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>my husband and I lost our son on Feb 1,2005. Our son >was diagnosed with Spinal Muscular Atrophy on Jan >7,2005 and we were told we had 3-6 months but we didnt >even get one month. Our son was at home surrounded by >people that loved him when he passed. This has been >the hardest thing to live with because I no longer get >to see my son's beautiful blue eyes and big smile and >I will never get to hold him in my arms again. Just >pray that it will get a little easier to bear because >i'll never get over having to watch my son die and >know that there wasnt anything i could do to make it >better.
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