This Is MS Multiple Sclerosis Community: Knowledge & Support

I started taking LDN 3mg at bedtime 3 days ago. I've noticed that it causes sleeplessness for me, which is counterproductive when it comes to my symptoms. When I sleep well, I feel much better throughout the day. Everything I've read about LDN says that everyone takes it at bedtime.

My questions are:

1)Does anyone take their dose at anytime other than bedtime (such as in the morning)?

2)Why should I HAVE to take it ...

I don't know if this is a stupid question, or not.

I live close to a local compounding pharmacy who has not compounded LDN but claims they have access to a US national pharmacological resource that provides directions on how they would take the standard dose of Naltrexone to the low-dose weight. I'm not sure who's database they're referring to.

Has anyone dealt with a local pharmacy (US) that has compounded LDN for them as ...

Passing this along ....


Dear Friends,

I have set up an LDN petition: "Sign & Support the campaign for Research & Trials in
'Low Dose Naltrexone for Multiple Sclerosis'"

I am campaigning for LDN with Lorna from Scotland and Linda from England who's working closely with Dr. Bob Lawrence. And I am from the Republic Ireland. We are trying to reach 100,000 signatures, and we need
YOUR HELP!

Please help by signing this petition to ...

Passing this along ....


Dear Friends,

I have set up an LDN petition: "Sign & Support the campaign for Research & Trials in
'Low Dose Naltrexone for Multiple Sclerosis'"

I am campaigning for LDN with Lorna from Scotland and Linda from England who's working closely with Dr. Bob Lawrence. And I am from the Republic Ireland. We are trying to reach 100,000 signatures, and we need
YOUR HELP!

Please help by signing this petition to ...

Hello All

This is my second post and it may seem a bit strange but what I'm looking for is information for our local MS Newsletter. I'm the new editor for it and I also write a column concerning any new research going on in regards to MS. For The May 1 edition I'm planning on writing about LDN. I have 2 motives for choosing this topic.
1. Many of our members are already using ...

could someone briefly explain LDN to me? There is so much out there and my internet connect SUCKS and I get disconnected....I would love it if someone could answer these questions for me...please and thanks!

where did it come from?
does the MS Society recognize it?
when should someone consider taking it?
what makes it different than the other options?

Please take a moment to answer this short survey on LDN:

http://home.earthlink.net/~dflomer/LDN/

You can also view the ongoing results to help you with your LDN research. This may also help sway medical opinion so that a clinical trial on LDN & MS gets underway. Researchers like stats!

I have read a lot about the importance of the compounding of, and the filler used in LDN. I was hoping someone could comment on Smith's or other Pharmas that they may use in Ontario.

Thanks,
Alan

I am suppose to pick an ABC or Ribif in 2 days. Diagnosed by MRI 2
weeks ago after bad optical Heuritis attack. Have been reading
everything on Vitmins, Nutrition, exercise, the main stream MS stuff
and came across LDN. Read as much as I could (still can't see well
in left eye).

All I have read so far about LDN sounds almost too good to be true.
Have any of you experienced or heard ...

Hi all,

I've heard from a friend who asked her neuro about starting the LDN treatment the LDN can be hard on the heart. Haven't read this anywhere else, but then I haven't done an in-depth search.

Anyone else out there have more details on this?