associationinformation


	Association for Glycogen Storage Disease

What is the
Association for
Glycogen Storage Disease (AGSD)?
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Association for Glycogen Storage Disease
P.O. Box 896
Durant, IA 52747
563-514-4022
www.agsdus.org Contact Us!

The Association for Glycogen Storage Disease [AGSD] is a parent and patient oriented support group that is advised by a group of experienced medical professionals.

The AGSD was established in 1979 in order to create an organization which would be a focus for parents of and individuals with all types of GSD to communicate by:
* sharing their successes and concerns
* sharing useful findings
* providing support
* creating an awareness of this condition for the public
* stimulating research in the various forms of glycogen storage diseases and have the results communicated to the parents, affected individuals, and the public as soon as possible.

Andrew O’Toole is the current President of the Association for Glycogen Storage Disease. You may contact him at: president @ agsdus.org. Hollie Swain is the founder of the AGSD, and the Membership Secretary and current Treasurer. She has worked tirelessly to make the AGSD what it is today.

The AGSD mails out a newsletter, The Ray, which is published quarterly. As a member of the AGSD, there is no charge to receive the newsletter.

Each year, the AGSD compiles a directory of all current active and associate members. The directory is distributed to AGSD members in the Spring issue of The Ray. These membership lists are to be used for SUPPORT ONLY - whether for emotional (parent - affected) guidance or professional guidance.

*Information about membership in the AGSD*
(including a printable version of the AGSD dues sheet)

The AGSD has also created a handbook, “Glycogen Storage Diseases, A Patient - Parent Handbook”, which has more in-depth information about each of the most common types of GSD.

The Association for Glycogen Storage Disease holds a family/medical conference each year for those affected with GSD, their families, and medical professionals involved in treatment or research of any type of GSD. The focus of these conferences is meeting other people and families affected by GSD, gaining a better understanding of the GSDs and their implications, and learning about the latest research findings and upcoming studies. The AGSD understands that having a family member with a rare medical condition is very difficult, so by gathering each year, we affirm and encourage each other.

The AGSD is active in fund-raising and encourages its members to participate in local fund raising projects. Funds that have been raised have gone to support research, provided help in obtaining the pumps for nocturnal nasogastric feeding, assist in providing supplies when needed, and granted awards to help defray college expenses for individuals with the disease. The association has fostered publicity about the condition in local newspapers to the public aware of the condition, the need for research, and the need for support by the individuals with GSD. As funds become available, we would hope to:

1. Greatly increase our publicity effort.
2. Solicit more actively to get Congress to increase research support.
3. Increase our help to individual families of patients.
4. Improve our educational tools and efforts for the families and the public.
5. Provide referral services to identified treatment facilities.
6. Respond quicker to requests from the medical community.
7. Support a fellowship for a young investigator in one of the universities active in
GSD research, so the individual could work full-time on GSD research.

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