LDN was no use to my partner.

[Guest guest]

My partner Margot has advanced secondary progressive MS.

She has taken 4.5mg LDN for six months and she has had NO benefit at

all from it.

I wish all MS sufferers well and hope that they have a better

experience than we did.

When we read of people who have been in a wheelchair for years taking

LDN and walking.... Well I hope it is true and wish them well.

I want people to realise that others like us for whom it didn't work

at all are in fact unlikely to do what i am doing now and saying so!

Thus anecdotes abound of 'success' (maybe)and our disappointments are

unspoken.

There is only one thing worse than the handwringing 'no hope' from

our neurologist and that is the pedlars of false hopes.

Pete

[Guest guest]

Pete

Pls remember that the purpose of low dose Naltrexone is to stop progression of disease, not necessarily symptom improvement. So, LDN may well be working..... just not the way you want it to work.

And, then, there is always the issue of fillers..... is the filler being used the best for the person..... would te transdermal version be a better option?

mjh

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