Guest guest Posted November 15, 2008 Report Share Posted November 15, 2008 We learned yesterday night that Charlie's Paternal Grandmother, (my Mother in Law)has been Dx with Muscular Dystrophy. In two weeks we will know the exact type. I am confident because I have watched her eat in slow motion and choke and tears would come out of her eyes for 10 years. B*tched and begged her sons and husband take her to a neurologist. What kind of doctor cannot look at that woman and see there is a problem is beyond me. Everyone outside of their family would ask me what he heck was wrong with her. Oculopharyngeal muscular dystrophy (OPMD): Symptoms of OPMD are confined to weakness in the muscles controlling the eyes and throat. Symptoms include drooping eyelids and difficulty swallowing (dysphagia). The weakness progresses to other muscles of the face and neck, and can occasionally affect the upper parts of the legs. Dysphagia can cause food or saliva to enter the airways, called " aspiration, " which can cause pneumonia. Anyway, do any of you have family members with this MD or this type of MD? With Charlie having Hypotonia of the mouth, born with tortocollis, I am just puzzled at if he woudl have this or not. It says MD can be passed from Mother to child. So I think he woudl be safe, my husband has a 50% chance it looks like. Thanks! Colleen Quote Link to comment Share on other sites More sharing options...
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