NeuroTalk Support Groups - View Single Post - LDN Information & Check-in 2

lady_express_44 · 06-12-2009, 02:10 AM

Quote:

Originally Posted by Lady

LDN check-in.

Hi All,
I went to my MS Specialist last week for my regular check-up. Again, she was very surprised at how many improvements since the last visit. She gave me a very long exam, with lots of testing, and said, "You are making me a believer in LDN."

She does not prescribe it for me, so I didn't ask her for a script. Let her keep tracking me and one day she will prescribe it to whomever asks for it.

I get it from my PCP. The MS doctor had her nurse call him, to ask him to write it for me. She only does the DMD's.

I was thinking. I bet someday they will come out with a drug, so similar to LDN for a MS treatment drug, and charge a high price for it.

We know there is no money to be made with LDN for the researchers. So if they change one ingredient or add something to it, they can get it to clinical trials and get it FDA approved for MS.

Just my late night thinking.

I've thought about that too, Lady. I even wondered at one point if I should be telling people about this stuff, in case someone catches on and finds a way to charge $50K a yr for it ...

My MS Specialist just says "I guess I'll see you next year then ...". I have to be her easiest patient.

I am thrilled that it's worked out so well for you, especially so far into the disease process. I know you were very nervous with all the other medical issues you had to contend with . . . but I haven't really run into anyone that has had any problems from LDN. I always think about potentially steering even one person wrong though ... even now.

They should just put it in the water supply, don't you think?

Cherie