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07-30-2007, 05:55 PM
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In Remembrance
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I didn't read your intro in the general intro forum, so, WELCOME to the MS Forum...I'll go read it now..
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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08-06-2007, 10:35 PM
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#3 | |||
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Junior Member
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Greetings!
 Just joined this forum, and am happy to report that though I was diagnosed with R/R MS in 1993,I've been very lucky and haven't had too a bad time of it. Ten years after my diagnosis,when I had some fleeting visual disturbances , my neuro had me get my first MRI since then. He said that the progression was slight enough that it looked almost like a new case, and recommended therapy to try to keep it that way. I've been on Copaxone for 4 years,and my only real side effect has been those dam lipo atrophy site dents(arms, thighs).I know I probably should not do this, but I only shoot my butt now-- WTH, it looks like chewed bubblegum anyway  (I'm 51) As for the disease and symptoms,(though I HATE the heat and do tire occasionally)nothing really major since '93, and thus far, the Copaxone seems to be effective. Cheers!
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08-07-2007, 11:25 AM
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In Remembrance
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Hi Bee, Welcome to your home away from home.
I'm glad to hear that you are stable early in the game. I hope Copaxone keeps doing it's thing for you. Jump right in and enjoy your stay. 
__________________
~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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09-28-2007, 05:30 PM
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New Member
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Hi, found your informative web site by accident while looking for a LDN prescriber
in Colorado, they all seem to fear someone cutting into thier pharmacy kick backs. I read a post by Sally C stating that she could help. Sally when you read this would you please help me find someone. I have had MS since 1994, tried all prescribed drugs with no relief , and just heard about LDN. Thanks Kathy P bkpal@comcast.net |
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09-28-2007, 06:26 PM
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Magnate
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 Hello Kathy and  to NeuroTalk.I'm sure Sally will be on soon to give you some information on LDN. We also have another member, LarryLDN who can give you some information about LDN. Again, welcome!
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Dx RRMS 1984 |
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09-28-2007, 06:41 PM
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Yappiest Elder Member
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hi kathy. ( hi snoopy
)i sent a pm to larry with a link to this post. sally is having some keyboard issues, so i'm not sure how much she will be posting the next few days. ladyexpress takes ldn too.
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09-28-2007, 07:07 PM
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Magnate
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Quote:
 I will see if I can send her over this way.
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Dx RRMS 1984 |
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09-28-2007, 07:16 PM
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Member
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how about some links?
http://www.larrygc.com/ms is my MS & LDN related links. http://www.ldninfo.org is the LDN main site http://www.gazorpa.com has helpful information for MS patients to share with their docs http://www.larrygc.com/mystory is my own personal story from the early days |
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Hi from new member
Hybrid Mode
