Michelle: I live in Illinois with my family. We have a farm and I have two small girls that are in school and work at a university as a college professor. It really hit in July of 2020, during the pandemic. And, I ended up with shingles. Those symptoms just kept going on for about two months. Itching, rash, I even got to the point where I was having nausea each day. And no answers.

It was just, "Take some anti-nausea pills." It was, it was very frustrating. When you live on a farm, you work hard, and to not work hard is kind of seen as laziness. And so I felt lazy. I felt like I couldn't support my family. I was asking my husband for a lot of help because I was too nauseous to even cook dinner. As a college professor, I wanted to have energy in the classroom and I just felt sick all the time.

It was very, very frustrating for those three months. It wasn't until October, that I woke up one morning and in this eye there was just a little spot that was fuzzy. And went to an ophthalmologist and they did a visual field test. And that visual field test showed that I had optic neuritis. What scared me the most about this optic neuritis is she said, "This could be your new normal." She said, "It may not go away."

She sent me to the neuro-ophthalmologists because they are the specialists, with eye diseases and other eye disorders. And I told him all of my symptoms. I told him all about the nausea. I told him all about the tingling in my skin, told him about the shingles, and it was like a light bulb clicked for him and he ordered a blood test. Two weeks later, I get the results and he said, "You have neuromyelitis optica."

Narrator: Michelle was diagnosed with neuromyelitis optica spectrum disorder or NMOSD, a rare, lifelong autoimmune disease caused by inflammation in the central nervous system (CNS), which is made up of the optic nerve, brain stem and spinal cord.

Her neuro-ophthalmologist immediately started her on treatment, but she continued to have relapses.

Michelle: I woke up one morning. This was my first relapse of the disease. It was about six months after my diagnosis, so I was doing good. I woke up and I just *hiccup, hiccup, hiccup,* I couldn't stop. And it lasted an hour. And then another hour later they start back up again. So they just kept going. Then I started vomiting, and that didn't stop. The relationship I had with my neuro-ophthalmologist was unlike one I'd had with any other doctor before.

NMO is such a rare disease that he actually gave me his cell phone number. So about three days into this, I call him and he said, "Yes, that is actually a relapse." Then my second relapse, the last one I've had, was in 2021. I had vertigo. This was all day, constant vertigo for a week. And so when I went to the hospital, that ended up being a five day stay. Longest I'd ever been in the hospital before.

At that point my neuro-ophthalmologist said, "You shouldn't be having relapses every two months." So, he actually referred me to another doctor who was more of a specialist. He gave me some brochures with the FDA-approved options for NMO. And, he talked me through each one and I was able to make a decision based on kind of the pros and cons of each one, and which one would work best for me.

Narrator: Together, Michelle and her doctor decided the best option for her was UPLIZNA. UPLIZNA is the only FDA-approved NMOSD therapy with treatment just two times a year, following two initial doses.

Michelle: The draw to UPLIZNA was absolutely the once every six month infusion. So with UPLIZNA, the doctor walked me through the potential side effects. But with any medication, there are side effects. And I felt like it was still worth going through the treatment based on the dosing schedule. That's really what I was looking for. And the data looked good. The data he was showing me was that there were a lot of patients that did not have relapses. And so that was intriguing. You know, I'd had three at this point and I was ready to try something.

After taking UPLIZNA, I have not had a relapse since. Is every day perfect? No, I still have days I'm tired. I still have days where I might have some nerve pain. I go to work, I teach my classes, I have my energy like I always do. I come home, I take my kids to scouting events, to church events. You know, I can be the mom I want to be. I can help out on the farm. And, UPLIZNA is part of that. Absolutely.

We went on vacation last year and I didn't have that worry that we would have to find a hospital somewhere. We're going on vacation this summer. My husband and I are thinking about going overseas next year for our 15th anniversary. And three years ago, I would have been very worried about doing that. Before, I felt like NMOSD was controlling me, and after starting treatments, it was the opposite. Rather than NMOSD controlling me, I felt like I was controlling it. That this medicine was helping me live the life I wanted to at work, with my family. As someone who likes some control in her life, it was nice to have that control back.

IMPORTANT SAFETY INFORMATION

What is UPLIZNA?

UPLIZNA is a prescription medicine used to treat adults with neuromyelitis optica spectrum disorder (NMOSD) who are anti-aquaporin-4 (AQP4) antibody positive.

It is not known if UPLIZNA is safe or effective in children.

Who should not receive UPLIZNA?

You should not receive UPLIZNA if you have:

• had a life-threatening infusion reaction to UPLIZNA.
• an active hepatitis B virus infection.
• active or untreated inactive (latent) tuberculosis.

Before receiving UPLIZNA, tell your healthcare provider about all of your medical conditions, including if you:

• have or think you have an infection.
• have ever taken, currently take, or plan to take medicines that affect your immune system, or other treatments for NMOSD. These medicines may increase your risk of getting an infection.
• have or have ever had hepatitis B or are a carrier of the hepatitis B virus.
• have or have ever had tuberculosis.
• have had a recent vaccination or are scheduled to receive any vaccinations. You should receive any required vaccines at least 4 weeks before you start treatment with UPLIZNA.
• are pregnant or plan to become pregnant. It is not known if UPLIZNA will harm your unborn baby. Females should use birth control (contraception) during treatment with UPLIZNA and for 6 months after your last infusion of UPLIZNA.
• are breastfeeding or plan to breastfeed. It is not known if UPLIZNA passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby if you receive UPLIZNA.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.