I am back for another round of ivig this morning 14th march.
My dr told me at the end of the last lot we are going to extend my treatment to every 8 weeks, from every 6 weeks.
So I agreed and away we went… well this is week 7… good heavens I’m bad. Very weak and wobbly. Feet, which are my main issue, are super numb and painful. My hands, which are normally ok, are terrible can’t feel my left at all. They are also very weak and have dropped a lot!!!
Oh well hopefully all will go with no issues and help ease things a bit.
Doesn’t sound good…I have CIDP-MGUS and IVIG didn’t help. I take 800mg of gabapentin and it controls the pain to a tolerable limit. Pray you will get some relief
My doctor suggested extending my IVIG from four weekly to six weekly “to see what happens”. I said, “let’s not!” I know I get worse the closer I get to the infusion date, and was not interested in making it longer.
I’ve found the titration rate significantly affects whether I’ll wind up with a headache. The nurses are now all over this, and all is okay (well … as okay as it can be).
This winter was particularly cold, we had 26 days below -20 (degrees Celsius that is, so -4 Fahrenheit). You would think after that cold ten degrees would feel like shorts weather!
Thanks CanadianGirl for the feedback.
It can be pretty hard at times when you feel that no one understands and
even the GP has to continually look up CIDP.