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MS & transdermal cream

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Darleen,

I absolutely agree with all you said

I have had SPMS (for last 15

years) and have seen fantastic benefits (after 7 months) in balance, mobility,

flexibility. I regained my sense of smell, taste, dexterity of my left hand, voice

strength. LDN stopped my sinus (which triggered MS exacerbations)

and choking. If I had known about it when I was RRMS I would never have

progressed. Why would someone with MS NOT TRY IT? What is there to

lose? There is a lot of info here Crystal's MS,TM & LDN Website Trish

“I have read many reports of folks with MS and they get better

on LDN. Read all you can. Because of my experience with the

LDN. I would never advise a person to take the pills. Start out with the

cream you rub on at night. It is called Trans dermal LDN. that has the least

side effects. and start with a very small dose”.

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