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#1 | |||
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In Remembrance
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Hi Gail, nice to meet you.
![]() Yes, LDN used to be a dirty word on most forums, because it was new, it was cheap and was not Big Pharma approved. ![]() I'm surprised you are still having problems talking about it, though, since a lot of the naysayers are now on it..LOL. We are free to talk about all our Med choices here, and debate them as well, so don't be shocked if someone does not agree that LDN is a good thing. I am glad Cherie steered you in our direction. ![]() Hugs,
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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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#2 | |||
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Junior Member
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Thanks Sally and Lee Ann -- Glad to be here.
I don't mind controversy == I like a good debate. And as far as meds go--its whatever works for you. Have a good evening ![]() |
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#3 | |||
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Magnate
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I joined awhile ago but never posted. I was on another message board for years which has been down for quite some time.
I was diagnosed 16 years ago and did pretty good until three years ago when my arms got very weak, followed by my legs last year. Now, I use a rollator or a wheelchair to get around because of weakness and because of falls. I was on Copaxone, then switched to Betaseron in September. So, I just wanted to say Hello to everyone. ![]()
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Mair . |
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#4 | |||
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Magnate
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Hello Ann!
I'm glad you decided to post and let us know your here - the more the merrier ![]() Have you noticed any difference with Beta?
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Dx RRMS 1984 |
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#5 | |||
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In Remembrance
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Welcome Ann, Nice to meet you..
![]() I'm so glad that you decided to join the group.
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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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#6 | |||
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Magnate
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Thank you LeeAnn and Sally. I haven't noticed any difference yet since starting on Beta. I switched because I was slowly getting worse on the Copaxone, and we decided to go with an interferon plus a 3-day IV Solu-Medrol infusion. I have hopes that between the two of them, my MS will stop getting worse.
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Mair . |
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