Eva's death
Hi, this is my first entry in this journal. First, I'm a french canadian, so I will try to write the best I can in my second language.
The main reason why I start a live journal was to follow and comment the LJ of Eva Markvoort who battle CF whit such a courage. I,Ve begin to read her LJ sinci november 2009 afer the broadcasting of the documentary '65_redroses' at CBC. She inspire me so much as well as people who followed her that I can say today that my view of life have change forever. I do not take for granted everything now, every breath a take and has she said "Life is not measured by breaths we take but by the moments that take our breath away...".Eva passed away on march 27 and I'm still in shock. So to have some closure, I've begenning to read her journal since her first entry in 2006 and she is still alive in my heart now that I see her pictures, read the comments of other people with CF warriors like Talana, Meg, Kina, and followed her before and after her transplant. For now on, even if I dont have CF, I'm gone be more active to the cause of Eva, for donneting organs, so that orther people could have a gift of life. Also, I will try to support others CF persons who have a LJ.
Now I'll return to Eva journal because I'm at the 30 november 2007 entry (after her transplant).
I will write more later.
Denis
The main reason why I start a live journal was to follow and comment the LJ of Eva Markvoort who battle CF whit such a courage. I,Ve begin to read her LJ sinci november 2009 afer the broadcasting of the documentary '65_redroses' at CBC. She inspire me so much as well as people who followed her that I can say today that my view of life have change forever. I do not take for granted everything now, every breath a take and has she said "Life is not measured by breaths we take but by the moments that take our breath away...".Eva passed away on march 27 and I'm still in shock. So to have some closure, I've begenning to read her journal since her first entry in 2006 and she is still alive in my heart now that I see her pictures, read the comments of other people with CF warriors like Talana, Meg, Kina, and followed her before and after her transplant. For now on, even if I dont have CF, I'm gone be more active to the cause of Eva, for donneting organs, so that orther people could have a gift of life. Also, I will try to support others CF persons who have a LJ.
Now I'll return to Eva journal because I'm at the 30 november 2007 entry (after her transplant).
I will write more later.
Denis