MMP | kleinelevinsyndrome

Living with Kleine-Levin Syndrome: The Unknown

With more than 100 confirmed cases in the UK, Kleine-Levin Syndrome is a rare and neurological disorder which affects young children and...

What a journey it has been - today marks the end of the editing process. I am typing this having just exported the final product after...

However, when I spoke to Helen Renouf (Jake's mum), and referred to it as this, she explained that some patients and family members may...

After weeks of constant emails and phone calls searching for a doctor or specialist to interview for my MMP, I finally managed to make...

It is important to me to remain ethical throughout my journalism career in order to stay true to what I am reporting about. This makes no...

We are now entering the early stages of editing the documentary together and the challenges I am facing are becoming clearer as the time...

In order to gain an understanding of what support is available to Kleine-Levin Syndrome patients, their families and their loved ones, I...

I met with my second case study for my documentary, Meg Gibson, on 4th December 2017. Like Jake, she also suffers with Kleine-Levin...

After meeting with Jake a second time to re-record his interview on Thursday 23rd November (as the computer didn’t record the entirety of...

Today, I met with Jake and and his sister Beck at university to discuss my documentary in more detail so they had an understanding of...