Letter Writing Campaign to Raise Funds for SDS
A letter writing/email campaign is an easy way to ask friends and family for help in fundraising. You can ask for stationary from SDSF and produce it and mail it via the USPS or copy and paste into an email. Let us know how we can help you create an effective and efficient letter. With an email, you will want to put the link to our Get Involved page that has our donation information and DONATE BUTTON on it for easy credit card donating. www.shwachman-diamond.org/donate.htm
Here below is a sample that you can copy and use or feel free to edit. Sometimes it is easier to edit/re-write than to start from scratch. It is helpful to keep things positive and informative and limited to one page.
Dear Family and Friends,
As you may or may not know, our (family member, relation to you, and name) has Shwachman Diamond Syndrome. This disease is diagnosed in patients with bone marrow dysfunction (anemia, neutropenia or pancytopenia, multiple infections, bone marrow failure and higher risks for MDS, AML or ALL leukemias), pancreatic insufficiency (children are unable to digest food without pancreatic enzymes), skeletal abnormalities (bone growth doesn’t match the age growth and other abnormalities), and other lesser reported symptoms involving the lungs, heart, liver.
We are writing to you to ask you to send in any amount of money that you can to help us help (name of patient) through the efforts of Shwachman Diamond Syndrome Foundation. A suggested amount is $100 so as to raise as much money as we can to support the research efforts of Shwachman Diamond Syndrome Foundation. They currently have a research grant offering to scientists/doctors for $35,000 in order to remain competitive in the research world.
Shwachman Diamond Syndrome Foundation was started in 1994 by a mother of an afflicted child and has grown to serve over 500 patients and their families in the US alone (others around the world too), plus hundreds of medical professionals who ask for and receive information from it. It was the first SDS organization in the world and it spawned numerous other support groups due to its leadership and vision. With only 7% of the revenue going to administrative costs, 93% of every dollar donated goes to the activities listed below.
Activities supported and funded by SDSF are sending New Family Packets comprising of pertinent information for new families to learn about SDS, advocating grants for and fund research, baskets to hospitalized patients, providing email/phone family support, publishing tri-annual newsletter, attending and funding pertinent medical conferences, hosting and maintaining an international web site, and hosting a bi-annual family conference. The gene was found (December 2002) through the financial help of SDSF and this has given way to a better understanding of the disease and to diagnostic tests that have been developed to help with faster diagnosis.
Our family has benefited from many of these supports and activities and wants to continue to do so. Please help by going online to www.shwachman-diamond.organd donating through Paypal on the home page or send a check in to: Shwachman-Diamond Syndrome Foundation, P. O. Box 40, Avon, NY 14414. We will have your name published in the newsletter as having contributed in (name of patient) honor.
This is not a case of ‘what if” (name of patient) takes a downturn,
but ‘what if” we help fund a cure!
Thank you for your consideration to donate. Please feel free to call or email me with any questions.
P.S. Don’t forget to fill out the Matching Gift fund paperwork from your employer to maximize your donation. The number is 9588351. The tax exempt number is 43-1709945