Guest guest Posted June 6, 2000 Report Share Posted June 6, 2000 I agree with Doug that we really don't know what our condition will be after 20 or more years. We have such a wide range of PLS in our group. From Kathy or Bettie Jo to Rita. All have had it a long time. Joe has said that his condition could possibly be from a fall he had. We can't lump every one together and say that we will end up as most ALS people do. My first Neurologolist that I had told me that the reason we have such a wide range PLS is that it depends in which part of the spinal cord the problem occurs. We have no way telling that without an autopsy. The area that is affected in me might lower or higher than the next person and that is the difference in our PLS. Does that make any sense to anyone? If it does then we have no way of telling to what extent PLS will affect us. M. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.