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Story


HLA

a FILM BY VALENTINA FEDONOS

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Story


HLA

a FILM BY VALENTINA FEDONOS

Story

"Above all is one's health. Often we just say that. But above all is one's health" 
Effie Streppa

"HLA"  

When his son dies from leukaemia, Michael Karaiskakis donates the money he raised for his son's treatment to create the first Bone Marrow Registry in Cyprus. The "HLA" feature length documentary follows the cases Karaiskakio Foundation is involved in while exploring the story of Karaiskaki's family.

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Progress


Progress


Progress

“HLA” is currently in the production stage. I started filming early January 2016. At the moment part 1 of the documentary is almost completed.

If everything goes as planned by June a rough cut will be ready and any additional filming needed, will be scheduled.

Please subscribe to the newsletter in order to receive updates. I also kindly ask you to follow the film on Facebook and keep an eye for any new posts.

“HLA” website will be regularly updated too so stick around. 

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Valentina Fedonos


Valentina Fedonos


Valentina Fedonos

 

 

London-based director with a main focus in trying to better the world through filmmaking. In my films I am exploring the theme of identity, migration, belonging and equality. Should you wish to find out more please feel free to have a look at my personal website here

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Karaiskakio Foundation


Karaiskakio Foundation


Karaiskakio Foundation

Karaiskakio Foundation is a non – profit organization established with the sole purpose of organizing a volunteer Bone Marrow Donor Registry. Today, by setting a dynamic vision “for a world without leukemia”, it combines volunteering and specialized scientific support, in order to serve the needs of patients with haematological malignancies both effectively and efficiently.

 

Should you wish to find out more – or even better become a donor – please visit Karaiskakio Foundation site by clicking on the button below

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How can you help


How can you help


How can you help

When I decided I wanted to do this film the idea was to raise awareness about leukemia as the percentage of new cases drastically increases and Bone Marrow Registries around the world need new volunteer donors to register, in order to treat new patients. What works against that is the lack of information or even worse the misinformation about the procedures of actually becoming a donor.

“HLA” will shed light and inform by following real cases and real people.

I can’t do that though by myself as I need as many people possible to help me spread the word about this attempt and the project. We need to start a dialogue with people and let them know what we are trying to do.

It will only take 5 minutes of your time to share this website on Twitter, Facebook and any other social networking platforms you are using. You can also email people you know and talk to them about “HLA”. The more people we manage to inform and urge them to join our team the better.

Please Like our Facebook page and invite your friends to like it too. And interact, my films are made in a way so that people will start talking with each other. 

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