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      Spinal 
      Muscular Atrophy is an inherited genetic condition that affects the 
      anterior horn cells of the spinal cord. These anterior horn cells are 
      responsible for controlling voluntary muscles such as crawling, walking, 
      head and neck control, swallowing and breathing.
 
      There 
      are 3 main types of SMA, all of which vary in severity and age of onset. 
      One common observation is that SMA children are unusually bright and 
      sociable.  
      TYPE 1(Werdnig-Hoffman disease)
      
      Diagnosis is usually made before the age of 6 months. This is the most 
      severe form of SMA. These babies rarely make it to the age of  2, most die 
      before 1 year due to breathing difficulties like pneumonia. SMA Type 1 
      babies never are able to lift their heads, or accomplish normal 
      milestones. Some children have a tongue tremor called tongue 
      fasciculation. This is seen in virtually no other disease other than SMA.  Because 
      this disease also affects swallowing and feeding, secretions become 
      increasingly hard to control and mechanical suctioning is needed. Upon 
      X-ray of the chest, Type I babies can have a bell shaped rib-cage due to 
      the general muscle weakness and diaphragmatic breathing (tummy breathing) 
        
      TYPE 2
       Diagnosis 
      is usually made before the age of 2. A less severe disease than Type 1, 
      these children may be able to sit unsupported. Some are even able to stand 
      with the help of braces or other aids. Feeding is not usually a problem 
      with type 2, although some may need to have a feeding tube put in. 
      
        
      TYPE 3
       This 
      type is diagnosed sometime after the age of 18 months, even up to 
      adolescence.  These children are able to stand by themselves and walk, but 
      may have some difficulties. 
  
      
       FACTS 
      ABOUT SMA
        
        
        
        SMA is the #1 
        genetic killer of babies under the age of 2
        
        SMA 
        children with the most severe form often face quickly increasing muscle 
        weakness, leading to paralysis and death.
        
        One out of 40 people, most unknowingly, carry this deadly gene.
        
        One of every 6,000 children born are affected by SMA.
        
        
        1 in 4 chance with 
        each pregnancy of having an affected child (25%)
        
        
        Some Statistics show SMA to be TWICE as common 
        as ALS.
        
        
        Does not 
        discriminate based on age or race or gender
        
        
        There 
        is no cure For more 
        specific details on SMA, visit www.smasupport.com! 
      
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