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CFF Fundraising
- Thread starter anonymous
- Start date
I am sure this has already been mentioned so sorry if it is repetative, but I just want to put it out there that in addition to the Cystic Fibrosis foundation and the great strides walk and all those wonderful things that help raise money for a cure, there is also the lungs for life foundation and the Milan foundation that take donations to assist Cystic fibrosis families who are struggling with financial issues associated with CF.
In the past I have raised money for CFF, but this year my focus is going to be for the lungs of life foundation and the Milan foundation. I Just thought it might be some useful information, because I feel that although it is very important to work for a cure, it is also very important to make sure that those living with CF right now are cared for and taken care of as much as possible financially.
Julie
In the past I have raised money for CFF, but this year my focus is going to be for the lungs of life foundation and the Milan foundation. I Just thought it might be some useful information, because I feel that although it is very important to work for a cure, it is also very important to make sure that those living with CF right now are cared for and taken care of as much as possible financially.
Julie
Hi Carey,
Would it be possible for you to e-mail me a copy of your letter too. That is so inspirational all the money you have raised for CF. I too have two children with CF (22 months old and 4 years old). I would love to send out a letter like that. It seems as if we are always asking the same people for donations to CF. I would also get my parents etc. to send copies to everyone they know as well.
Thanks.
bianchin_strong@hotmail.com
Would it be possible for you to e-mail me a copy of your letter too. That is so inspirational all the money you have raised for CF. I too have two children with CF (22 months old and 4 years old). I would love to send out a letter like that. It seems as if we are always asking the same people for donations to CF. I would also get my parents etc. to send copies to everyone they know as well.
Thanks.
bianchin_strong@hotmail.com
Augustmoon
New member
Carey,
Hopefully you are still checking this topic. I'd love a copy of the letter! My email is: Augustmoon0003@aol.com.
Thank you so much!!!!!
Hopefully you are still checking this topic. I'd love a copy of the letter! My email is: Augustmoon0003@aol.com.
Thank you so much!!!!!
Okay,
Having troubles getting logged on. Kay here. I have 2 siblings with cf. I do the Great Strides walks every year. I am starting my own fund raiser with the help of my yacht club called Sail for the Cure. Lake wide race all proceeds going to CFF. Don't know if I will get this pulled off for this coming year, but for sure in 2006. I am trying REALLY hard to get this going for '05. With the help of a few of my friends, I hope to raise ALOT of money. Wish me luck.
Kay Isom 19 days from being 30
sis 31 w/cfrd
brother 24 w/cf
Having troubles getting logged on. Kay here. I have 2 siblings with cf. I do the Great Strides walks every year. I am starting my own fund raiser with the help of my yacht club called Sail for the Cure. Lake wide race all proceeds going to CFF. Don't know if I will get this pulled off for this coming year, but for sure in 2006. I am trying REALLY hard to get this going for '05. With the help of a few of my friends, I hope to raise ALOT of money. Wish me luck.
Kay Isom 19 days from being 30
sis 31 w/cfrd
brother 24 w/cf