Need info on LDN

A board to discuss Low Dose Naltrexone (LDN) as a treatment for Multiple Sclerosis

Postby hopecomesnow » Mon Mar 01, 2010 4:33 pm

thanks...I was confused with the blockage and endorphines think!
thanks for clearing me!!!
HCN :D
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Postby Vhoenecke » Sun Mar 14, 2010 11:47 am

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
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Postby bebop » Sun Mar 14, 2010 1:19 pm

Val,

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

bebop
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LDN

Postby GinaMass » Sat Mar 20, 2010 8:53 am

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?
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Postby Sharon » Sat Mar 20, 2010 9:15 am

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
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Postby shye » Thu Apr 01, 2010 2:35 pm

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
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Postby Vhoenecke » Sun Apr 04, 2010 8:50 pm

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
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