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Sometimes it is hard to be special and not eat some of the foods that other kids eat. Sometimes I have different feelings about having .

Here's a list of some of the feelings I have:

  • is not a huge deal.
  • Having doesn't feel special.
  • Sad that I have and others don't.
  • Confused.
  • Tired of going to the clinic.
  • is not the most important thing about me.
  • But I just remember that everyone is different and that I am not alone. There are lots of other kids with .


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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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