We need your help

Families of children and adults with AGS have the odds stacked against them.  Since AGS is incredibly rare and has no government funding, the responsibility is on families to find a cure for our loved ones.

We need YOU to help make this happen. Any of our board members are always willing to discuss and help facilitate ideas that will result in raising awareness and/or funds for AGS research.

Find out what we've achieved so far!


set up a monthly donation

The easiest & greatest way to help is to set up a monthly donation. Once you've selected your donation amount, click 'Monthly' before moving on. We assure you, your credit card information is safe & secure.

 

OR SEND A CHECK

Online credit card processing platforms take a percentage of your donation: 2.2% – 2.9% + $0.30 per donation. If you'd rather send a check please send to: 

AGSAA
PO Box 1181
La Plata, MD 20646

 

Spread the Word

Once you make a donation click the share button to share to your Facebook page! It won't show your amount, it will just direct people to this page so they can offer support, too! Social media is an incredible outlet for getting awareness out there.