Hello there, is there anyone I can talk to who has been told that they are suffering from the awful symptons of spastic parapersis? I have been suffering with this condition since 1997 and although I am on a lot of medication to help control it I still am in constant pain, having loads of spasms, the unpleasant sensations in my feet, legs arms and hands seem to be getting worse as does the myoclonus. The frustating thing is that I have been told it is not an illness in its own right and despite having every test imaginable no cause has been found. It is a lonely kind of illness not fitting into any category. I do not know anyone else who these symptons, it would be nice to hear from anyone who has been told they have this.Reply Follow This Thread Stop Following This Thread Flag this Discussion
Know the five types of psoriasis and how to spot flares.
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Is it sensitive skin or something else?