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G'day Tasmaid here using hubbies membership. You mention being cpms

and whether LDN will work. I belong to neuro-mancer forum which is

the Mass. General Hospital site for all neurology and a woman named

Jeannie Zeis posts about her success going from wheelchair and from

using different injectables which in cp no longer work to now only

using LDN, 4AP and antivirals. She has quality of life and has

regained things she lost over many years. She has been on LDN nearly

3 years and knows of many in her MS group who have improved.

I can't speak of this myself since my MS is relatively mild but you

could read the archived ms pages using her name to get some answers

for yourself. I'll try a link, hope it works.

http://www.neuro-mancer.mgh.harvard.edu/cgi-bin/forumdisplay.cgi?...

If all else fails just go to neuro-mancer and select ms forum. They

are a great bunch of people with all shades of MS and all points of

view as to therapies, research etc.

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