diagnisis

I was diagnosed with ms in 2014 and i have never felt so crushed. All my dreams of travelling, jogging, doing marathons, hiking the inca trails and even as already barely functioning because of my mental health, went away.

It's really hard to have ms. 

I was started on tecfidera but the pain was so bad within two years that I wound up taking heavy doses of cbd daily which maybe worsened my fatigue. The fatigue was crippling. Some days I just didn't even wake up until 3pm even if i went to sleep at 7pm..

In 2022 i was switched to maven clad (immunotherapy) and at least I could stop taking cbd. So the fatigue reduced although the pain came back but less frequently. I also got severe cognitive fogginess si then working or having a life became impossible.

Don't joke about ms, it's a horrific disease.