Menu Close

You wonder whether they can put the pieces of your broken daughter together again


When your child has shown serious signs of disordered eating and goes off to college you are not really sure what is going to happen. Things might go well for her. Or they might not. Your daughter goes off to her dream university with a generous scholarship. Your beloved amazing daughter, who has always had friends and interests and is beautiful and a little too perfect but who you always believed had only the most unquestionably bright future in front of her. That child becomes critically ill the first semester of freshman year. You find yourself in emergency mode driving to pick her up after frantically throwing some hefty bags and boxes in your car and bringing her home on medical leave because she is suicidal and self-harming and has been diagnosed with anorexia binge-purge subtype. You help move her out of her cute dorm room and bring her too tiny jeans home, and sadly remember the optimistic shopping trip you took together to Bed, Bath and Beyond to buy her first living-away-from-home items for her-new-grown-up-life. You drive home at night digging your fingernails into your palms to keep awake at 3 am while your emaciated, vanishing daughter who suddenly seems like a stranger sleeps an uneasy sleep next to you and you drive 65 miles an hour down the highway into an uncertain and frightening and heartbreaking future. But you don’t really know how heartbreaking or how difficult it will be, yet. Or that you will fight against this eating disorder for many years and sometimes it will feel at though you are fighting your daughter because the illness won’t let her understand why she needs to weigh enough in order to help kick the eating disorder to the curb. It is still the beginning and you are still a little innocent.

A year ago you were buying her a nice outfit to wear for her college interviews. You watched her win academic awards at her high school, get her braces off and go to prom looking like a princess. Now you drive her to a psychiatric institute, and she will stay there behind locked doors for 3 months while she learns how to eat again and receives enough therapy to last several lifetimes, in order to try to quiet the demons in her head screaming at her that she is fat even though in reality she is frighteningly malnourished when you leave her there in the florescent-lit hospital corridor with the doctors and therapists, nurses, dietitians, and psychiatrists. You wonder whether they can put the pieces of your broken daughter together again and back to some semblance of herself. You read that eating disorders have the highest mortality rate of any mental illnesses and that only about a third of people who suffer from anorexia nervosa make a full and lasting recovery. You learn that these serious and life-threatening diseases receive the smallest dollar amount of research funding of any mental health condition.

Your daughter is in a world of indescribable pain and so is the rest of your family. You soon learn of her secret life and the lies and the symptoms that she had been hiding from you during high school while pretending to be that perfect daughter who you thought you knew until things spun so far out of control when she left home and stopped eating that she could no longer manage. You learn that these are biological brain disorders with metabolic and genetic underpinnings and that families are not to blame even though you still look for reasons to blame yourself. You continue to get up every day and go to work and visit her in the hospital while her brain starts to come back online again after the period of starvation, and you attend family therapy sessions where you try to envision a life after the hospital and what it will be like and what you need to learn in order to help her get well again. You go on a self-inflicted crash course to learn about eating disorders and read every book you can get your hands on. You watch a video about what to do and say during mealtimes. You reach out to other parents experiencing the same thing on a message board and feel supported and comforted. You feel relieved that your daughter is safe behind the walls of the hospital and that the program is very structured and serious about re-feeding her. You feel calmed that she is cooperating with the doctors and eating her meals and going for walks on the hospital grounds and making friends with some of the other women there and that there are a lot of visiting hours. But you also feel that you have blundered into some sort of nightmare you can never fully wake up from and you are numb and you cry a lot and isolate from your friends and family because, well really, who could ever understand this?

After a long time with lots of challenging ups and downs and steps forward and backward, she tries college again. And you wish you could be like the other empty-nester moms who worry about what bus their child will take home for break, or whether their kid has enough storage in their dorm room, or whether they will meet lasting friends and where they can order a cake in the neighborhood for their daughter’s birthday, and if they will do well in their classes and did they fill out the FAFSA correctly and when is it due. Instead, you visit your daughter often and try to encourage her to be motivated to be recovery minded. You eat meals with her and take her food shopping and watch for any signs of the anorexia creeping back in and when your stomach clenches because you see that it is still there lurking, you do everything you can to keep encouraging her to eat and weigh enough. And you applaud all of her successes, small and large because she worked so unbelievably hard to be able to be where she is right now. Because those SATs, ACT, and AP classes she took and those grades she earned in high school were easy compared to the real work she had to do in order to be able to be this college student now and to move ahead with her life. And you forgive anorexia, and you forgive your daughter for her outbursts and food refusals and emotional dysregulation, and you forgive yourself for what you didn’t do to cause this and most of all, you forgive the universe for sending this terrible, terrible thing into your lives.

Don’t ever give up hope. Just keep going, one meal at a time.


Share this post:


  1. Jen

    This is so on target. It’s amazing how little material and discussion is available for caregivers sending their child to college and either letting go -respecting her hard journey and allowing her to find her way, because this illness is one that will be on the path to recovery when the patient finds herself ready-OR-striving to continue FBT as much as possible, hoping she’ll use us and her team as a resource to help her get to the table and eat. We have done both in these theee years of college. We’ve hoped, we’ve worked with her team, we’ve written and agreed upon contracts, we’ve pulled her home, threats of residential treatment have not been implemented because she refuses to go saying it’s not for her(what’s the point if she won’t buy in even a little? She has been in 2 php programs). Balancing the concept of letting her live her path and doing everything we can to help is confusing and so very uncertain. She does just enough to keep herself afloat and alive (physically), but is still mentally tortured every day from ED. She does very well in school (how when her brain is working without nutrients I have no idea!) We read of stories of those who self recovered, after many many years-I wonder if this is truly the way for her, or is this just the “easy” route for us. Ha. When she’s home it’s torture for her 18 yr H.S. old sister who won’t come to the dinner table, mainly because of the tension and she can’t stand the vegetarian food sister eats. Our ED daughter is always the special one, little sister seems to always be not enough in her mind. It is heart breaking. So, I loved hearing about someone with the experience of sending the kid to college and wish I’d found more to read on this 3 1/2 years ago. I hope to God that your daughter has found her path to recluyera. Thank you for posting.

  2. Debbie Chavarria

    Beautifully written.
    It brought me to tears.
    And although crying can be therapeutic, it has made me ill. Literally. My sinuses are congested. But thank you for writing this. I will save it.
    Love you, Warrior Mama.

  3. Leslie

    I needed that. Thank you. My 13 yr old has just been diagnosed. And I wonder how long it will take to know she’s ok to manage this on her own. I’m guessing years.

Leave a Reply

Your email address will not be published.

Social media & sharing icons powered by UltimatelySocial