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Holly’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

A day in the life of a BDD sufferer

Imagine you are at a conference and as you look around you notice the room is packed full of gorgeous people that you admire and want to impress or perhaps even date (let’s say for the sake of argument, Barack Obama, Richard Branson, famous supermodels, Angelina Jolie, Brad Pitt and more). Imagine the organiser suddenly dims the lights, puts an extremely bright spotlight on you and asks you to deliver a speech on why you are all gathered there; you are unprepared and the topic is on something they all know more about than you (I don’t know, maybe ‘Why America is the best’… but you are British and have never been across the pond, while clearly the above attendees have).

You start to mumble and blag your way through, knowing that all the attendees know more about that topic than you and will immediately spot all the mistakes you are making. In fact, one by one, you start seeing each of them rolling their eyes, smirking with distain and even whispering conspiratorially to the person next to them as they turn to stare at you. You feel yourself going red, you start to visibly sweat and your shaky voice is giving you away even more and causing a scene. The organiser takes pity and interrupts you to say “thank you for your… contribution” and proceeds to deliver the finest, most eloquent, witty and intelligent speech you have ever heard on the topic. The crowd love him and give him a standing ovation, as some glance over uncomfortably because they clearly feel sorry for you, considering how awkward the situation is and the obvious ‘elephant in the room’.

“You glance in the mirror as you pass it, and immediately freeze”

Afterwards, you head home. On your way to the kitchen to make dinner and take care of important ‘life admin’, you glance in the mirror as you pass it, and immediately freeze. Oh no. Your hair must have gotten caught in the rain before the conference and has done that unique frizzy thing that only your hair can do, which makes the bowl haircut disaster that the hairdresser created the other day even worse. You also appear to have the largest, pusiest, ugliest, angriest, reddest spot known to man that has set up home right on the tip of your nose! You have large bits of black food from breakfast stuck between most of your teeth, your skirt is visibly tucked into your granny pants and you have a large stream of toilet roll stuck to your shoe. You also have mascara stains down your cheeks from a panic attack you had that morning just before you went into the conference, so it must have been obvious to everyone that you were not confident and knew you didn’t deserve to be there. In fact, your whole appearance most likely accounts for at least some of the looks you received that day.

When your partner arrives home, you tell them all about the scandal that happened that day, waiting for them to be as outraged as you at the unfairness of what you’ve had to go through; but instead, they tell you “you look beautiful today” and “in fact, this is the best I have ever seen you look”. You feel shocked and betrayed that they are mocking you by telling you such a lie or, more scarily, that they think this is actually what you normally look like and is the best you could ever look. You withdraw from them and make a note to store up that resentment for later. You go to bed feeling humiliated and ashamed, hoping tomorrow will be better. When morning comes, you get up and make your way to the second day of the conference, determined that today will be the day you will prove your worth to these amazing people. But wait – you get home that day, look in the mirror and you have somehow managed to make all the same mistakes again!! How is this possible?! As you fall asleep that day, you start to lose confidence that tomorrow will be different.

The following day, remembering how you must have been appearing to others the last couple of days and the growing likelihood that today is no different, you are quiet at the conference. You do not speak unless you must, you avoid eye contact, and you pull your hair forward to cover some of the likely abominations on your face (such as the spot and possible food between your teeth). In fact, whenever someone starts to talk to you, you make an excuse as soon as possible and go hide in the bathroom before they notice any such deficiencies. You see someone else observing this and through their eyes and body language they communicate an unspoken message that they understand why you are doing this, having witnessed your aesthetic disasters the last couple of days, and would indeed be taking the same action if god forbid they were in your position. At the end of the day, you rush home as quickly as possible, head down when passing people in the street. When you get in, you let out a sigh of relief that you are now in a safe place and spend the rest of the evening focusing on what you can do to avoid such future disasters, whilst crying tears of frustration and sadness.

“This is the reality of a BDD sufferer”

This is the reality of a BDD sufferer – they go through the exact same scenario, except that the ‘abominations’ they see are skin-deep and cannot be washed away or covered. They also go through this humiliation EVERY SINGLE DAY, without any break in-between to build themselves up again; in other words, the conference never ends. BDD afflicts 1 in every 50 of us, which is rather common – this means there are people in your school or workplace going through this battle right now. The private shame of sufferers and misdiagnosis (for example, of anxiety or depression) mean that this horrific illness is often not well known about or given appropriate treatment. The unrelenting pervasive pain experienced can lead to devastating consequences – BDD sufferers are 45 times more likely to commit suicide than the general population and suicidal thoughts are more common than in ANY other mental health condition including major depression. Thus, in many ways, it must be handled with the upmost respect and viewed as a potentially fatal illness if left untreated.

“BDD is NOT about wanting to look good, it is about wanting to look ‘normal’”

BDD is NOT about wanting to look good, it is about wanting to look ‘normal’ or even ‘below average’ but without being a walking freak show (hoping to be considered ‘attractive’ would be too high an aim). It is about being able to see the beauty and worth of EVERYONE you come across, except yourself. It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

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Felipe’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

Hi, my name is Felipe and I used to suffer from BDD and Depression. I don’t know how it started but I think it was at some point when I was between 13 and 15 years old. In my case I felt I had a problem with my speech. I couldn’t explain it to doctors; I knew I didn’t have a stutter or anything and there were times when I spoke normally – mainly when I was with my family. So my problem must be psychological.

“My parents thought it was just their teenage kid going through an undefined crisis”

I struggled on my own for about 6 years, and during this time I got low grades, had almost no social life, lacked the will to do anything, and didn’t attend school very often. In fact the only positive thing I can say about this period is that, while I stayed home, almost all my free time I spent reading, which is a good habit I still have. My parents thought it was just their teenage kid going through an undefined crisis or something, but didn’t think it was very important. Not even when their son remained in the car when they went out, remained in the hotel when they went travelling abroad, and had no social life.

One thing that helped me was Buddhism, and meditation. When I started doing meditation it hit me like a rock that life was very short, and I had to live it no matter what. So, still under the effects of BDD I started making the effort to go out, use the bus and underground, even though I still thought everyone was looking at me for being so utterly hideous and different from other people. Eventually I sought psychiatric help, and went on to have regular therapy. It’s helped me a lot. I’m taking an antidepressant, and it helps too. Knowing that there is an illness with the very symptoms you have is the first step to recovery, I think.

Thank you.

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Erin’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

I have suffered from BDD for 10 years; it started when I was 18. I was convinced that there was a patch of bumpy, scarred skin on my face and became obsessed with it. I only liked to go out at night as I thought that way people couldn’t see my hideous flaw. I had a boyfriend but was sure he thought I was disgusting and just didn’t say so. I couldn’t look people in the eyes, and had really low self-esteem. I tried various creams, would sleep with scar pads on the area, and spend hours a day in front of the mirror inspecting it. When I went out, I would cover the patch with makeup, wash it off and reapply it 4 or 5 times. I was convinced I was disfigured. I was living less than a life, unable to enjoy anything.

“My best friend came up to my face and peered closely. ‘What bumps?’”

Things came to a head in 2005. I was breaking up with my boyfriend – totally mutual and friendly, I wasn’t really upset about it, but I started panicking because I was convinced I would never find anyone who would overlook my flaw. Finally I broke down and told my best friend about the bumps. I had never told anyone, I was too embarrassed and I thought everyone knew I was very ugly but felt pity for me. It was also that I didn’t want to hear ‘but you’re a great person’ or ‘it’s not so bad’. My best friend came up to my face and peered closely. ‘What bumps?’ She said she didn’t see what I was talking about. I thought she was just being nice.

I felt angry, and in a fit of BDD picked at the bumps I saw, which left what I thought was a huge gaping scar. For weeks, it was all I could talk about. I was no longer hiding my flaw but instead obsessing about it – on the phone to my sister, to my friends, who couldn’t understand what I was talking about. They listened patiently though. I was spending about 6 hours a day in front of the mirror. I would feel tears start up while at my desk at work, and go into the bathroom to sit in front of the mirror, hating my scarring. I hid in my house for weeks, drinking a lot and making excuses to friends so I didn’t have to go out.

Finally, one night, I broke down. I couldn’t stand it anymore. I was becoming increasingly paranoid that people on the street were talking about my skin. I had mirrors all over the house in order to look at my face from different angles and in different lighting, and it always looked horrible. I had a crush on a guy but ‘knew’ I could never get him because he’d only seen me in a dark pub and if I actually went on a date with him he would see how scarred I was. I called my parents in tears. My dad answered; he’d never heard me like this. He knew something was wrong and he told me my mom would fly out the next day to spend some time with me. I cried and told him about the big scar I had and how my skin was ruined, destroyed, and I couldn’t stand being so ugly anymore.

“She kept telling me all she could see was a little scratch”

My mom came out the next day. She hugged me and I felt a bit better, and took the next two days off work sick. She kept telling me all she could see was a little scratch, but I didn’t believe her. We went to A&E and I was given medication, but I just told the nurse I was feeling suicidal, and didn’t get into the skin ‘problem’. My mom tried to help cheer me up at home, but I felt worse and worse. She forced me to go to casualty with her again, and this time, the psychiatrist came in. I broke down and told him my suicidal thoughts were because of my awful skin problems. He got me to point out what I meant, and then said, ‘We would like to admit you.’ My mind raced: I hadn’t thought that would happen. Still, I had no idea about BDD; I thought they were admitting me solely because of my suicide risk.

I spent the next three days in the common area waiting for a bed in the psych ward. Thank God for my mom, she came every day to visit. That time is very hazy, I was on a lot of medication and it wasn’t very comfortable. I moved up to the psych ward where I stayed for seven days. I was assigned a nurse and a psychiatrist, who I talked to every day. Despite my extreme embarrassment about my skin, I showed the doctor my problems, including this new scar, and the other bumps and scars I thought I had. But at this point the doctors and nurses just listened to me, and didn’t offer any advice.

My mom and I met with the psychiatrist on the 3rd or 4th day, and he said he had a diagnosis. Body Dysmorphic Disorder: I’d heard of it but didn’t know a lot about it. He said it was severe, to the point where it was paranoid and delusional. I was shocked. I asked him if he was sure, if maybe it wasn’t just the lighting in the room or something. He said yes, we’re sure. Back on the ward I asked the nurse, ‘But can’t you see the bumps and redness?’ She said, almost sadly, ‘No, I really can’t.’ It was like a light bulb went on: there was nothing there.

It was good to have a name for what I was suffering from, and in a way I felt like I had a new chance at life. For 10 years, I had hid my face in shame, thinking that I was scarred, avoiding social situations and opportunities. But it wasn’t really there – I was attractive after all! I felt so happy that I wasn’t disfigured, but sad that I had wasted so much time thinking that I was. It was difficult because I still saw the scarring but had to come to terms with the fact it wasn’t there.

“It’s as though most of the time I realize it’s not real, but sometimes my mind is powerful enough to convince myself that perhaps it is”

It’s been a year and a half since that time. I’m slowly weaning off my medication. I have also been able to stop the compulsive mirror checking and reapplying of makeup. I am happy in my job, and was married last year to a great guy. I’m not saying everything about my BDD is gone; I still suffer from symptoms if I catch myself in a brightly lit department store, or if someone is close to my face, especially in the daytime. It’s as though most of the time I realize it’s not real, but sometimes my mind is powerful enough to convince myself that perhaps it is, even though deep down I know it’s not. But all in all, I feel good, and I’m glad for my journey. Although I had to hit rock bottom and struggle for a while, it made me stronger, and I got my life back.

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Nicole’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

My name is Nicole and I am 20 years old. I was diagnosed with BDD a little over a year ago and have spent my time since then trying to learn about this disorder. When I was first told I had it I felt relieved that there was a name for what was wrong with me, but I also felt sad because there was definitely something wrong with me. I remember when I was only nine years old I thought about cutting off my nose because it was too big. I was already tired of the snide remarks from friends and even strangers about how big it was.

“On school picture days I would come home bawling because I knew that my nose would be posted everywhere”

When I was in junior high, my self-esteem issues went far beyond the average teenager angst. I couldn’t bear to look in a mirror or have my picture taken. On school picture days I would come home bawling, because I knew that my nose would be posted everywhere. I wore a windbreaker with long sleeves so I could use the sleeve to cover up my face. It made me feel better. In high school I discovered my knack for humour. I made fun of myself before anyone else could get to me first. Deep inside the demon was ready to come bursting out. I suffered from anorexia for years, as well as addiction to painkillers.

After I was diagnosed with BDD, along with panic disorder, I was put on an anti-depressant that has saved me. No, it doesn’t take away the thoughts about my nose or body; no, it doesn’t give me hallucinations that I am a supermodel. It helps me to think clearly, and not dwell on my ‘physical problems’. I know that no matter how many times people might tell someone with BDD that you are beautiful, you still won’t believe it. And what if you were absolutely the most gorgeous woman on the inside? Doesn’t that matter too? That’s what I try to tell myself each and every day. It’s sort of my mantra now. I’ve noticed that, once I stopped openly complaining about the way I looked, I began to receive more positive vibes from people. I am still not ready to be photographed, but hopefully with time and my therapy I will make that giant step!

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Val’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

For as long as I can remember I had self-esteem issues. My first BDD attack was when I was 12. My Grandparents sent me off to an all-girls boarding school to get me out of my mother and stepfather’s house. I was there until the age of 14. Anyway, I saw a picture of a very thin blonde girl and something snapped. I got out my secret stash of extra-strength Tylenol and locked myself into the bathroom. It was a room with only a bathtub in it; the shower cubicles, toilets and sinks were in a different room altogether. I ran a nice hot bath and swallowed the whole bottle; when I woke I was having my stomach pumped.

“Eventually my mother and stepfather kicked me out of the house because of my ‘attitude problem’”

That was the first of several suicide attempts. I was sent home for a week to ‘recover’. By the time I was in grade 9 I was in full self-hatred self-mutilating mode. I insisted I wouldn’t go back to boarding school and told them if they tried to send me back I’d find a way to get expelled. That year I was in two different schools in different cities (my parents moved in the middle of the school year) and in each one I fell in with a group of kids that weren’t of the greatest mindset. They did drugs, drank, pulled B-n-E’s, etc. Eventually my mother and stepfather kicked me out of the house because of my ‘attitude problem’. I ended up living with people that I would deem pretty ‘seedy’ but I had no where else to go. My grandparents lived 3000 miles away and I had no family to speak of other than my dad, who was working in the camps up in the Yukon.

I never pulled any B-n-E’s but to earn my keep I had to do equally if not worse things. After another failed suicide attempt, my parents moved back to my original city and my grandparents gave them the money to enrol me in a local private school, hoping that would turn me around. I was there for my grade 10 year and absolutely refused to return the following year, again making my point by slashing my wrists. I went to the senior high school in my area for my grades 11 and 12; there I made many friends, almost all of whom were just as messed up as I was.

“I had stopped eating and was surviving on an apple and two pieces of bread a week”

By this time I had stopped eating and was surviving on an apple and two pieces of bread a week, along with lots of coffee, water and cigarettes. I was working out excessively and doing any type of drug that I could get my hands on. The drugs took away the hunger pains as well as the emotional pains. I graduated with a not-so-bad GPA, considering I was in the mall across the road smoking and drinking coffee the majority of the time.

After graduation my parents moved and left me to my own devices. Not long after that my dad shot himself and that sent me into a downward spiral. I got in really deep with the coke, bingeing for days – no sleep, no food, and finally crashing. Then the cycle would begin again. I knew the coke was ageing me and I didn’t want that, I HATED that! I looked like a shrivelled-up used piece of goods at the age of 21. At the time I thought it was vanity that saved me. I went back to school and have been in the same sort of business since then.

I met my husband when I was 24 and clean. Things were definitely looking up for me. I still hated myself and my appearance, but I somehow managed to put it on the back burner – until January of 2006. It was a month before my 30th birthday and I snapped. I couldn’t sleep, I couldn’t concentrate at work, my marriage was suffering terribly and it was all because of my body and my hatred of it.

“I absolutely loathed myself, everything about myself”

Throughout all those years I absolutely loathed myself, everything about myself, especially my body: everything about it, from the shape to the length to the width. No matter how thin I got it was never good enough for me. If my hatred wasn’t in the front of my mind it was in the back of it. I constantly compared myself to others. I went though stages of not looking in mirrors, and of being mesmerized by them for hours. All shiny surfaces were up for securitization; anywhere I could get a glimpse of myself I would. Most of the time I walked away feeling defeated, angry and sad, because nothing changed. I was constantly trying to figure out ways I could get skinnier. I was envious of every female that I saw because they were all prettier and skinnier than me. I NEVER asked for reassurance from others because I was terrified of the answer. On the rare occasion I did go out I would wear the biggest, droopiest cloths and a hat, so no one could see me.

Just before my birthday I went to one of my many ‘quest-for-perfection’ appointments and the nutritionist asked if I had ever heard of BDD. She had asked how many inches I wanted to loose and I guess to her my answer seemed unreasonable. That night I went home and started surfing. I was glued for hours. I was in tears for hours. I had no idea there were others out there like me. I thought I was the most vain, selfish, narcissistic person ever, but reading about BDD, and in particular the personal stories of other sufferers, I knew I had found my answer! I finally knew what was wrong with me, and for me that was half the battle. I had spent years in and out of therapy without being properly diagnosed.

I made an appointment with my doctor the next day and told him my story, and about my recent ‘breakdown’. He started me on medication and referred me to a psychiatrist who specializes in CBT. It took several months of being on a waiting list, but I tell you, it was well worth the wait. My psychiatrist has diagnosed me with BDD, along with several other disorders, and we’re actually gaining on them, slowly but surely. I still have my rituals; I still compare and get envious, but it is diminishing as I catch myself, and correct myself. The therapy is very hard work, but I think in the end it will be well worth the effort.

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Sue’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

I now realise that I experienced symptoms of BDD from a very early age. I was always sensitive and self-conscious and felt that I was different from the other girls. My confidence increased slightly when I reached my mid-teens and I was able to camouflage my appearance with make-up, and straighten and control my hair. With the arrival of a few boyfriends and my marriage at 18 I felt a little more ‘normal’, but by this time the obsessive behaviours had set in.

At 21 my marriage broke down and I became severely depressed. At that point BDD took over my life. I was so repulsed and disgusted by my appearance that I thought no one would ever want me again. My parents took me to the GP who treated me for depression and prescribed Valium. The BDD and depression became so unbearable that I took an overdose and was then referred to a psychiatrist. The next seven years of my life were spent in and out of hospital, trying countless different types of medication. But the symptoms persisted and I took more overdoses. I explained that I felt distressed because of the way that I looked, but I was dismissed. This increased my feelings of embarrassment and shame and I felt that I was also a ‘sinner’ for worrying so much about the way that I looked. The BDD increased and my life revolved around the level of satisfaction I could achieve with the never-ending cycle of camouflage.

“I felt repulsive and hideous and didn’t feel that I looked human or deserved to live.”

When I reached 28 I met my second husband and the years that followed were much better, with the distraction of my home, children, and career. Social activities were still affected, as it was difficult to be around others who were attractive and therefore ‘adequate’, unlike myself. Then, at 45, things took a serious turn for the worse with the failure of my second marriage, and the BDD became severe. I began checking my refection in the mirror for up to four hours at a time. I felt repulsive and hideous and didn’t feel that I looked human or deserved to live. I would constantly compare myself to others and to old photographs, always focusing on what I considered to be my worst features, for several hours at a time.

I thought about my ugly appearance every moment of the day, and again became suicidal. I couldn’t talk to family and friends about my feelings because I was frightened that they would think that I was vain, or mad. I couldn’t understand how anyone could bear to look at me and not recoil in horror. I was being treated at this time by a psychiatrist who tried different medications, including anti-psychotics, and referred me to two different psychologists who didn’t help at all. I was not offered CBT, and no one seemed able to help me.

“I visited the beauty salon and spent over £300 on the treatment”

Then I saw an advertisement in the local paper for a ‘non-surgical facelift’ and I visited the beauty salon and spent over £300 on the treatment. Any positive results were short-lived but it was at this time that the owner started to talk to me about cosmetic surgery. Despite having these disturbing thoughts about my appearance I hadn’t really thought about it before. But the more I researched it the more I was convinced that it might just save my life. This seemed my last chance.

Having once made up my mind I wanted surgery immediately, and I arranged an appointment with a surgeon within days. My main appearance concern at this time was lines on my face, although over the years I had focused on my eyes and my hair. I went into hospital two weeks later and had a facelift and lower-eye surgery at a cost of £3,500. I wasn’t nervous or hesitant at all. This was an emergency, and although I was battered and bruised afterwards it didn’t matter: there was at least some hope, or so I thought. As the days passed and my face healed I could still see imperfections on my face and my anxiety soared. I scrutinised every area of my face and was convinced that I had made things worse and now it was ‘all my own fault’. How could I have been so stupid?

Within months I was back at the clinic, having injectable fillers that were very painful and expensive, and only lasted a few months. The next year I went back into hospital for more surgery: another £3,000 for tissue implants under the lines and more eye surgery. Afterwards I felt the same. Disgusted by my appearance and horrified at what I had done. Despite all this, and because my BDD was so bad, I continued with injectable fillers and spent a fortune on various products over the next two years.

This unhealthy cycle of behaviour carried on until the year 2000. I was suicidal and didn’t know where to turn. I was still seeing a psychiatrist, and a psychologist, but my BDD remained undiagnosed. The psychologist discharged me after pointing out that despite all the help I had had from mental health professionals and cosmetic surgery intervention no one could help me. I returned home feeling that the end had come. I survived another overdose around that time, but it was followed by a spell of taking tablets day and night, because I could not stand the torturous thoughts.£8,500 for another face-lift, chin tuck, eye-brow lift and laser treatment.

“I returned home feeling that the end had come.”

I decided to give cosmetic surgery another chance. After all, it may just ‘work’ this time, and if it didn’t I would end my life, which seemed inevitable anyway. Again, having made up my mind, I went to see a different surgeon and was operated on within the week, taking a cancellation slot. The surgery was more costly this time, £8,500 for another face-lift, chin tuck, eye-brow lift and laser treatment. The money didn’t matter though. I cashed in my mortgage endowment policy without a second thought.

As is usually the case (I know now) I felt worse afterwards, and whilst nothing much had improved there were now new areas of concern. It was at this time that I saw a TV programme about a girl who didn’t like the way she looked, and who had a condition called BDD. I couldn’t believe that I was not the only one who felt this way, and I phoned the helpline and got information about BDD from OCD Action. Now, nearly seven years on, after years of excellent CBT treatment from David Veale and Rob Willson, I understand that all the surgery I had was not helpful at all. It made my BDD worse and far more dangerous.

I have learnt not to make demands on myself to look or be a certain way to be accepted. It is ‘enough’ just to be me, and I am grateful for the life I am now living which could so easily have been lost.

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Stephen’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

At the age of 18 here I was, the survivor of a huge overdose. I lay in the hospital bed with my family around me, their faces stricken, pale and afraid, asking, ‘Why?’ I had my reasons. Every second was a struggle, and with every waking breath I thought about one thing: my monstrous ugliness. I don’t remember when I started to believe that my skin had begun to thin, to redden and to grow pimples. But one morning as I got ready for school I just couldn’t bear the thought of being exposed and so I raided my mother’s make-up box. I covered my face with her foundation and caught the bus as normal. No one seemed to notice. The taunts of ‘ugly’ and the sarcastic comments of ‘nice hair’ continued unabated, but they were not accompanied by jibes about the fact that I was a man in make-up. I thought about my face all day, worrying that I still looked ugly and worrying that I stuck out like a sore thumb, but no one said anything, and it was better than having no cover for my skin. I was so pleased to get home but I knew it would be the same the next day. From that day on I had to wear make-up.

“Every morning was a battle with the mirror.”

When I left school and got a job as a hospital porter I thought things would change, but they didn’t. Every morning was a battle with the mirror. I would put on make-up, pick at my skin and try to make myself look normal. I didn’t have to be outstandingly handsome; I wasn’t vain. I was a deformed monster and I just wanted to look acceptable. I would be late most days and I was so miserable being on display to the public that I couldn’t do my job. I would hide in the toilets and stare into the mirrors and just wish that I was back home in my dark bedroom where no one could see me. I lost my job, and when I seemed to lose everything else I tried to end my life.

“I dreaded sweating and losing my make-up”

I didn’t tell anyone about my fears relating to my skin; I was too embarrassed by it. And I didn’t think that there was anything anyone could do. I started to see a counsellor and went on prozac. I felt a little better but the problems were still there, my dark secret: that I felt like the phantom of the opera hiding behind my mask. I had to avoid getting wet, so I never went swimming and tried not to leave the house in the rain. I dreaded sweating and losing my make-up. Everyone has thoughts about their appearance, about wanting to look their best, but I was disabled by it. I was in mental anguish every day. All I wanted was to look normal.

When my long-term relationship ended it was at its worst. I was living alone, lonely and at the mercy of my mind. I had a job again, but it was getting harder and harder to make it in each day. I began to set my alarm earlier and earlier so that I had time to sort out my face before facing the guys at work. It went from one hour to three, and I was still late most days, if I made it in at all. I would look from the mirror to my watch, going from room to room to look at myself in different mirrors where the light was different, and might make my reflection more favourable. I would pick at my skin with tweezers and finger nails. I would put the make-up on, smooth it in, and then wash it all off again. I just couldn’t make it go right. I was never happy with how I looked. And when I glanced at my watch and saw that it was already time to be at work and my face still looked awful I would panic, and try to sort it one last time with my heart racing and my breath coming too quick. Then it would seem impossible for me to go to work at all, and I would fall to the bathroom floor and cry pitifully.

“I despaired, and before long the pressure and the pain had got too much for me and I tried to slit my wrists”

I told my boss that I was depressed and that some days it was too hard for me to be at work. That was only half of the story. I was depressed but it wasn’t as simple as that. I couldn’t tell him that even on the days I made it to work I was thinking about how bad I looked and comparing my skin to everyone else wishing I looked human. How could I tell anyone the embarrassing truth? No one would understand, and if I told them I had a problem with my face they would all notice my ugliness even more. I despaired, and before long the pressure and the pain had got too much for me and I tried to slit my wrists.

Despite the help I received from the mental health system it wasn’t long before I was back in hospital, having overdosed on my antidepressant pills. I was getting deeper and deeper into misery and couldn’t cope with even the smallest problem. I was cutting my arms regularly and isolating myself from former friends, even shutting out my family. I would ignore the phone and hide if there was a knock at the door, afraid to let anyone see me without first sorting out my make up.

I didn’t tell the doctors about the main problem because I didn’t want to admit that my face was my main problem. I understood my feelings of depression but I couldn’t justify my appearance worries, they just seemed too trivial. I didn’t tell anyone because I thought the problem was physical, not mental. I really was ugly. I researched online the possibility of having a chemical peel but it was too expensive. I stole tablets from my sister’s house and took a massive overdose that put me in a coma for a day and two nights. I survived, and it made sense that I should now tell my new doctor everything.

That was the best thing I could ever have done. He prescribed me a new antidepressant called Clomipramine that he thought might help with my other worries. I could not have imagined the dramatic effect it would have. Within a few weeks of taking it my skin seemed to improve. The redness of my nose dulled and the pimples seemed less intrusive. I still put on make-up but I did it more from habit than any actual need. I stopped taking the make-up to work with me, stopped thinking about my face for twenty-four hours a day. I would never be completely free from my thoughts but they were not so strong or so all-encompassing as they used to be.

I could begin to live normally, to go out of the house without hours of trauma. My doctor had truly helped me and the reason was a simple one: there had never been anything wrong with my skin. I had a mental condition called Body Dysmorphic Disorder, and the pills were easing the symptoms. My silence had been my enemy: an enemy that had ostracised me from the waking world for fifteen years.

I am now happily married. I still have occasional attacks of BDD but I have had the strength to write about my problems and turn my darkest thoughts into literature. My autobiographical work Suicide Junkie, which goes into detail about my battle with mental health, has now been published by the mental health publisher www.chipmunkapublishing.co.uk.

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Louise’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

Looking back, I think I have had BDD all my life. There has always been something to worry about. I remember a year of obsessively looking at my fringe in shop mirrors, thinking I was going bald, and an obsession about brown marks on my teeth for a whole summer. My obsessions moved around my body until, four years ago, they took over my life. I noticed I had facial hair that was quite long, and got very upset. I was travelling at the time, and started to check it in different mirrors, from different angles, at regular intervals during the day. When I returned from travelling I tried different treatments to remove the hair. I felt very self-conscious sitting in certain lights. This carried on even though my Mum said she couldn’t see it. The treatments only worked temporarily, and I became convinced they were making the hair worse and worse and worse until one day I decided I wouldn’t look any more and would only think positive thoughts about my facial hair whenever it came up in my mind.

Amazingly I managed to avoid looking at my facial hair for about two years, and if I ever did see it I would look away. I felt like I was lying to myself, but it meant I could get on with my life. This seemed to work until my Mum bought me a magnetising mirror, and I noticed that the skin on my cheeks had got looser and more wrinkly, and felt very upset that one of the treatments might have ‘damaged my skin’. I remember sitting in a meeting at work for two hours with my jumper pulled up around my face!

“I became more and more upset about it until I started looking for a treatment to fix it”

I became more and more upset about it until I started looking for a treatment to fix it and discovered microdermabrasion. This magic treatment promised to smooth out my skin and get rid of wrinkles and the first treatment did seem to make my skin look smoother. But each treatment after that seemed to make it worse, even though I followed the instructions on how often to do it and how to look after my skin. I became more and more worried that I had now damaged my skin more, and this is when my BDD got really bad.

I visited a dermatologist who said my skin was fine and completely undamaged by the microdermabrasion and previous hair removal treatment. He even said my skin was quite good for my age and another dermatologist has since said the same – and that I should see a psychiatrist! But although I felt better for a few hours I found his words of reassurance very hard to believe. Subsequent reassurance from family and my boyfriend did nothing to make me feel any better, as there was no way my skin looked okay to me. I thought they must have low standards, or that they were being nice or just not looking close enough. The more I looked at my skin the worse it looked, and I became transfixed and increasingly horrified by how bad it was and how it was getting worse and worse.

“Out of work I had too much time to look in the mirror”

I started piling on expensive anti-aging creams, and when I saw some new lines by my eyes I started to worry that the positions I was sleeping in was making it worse. I tried lots of different pillows and positions – some of them very uncomfortable! It got to the point I would look in the mirror over and over again, sometimes for hours on end, and not be able to go out because I was so self-conscious and panicked. Instead I would hide under a pillow and cry. It became difficult to see friends who had ‘good skin’. I looked at numerous magazines to see if I could find anyone with skin like mine. Sometimes I could, but I would only feel better for a short times. Nothing could make me feel better for more than a few minutes. It felt like being in a nightmare I couldn’t wake up from. Sleep was my best escape, although I would often dream about it. My poor parents caught the brunt of it, as I would phone them regularly, completely distraught and inconsolable. Out of work I had too much time to look in the mirror, but when I did eventually go back to work part-time it was stressful and I found it very difficult to concentrate whilst sitting under a strip light. My output was pretty low!

This went on for quite a few months. Every day it took a huge effort just to get up and out of the house with people looking at me. Tubes were a nightmare and the mirrors in plane toilets caused massive upsets. I spent hours upset or worrying about or looking at my skin, to the point where it became what I thought about most of the time. I found it very difficult to think how I would live with looking so bad, and with it getting worse the older I got. Although I was in a relationship, that in some ways made it harder, as someone was looking at me close up and seeing how awful my skin was.

I started CBT at the end of last year and have had 5 sessions. It is the most difficult thing I have ever done, as I am having to give up habits that seem impossible to resist. I have done better at some than others, and sometimes I have to start all over again when I slip into my old habits. But overall I am better able to concentrate on other things. It’s difficult to imagine fully recovering, but my CBT therapist, who specialises in BDD, has a very high recovery rate. I know that, one day at a time, I will get there.

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Cari’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

How do you feel when you look in the mirror? Happy? Not fussed? Whenever I saw my face in the mirror, I felt so sick I wanted to smash the glass. I thought I looked like a monster. It all started my first term of secondary school. A bunch of girls and boys in my class began bullying me about my acne, calling me ‘Spotty’. I tried to ignore them, but the insults made me feel really self-conscious. They started taking the mick out of my forehead, saying it was ‘massive’, and that I had a voice like a man just ’cause it was deeper than some of the other girls in the class.

“By the time I was 13 the way I looked was all I thought about”

As the months passed I got more and more upset. When you’re told over and over again that you’re ugly, you start to believe it. I began studying my face in the mirror, worrying about the way I looked. I decided I hated my nose: it was too big. My eyes squinted when I laughed, and my hair was too thin. And I was fat. I’d try holding my stomach in and pulling the skin taut, wondering if I’d be prettier if I was skinny. By the time I was 13 the way I looked was all I thought about.

I tried to talk to my school friends about how I felt. ‘Don’t be silly, Cari,’ they’d say. ‘We all feel like that.’ But I knew they didn’t. It wasn’t like I was having an ‘off day’; I felt like this constantly. If I was going out with mates I’d spend the entire day getting ready, changing my outfit and make-up about 20 times. Each time I’d hate the way I looked, take off my make-up and start again, only to hate what I saw and end up in floods of tears. In the end I’d refuse to go out at all. Gradually my friends stopped including me in their plans, which made me feel even more isolated.

When I was 14 I started self harming, cutting my wrists and neck with knives from the kitchen, or razor blades. I wanted to punish myself for being so ugly and worthless. Nothing made me feel better about myself. If someone paid me a compliment I wouldn’t believe it. If a boy glanced at me I’d imagine he was looking at me in disgust. As I got older I started finding other ways to hide. I had a fringe cut to hide my forehead and began getting tattoos and piercings. I felt that if I had something beautiful on my body, I wouldn’t be quite so revolting. Plus, if people were looking at my body art they wouldn’t be looking at me.

“You silly girl,’ she told me as she hugged me, ‘there’s nothing wrong with you.”

I knew my family were worried about how withdrawn I’d become, yet when they tried to talk to me I’d just snap at them. But as time passed I found it harder to keep my feelings to myself. Finally, one New Year’s Eve (as usual I was at home instead of out partying), I found myself blurting out everything I felt to Mum. How ugly I was. How I’d cut myself. Mum was shocked. ‘You silly girl,’ she told me as she hugged me, ‘there’s nothing wrong with you.’ She didn’t understand that her words couldn’t make me feel better. I wasn’t just feeling insecure; I hated myself.

Mum was convinced I had depression, so she took me to the doctor who put me on anti-depressants. They made me feel a bit better, but I still couldn’t shake the repulsion I felt about my own appearance. Months passed. Then one day, when I was 17, I sat down in front of the TV and started watching a documentary called Too Ugly for Love. It was about people who couldn’t have relationships because they felt they were so ugly. None of the people in the show were ugly, but their behaviour was like mine: they’d look at themselves for ages and hate what they saw. They all had something called Body Dysmorphic Disorder, or BDD: a condition that meant they couldn’t see themselves the way other people saw them; their self-image was so distorted they thought they were hideously ugly, when they were perfectly normal.

It was like a light bulb going on in my head. I knew this was what I had, too. Weirdly, just knowing what was wrong with me helped me to feel better. I found a counsellor, which meant I had someone to talk to, and having an actual diagnosis made it easier for my family to understand what I was going through. I still struggled to accept my body, but gradually I recognised that I didn’t see it the way other people did, and that it was possible for me to live a normal life. I even said yes when an old friend, Mike, asked me out. I’m working on the way I feel. I hope that one day I’ll feel truly confident in myself.

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Matt’s Story

It is a medically-recognised illness, much like diabetes, that anyone is susceptible to given the right combination of genetics and environmental factors. It is NOT what defines someone or their personality, in fact given the right treatment it can largely be successfully ‘removed’ and the person, not ill or in pain anymore, shines bright and can be who they were before this insidious illness attached itself to them.

I would like to share my experience. Forgive me if I give advice or offend; I’m quite passionate about my recovery and want to share with you my sense of hope. I did not realise that my Body Dysmorphic Disorder had gradually changed me into someone that I didn’t want to be. A person who was at odds with himself and his fellow man. I picked my skin until I gave myself scars, then I stayed in my room to pick at the scars rather than go outside the house with family or friends. One of the things I used to do was to keep looking at my scars in the mirror until they became out of focus, as my eyes grew tired. Gazing from different angles and not wanting to blink, I was drawn to the things that I hated and it caused me a lot of distress. It felt as if the mirror would drag me towards it and scream ugly names at me. Later I tried to remove the scars with unnecessary surgery, which only caused larger and redder scars.

I had painful steroid injections into the scar tissue to try to soften them. I had laser surgeries to try to reduce their redness. I filed my own teeth with a razor to try to make them even. I dreamt incessantly of nose surgery. I thought my arm and leg hair was ugly and dirty and tried to cover it up. I saw uneven ears, uneven nostrils, over-developed muscles on one side of my forehead, to name just a few of my ‘flaws’. And that’s not even going into the rituals and tricks that took up hours of my day in an effort to camouflage.

“I thought I didn’t deserve love, but punishment”

For many years I tried to keep people from knowing about my pain and my negative thoughts. I isolated myself, and lived in a prison of my own making. I avoided intimate relationships for fear of rejection because of my defects. If I felt rejected I put it down to the way I looked. I thought I didn’t deserve love, but punishment. I told myself no one would love me because of these ugly, grotesque parts of my appearance. In my head I went over every conversation, every social interaction, trying to account for my feelings of rejection. I was trying to use my insight, not realising that my insight was distorted. Later I came to realise that, unknowingly, I was using my ‘insight’ to keep myself stuck.

My BDD was a destructive force in my life. My best efforts resulted in ever-greater destruction and despair. At some point I realised that I needed the help of professionals. With therapy I came to realise that holding on to these rituals, tricks, safety behaviours and obsessions would eventually sicken me and stop me from taking part in a new way of life. I realised that if I kept entertaining these obsessive thoughts it would lead me to a worse state. I have learnt that if I let an obsessive thought surge, it maintains its own momentum, until it boggles my mind and alters my mood. It is the old, unhealthy mindset that BDD is preserving.

“Many of us with BDD cling to our fears, doubts, self-loathing or hatred because there is a certain security in our pain”

How sincerely I worked at each Cognitive Behavioural Exposure exercise (or what I term a recovery step). My effort was proportionate to my desire for change. And this next part was an important one for me: for a long time it didn’t seem safe to embrace what I now knew, and to let go of the familiar for the unknown. Many of us with BDD cling to our fears, doubts, self-loathing or hatred because there is a certain security in our pain. But I started to liken my behaviour to that of an addict, and I realised that each ritual starts the deadly cycle all over again. Drug addicts try to control their addictions, to ‘use in moderation’ or to use just ‘certain drugs’. None of these control methods work. I too had to admit my powerlessness over my rituals. I couldn’t substitute one ritual for another. I couldn’t take the view that I could do my rituals in moderation. My therapist gave me a great example: if you have an infected wound and you wipe 90% of the infection away, the infection spreads again.

My therapist told me to view any current or new behaviour in that way. If it was even partly BDD-related, e.g. 20% BDD, and 80% a ‘normal’ appearance concern, then I had to stop doing it because substituting one trick for another was releasing my compulsions all over again. BDD is great for manipulating the truth. BDD is always a step ahead. I said to my therapist: yes, I need help, yes, I am willing to do whatever it takes to stop my rituals/tricks, but in the back of my mind I was like an addict, telling myself that ‘when’ I get my life together, then I can handle my drug habits. Or, ‘when’ I get out of rehab, I can handle the occasional drug. Such ways of thinking and acting lead us back to what Narcotics Anonymous call ‘active addiction’.

I came to realise that I had no choice except to completely change my old ways of thinking. From that point forward I began to see that every ritual-free day is a successful day, no matter what happens. Surrender means not having to fight anymore. We accept life the way it is. We become willing to do whatever it takes to stay ritual-free, even things we don’t like doing. I had to learn, and did learn, that I was growing when I made new mistakes instead of repeating old ones. I came to know myself through therapy. I found myself growing into a mature consciousness. I began to feel better, as willingness grew into hope. For the first time I could see my new life. With this in sight, I put my willingness into action, and that brought results. I examined my actions during the day. Writing them down helped. I could ask myself whether I was being drawn into old BDD patterns of fear. That way I could see if I was setting myself up for trouble.

I have come to realise that when someone points out a shortcoming in me, my first reaction doesn’t have to be defensive. I have had to realise, and do realise through recovery, that it is okay to have some not-so-great things about you. In appearance or otherwise, it is okay! Some parts of yourself might be a work in progress; other parts have to be lived with. But constantly thinking about changing a defect keeps the crazy thoughts going.

My recovery from BDD involved much more than simple abstinence from BDD tricks. If we had problems in the past, it is unlikely that simple abstinence will solve our problems. The recovery process involves an active change in our ideas and attitudes; attacking our ‘cognitive distortions’ such as catastrophising, mind-reading, disqualifying the positive, etc. We need to face up to our problems in order to stop the preoccupations which lie at the core of our disorder. If we allow ourselves to plateau and cling to ‘fatal’ safety behaviours, we are giving into the symptoms of our disorder. Continually ask yourself: would I be doing this if I didn’t have BDD?

Moreover, don’t let BDD dictate what you do or don’t do. I had to learn new ways to live, to replace old BDD habits with new ways of living. I have learnt from experience that a wave of peacefulness washes over me after I have successfully reduced or eliminated a ritual. Of course, at first it was hard and anxiety-provoking. But when I really kicked the trick, my internal fires died out. That which opposed me was less troubling, maybe even gone. I no longer feel the need to struggle today. Trusting that relief awaits me insures its arrival. Amelia Earhart said, ‘Courage is the price that life exacts for granting peace’. I am starting to be spirit-filled and I get the feeling my greatest contributions will be discovered now that my BDD has taken a rest. Our creativity awaits our discovery; we just have to release it from the clutches of our BDD.

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The Body Dysmorphic Disorder Foundation. Charity no. 1153753.

Online BDD Conference

An opportunity for professionals, researchers, students, and those with lived experience to find community and to learn more about BDD.

Join this virtual event on Saturday, May 31, 2025!

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