The Lauren Mantz OMS Research Fund was created by the parents of Lauren Mantz at Childrens Hospital Boston to address some of the many shortcomings today in the diagnosis and treatment of OMS. After our daughter Lauren was diagnosed with OMS, we were very surprised to find such little information and research existed about OMS. This has improved the last few years, but still has a long ways to go.
Research Fund Goals
Who is behind this research?
|The Lauren Mantz Fund for OMS Research was created at Childrens Hospital Boston, one of the premier medical facilities for children in the United States. Research in OMS is headed by Dr. Mark Gorman, head of the nuero immuniology program for the neurology department at Childrens Hospital. Dr. Gorman recognizes the many shortcomings in diagnosing and treating OMS and is dedicated to working towards the goals of the fund.||
Dr. Mark Gorman
How can I help?
We are putting together a Mother-Son OMS Fundraising Dance in the Ocala, FL area. If you would like to attend, all proceeds are for OMS research at Children's Hospital Boston. If you cannot attend the event, do not have a son or do not have children, you may still help by donating to the fund at Childrens Hospital Boston. If you wish to make a donation, please click the link below: