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idea for new website for LDN survey

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I posted this earlier but under a heading where no one probably saw

it. Thought it worth reposting. Anyone have any ideas?

" Maybe, we should get everyone in the group who has a personal

neuro/GP other than Dr. Bahari/Dr. Lawrence or the guys who do the

phone consults, to write letters on their patients experience with

LDN. If they wrote letters that they too were skeptical, but allowed

their patients to try it anyway because " it couldn't hurt " and how

surprised they are by the results, maybe others could use these

letters to get their own neuro /GP to write them scripts.

If some one in this group had a scanner, where the letters could be

scanned into their computer and then posted on the website so anyone

who needed them could go and print the doctor letters or the doctors

could be directed where to find them on the Internet, this would be

great. There would probably need to be some type of release form

signed by each group member that is willing to have their letter

posted on the website. I am not sophisticated enough in the

technology to know how to do this but for someone who is good with

the computer, I think its very easy.

I think most doctors are not into testimonials but letters from other

doctors might help them make the right decision.

I have thought for a long time that it would be great to have

somewhere on the Internet to go and see how many members there are in

this group, the breakdown of their illnesses, the amount of LDN they

take, what time they take it, how long they have been taking it, what

other drugs they do, what supplements they take and how much.

I wish that I was extremely computer literate. I would have my own

website with a very detailed survey that automatically updated itself

with the results. It would be kind of like having our own study on

an on going. Anyone out there retired, computer literate, that could

take on something like this?

Debbie

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