Re: Road to ville donation-

[Guest guest]

If you go to the website and then click on the "Fundraising" link it'll take you to it. Let me know if you need more assistance.

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[Guest guest]

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What I just did was print off the website. I printed what was on the site, which was two pages, and stapled it together. That's what I gave to the president of the Lions.

Check out AOL Money Finance's list of the hottest products and top money wasters of 2007.

[Guest guest]

I don't see any paper work on there, though, just a website describing what the fundraiser is. Is there something I can print out to give to people to ask them to donate? I know some people who would probably be happy to make a donation, but I would rather hand them something about it, rather than just giving a website address. Re: Road to ville

donation-

If you go to the website and then click on the "Fundraising" link it'll take you to it. Let me know if you need more assistance.

Check out AOL Money Finance's list of the hottest products and top money wasters of 2007.

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[Guest guest]

Oh, I see. Thanks! Re: Road to ville donation-

,

What I just did was print off the website. I printed what was on the site, which was two pages, and stapled it together. That's what I gave to the president of the Lions.

Check out AOL Money Finance's list of the hottest products and top money wasters of 2007.

Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now.

[Guest guest]

Dear ,Thank you for being willing to join us raising funds on The Road To ville.Below is a letter that Deb Wente used to raise funds from her family, friends and business contacts.She generously shared it with the group to copy. Just personalize it to your situation.Thanks to and  our newest travelers for joining us !!Together in the fight whatever it takes !LeeIf need more help you can email me at:leedeubert@...Dear Family and Friends of the Wentes and Grovers,As many of you know, in August, 2004, our daughter, Wente, was diagnosed with Primary Sclerosing Cholangitis (PSC), an uncommon and currently incurable liver disease that may require a transplant some time down the road unless a cure is found. Up until recently, has been asymptomatic – after a recent procedure to "unclog" her bile ducts, it is our goal to keep her that way for another few years.In January 2005, a 501©(3) not for profit Foundation dedicated to finding a cure for PSC and providing education and support for PSC patients and caregivers was created. Following is a partial list of our successes since our inception:-We are a totally volunteer foundation with an administrative expense of only 1.5% (Deb is the Treasurer).-Our active website (with information regarding our educational, support, and research activities) has an average of 30,000 hits per month.-Our PSC Literature site has 53,000 abstracts in the database covering all aspects of PSC and related diseases, which is accessed by physicians, researchers, and patients.-We created a brochure entitled "Living With PSC" which is available to PSCers, physicians, and caregivers. So far, 2800 brochures have been handed out nationally.-We hold annual national conferences for PSCers and caregivers. The first three were attended by about 100 participants each. -Our Medical Scientific Advisory Committee is actively engaged in deciding where to allocate our funds for PSC research. In 2006, our board of directors approved financial support for two types of PSC research:-$20,000 donated to STOPSC registry run by The Foundation-$3000 prize donated to the most promising junior PSC researcher to be awarded at the 2007 annual meeting of AASLD (American Association for the Study of Liver Diseases).The 2008 PSC Partners Seeking a Cure Conference will be held May 2-4, 2008 at the Mayo Clinic in ville Florida. Mile by mile we will walk/run/ride/swim across the country from the Denver Hyatt Tech Center to our next conference in ville, FL. We have 2,000 miles to cover!! Let's get going! Each mile is covered by raising $50.Please consider making a donation in 's name. All donations are tax deductible and go toward researching a cure for this specific disease and providing support and information to those who have it. Thank you,Deb, , and A tax-deductible donation of $50/mile in honor of Wente can be sent to: PSC Partners Seeking a CureThe Road to ville5237 So. Kenton WayEnglewood, CO 80111I don't see any paper work on there, though, just a website describing what the fundraiser is. Is there something I can print out to give to people to ask them to donate? I know some people who would probably be happy to make a donation, but I would rather hand them something about it, rather than just giving a website address.