LUPUS COMMUNITY
99% better

99% better

I HAVE BEEN diagnosed with Lupus, Sjogren's, Rheumatoid Arthritis, and Autoimmune Hepatitis, and now they SUSPECT MS.  I started taking low dose naltrexone on November 13th, and was able to drop SIX other medications for it, and am feeling MUCH BETTER!  It's been 3 weeks and I have minor swelling in my hands, but no pain, no heat in my joints, I'm stronger where I was weak, I no longer have urinary dribbles and can urinate when I need to instead of sitting in there waiting for my brain to decide it's time to go.... and I have much more energy.  I am still having trouble with my ability to type a word that I want to type; I keep mixing the letters up.  That started when all the other symptoms started in 2001.  But for the most part, I am 99% better and loving it.  I wish they would put this medication out there for the world to choose, like a vitamin, over the counter!  It's awesome.  There are issues for some people that take it, and it doesn't work for all..... but it DOES work for MOST!    I truly wish everyone could have it.  
Tags: LDN
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  • 99% BETTER (5 replies):
    I have not been diagnosed with MS, and hope I won't be. ...[more]
434278_tn?1324709825
Hey girly, So happy to hear your wonderful news.  You have so much going on.  We missed you, but am so glad you are back!

I'll have to check this medicine out.  I've had some trouble since the weather has turned cold here.  Does it get cold where you live?

I have trouble with urine hesitancy and getting my letters jumbled up when I type too.  And not being able to say of the right word.  I call things they are not.  Another strange thing that is happening is, it feels like something is crawling down my head or someone has placed their hands on my head and moving their hands down my hair.  There is a tingly feeling that happens along with that.  What kinds of MS symptoms are you having?
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