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Annual Lymphedema Fund Drive
YES we are beating the ignorance and lack of support!
When we first began to fight for Lymphedema Awareness in March 1997, people seemed to ''come out of the woodwork'' and be taken by surprise that they could do something about their Lymphedema and not just live with it. Now thousands of people are getting access to information and support in their communities, through the Lymphedema Awareness Foundation's events, seminars, educational forums/support groups and a complementary online magazine, eLymphNotes. It's a fact: every dollar you contribute helps improve the quality of life for a Lymphedema patient! Could any gift be more important?
The Lymphedema Awareness Foundation (LAF) is a 501 (c) 3 tax exempt, not-for-profit corporation filed in Florida, USA. Federal EIN # 59-3604229. website: www.elymphnotes.org email: lafinfo@elymphnotes.org tel/fax: 407 324 3255 USAPlease make checks out: In US dollars and make payable to the LAF and mail your donation WITH this completed page to the: LAF, 172 Lakeside Circle, Sanford, FL 32773 USA
Receipts will be issued for individual contribution of $200 or more. A canceled check serves as a receipt.
CONTRIBUTIONS ARE TAX DEDUCTIBLE UNDER INTERNAL REVENUE CODE SECTION 501(c)3. A COPY OF THE OFFICIAL REGISTRATION AND FINANCIAL INFORMATION MAY BE OBTAINED IN FLORIDA FROM THE DIVISION OF CONSUMER SERVICES BY CALLING TOLL FREE, 800-435-7352, WITHIN THE STATE, OR OUTSIDE FLORIDA 850-488-2221; OR FROM THE PENNSYLVANIA DEPARTMENT OF STATE BY CALLING TOLL FREE WITHIN PENNSYLVANIA 800-732-9000. REGISTRATION DOES NOT IMPLY ENDORSEMENT, APPROVAL, OR RECOMMENDATION BY THE STATE.
Please click here to donate to load/print a donation form to send with your donation. Thanks for your participation.
See LAF Financial Information |
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