The quality of learning achieved in university depends on many factors, with approaches to learning and studying being only one important aspect. To optimize learning among our university students, it is necessary to understand the learning processes that make high-quality learning outcomes possible. How students learn and study has been described extensively encompassing many overlapping aspects, using different terms: eg. learning approaches, learning styles, learning orientations, learning strategies and study skills. Approaches to learning and studying can be described in simple terms as ‘how students tackle their everyday academic tasks’. There are three main approaches to learning and studying eg. deep approach, surface apathetic approach and strategic approach. Identifying learning approaches and taking necessary actions to promote the more desirable learning approaches is necessary to achieve optimum learning. This presentation describes learning approaches and how to optimize them.
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This guidance was released today in the UK and if you haven't read it, it comes into effect in April and essentially is saying: we are allowed to maintain private online social profiles but must be aware if patients can access these and how we handle it if they contact us; any opinions voiced we have to make it clear it is our own and conduct yourself online as you would face to face with regards to confidentiality and boundaries.
This is quite interesting for me, as in our medical school there have been select cases of social media being used in disciplinary processes and I know myself that some of the photos I had on Facebook (I have deleted it) were not exactly portraying myself as the 100% professional doctor the GMC would love me to be.
But then reading the guidance, it makes no mention of content from when you were younger. When I'm an F1 will anybody really care about the drunk photos of me from freshers week 6 years ago and will these be taken out of context? I get the impression most people won't, but some might.
I really think they should have put a summarising take-home message in there somewhere: don't take the p**s, think before you post, don't give out medical advice as anything but your opinion and you'll be fine.
So, I think its about time I posted another blog post!
A few weeks ago I received the results from my most recent scan. I was both nervous and excited to find out my results, after months of tests and being misdiagnosed several times I just wanted to know what was wrong with me. However, as I read through the letter from my consultant I realised that my journey was just beginning. I was diagnosed with a rare stomach condition.
Gastroparesis. A chronic illness. There is no known cure, just various treatments with limited success. I didn’t really know how to react to this news. Shouldn’t I be happy that I finally knew what was wrong?
I had convinced myself for months that as soon as the doctors found out what was wrong, they could fix it and I’d be better in no time, but this wasn’t to be. I couldn’t understand how this could happen. Slowly the reality began to sink in, I’ll probably be fighting this battle for the rest of my life.
I think the mental aspect of chronic conditions is so commonly overlooked. I’ve sat through endless lectures about the pathophysiology of illnesses but I’ve never once stopped to think what it must be like to actually have it. The way it can limit your life, from not being able to go for a drink with friends because you’re in too much pain to the countless hospital appointments that your life seems to revolve around. The thing that hit me the most is the amount of medications I have to take on a daily basis just to make my symptoms bearable. I no longer have full control of my life and that's the worst part.
This experience has given me an invaluable insight into how patients with chronic illness feel. It affects almost every aspect of your life and you can never escape. It scares me to think of the future, I never know when I’m going to get my next flare up or how long its going to last. I just have to take one day at a time and hope that when I wake up tomorrow I won’t be too nauseous.
After spending a few weeks feeling down about it all, I’ve realised that I just have to enjoy life when I can and be grateful that I can still live a normal-ish life. It doesn’t matter how much I complain, it's not going to go away, and I think I’ve finally accepted that fact.
If anything, this experience has made me more determined to achieve my dream of becoming a doctor. I’ve been a lot more motivated to work harder so that one day I can help others like me through some of their toughest times, hopefully bringing them some comfort and relief.