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GBS-chance of recurrence - GBS|CIDP Foundation International Forums I had GBS – Miller Fisher Variant in 1997 when I was a teenager, we don’t know what caused my GBS it was either infection or vaccine since both happened at that time Would it still be very rare to get GBS a second time around with this medicine, or would I be “playing with fire” in this case?
Axonal Guillan Barre (AMAN) - GBS\|CIDP Hello! I’m reaching out to the few of us that have been diagnosed with the AMAN form of Guillan Barre (Acute Axonal Motor Neuropathy ) I say the “few of us” because from what I know, we are the exceedingly rare form of Guillan Barre… perhaps 3,000 cases world-wide and most of them are in Asia The viral nervous system damage we suffered is due to an attack on our actual nerves (axons
Effects of GBS over 2 years later Hello, I had GBS and was hospitalized for two weeks in August of 2015 Recovery took a long time Now, 2 years and 4 months later, I have concerns that I can’t find a concrete answer on I still experience muscle soreness and pain, in my knees and down to my feet, and in my forearms and hands At times, my hands can be very shaky, especially in my fingers Also when doing physical things
Average time for full recovery? - GBS\|CIDP So anything is possible There may be an average period of recovery of the motor nerves for GBS sufferers which is less than 2 years, but for muscle recovery, I think that the average recovery for those who had severe GBS, the average recovery period must be several years
For those who get regular IVIG infusions, how often do you . . . - GBS\|CIDP Just out of curiosity, for those who get regular IVIG treatments for their CIDP, how often do you get them? Once a week, once a month? Do you feel that such a maintenance keeps symptom free or something close to it? Thanks, Bryan
Cold weather and muscle weakness - GBS\|CIDP Has anyone had the experience that their muscle weakness increases as the weather gets colder? We are having an early cold snap and I seem to be weaker than normal This seems to be effecting my balance as well Any suggestions
Flare Up at 6 months post GBS diagnosis - GBS\|CIDP I was admitted on October 6, 2016 with advanced GBS I spent 4 weeks in ICU on a ventilator receiving IVIG during that time and then an additional 4 weeks in rehabilitation hospitals before returning home for outpatient therapy The 6th of April was 6 months since I was admitted About 4 days ago (April 11) I started to struggle with tingling in my feet again It has since spread up to my
Your top signs that your CIDP is coming back getting worse Here is the order for myself: 1) Numbness in the fingertips (both hands but right hand worse) and then numbness in my left foot (right foot has zero problems) 2) Problems walking up stairs and getting up from chair, bed etc 3) Loss of strength in my hands (again right hand much worse than left)