BryanF

Your Replies

  • February 23, 2017 at 7:28 pm

    One must distinguish between fatigue and relapse. Fatigue is normal, but it is not persistent. Weakness caused by demyelination will persist and progress. It is important not to overexert yourself during recovery. Cycles of exercize and rest are good but one should not work to the point of exhaustion.

    That’s a great way to put it. So far, I’ve been getting a bit more endurance each day, though in the back of mind, I’m acutely vigilant to make sure the demyelination process isn’t coming back. Thanks for you insight.

    February 22, 2017 at 9:53 pm

    Thank you Amanda. Hope things turn around for you.

    February 22, 2017 at 9:52 pm

    has he had a lumbar puncture? That’s sure way to diagnose CIDP.

    February 22, 2017 at 9:50 pm

    Its interesting how different neurologist treat CIDP. My course was prednisone, but I got worse. The doc sent me to hospital where I received 5 days of IVIG treatment which turned things around, all the while still taking 60mg of prednisone. Since my release, on January 6th, I’ve been on 40mg of prednisone, which will last at that dose for 2 more months, at which time he said we would taper it down over the course of 2 more additional months. I haven’t had IVIG since, though he said if things turn south, it would be used to once again turn things around.

    Not sure what to expect in long term healing. My chiropractor said I complained of numbness in hands and feet beginning mid-August(but I had been feeling fatigued, with back pain for months earlier). By mid-September I wasn’t better and said go see my GP. He did blood tests which showed a crashed B-12 level. Low B-12 can cause numb hands and feet. 3 weeks later, another blood test, B-12 levels were back to normal, but my neuropathy was worse. Finally late October he sent to the neurologist. A week of tests were negative and by then it was early/mid November when I had a lumbar puncture which confirmed CIDP. So he put me on 60mg of predisone and said give it a month to improve. Unfortunately I got worse.

    So the question is, how much irreversible damage was done in that period? He’s hopeful its minimal, but also cautioned that myelin repair only progresses at 1mm a day. Haven’t measured my legs, but that has to translate into 4-5-6-7 months!

    I tried Gabapentin and was taking it up to last week, but it does absolutely nothing for me. I asked for some type of pain pill, but he doesn’t want to go the route. I’d sure like to! : ) I finish physical therapy next week and plan on taking the hospital up on a 60 day free membership for their gym.

    If you’d like to get in touch, its ncc1701a “at” fuse.net

    February 22, 2017 at 12:10 pm

    I just put in full first week at work after being off for 7 weeks. I guess I hadn’t realized how deeply CIDP had atrophied my muscles from my knees on down. I’m worn out after standing all day. Plus, the neuropathy hasn’t healed yet in my feet, so they are stiff at the end of my shift as well.

    From reading the various accounts from our fellow suffers, it just seems everyone heals at different rates and my neurologist last Friday, after (can’t remember the name of it) the electrical test, that it might be another 60 days or more before we find out the true extent of what heals.

    I’m happy to be walking unaided, but I definitely want to heal a lot more than this. Then again, some of my weakness I’m putting towards the high does of steroids on still on for at least the next couple of months. It still throws me for a loop each day. And like the CIDP effects, the steroid side effects are new and different each and every day! : )

    So I think, if others are like me, you wonder a bit, when your pains and symptoms change, “Is the CIDP coming back?” or am I just tired?

    I’m always interested in seeing how others feel, how they react to exertion.

    February 21, 2017 at 4:49 pm

    Have you tried other treatments for CIDP beside CIDP? Maybe a different immune suppression drug or another treatment besides IVIG?

    I hope things turn around for you. I remember not being able to lift my legs to negotiate a curb from December and thought what is happening to me. That you’ve recovered and relapsed must be difficult.

    I’d definitely have a heart to heart with your neurologist and look into different treatments that might break the cycle you find yourself in.

    February 12, 2017 at 7:53 pm

    Wow, just read your blog. What a story and ordeal you went through. How are you doing now?

    February 11, 2017 at 12:51 pm

    51, male, white

    February 10, 2017 at 1:08 pm

    I wrote a pretty long summary of my symptoms and road to recovery here: https://forum.gbs-cidp.org/topic/cidp-progess-and-retrosepction-long/

    February 9, 2017 at 7:57 pm

    I don’t have any photos to share, but you are welcome to share my post and give me link to your blog when posted. You can email me at ncc1701@ “at” fuse.net

    Bryan

    February 5, 2017 at 1:44 pm

    I lost taste for about 3 months with onset of CIDP symptoms. Slowly came back this month after IVIG treatments.

    February 3, 2017 at 9:08 am

    Thanks for the responses. I’ll have talk with my neurologist

    January 30, 2017 at 10:47 am

    My CIDP made me short of breath upon exertion. Has gotten better. But I’m still winded more easily than I was before I got sick.

    January 30, 2017 at 10:08 am

    I just got one hour of sleep tonight. Miserable.

    January 30, 2017 at 10:06 am

    Can I ask the cost of the maintenance IVIg with or without insurance for you?