Guest guest Posted January 20, 2008 Report Share Posted January 20, 2008 Hi , It's different for everyone, but your symptoms remind me of the first symptoms that I had, two years before being diagnosed. I hope that you start taking care of yourself early on instead of waiting until you get like I am, in a wheelchair. msedup wrote: , Is what I am describing the usual type of spasticty in MS or does mine sound more like an injury related pain. (your opinion only of course) Thanks, --------------------------------- Looking for last minute shopping deals? Find them fast with Yahoo! Search. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2008 Report Share Posted January 20, 2008 Thanks Rich. I should add those to the home page. rich perillo wrote: Hi , don't forget " cavitations " , " root canals " . Could be THE issue. Jaw Thermogram. ...RP --------------------------------- Looking for last minute shopping deals? Find them fast with Yahoo! Search. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2008 Report Share Posted January 20, 2008 Already on the home page. rich perillo wrote: Hi , don't forget " cavitations " , " root canals " . Could be THE issue. Jaw Thermogram. ...RP --------------------------------- Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2008 Report Share Posted January 21, 2008 My wife also has spasticity in Legs and in her back. Seems like constant spasming.  She is in a wheel chair but not diagnosed with MS though she can't walk, has spasticity, legs don't work.  I had things similar but after mercury detox I recovered. But her doctor told her to wait until she is more healthy before replacing amalgam and doing detox. I think thats a big mistake, since the medical lit documents that although there is a big exposure when you have amalgam work, you can protect by using activated carbon supps on day of work and lots of Vit C and nutritiional support before and after, including maybe Vit C IV.  And after replacement daily exposure levels decline over 90% from then on.   But so far I'm losing that argument. We have one more doctor appt she wants to here from before understanding she's going to have to take her own treatment into her hands. She's been through 2 rounds of MRIs with orthapedic doctos and 2 rounds of neurological tests by 2 neurologists, with no suggestion by them of what will make her better.   Maybe after this Wed. when she will hear the same thing, she will do something more productive. Long story here, her father was an MD, but not familiar with mercury effects and such or alternative treatments.  My experience should convince her I think after her appt this week. Is spasticity and spasming of the muscles in leg and back indicative of MS, if the doctor didn't see anything in MRI?  If not, what could be the cause, other than mercury .  I have lots of documentation that mercury causes ataxia and other such conditions and people usually improve after detox, but her doctor and dentist have different orientations than those I go to. She likes them, but I don't think they know what they are doing regarding things like this. Bernie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2008 Report Share Posted January 21, 2008 Definetly time for an MS/MRI ________________________________________________________________________________\ ____ Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ Quote Link to comment Share on other sites More sharing options...
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