At the Lewy Body Dementia Association, we understand that many families are touched by Lewy body dementia. Whether you’ve been recently diagnosed, you’re a caregiver, a healthcare professional, or you’re looking for more information – we’re here for you. We’ve created our homepage to help LBD families quickly access up-to-date information about LBD to help prepare for some of the changes ahead.
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Learn more about LBD:
What is LBD?
Diagnosis
Symptoms
Treatment Options
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Join our Online Communities!
Caregiver and Patient Forums
LinkedIn Community (brand new!)
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We Need Your Help!
Did you know:
- $500 provides the latest information on LBD diagnosis and treatment options to 50 families.
- $250 provides vital information on Lewy body dementias to 20 physicians.
- $100 enables an LBDA Support Group to offer help and support to families for six months.
- $50 provides support to caregivers through the Caregiver Helpline for one week.
Click here to make your donation to the 2nd Annual Friends Asking Friends! Campaign.
Click here to get details on how you can invite your family and friends to join you!
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New LBDA Publication
An Introduction to Lewy Body Dementia:
A special publication for people newly diagnosed with
Lewy Body Dementia and those still seeking answers.
LBDA’s latest publication is now available. An Introduction to Lewy Body Dementia provides easy-to-read clinical information on LBD in a patient-friendly manner. This booklet was made possible by a generous grant from Novartis Pharmaceuticals Corporation and through the guidance of LBDA’s Scientific Advisory Council.
In this booklet, you will learn the symptoms of LBD, what to do if someone hasn’t received a diagnosis and the first steps to take after receiving a diagnosis. The booklet also includes a detachable medical alert wallet card to help ensure proper medical care in an emergency.
Click here to read An Introduction to Lewy Body Dementia.
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NEWS FLASH!
Lewy Body Dementia Association reaches major milestone!
The Lewy Body Dementia Association (LBDA) now has 40 support groups spanning 21 states plus the province of Ontario, Canada.
If you know of family caregivers who might be interested in becoming an LBDA Support Group Facilitator, they can learn more by clicking here.
Our thanks to Board Member Ronnie Genser, National Support Group Coordinator, and the growing pool of support group facilitators, for your continued commitment to lift the burden on families affected by Lewy body dementia!
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In Remembrance
The Lewy Body Dementia Association mourns the passing of Harry T. Mangurian, Jr., Sunday, October 19, 2008. Mr. Mangurian was a true friend and supporter of LBDA in myriad ways.
Click here to learn more about Mr. Mangurian and how he supported LBDA's mission.
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Here are some helpful materials to print out and read at your convenience. (These materials can be viewed with Adobe Reader, which can be downloaded for free from Adobe.)
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