion sizes can turn into another type of obsessive compulsive eating behaviour.   Teach people that normalized eating can vary from day to day and that is okay.   You aren’t a bad person or shameful because you ate 3 cookies instead of 2.  You aren’t broken or weird if you are still hungry after a 1 cup serving of cereal.  Meal plans are important in early recovery, but they are NOT the be all and end all of treatment.     Don’t treat people who are thin as morally superior to people who are overweight.  Ideally, don’t make comments on people’s bodies at all.

3. Do NOT assume you can tell whether or not someone has an eating disorder based on their appearance.  If someone is struggling with disordered eating symptoms, they deserve care, help and compassion.  It makes NO sense to only provide services to the very sickest people who are basically on the verge of death.  By this point the health consequences can be severe and the behaviours are SO entrenched it can be extremely difficult to recover.  As with most illnesses and mental illnesses early intervention and prevention are KEY.   Providing services based on how medically unstable someone is only encourages people to compete to see who is the sickest.  It makes people who have larger bodies feel they don’t deserve help or aren’t sick enough to MATTER.  It perpetuates the stereotype that only young, white, rich VERY thin women can have eating disorders.  An eating disorder is a serious mental and physical illness and ALL people who suffer, regardless of race, gender, size etc deserve treatment.

Instead:  Stop using BMI alone as a measure of health.  The newest version of the DSM has removed BMI criteria from the anorexia criteria.  Doctors need to follow suit.  Even if someone is at a BMI of 19.5 or 20, or even higher, they can still be struggling with anorexia. Being weight restored or reaching a minimum BMI of 18.5 is NOT the only indicator of recovery.   Ideally body positivity should be encouraged and fostered at all stages of the recovery process.  Governments need to increase funding for eating disorder treatment to make it more readily accessible to folks who are at risk or at the early stages of illness.   Fight fatphobia and discrimination based on weight (and class) when you see it happening around you.

4. Do NOT make negative comments about food at ALL.  I can’t even count the number of times I’ve heard people say things like “I’m so bad for eating this cake”  or even “I feel so guilty for eating a sandwich instead of a salad.”   Don’t promote fad diets.  Don’t promote cutting out whole food categories. Don’t promote the idea of “clean” eating as morally superior.  Don’t imply that eating a salad is virtuous and eating cake is dirty.  Just stop.  PLEASE.  People around you are listening.  Impressionable people. Young kids whose opinions about food are just forming.   Friends and family members who may be struggling with eating disorders themselves.   This may be controversial, but unless you have a food allergy, there is NO need to obsessively eliminate particular foods from your diet.  Everyone has preferences, but that is NOT the same as conferring MORAL value on food.

Instead:  Remember that food can serve many purposes including enjoyment, nourishment, connection (sharing a meal with friends and family), ritual, celebration etc.  but food’s purpose is NOT to cause shame and guilt.  Be vigilant about situations when food is given a moral value (good or bad, clean or dirty).  If you feel confident, let people around you know that judgmental comments about food are not welcome and can be triggering for those in eating disorder recovery and those who are predisposed to developing eating disorders.

We all deserve to have a positive relationship with our bodies and the food we eat.

I wish I didn’t care.

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Intellectually I know that it is counter productive and makes no sense to expect anything at all, anything even remotely approaching care or consideration, from my children’s father.  I know he is a narcissist and I know that he hates me.  I know that he will always be the victim in every situation and that I will always be wrong, bad, crazy or plain evil.  I know that it is unhealthy to expect anything else.  I know that the very definition of insanity would be expecting him to change.   In a way, it is easy to accept that he abhors me and probably wishes me dead.  I can accept that he wanted to be on the other side of the country to me and basically never speak to me again.  I’m okay with that.

What I’m not okay with is how completely he disregards the needs and feelings of his children.  I find myself entirely filled with rage, disgust and despair.   And I get disappointed, angry and upset EVERY SINGLE TIME he fails to meet even a minimum standard of decent parenting.

In March, my younger daughter scratched her eye on a school field trip.  It was luckily fairly minor and healed within a few days with antibiotic drops, but it was still her eye, and it was still scary.  I took her to the ER at the children’s hospital here and I notified her father about the injury and need to seek medical care.   I’m legally required to notify him of doctor’s appointments and medical information, but he never replies or acknowledges the information I send.   It makes me SO angry that a parent, living across the country, would not even text or call to check to make sure his kid was okay.

This week my daughter fell playing soccer and got a concussion.  Again, I took her to the ER and again I notified her father.  I sent him the handouts the Dr gave us and let him know how the injury occurred.  His child has a mild brain injury and he couldn’t even text or reply to the email to check on her?  Really?

I can’t imagine under any circumstances that I would not want to check to make sure my child was okay.   I would be on the phone or texting back the minute I got the email.  I’d be calling her myself to see how she was feeling.

An empathetic, kind person might even ask me how I was doing.  Thank me for taking her to get prompt medical attention.  Thank me for taking care of her during the recovery period.  Apologize for not being there.  React like a normal human and a loving parent.

It’s isolating being a solo parent.  It can be lonely and it can be scary when your child is sick or hurt.  It is a lot of responsibility making the decisions alone.   It’s hard caring for children without much of a break.   It’s bad enough if you are fully alone, or if the other parent is supportive but far away, but it is terrible when the other parent is absent, but not gone and completely working at cross purposes to co-parenting.

I find it very triggering.  I’m so angry and I just want to scream at him.  But he isn’t here and he won’t be here.  I don’t even know if he reads the emails I send, so there isn’t much point in screaming endlessly into a void.  On the other hand, I’m legally required to continue keeping him informed so I feel trapped.

Sending him a message about his child’s health and not getting a response makes me angry.  But if he replied I can almost guarantee that the response would upset me just as much, if not more.  It’s a lose-lose-lose situation.   And the worst part of it is that my kids can see just how little he cares.   He almost only ever engages with them on his terms.  He rarely directly answers their questions (if at all) and often gives roundabout confusing half-answers and suspects them of sneaking around (when they are just asking for a simple password!).   It is truly maddening.

We are all trying to get on with our lives.  A lot of positive things have happened over the last few months.  A greater sense of stability and normalcy has settled into our days.  I’ve been struggling to know exactly what to write about in this blog and what direction to take it in going forward.

For much more of our day to day lives we are freer now.  I can make decisions more easily and accomplish more in a shorter amount of time.  But weeks like this I still feel caged.  I rage at the legal system which has literally forced me to stay in regular contact with my abuser, no matter whether or not he actual responds (or even reads my messages).  I still don’t feel free because he still has some level of control over aspects of our lives.  I try to rise above and to think as little as possible about him and the harm he has caused, but it’s not always possible to block it out.

It’s difficult to move forward knowing that he will never face any legal consequences.  He was able to pick up, move to another province and more or less start over.  He still thinks that I’m “mental” and his mother still thinks that I belong in a mental hospital.  “Once a mental person, always a mental person” she told my daughter.

People who can repeatedly call a child’s mother “mental” to their own children are not good people.  He is not a good person.  I know that, but I’m still angry.  And I’m angry at myself for the strange twisted hope and disappointment I feel every time he fails, yet again to ACTUALLY CARE about any of us.

And the fact that I care SO MUCH means that I am an empathetic, kind, loving human who wants what most people want: connection.   My humanity allows me to be deeply hurt, but I would not trade it for his empty life.