Author Archives: abtadmin
Give to the Annual Fund: Chair Beth Karas
Your donation to the National MPS Society’s Annual Fund helps move our Mission forward in finding therapies and cures for children who need them and supporting our families.
MPS IV phase III clinical trial
The MPS IV phase III clinical trial is now underway in several centers in the U.S. For more information, please refer to the study brochure. Patients Brochure
Illinois legislature approves MPS I and MPS II newborn screening
The Illinois legislature approved newborn screening for several lysosomal diseases in November 2010, and recently added MPS I and MPS II to their list. Illinois Public Act 097-0532
2011 Research Grants Awarded
The National MPS Society awarded $421,500 in grant funding for 2011. The funding the Society provides has been and continues to be crucial as we move forward with our mission …
New California Law Ensures Affordable Health Coverage for Kids
Insurance Commissioner Jones And Assembly Member Feuer Highlight Critical Window For Children’s Health Insurance New Law Ensures Affordable Coverage for Kids, Regardless of Pre-Existing Conditions; Open Enrollment Period Ends March …
Help us secure May 15, 2011 as National MPS Awareness Day!
Dear Friends: The Time for Action is NOW to secure co-sponsors for Senate resolution designating May 15, 2011 as National MPS Awareness Day. The deadline for co-sponsors is May 11, …
Research Grants 2011
The National MPS Society awarded $421,500 in grant funding for 2011. The funding the Society provides has been and continues to be crucial as we move forward with our mission to find the cures.
