Do you have MS but it does not effect your quality of life?

In 2017 at the age of 23 I was diagnosed with MS. I developed a limp, the fine motor movement in my fingers were severely impaired, I had a burning sensation on my chest and a few other small things. It was scary, but I went on Tecfidera, started working out almost daily and made a few small changes to my diet and luckily within 6 months everything basically went back to normal.

7 years have now gone by without an attack/relapse and thankfully MS has effectively no impact on my quality of life. As a result of it not having an impact on my quality of life, very few people know I have MS because there is no reason to share it.

The other day I was googling and learned that 1m people in the US have MS and it got my wondering, of those 1m people, how many people are like me where it is very little impact on their quality of life?

I have tried to ask my doctors this before and they are generally reluctant to answer, so I figured I would ask here!