I have a dream.

                               I have a dream that no child will ever suffer, or die from Spinal Muscular Atrophy (SMA).

                       I have a dream that no mother and father will have to endure the loss of their child because of SMA.

                       I have a dream that no family will have to observe the struggle of their loved ones.

                    I have a dream that we will live in a nation where children with SMA will not be judged by their disabilities,

                      but by the content of their character.

              I have a dream that friends will no longer have to wonder how they can help, but rather what fun can we have.

                I have a dream that people will know what Spinal Muscular Atrophy is, and how it may affect their friends and family.

                   I have a dream that people will have the option of getting carrier testing done so they can prevent

                                         SMA from entering their home.

                                        This is our hope. I have a dream that one day this nation will rise up and this site, this foundation,

                                            and this community support will no longer be needed because we have all worked together

                                                                                 to overcome SMA, and a CURE has been found.