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#1 | |||
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Magnate
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Hi zipfed!
Welcome to NT! ![]() I'm not on LDN, but there's a sticky at the top of the MS forum with loads of support for those who are on LDN!
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I know the sound the river makes, by dawn, by night, by day. But can it stay me through tomorrows that find me far away? . I have this mental picture in my mind of you all, shaking bones and bells and charms, muttering prayers and voodoo curses, dancing around in a circle of salt, with leetle glasses and tiny bottles of cheer in the middle...myyyyyy friends! diagnosed 09/03/2004 scheduled to start Tysabri 03/05 Tysabri withdrawn from market 02/28/05 Copaxone 05/05-12/06 Tysabri returned to market 06/05/06 Found a new neuro 04/07 Tysabri 05/25/07-present Medical Marijuana legally 12/03/09 . Negative for JC virus antibodies! . I'm doing alright and making good grades, The future's so bright, I gotta wear shades! . |
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#2 | |||
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Grand Magnate
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I am only on LDN, and it's all I've ever used.
If I was on Copaxone and managing ok, I would stick with both ... if only for double protection. I am very satisfied with LDN alone. Cherie
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I am not a Neurologist, Physician, Nurse, or Hairdresser ... but I have learned that it is not such a great idea to give oneself a haircut after three margaritas
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"Thanks for this!" says: | dmplaura (09-01-2009), Jappy (08-25-2009), Lady (08-25-2009), SallyC (08-25-2009), Twinkletoes (08-25-2009) |
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#3 | |||
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Wisest Elder Ever
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I've been on LDN for a year now. It's the only med I take for MS. I've been very pleased with it. I was on Copaxone (my first DMD) and it didn't work for me. LDN has been a blessing.
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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