PML- symptoms
Hi all,
Has anyone had PML before? The symptoms are the same as an MS relapse so I’m so scared it’s that after ten years on Tysabri.
Thank you.
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Last reply
After circa 20yrs of use, neurologists have become wise to the risk of PML caused by Tysabri. The 1 in 250 risk Is almost historic IMO. Aaron Boster has a YouTube video on it. If you opt for 5 weekly infusions then it drops to 1 in thousands. I believe your neurologist should monitor your JCV count and Lymphocyte count and recommend you stop taking it. Being JCV + isn't the end if the world - half the worlds population are JCV+. You just need monitoring by blood tests.
I would contact your doctor if you're concerned about new symptoms and JC+