I care very much…
Linda,
Don’t ever doubt how much the people on this forum care about how you feel. We can understand so much better than the neurologists how you actually feel. I got up at 11:00 & feel like I need a nap already; this has been my life for the past 5 1/2 years. No one can understand this fatigue unless you have been through it. My husband tries very hard, but I know he can’t really feel what I feel. Not to mention all of the pain, it can be so overwhelming…
About your treatment, I have read other posts by you & personally feel that methotrexate is probably not helping you. Listen to your own body & if it not helping you by now, it probably won’t. I also don’t believe that this is your last resort. Besides, I think that drug is mostly for RA, not CIDP. If you ever want to talk just email your phone number & I can call you. I had/have a very severe case of CIDP & ran the gamut of all of the treatments out there.
Blessings, Pam