Making a difference, one person at a time!

Imagine the impact you can make if you and five of your family and friends participate in the 2nd Annual Friends Asking Friends campaign! We will be able to increase our services and programs for the women and men impacted by Lewy body dementia.

This year alone, we have:

• Opened 22 new support groups, bringing the total to 40 groups run by volunteer facilitators.
• Distributed more than 100,000 booklets for newly diagnosed patients and their families to local service agencies across the United States.
• Launched a redesigned website that offers current scientific information on LBD as well as new features including online video presentations from experts in the field of Lewy body disorders. Website users can now logon and find more resources than ever before.

We have a full agenda for next year. LBDA will:

• Host an LBD Biomarker Symposium with Washington University, St. Louis, under the auspices of LBDA’s Scientific Advisory Council.
• Train more Helpline volunteers to answer questions and lead callers to critical resources.
• Launch a national program designed to educate physicians about LBD and new trends in diagnosis and treatments.

It’s easy to participate!

 First, please show your personal support with a gift today. Press here to contribute.

Then contact your family and friends, through mail or email, and encourage them to join you in supporting the Lewy Body Dementia Association. Click here to find a sample letter or email for your use. Need return envelopes to include with your letters? Please let the office know how many. Contact LBDA using the email form below.

Please send out your letters and email as soon as possible, so that your family and friends are contacted before the holiday rush. Would you like LBDA to know your friends’ donations are from you? Please ask them to put your name on the reference line of the donation page. Or, if you’re sending letters, mark your name on the back of the return envelope.

The fear and isolation Lewy body dementia brings to a family is staggering. LBDA needs to continue to be available when those impacted by this life-changing disease need help.

Thank you for all you do for LBDA!