Originally posted by SuzE-Q
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What guts!
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Desperate people will try anything. I have no idea if I'd want this and hope I never have to decide. But I have noticed that I'll do things I wouldn't have thought I was capable of doing if I'm desperate.Originally posted by SalpalSally View PostIt's. All Stinky stuff!!!SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.
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I think I'd rather try a fecal transplant, likely in the form of an enema(?) that's been properly sanitized in some way than many of the standard MS treatments that have such severe risks, even though unlikely to occur, attached to them.
This at least seems safer since our colons are populated with microbes, albeit different varieties, to begin with.
I take probiotics that essentially is the same idea.
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Per Mike Weins: "...the admin/mod team doesn't have to provide a forewarning/warning/mention about altering a members post. It doesn't matter if they fix a link, remove a link, fix a typo, or whatever...."
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I agree, Sally, experiencing a scary and debilitating MS event is quite a motivating factor that makes us far more willing to take chances and try treatments we would not have contemplated before when our disease was more stable!
Please Note that my posts may have been arbitrarily altered by a Moderator and may not reflect my original content.
Per Mike Weins: "...the admin/mod team doesn't have to provide a forewarning/warning/mention about altering a members post. It doesn't matter if they fix a link, remove a link, fix a typo, or whatever...."
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