A board to discuss the Multiple Sclerosis modifying drug Rebif


Postby julieg » Mon Jan 14, 2013 8:15 am

I have been on Rebif since Nov 24, was on copaxone for almost 13 years, and it stopped working. I really do not like the way this rebif makes me feel, it seems to really bother my eyes like the pressure in my eyes is really high, does any one else have that problem and it just makes me feel so tired and rotten
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Re: rebif

Postby mrbarlow » Sun Jan 20, 2013 7:02 am

I was on Rebif for 18 months after Optic Neuritis. Felt dreadful for 18 months. Now completely off it and feel a million times better and less symptoms. My natural approach is low dose hookworms, a mineral, vitamin and anti oxidant regimen, anti inflammatory diet, sunbathing and lots of green tea.

I don't discount that I got some benefit from Rebif in the early days but IMO it isn't a long term solution as it is hell on the liver.
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