How is a person with MS affected by being a COVID-19 long-hauler?

I've had COVID-19 twice. The first time was in January, 2021 and the second time was in October, 2021. The first time I lost my sense of taste and it hasn't come back yet. I can taste whether things taste good or bad or a little salty but nothing more. My fatigue had increased as has my breathing problems. Do folks with MS become long-haulers more than the general public?