Have you ever felt like you don’t belong? Like any second now your friends or work mates will discover that you are a fraud? Do you ever think that your successes are attributed to luck, rather than your own skills or qualifications? Or, do you try to keep more and more balls juggling in the air; always trying to maintain impossibly high standards, and with each success you achieve the greater the feeling that you aren’t enough?
If so, you’ve probably experienced imposter syndrome, right along with an estimated 70% of the population.
Imposter syndrome was first described back in the late 70’s by psychologists Pauline Rose Clance and Suzanne Imes who recognised that this imposter phenomenon was particularly prevalent amongst a select group of high achieving women. But, it is known to affect all kinds of people from all walks of life, men, women, medical students and managers.
Even international superstars are not immune to its effects. Emma Watson, star of the Harry Potter movies told Rookie magazine, in an interview (2013), “It’s almost like the better I do, the more my feeling of inadequacy actually increases, because I’m just going, ‘Any moment, someone’s going to find out I’m a total fraud, and that I don’t deserve any of what I’ve achieved.”
More and more imposter syndrome is being seen in marginalised groups and shows up regularly in the disabled and chronic illness communities. It makes perfect sense that your feelings of self doubt and being a fraud are more likely to show up if you have grown up belonging to a group that was historically believed to be less capable.
According to the department of health, fifteen million people in England have one or more long-term health conditions, and the number of people with multiple chronic illness’ is rising. These are conditions which cannot be cured in most cases, but which can have a major impact on people’s everyday lives. Aside from the physical symptoms, people with long-term conditions are 2-3 times more likely to suffer mental health problems than the general population (King’s Fund) and with 15% of all long term conditions seen in young adults aged 11-15, this group is too important to ignore.
With the pressures in society increasing, imposter syndrome is likely to be seen more and more.
How does imposter syndrome show up when you have a chronic illness or disability?
The more I delve into this topic the more I can recognise my imposter showing up for me during the different stages of my chronic illness journey. As a young adult before my diagnosis, after diagnosis (while simultaneously trying to juggle work and hide from everyone the struggles with my health), when I was a new mum (and my health crashed to an all-time low), and even now, when I feel like I am not well enough to be ‘normal’ but don’t look disabled enough to fit into that space either.
Expert on the subject, Dr. Valerie Young, has categorised imposter syndrome into five subgroups in her book, ‘The Secret Thoughts of Successful Women: Why Capable People Suffer From The Imposter Syndrome and How to Thrive in Spite of It’: the Perfectionist, the Superhero, the Expert, the Soloist, and the Natural Genius. I can recognise elements of myself in most of these Imposter archetypes, particularly the perfectionist, the expert and the superhero. Read more here – What Is Imposter Syndrome and Do I have It?
Feeling like a fraud in your own body
I was diagnosed in my 20 with Charcot Marie Tooth disease (CMT) and in my 30’s with Ehlers-Danlos syndrome (hEDS), despite living with the symptoms since being a small child, at points hospitalised unable to walk. I encountered decades of normal blood test results and doctors telling me that there was nothing wrong, when in fact the doctors were never looking in the right place.
Now we know that imposter syndrome makes you feel like a phoney. Imagine being told all your life that your symptoms are in your head, that the pain that you are experiencing has no cause, so much so that you begin to doubt that it is real yourself. Then when, often as an adult, you finally get a diagnosis you still doubt yourself. The decades of feeling like a fraud in your own body are hard to shift. When you feel pain, even after the validation of a diagnosis, you question if it is as bad as you are imagining. This feeling of being an imposter can be as crippling as the pain itself.
Imposter syndrome and refusing your own success
These feelings spilled over into my studies at university. I came from a very working-class background and was the first person in my family to go to Uni. My symptoms continued throughout my teens and my time studying and I began to just push them aside more and more. If no one could find a reason then I must be imagining it, right? Dislocations would happen more often than brushing my teeth and I could relocate my patella as easily as zipping up my trousers. I worked hard and my grades steadily got better and better and I left university with a 1st degree. But, I didn’t believe that I deserved it, nor had I earned it and I put it all down to a fluke. Applying for jobs I would often downplay my expertise even though I was genuinely more skilled than the other candidates. Thankfully they saw me for who I was, sat in front of them with the skills I possessed and viewed my modesty as an admirable quality rather than the imposter around my neck holding me hostage.
Your imposter making you doubt your symptoms or disability
Occasionally I have to use a wheelchair to get about, when I can’t weight bear as my labral tear or hip impingement is flaring or if I have had a dislocation. There have been points over the last few years where our son would not have been able to leave the house without one. And, our daughter uses a wheelchair regularly when out and about to manage pain and fatigue. We can walk, mostly we look well (although that is not always the case with my son, but you generally won’t see him on those days), and we are happy. Which begs the question where do we fit? We certainly do not ‘fit’ into the disabled criteria, neither are we able bodied. Using a wheelchair part time can make you feel like a fraud and question your reasons for using it at all. Should I just manage without, even if it leaves me unable to walk for the next few days? That nagging doubt begins to creep back in.
Imposter syndrome fuelled by medical gaslighting
With my diagnoses’ I entered two worlds; One where I had a genetic test to confirm it (CMT) and one where I didn’t (hEDS). And what I have noted time and time again is that the imposter phenomenon is far more present in the latter due to the continuing doubt form the medical community that hEDS exists at all. Similar practices are echoed in the M.E. (myalgic encephalomyelitis) community. Another condition is diagnosed clinically and at present has no conclusive test to diagnose. Medical practitioner’s gaslight patients by blaming their illness or symptoms on psychological factors, or by denying a patient’s illness entirely, for example by wrongly telling patients that they are not sick. After enduring decades of ‘normal’ test results I was adamant that I did not need nor want any support with my psychological wellbeing. I was not going to let anyone tell me that these conditions were in my head. This narrative caused by medical gaslighting is damaging, many people with long term conditions would benefit from support to process their emotions and thoughts surrounding the impact their health condition has on their life and move forward positively, but like me will refuse it.
Being a perfectionist and self sabotage
Being a perfectionist is the imposter avatar I relate to the most, this probably has something to do with my personality type but also relates to my experiences with disability and chronic illness. As a young teacher, quickly progressing through the ranks in school I placed impossibly high standards on myself to match up to my peers. I worked longer and longer hours, weekends, volunteered for things that I did not really want to do all in a bit to prove to others (and myself) that I matched up. That my disability did not need to get in the way and that I did not need special treatment. The truth was that my colleagues probably never thought about my health because I hid it so well and what I projected was so ‘normal’ and capable. What I did was place an impossibly high bar for myself to achieve and made myself more sick in the process. If I had been honest with myself then I may have stayed in the profession, either way I would have had a choice. My fear of failure and insecurities had a hand in sabotaging my own success.
Asking for help is sign of weakness
As a new mother my body actually started to fall apart. Surgery after surgery came and when I wasn’t recovering from a procedure, I just felt generally awful. On top of that I felt guilty that I wasn’t the mum to my young son I had visualised in my head. In a bid to prove to the world that I could cope I tried to do everything on my own, firmly believing that asking for help would be a sign of weakness. I felt ashamed that I couldn’t do everything (although people rarely saw because I didn’t let them). I was always striving to be better, not less than. Looking back with fresh eyes I can see that this time of my life was actually quite precious, I was present with all of my children every day. Had my body not been falling apart I would have undoubtedly been trying to conquer the world and having it all. The bond I now have with each of my three children is unbreakable and it is due to the fact that we have always spent so much time together.
Ableism fuelling imposter syndrome
Ableism, the discrimination towards able-bodied people is strong throughout them educational system in the UK, particularly when you have a disability or medical need but are academically bright. You are entitled to educational accommodations to help with your studies or tests, to level the playing field so to speak, maybe because you get brain fog and need regular rest breaks, or get hand pain when writing and need to use technology or a scribe. Many people with a disability or illness are made to fight for any real support leaving them with feelings of doubt questioning if they really deserve the accommodations in the first place. To get the right support in place for my teen, who was too sick to attend school at all took twenty months rather than the twenty weeks suggested by the UK government and we ended up in court. Twenty months and a court case to secure at home online education, that is now so commonplace. Seems ridiculous. Many give up as the system is stacked against them. I see the feelings of uncertainty in this population time and time again. It stems from this deep rooted ableism, a lack of money and a system that is stacked against them.
Comparison feeding the feeling of not matching up
As someone with a (mostly invisible) disability, I am guilty of comparing myself to others. From my best friend would literally looked a stone lighter on a night out when she popped on her 6″ stilettos, while I donned sensible flats. To the mums in the playground with their perfect car and child and hair, that seemed to have it all. Fuelling the feelings of not being good enough that stemmed from my body letting me down. What I have come to realise is that no one actually has it all, least of all the mum who hid behind her perfect life to hide her own crippling insecurities and debt.
Facing my Imposter feelings
As I have aged and am now well into my 40’s I can look back on my life with reflective eyes, both on the progression of my chronic illness’, my work, my growing family and my feelings of being an imposter.
My feelings of being a fraud have pushed me out of my comfort zone at many times during my life, like when my tutor said I wasn’t bright enough to be in his A level biology class (note the first degree), or when I spoke to a room full of paediatric consultants about my children’s conditions and each year when I guest lecture at Brunel University. Credit where it is due, at points in my life my imposter has truly been the driving force behind my successes.
I am still a perfectionist, but I can recognise when that is not serving me and know that done is better than perfect. I know that I can play to my strengths, because I have many of them and am happy to ditch or delegate the other things to other people. I know that asking for help is a sign of strength not of weakness and by working together with others I can achieve so much more.
Will we still have to face gaslighting from the medical profession? probably. It saddens me to think that this still goes on. I stand strong in appointments with professionals and where our opinion differs, for example where a consultant told us he didn’t actually believe our son’s condition existed at all, (clinically diagnosed by an esteemed colleague). I thank them for their comments and move on… quickly.
Do I care that my daughter uses her wheelchair to ride to the park so that she has enough energy to play while she is there and still be awake at teatime? Of course not! Do we get funny looks when she gets out of her wheelchair and her older brother shouts ‘IT’S A MIRACLE’ for all to hear? Most definitely, but we laugh and carry on with our day.
What I am noticing is that I am raising children with their own health issues who are confident and proud, of who they are and of all their abilities and achievements. Disabilities or not they have a strong and positive self-concept and I am proud of each of them as they grow.
What has changed over the years is not my disability or illness or the world in which I live but my own thought processes surrounding everything to do with my life and my health. My mindset, my own attitude towards myself and my illness has grown, and what has followed is a freedom I could have only dreamed of in my early 30’s.
Do I wish I could wear high heels? Sometimes. But if that meant giving up who I have become I will keep this version thanks.
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Right now you may feel like no-one understands what it’s like living with your chronic illness. That you are hanging on by a thread or the future may feel a little uncertain. Here in the Tribe we get that.
You value life and want to be the best version of you. To get your head around your diagnosis, manage your symptoms effectively and have open and honest relationships – so that you can live your best life and feel in control of your health condition.
In the community we will be having real, open conversations about how you can do this. With my experience of living with multiple chronic illness’ and raising kids with CMT, EDS, PoTS and ME. I know that the struggle is real. I will be sharing guidance, challenges, my personal tips and real life stories to remind you of how this can become a reality for YOU now!
I am passionate about this because I know the positive impact that my mindset has on managing my chronic illness and helping my children to live their best lives.
It has changed my life.