Little Lauren.org was created to raise awareness about opsoclonus-myoclonus syndrome (OMS), a very rare neurological autoimmune disease that Lauren has been ill with and fighting since January 2009.
Because it is such a rare disease, very little research is being done to assist in diagnosis and treatment. We are trying to raise money for OMS research so that those affected with the disease can be diagnosed as quickly as possible and receive the most effective treatments, including our "Little Lauren". We hope you will join us. :)
How can you help?
Donate to OMS Research
A research fund for OMS has been setup at Childrens Hospital Boston named the "The Lauren Mantz Fund for OMS Research". Your help is needed to improve the outcome for future OMS children. Donations can be made online to this fund. Click the link below for details about the research and the online donation page.
Click Here - Donation Link and Research Fund Details
Attend the local Ocala fundraiser
Tickets will go on sale April 2 at The Learning Wheel in Ocala and are $30/couple and $10/additional son.
Hawaiian Themed or Dressy Casual Attire Recommended
All proceeds from the event are donated to Boston Childrens Hospital and allocated to the Lauren Mantz fund for OMS Research. We hope to see you there!
We would like to extend a big Thank You to following who have already committed to being a 2013 Dance Sponsors:
|Bill Barker & Ida Prince||Ocala Psychiatric Associates|| Lauren's Grandma|
|The Ryan Family||Todd Panzer |