We NEED to find better treatments for all of the symptoms of dup15q syndrome. We NEED to know how those with dup15q syndrome develop over time. We NEED to know why some children affected by dup15q syndrome have seizures and some don’t. We NEED to emphasize the importance of research. Direct patient and family research is critical to meet these needs, identify other needs, get better treatments and make positive changes to the lives of all those affected by dup15q syndrome.
We NEED your HELP!
Your donation will go directly towards our clinical research.
Provided by CoolFundraisingIdeas.net