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Do you have a loved one living with Alzheimer’s disease and dementia? As a caregiver you know the challenges of the daily routines needed to ensure your loved one is comfortable and safe. A new federal grant is on its way to help support families and loved one.

 
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$1.3 Million Federal Grant for Alzheimer’s and Dementia Treatment

A San Diego research institute has been recently awarded a federal grant to do important research for families living with Alzheimer’s disease. The institute has been awarded $1.3 million.

The Conrad Prebys Center for Chemical Genomics is the recipient of the federal grant. The researchers there aim to identify chemical compounds that may be used in a new medicine to slow Alzheimer’s and dementia progression.

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Three Year Grant from National Institutes of Health (NIH)

The National Institutes of Health is funding the research for the treatment to slow the disease’s progression. It will be for a length of three years.

The San Diego County has a large number of people over 55 years old, and expected to increase by 36 percent in less than 15 years. The treatment research may be useful locally and globally.

Currently there is no cure or known treatment that modifies the disease, but researchers aim to change this. They have pinpointed a specific gene that appears to be problematic in the progression of the disease.

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Drug Screening Robots are Helping Researchers Find Alzheimer’s Treatment

Interestingly, drug screening robots are assisting in testing over a million compounds to find the right one to attack the problem gene researchers have identified. This can help caregivers and families of people living with Alzheimer’s and dementia significantly.

The institutions involved in the research and federal grant are Sanford Burnham Prebys, C4C, The Salk Institute, The Scripps Research Institute, J. Craig Venter Institute and the University of California, San Diego.

Alzheimer’s disease is the sixth leading cause of death for Americans. In San Diego County it is the third. The grant signals the need for more research and a treatment option for families and those living with the disease.

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