Radio | 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...

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...

Over the weekend, I reached out to Jake (who has KLS) and Beck Renouf, son and daughter of Helen, author of the blog Kleine-Levin...