The FVL Project

The FVL Project is a new initiative I created in March 2014 to continue my goal of raising more awareness about the little known blood disorder Factor V Leiden mutation. Here you will find stories written by every day people about their experiences with FVL from all over the world in the hope you will find there are people out there just like you.

*The stories told here are all personal accounts and opinions; when in doubt about a medical condition, always consult your doctor or specialist.

Natale Caliendo – Maryland, USA
March, 2014
(A collaboration between Natale Caliendo, Louise Bensky and Berenice Vera Nieto)

Natale with son Noah

Natale with son Noah

Anyone living with Factor V Leiden (FVL) knows that it doesn’t just manifest into our system. It is a part of us; it has always been there, from our birth to our first breath, through childhood to adulthood and beyond.
Natale Caliendo calls it The Beast. He chose to give it a personality because you don’t mess with it…

Read more here

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Comments

  1. *The stories told here are all personal accounts and opinions; when in doubt about a medical condition, always consult your doctor or specialist.
    They are standing idly by, feeding rat poison to those who have a DVT.
    Serrapeptase and Nattokinase dissolve clots and reverse some of the accumulated organ damage. Stand up for your rights, you are not a slave of the medical establishment!

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