When you’re applying for a job, you often get asked the question: “Tell me about yourself.” This gives your interviewer an idea of what kind of person you are and allows them to figure out if they think you can do the job well. There are some things you should avoid when answering this question, though.
One of the most important aspects of a good self-description is to be specific about your skills and qualities. You want to describe yourself in ways that will make you more memorable and believable, so your interviewer can imagine what it would be like to work with you. This is why it’s important to be creative in the way you answer this question, but also to focus on your strengths and how you can benefit the company or organization.
You should use this opportunity to highlight your best qualities and explain how they relate to the position you’re applying for. It’s also a great time to discuss any accomplishments that you are particularly proud of. This can help your interviewer understand why you are the best candidate for the role.
Many people who have ME/CFS struggle to get a diagnosis and can be misdiagnosed or diagnosed with another condition. This is partly because there is no test for ME/CFS and doctors can only diagnose the disease based on symptoms and using recognised criteria. It is therefore important that you work with your healthcare professional and keep a detailed log of your symptoms.
ME/CFS is a complex neuroimmune illness that is not well understood and can have devastating effects on people’s lives. The illness can appear suddenly or more slowly over time and is triggered by certain infections, usually viruses.
There is no cure and no known cause for the illness, but treatments can help manage symptoms, such as pacing activity to match your energy levels; sleep aids; painkillers; and physiotherapy. Keeping up to date with current research can also be helpful, and contacting local support groups is a good place to start (e.g. ALISS and Action for ME).
ME/CFS can affect anyone from any background, although it is more common in women than men. It can be a debilitating and isolating illness, especially when symptoms are severe, and it is sometimes not taken seriously by family and friends. The lack of understanding and awareness about the illness means that it can be difficult to access social care, employment, and NHS treatment, and may lead to disbelief and discrimination from others. Those with ME/CFS who require additional support should contact a local ME/CFS service or call the helpline at Emerge Australia (0800 865 321) for more information and advice.