Following are comments from letters received by Sandy Bulcher since the Symposium.

Young adult with MSUD (PA): I wish there would be an MSUD meeting every day.

MSUD Mom (PA): It gave us fresh courage to come home and keep trying to fulfill our duties in caring for our MSUD child and the rest of the family.

MSUD Mom (CO): It is great to be with people who walk the same path. At least we know we are not alone.

MSUD Mom (Canada): The ambiance that was created by the presence of so many families (old and new) was impressive and most of all heartwarming.

MSUD Mom (Canada): The input at the parents meeting helped shape the program and made the atmosphere congenial and warm. We loved it.

Rosemary from Australia: Sam & myself have been on the local ABC radio here talking about MSUD and the Symposium in Ohio. After traveling all the way to America and talking in front of the group, I must admit we sounded pretty professional, even if I say so myself!"


The MSUD Family Support Group is currently funding several research projects and we are proactively looking for researchers interested in developing new treatments or finding a cure for MSUD. Significant funding is necessary if we are to accomplish this goal.
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