fear

Weight gain in eating disorder recovery

Recovery belly

For most of us recovery means committing to weight gain. Learning to accept our bodies unsuppressed natural weight. Getting there has for me been far harder than simply just putting on weight. It’s weight we were never meant to have lost, our bodies didn’t want us to lose this weight but learning to accept this doesn’t happen overnight. We taught it that losing weight feels good, gaining weight feels bad. We taught our brains to believe “skinny = happy” but we know this isn’t the truth. I was never more unhappy than when I was at my sickest. My emotions blunted, isolated from friends, family and bound by strict rules that my life revolved around. No I was not happy. I was a ghost.

But that doesn’t mean accepting weight gain was/ is easy. It’s going against everything I’ve taught myself to believe is ideal. The weight restoration phase on ED recovery is a small part but is so painful because of our neural pathways and our beliefs and distortions.

Weight restoration is messy. I think if no one has told you, now is a good time to tell you. When you gain weight after waging war against your body, your body no longer trusts you. Whether this is from diet cycling, restriction, purging or over exercising. Your body likes to be in homeostasis and sits at a steady weight when left to its own devices. But when we intervene everything slows down, the body has a massive freak out. It thinks its starving (which in many of our cases it literally is) and when we start eating again the body is like, oh thank fuck. It holds on to everything initially in case we are cruel enough to inflict war on it again. The most common place this extra weight/ fat goes to is the tummy a.k.a the “recovery belly”. You can easily look 6 months pregnant. I look pregnant now. Staving off unwanted comments can be an unwanted side effect. But if this happens it’s because you are recovering and doing well so don’t give in. This is hard. My belly has been here a while and likely It’s here to stay for a while yet. I have made peace with it, doesn’t mean I don’t freak out when I see it in reflections some days. Today has been a hard day. But I know it’s keeping me alive and acts as a reminder to not go backwards and the progress I’m making. I know it will redistribute and if it doesn’t well then I’ll learn accept that too. I did a lot of googling when I started my weight restoration journey and so I expect with time my body will trust me once more, so long as I am kind to it.

Doesn’t matter how much I hated how I looked at my sickest, I was still terrified of weight gain. I have had to and am working very hard on rewiring this fear. By challenging it every day. This has involved many melt downs, sobbing in the shower but it’s so much easier with time as your brain shifts with you. This takes a bit of time.

Ditch the scales..

Ditch the scales. They are not your friend. You should break up with this unloving/ non compassionate partner, it’s a one sided relationship. ( *There may be times where you have to be weighed for medical reasons) this does not mean YOU need to know your weight. If this scenario occurs request it to be blind, because no matter what the number, it will not serve your recovery but it will fuel your ED.

My relationship with the scales was messy, unforgiving. In my depths of my ED, I would live my days by the number in the morning. It would stipulate whether I was going to have a good day or bad day, whether I deserved to eat. I would weigh myself multiple times a day and go to great lengths to do it. In early recovery I used it as an excuse I was making progress. BULLSHIT, I was still using it as an excuse not to gain “too fast”, “too much” this is not recovery.

You do not need to deserve to eat. Eating is a necessity every one shares. Your weight does not define you. It is a number. It means nothing in relation to health, your worth. So ditch them. I binned mine. I have no idea what I weigh now. It’s not relevant because I am getting healthy. Sure in early recovery teams may need to know our weights. We do not. Be free and kind to yourself.

Ditch the things that are holding you back in ED recovery

Fitness trackers. These are not our friends in ED recovery. I do not think anyone with an ED history should EVER wear a fitness tracker watch etc. similarly to the scales my day revolves around steps, calories burned, moving raising my HR bla bla bla. Why would you need it unless training for an Olympic event? I don’t even really see the necessity for my patients because if they have problems with HR etc it’s monitored formally. So like my scales I binned my watch. It wasn’t easy but it will be liberating I assure you.

So I hope if this resonates you can make some changes and move forward. You deserve better. Your worth cannot be defined by a number.

Eating disorders don’t discriminate

Eating disorders affect any age, gender, body size, ethnicity and socioeconomic background

One of my main motivations for starting this blog was to contribute from the ground up in informing misconceptions surrounding eating disorders.

Look at the person to your right, look at the person to your left and in front of you. (If you’re currently alone try this next time you’re in a room full of people). Chances are one of those people has had some form of struggle at some point in their life with relationship with food/ body image.

If you’re like me, you had possibly never thought about what a person with an eating disorder looked like before you had one or supported a person suffering with one. Eating disorders affect ANYONE. The sad truth is, society has helped create an image of what an eating disorder should look like. Typically a white, emaciated, teenage girl with anorexia nervosa. Although I fitted this demographic, this is actually the rarity. I want to help change people’s understanding of this. I want treatment to be available to everyone, this happens with awareness of what an eating disorder really looks like.

A person in a “larger” body may be as unwell as the stereotypical emaciated person. Anorexia, can affect any size, weight and BMI cannot identify this. A person in a larger body is less likely to seek help when they are significantly impaired by disordered thoughts or physiological consequences of eating disorder. They can be as malnourished as a person who appears emaciated. Seeking help is harder, why? Because when a person in a larger body loses weight they are often rewarded by society, health professionals. Making it impossible for them to find help or feel like they need help. Health professionals carry their own biases and this needs to change.

Additionally anorexia although the most portrayed eating disorder, is the least common eating disorder. Binge eating disorder, Bulimia, OFSED are more common but talked about less. Why? Because often they are not the stereotypical image.

Globally eating disorders affect close to 1 in 10 people (10% roughly)

Eating disorders have the highest mortality than any other psychiatric illness. Startling.

Before I started recovery, I used to get angry with myself. I questioned how as a doctor I could possibly be having this struggle. I have seen first hand the consequences of eating disorders. Even in the thick of my disorder I treated patients medically, this makes me feel sad now. There was a constant dissonance within. It was like a DVD playing on repeat in my brain, you should know better, you’re a doctor, why don’t you stop? This highlights beautifully the grip an ED can have on someone. It is a mental illness. I could not stop. It was not a choice. It was not a diet “gone wrong” I didn’t like being thin, although I couldn’t stop. So how can we expect others to understand when we don’t understand ourselves.

Not only was I a doctor, I was an adult and in healthcare there is a stigma towards anything other than being 100% all the time, let alone suffering from a mental health problem. Not only did I question myself, how could I be so irresponsible as a doctor. I received the same judgement, confusion from those I chose to share my struggle with. They could not understand how a healthcare professional could behave this way. That made the inner disgust and struggle that the ED likes to feed on so much more powerful. This was not their fault, this is society’s lack of understanding of mental health full stop.

This, I hope highlights how EDs sink their ugly claws in, and become an unwanted hitchhiker. The sufferer may think they have control, but when challenged to stop behaviours, thoughts they cannot. It adds to shame when people describe eating disorders as a choice. Some EDs may have started from “good intentions” like a special diet for health reasons etc, but once the disorder develops, takes hold it is crippling. My ED was a perfect storm, I had the “perfectionism traits” genetic vulnerability and I dieted. I wanted to stop, I did know better, I couldn’t stop until I sought help. But once I knew it was an illness, even if others didn’t understand (they don’t have to) I could use it to my advantage and make choices towards recovery. EATING DISORDERS are not a choice, or a lifestyle. They are a mental illness.

The earlier someone seeks intervention for an eating disorder the better the outcome. That’s not to say that someone who has had an ED for many years cannot recover, because ANYONE can recover. But recognising signs you or someone has an eating disorder is the first step towards recovery. Understanding the diversity within eating disorders is fundamental to change.

When will I be done?! Anorexia recovery

If you’ve read my “About page” you know how my eating disorder started.

Let’s get real about some things I wish I’d known when I started recovery. I hope being for-warned is forearmed.

When I finally sought help, I couldn’t bring myself to acknowledge or repeat the diagnosis I was given Anorexia nervosa, restrictive type.
My therapist was patient, despite my denial. She normalised the name, she used the term anorexia as if it was as routine to her as me diagnosing my patients with asthma, diabetes- no judgement. And really why should it be any different. But still, It felt dirty and shameful, I know now this was the ED talking. The ED does that, makes you think it’s your fault that your eating disorder does not deserve the same care or compassion any other diagnosis would. It’s a choice right? You can stop anytime. If you could- it’s not an eating disorder, eating disorders lull you into a false state of security and control. You think you are in control. But when asked to stop, why can’t you? Because you are unwell, you are not in control, it’s not your fault and it’s not a choice. Recovery is a choice. It is the best choice you will ever make.

After I was officially diagnosed with anorexia, orthorexia, perfectionism and over exercising my first question was; if what you say is true, when will I be done?

SO WHEN WILL I BE DONE?

This is a common question I’ve come to learn many of us ask. You will be done when you are done. Some people’s recovery takes months, some much longer, years. BUT I think the most important take home from this is, this is your journey, no one can tell you “when you’ll be done”

“your worst day in recovery is never as bad as your worst day in the ED” .

If I think I’m having a bad day, be it loud “HH” thoughts, criticism or self image, I remind myself of how far I’ve come and repeat this phrase. Thankfully the “HH” thoughts are now just a mere fleeting whisper in the wind.

Who knows how much healing you have to do, physically & mentally. The years, months of damage you’ve done by going into war with your body. But one thing is true…each step towards recovery gets easier, each step outside of the grips of your ED. Each positive step is a little bit further than the day before. I heard this phrase early in my recovery and I think there is nothing more true:

The next thing that I wish I knew when I first started recovery…

RECOVERY IS NOT LINEAR, it is NOT PERFECT

Since then I’ve had some pretty big lapses and one full relapse. But I learnt from them. I feel stronger for them.

Slips happen. It’s how you get over them that counts.

3. Recovery is hard.

There are many things we are told about when starting recovery, looking out for signs of refeeding syndrome ( metabolic disruption when nutrition is reinstated, can be life-threatening), but no one tells you: Healing is painful. It will always get worse before it gets better. But it does get better. Stick with it.

The oedema, the irratic bowels, bloating, nausea, fluid retention, acne, night sweats, second puberty, growing pains, awakening of your numbed emotions ( often leading to a clusterfuck of emotions all at once without warning), the changing body shape, uneven weight distribution. I will write a seperate post on this. I think this is a blog in itself. It takes strength to recover, it is easy to continue in what comes easily and takes a lot of unlearning of many beliefs and behaviours. It’s exhausting. BUT IT GETS better. It’s also not complicated. Food is medicine. Resting is healing. These are just a few things I wish I’d known early on in the recovery process. There’s many more thing’s iv’e learnt along the way that have been helpful, some not so much. I intend to share these on this blog, hopefully by sharing my experience you may find something to help you in your recovery.

Sharing is promoting awareness and I hope changing the stigma.