@moonannr 

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moonannr

Medication and Navigating This New Diagnosis

Hi there. I was diagnosed in Dec. 2021 and my neurologist wanted to start me on Aubagio. After doing the necessary lab work prior to starting any meds, it was discovered that my JC Virus index was on the higher side, putting me at risk for PML. He wanted to start me on the medication anyway, and continue to have me monitored. I do not feel comfortable with this. Does anyone have any experience with this or something similar? Additionally, since this diagnosis is new for me and I am still learning and doing as much research as possible, I would gladly welcome any advice that pertains to building a medical care team (as far as what other specialists, if any, I should be seeing), and tips for navigating the financial aspect. I decided to leave my work in the education field as it was taking a toll on me mentally and physically even before being diagnosed, and with the constant COVID exposure in a school setting, I determined this was the best course of action for me right now. I’ve been doing a lot of online research, but am open to learning from the personal experiences of others, as not all of my questions can be answered online.
@jamoranto

Got it @moonannr if feel uncomfortable with anyone not on a medication for MS get on a medication asap is what most people’s advise would be. I have had a few of the medications including copaxone with the morning wake ups and tummy rubs. You will understand what I’m speaking of if you get copaxone. Number one advise is keep ur head up don’t stop succeeding in anything you do. Best Jorge

@jamoranto

* I feel uncomfortable