Progress - GBS Miller Fisher Syndrome (65 days since diagnosis)

Just a quick update. 2 months or so back I was fully paralyzed, swallow, vision impacted, couldn’t even hold my phone. Doctors and therapists were trying to get me into long term nurse care, and at one point measuring me for a customized wheelchair as they said I wouldn’t walk for 6 month if not longer…. Fast forward to 2 months later I can lightly jog and even run drill. Mind you, the pain on my hands and feet are still terrifying, learning to live with it though and my face has some ways to go. I’m still not able to fully smile, and still ongoing speech therapy to help. Hope this helps anyone in here with their journey! I’ll continue to always pray for those impacted by this. Stay strong!