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Tysabri/Naltroxone

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Hi ~ My daughter has relapsing-remitting MS....diagnosed 3 years ago-no

remission though treated...experiencing more and more symptoms and brain and

spine MRI's that are ptretty bad.  They are encouraging her to try Tysabri,

however the caveat is the 'chance' of contracting PML which is a

deadly/seriously disabling brain infection  which can arise using Tysabri.  If

they said it is a tough problem, but they could treat the PML it would be one

thing.  But the specialists are saying if you do contract PML there is NOTHING

they can do to treat or cure it.  My daughter's stance right now is that she

rather have the MS progress than contract PML.  She is BEYOND terrified, and

emotionally drained from all the bad news the past few weeks.  She is currently

doing the Dr. Swank MS Diet and using the drug Copaxone, this drug which if not

useless for her has not done enough as her MS and MRI's are worse.

Has anyone here any experience, pro or con, with Tysabri?

I have read about a low dose of Naltroxone, which at high doses is used to treat

drug withdrawls, being found helpful in MS as well as RA and other autoimmune

diseases.  Any experiences with that either?

Thanks so much...

Cheryle, in Oregon

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