I'm in the majority

I choose the risk of death via PML to effectively combat my MS. It's a common feeling amongst MS patients on Tysabri.

I am not alone on this cliff that is treating my MS with Tysabri. I hope, as I assume so many others on this drug do also, that I may never fall over the cliff. My neuro has reduced the frequencies of treatments from every 4 weeks to every 6 weeks. This is done in the hope that it will allow antibodies to pass the BBB and prevent infection of my brain by the JC virus, which in turn brings PML - and that ain't good. Let's just say all those years of not sniffing glue will have been in vain. That is what I am willing to risk to stop the progression of my MS.

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