Re: One Year ago--To tell your doc or not about LDN

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CJ

Congratulations on stopping your progression with LDN, glad you could

join this happy club :-)

Everybody needs to respect everyone's choice about telling their doc

about LDN, I remember that paralyzing dependence I had on my docs

before LDN, because there was no hope except what they could offer.

And even with LDN, there is always that unknown future when you might

need their help again.

All I can do is report my experience with telling my docs, for those

who are pondering this. My TX neuro back in 2004 said No when I asked

for LDN, so I got it elsewhere, then converted him to an LDN scripter

when I went back in 4 weeks no longer using my cane and so much

better. Since then I have told my story to 2 GP's who wrote scripts.

I went back to my WA neuro a few weeks ago, I was happy to find that

she has been hearing LDN stories, and has no problem writing the

script, and this is at a major Seattle MS center. So this is a major

way we can keep chipping away and spread clinical experience with

LDN, so docs won't be afraid of it.

The other way is research. Please contribute if you can!

http://ldninfo.org/research_funding.htm

SammyJo