Funding more than one million dollars in research grants to date, ASAP is the leading 501(c)(3) donor- supported organization dedicated to promoting awareness, advancing research, and providing support to individuals and families affected by syringomyelia and Chiari malformation. ASAP aims to improve the quality of life for those impacted by these conditions through education, advocacy and collaborative initiatives with the medical community.ASAP offers a wide range of resources for patients, caregivers and medical professionals. If you are newly diagnosed, please see our Patient Handbook for a comprehensive resource guide for patients and families affected by Chiari Malformation and syringomyelia. The ASAP Annual Conference is our most valuable resource available. This event brings together leading experts, researchers, medical professionals and individuals affected by syringomyelia (SM) and Chiari malformation (CM) and related disorders for a collaborative exchange of knowledge, insights and support.Watch presentations from our latest conferences for free: https://www.youtube.com/@ChiariSyringomyeliaASAPorgFollow us for support group information, updates on the latest research and much more:https://www.facebook.com/asapcmsmhttps://www.instagram.com/asaporg/https://twitter.com/ASAPorghttps://www.facebook.com/groups/asapcmsmhttps://asap.org/chiari-and-syringomyelia-patient-information/patient-handbook/