Whatch the film. Join the movment. #4Eva
 

MEG WILL BE AT SPOKANE FILM FEST!

By · January 30, 2010
Filed in Blog, Film

65_RedRoses will be screening as a part of the Spokane International Film Festival…

AND MEG (aka ‘megmucus’) FROM THE FILM WILL BE IN ATTENDANCE!!!

IMG_3920megmucus & 65_RedRoses

PVR OR TVO THE SUPER BOWL AND COME SHOW YOUR SUPPORT FOR CYSTIC FIBROSIS AND ORGAN DONATION!

SCREENING INFORMATION:

When: Sunday February 7th, 2010 at 12pm

Where: Magic Lantern Theatre, Downtown Spokane, WA

PLEASE CHECK OUT THIS SCREENING IF YOU’RE IN THE USA!!!

www.spokanefilmfestival.org

Comments

And I will be there!!!!

Damn…..I’d love to be there but that is one of the CRAPPIEST weekends to hold a film festival in the US. It’s Superbowl Sunday and thus I already have a group of friends coming over to watch it. If you are driving back and are going through Seattle area I live just outside of it and would love to meet ya. If you can’t guess from my e-mail I have CF too. So does my sister who still lives in California. I’m under my same name on FB if you want to reach me there. Hope the screening goes well.

It is the second entry I really enjoyed tonight. Thank you.

Hey Meg,
Not sure if you are going to get this or not but I saw the documentary two days a ago and Eva passed away yesterday. I am so sorry. You all have tremendous strength and courage and I am rooting for you. Whatever your decision may be. You touched me in ways you cannot even imagine.
Stay strong.
Rachel

follow this webpage for to the 2010 riders link, I need your support to help research and cure CF. 65_Red Roses gave me a glimpse of life with CF and we the 24 riders for CF will be doing a 9 day trek on our bikes from Vancouver B.C. to Banff in June 2010–your support is necessary to make these childrens and young adults life more livable

Remember GearUp4CF, 2010 Riders, Kitty Chavarie…please give so others may live

i,m from nova scotia. and my little princess has c.f.she is now 20 and so far so good. i,ve seen the movie 65_redroses last night and at that end they said eva had passed last week. god bless you eva and your family.you,s are so strong. i just hope if the time comes that i will be as strong as you. i have lung trouble myself so i,m hopeing that i will go long before any of my kids. i just want you,s to know that we here on the east coast are thinking of you,s and that eva has got the org. message out and hopefully they will have a cure soon. i know when our princess was born in 1990 they said she would be here for around15 yrs or so but in that time it has gone up to 40+and it is because of the love of people like eva.so lets hope that they will have a cure soon so know other has to fight to breath.all the best to all .

Eva, our Red Girl;

The light is a little dimmer now. Memories of your smile inspire our hope. Surely the dawn must be coming?

Damn…..I’d love to be there but that is one of the CRAPPIEST weekends to hold a film festival in the US. It’s Superbowl Sunday and thus I already have a group of friends coming over to watch it. If you are driving back and are going through Seattle area I live just outside of it and would love to meet ya. If you can’t guess from my e-mail I have CF too. So does my sister who still lives in California. I’m under my same name on FB if you want to reach me there. Hope the screening goes well.

follow this webpage for to the 2010 riders link, I need your support to help research and cure CF. 65_Red Roses gave me a glimpse of life with CF and we the 24 riders for CF will be doing a 9 day trek on our bikes from Vancouver B.C. to Banff in June 2010–your support is necessary to make these childrens and young adults life more livable

Remember GearUp4CF, 2010 Riders, Kitty Chavarie…please give so others may live

It is the second entry I really enjoyed tonight. Thank you.

And I will be there!!!!

i,m from nova scotia. and my little princess has c.f.she is now 20 and so far so good. i,ve seen the movie 65_redroses last night and at that end they said eva had passed last week. god bless you eva and your family.you,s are so strong. i just hope if the time comes that i will be as strong as you. i have lung trouble myself so i,m hopeing that i will go long before any of my kids. i just want you,s to know that we here on the east coast are thinking of you,s and that eva has got the org. message out and hopefully they will have a cure soon. i know when our princess was born in 1990 they said she would be here for around15 yrs or so but in that time it has gone up to 40+and it is because of the love of people like eva.so lets hope that they will have a cure soon so know other has to fight to breath.all the best to all .

follow this webpage for to the 2010 riders link, I need your support to help research and cure CF. 65_Red Roses gave me a glimpse of life with CF and we the 24 riders for CF will be doing a 9 day trek on our bikes from Vancouver B.C. to Banff in June 2010–your support is necessary to make these childrens and young adults life more livable

Remember GearUp4CF, 2010 Riders, Kitty Chavarie…please give so others may live

i,m from nova scotia. and my little princess has c.f.she is now 20 and so far so good. i,ve seen the movie 65_redroses last night and at that end they said eva had passed last week. god bless you eva and your family.you,s are so strong. i just hope if the time comes that i will be as strong as you. i have lung trouble myself so i,m hopeing that i will go long before any of my kids. i just want you,s to know that we here on the east coast are thinking of you,s and that eva has got the org. message out and hopefully they will have a cure soon. i know when our princess was born in 1990 they said she would be here for around15 yrs or so but in that time it has gone up to 40+and it is because of the love of people like eva.so lets hope that they will have a cure soon so know other has to fight to breath.all the best to all .

follow this webpage for to the 2010 riders link, I need your support to help research and cure CF. 65_Red Roses gave me a glimpse of life with CF and we the 24 riders for CF will be doing a 9 day trek on our bikes from Vancouver B.C. to Banff in June 2010–your support is necessary to make these childrens and young adults life more livable

Remember GearUp4CF, 2010 Riders, Kitty Chavarie…please give so others may live

Damn…..I’d love to be there but that is one of the CRAPPIEST weekends to hold a film festival in the US. It’s Superbowl Sunday and thus I already have a group of friends coming over to watch it. If you are driving back and are going through Seattle area I live just outside of it and would love to meet ya. If you can’t guess from my e-mail I have CF too. So does my sister who still lives in California. I’m under my same name on FB if you want to reach me there. Hope the screening goes well.

Hey Meg,
Not sure if you are going to get this or not but I saw the documentary two days a ago and Eva passed away yesterday. I am so sorry. You all have tremendous strength and courage and I am rooting for you. Whatever your decision may be. You touched me in ways you cannot even imagine.
Stay strong.
Rachel

abbreviation is along word because they want you to abreviate it

Leave a Comment

Whatch the film. Join the movment. #4Eva