Having an excellent answer for the “Describe yourself in one word” question can be the difference between getting or not getting a job interview. Hiring managers ask this question because they want to understand if your personality and character are the best fit for their company and role. It’s a good idea to practice answering this question beforehand so you can give an appropriate and confident response. You can do this by writing down all of the qualities you associate with yourself and then narrowing them down to a selective bunch. Then choose the word that best describes you the most.
Myalgic Encephalomyelitis (ME) or Chronic Fatigue Syndrome (CFS), also known as post-viral fatigue syndrome (PVFS) and Systemic Exertion Syndrome, is a global disease with symptoms that affect multiple body systems. It is one of the most complex and challenging diseases to diagnose because it has broad and overlapping symptoms with other diseases such as Lyme disease, fibromyalgia and rheumatoid arthritis. Currently there is no laboratory test for ME/CFS, and accurate diagnosis requires in-depth clinical assessment of all the symptoms and exclusion of other diseases. Often people with ME go years before they receive a correct diagnosis.
It is estimated that 1 in 4 people are housebound or bedbound by ME/CFS, and many are unable to work full or part time. People who are severely impacted may need around the clock care. This can have a devastating impact on relationships, health and well-being, and financial security for the person with ME and their family.
There is no cure for ME, but there are ways to help manage the symptoms, including exercise, sleep, and medications. It is important for everyone to have an understanding of the illness and to support those living with it.
People who have ME/CFS and their loved ones have a voice that needs to be heard. We need to be an advocate for ourselves and others, to let our community know we’re not alone. There are a variety of resources available, including the ME Association, which offers information, support and practical advice. You can also join the Facebook ME Support Group or watch UNREST, a documentary about how the disease impacts individuals and their families. The National Institutes of Health has awarded ME research centers, which will help speed up research on this underfunded and misunderstood condition.