Research and FundRaising
Research is Continuing
The Foundation for Children with Atypical HUS, a United States Charity, has now sponsored over 4 grants. The grant are awarded on a comnpetitive basis, and are awarded based on "Research which fosters a better understanding of the mechanisms which cause Atypical HUS. Preferential treatment will be given to any study which also attempts to find a better method of treatment for Atypical HUS."
Over $250,000 has now been awarded to cutting edge researchers. The top European researchers have been awarded the grants in the past. These included Dr. Guiseppe Remuzzi, Dr.Timothy Goodship, and Dr. Peter Zipfel.
The proposals included a study of the Factor H Genes, and also the ADAMTS13, a gene which is suspect in TTP and in Atypical HUS.
The grant was awarded on a competitive bid process involving researchers throughout the world. Many thanks to all participants. The Foundation for Children with Atypical HUS has plans to sponsor additional promising research as funding allows. For more information, contact BBiermann@Premier-ks.com
In 2007, the Foundation announced the funding of a United States Graduate student at the University of Iowa. Dr. Richard Smith, Professor at the University of Iowa, will oversee a graduate student. To our knowledge, this is the first private funding of any research project on Atypical HUS in the United States.
One of the most important goals of the project is the development of a testing sytem for all of the suspect Genes. A second goal is the registry information that accompanies the testing. Also, the development of a synthetic Factor H replacment would be a dream come true.
-THE FOUNDATION FOR CHILDREN WITH ATYPICAL HUS
The "Foundation for Children with Atypical HUS" is IRS approved, not for profit organization.
The primary purpose of the foundation is to fund research for this disease.
A secondary purpose is to generate information on the disease so parents and medical professionals can be more informed.
The organization will also function as a support group for parents and siblings who have a loved one with the disease.
Fundraisers are occurring throughout the year. If you would like information on how you can help, EMail me, Bill Biermann, at SaturnRacer1@cs.com, or call me at 636-942-4425
Contributions can be made to:
Foundation for Children with Atypical HUS
c/o Missouri State Bank
101 South Hanley
Clayton MO 63105
Attn: Debbie Hanak
If you want more Information
Contact BBiermann@Premier-ks.com
