Blind MasterChef Christine Ha Gives Voice to Disabled, Women of Color

by Debra Lau Whelan


Christine HaChristine Ha shot to fame in 2012 when she became the first blind winner of MasterChef with Gordon Ramsay. Since then, the 44-year-old has made it her mission to advocate for women, Asian Americans, and the visually impaired. Whether it’s through TED Talks or her recent “NMOSD Won’t Stop Me” campaign, Ha says she’s using her elevated platform to empower the disadvantaged and to give them hope. Ha was a 19-year-old student at the University of Texas at Austin when she first experienced blurred vision in her right eye. It took doctors four years to properly diagnose her with neuromyelitis optica spectrum disorder (NMOSD), a rare inflammatory autoimmune disease of the central nervous system that can lead to blindness and paralysis.

It was the second time that disaster struck for Ha; at 14, she lost her mother to lung cancer. But somehow Ha persevered. “I had to figure out a way to live my best life, the way I saw it, regardless of whatever hand I was dealt with,” she says. While coping with her vision loss, Ha sought to reconnect with her mother by recreating her favorite Vietnamese dishes using trial and error, her father’s help, and assistive technology. Ha’s blog, the Blind Cook, caught the attention of MasterChef producers--and the rest is history.

We spoke to Ha, who describes her vision as “looking at a very foggy mirror after a hot shower,” about inner strength, the importance of self-advocacy, and why she values Asian culture.


_____________________________


How did winning Master Chef change your life?

I’m naturally an introvert and pretty reserved around people, and suddenly my life was in public view. That took a long time to adjust to, but it opened up a lot of opportunities like being able to do more cooking on television, to write a cookbook, and eventually open restaurants. The biggest thing is having my voice be a beacon of hope for a lot of people, whether it be women, people of color, Asians all over the world, or people with vision impairment and other disabilities. Giving them hope is the biggest reward of all.

It must have been terrifying when you were diagnosed with NMOSD at such a young age.

It was pretty scary. My first symptom was optic neuritis, or inflammation of the optic nerve, and I was in college. At that age, you don't think about dealing with a serious illness. I went through bouts of numbness and tingling in my legs, as well. I was initially misdiagnosed with MS (multiple sclerosis), and it wasn't until some years later that I was finally correctly diagnosed.

Did you lose precious time from your misdiagnosis?

I was put on MS therapies, which weren’t working because I had an incorrect diagnosis. So I was still getting a lot of flare ups and attacks, and it was taking a toll on my vision. I gradually lost my vision because my optic nerves just atrophied after so many bouts of inflammation. It was actually a relief to find out I had NMOSD because I finally felt like “OK, I think this is correct.”

Do you think you’d still have your vision if you were properly diagnosed?

If I was correctly diagnosed, and I was put on the right treatment, and if my doctors would have listened to me when I said, “I feel another bout of optic neuritis coming, and I need the steroids right away; I feel like a combination of these things could have prevented me from losing as much vision as I have.”

Did doctors dismiss some of your concerns because you were so young at the time?

I’ve had doctors talk down to me and made me feel like my symptoms weren't validated. I was asked if it was because I’m a woman and a woman of color. I didn't think it was really a racial thing, but I definitely think it was an age thing. Because I was so young, I was probably dismissed for not knowing enough or being too inexperienced to know my body. Part of it was also perhaps being a woman.

So your message is to stay informed and speak up?

I've learned that it’s really important to be an educated patient, and it's important to find a support network, whether it's other patients that have the same disease or a healthcare team that understands and listens to you--and makes you feel like your feelings and your thoughts are valid. I felt very passive in my treatment plan, and I didn't realize how disempowering that felt until I finally found doctors and nurses who participated more fully and allowed me to participate more fully in my health care plan.

Is that why you’re such an advocate for NMOSD awareness?

NMOSD Won't Stop Me Now GroupIt’s exactly why I like to speak up about this--not only to raise awareness about NMOSD, but about rare diseases in general. My experience was so isolating, scary, and frustrating that I want to prevent another person from going through that same experience. I want to raise awareness because NMOSD primarily affects the Asian and African American population, so I'm trying to help others who were initially misdiagnosed with another disease like MS. Even broader, I’d like to help minimize the loneliness by connecting patients with other patients and caregivers with other caregivers, and giving them the right resources so that they can make educated decisions about their health care teams and the right treatment plans. That’s why I partnered with Horizon on this NMOSD Won't Stop Me campaign.

How did you find the inner strength to handle going blind?

I survived it by taking it day by day, even sometimes hour by hour, or minute by minute. It was a lot of mental strength and determination. All of us are a lot more resilient than we think we are. We don't really know how we’ll survive until we're put to that test. My mom wasn't around, and I love my dad, but he was a very typical Asian dad, so I couldn't really talk to him. I have great friends, but none of them were going through what I was going through. It’s important to acknowledge that I was down and depressed. As I got older and had more life experience, I realized that everything is temporal and time will pass at some point. I was able to get through it by knowing that eventually there was an endpoint.

Do you think your resilience comes from hearing your parents talk about their hardships in Vietnam and how they escaped the Vietcong?

I do attribute a lot of my personality and perseverance to my parents. I was taught that life is never easy, and you have to fight for what you want. It would have been better if my parents sat with me and let me be in that pain and feel the grief. But a lot of how they parented was how they were brought up. I didn't understand their experience because I didn't come here on a ship, and I wasn't a refugee. Until you’re older, it's hard to empathize and understand the sacrifices they made.

How did your parents escape Saigon during the last days of the Vietnam War?

They were courting and had just graduated university, and it was a few days before the fall of Saigon, so it was late April 1975. My dad ran to my mom's house to ask her to escape to Vietnam, so basically he was asking for permission to marry her. So they ran to the US naval ship at the port and fought their way onto the ship. They escaped before the official fall of Saigon and were at sea for a while. Their ship broke down and they eventually made their way to the Philippines and flew to Guam, where they were in a refugee camp before they were sponsored by a church in Pennsylvania. They ended up moving to Pennsylvania, then Chicago, and then to LA where I was born.

Did you start cooking because you missed your mom’s Vietnamese dishes?

I missed my mom's food because she never taught me how to cook. But, when I was in college, I had to figure out a way to feed myself. After several attempts at cooking, I realized that I enjoyed it. There was something very zen about chopping things up and cooking them and then being able to feed my friends and my roommates, too. That’s what sparked my first love for cooking.

Did you have any formal training as a chef?

No, I’m 100 percent self-taught.

You wrote a cookbook, hosted MasterChef Vietnam, and opened a few restaurants. What else is going on?

Recipes from My Home Kitchen: Asian and American Comfort Food by Christine HaThe cookbook was part of winning [MasterChef], so I wrote it right after and published it the year after. I also did guest appearances on MasterChef Vietnam and was a full-fledged judge on season three. I did a lot of guest judging on MasterChef U.S. I did a cooking show, Four Senses, in Canada that was geared toward the visually impaired cook. I did a lot of events and public speaking about what it's like to be an Asian woman in this industry as someone with a disability. I’ve also worked with the US Embassy doing culinary diplomacy tours overseas. Then in 2019, I opened my first restaurant, The Blind Goat, in Houston.

Tell us about the Blind Goat and Xin Chao.

I named my first restaurant the Blind Goat because I’m known as the blind chef and the goat is my Vietnamese astrological sign. I wanted to give it a fun name because it's a whimsical modern Vietnamese restaurant that showcases Vietnamese street food and seafood.

Xin Chao means ‘hello” in Vietnamese. I partnered with Chef Tony Nguyen. We grew up eating a lot of traditional Vietnamese food, along with barbecue, Tex Mex, and Gulf Coast cajun food. So I describe Xin Chao as a contemporary Vietnamese space with traditional Vietnamese dishes, but with a Texas Gulf Coast twist on it.

And you just opened Stuffed Belly.

In June, I opened my third restaurant, called Stuffed Belly, and this one is a drive thru casual craft sandwich joint with Asian elements throughout some of the sandwiches. It’s mainly classic American childhood sandwiches with my fun twist on them.

You have a BA in finance. Why did you switch gears and get an MA in creative writing?

I was going to take the business route but it was during my corporate job that I started experiencing all of these NMOSD symptoms. I had to leave work for a long time because of the attacks that left me paralyzed from the neck down for a while. I left the corporate world and started thinking, “What do I really want to do?” I've always loved to read and rediscovered my love for literature, so I decided to go back to school and learn the craft of creative writing.

Is a novel on the horizon?

I've been working on my memoir and I tabled it because of all this restaurant stuff. But I hope to finish it once these restaurants can stand on their own.

Do you feel close to your Vietnamese roots?

I identify more as American than Vietnamese because I was born and raised in America. I think we're taught to be independent thinkers. And while that's great, I also hold the value of a lot of Asian thought, where you think about the communal good. But it’s a balance. It’s important to get along with others and to think everyone's needs are as important as our own. At the same time, I value independence and being vocal. I always try to encourage young Asian girls to find their voice and not be afraid to speak their minds.

You have three strikes against you--you’re a woman, you're Asian, and you have a disability. What advice do you have for those at a disadvantage?

It’s not easy. I have to be two to three times as vocal to be heard. I grew up as an Asian daughter, so I was always taught to kind of suck it up; be quiet, be obedient, and just say yes. My mom believed in some very traditional gender roles, but she was a feminist based on the things she taught me, like, “Be a strong person and say what you think.” A lot of my personality comes from her. I understand now as a business owner that sometimes you have to address things or it'll just fester. My advice is to be kind and compassionate towards other people, but don't be afraid to use your voice.