Guest guest Posted October 13, 2003 Report Share Posted October 13, 2003 There is another group called Living-with-ALS. They too are a wonderful group and will answer so many of your question. <A HREF= " http://groups.yahoo.com/group/living-with-als " >Yahoo! Groups : living-with-als</A> There is also this group, not as big but just as nice. <A HREF= " http://groups.yahoo.com/group/ALS-discuss/?yguid=26797479 " >Yahoo! Groups : ALS-discuss</A> My brother has sporadic ALS and I have recently been DX with PLS. As I was told when I joined this group it was the better of the evils so I hope to stay here but only God knows my destiny. I too suffered from reflux for years and was up to 120mg a day at times. The vomiting, ect was horrible. Then the choking episodes started and that lasted about 6-8 months. My neruo said I have no gag reflex. My reflex of the chin is brisk. After test for swallowing, I do not have a digestive disease and that the muscles and nerves don't work properly and was given all kinds of tips. I listened patiently as it was obvious that this tech had no idea why it wasn't working. After she was done I explained and she had this look of, oh! Of course they offer and suggest all kinds of things. My neuros try to be positive and express hope that I do not progress further. However, as most know, they don't really know themselves. Just like certain types of cancer require specialist, it is just as important to find a doctor that knows about ALS. Quote Link to comment Share on other sites More sharing options...
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