This Is MS Multiple Sclerosis Community: Knowledge & Support

thanks...I was confused with the blockage and endorphines think!
thanks for clearing me!!!
HCN

I am from Canada and interested in starting LDN or finding someone to help me. Let me know if anyone is out there. Thanks

Val

Val,

If you go to www.LDNaware.org there is a Canadian page and Facebook group. I'm sure they can help.

bebop

I started LDN a couple of months ago. My energy is definately better. Legs seem to be a bit better too, but I also started 10000 IU of vit d at the same time. Stopped Avonex/
My only complaint so far is some mid night waking up. a couple of times at midnight/unable to get back to sleep at all.
I am looking for someone in Texas to test me for CCSVi. Anyone?

Ginamass

Go to the local universities -- ask around the IR departments to see if you can get someone to test you for CCSVI. Print off and hand out the information from Dr. Mark Haacke's website http://www.ms-mri.com/

I have not heard of anyone getting the testing completed in Texas --- maybe you can be the first!

Sharon

Erika and Sharon,
It would be a great help if you said the dosage of LDN tht you take--read some literature tht says 4.5 best, others 3, others 2 ! So how to decide..
Thanks

Thanks Bebop,

I am looking into starting LDN I have RRMS dx Jan 2009. On copaxone and wanting to try LDN. Will piggyback both for a bit then if things go well drop Copaxone. I appreciate hearing from people who have been liberated and still on LDN. Thanks for all of the stories.

Val