Hello ladies. Thank you for sharing your story. I can relate to Jennifer. I was diagnosed with MMN back in 2017. I was originally diagnosed with ALS, but after a barrage of diagnostics (including the EMG/Nerve Conduction testing) I was finally diagnosed with MMN. My disease affects both of my hands pretty severely and my feet, to a lesser extent. I have been receiving IVIG for two consecutive days every 28 days and it has helped, though I feel like I’ve plateaued with any progress for the last couple of years. Best wishes to you, Jennifer. It’s so comforting to hear someone else who is going through this journey since there aren’t many of us. ❤😊
My symptoms are exactly like Jennifers. I just went to the Facebook page. And I had the most stress in my life before this started. So much stress that I thought for sure I would have a heart attack.
Glad I found y’all
Thanks for sharing yr story
Multifocal Motor Neuropathy has changed my life.
Hello ladies. Thank you for sharing your story. I can relate to Jennifer. I was diagnosed with MMN back in 2017. I was originally diagnosed with ALS, but after a barrage of diagnostics (including the EMG/Nerve Conduction testing) I was finally diagnosed with MMN. My disease affects both of my hands pretty severely and my feet, to a lesser extent. I have been receiving IVIG for two consecutive days every 28 days and it has helped, though I feel like I’ve plateaued with any progress for the last couple of years. Best wishes to you, Jennifer. It’s so comforting to hear someone else who is going through this journey since there aren’t many of us. ❤😊
My symptoms are exactly like Jennifers. I just went to the Facebook page. And I had the most stress in my life before this started. So much stress that I thought for sure I would have a heart attack.
😢
How do I find Jennifer on Facebook MMN support groupm
Here: MMN Multifocal Motor Neuropathy WARRIORS