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LDN update

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When I first started LDN, my legs became very spastic. I stopped for

a while and then started again about 4 weeks ago, and increased my

Baclofen. That took care of the spasticity.

So far, the only change I've seen is that I get up once a night

instead of 2-3 times, and that is worth taking LDN.

I do not have MS. I have PLS, an upper motor neuron disease similar

to Lou Gehrig's.

Edith

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