Guest guest Posted April 16, 2005 Report Share Posted April 16, 2005 PLS affects the nerves so it can and besides most woman say their husbands have selective hearing so it must be voluntary! dale Sensory problems > > > I was wondering about something. The 'specialists' say that PLS only > affects the voluntary muscles...with some indirect effect on the > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 16, 2005 Report Share Posted April 16, 2005 PLS affects the nerves so it can and besides most woman say their husbands have selective hearing so it must be voluntary! dale Sensory problems > > > I was wondering about something. The 'specialists' say that PLS only > affects the voluntary muscles...with some indirect effect on the > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 16, 2005 Report Share Posted April 16, 2005 PLS affects the nerves so it can and besides most woman say their husbands have selective hearing so it must be voluntary! dale Sensory problems > > > I was wondering about something. The 'specialists' say that PLS only > affects the voluntary muscles...with some indirect effect on the > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2005 Report Share Posted April 18, 2005 , I do have some sensory loss on my legs and 'cape' area. Like y ou this was thought to be more MS related but it has been proven time and time again, there is no CNS involvement. My neuro think it is some sort of varient form of PLS. Interestingly, he also said that with HSP you can get sensory involvement. I have 'above the waiste' issues that make it PLS. But since HSP and PLS are both UMN diseases, it seems reasonable there could be sensory involvement. Colleen > > I was wondering about something. The 'specialists' say that PLS only > affects the voluntary muscles...with some indirect effect on the > organs they surround. I was told not to expect ANY sensory problems. > > Well......maybe they are right....but I sometimes get the following: > Numbness and tingling in my hands and feet (MS has been excluded) > > Hearing loss > > Ringing in my ears > > Bladder and bowel troubles, although they could be an indirect > thing...for muscle spasms. > > Has anyone else had sensory...involuntary muscle-type symptoms? > > Di....PLS....Canada Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2005 Report Share Posted April 18, 2005 Thanks colleen, That is info I didn't have. Makes sense. Take good care! Di...PLS....Canada > > > > I was wondering about something. The 'specialists' say that PLS > only > > affects the voluntary muscles...with some indirect effect on the > > organs they surround. I was told not to expect ANY sensory > problems. > > > > Well......maybe they are right....but I sometimes get the > following: > > Numbness and tingling in my hands and feet (MS has been excluded) > > > > Hearing loss > > > > Ringing in my ears > > > > Bladder and bowel troubles, although they could be an indirect > > thing...for muscle spasms. > > > > Has anyone else had sensory...involuntary muscle-type symptoms? > > > > Di....PLS....Canada Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2005 Report Share Posted April 18, 2005 Thanks colleen, That is info I didn't have. Makes sense. Take good care! Di...PLS....Canada > > > > I was wondering about something. The 'specialists' say that PLS > only > > affects the voluntary muscles...with some indirect effect on the > > organs they surround. I was told not to expect ANY sensory > problems. > > > > Well......maybe they are right....but I sometimes get the > following: > > Numbness and tingling in my hands and feet (MS has been excluded) > > > > Hearing loss > > > > Ringing in my ears > > > > Bladder and bowel troubles, although they could be an indirect > > thing...for muscle spasms. > > > > Has anyone else had sensory...involuntary muscle-type symptoms? > > > > Di....PLS....Canada Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2005 Report Share Posted April 18, 2005 Thanks colleen, That is info I didn't have. Makes sense. Take good care! Di...PLS....Canada > > > > I was wondering about something. The 'specialists' say that PLS > only > > affects the voluntary muscles...with some indirect effect on the > > organs they surround. I was told not to expect ANY sensory > problems. > > > > Well......maybe they are right....but I sometimes get the > following: > > Numbness and tingling in my hands and feet (MS has been excluded) > > > > Hearing loss > > > > Ringing in my ears > > > > Bladder and bowel troubles, although they could be an indirect > > thing...for muscle spasms. > > > > Has anyone else had sensory...involuntary muscle-type symptoms? > > > > Di....PLS....Canada Quote Link to comment Share on other sites More sharing options...
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