Thread: ALS/Lyme Help
View Single Post
Old 04-06-2010, 02:26 PM #15 (permalink)
kelly11016's Avatar
kelly11016 kelly11016 is offline
New Member
 
Join Date: 2010
Posts: 71
kelly11016 is on a distinguished road
kelly11016 kelly11016 is offline
New Member
kelly11016's Avatar
Join Date: 2010
City: Auburn
State: Alabama
Country: US
Posts: 71
kelly11016 is on a distinguished road
Default Re: ALS/Lyme Help

Ive read your posts about your symptoms..Do you take magnesium..my doctor told me to take as much as I could without getting diarrhea..right now I can only handle 500mg at bedtime but within a week on the Mag..my spasms cut in half seriously and my fasciculations are almost gone..my LLMD said that with PNH that you sometimes get from a virus or infections magnesium will help restore the levels lost with the infection in that improving hyperflexia, twitching, cramps, and spasms. Just wondering if you are on them and seeing improvements..He said if my spasms and things were due to Lou then they would not be improving on magnesium..not sure what to make of it.
kelly11016 is offline