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With solely natural approach, how do you manage your neuro?

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I was taken first of Copaxone and then put on and then removed off avonex

and I am no longer on any MS medications at all. My neuro states he doesn't

know what to do with me and says I will continue to get progressively worse

etc.

I find it ridiculous to even keep seeing this neuro. I had my MRI this month

while in hospital so otherwise I see no reason at all to keep going to see

this guy. How do others address their medical needs when they are taking

solely natural approaches to their treatment? Can I just keep going to my

primary care doc etc and that's it. I'm already on SSDI so I don't need a

neuro for that.

For the record, I did LDN trial for 30 days and the spasticity got

significantly worse so that I couldn't use my feet to walk so I stopped that

as well. I was doing 3mg in liquid put under tongue sublingual.

Anyway input appreciated on managing your neuro when you refuse to take the

normal MS medications.

Okay time now for my home physical therapy program this morning and then

going to go outside and look at the beautiful changing leaves.

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