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secondary progressive MS

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Hi i have secondary progressive ms i started on ldn 3.0 mg in march and

april i was on copaxone for 2 years before that . since i started ldn i

feel much better got more strengh in my right arm can hold and drink a

cup of coffee only get up about 3 times at night for bath room trips

instude of 6 or 8 times stopped copaxone. walk better with walker had

less muscel cramps and back pain but started 4.5 in may now i have more

back pain and muscel cramps at night so i am going to go back to 3.0

again my hole body feels better than before.hope this helps.

bodie_lister wrote:

>Is there anyone with secondary progressive MS that has used naltrexone? If so,

what

>were the results?

>

>

>

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Sue,

Thank you for your reply. My wife has had RRMS since 1972 evolved into SPMS

around 1992. Would be very interested in your progress on LDN.

Bodie

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