My LDN update

[Guest guest]

Hi, all-

Just wanted to give you all an update on my LDN usage. I started on 4.5

at the end of May. I had tightness in my legs after just a couple of

days so I started pouring out the capsule. Started feeling better and

ordered a script for 3.0 thinking I would stay on that.

Then after a few weeks I started getting new symptoms.. .numbness and

weakness in my right hand. (I had numbness in my left hand and numbness

from my stomach to my toes already going on). I called Bihari and he

told me up to my dosage back to 4.5. I was scared that the stiffness

would return but it didn't and the weakness in my hand went away. It's

still a little numb but all the numbness is very slowly going away. The

healing is so subtle that I can't even notice from day to day, but when

I think back to how I felt a few weeks ago, I can tell there are changes

going on.

The point of my story is to try to stick it out, even when it seems you

are getting worse. My neuros tell me my hand problems are from pinched

nerves in my elbows and not MS. Who knows!! My last neuro appt was this

past Monday and he wanted me to go to the hospital for a few days and

get IV steroids. I told him I have to think about it (it's almost

tempting if it would take away all this numbess but I think it will mess

my immune system even more). He couldn't say if if would help or not

and then he gave me all the info on the ABCRs. I mentioned LDN and all

he could say is it is not FDA approved. I wanted to say that it is but

I really didn't want to get into it. I thought it would just get me

upset so I stayed silent. But in a year from now if I do not have any

more relapses I am definitely going to give him my piece of mind and

push him to look into LDN. He is a really nice guy but he is ignorant.

A typical western medicine doctor.

So here I am on 4.5 and doing better each day. I hope and pray all of

you are doing well and that someday we can all be on the news and tell

the world about LDN!!